TY  - JOUR
AU  - Labus, Nebojsa
AU  - Krstić, Jugoslav
AU  - Matijašević, Srđan
AU  - Pavlović, Vladimir
PY  - 2023
UR  - https://dais.sanu.ac.rs/123456789/15141
AB  - Powder mixture consisted of ZnO, Mn2O3 (MnCO3) and Fe2O3 blended powders, was found laminating during compaction. Polyvinyl alcohol (PVA) and a combination of PVA with polyethylene glycol (PEG) added as a plasticizer, were introduced as polymer binders to improve the compaction of oxide mixtures. It has been done by forming a suspension of oxide mixture and varying the polymer solution concentration and composition. By evaporating the solvent, new materials were obtained, which consist of oxide particles bound via polymer. In such a manner obtained hybrid materials were characterized with attenuated total reflection Fourier transformed infrared (ATR-FTIR) spectroscopy, differential thermal analysis (DTA) and transmission electron microscopy (TEM). The oxide polymer material was compacted at 200 MPa and the expansion of this compact during heating was monitored in temperature range up to 550ºC with dilatometer. It was found that PVA forms graft polymer with PEG and specific interaction with oxide particles surface was revealed.
AB  - Смеша прахова састављена од ZnO, Mn2O3 (MnCO3) и Fe2O3 комбинацијепрахова је показивала ламинацију током пресовања. Поливинил алкохол (PVA) икомбинација PVA са полиетилен гликолом (PEG) који је додат као пластификатор, сууведени као полимерно везиво за пресовање оксидних прахова. Везиво је уведено такошто је формирана суспензија смеше различитих оксида прахова у полимерномраствору. Концентрације полимера и састави су варирани. Уклањањем растварачадобијени су нови материјали који се састоје од честица оксида повезаних полимерима.Ови хибридни материјали окарактерисани су методама ометене тоталне рефлексијефурије трансформисане инфрацрвене спектроскопије (ATR-FTIR) као идиференцијалне термичке анализе (DTA). Микроструктура је посматранатрансмисоном електронском микроскопијом (TEM). Оксид-полимер материјали супресовани на притиску од 200 MPa и ширење испреска током грејања је праћено у температурском опсегу од собне до 550ºC употребом дилатометра. Нађено је да PVAформира графт полимер са PEG и да постоји специфична интеракција полимера саповршином честица оксида.
PB  - Belgrade : Association for ETRAN Society
T2  - Science of Sintering
T1  - Oxide Powder Mixture with Poly-vinyl Alcohol (PVA) and added Polyethylene Glycol (PEG) as Plasticizer
SP  - 189
EP  - 2023
VL  - 55
DO  - 10.2298/SOS220828005L
UR  - https://hdl.handle.net/21.15107/rcub_dais_15141
ER  - 

@article{
author = "Labus, Nebojsa and Krstić, Jugoslav and Matijašević, Srđan and Pavlović, Vladimir",
year = "2023",
abstract = "Powder mixture consisted of ZnO, Mn2O3 (MnCO3) and Fe2O3 blended powders, was found laminating during compaction. Polyvinyl alcohol (PVA) and a combination of PVA with polyethylene glycol (PEG) added as a plasticizer, were introduced as polymer binders to improve the compaction of oxide mixtures. It has been done by forming a suspension of oxide mixture and varying the polymer solution concentration and composition. By evaporating the solvent, new materials were obtained, which consist of oxide particles bound via polymer. In such a manner obtained hybrid materials were characterized with attenuated total reflection Fourier transformed infrared (ATR-FTIR) spectroscopy, differential thermal analysis (DTA) and transmission electron microscopy (TEM). The oxide polymer material was compacted at 200 MPa and the expansion of this compact during heating was monitored in temperature range up to 550ºC with dilatometer. It was found that PVA forms graft polymer with PEG and specific interaction with oxide particles surface was revealed., Смеша прахова састављена од ZnO, Mn2O3 (MnCO3) и Fe2O3 комбинацијепрахова је показивала ламинацију током пресовања. Поливинил алкохол (PVA) икомбинација PVA са полиетилен гликолом (PEG) који је додат као пластификатор, сууведени као полимерно везиво за пресовање оксидних прахова. Везиво је уведено такошто је формирана суспензија смеше различитих оксида прахова у полимерномраствору. Концентрације полимера и састави су варирани. Уклањањем растварачадобијени су нови материјали који се састоје од честица оксида повезаних полимерима.Ови хибридни материјали окарактерисани су методама ометене тоталне рефлексијефурије трансформисане инфрацрвене спектроскопије (ATR-FTIR) као идиференцијалне термичке анализе (DTA). Микроструктура је посматранатрансмисоном електронском микроскопијом (TEM). Оксид-полимер материјали супресовани на притиску од 200 MPa и ширење испреска током грејања је праћено у температурском опсегу од собне до 550ºC употребом дилатометра. Нађено је да PVAформира графт полимер са PEG и да постоји специфична интеракција полимера саповршином честица оксида.",
publisher = "Belgrade : Association for ETRAN Society",
journal = "Science of Sintering",
title = "Oxide Powder Mixture with Poly-vinyl Alcohol (PVA) and added Polyethylene Glycol (PEG) as Plasticizer",
pages = "189-2023",
volume = "55",
doi = "10.2298/SOS220828005L",
url = "https://hdl.handle.net/21.15107/rcub_dais_15141"
}

Labus, N., Krstić, J., Matijašević, S.,& Pavlović, V.. (2023). Oxide Powder Mixture with Poly-vinyl Alcohol (PVA) and added Polyethylene Glycol (PEG) as Plasticizer. in Science of Sintering
Belgrade : Association for ETRAN Society., 55, 189-2023.
https://doi.org/10.2298/SOS220828005L
https://hdl.handle.net/21.15107/rcub_dais_15141

Labus N, Krstić J, Matijašević S, Pavlović V. Oxide Powder Mixture with Poly-vinyl Alcohol (PVA) and added Polyethylene Glycol (PEG) as Plasticizer. in Science of Sintering. 2023;55:189-2023.
doi:10.2298/SOS220828005L
https://hdl.handle.net/21.15107/rcub_dais_15141 .

Labus, Nebojsa, Krstić, Jugoslav, Matijašević, Srđan, Pavlović, Vladimir, "Oxide Powder Mixture with Poly-vinyl Alcohol (PVA) and added Polyethylene Glycol (PEG) as Plasticizer" in Science of Sintering, 55 (2023):189-2023,
https://doi.org/10.2298/SOS220828005L .,
https://hdl.handle.net/21.15107/rcub_dais_15141 .

TY  - CONF
AU  - Stefanović, Milica
AU  - Vujančević, Jelena
AU  - Petrović, Rada
AU  - Janaćković, Đorđe
PY  - 2021
UR  - https://dais.sanu.ac.rs/123456789/12075
AB  - The organo-inorganic perovskites are materials that have recently revolutionized the field of
photovoltaics due to their low-cost fabrication and high optical absorption. The hybrid organoinorganic perovskite absorbs the visible part of the spectrum resulting in the creation of electron-hole pair. To decrease the recombination of charge carriers, the construction of solar cells requires the existence of separate layers for holes and for electrons. TiO2 is usually used as an electron transport layer because its conduction band (CB) lies under the CB of perovskite. In that way, electrons diffuse from CB of perovskite to CB of TiO2. For these experiments, TiO2 nanotubular structure was used as an electron transport layer due to its advantages compared to nanoparticular TiO2. TiO2 nanotubes can provide a one-dimensional transmission channel for the charge carriers, so it will reduce the recombination rate of the carriers and provide a channel for fast carrier transport. However, there is a problem with the contact surface between perovskite and TiO2 nanotubes. The aim of this study is to increase the contact surface of perovskite and TiO2 nanotubes by filling the nanotubes with perovskite material in order to improve electron transport. Methylammonium lead bromide perovskite (MAPbBr3) was deposited on anodically synthesized TiO2 nanotubes which were annealed at 450 °C for 1 h. After degassation of the sample under high vacuum for 3 h at 200 °C, the cooled sample was put in a solution of MAPbBr3 in dimethylformamide (DMF) and it was treated with inert gas (N2), which enabled the filling of the nanotubes with perovskite material to some extent. FESEM and XRD analyses were used for morphological and chemical characterization of the sample. The diffuse reflectance spectroscopy measurement of the sample proved that deposition of MAPbBr3 improves the absorption properties of TiO2 nanotubes. By measuring the I-V characteristics of the sample in the dark and under visible light, a hysteresis curve was obtained.
PB  - Belgrade : Materials Research Society of Serbia
C3  - Programme and the Book of abstracts / Twenty-second Annual Conference YUCOMAT 2021 Herceg Novi, Montenegro, August 30 - September 3, 2021
T1  - Synthesis and deposition of MAPbBr3 perovskite on titania nanotube arrays
SP  - 111
EP  - 111
UR  - https://hdl.handle.net/21.15107/rcub_dais_12075
ER  - 

@conference{
author = "Stefanović, Milica and Vujančević, Jelena and Petrović, Rada and Janaćković, Đorđe",
year = "2021",
abstract = "The organo-inorganic perovskites are materials that have recently revolutionized the field of
photovoltaics due to their low-cost fabrication and high optical absorption. The hybrid organoinorganic perovskite absorbs the visible part of the spectrum resulting in the creation of electron-hole pair. To decrease the recombination of charge carriers, the construction of solar cells requires the existence of separate layers for holes and for electrons. TiO2 is usually used as an electron transport layer because its conduction band (CB) lies under the CB of perovskite. In that way, electrons diffuse from CB of perovskite to CB of TiO2. For these experiments, TiO2 nanotubular structure was used as an electron transport layer due to its advantages compared to nanoparticular TiO2. TiO2 nanotubes can provide a one-dimensional transmission channel for the charge carriers, so it will reduce the recombination rate of the carriers and provide a channel for fast carrier transport. However, there is a problem with the contact surface between perovskite and TiO2 nanotubes. The aim of this study is to increase the contact surface of perovskite and TiO2 nanotubes by filling the nanotubes with perovskite material in order to improve electron transport. Methylammonium lead bromide perovskite (MAPbBr3) was deposited on anodically synthesized TiO2 nanotubes which were annealed at 450 °C for 1 h. After degassation of the sample under high vacuum for 3 h at 200 °C, the cooled sample was put in a solution of MAPbBr3 in dimethylformamide (DMF) and it was treated with inert gas (N2), which enabled the filling of the nanotubes with perovskite material to some extent. FESEM and XRD analyses were used for morphological and chemical characterization of the sample. The diffuse reflectance spectroscopy measurement of the sample proved that deposition of MAPbBr3 improves the absorption properties of TiO2 nanotubes. By measuring the I-V characteristics of the sample in the dark and under visible light, a hysteresis curve was obtained.",
publisher = "Belgrade : Materials Research Society of Serbia",
journal = "Programme and the Book of abstracts / Twenty-second Annual Conference YUCOMAT 2021 Herceg Novi, Montenegro, August 30 - September 3, 2021",
title = "Synthesis and deposition of MAPbBr3 perovskite on titania nanotube arrays",
pages = "111-111",
url = "https://hdl.handle.net/21.15107/rcub_dais_12075"
}

Stefanović, M., Vujančević, J., Petrović, R.,& Janaćković, Đ.. (2021). Synthesis and deposition of MAPbBr3 perovskite on titania nanotube arrays. in Programme and the Book of abstracts / Twenty-second Annual Conference YUCOMAT 2021 Herceg Novi, Montenegro, August 30 - September 3, 2021
Belgrade : Materials Research Society of Serbia., 111-111.
https://hdl.handle.net/21.15107/rcub_dais_12075

Stefanović M, Vujančević J, Petrović R, Janaćković Đ. Synthesis and deposition of MAPbBr3 perovskite on titania nanotube arrays. in Programme and the Book of abstracts / Twenty-second Annual Conference YUCOMAT 2021 Herceg Novi, Montenegro, August 30 - September 3, 2021. 2021;:111-111.
https://hdl.handle.net/21.15107/rcub_dais_12075 .

Stefanović, Milica, Vujančević, Jelena, Petrović, Rada, Janaćković, Đorđe, "Synthesis and deposition of MAPbBr3 perovskite on titania nanotube arrays" in Programme and the Book of abstracts / Twenty-second Annual Conference YUCOMAT 2021 Herceg Novi, Montenegro, August 30 - September 3, 2021 (2021):111-111,
https://hdl.handle.net/21.15107/rcub_dais_12075 .

TY  - JOUR
AU  - Obradović, Nina
AU  - Fahrenholtz, William G.
AU  - Filipović, Suzana
AU  - Marković, Smilja
AU  - Blagojević, Vladimir A.
AU  - Lević, Steva
AU  - Savić, Slobodan
AU  - Đorđević, Antonije
AU  - Pavlović, Vladimir B.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/10027
AB  - Solid-state mechanical activation of MgO and α-Al2O3 powders was used to produce MgAl2O4. The cation site occupancy in the resulting MgAl2O4 spinel was investigated using different methods. Differential thermal analysis and thermal gravimetry showed that mechanical activation reduced the spinel formation temperature by around 200 °C, and the corresponding activation energy by about 25%. In addition, characteristic temperatures for evaporation of physisorbed water and decomposition of Mg(OH)2 shifted to lower values, and peaks were more pronounced. Raman spectra were used to characterize the degree of inversion as a function of the sintering temperature for all of the sintered specimens, indicating that the breaking point for ordering of the crystal structure was around 1500 °C for non-activated samples, and 1400 °C for activated samples.
PB  - Springer
T2  - Journal of Thermal Analysis and Calorimetry
T1  - Formation kinetics and cation inversion in mechanically activated MgAl2O4 spinel ceramics
SP  - 95
EP  - 107
VL  - 140
DO  - 10.1007/s10973-019-08846-w
UR  - https://hdl.handle.net/21.15107/rcub_dais_10027
ER  - 

@article{
author = "Obradović, Nina and Fahrenholtz, William G. and Filipović, Suzana and Marković, Smilja and Blagojević, Vladimir A. and Lević, Steva and Savić, Slobodan and Đorđević, Antonije and Pavlović, Vladimir B.",
year = "2020",
abstract = "Solid-state mechanical activation of MgO and α-Al2O3 powders was used to produce MgAl2O4. The cation site occupancy in the resulting MgAl2O4 spinel was investigated using different methods. Differential thermal analysis and thermal gravimetry showed that mechanical activation reduced the spinel formation temperature by around 200 °C, and the corresponding activation energy by about 25%. In addition, characteristic temperatures for evaporation of physisorbed water and decomposition of Mg(OH)2 shifted to lower values, and peaks were more pronounced. Raman spectra were used to characterize the degree of inversion as a function of the sintering temperature for all of the sintered specimens, indicating that the breaking point for ordering of the crystal structure was around 1500 °C for non-activated samples, and 1400 °C for activated samples.",
publisher = "Springer",
journal = "Journal of Thermal Analysis and Calorimetry",
title = "Formation kinetics and cation inversion in mechanically activated MgAl2O4 spinel ceramics",
pages = "95-107",
volume = "140",
doi = "10.1007/s10973-019-08846-w",
url = "https://hdl.handle.net/21.15107/rcub_dais_10027"
}

Obradović, N., Fahrenholtz, W. G., Filipović, S., Marković, S., Blagojević, V. A., Lević, S., Savić, S., Đorđević, A.,& Pavlović, V. B.. (2020). Formation kinetics and cation inversion in mechanically activated MgAl2O4 spinel ceramics. in Journal of Thermal Analysis and Calorimetry
Springer., 140, 95-107.
https://doi.org/10.1007/s10973-019-08846-w
https://hdl.handle.net/21.15107/rcub_dais_10027

Obradović N, Fahrenholtz WG, Filipović S, Marković S, Blagojević VA, Lević S, Savić S, Đorđević A, Pavlović VB. Formation kinetics and cation inversion in mechanically activated MgAl2O4 spinel ceramics. in Journal of Thermal Analysis and Calorimetry. 2020;140:95-107.
doi:10.1007/s10973-019-08846-w
https://hdl.handle.net/21.15107/rcub_dais_10027 .

Obradović, Nina, Fahrenholtz, William G., Filipović, Suzana, Marković, Smilja, Blagojević, Vladimir A., Lević, Steva, Savić, Slobodan, Đorđević, Antonije, Pavlović, Vladimir B., "Formation kinetics and cation inversion in mechanically activated MgAl2O4 spinel ceramics" in Journal of Thermal Analysis and Calorimetry, 140 (2020):95-107,
https://doi.org/10.1007/s10973-019-08846-w .,
https://hdl.handle.net/21.15107/rcub_dais_10027 .

TY  - JOUR
AU  - Mitić, Vojislav V.
AU  - Lazović, Goran
AU  - Lu, Chun-An
AU  - Paunović, Vesna
AU  - Radović, Ivana
AU  - Stajčić, Aleksandar
AU  - Vlahović, Branislav
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/8957
AB  - The BaTiO3 ceramics applications based on electronic properties have very high gradient scientific and industrial-technological interests. Our scientific research has been based on nano BaTiO3 modified with Yttrium based organometallic salt (MOD-Y). The samples have been consolidated at a sintering temperature of 1350 °C. Within the study, the new frontiers for different electronic properties between the layers of BaTiO3 grains have been introduced. The research target was grain boundary investigations and the influence on dielectric properties. After scanning electron microscopy and dielectric measurements, it has been established that modified BaTiO3 samples with larger grains showed a better compact state that led to a higher dielectric constant value. DC bias stability was also investigated and showed a connection between the grain size and capacitance stability. Analyses of functions that could approximate experimental curves were successfully employed. Practical application of fractal corrections was performed, based on surface (αs) and pore size (αp) corrections, which resulted in obtainment of the relation between the capacitance and Curie temperature. Successful introduction of fractal corrections for capacitance-Curie temperature dependence for a set of experimental data is an important step towards further miniaturization of intergranular capacitors. © 2020 by the authors.
PB  - Basel : MDPI
T2  - Applied Sciences (Switzerland)
T1  - The Nano-Scale Modified BaTiO3 Morphology Influence on Electronic Properties and Ceramics Fractal Nature Frontiers
SP  - 3485
VL  - 10
IS  - 10
DO  - 10.3390/app10103485
UR  - https://hdl.handle.net/21.15107/rcub_dais_8957
ER  - 

@article{
author = "Mitić, Vojislav V. and Lazović, Goran and Lu, Chun-An and Paunović, Vesna and Radović, Ivana and Stajčić, Aleksandar and Vlahović, Branislav",
year = "2020",
abstract = "The BaTiO3 ceramics applications based on electronic properties have very high gradient scientific and industrial-technological interests. Our scientific research has been based on nano BaTiO3 modified with Yttrium based organometallic salt (MOD-Y). The samples have been consolidated at a sintering temperature of 1350 °C. Within the study, the new frontiers for different electronic properties between the layers of BaTiO3 grains have been introduced. The research target was grain boundary investigations and the influence on dielectric properties. After scanning electron microscopy and dielectric measurements, it has been established that modified BaTiO3 samples with larger grains showed a better compact state that led to a higher dielectric constant value. DC bias stability was also investigated and showed a connection between the grain size and capacitance stability. Analyses of functions that could approximate experimental curves were successfully employed. Practical application of fractal corrections was performed, based on surface (αs) and pore size (αp) corrections, which resulted in obtainment of the relation between the capacitance and Curie temperature. Successful introduction of fractal corrections for capacitance-Curie temperature dependence for a set of experimental data is an important step towards further miniaturization of intergranular capacitors. © 2020 by the authors.",
publisher = "Basel : MDPI",
journal = "Applied Sciences (Switzerland)",
title = "The Nano-Scale Modified BaTiO3 Morphology Influence on Electronic Properties and Ceramics Fractal Nature Frontiers",
pages = "3485",
volume = "10",
number = "10",
doi = "10.3390/app10103485",
url = "https://hdl.handle.net/21.15107/rcub_dais_8957"
}

Mitić, V. V., Lazović, G., Lu, C., Paunović, V., Radović, I., Stajčić, A.,& Vlahović, B.. (2020). The Nano-Scale Modified BaTiO3 Morphology Influence on Electronic Properties and Ceramics Fractal Nature Frontiers. in Applied Sciences (Switzerland)
Basel : MDPI., 10(10), 3485.
https://doi.org/10.3390/app10103485
https://hdl.handle.net/21.15107/rcub_dais_8957

Mitić VV, Lazović G, Lu C, Paunović V, Radović I, Stajčić A, Vlahović B. The Nano-Scale Modified BaTiO3 Morphology Influence on Electronic Properties and Ceramics Fractal Nature Frontiers. in Applied Sciences (Switzerland). 2020;10(10):3485.
doi:10.3390/app10103485
https://hdl.handle.net/21.15107/rcub_dais_8957 .

Mitić, Vojislav V., Lazović, Goran, Lu, Chun-An, Paunović, Vesna, Radović, Ivana, Stajčić, Aleksandar, Vlahović, Branislav, "The Nano-Scale Modified BaTiO3 Morphology Influence on Electronic Properties and Ceramics Fractal Nature Frontiers" in Applied Sciences (Switzerland), 10, no. 10 (2020):3485,
https://doi.org/10.3390/app10103485 .,
https://hdl.handle.net/21.15107/rcub_dais_8957 .

TY  - JOUR
AU  - Paunović, Vesna
AU  - Mitić, Vojislav V.
AU  - Đorđević, M.
AU  - Prijić, Z.
PY  - 2020
UR  - http://www.sciencedirect.com/science/article/pii/S0272884219335205
UR  - https://dais.sanu.ac.rs/123456789/8964
AB  - The effect of Nb on the microstructure and dielectric properties of BaTiO3 ceramics was investigated. The Nb/Mn–BaTiO3 ceramics were prepared using a conventional solid-state method. The concentration of Nb varied from 0.1 to 5.0 at% but Mn was fixed at 0.05 at%. The SEM indicated that compositions of 0.1 and 0.5 at% Nb displayed a fairly uniform microstructure and homogeneous distribution of additives, with a grain size of less than 2 μm. In highly doped samples a wide range of microstructural features was observed, from homogeneous and completely fine-grained microstructure to the appearance of secondary abnormal grains with core-shell structure. The dielectric constant and the loss tangent of modified ceramics were measured as a function of temperature (20–180 °C) and frequency (100 Hz-1MHz) for different concentrations of additives. The obtained results have shown that the dielectric constant at, both, room temperature (εr) and Curie temperature (εrmax), decreased as the concentration of Nb5+ increased. Thus, the highest values for the dielectric constant at room temperature (εr = 6648) as well as at Curie temperature (εrmax = 7680) were measured for the 0.1Nb/Mn–BaTiO3 samples sintered at 1350 °C. The highly doped BaTiO3 ceramics were found to exhibit lower values of the dielectric constant and low dielectric losses at room temperature. In these samples, stable dielectric permittivity with a flat dielectric behavior over a wide temperature range is observed. The Curie constant for all series of samples decreases with an increase of dopant concentration and the highest values were measured from samples doped with 0.1 at% Nb. The effect of additives on the Curie constant change is more pronounced at higher sintering temperatures. The analysis of the critical nonlinearity exponent (γ = 1.07–1.27), for lower dopant concentrations, shows a sharp phase transformation. For samples with increased Nb content, the degree of nonlinearity γ is higher indicating a diffuse phase transformation.
PB  - Elsevier
T2  - Ceramics International
T1  - Niobium doping effect on BaTiO3 structure and dielectric properties
SP  - 8154
EP  - 8164
VL  - 46
IS  - 6
DO  - 10.1016/j.ceramint.2019.12.043
UR  - https://hdl.handle.net/21.15107/rcub_dais_8964
ER  - 

@article{
author = "Paunović, Vesna and Mitić, Vojislav V. and Đorđević, M. and Prijić, Z.",
year = "2020",
abstract = "The effect of Nb on the microstructure and dielectric properties of BaTiO3 ceramics was investigated. The Nb/Mn–BaTiO3 ceramics were prepared using a conventional solid-state method. The concentration of Nb varied from 0.1 to 5.0 at% but Mn was fixed at 0.05 at%. The SEM indicated that compositions of 0.1 and 0.5 at% Nb displayed a fairly uniform microstructure and homogeneous distribution of additives, with a grain size of less than 2 μm. In highly doped samples a wide range of microstructural features was observed, from homogeneous and completely fine-grained microstructure to the appearance of secondary abnormal grains with core-shell structure. The dielectric constant and the loss tangent of modified ceramics were measured as a function of temperature (20–180 °C) and frequency (100 Hz-1MHz) for different concentrations of additives. The obtained results have shown that the dielectric constant at, both, room temperature (εr) and Curie temperature (εrmax), decreased as the concentration of Nb5+ increased. Thus, the highest values for the dielectric constant at room temperature (εr = 6648) as well as at Curie temperature (εrmax = 7680) were measured for the 0.1Nb/Mn–BaTiO3 samples sintered at 1350 °C. The highly doped BaTiO3 ceramics were found to exhibit lower values of the dielectric constant and low dielectric losses at room temperature. In these samples, stable dielectric permittivity with a flat dielectric behavior over a wide temperature range is observed. The Curie constant for all series of samples decreases with an increase of dopant concentration and the highest values were measured from samples doped with 0.1 at% Nb. The effect of additives on the Curie constant change is more pronounced at higher sintering temperatures. The analysis of the critical nonlinearity exponent (γ = 1.07–1.27), for lower dopant concentrations, shows a sharp phase transformation. For samples with increased Nb content, the degree of nonlinearity γ is higher indicating a diffuse phase transformation.",
publisher = "Elsevier",
journal = "Ceramics International",
title = "Niobium doping effect on BaTiO3 structure and dielectric properties",
pages = "8154-8164",
volume = "46",
number = "6",
doi = "10.1016/j.ceramint.2019.12.043",
url = "https://hdl.handle.net/21.15107/rcub_dais_8964"
}

Paunović, V., Mitić, V. V., Đorđević, M.,& Prijić, Z.. (2020). Niobium doping effect on BaTiO3 structure and dielectric properties. in Ceramics International
Elsevier., 46(6), 8154-8164.
https://doi.org/10.1016/j.ceramint.2019.12.043
https://hdl.handle.net/21.15107/rcub_dais_8964

Paunović V, Mitić VV, Đorđević M, Prijić Z. Niobium doping effect on BaTiO3 structure and dielectric properties. in Ceramics International. 2020;46(6):8154-8164.
doi:10.1016/j.ceramint.2019.12.043
https://hdl.handle.net/21.15107/rcub_dais_8964 .

Paunović, Vesna, Mitić, Vojislav V., Đorđević, M., Prijić, Z., "Niobium doping effect on BaTiO3 structure and dielectric properties" in Ceramics International, 46, no. 6 (2020):8154-8164,
https://doi.org/10.1016/j.ceramint.2019.12.043 .,
https://hdl.handle.net/21.15107/rcub_dais_8964 .

TY  - JOUR
AU  - Veljković, Sandra
AU  - Mitić, Vojislav V.
AU  - Paunović, Vesna
AU  - Lazović, Goran
AU  - Mohr, Marcus
AU  - Fecht, Hans
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/10046
AB  - There is a progressing interests for polycrystalline diamonds and they have been more extensively used recently. This area has been intensively researched due to the outstanding potential of this material, and this necessitated presenting some of the latest application related to engineering in this paper. A better insight of polycrystalline diamonds properties can be achieved by intensively researching the surface structure. Samples of nanocrystalline diamonds grown by the chemical vapor deposition method are analyzed and accordingly, the focus of the research was the surface parameters and their structure. It is observed that waviness and texture are unique for any direction, their values are almost the same for the chosen directions and they vary approximately from -0.2 nm to 0.4 nm. Analyses of the parameters allowed a more detailed insight into the morphology of the surfaces of polycrystalline films.
PB  - Čačak : University of Kragujevac, Faculty of Technical Sciences
T2  - Serbian Journal of Electrical Engineering
T1  - Analyses of the surface parameters in polycrystalline diamonds
SP  - 111
EP  - 129
VL  - 17
IS  - 1
DO  - 10.2298/SJEE2001111V
UR  - https://hdl.handle.net/21.15107/rcub_dais_10046
ER  - 

@article{
author = "Veljković, Sandra and Mitić, Vojislav V. and Paunović, Vesna and Lazović, Goran and Mohr, Marcus and Fecht, Hans",
year = "2020",
abstract = "There is a progressing interests for polycrystalline diamonds and they have been more extensively used recently. This area has been intensively researched due to the outstanding potential of this material, and this necessitated presenting some of the latest application related to engineering in this paper. A better insight of polycrystalline diamonds properties can be achieved by intensively researching the surface structure. Samples of nanocrystalline diamonds grown by the chemical vapor deposition method are analyzed and accordingly, the focus of the research was the surface parameters and their structure. It is observed that waviness and texture are unique for any direction, their values are almost the same for the chosen directions and they vary approximately from -0.2 nm to 0.4 nm. Analyses of the parameters allowed a more detailed insight into the morphology of the surfaces of polycrystalline films.",
publisher = "Čačak : University of Kragujevac, Faculty of Technical Sciences",
journal = "Serbian Journal of Electrical Engineering",
title = "Analyses of the surface parameters in polycrystalline diamonds",
pages = "111-129",
volume = "17",
number = "1",
doi = "10.2298/SJEE2001111V",
url = "https://hdl.handle.net/21.15107/rcub_dais_10046"
}

Veljković, S., Mitić, V. V., Paunović, V., Lazović, G., Mohr, M.,& Fecht, H.. (2020). Analyses of the surface parameters in polycrystalline diamonds. in Serbian Journal of Electrical Engineering
Čačak : University of Kragujevac, Faculty of Technical Sciences., 17(1), 111-129.
https://doi.org/10.2298/SJEE2001111V
https://hdl.handle.net/21.15107/rcub_dais_10046

Veljković S, Mitić VV, Paunović V, Lazović G, Mohr M, Fecht H. Analyses of the surface parameters in polycrystalline diamonds. in Serbian Journal of Electrical Engineering. 2020;17(1):111-129.
doi:10.2298/SJEE2001111V
https://hdl.handle.net/21.15107/rcub_dais_10046 .

Veljković, Sandra, Mitić, Vojislav V., Paunović, Vesna, Lazović, Goran, Mohr, Marcus, Fecht, Hans, "Analyses of the surface parameters in polycrystalline diamonds" in Serbian Journal of Electrical Engineering, 17, no. 1 (2020):111-129,
https://doi.org/10.2298/SJEE2001111V .,
https://hdl.handle.net/21.15107/rcub_dais_10046 .

TY  - JOUR
AU  - Spasojević, Milica
AU  - Ribić Zelenović, Lenka
AU  - Spasojević, Miroslav
AU  - Trišović, Tomislav
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/10033
AB  - A catalytic coating composed of a mixture of RuO2 and Pt nanocrystals was prepared by a thermal procedure on a titanium substrate and used for the electrochemical oxidation of methanol. The adsorption of the intermediate CO, formed by methanol oxidation on Pt nanocrystals, depended on potential and the coating composition. An increase in the RuO2 content decreased the rate of methanol dehydrogenation and increased the rate of oxidation of the strongly bound intermediate COad. This caused a decrease in the maximum coverage of Pt nanocrystals with COad and a shift of the rapid linear drop in COad coverage to more negative potentials.
PB  - Editura Academiei Romane
T2  - Revue Roumaine de Chimie
T1  - The effect of the composition of the alloy of RuO2 and Pt nanocrystals on intermediate adsorption during methanol oxidation
SP  - 481
EP  - 489
VL  - 65
IS  - 5
DO  - 10.33224/rrch.2020.65.5.08
UR  - https://hdl.handle.net/21.15107/rcub_dais_10033
ER  - 

@article{
author = "Spasojević, Milica and Ribić Zelenović, Lenka and Spasojević, Miroslav and Trišović, Tomislav",
year = "2020",
abstract = "A catalytic coating composed of a mixture of RuO2 and Pt nanocrystals was prepared by a thermal procedure on a titanium substrate and used for the electrochemical oxidation of methanol. The adsorption of the intermediate CO, formed by methanol oxidation on Pt nanocrystals, depended on potential and the coating composition. An increase in the RuO2 content decreased the rate of methanol dehydrogenation and increased the rate of oxidation of the strongly bound intermediate COad. This caused a decrease in the maximum coverage of Pt nanocrystals with COad and a shift of the rapid linear drop in COad coverage to more negative potentials.",
publisher = "Editura Academiei Romane",
journal = "Revue Roumaine de Chimie",
title = "The effect of the composition of the alloy of RuO2 and Pt nanocrystals on intermediate adsorption during methanol oxidation",
pages = "481-489",
volume = "65",
number = "5",
doi = "10.33224/rrch.2020.65.5.08",
url = "https://hdl.handle.net/21.15107/rcub_dais_10033"
}

Spasojević, M., Ribić Zelenović, L., Spasojević, M.,& Trišović, T.. (2020). The effect of the composition of the alloy of RuO2 and Pt nanocrystals on intermediate adsorption during methanol oxidation. in Revue Roumaine de Chimie
Editura Academiei Romane., 65(5), 481-489.
https://doi.org/10.33224/rrch.2020.65.5.08
https://hdl.handle.net/21.15107/rcub_dais_10033

Spasojević M, Ribić Zelenović L, Spasojević M, Trišović T. The effect of the composition of the alloy of RuO2 and Pt nanocrystals on intermediate adsorption during methanol oxidation. in Revue Roumaine de Chimie. 2020;65(5):481-489.
doi:10.33224/rrch.2020.65.5.08
https://hdl.handle.net/21.15107/rcub_dais_10033 .

Spasojević, Milica, Ribić Zelenović, Lenka, Spasojević, Miroslav, Trišović, Tomislav, "The effect of the composition of the alloy of RuO2 and Pt nanocrystals on intermediate adsorption during methanol oxidation" in Revue Roumaine de Chimie, 65, no. 5 (2020):481-489,
https://doi.org/10.33224/rrch.2020.65.5.08 .,
https://hdl.handle.net/21.15107/rcub_dais_10033 .

TY  - JOUR
AU  - Spasojević, Miroslav
AU  - Ranđić, Siniša
AU  - Maričić, Aleksa
AU  - Trišović, Tomislav
AU  - Spasojević, Milica
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/9451
AB  - Nanostructured Ni-Fe-W-Cu alloy powders were electrodeposited from an alkaline ammonium citrate solution on a titanium cathode. Powder particles were dendrite- and cauliflower-shaped. The dendritic particles had a high density of branches made up of interconnected globules. XRD analysis showed that the powder contained an amorphous matrix and FCC nanocrystals of the solid solution of Fe, W and Cu in Ni. As the deposition current density increased, the mean nanocrystal size decreased, and the mean value of internal microstrain and the total weight percent of Fe and Ni in the alloy increased. The powders deposited at higher current densities exhibited higher magnetization. During annealing at temperatures up to 460 °C, the powders underwent short-range ordering, which caused an increase in magnetization, whereas at temperatures above 460 °C, the magnetization decreased due to the formation of large FCC crystalline grains.
PB  - Springer
T2  - Science of Sintering
T1  - Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders
SP  - 109
EP  - 121
VL  - 52
IS  - 1
DO  - 10.2298/SOS2001109S
UR  - https://hdl.handle.net/21.15107/rcub_dais_9451
ER  - 

@article{
author = "Spasojević, Miroslav and Ranđić, Siniša and Maričić, Aleksa and Trišović, Tomislav and Spasojević, Milica",
year = "2020",
abstract = "Nanostructured Ni-Fe-W-Cu alloy powders were electrodeposited from an alkaline ammonium citrate solution on a titanium cathode. Powder particles were dendrite- and cauliflower-shaped. The dendritic particles had a high density of branches made up of interconnected globules. XRD analysis showed that the powder contained an amorphous matrix and FCC nanocrystals of the solid solution of Fe, W and Cu in Ni. As the deposition current density increased, the mean nanocrystal size decreased, and the mean value of internal microstrain and the total weight percent of Fe and Ni in the alloy increased. The powders deposited at higher current densities exhibited higher magnetization. During annealing at temperatures up to 460 °C, the powders underwent short-range ordering, which caused an increase in magnetization, whereas at temperatures above 460 °C, the magnetization decreased due to the formation of large FCC crystalline grains.",
publisher = "Springer",
journal = "Science of Sintering",
title = "Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders",
pages = "109-121",
volume = "52",
number = "1",
doi = "10.2298/SOS2001109S",
url = "https://hdl.handle.net/21.15107/rcub_dais_9451"
}

Spasojević, M., Ranđić, S., Maričić, A., Trišović, T.,& Spasojević, M.. (2020). Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders. in Science of Sintering
Springer., 52(1), 109-121.
https://doi.org/10.2298/SOS2001109S
https://hdl.handle.net/21.15107/rcub_dais_9451

Spasojević M, Ranđić S, Maričić A, Trišović T, Spasojević M. Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders. in Science of Sintering. 2020;52(1):109-121.
doi:10.2298/SOS2001109S
https://hdl.handle.net/21.15107/rcub_dais_9451 .

Spasojević, Miroslav, Ranđić, Siniša, Maričić, Aleksa, Trišović, Tomislav, Spasojević, Milica, "Morphological, microstructural and magnetic characteristics of electrodeposited Ni-Fe-W-Cu alloy powders" in Science of Sintering, 52, no. 1 (2020):109-121,
https://doi.org/10.2298/SOS2001109S .,
https://hdl.handle.net/21.15107/rcub_dais_9451 .

TY  - JOUR
AU  - Obradović, Nina
AU  - Fahrenholtz, William G.
AU  - Filipović, Suzana
AU  - Marković, Smilja
AU  - Blagojević, Vladimir A.
AU  - Lević, Steva
AU  - Savić, Slobodan
AU  - Đorđević, Antonije
AU  - Pavlović, Vladimir B.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/6910
AB  - Solid-state mechanical activation of MgO and α-Al2O3 powders was used to produce MgAl2O4. The cation site occupancy in the resulting MgAl2O4 spinel was investigated using different methods. Differential thermal analysis and thermal gravimetry showed that mechanical activation reduced the spinel formation temperature by around 200 °C, and the corresponding activation energy by about 25%. In addition, characteristic temperatures for evaporation of physisorbed water and decomposition of Mg(OH)2 shifted to lower values, and peaks were more pronounced. Raman spectra were used to characterize the degree of inversion as a function of the sintering temperature for all of the sintered specimens, indicating that the breaking point for ordering of the crystal structure was around 1500 °C for non-activated samples, and 1400 °C for activated samples.
PB  - Springer
T2  - Journal of Thermal Analysis and Calorimetry
T1  - Formation kinetics and cation inversion in mechanically activated MgAl2O4 spinel ceramics
SP  - 95
EP  - 107
VL  - 140
DO  - 10.1007/s10973-019-08846-w
UR  - https://hdl.handle.net/21.15107/rcub_dais_6910
ER  - 

@article{
author = "Obradović, Nina and Fahrenholtz, William G. and Filipović, Suzana and Marković, Smilja and Blagojević, Vladimir A. and Lević, Steva and Savić, Slobodan and Đorđević, Antonije and Pavlović, Vladimir B.",
year = "2020",
abstract = "Solid-state mechanical activation of MgO and α-Al2O3 powders was used to produce MgAl2O4. The cation site occupancy in the resulting MgAl2O4 spinel was investigated using different methods. Differential thermal analysis and thermal gravimetry showed that mechanical activation reduced the spinel formation temperature by around 200 °C, and the corresponding activation energy by about 25%. In addition, characteristic temperatures for evaporation of physisorbed water and decomposition of Mg(OH)2 shifted to lower values, and peaks were more pronounced. Raman spectra were used to characterize the degree of inversion as a function of the sintering temperature for all of the sintered specimens, indicating that the breaking point for ordering of the crystal structure was around 1500 °C for non-activated samples, and 1400 °C for activated samples.",
publisher = "Springer",
journal = "Journal of Thermal Analysis and Calorimetry",
title = "Formation kinetics and cation inversion in mechanically activated MgAl2O4 spinel ceramics",
pages = "95-107",
volume = "140",
doi = "10.1007/s10973-019-08846-w",
url = "https://hdl.handle.net/21.15107/rcub_dais_6910"
}

Obradović, N., Fahrenholtz, W. G., Filipović, S., Marković, S., Blagojević, V. A., Lević, S., Savić, S., Đorđević, A.,& Pavlović, V. B.. (2020). Formation kinetics and cation inversion in mechanically activated MgAl2O4 spinel ceramics. in Journal of Thermal Analysis and Calorimetry
Springer., 140, 95-107.
https://doi.org/10.1007/s10973-019-08846-w
https://hdl.handle.net/21.15107/rcub_dais_6910

Obradović N, Fahrenholtz WG, Filipović S, Marković S, Blagojević VA, Lević S, Savić S, Đorđević A, Pavlović VB. Formation kinetics and cation inversion in mechanically activated MgAl2O4 spinel ceramics. in Journal of Thermal Analysis and Calorimetry. 2020;140:95-107.
doi:10.1007/s10973-019-08846-w
https://hdl.handle.net/21.15107/rcub_dais_6910 .

Obradović, Nina, Fahrenholtz, William G., Filipović, Suzana, Marković, Smilja, Blagojević, Vladimir A., Lević, Steva, Savić, Slobodan, Đorđević, Antonije, Pavlović, Vladimir B., "Formation kinetics and cation inversion in mechanically activated MgAl2O4 spinel ceramics" in Journal of Thermal Analysis and Calorimetry, 140 (2020):95-107,
https://doi.org/10.1007/s10973-019-08846-w .,
https://hdl.handle.net/21.15107/rcub_dais_6910 .

TY  - JOUR
AU  - Anđelković, Ljubica
AU  - Jeremić, Dejan
AU  - Milenković, Milica R.
AU  - Radosavljević, Jelena
AU  - Vulić, Predrag
AU  - Pavlović, Vladimir B.
AU  - Manojlović, Dragan D.
AU  - Nikolić, Aleksandar S.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/6901
AB  - A simple organic-phase synthesis process was used to produce bare NiFe2O4 and ZnFe2O4 and core-shell ZnFe2O4@NiFe2O4 ferrite nanoparticles. X-ray powder diffractograms for all investigated powders show characteristic peaks of a spinel cubic structure without a secondary phase. Transmission electron microscopy (TEM) indicated the presence of nanoparticles that are smaller than 20 nm. The release of divalent ions (Ni2+ and Zn2+) from synthesized nanoparticles that were dispersed in saline solution, phosphate-buffered saline (PBS) and human serum, as determined by the inductively coupled plasma mass spectrometry (ICP-MS) method, was lower than 2 wt %. These results demonstrate the stability of the investigated nanoparticles in biologically relevant media and exclude the toxicity of Ni2+ and Zn2+ due to metal ion release, thereby opening a broad range of (bio)medical applications.
PB  - Elsevier
T2  - Ceramics International
T1  - Synthesis, characterization and in vitro evaluation of divalent ion release from stable NiFe2O4, ZnFe2O4 and core-shell ZnFe2O4@NiFe2O4 nanoparticles
SP  - 3528
EP  - 3533
VL  - 46
IS  - 3
DO  - 10.1016/j.ceramint.2019.10.068
UR  - https://hdl.handle.net/21.15107/rcub_dais_6901
ER  - 

@article{
author = "Anđelković, Ljubica and Jeremić, Dejan and Milenković, Milica R. and Radosavljević, Jelena and Vulić, Predrag and Pavlović, Vladimir B. and Manojlović, Dragan D. and Nikolić, Aleksandar S.",
year = "2020",
abstract = "A simple organic-phase synthesis process was used to produce bare NiFe2O4 and ZnFe2O4 and core-shell ZnFe2O4@NiFe2O4 ferrite nanoparticles. X-ray powder diffractograms for all investigated powders show characteristic peaks of a spinel cubic structure without a secondary phase. Transmission electron microscopy (TEM) indicated the presence of nanoparticles that are smaller than 20 nm. The release of divalent ions (Ni2+ and Zn2+) from synthesized nanoparticles that were dispersed in saline solution, phosphate-buffered saline (PBS) and human serum, as determined by the inductively coupled plasma mass spectrometry (ICP-MS) method, was lower than 2 wt %. These results demonstrate the stability of the investigated nanoparticles in biologically relevant media and exclude the toxicity of Ni2+ and Zn2+ due to metal ion release, thereby opening a broad range of (bio)medical applications.",
publisher = "Elsevier",
journal = "Ceramics International",
title = "Synthesis, characterization and in vitro evaluation of divalent ion release from stable NiFe2O4, ZnFe2O4 and core-shell ZnFe2O4@NiFe2O4 nanoparticles",
pages = "3528-3533",
volume = "46",
number = "3",
doi = "10.1016/j.ceramint.2019.10.068",
url = "https://hdl.handle.net/21.15107/rcub_dais_6901"
}

Anđelković, L., Jeremić, D., Milenković, M. R., Radosavljević, J., Vulić, P., Pavlović, V. B., Manojlović, D. D.,& Nikolić, A. S.. (2020). Synthesis, characterization and in vitro evaluation of divalent ion release from stable NiFe2O4, ZnFe2O4 and core-shell ZnFe2O4@NiFe2O4 nanoparticles. in Ceramics International
Elsevier., 46(3), 3528-3533.
https://doi.org/10.1016/j.ceramint.2019.10.068
https://hdl.handle.net/21.15107/rcub_dais_6901

Anđelković L, Jeremić D, Milenković MR, Radosavljević J, Vulić P, Pavlović VB, Manojlović DD, Nikolić AS. Synthesis, characterization and in vitro evaluation of divalent ion release from stable NiFe2O4, ZnFe2O4 and core-shell ZnFe2O4@NiFe2O4 nanoparticles. in Ceramics International. 2020;46(3):3528-3533.
doi:10.1016/j.ceramint.2019.10.068
https://hdl.handle.net/21.15107/rcub_dais_6901 .

Anđelković, Ljubica, Jeremić, Dejan, Milenković, Milica R., Radosavljević, Jelena, Vulić, Predrag, Pavlović, Vladimir B., Manojlović, Dragan D., Nikolić, Aleksandar S., "Synthesis, characterization and in vitro evaluation of divalent ion release from stable NiFe2O4, ZnFe2O4 and core-shell ZnFe2O4@NiFe2O4 nanoparticles" in Ceramics International, 46, no. 3 (2020):3528-3533,
https://doi.org/10.1016/j.ceramint.2019.10.068 .,
https://hdl.handle.net/21.15107/rcub_dais_6901 .

TY  - THES
AU  - Živojinović, Jelena A.
PY  - 2020
UR  - http://eteze.bg.ac.rs/application/showtheses?thesesId=7481
UR  - https://fedorabg.bg.ac.rs/fedora/get/o:22343/bdef:Content/download
UR  - http://vbs.rs/scripts/cobiss?command=DISPLAY&base=70036&RID=17167369
UR  - http://nardus.mpn.gov.rs/handle/123456789/17287
UR  - https://dais.sanu.ac.rs/123456789/9154
AB  - Cilj ove doktorske disertacije je bio da se analizira i sagleda uticaj mehaničke aktivacije nastrukturu i svojstva nedopiranog i dopiranog SrTiO3 praha, kao i uticaj na strukturu i svojstvakeramike dobijene sinterovanjem ispresaka pomenutih prahova. U slučaju sinterovanih nedopiranihSrTiO3 uzoraka dodatno su razmatrane promene u brzini densifikacije i kinetici sinterovanja. Uticajmehaničke aktivacije i dopanta na električna svojstva stroncijum-titanatne keramike je analiziranmerenjem frekventne zavisnosti relativne dielektrične permitivnosti i tangensa ugla dielektričnihgubitaka na sobnoj temperaturi. Magnetnim merenjima, kod dopiranih SrTiO3 uzoraka dobijenihdodavanjem mangan(IV)-oksida, praćen je uticaj mehaničke aktivacije, koncentracije dopanta ijačine magnetnog polja na vrednost specifične magnetizacije.Mehanička aktivacija SrTiO3 praha je vršena u visoko-energetskom planetarnom mlinu sakuglama, pri čemu je vreme aktivacije nedopiranog praha iznosilo: 5, 10, 30, 60, 90 i 120 minuta,dok je efekat dopiranja razmatran za aktivaciju od 10, 30 i 120 minuta. U cilju dobijanja SrTiO3:Mnsistema, tipa Sr1-xMnxTiO3 (SMnT) ili SrTi1-xMnxO3 (STMn), u polazni SrTiO3 prah je dodatmangan(IV)-oksid (MnO2), pri čemu su izabrane vrednosti za x bile: 0,03, 0,06 i 0,12. Raspodelaveličina čestica je ukazala da je mehanička aktivacija dovela do usitnjavanja čestica polaznog praha,uz istovremenu pojavu šire raspodele veličina čestica pri dužim vremenima aktivacije.Skenirajućom i transmisionom elektronskom mikroskopijom (SEM i TEM) analizirana jemikrostruktura i morfologija polaznog i mehanički aktiviranih prahova. BET metodom je utvrđenoda se najviša vrednost specifične površine kod nedopiranih prahova postiže pri aktivaciji u trajanjuod 60 minuta, dok pri daljoj aktivaciji specifična površina ostaje približno konstantne vrednosti,usled povećane sekundarne aglomerizacije. Pokazano je da je gustina ispreska kod prahaaktiviranog tokom 10-30 minuta najveća. Zapaženo je sniženje intenziteta XRD pikova sa porastomvremena aktivacije, kao i širenje difrakcionih linija, usled smanjenja veličine kristalita i porastamikronaprezanja. Primenjena mehanička aktivacija je omogućila formiranje kubnog nanokristalnogSrTiO3 praha, pri čemu veličina kristalita opada i do ~20 nm sa uvećanjem vremena aktivacije.Uočena promena u vrednosti parametra kristalne rešetke a je posredno ukazala i na mogućepromene u koncentraciji kiseonikovih vakancija. Analizom Ramanovih spektara je praćen uticajmehaničke aktivacije na promene u fononskom spektru prahova, sa posebnim akcentom na polarneTO mode, čiji oblik i intenzitet bitno zavise od defekata kao što su kiseonikove vakancije. Analizaoptičkih svojstava kristalnih materijala pomoću UV-Vis spektroskopije je ukazala na sniženjeenergije zabranjene zone sa uvećanjem vremena aktivacije. Primenom dilatometrije je ispitivanuticaj mehaničke aktivacije na početni stadijum sinterovanja dvostrano presovanih SrTiO3 prahova.Uočeno je značajno smanjenje temperature početka skupljanja ispreska, kao i uticaj na brzinuskupljanja i na konačne gustine sinterovanih uzoraka. Primena Dornove metode je ukazala naznačajno smanjenje efektivne energije aktivacije transporta mase u početnom stadijumusinterovanja, sa porastom vremena mehaničke aktivacije polaznog praha. Za uzorke dobijenesinterovanjem do 1300 oC, uz izotermsko zadržavanje na maksimalnoj temperaturi u trajanju od 2h,je izvršena korelacija između zapaženih strukturnih promena i promena u dielektričnim svojstvima,nastalim usled mehaničke aktivacije. Posebna pažnja je posvećena uticaju promena: gustine,poroznosti, veličine zrna i kristalita, kao i uticaju promena parametra kristalne rešetke, nadielektrična svojstva. Promene vrednosti relativne dielektrične permitivnosti su razmatrane i sastanovišta promena u oblasti granice zrna, posebno imajući u vidu rezultate koji su ukazali napromenu koncentracije kiseonikovih vakancija...
AB  - The aim of this doctoral dissertation is to analyze and evaluate the effect of mechanicalactivation on the structure and properties of undoped and doped SrTiO3 powders, as well as theeffect on the structure and properties of the ceramics obtained by sintering these powders. For thesintered undoped SrTiO3 samples, changes in the densification rate were also analyzed. The effectof mechanical activation and dopant on the electrical properties of strontium titanate ceramics wasanalyzed by measuring the frequency-dependent relative dielectric permittivity and the loss tangentat room temperature. Magnetic measurements performed on the doped SrTiO3 samples obtained bythe addition of manganese(IV) oxide were used to monitor the influence of mechanical activation,dopant concentration and magnetic field strength on magnetization.The mechanical activation of the SrTiO3 powder was performed in a high-energy planetaryball mill; the activation times of the undoped powder were: 5, 10, 30, 60, 90, and 120 minutes,while the doping effect was analyzed for the activation periods of 10, 30, and 120 minutes. In orderto obtain SrTiO3:Mn systems belonging to Sr1-xMnxTiO3 (SMnT) or SrTi1-xMnxO3 (STMn)compound types, manganese(IV) oxide (MnO2) was added to the starting SrTiO3 powder, where thevalues selected for x were: 0.03, 0.06 and 0.12. The particle size distribution indicated thatmechanical activation resulted in the comminution of the starting powder particles, accompaniedwith a wider particle size distribution at longer activation times. The microstructural andmorphological analysis of the starting and mechanically activated powders was performed usingscanning and transmission electron microscopy (SEM and TEM). The BET method revealed that60-minute activation resulted in the highest specific surface area in undoped powders, while furtheractivation led to a relatively constant specific surface due to increased secondary agglomeration.The density of the powder activated for 10-30 minutes was the highest. The intensity of XRD peaksdecreased with longer activation times and diffraction lines broadened due to decreased crystallitesizes and increased microstrain. Mechanical activation led to the formation of cubic nanocrystallineSrTiO3 powder, with the minimum crystallite size of 20 nm. The observed change in the value ofthe crystal lattice parameter indirectly indicated possible changes in the concentration of oxygenvacancies. The analysis of Raman spectra revealed the effect of mechanical activation on thephonon spectrum of powders, with particular emphasis on polar TO modes which shape andintensity generally depend on defects such as oxygen vacancies. The analysis of the opticalproperties of crystalline materials by UV-Vis spectroscopy indicated a correlation betweendecreased band gap energy and increased activation times. The effect of mechanical activation onthe initial stage of sintering of bilaterally pressed SrTiO3 powders was investigated by dilatometry.A significant decrease in the temperature of the onset of densification was observed, as well as theeffect of mechanical activation on the densification rate and on the final density of the sinteredsamples. The application of the Dorn method indicated a significant decrease in the effectiveactivation energy of mass transport in the initial sintering stage, with a longer time of themechanical activation of the starting powder. For the samples obtained by sintering up to 1300 °C,with isothermal retention at the maximum temperature for 2 h, a correlation between the structuralchanges and the changes in dielectric properties resulting from mechanical activation was observed.Particular attention was paid to the effect of changes: density, porosity, grain and crystallite size, as well as the effect of crystal lattice parameter changes on the dielectric properties. The changed values of the relative dielectric permittivity were analyzed in the context of the changes in the grainboundary region, with special respect to the results indicating changes in the oxygen vacancy concentration.
PB  - Универзитет у Београду, Технолошко-металуршки факултет
T2  - Универзитет у Београду
T1  - Uticaj mehaničke aktivacije na strukturu i svojstva stroncijum-titanatne keramike
UR  - https://hdl.handle.net/21.15107/rcub_dais_9154
ER  - 

@phdthesis{
author = "Živojinović, Jelena A.",
year = "2020",
abstract = "Cilj ove doktorske disertacije je bio da se analizira i sagleda uticaj mehaničke aktivacije nastrukturu i svojstva nedopiranog i dopiranog SrTiO3 praha, kao i uticaj na strukturu i svojstvakeramike dobijene sinterovanjem ispresaka pomenutih prahova. U slučaju sinterovanih nedopiranihSrTiO3 uzoraka dodatno su razmatrane promene u brzini densifikacije i kinetici sinterovanja. Uticajmehaničke aktivacije i dopanta na električna svojstva stroncijum-titanatne keramike je analiziranmerenjem frekventne zavisnosti relativne dielektrične permitivnosti i tangensa ugla dielektričnihgubitaka na sobnoj temperaturi. Magnetnim merenjima, kod dopiranih SrTiO3 uzoraka dobijenihdodavanjem mangan(IV)-oksida, praćen je uticaj mehaničke aktivacije, koncentracije dopanta ijačine magnetnog polja na vrednost specifične magnetizacije.Mehanička aktivacija SrTiO3 praha je vršena u visoko-energetskom planetarnom mlinu sakuglama, pri čemu je vreme aktivacije nedopiranog praha iznosilo: 5, 10, 30, 60, 90 i 120 minuta,dok je efekat dopiranja razmatran za aktivaciju od 10, 30 i 120 minuta. U cilju dobijanja SrTiO3:Mnsistema, tipa Sr1-xMnxTiO3 (SMnT) ili SrTi1-xMnxO3 (STMn), u polazni SrTiO3 prah je dodatmangan(IV)-oksid (MnO2), pri čemu su izabrane vrednosti za x bile: 0,03, 0,06 i 0,12. Raspodelaveličina čestica je ukazala da je mehanička aktivacija dovela do usitnjavanja čestica polaznog praha,uz istovremenu pojavu šire raspodele veličina čestica pri dužim vremenima aktivacije.Skenirajućom i transmisionom elektronskom mikroskopijom (SEM i TEM) analizirana jemikrostruktura i morfologija polaznog i mehanički aktiviranih prahova. BET metodom je utvrđenoda se najviša vrednost specifične površine kod nedopiranih prahova postiže pri aktivaciji u trajanjuod 60 minuta, dok pri daljoj aktivaciji specifična površina ostaje približno konstantne vrednosti,usled povećane sekundarne aglomerizacije. Pokazano je da je gustina ispreska kod prahaaktiviranog tokom 10-30 minuta najveća. Zapaženo je sniženje intenziteta XRD pikova sa porastomvremena aktivacije, kao i širenje difrakcionih linija, usled smanjenja veličine kristalita i porastamikronaprezanja. Primenjena mehanička aktivacija je omogućila formiranje kubnog nanokristalnogSrTiO3 praha, pri čemu veličina kristalita opada i do ~20 nm sa uvećanjem vremena aktivacije.Uočena promena u vrednosti parametra kristalne rešetke a je posredno ukazala i na mogućepromene u koncentraciji kiseonikovih vakancija. Analizom Ramanovih spektara je praćen uticajmehaničke aktivacije na promene u fononskom spektru prahova, sa posebnim akcentom na polarneTO mode, čiji oblik i intenzitet bitno zavise od defekata kao što su kiseonikove vakancije. Analizaoptičkih svojstava kristalnih materijala pomoću UV-Vis spektroskopije je ukazala na sniženjeenergije zabranjene zone sa uvećanjem vremena aktivacije. Primenom dilatometrije je ispitivanuticaj mehaničke aktivacije na početni stadijum sinterovanja dvostrano presovanih SrTiO3 prahova.Uočeno je značajno smanjenje temperature početka skupljanja ispreska, kao i uticaj na brzinuskupljanja i na konačne gustine sinterovanih uzoraka. Primena Dornove metode je ukazala naznačajno smanjenje efektivne energije aktivacije transporta mase u početnom stadijumusinterovanja, sa porastom vremena mehaničke aktivacije polaznog praha. Za uzorke dobijenesinterovanjem do 1300 oC, uz izotermsko zadržavanje na maksimalnoj temperaturi u trajanju od 2h,je izvršena korelacija između zapaženih strukturnih promena i promena u dielektričnim svojstvima,nastalim usled mehaničke aktivacije. Posebna pažnja je posvećena uticaju promena: gustine,poroznosti, veličine zrna i kristalita, kao i uticaju promena parametra kristalne rešetke, nadielektrična svojstva. Promene vrednosti relativne dielektrične permitivnosti su razmatrane i sastanovišta promena u oblasti granice zrna, posebno imajući u vidu rezultate koji su ukazali napromenu koncentracije kiseonikovih vakancija..., The aim of this doctoral dissertation is to analyze and evaluate the effect of mechanicalactivation on the structure and properties of undoped and doped SrTiO3 powders, as well as theeffect on the structure and properties of the ceramics obtained by sintering these powders. For thesintered undoped SrTiO3 samples, changes in the densification rate were also analyzed. The effectof mechanical activation and dopant on the electrical properties of strontium titanate ceramics wasanalyzed by measuring the frequency-dependent relative dielectric permittivity and the loss tangentat room temperature. Magnetic measurements performed on the doped SrTiO3 samples obtained bythe addition of manganese(IV) oxide were used to monitor the influence of mechanical activation,dopant concentration and magnetic field strength on magnetization.The mechanical activation of the SrTiO3 powder was performed in a high-energy planetaryball mill; the activation times of the undoped powder were: 5, 10, 30, 60, 90, and 120 minutes,while the doping effect was analyzed for the activation periods of 10, 30, and 120 minutes. In orderto obtain SrTiO3:Mn systems belonging to Sr1-xMnxTiO3 (SMnT) or SrTi1-xMnxO3 (STMn)compound types, manganese(IV) oxide (MnO2) was added to the starting SrTiO3 powder, where thevalues selected for x were: 0.03, 0.06 and 0.12. The particle size distribution indicated thatmechanical activation resulted in the comminution of the starting powder particles, accompaniedwith a wider particle size distribution at longer activation times. The microstructural andmorphological analysis of the starting and mechanically activated powders was performed usingscanning and transmission electron microscopy (SEM and TEM). The BET method revealed that60-minute activation resulted in the highest specific surface area in undoped powders, while furtheractivation led to a relatively constant specific surface due to increased secondary agglomeration.The density of the powder activated for 10-30 minutes was the highest. The intensity of XRD peaksdecreased with longer activation times and diffraction lines broadened due to decreased crystallitesizes and increased microstrain. Mechanical activation led to the formation of cubic nanocrystallineSrTiO3 powder, with the minimum crystallite size of 20 nm. The observed change in the value ofthe crystal lattice parameter indirectly indicated possible changes in the concentration of oxygenvacancies. The analysis of Raman spectra revealed the effect of mechanical activation on thephonon spectrum of powders, with particular emphasis on polar TO modes which shape andintensity generally depend on defects such as oxygen vacancies. The analysis of the opticalproperties of crystalline materials by UV-Vis spectroscopy indicated a correlation betweendecreased band gap energy and increased activation times. The effect of mechanical activation onthe initial stage of sintering of bilaterally pressed SrTiO3 powders was investigated by dilatometry.A significant decrease in the temperature of the onset of densification was observed, as well as theeffect of mechanical activation on the densification rate and on the final density of the sinteredsamples. The application of the Dorn method indicated a significant decrease in the effectiveactivation energy of mass transport in the initial sintering stage, with a longer time of themechanical activation of the starting powder. For the samples obtained by sintering up to 1300 °C,with isothermal retention at the maximum temperature for 2 h, a correlation between the structuralchanges and the changes in dielectric properties resulting from mechanical activation was observed.Particular attention was paid to the effect of changes: density, porosity, grain and crystallite size, as well as the effect of crystal lattice parameter changes on the dielectric properties. The changed values of the relative dielectric permittivity were analyzed in the context of the changes in the grainboundary region, with special respect to the results indicating changes in the oxygen vacancy concentration.",
publisher = "Универзитет у Београду, Технолошко-металуршки факултет",
journal = "Универзитет у Београду",
title = "Uticaj mehaničke aktivacije na strukturu i svojstva stroncijum-titanatne keramike",
url = "https://hdl.handle.net/21.15107/rcub_dais_9154"
}

Živojinović, J. A.. (2020). Uticaj mehaničke aktivacije na strukturu i svojstva stroncijum-titanatne keramike. in Универзитет у Београду
Универзитет у Београду, Технолошко-металуршки факултет..
https://hdl.handle.net/21.15107/rcub_dais_9154

Živojinović JA. Uticaj mehaničke aktivacije na strukturu i svojstva stroncijum-titanatne keramike. in Универзитет у Београду. 2020;.
https://hdl.handle.net/21.15107/rcub_dais_9154 .

Živojinović, Jelena A., "Uticaj mehaničke aktivacije na strukturu i svojstva stroncijum-titanatne keramike" in Универзитет у Београду (2020),
https://hdl.handle.net/21.15107/rcub_dais_9154 .

TY  - THES
AU  - Vujančević, Jelena
PY  - 2020
UR  - http://eteze.bg.ac.rs/application/showtheses?thesesId=8054
UR  - https://fedorabg.bg.ac.rs/fedora/get/o:23509/bdef:Content/download
UR  - http://vbs.rs/scripts/cobiss?command=DISPLAY&base=70036&RID=35998985
UR  - https://nardus.mpn.gov.rs/handle/123456789/18222
UR  - https://dais.sanu.ac.rs/123456789/11714
AB  - Ekološki izvori energije i ekonomične metode prečišćavanja vode i vazduha velika supotreba današnjeg tehnološki razvijenog sveta. Fotoaktivni materijali mogu da obezbede ekološkualternativu fosilnim gorivima kada je u pitanju proizvodnja energije i omoguće saniranje nastalihpromena u životnoj sredini. Naime, fotoaktivni materijali apsorbuju svetlost i tada dolazi dopobuđivanja elektrona, koji su odgovorni za prenos električne struje ili učestvuju u procesurazgradnje zagađujućih materija. Postoji veliki broj fotoaktivnih materijala, među kojima se izdvajaTiO2, kojeg odlikuje hemijska inertnost, otpornost na fotoindukovanu i hemijsku koroziju inetoksičnost. Na fotoaktivnost TiO2 utiču mnogi faktori, kao što su morfologija, kristalna struktura istepen rekombinacije nosilaca naelektrisanja.Cilj ove doktorske disertacije je poboljšanje fotokatalitičke i fotoelektrične aktivnosti TiO2nanocevi. U tu svrhu, TiO2 nanocevi su sintetisane metodom elektrohemijske anodizacije pločicetitana. Ispitivan je uticaj procesnih parametara anodizacije na morfologiju i fotokatalitičku aktivnostnanocevi TiO2 u procesu razgradnje boje. Utvrđeno je da sa porastom napona anodizacije rastuvisina i prečnik nanocevi, što utiče na pomeraj apsorpcione granice ka vidljivom delu spektra i napoboljšanje fotokatalitičke aktivnosti. Određen je uticaj temperature žarenja na kristalnu strukturu,morfologiju i fotokatalitičku aktivnost TiO2 nanocevi. Žarenjem nanocevi na 450 °C dobijena jekristalna modifikacija anatasa sa veoma malim sadržajem faze rutila. Sa daljim porastomtemperature žarenja (600 i 650 °C) uočeno je prisustvo obe faze, anatasa i rutila, u različitimodnosima, a do kompletne transformacije anatasa u rutil došlo je na 700 °C. Pored promenekristalne strukture, uočen je uticaj temperature žarenja na morfologiju nanocevi. Sa povišenjemtemperature žarenja, visina nanocevi se smanjivala, kao i poroznost nanocevi, da bi na 700 °C došlodo kolapsa nanocevne morfologije. Sagledan je uticaj kristalne strukture i morfologije TiO2nanocevi na fotokatalitičku razgradnju boje metil-oranž. Zaključeno je da istovremeno prisustvoanatasa i rutila obezbeđuje bolju fotokatalitičku aktivnost u odnosu na čist anatas i čist rutil.Kako bi se ispitao uticaj dopiranja TiO2 azotom na fotokatalitičku aktivnost, nanocevi TiO2su žarene u atmosferi amonijaka, na temperaturi od 450 °C, pri različitim dužinama žarenja.Ispitivan je uticaj vremena žarenja na količinu i vrstu dopiranja. Uočeno je da žarenje u atmosferiamonijaka, pri različitim vremenima, nije uticalo na morfologiju nanocevi. Hemijska analizapovršine TiO2 nanocevi rendgenskom fotoelektronskom spektroskopijom pokazala je da sa dužimvremenom žarenja opada ukupan sadržaj azota u nanocevima. Osim toga, dužina žarenja uamonijaku je uticala i na prirodu inkorporiranja azota u TiO2. Pri kraćem vremenu žarenja zapaženje veći sadržaj intersticijskog azota, a manji sadržaj supstitucijskog azota. S dužim vremenomžarenja u amonijaku, sadržaj intersticijskog azota opada, dok sadržaj supstitucijskog raste.Apsorpcioni spektri su pokazali da uzorak sa najvećom količinom azota i najvećim sadržajemintersticijskog azota pokazuje najveći pomeraj granice apsorpcije ka većim talasnim dužinama. Istoje uočeno i za fotokatalitičku efikasnost. Najveću fotokatalitičku razgradnju boje postigao je uzorakžaren u amonijaku pri najkraćem vremenu.Dalje istraživanje je išlo u smeru proširenja saznanja o pojedinačnim i kombinovanimuticajima dopiranja azotom i deponovanja kvatnih tačaka neorganskog senzivatora nafotokatalitičku aktivnost TiO2 nanocevi. Zapaženo je da deponovanje kvantnih tačaka CdS nijeuticalo na morfologiju nanocevi, ali je na pojedinim mestima došlo do aglomeracije CdSnanočestica, što je dovelo do zatvaranja otvora nanocevi. Utvrđeno je da je fotokatalitičkaefikasnost azotom dopiranih nanocevi poboljšana nakon deponovanja CdS nanočestica. Najvećufotokatlitiču efikasnost pokazao je uzorak sa najvećim sadržajem ukupnog azota i intersticijskogazota u kombinaciji sa deponovanim CdS nanočesticama...
AB  - Environmental friendly power sources and cost-effective methods for water and airpurification, are a necessity in modern technologically developed world. Photoactive materials canprovide an environmentally friendly alternative to fossil fuels in power production and enable theremediation of changes in the environment. Namely, photoactive materials absorb light, whichexcites electrons that are responsible for generating electricity or participate in the process ofdecomposition of pollutants. There are a large number of photoactive materials, among which TiO2has attracted particular attention, due to its chemical inertness, resistance to photo and chemicalcorrosion and non-toxicity. The photoactivity of TiO2 depends on many factors, such asmorphology, crystal structure and the degree of recombination of charge carriers.The aim of this doctoral dissertation is to improve the photocatalytic and photoelectricactivity of TiO2 nanotubes. For this purpose, TiO2 nanotubes were synthesized by theelectrochemical anodization of a titanium plate. The influence of the anodization process parameterson the morphology and photocatalytic activity of TiO2 nanotubes for color degradation wasinvestigated. It was found that an increased anodization voltage leads to increased heights anddiameters of nanotubes, causing the shift of the absorption limit towards the visible part of thespectrum and the improvement of the photocatalytic activity. The influence of the annealingtemperature on the crystal structure, morphology and the photocatalytic activity of TiO2 nanotubeswas determined. The anatase crystalline modification with a very low rutile phase content wasobtained by annealing nanotubes at 450 °C. When the annealing temperature was further increased(600 and 650 °C), the presence of both phases, anatase and rutile, was observed in different ratios,and the complete transformation of anatase to rutile occurred at 700 °C. Besides the change in thecrystal structure, the influence of the annealing temperature on the morphology of the nanotubeswas observed as well. As the annealing temperature increased, the height and porosity of nanotubesdecreased, so that the nanotube morphology collapsed at 700 °C. The influence of the crystalstructure and morphology of TiO2 nanotubes on the photocatalytic degradation of methyl-orangewas observed. It was concluded that the simultaneous presence of anatase and rutile provides betterphotocatalytic activity than pure anatase and pure rutile.In order to investigate the effect of nitrogen doping of TiO2 on photocatalytic activity, TiO2nanotubes were annealed in an ammonia atmosphere, at a temperature of 450 °C, for differentannealing times. The influence of the annealing time on the amount and type of doping wasinvestigated. It was observed that annealing in an ammonia atmosphere, for different periods, didnot affect the morphology of nanotubes. A chemical analysis of the surface of TiO2 nanotubes by Xray photoelectron spectroscopy showed that the total nitrogen content in nanotubes decreased withlonger annealing times. In addition, the annealing duration in ammonia also influenced the nature ofnitrogen incorporation into TiO2. With a shorter annealing time, a higher content of interstitialnitrogen and a lower amount of substitution nitrogen were observed. With a longer annealing timein ammonia, the amount of interstitial nitrogen decreased, while the substitution nitrogen increased.The absorption spectra showed that the sample with the highest amount of nitrogen and the highestcontent of interstitial nitrogen showed the largest shift towards higher wavelengths. The sameapplies to the photocatalytic efficiency. The greatest photocatalytic degradation of the dye wasachieved in the sample annealed in ammonia for the shortest time.Further research was directed towards expanding the knowledge of individual and combinedeffects of nitrogen doping and deposition of the quantum dots of inorganic sensors on thephotocatalytic activity of TiO2 nanotubes. It was observed that the deposition of CdS quantum dotsdid not affect the morphology of nanotubes, but in some places agglomeration of CdS nanoparticlesoccurred, due to which nanotube openings closed. The photocatalytic efficiency of nitrogen-dopednanotubes was improved after CdS nanoparticle deposition. The sample with the highest amount oftotal nitrogen and interstitial nitrogen in combination with deposited CdS nanoparticles exhibitedthe highest photocatalytic efficiency...
PB  - Универзитет у Београду, Технолошко-металуршки факултет
T1  - Modifikovanje strukture i fotoaktivnosti nanocevi titan(IV)-oksida dopiranjem i primenom fotoosetljivih komponenata
UR  - https://hdl.handle.net/21.15107/rcub_nardus_18222
ER  - 

@phdthesis{
author = "Vujančević, Jelena",
year = "2020",
abstract = "Ekološki izvori energije i ekonomične metode prečišćavanja vode i vazduha velika supotreba današnjeg tehnološki razvijenog sveta. Fotoaktivni materijali mogu da obezbede ekološkualternativu fosilnim gorivima kada je u pitanju proizvodnja energije i omoguće saniranje nastalihpromena u životnoj sredini. Naime, fotoaktivni materijali apsorbuju svetlost i tada dolazi dopobuđivanja elektrona, koji su odgovorni za prenos električne struje ili učestvuju u procesurazgradnje zagađujućih materija. Postoji veliki broj fotoaktivnih materijala, među kojima se izdvajaTiO2, kojeg odlikuje hemijska inertnost, otpornost na fotoindukovanu i hemijsku koroziju inetoksičnost. Na fotoaktivnost TiO2 utiču mnogi faktori, kao što su morfologija, kristalna struktura istepen rekombinacije nosilaca naelektrisanja.Cilj ove doktorske disertacije je poboljšanje fotokatalitičke i fotoelektrične aktivnosti TiO2nanocevi. U tu svrhu, TiO2 nanocevi su sintetisane metodom elektrohemijske anodizacije pločicetitana. Ispitivan je uticaj procesnih parametara anodizacije na morfologiju i fotokatalitičku aktivnostnanocevi TiO2 u procesu razgradnje boje. Utvrđeno je da sa porastom napona anodizacije rastuvisina i prečnik nanocevi, što utiče na pomeraj apsorpcione granice ka vidljivom delu spektra i napoboljšanje fotokatalitičke aktivnosti. Određen je uticaj temperature žarenja na kristalnu strukturu,morfologiju i fotokatalitičku aktivnost TiO2 nanocevi. Žarenjem nanocevi na 450 °C dobijena jekristalna modifikacija anatasa sa veoma malim sadržajem faze rutila. Sa daljim porastomtemperature žarenja (600 i 650 °C) uočeno je prisustvo obe faze, anatasa i rutila, u različitimodnosima, a do kompletne transformacije anatasa u rutil došlo je na 700 °C. Pored promenekristalne strukture, uočen je uticaj temperature žarenja na morfologiju nanocevi. Sa povišenjemtemperature žarenja, visina nanocevi se smanjivala, kao i poroznost nanocevi, da bi na 700 °C došlodo kolapsa nanocevne morfologije. Sagledan je uticaj kristalne strukture i morfologije TiO2nanocevi na fotokatalitičku razgradnju boje metil-oranž. Zaključeno je da istovremeno prisustvoanatasa i rutila obezbeđuje bolju fotokatalitičku aktivnost u odnosu na čist anatas i čist rutil.Kako bi se ispitao uticaj dopiranja TiO2 azotom na fotokatalitičku aktivnost, nanocevi TiO2su žarene u atmosferi amonijaka, na temperaturi od 450 °C, pri različitim dužinama žarenja.Ispitivan je uticaj vremena žarenja na količinu i vrstu dopiranja. Uočeno je da žarenje u atmosferiamonijaka, pri različitim vremenima, nije uticalo na morfologiju nanocevi. Hemijska analizapovršine TiO2 nanocevi rendgenskom fotoelektronskom spektroskopijom pokazala je da sa dužimvremenom žarenja opada ukupan sadržaj azota u nanocevima. Osim toga, dužina žarenja uamonijaku je uticala i na prirodu inkorporiranja azota u TiO2. Pri kraćem vremenu žarenja zapaženje veći sadržaj intersticijskog azota, a manji sadržaj supstitucijskog azota. S dužim vremenomžarenja u amonijaku, sadržaj intersticijskog azota opada, dok sadržaj supstitucijskog raste.Apsorpcioni spektri su pokazali da uzorak sa najvećom količinom azota i najvećim sadržajemintersticijskog azota pokazuje najveći pomeraj granice apsorpcije ka većim talasnim dužinama. Istoje uočeno i za fotokatalitičku efikasnost. Najveću fotokatalitičku razgradnju boje postigao je uzorakžaren u amonijaku pri najkraćem vremenu.Dalje istraživanje je išlo u smeru proširenja saznanja o pojedinačnim i kombinovanimuticajima dopiranja azotom i deponovanja kvatnih tačaka neorganskog senzivatora nafotokatalitičku aktivnost TiO2 nanocevi. Zapaženo je da deponovanje kvantnih tačaka CdS nijeuticalo na morfologiju nanocevi, ali je na pojedinim mestima došlo do aglomeracije CdSnanočestica, što je dovelo do zatvaranja otvora nanocevi. Utvrđeno je da je fotokatalitičkaefikasnost azotom dopiranih nanocevi poboljšana nakon deponovanja CdS nanočestica. Najvećufotokatlitiču efikasnost pokazao je uzorak sa najvećim sadržajem ukupnog azota i intersticijskogazota u kombinaciji sa deponovanim CdS nanočesticama..., Environmental friendly power sources and cost-effective methods for water and airpurification, are a necessity in modern technologically developed world. Photoactive materials canprovide an environmentally friendly alternative to fossil fuels in power production and enable theremediation of changes in the environment. Namely, photoactive materials absorb light, whichexcites electrons that are responsible for generating electricity or participate in the process ofdecomposition of pollutants. There are a large number of photoactive materials, among which TiO2has attracted particular attention, due to its chemical inertness, resistance to photo and chemicalcorrosion and non-toxicity. The photoactivity of TiO2 depends on many factors, such asmorphology, crystal structure and the degree of recombination of charge carriers.The aim of this doctoral dissertation is to improve the photocatalytic and photoelectricactivity of TiO2 nanotubes. For this purpose, TiO2 nanotubes were synthesized by theelectrochemical anodization of a titanium plate. The influence of the anodization process parameterson the morphology and photocatalytic activity of TiO2 nanotubes for color degradation wasinvestigated. It was found that an increased anodization voltage leads to increased heights anddiameters of nanotubes, causing the shift of the absorption limit towards the visible part of thespectrum and the improvement of the photocatalytic activity. The influence of the annealingtemperature on the crystal structure, morphology and the photocatalytic activity of TiO2 nanotubeswas determined. The anatase crystalline modification with a very low rutile phase content wasobtained by annealing nanotubes at 450 °C. When the annealing temperature was further increased(600 and 650 °C), the presence of both phases, anatase and rutile, was observed in different ratios,and the complete transformation of anatase to rutile occurred at 700 °C. Besides the change in thecrystal structure, the influence of the annealing temperature on the morphology of the nanotubeswas observed as well. As the annealing temperature increased, the height and porosity of nanotubesdecreased, so that the nanotube morphology collapsed at 700 °C. The influence of the crystalstructure and morphology of TiO2 nanotubes on the photocatalytic degradation of methyl-orangewas observed. It was concluded that the simultaneous presence of anatase and rutile provides betterphotocatalytic activity than pure anatase and pure rutile.In order to investigate the effect of nitrogen doping of TiO2 on photocatalytic activity, TiO2nanotubes were annealed in an ammonia atmosphere, at a temperature of 450 °C, for differentannealing times. The influence of the annealing time on the amount and type of doping wasinvestigated. It was observed that annealing in an ammonia atmosphere, for different periods, didnot affect the morphology of nanotubes. A chemical analysis of the surface of TiO2 nanotubes by Xray photoelectron spectroscopy showed that the total nitrogen content in nanotubes decreased withlonger annealing times. In addition, the annealing duration in ammonia also influenced the nature ofnitrogen incorporation into TiO2. With a shorter annealing time, a higher content of interstitialnitrogen and a lower amount of substitution nitrogen were observed. With a longer annealing timein ammonia, the amount of interstitial nitrogen decreased, while the substitution nitrogen increased.The absorption spectra showed that the sample with the highest amount of nitrogen and the highestcontent of interstitial nitrogen showed the largest shift towards higher wavelengths. The sameapplies to the photocatalytic efficiency. The greatest photocatalytic degradation of the dye wasachieved in the sample annealed in ammonia for the shortest time.Further research was directed towards expanding the knowledge of individual and combinedeffects of nitrogen doping and deposition of the quantum dots of inorganic sensors on thephotocatalytic activity of TiO2 nanotubes. It was observed that the deposition of CdS quantum dotsdid not affect the morphology of nanotubes, but in some places agglomeration of CdS nanoparticlesoccurred, due to which nanotube openings closed. The photocatalytic efficiency of nitrogen-dopednanotubes was improved after CdS nanoparticle deposition. The sample with the highest amount oftotal nitrogen and interstitial nitrogen in combination with deposited CdS nanoparticles exhibitedthe highest photocatalytic efficiency...",
publisher = "Универзитет у Београду, Технолошко-металуршки факултет",
title = "Modifikovanje strukture i fotoaktivnosti nanocevi titan(IV)-oksida dopiranjem i primenom fotoosetljivih komponenata",
url = "https://hdl.handle.net/21.15107/rcub_nardus_18222"
}

Vujančević, J.. (2020). Modifikovanje strukture i fotoaktivnosti nanocevi titan(IV)-oksida dopiranjem i primenom fotoosetljivih komponenata. 
Универзитет у Београду, Технолошко-металуршки факултет..
https://hdl.handle.net/21.15107/rcub_nardus_18222

Vujančević J. Modifikovanje strukture i fotoaktivnosti nanocevi titan(IV)-oksida dopiranjem i primenom fotoosetljivih komponenata. 2020;.
https://hdl.handle.net/21.15107/rcub_nardus_18222 .

Vujančević, Jelena, "Modifikovanje strukture i fotoaktivnosti nanocevi titan(IV)-oksida dopiranjem i primenom fotoosetljivih komponenata" (2020),
https://hdl.handle.net/21.15107/rcub_nardus_18222 .

TY  - DATA
AU  - Ristić, Predrag
AU  - Blagojević, Vladimir A.
AU  - Janjić, Goran V.
AU  - Rodić, Marko
AU  - Vulić, Predrag J.
AU  - Donnard, Morgan
AU  - Gulea, Mihaela
AU  - Chylewska, Agnieszka
AU  - Makowski, Mariusz
AU  - Todorović, Tamara
AU  - Filipović, Nenad R.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/9455
AB  - Figure S1.IR spectra of gaseous decomposition products obtained during TGexperiments with 1(A) and 2(B);Figure S2.The 3D presentation of thermal decompositions versustime together with IR spectra of their gaseous products: (a)1; (b)2; Figure S3. Overlapped experimental (blue) and calculated (red) powder XRD diffractograms of 1 (A) and 2 (B); Figure S4.Comparison between experimental powder XRD patterns of 1(left) and 2(right) with simulated  patterns  of  their  analogues  with  different positionof M‒Sbondwith  respect  to  the TM-CN ring chair conformation; Figure S5. Optical microscope images of Pt-(left) and Pd-complex (right)showing as-obtained single crystals; Figure S6.SEM images of Pt-(left) and Pd-complex (right)after reduction to powder for XRD measurements; Figure S7. 1H NMR spectra of TM-CN in DMSO-d6(A) and CD3NO2(B); Figure S8. 13CNMR spectra of TM-CN in DMSO-d6(A) and CD3NO2(B); Figure S9. 1H (A) and 13CNMR (B) spectra of 1in DMSO-d6; Figure S10. COSY spectrum of 1in DMSO-d6; Figure S11. NOESY spectrum of 1in DMSO-d6; Figure S12. 1H–13CHSQC spectrum of 1in DMSO-d6, Figure S13. 1H (A) and 13CNMR (B) spectra of 1in CD3NO2; Figure S14. 1H (A) and 13CNMR (B) spectra of 2in DMSO-d6; Figure S15. 1H (A) and 13CNMR (B) spectra of 2in CD3NO2; Scheme S1. Labellingof atoms used for NMR signal assignments;
Table  S1.Experimental  vibrational  frequencies  (cm-1)  and  signals  description  of  complexes studied;Table S2.Crystal data and structure refinement for 1and 2; Table S3.Selected bond lengths (Å) and angles (°) for complexes 1 and 2;Table  S4. Results  of  energy  calculations  for  C-H/Cl-M,  C-H/S-M,  C-H/M  and C-H/NCinteractions  (M=  Pd(II)  and  Pt(II))  at wb97xd/6-31+g**  +lanl2dzlevel  of  theory.  Energies  are expressed in kcal/mol; Table  S5.C-H/M  interactions  obtained  from  the  periodic  calculations  of  axial  and  equatorially coordinated Pd and Pt; Table S6.1H NMR spectral data (399.74 MHz)in DMSO-d6and CD3NO2at 298 K for TM-CN and complexes 1and 2; Table S7. 13C NMR spectral data (100.53 MHz)in DMSO-d6and CD3NO2at 298 K for TM-CN and complexes 1and 2.
PB  - American Chemical Society
T2  - Crystal Growth & Design
T1  - Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661
UR  - https://hdl.handle.net/21.15107/rcub_dais_9455
ER  - 

@misc{
author = "Ristić, Predrag and Blagojević, Vladimir A. and Janjić, Goran V. and Rodić, Marko and Vulić, Predrag J. and Donnard, Morgan and Gulea, Mihaela and Chylewska, Agnieszka and Makowski, Mariusz and Todorović, Tamara and Filipović, Nenad R.",
year = "2020",
abstract = "Figure S1.IR spectra of gaseous decomposition products obtained during TGexperiments with 1(A) and 2(B);Figure S2.The 3D presentation of thermal decompositions versustime together with IR spectra of their gaseous products: (a)1; (b)2; Figure S3. Overlapped experimental (blue) and calculated (red) powder XRD diffractograms of 1 (A) and 2 (B); Figure S4.Comparison between experimental powder XRD patterns of 1(left) and 2(right) with simulated  patterns  of  their  analogues  with  different positionof M‒Sbondwith  respect  to  the TM-CN ring chair conformation; Figure S5. Optical microscope images of Pt-(left) and Pd-complex (right)showing as-obtained single crystals; Figure S6.SEM images of Pt-(left) and Pd-complex (right)after reduction to powder for XRD measurements; Figure S7. 1H NMR spectra of TM-CN in DMSO-d6(A) and CD3NO2(B); Figure S8. 13CNMR spectra of TM-CN in DMSO-d6(A) and CD3NO2(B); Figure S9. 1H (A) and 13CNMR (B) spectra of 1in DMSO-d6; Figure S10. COSY spectrum of 1in DMSO-d6; Figure S11. NOESY spectrum of 1in DMSO-d6; Figure S12. 1H–13CHSQC spectrum of 1in DMSO-d6, Figure S13. 1H (A) and 13CNMR (B) spectra of 1in CD3NO2; Figure S14. 1H (A) and 13CNMR (B) spectra of 2in DMSO-d6; Figure S15. 1H (A) and 13CNMR (B) spectra of 2in CD3NO2; Scheme S1. Labellingof atoms used for NMR signal assignments;
Table  S1.Experimental  vibrational  frequencies  (cm-1)  and  signals  description  of  complexes studied;Table S2.Crystal data and structure refinement for 1and 2; Table S3.Selected bond lengths (Å) and angles (°) for complexes 1 and 2;Table  S4. Results  of  energy  calculations  for  C-H/Cl-M,  C-H/S-M,  C-H/M  and C-H/NCinteractions  (M=  Pd(II)  and  Pt(II))  at wb97xd/6-31+g**  +lanl2dzlevel  of  theory.  Energies  are expressed in kcal/mol; Table  S5.C-H/M  interactions  obtained  from  the  periodic  calculations  of  axial  and  equatorially coordinated Pd and Pt; Table S6.1H NMR spectral data (399.74 MHz)in DMSO-d6and CD3NO2at 298 K for TM-CN and complexes 1and 2; Table S7. 13C NMR spectral data (100.53 MHz)in DMSO-d6and CD3NO2at 298 K for TM-CN and complexes 1and 2.",
publisher = "American Chemical Society",
journal = "Crystal Growth & Design",
title = "Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661",
url = "https://hdl.handle.net/21.15107/rcub_dais_9455"
}

Ristić, P., Blagojević, V. A., Janjić, G. V., Rodić, M., Vulić, P. J., Donnard, M., Gulea, M., Chylewska, A., Makowski, M., Todorović, T.,& Filipović, N. R.. (2020). Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661. in Crystal Growth & Design
American Chemical Society..
https://hdl.handle.net/21.15107/rcub_dais_9455

Ristić P, Blagojević VA, Janjić GV, Rodić M, Vulić PJ, Donnard M, Gulea M, Chylewska A, Makowski M, Todorović T, Filipović NR. Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661. in Crystal Growth & Design. 2020;.
https://hdl.handle.net/21.15107/rcub_dais_9455 .

Ristić, Predrag, Blagojević, Vladimir A., Janjić, Goran V., Rodić, Marko, Vulić, Predrag J., Donnard, Morgan, Gulea, Mihaela, Chylewska, Agnieszka, Makowski, Mariusz, Todorović, Tamara, Filipović, Nenad R., "Supplementary data for the article: Ristić, P.; Blagojević, V.; Janjić, G.; Rodić, M.; Vulić, P.; Donnard, M.; Gulea, M.; Chylewska, A.; Makowski, M.; Todorović, T.; Filipović, N. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-Carbonitrile: Crystallographic, Thermal, and DFT Study. Crystal Growth & Design 2020, 20 (5), 3018–3033. https://doi.org/10.1021/acs.cgd.9b01661" in Crystal Growth & Design (2020),
https://hdl.handle.net/21.15107/rcub_dais_9455 .

TY  - JOUR
AU  - Ristić, Predrag
AU  - Blagojević, Vladimir A.
AU  - Janjić, Goran V.
AU  - Rodić, Marko
AU  - Vulić, Predrag J.
AU  - Donnard, Morgan
AU  - Gulea, Mihaela
AU  - Chylewska, Agnieszka
AU  - Makowski, Mariusz
AU  - Todorović, Tamara
AU  - Filipović, Nenad R.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/9454
AB  - Pt(II) and Pd(II) complexes (1 and 2, respectively) with thiomorpholine-4-carbonitrile (TM-CN), an N-substituted thiomorpholine derivative, were synthesized from tetrachlorido precursors in water. Structural analysis has shown that 1 represents the first monomeric metal complex with this ligand type with an axial M-S bond with respect to the TM-CN ring chair conformation, while in 2 a typical equatorial M-S bond position with respect to the ring chair conformation was observed. A detailed DFT investigation revealed that axial conformers are more stable for molecular forms of both metals, while intermolecular interactions in the crystals stabilize the axial conformer for Pt(II) and the equatorial conformer for Pd(II). The magnitude of this stabilization in the case of 2 is large enough to change the most stable axial conformer in the molecular form to the equatorial conformer in the crystal. Further investigation of the strength of individual intermolecular interactions revealed significant differences of some interactions between the two structures. The likely cause of the difference in the crystal structures of experimentally obtained complexes is the fact that 1 and 2 exhibit different dominant interactions: C-H/M and C-H/S are more dominant in 1 and C-H/Cl interactions are more dominant in 2. In addition, DFT calculations have shown that while the axial position of the Pt-S bond with respect to the ring chair conformation results in a significantly shorter C-H/Pt interaction distance than that in the hypothetical equatorial conformer, there is very little difference in C-H/Pd interaction distances in conformers with axial and equatorial positions of Pd-S bond with respect to the ring chair conformation.
PB  - American Chemical Society
T2  - Crystal Growth & Design
T1  - Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study
SP  - 3018
EP  - 3033
VL  - 20
IS  - 5
DO  - 10.1021/acs.cgd.9b01661
UR  - https://hdl.handle.net/21.15107/rcub_dais_9454
ER  - 

@article{
author = "Ristić, Predrag and Blagojević, Vladimir A. and Janjić, Goran V. and Rodić, Marko and Vulić, Predrag J. and Donnard, Morgan and Gulea, Mihaela and Chylewska, Agnieszka and Makowski, Mariusz and Todorović, Tamara and Filipović, Nenad R.",
year = "2020",
abstract = "Pt(II) and Pd(II) complexes (1 and 2, respectively) with thiomorpholine-4-carbonitrile (TM-CN), an N-substituted thiomorpholine derivative, were synthesized from tetrachlorido precursors in water. Structural analysis has shown that 1 represents the first monomeric metal complex with this ligand type with an axial M-S bond with respect to the TM-CN ring chair conformation, while in 2 a typical equatorial M-S bond position with respect to the ring chair conformation was observed. A detailed DFT investigation revealed that axial conformers are more stable for molecular forms of both metals, while intermolecular interactions in the crystals stabilize the axial conformer for Pt(II) and the equatorial conformer for Pd(II). The magnitude of this stabilization in the case of 2 is large enough to change the most stable axial conformer in the molecular form to the equatorial conformer in the crystal. Further investigation of the strength of individual intermolecular interactions revealed significant differences of some interactions between the two structures. The likely cause of the difference in the crystal structures of experimentally obtained complexes is the fact that 1 and 2 exhibit different dominant interactions: C-H/M and C-H/S are more dominant in 1 and C-H/Cl interactions are more dominant in 2. In addition, DFT calculations have shown that while the axial position of the Pt-S bond with respect to the ring chair conformation results in a significantly shorter C-H/Pt interaction distance than that in the hypothetical equatorial conformer, there is very little difference in C-H/Pd interaction distances in conformers with axial and equatorial positions of Pd-S bond with respect to the ring chair conformation.",
publisher = "American Chemical Society",
journal = "Crystal Growth & Design",
title = "Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study",
pages = "3018-3033",
volume = "20",
number = "5",
doi = "10.1021/acs.cgd.9b01661",
url = "https://hdl.handle.net/21.15107/rcub_dais_9454"
}

Ristić, P., Blagojević, V. A., Janjić, G. V., Rodić, M., Vulić, P. J., Donnard, M., Gulea, M., Chylewska, A., Makowski, M., Todorović, T.,& Filipović, N. R.. (2020). Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study. in Crystal Growth & Design
American Chemical Society., 20(5), 3018-3033.
https://doi.org/10.1021/acs.cgd.9b01661
https://hdl.handle.net/21.15107/rcub_dais_9454

Ristić P, Blagojević VA, Janjić GV, Rodić M, Vulić PJ, Donnard M, Gulea M, Chylewska A, Makowski M, Todorović T, Filipović NR. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study. in Crystal Growth & Design. 2020;20(5):3018-3033.
doi:10.1021/acs.cgd.9b01661
https://hdl.handle.net/21.15107/rcub_dais_9454 .

Ristić, Predrag, Blagojević, Vladimir A., Janjić, Goran V., Rodić, Marko, Vulić, Predrag J., Donnard, Morgan, Gulea, Mihaela, Chylewska, Agnieszka, Makowski, Mariusz, Todorović, Tamara, Filipović, Nenad R., "Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study" in Crystal Growth & Design, 20, no. 5 (2020):3018-3033,
https://doi.org/10.1021/acs.cgd.9b01661 .,
https://hdl.handle.net/21.15107/rcub_dais_9454 .

TY  - JOUR
AU  - Ristić, Predrag
AU  - Blagojević, Vladimir A.
AU  - Janjić, Goran V.
AU  - Rodić, Marko
AU  - Vulić, Predrag J.
AU  - Donnard, Morgan
AU  - Gulea, Mihaela
AU  - Chylewska, Agnieszka
AU  - Makowski, Mariusz
AU  - Todorović, Tamara
AU  - Filipović, Nenad R.
PY  - 2020
UR  - https://dais.sanu.ac.rs/123456789/9453
AB  - Pt(II) and Pd(II) complexes (1 and 2, respectively) with thiomorpholine-4-carbonitrile (TM-CN), an N-substituted thiomorpholine derivative, were synthesized from tetrachlorido precursors in water. Structural analysis has shown that 1 represents the first monomeric metal complex with this ligand type with an axial M-S bond with respect to the TM-CN ring chair conformation, while in 2 a typical equatorial M-S bond position with respect to the ring chair conformation was observed. A detailed DFT investigation revealed that axial conformers are more stable for molecular forms of both metals, while intermolecular interactions in the crystals stabilize the axial conformer for Pt(II) and the equatorial conformer for Pd(II). The magnitude of this stabilization in the case of 2 is large enough to change the most stable axial conformer in the molecular form to the equatorial conformer in the crystal. Further investigation of the strength of individual intermolecular interactions revealed significant differences of some interactions between the two structures. The likely cause of the difference in the crystal structures of experimentally obtained complexes is the fact that 1 and 2 exhibit different dominant interactions: C-H/M and C-H/S are more dominant in 1 and C-H/Cl interactions are more dominant in 2. In addition, DFT calculations have shown that while the axial position of the Pt-S bond with respect to the ring chair conformation results in a significantly shorter C-H/Pt interaction distance than that in the hypothetical equatorial conformer, there is very little difference in C-H/Pd interaction distances in conformers with axial and equatorial positions of Pd-S bond with respect to the ring chair conformation.
PB  - American Chemical Society
T2  - Crystal Growth & Design
T1  - Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study
SP  - 3018
EP  - 3033
VL  - 20
IS  - 5
DO  - 10.1021/acs.cgd.9b01661
UR  - https://hdl.handle.net/21.15107/rcub_dais_9453
ER  - 

@article{
author = "Ristić, Predrag and Blagojević, Vladimir A. and Janjić, Goran V. and Rodić, Marko and Vulić, Predrag J. and Donnard, Morgan and Gulea, Mihaela and Chylewska, Agnieszka and Makowski, Mariusz and Todorović, Tamara and Filipović, Nenad R.",
year = "2020",
abstract = "Pt(II) and Pd(II) complexes (1 and 2, respectively) with thiomorpholine-4-carbonitrile (TM-CN), an N-substituted thiomorpholine derivative, were synthesized from tetrachlorido precursors in water. Structural analysis has shown that 1 represents the first monomeric metal complex with this ligand type with an axial M-S bond with respect to the TM-CN ring chair conformation, while in 2 a typical equatorial M-S bond position with respect to the ring chair conformation was observed. A detailed DFT investigation revealed that axial conformers are more stable for molecular forms of both metals, while intermolecular interactions in the crystals stabilize the axial conformer for Pt(II) and the equatorial conformer for Pd(II). The magnitude of this stabilization in the case of 2 is large enough to change the most stable axial conformer in the molecular form to the equatorial conformer in the crystal. Further investigation of the strength of individual intermolecular interactions revealed significant differences of some interactions between the two structures. The likely cause of the difference in the crystal structures of experimentally obtained complexes is the fact that 1 and 2 exhibit different dominant interactions: C-H/M and C-H/S are more dominant in 1 and C-H/Cl interactions are more dominant in 2. In addition, DFT calculations have shown that while the axial position of the Pt-S bond with respect to the ring chair conformation results in a significantly shorter C-H/Pt interaction distance than that in the hypothetical equatorial conformer, there is very little difference in C-H/Pd interaction distances in conformers with axial and equatorial positions of Pd-S bond with respect to the ring chair conformation.",
publisher = "American Chemical Society",
journal = "Crystal Growth & Design",
title = "Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study",
pages = "3018-3033",
volume = "20",
number = "5",
doi = "10.1021/acs.cgd.9b01661",
url = "https://hdl.handle.net/21.15107/rcub_dais_9453"
}

Ristić, P., Blagojević, V. A., Janjić, G. V., Rodić, M., Vulić, P. J., Donnard, M., Gulea, M., Chylewska, A., Makowski, M., Todorović, T.,& Filipović, N. R.. (2020). Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study. in Crystal Growth & Design
American Chemical Society., 20(5), 3018-3033.
https://doi.org/10.1021/acs.cgd.9b01661
https://hdl.handle.net/21.15107/rcub_dais_9453

Ristić P, Blagojević VA, Janjić GV, Rodić M, Vulić PJ, Donnard M, Gulea M, Chylewska A, Makowski M, Todorović T, Filipović NR. Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study. in Crystal Growth & Design. 2020;20(5):3018-3033.
doi:10.1021/acs.cgd.9b01661
https://hdl.handle.net/21.15107/rcub_dais_9453 .

Ristić, Predrag, Blagojević, Vladimir A., Janjić, Goran V., Rodić, Marko, Vulić, Predrag J., Donnard, Morgan, Gulea, Mihaela, Chylewska, Agnieszka, Makowski, Mariusz, Todorović, Tamara, Filipović, Nenad R., "Influence of C–H/X (X = S, Cl, N, Pt/Pd) Interactions on the Molecular and Crystal Structures of Pt(II) and Pd(II) Complexes with Thiomorpholine-4-carbonitrile: Crystallographic, Thermal, and DFT Study" in Crystal Growth & Design, 20, no. 5 (2020):3018-3033,
https://doi.org/10.1021/acs.cgd.9b01661 .,
https://hdl.handle.net/21.15107/rcub_dais_9453 .

TY  - JOUR
AU  - Obradović, Nina
AU  - Pavlović, Vera P.
AU  - Kachlik, Martin
AU  - Maca, Karel
AU  - Olćan, Dragan
AU  - Đorđević, Antonije
AU  - Tshantshapanyan, Ani
AU  - Vlahović, Branislav
AU  - Pavlović, Vladimir B.
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/4557
AB  - Sintering of pure cordierite 2MgO:2Al2O3:5SiO2, and cordierite with the addition of 5 mass % TeO2 was studied. Green bodies were prepared from powder mixtures mechanically activated in a high-energy planetary mill, shaped by uniaxial (20 MPa) and cold isostatic pressing (1000 MPa). The pressure-less sintering of these specimens was performed at 1350°C for 1 h. High relative density over 95% of the theoretical value was obtained through solid-state reaction and pressure-less sintering of powder activated for 40 min, and for the first time reported in the literature. Phase composition and microstructures of sintered samples were determined by XRD and SEM, coupled with EDS mapping. The real part of the complex relative permittivity of the samples was measured at 200 MHz. The loss tangent of all samples was below the resolution of the measurement setup. A strong correlation between the relative permittivity and the density agrees with previously published data.
PB  - Taylor and Francis
T2  - Advances in Applied Ceramics
T1  - Processing and properties of dense cordierite ceramics obtained through solid-state reaction and pressure-less sintering
SP  - 241
EP  - 248
VL  - 118
IS  - 5
DO  - 10.1080/17436753.2018.1548150
UR  - https://hdl.handle.net/21.15107/rcub_dais_4557
ER  - 

@article{
author = "Obradović, Nina and Pavlović, Vera P. and Kachlik, Martin and Maca, Karel and Olćan, Dragan and Đorđević, Antonije and Tshantshapanyan, Ani and Vlahović, Branislav and Pavlović, Vladimir B.",
year = "2019",
abstract = "Sintering of pure cordierite 2MgO:2Al2O3:5SiO2, and cordierite with the addition of 5 mass % TeO2 was studied. Green bodies were prepared from powder mixtures mechanically activated in a high-energy planetary mill, shaped by uniaxial (20 MPa) and cold isostatic pressing (1000 MPa). The pressure-less sintering of these specimens was performed at 1350°C for 1 h. High relative density over 95% of the theoretical value was obtained through solid-state reaction and pressure-less sintering of powder activated for 40 min, and for the first time reported in the literature. Phase composition and microstructures of sintered samples were determined by XRD and SEM, coupled with EDS mapping. The real part of the complex relative permittivity of the samples was measured at 200 MHz. The loss tangent of all samples was below the resolution of the measurement setup. A strong correlation between the relative permittivity and the density agrees with previously published data.",
publisher = "Taylor and Francis",
journal = "Advances in Applied Ceramics",
title = "Processing and properties of dense cordierite ceramics obtained through solid-state reaction and pressure-less sintering",
pages = "241-248",
volume = "118",
number = "5",
doi = "10.1080/17436753.2018.1548150",
url = "https://hdl.handle.net/21.15107/rcub_dais_4557"
}

Obradović, N., Pavlović, V. P., Kachlik, M., Maca, K., Olćan, D., Đorđević, A., Tshantshapanyan, A., Vlahović, B.,& Pavlović, V. B.. (2019). Processing and properties of dense cordierite ceramics obtained through solid-state reaction and pressure-less sintering. in Advances in Applied Ceramics
Taylor and Francis., 118(5), 241-248.
https://doi.org/10.1080/17436753.2018.1548150
https://hdl.handle.net/21.15107/rcub_dais_4557

Obradović N, Pavlović VP, Kachlik M, Maca K, Olćan D, Đorđević A, Tshantshapanyan A, Vlahović B, Pavlović VB. Processing and properties of dense cordierite ceramics obtained through solid-state reaction and pressure-less sintering. in Advances in Applied Ceramics. 2019;118(5):241-248.
doi:10.1080/17436753.2018.1548150
https://hdl.handle.net/21.15107/rcub_dais_4557 .

Obradović, Nina, Pavlović, Vera P., Kachlik, Martin, Maca, Karel, Olćan, Dragan, Đorđević, Antonije, Tshantshapanyan, Ani, Vlahović, Branislav, Pavlović, Vladimir B., "Processing and properties of dense cordierite ceramics obtained through solid-state reaction and pressure-less sintering" in Advances in Applied Ceramics, 118, no. 5 (2019):241-248,
https://doi.org/10.1080/17436753.2018.1548150 .,
https://hdl.handle.net/21.15107/rcub_dais_4557 .

TY  - CONF
AU  - Đorđević, Nataša
AU  - Obradović, Nina
AU  - Sokić, Miroslav D.
AU  - Marković, Branislav R.
AU  - Patarić, Aleksandra
AU  - Petronijević, Nela
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/14867
AB  - Mechanochemical activation of 2MgO•2Al2O3•5SiO2, starting components of cordierite, was used in aim to decrease the sintering temperature. Cordierite is very attractive ceramic material due to its properties, excellent thermal shock resistance, low dielectric constants (~5) and low thermal expansions (20•10-7 ºC-1). Specific surface area of the activated components was detected by the BET method. TG and DTA methods have followed behaviors of the three-component system. To see the influence of relaxation time on the activated components, FT IR has analyzed the starting components as well as activated mixture after 24h and 24 months. TG analyses of starting cordierite mixture activated 5 to 240 minutes showed a mass decrease from 8 to12%. DT analyses showed the influence of mechanochemical activation of the starting components as increasing energy of the starting cordierite mixture, which resulted in moving the endothermic and exothermic effects to lower temperatures. The increasing of the temperatures of these effects was about 100°C, depending on activation time. IR analyses showed that relaxation time, that is laying-off time to the moment of sintering, do not influence changes of activated mixtures. Since the given results, it can be concluded that the activated sample has no changes to the moment of using for a certain purpose (sintering) for any time since activation.
PB  - Belgrade : Association of Metallurgical Engineers of Serbia (AMES)
C3  - Book of Abstracts / Metallurgical & Materials Engineering Congress of South-East Europe (MME SEE 2019), June 5-7, 2019, Belgrade, Serbia
T1  - Activation and relaxation time influence on cordierite ceramics
SP  - 61
EP  - 61
UR  - https://hdl.handle.net/21.15107/rcub_dais_14867
ER  - 

@conference{
author = "Đorđević, Nataša and Obradović, Nina and Sokić, Miroslav D. and Marković, Branislav R. and Patarić, Aleksandra and Petronijević, Nela",
year = "2019",
abstract = "Mechanochemical activation of 2MgO•2Al2O3•5SiO2, starting components of cordierite, was used in aim to decrease the sintering temperature. Cordierite is very attractive ceramic material due to its properties, excellent thermal shock resistance, low dielectric constants (~5) and low thermal expansions (20•10-7 ºC-1). Specific surface area of the activated components was detected by the BET method. TG and DTA methods have followed behaviors of the three-component system. To see the influence of relaxation time on the activated components, FT IR has analyzed the starting components as well as activated mixture after 24h and 24 months. TG analyses of starting cordierite mixture activated 5 to 240 minutes showed a mass decrease from 8 to12%. DT analyses showed the influence of mechanochemical activation of the starting components as increasing energy of the starting cordierite mixture, which resulted in moving the endothermic and exothermic effects to lower temperatures. The increasing of the temperatures of these effects was about 100°C, depending on activation time. IR analyses showed that relaxation time, that is laying-off time to the moment of sintering, do not influence changes of activated mixtures. Since the given results, it can be concluded that the activated sample has no changes to the moment of using for a certain purpose (sintering) for any time since activation.",
publisher = "Belgrade : Association of Metallurgical Engineers of Serbia (AMES)",
journal = "Book of Abstracts / Metallurgical & Materials Engineering Congress of South-East Europe (MME SEE 2019), June 5-7, 2019, Belgrade, Serbia",
title = "Activation and relaxation time influence on cordierite ceramics",
pages = "61-61",
url = "https://hdl.handle.net/21.15107/rcub_dais_14867"
}

Đorđević, N., Obradović, N., Sokić, M. D., Marković, B. R., Patarić, A.,& Petronijević, N.. (2019). Activation and relaxation time influence on cordierite ceramics. in Book of Abstracts / Metallurgical & Materials Engineering Congress of South-East Europe (MME SEE 2019), June 5-7, 2019, Belgrade, Serbia
Belgrade : Association of Metallurgical Engineers of Serbia (AMES)., 61-61.
https://hdl.handle.net/21.15107/rcub_dais_14867

Đorđević N, Obradović N, Sokić MD, Marković BR, Patarić A, Petronijević N. Activation and relaxation time influence on cordierite ceramics. in Book of Abstracts / Metallurgical & Materials Engineering Congress of South-East Europe (MME SEE 2019), June 5-7, 2019, Belgrade, Serbia. 2019;:61-61.
https://hdl.handle.net/21.15107/rcub_dais_14867 .

Đorđević, Nataša, Obradović, Nina, Sokić, Miroslav D., Marković, Branislav R., Patarić, Aleksandra, Petronijević, Nela, "Activation and relaxation time influence on cordierite ceramics" in Book of Abstracts / Metallurgical & Materials Engineering Congress of South-East Europe (MME SEE 2019), June 5-7, 2019, Belgrade, Serbia (2019):61-61,
https://hdl.handle.net/21.15107/rcub_dais_14867 .

TY  - CONF
AU  - Đorđević, Nataša
AU  - Obradović, Nina
AU  - Sokić, Miroslav D.
AU  - Marković, Branislav
AU  - Patarić, Aleksandra
AU  - Petronijević, Nela
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/14866
AB  - The influence of Bi2O3 as a functional additive on the process of obtaining cordierite, 2MgO-2Al2O3-5SiO2 (MAS) was studied by sintering the MgO / Bi2O3 system (sintered at 820 °C and 1100 °C), Al2O3 / Bi2O3 and SiO2 / Bi2O3 (sintered at 1100 °C ), the composition being 80% oxide and 20% Bi2O3. The effects of sintering, composition, and morphology were followed by X-ray diffraction, scanning electron microscopy and EDS analysis. It has been found that, in addition to the liquid phase, Bi2O3 produces intermediate metastable compounds with MgO and Al2O3. The sintering of MAS ceramics with 10% Bi2O3 at 1000 °C, 1100 °C and 1200 °C was also performed. Binary systems MgO / Bi2O3 at 820 ºC and 1100 ºC, Al2O3 / Bi2O3 and SiO2 / Bi2O3 were sintered at 1100 ºC, as well as MgO, Al2O3, SiO2 / Bi2O3 at 1000 ºC, 1100 ºC and 1200 ºC to examine the reaction of the cordierite synthesis. The results show the formation of a liquid phase at 820 °C (melting temperature Bi2O3), as well as the formation of metastable compounds forming MgO and Al2O3 with Bi2O3 at 1100 °C and which diffuse through the liquid phase, thus enabling the mechanism of reaction in the multi-component system to be accelerated from two aspects. By the sintering of a three-component MAS system in the presence of Bi2O3, the existence of cordierite was established. The lowest temperature at which the tracer cordierite was observed (in hexagonal form - indialite) is 1100 °C, while in the sintered system at 1200 ºC the most frequent phase is indialite. This study found that the presence of Bi2O3 in basic cordierite mixture allows the sintering temperature to decrease by ~ 170 ºC relative to the temperature of the formation of cordierite ceramics from the mixture without the presence of functional additives.
PB  - Belgrade : Association of Metallurgical Engineers of Serbia (AMES)
C3  - Book of Abstracts / Metallurgical & Materials Engineering Congress of South-East Europe (MME SEE 2019), June 5-7, 2019, Belgrade, Serbia
T1  - Bi2O3 influence on electronic ceramics sintering process and final properties
SP  - 60
EP  - 60
UR  - https://hdl.handle.net/21.15107/rcub_dais_14866
ER  - 

@conference{
author = "Đorđević, Nataša and Obradović, Nina and Sokić, Miroslav D. and Marković, Branislav and Patarić, Aleksandra and Petronijević, Nela",
year = "2019",
abstract = "The influence of Bi2O3 as a functional additive on the process of obtaining cordierite, 2MgO-2Al2O3-5SiO2 (MAS) was studied by sintering the MgO / Bi2O3 system (sintered at 820 °C and 1100 °C), Al2O3 / Bi2O3 and SiO2 / Bi2O3 (sintered at 1100 °C ), the composition being 80% oxide and 20% Bi2O3. The effects of sintering, composition, and morphology were followed by X-ray diffraction, scanning electron microscopy and EDS analysis. It has been found that, in addition to the liquid phase, Bi2O3 produces intermediate metastable compounds with MgO and Al2O3. The sintering of MAS ceramics with 10% Bi2O3 at 1000 °C, 1100 °C and 1200 °C was also performed. Binary systems MgO / Bi2O3 at 820 ºC and 1100 ºC, Al2O3 / Bi2O3 and SiO2 / Bi2O3 were sintered at 1100 ºC, as well as MgO, Al2O3, SiO2 / Bi2O3 at 1000 ºC, 1100 ºC and 1200 ºC to examine the reaction of the cordierite synthesis. The results show the formation of a liquid phase at 820 °C (melting temperature Bi2O3), as well as the formation of metastable compounds forming MgO and Al2O3 with Bi2O3 at 1100 °C and which diffuse through the liquid phase, thus enabling the mechanism of reaction in the multi-component system to be accelerated from two aspects. By the sintering of a three-component MAS system in the presence of Bi2O3, the existence of cordierite was established. The lowest temperature at which the tracer cordierite was observed (in hexagonal form - indialite) is 1100 °C, while in the sintered system at 1200 ºC the most frequent phase is indialite. This study found that the presence of Bi2O3 in basic cordierite mixture allows the sintering temperature to decrease by ~ 170 ºC relative to the temperature of the formation of cordierite ceramics from the mixture without the presence of functional additives.",
publisher = "Belgrade : Association of Metallurgical Engineers of Serbia (AMES)",
journal = "Book of Abstracts / Metallurgical & Materials Engineering Congress of South-East Europe (MME SEE 2019), June 5-7, 2019, Belgrade, Serbia",
title = "Bi2O3 influence on electronic ceramics sintering process and final properties",
pages = "60-60",
url = "https://hdl.handle.net/21.15107/rcub_dais_14866"
}

Đorđević, N., Obradović, N., Sokić, M. D., Marković, B., Patarić, A.,& Petronijević, N.. (2019). Bi2O3 influence on electronic ceramics sintering process and final properties. in Book of Abstracts / Metallurgical & Materials Engineering Congress of South-East Europe (MME SEE 2019), June 5-7, 2019, Belgrade, Serbia
Belgrade : Association of Metallurgical Engineers of Serbia (AMES)., 60-60.
https://hdl.handle.net/21.15107/rcub_dais_14866

Đorđević N, Obradović N, Sokić MD, Marković B, Patarić A, Petronijević N. Bi2O3 influence on electronic ceramics sintering process and final properties. in Book of Abstracts / Metallurgical & Materials Engineering Congress of South-East Europe (MME SEE 2019), June 5-7, 2019, Belgrade, Serbia. 2019;:60-60.
https://hdl.handle.net/21.15107/rcub_dais_14866 .

Đorđević, Nataša, Obradović, Nina, Sokić, Miroslav D., Marković, Branislav, Patarić, Aleksandra, Petronijević, Nela, "Bi2O3 influence on electronic ceramics sintering process and final properties" in Book of Abstracts / Metallurgical & Materials Engineering Congress of South-East Europe (MME SEE 2019), June 5-7, 2019, Belgrade, Serbia (2019):60-60,
https://hdl.handle.net/21.15107/rcub_dais_14866 .

TY  - CONF
AU  - Obradović, Nina
AU  - Đorđević, Antonije
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/6962
AB  - Mechanical activation is commonly used as a pre-sintering process in order to enhance the reactivity of materials, reduce the particle size, increase diffusion rates, accelerate the reaction, and lower the sintering temperature. The mechanical activation can affect the final electrical and mechanical characteristics. In this paper we consider the influence of the mechanical activation on the permittivity and the loss tangent. We outline methods for evaluation of these parameters, with emphasis on our coaxial-chamber technique for measurements in the VHF band.
PB  - Belgrade : ETRAN
PB  - Belgrade : Academic Mind
C3  - Proceedings of Papers – 6th International Conference on Electrical, Electronic and Computing Engineering, IcETRAN 2019, Silver Lake, Serbia, June 03 – 06, 2019 / Zbornik radova - 63. Konferencija za elektroniku, telekomunikacije, računarstvo, automatiku i nuklearnu tehniku, Srebrno jezero, 03 – 06. juna, 2019. godine
T1  - Influence of Mechanical Activation on Electrical Properties of Ceramic Materials in VHF Band
SP  - 636
EP  - 645
UR  - https://hdl.handle.net/21.15107/rcub_dais_6962
ER  - 

@conference{
author = "Obradović, Nina and Đorđević, Antonije",
year = "2019",
abstract = "Mechanical activation is commonly used as a pre-sintering process in order to enhance the reactivity of materials, reduce the particle size, increase diffusion rates, accelerate the reaction, and lower the sintering temperature. The mechanical activation can affect the final electrical and mechanical characteristics. In this paper we consider the influence of the mechanical activation on the permittivity and the loss tangent. We outline methods for evaluation of these parameters, with emphasis on our coaxial-chamber technique for measurements in the VHF band.",
publisher = "Belgrade : ETRAN, Belgrade : Academic Mind",
journal = "Proceedings of Papers – 6th International Conference on Electrical, Electronic and Computing Engineering, IcETRAN 2019, Silver Lake, Serbia, June 03 – 06, 2019 / Zbornik radova - 63. Konferencija za elektroniku, telekomunikacije, računarstvo, automatiku i nuklearnu tehniku, Srebrno jezero, 03 – 06. juna, 2019. godine",
title = "Influence of Mechanical Activation on Electrical Properties of Ceramic Materials in VHF Band",
pages = "636-645",
url = "https://hdl.handle.net/21.15107/rcub_dais_6962"
}

Obradović, N.,& Đorđević, A.. (2019). Influence of Mechanical Activation on Electrical Properties of Ceramic Materials in VHF Band. in Proceedings of Papers – 6th International Conference on Electrical, Electronic and Computing Engineering, IcETRAN 2019, Silver Lake, Serbia, June 03 – 06, 2019 / Zbornik radova - 63. Konferencija za elektroniku, telekomunikacije, računarstvo, automatiku i nuklearnu tehniku, Srebrno jezero, 03 – 06. juna, 2019. godine
Belgrade : ETRAN., 636-645.
https://hdl.handle.net/21.15107/rcub_dais_6962

Obradović N, Đorđević A. Influence of Mechanical Activation on Electrical Properties of Ceramic Materials in VHF Band. in Proceedings of Papers – 6th International Conference on Electrical, Electronic and Computing Engineering, IcETRAN 2019, Silver Lake, Serbia, June 03 – 06, 2019 / Zbornik radova - 63. Konferencija za elektroniku, telekomunikacije, računarstvo, automatiku i nuklearnu tehniku, Srebrno jezero, 03 – 06. juna, 2019. godine. 2019;:636-645.
https://hdl.handle.net/21.15107/rcub_dais_6962 .

Obradović, Nina, Đorđević, Antonije, "Influence of Mechanical Activation on Electrical Properties of Ceramic Materials in VHF Band" in Proceedings of Papers – 6th International Conference on Electrical, Electronic and Computing Engineering, IcETRAN 2019, Silver Lake, Serbia, June 03 – 06, 2019 / Zbornik radova - 63. Konferencija za elektroniku, telekomunikacije, računarstvo, automatiku i nuklearnu tehniku, Srebrno jezero, 03 – 06. juna, 2019. godine (2019):636-645,
https://hdl.handle.net/21.15107/rcub_dais_6962 .

TY  - JOUR
AU  - Mitić, Vojislav V.
AU  - Lazović, Goran
AU  - Paunović, Vesna
AU  - Cvetković, Nenad
AU  - Jovanović, Dejan
AU  - Veljković, Sandra
AU  - Ranđelović, Branislav
AU  - Vlahović, Branislav
PY  - 2019
UR  - http://www.sciencedirect.com/science/article/pii/S0272884219300227
UR  - https://dais.sanu.ac.rs/123456789/5252
AB  - The world's perennial need for energy and microelectronic miniaturization brings with it a broad set of technological and scientific challenges. Materials characterized by precise microstructural architectures based on fractal analysis and ranging in size down to nano scale represent an important avenue for finding novel solutions. Deep materials structure hierarchies of this type open new possibilities in capacity according to the Heywang model, especially when extended by a fractals approach and intergranular relationships supported and recognized by their fractal nature. These developments are opening new frontiers in microelectronics miniaturization. They build on early fractal applications that were used as tools in miniaturization research and also provided application perspectives for diverse energy technologies. In other words, fractals, as a crucial concept of modern theoretical-experimental physics and materials sciences, are tightly linked to higher integration processes and microelectronics miniaturization. They also hold potential for meeting the energy exploitation challenge. In this research context, for the first time we experimentally and theoretically investigated the electrostatic field between the grains within fractal nature aspects. It is essentially a theoretical experiment based on samples of experimental microstructures imaged with SEM, as previously published in a number of other papers. We now take the research a step further by consolidating the experimental samples with respect to the predicted distribution of grains and pores within the sample mass. We make an original contribution by opening the frame of scale sizes with respect to the technical processes of consolidation. This lets us predict the constitutive elements of the microstructures – approximately equidistant grains and pores. In this paper we define in a practical manner the final target elements for experimental consolidation of real samples. It is the main bridge between a designed microstructure and related characteristics – for example, fractal dimensions and final properties of next-generation fractal microelectronics.
PB  - Elsevier
T2  - Ceramics International
T1  - Fractal frontiers in microelectronic ceramic materials
SP  - 9679
EP  - 9685
VL  - 45
DO  - 10.1016/j.ceramint.2019.01.020
UR  - https://hdl.handle.net/21.15107/rcub_dais_5252
ER  - 

@article{
author = "Mitić, Vojislav V. and Lazović, Goran and Paunović, Vesna and Cvetković, Nenad and Jovanović, Dejan and Veljković, Sandra and Ranđelović, Branislav and Vlahović, Branislav",
year = "2019",
abstract = "The world's perennial need for energy and microelectronic miniaturization brings with it a broad set of technological and scientific challenges. Materials characterized by precise microstructural architectures based on fractal analysis and ranging in size down to nano scale represent an important avenue for finding novel solutions. Deep materials structure hierarchies of this type open new possibilities in capacity according to the Heywang model, especially when extended by a fractals approach and intergranular relationships supported and recognized by their fractal nature. These developments are opening new frontiers in microelectronics miniaturization. They build on early fractal applications that were used as tools in miniaturization research and also provided application perspectives for diverse energy technologies. In other words, fractals, as a crucial concept of modern theoretical-experimental physics and materials sciences, are tightly linked to higher integration processes and microelectronics miniaturization. They also hold potential for meeting the energy exploitation challenge. In this research context, for the first time we experimentally and theoretically investigated the electrostatic field between the grains within fractal nature aspects. It is essentially a theoretical experiment based on samples of experimental microstructures imaged with SEM, as previously published in a number of other papers. We now take the research a step further by consolidating the experimental samples with respect to the predicted distribution of grains and pores within the sample mass. We make an original contribution by opening the frame of scale sizes with respect to the technical processes of consolidation. This lets us predict the constitutive elements of the microstructures – approximately equidistant grains and pores. In this paper we define in a practical manner the final target elements for experimental consolidation of real samples. It is the main bridge between a designed microstructure and related characteristics – for example, fractal dimensions and final properties of next-generation fractal microelectronics.",
publisher = "Elsevier",
journal = "Ceramics International",
title = "Fractal frontiers in microelectronic ceramic materials",
pages = "9679-9685",
volume = "45",
doi = "10.1016/j.ceramint.2019.01.020",
url = "https://hdl.handle.net/21.15107/rcub_dais_5252"
}

Mitić, V. V., Lazović, G., Paunović, V., Cvetković, N., Jovanović, D., Veljković, S., Ranđelović, B.,& Vlahović, B.. (2019). Fractal frontiers in microelectronic ceramic materials. in Ceramics International
Elsevier., 45, 9679-9685.
https://doi.org/10.1016/j.ceramint.2019.01.020
https://hdl.handle.net/21.15107/rcub_dais_5252

Mitić VV, Lazović G, Paunović V, Cvetković N, Jovanović D, Veljković S, Ranđelović B, Vlahović B. Fractal frontiers in microelectronic ceramic materials. in Ceramics International. 2019;45:9679-9685.
doi:10.1016/j.ceramint.2019.01.020
https://hdl.handle.net/21.15107/rcub_dais_5252 .

Mitić, Vojislav V., Lazović, Goran, Paunović, Vesna, Cvetković, Nenad, Jovanović, Dejan, Veljković, Sandra, Ranđelović, Branislav, Vlahović, Branislav, "Fractal frontiers in microelectronic ceramic materials" in Ceramics International, 45 (2019):9679-9685,
https://doi.org/10.1016/j.ceramint.2019.01.020 .,
https://hdl.handle.net/21.15107/rcub_dais_5252 .

TY  - JOUR
AU  - Terzić, Anja
AU  - Obradović, Nina
AU  - Kosanović, Darko
AU  - Stojanović, Jovica
AU  - Đorđević, Antonije
AU  - Andrić, Ljubiša
AU  - Pavlović, Vladimir B.
PY  - 2019
UR  - http://www.sciencedirect.com/science/article/pii/S0272884218329262
UR  - https://dais.sanu.ac.rs/123456789/4635
AB  - Steatite, as ceramic with composition predominantly resting on magnesium silicate, was produced from economic resources – talc, aluminosilicate clays, and either BaCO3 or feldspar as flux. Titanium dioxide was a doping agent. Four steatite mixtures were mechanically activated in a planetary ball mill for 30, 45 or 60 min, prior to the thermal treatment. Two-step sintering with initial phase set at 1350 °C and holding period conducted at 1250 °C was applied to initiate diffusion and prevent grain growth. Thereby, a high density ceramic material with low-porous submicron structure was acquired. The effects of TiO2 addition on densification, microstructure, and dielectric characteristics of steatites were monitored. The thermal stability of green mixtures was tested by differential thermal and thermogravimetric analyses. Changes in crystallinity and mineral phase composition were observed by the X-ray diffraction technique. Microstructural visualization with spatial arrangements of individual chemical elements on surface of the sintered ceramics was acquired by scanning electron microscopy accompanied with EDS mapping. In order to test the possibility of employment of the obtained steatites in insulation materials, electrical measurements were conducted by recording variations of the dielectric constant and loss tangent as a function of alternations in the mix-design and the mechanical activation period.
PB  - Elsevier
T2  - Ceramics International
T1  - Effects of mechanical-activation and TiO2 addition on the behavior of two-step sintered steatite ceramics
SP  - 3013
EP  - 3022
VL  - 45
IS  - 3
DO  - 10.1016/j.ceramint.2018.10.120
UR  - https://hdl.handle.net/21.15107/rcub_dais_4635
ER  - 

@article{
author = "Terzić, Anja and Obradović, Nina and Kosanović, Darko and Stojanović, Jovica and Đorđević, Antonije and Andrić, Ljubiša and Pavlović, Vladimir B.",
year = "2019",
abstract = "Steatite, as ceramic with composition predominantly resting on magnesium silicate, was produced from economic resources – talc, aluminosilicate clays, and either BaCO3 or feldspar as flux. Titanium dioxide was a doping agent. Four steatite mixtures were mechanically activated in a planetary ball mill for 30, 45 or 60 min, prior to the thermal treatment. Two-step sintering with initial phase set at 1350 °C and holding period conducted at 1250 °C was applied to initiate diffusion and prevent grain growth. Thereby, a high density ceramic material with low-porous submicron structure was acquired. The effects of TiO2 addition on densification, microstructure, and dielectric characteristics of steatites were monitored. The thermal stability of green mixtures was tested by differential thermal and thermogravimetric analyses. Changes in crystallinity and mineral phase composition were observed by the X-ray diffraction technique. Microstructural visualization with spatial arrangements of individual chemical elements on surface of the sintered ceramics was acquired by scanning electron microscopy accompanied with EDS mapping. In order to test the possibility of employment of the obtained steatites in insulation materials, electrical measurements were conducted by recording variations of the dielectric constant and loss tangent as a function of alternations in the mix-design and the mechanical activation period.",
publisher = "Elsevier",
journal = "Ceramics International",
title = "Effects of mechanical-activation and TiO2 addition on the behavior of two-step sintered steatite ceramics",
pages = "3013-3022",
volume = "45",
number = "3",
doi = "10.1016/j.ceramint.2018.10.120",
url = "https://hdl.handle.net/21.15107/rcub_dais_4635"
}

Terzić, A., Obradović, N., Kosanović, D., Stojanović, J., Đorđević, A., Andrić, L.,& Pavlović, V. B.. (2019). Effects of mechanical-activation and TiO2 addition on the behavior of two-step sintered steatite ceramics. in Ceramics International
Elsevier., 45(3), 3013-3022.
https://doi.org/10.1016/j.ceramint.2018.10.120
https://hdl.handle.net/21.15107/rcub_dais_4635

Terzić A, Obradović N, Kosanović D, Stojanović J, Đorđević A, Andrić L, Pavlović VB. Effects of mechanical-activation and TiO2 addition on the behavior of two-step sintered steatite ceramics. in Ceramics International. 2019;45(3):3013-3022.
doi:10.1016/j.ceramint.2018.10.120
https://hdl.handle.net/21.15107/rcub_dais_4635 .

Terzić, Anja, Obradović, Nina, Kosanović, Darko, Stojanović, Jovica, Đorđević, Antonije, Andrić, Ljubiša, Pavlović, Vladimir B., "Effects of mechanical-activation and TiO2 addition on the behavior of two-step sintered steatite ceramics" in Ceramics International, 45, no. 3 (2019):3013-3022,
https://doi.org/10.1016/j.ceramint.2018.10.120 .,
https://hdl.handle.net/21.15107/rcub_dais_4635 .

TY  - JOUR
AU  - Terzić, Anja
AU  - Obradović, Nina
AU  - Kosanović, Darko
AU  - Stojanović, Jovica
AU  - Đorđević, Antonije
AU  - Andrić, Ljubiša
AU  - Pavlović, Vladimir B.
PY  - 2019
UR  - http://www.sciencedirect.com/science/article/pii/S0272884218329262
UR  - https://dais.sanu.ac.rs/123456789/4645
AB  - Steatite, as ceramic with composition predominantly resting on magnesium silicate, was produced from economic resources – talc, aluminosilicate clays, and either BaCO3 or feldspar as flux. Titanium dioxide was a doping agent. Four steatite mixtures were mechanically activated in a planetary ball mill for 30, 45 or 60 min, prior to the thermal treatment. Two-step sintering with initial phase set at 1350 °C and holding period conducted at 1250 °C was applied to initiate diffusion and prevent grain growth. Thereby, a high density ceramic material with low-porous submicron structure was acquired. The effects of TiO2 addition on densification, microstructure, and dielectric characteristics of steatites were monitored. The thermal stability of green mixtures was tested by differential thermal and thermogravimetric analyses. Changes in crystallinity and mineral phase composition were observed by the X-ray diffraction technique. Microstructural visualization with spatial arrangements of individual chemical elements on surface of the sintered ceramics was acquired by scanning electron microscopy accompanied with EDS mapping. In order to test the possibility of employment of the obtained steatites in insulation materials, electrical measurements were conducted by recording variations of the dielectric constant and loss tangent as a function of alternations in the mix-design and the mechanical activation period.
PB  - Elsevier
T2  - Ceramics International
T1  - Effects of mechanical-activation and TiO2 addition on the behavior of two-step sintered steatite ceramics
SP  - 3013
EP  - 3022
VL  - 45
IS  - 3
DO  - 10.1016/j.ceramint.2018.10.120
UR  - https://hdl.handle.net/21.15107/rcub_dais_4645
ER  - 

@article{
author = "Terzić, Anja and Obradović, Nina and Kosanović, Darko and Stojanović, Jovica and Đorđević, Antonije and Andrić, Ljubiša and Pavlović, Vladimir B.",
year = "2019",
abstract = "Steatite, as ceramic with composition predominantly resting on magnesium silicate, was produced from economic resources – talc, aluminosilicate clays, and either BaCO3 or feldspar as flux. Titanium dioxide was a doping agent. Four steatite mixtures were mechanically activated in a planetary ball mill for 30, 45 or 60 min, prior to the thermal treatment. Two-step sintering with initial phase set at 1350 °C and holding period conducted at 1250 °C was applied to initiate diffusion and prevent grain growth. Thereby, a high density ceramic material with low-porous submicron structure was acquired. The effects of TiO2 addition on densification, microstructure, and dielectric characteristics of steatites were monitored. The thermal stability of green mixtures was tested by differential thermal and thermogravimetric analyses. Changes in crystallinity and mineral phase composition were observed by the X-ray diffraction technique. Microstructural visualization with spatial arrangements of individual chemical elements on surface of the sintered ceramics was acquired by scanning electron microscopy accompanied with EDS mapping. In order to test the possibility of employment of the obtained steatites in insulation materials, electrical measurements were conducted by recording variations of the dielectric constant and loss tangent as a function of alternations in the mix-design and the mechanical activation period.",
publisher = "Elsevier",
journal = "Ceramics International",
title = "Effects of mechanical-activation and TiO2 addition on the behavior of two-step sintered steatite ceramics",
pages = "3013-3022",
volume = "45",
number = "3",
doi = "10.1016/j.ceramint.2018.10.120",
url = "https://hdl.handle.net/21.15107/rcub_dais_4645"
}

Terzić, A., Obradović, N., Kosanović, D., Stojanović, J., Đorđević, A., Andrić, L.,& Pavlović, V. B.. (2019). Effects of mechanical-activation and TiO2 addition on the behavior of two-step sintered steatite ceramics. in Ceramics International
Elsevier., 45(3), 3013-3022.
https://doi.org/10.1016/j.ceramint.2018.10.120
https://hdl.handle.net/21.15107/rcub_dais_4645

Terzić A, Obradović N, Kosanović D, Stojanović J, Đorđević A, Andrić L, Pavlović VB. Effects of mechanical-activation and TiO2 addition on the behavior of two-step sintered steatite ceramics. in Ceramics International. 2019;45(3):3013-3022.
doi:10.1016/j.ceramint.2018.10.120
https://hdl.handle.net/21.15107/rcub_dais_4645 .

Terzić, Anja, Obradović, Nina, Kosanović, Darko, Stojanović, Jovica, Đorđević, Antonije, Andrić, Ljubiša, Pavlović, Vladimir B., "Effects of mechanical-activation and TiO2 addition on the behavior of two-step sintered steatite ceramics" in Ceramics International, 45, no. 3 (2019):3013-3022,
https://doi.org/10.1016/j.ceramint.2018.10.120 .,
https://hdl.handle.net/21.15107/rcub_dais_4645 .

TY  - JOUR
AU  - Vujančević, Jelena
AU  - Andričević, Pavao
AU  - Bjelajac, Anđelika
AU  - Đokić, Veljko
AU  - Popović, Maja
AU  - Rakočević, Zlatko
AU  - Horváth, Endre
AU  - Kollár, Márton
AU  - Náfrádi, Bálint
AU  - Schiller, Andreas
AU  - Domanski, Konrad
AU  - Forró, Laszlo
AU  - Pavlović, Vera P.
AU  - Janaćković, Đorđe
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/5084
AB  - Highly ordered, anodically grown TiO 2 nanotubes on titanium supports were annealed in ammonia atmosphere in order to incorporate nitrogen doping (≤2 at.%) in the titanium oxide lattice. FESEM micrographs revealed nanotubes with an average outer diameter of 101.5 ± 1.5 nm and an average wall thickness of about 13 nm. Anatase crystals were formed inside the tubes after annealing in ammonia atmosphere for 30 min. With further annealing, rutile peaks appeared due to the thermal oxidation of the foil and rise as the duration of heat treatment was increased. The concentration and chemical nature of nitrogen in the nanotube arrays can be correlated to the optical response of dry-pressed heterojunctions of doped TiO 2 /CH 3 NH 3 PbI 3 single crystals. The N-TiO 2 /perovskite heterojunction with the highest amount of interstitial nitrogen exhibited an improved photocurrent, indicating the importance of the semiconductor doping-based heterojunction optimization strategies to deliver competitive levels of halide perovskite-based optoelectronic devices to be envisioned for urban infrastructures. © 2019
PB  - Elsevier
T2  - Ceramics International
T1  - Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping
SP  - 10013
EP  - 10020
VL  - 45
IS  - 8
DO  - 10.1016/j.ceramint.2019.02.045
UR  - https://hdl.handle.net/21.15107/rcub_dais_5084
ER  - 

@article{
author = "Vujančević, Jelena and Andričević, Pavao and Bjelajac, Anđelika and Đokić, Veljko and Popović, Maja and Rakočević, Zlatko and Horváth, Endre and Kollár, Márton and Náfrádi, Bálint and Schiller, Andreas and Domanski, Konrad and Forró, Laszlo and Pavlović, Vera P. and Janaćković, Đorđe",
year = "2019",
abstract = "Highly ordered, anodically grown TiO 2 nanotubes on titanium supports were annealed in ammonia atmosphere in order to incorporate nitrogen doping (≤2 at.%) in the titanium oxide lattice. FESEM micrographs revealed nanotubes with an average outer diameter of 101.5 ± 1.5 nm and an average wall thickness of about 13 nm. Anatase crystals were formed inside the tubes after annealing in ammonia atmosphere for 30 min. With further annealing, rutile peaks appeared due to the thermal oxidation of the foil and rise as the duration of heat treatment was increased. The concentration and chemical nature of nitrogen in the nanotube arrays can be correlated to the optical response of dry-pressed heterojunctions of doped TiO 2 /CH 3 NH 3 PbI 3 single crystals. The N-TiO 2 /perovskite heterojunction with the highest amount of interstitial nitrogen exhibited an improved photocurrent, indicating the importance of the semiconductor doping-based heterojunction optimization strategies to deliver competitive levels of halide perovskite-based optoelectronic devices to be envisioned for urban infrastructures. © 2019",
publisher = "Elsevier",
journal = "Ceramics International",
title = "Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping",
pages = "10013-10020",
volume = "45",
number = "8",
doi = "10.1016/j.ceramint.2019.02.045",
url = "https://hdl.handle.net/21.15107/rcub_dais_5084"
}

Vujančević, J., Andričević, P., Bjelajac, A., Đokić, V., Popović, M., Rakočević, Z., Horváth, E., Kollár, M., Náfrádi, B., Schiller, A., Domanski, K., Forró, L., Pavlović, V. P.,& Janaćković, Đ.. (2019). Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping. in Ceramics International
Elsevier., 45(8), 10013-10020.
https://doi.org/10.1016/j.ceramint.2019.02.045
https://hdl.handle.net/21.15107/rcub_dais_5084

Vujančević J, Andričević P, Bjelajac A, Đokić V, Popović M, Rakočević Z, Horváth E, Kollár M, Náfrádi B, Schiller A, Domanski K, Forró L, Pavlović VP, Janaćković Đ. Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping. in Ceramics International. 2019;45(8):10013-10020.
doi:10.1016/j.ceramint.2019.02.045
https://hdl.handle.net/21.15107/rcub_dais_5084 .

Vujančević, Jelena, Andričević, Pavao, Bjelajac, Anđelika, Đokić, Veljko, Popović, Maja, Rakočević, Zlatko, Horváth, Endre, Kollár, Márton, Náfrádi, Bálint, Schiller, Andreas, Domanski, Konrad, Forró, Laszlo, Pavlović, Vera P., Janaćković, Đorđe, "Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping" in Ceramics International, 45, no. 8 (2019):10013-10020,
https://doi.org/10.1016/j.ceramint.2019.02.045 .,
https://hdl.handle.net/21.15107/rcub_dais_5084 .

TY  - JOUR
AU  - Vujančević, Jelena
AU  - Andričević, Pavao
AU  - Bjelajac, Anđelika
AU  - Đokić, Veljko
AU  - Popović, Maja
AU  - Rakočević, Zlatko
AU  - Horváth, Endre
AU  - Kollár, Márton
AU  - Náfrádi, Bálint
AU  - Schiller, Andreas
AU  - Domanski, Konrad
AU  - Forró, Laszlo
AU  - Pavlović, Vera P.
AU  - Janaćković, Đorđe
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/5765
AB  - Highly ordered, anodically grown TiO 2 nanotubes on titanium supports were annealed in ammonia atmosphere in order to incorporate nitrogen doping (≤2 at.%) in the titanium oxide lattice. FESEM micrographs revealed nanotubes with an average outer diameter of 101.5 ± 1.5 nm and an average wall thickness of about 13 nm. Anatase crystals were formed inside the tubes after annealing in ammonia atmosphere for 30 min. With further annealing, rutile peaks appeared due to the thermal oxidation of the foil and rise as the duration of heat treatment was increased. The concentration and chemical nature of nitrogen in the nanotube arrays can be correlated to the optical response of dry-pressed heterojunctions of doped TiO 2 /CH 3 NH 3 PbI 3 single crystals. The N-TiO 2 /perovskite heterojunction with the highest amount of interstitial nitrogen exhibited an improved photocurrent, indicating the importance of the semiconductor doping-based heterojunction optimization strategies to deliver competitive levels of halide perovskite-based optoelectronic devices to be envisioned for urban infrastructures. © 2019
PB  - Elsevier
T2  - Ceramics International
T1  - Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping
SP  - 10013
EP  - 10020
VL  - 45
IS  - 8
DO  - 10.1016/j.ceramint.2019.02.045
UR  - https://hdl.handle.net/21.15107/rcub_dais_5765
ER  - 

@article{
author = "Vujančević, Jelena and Andričević, Pavao and Bjelajac, Anđelika and Đokić, Veljko and Popović, Maja and Rakočević, Zlatko and Horváth, Endre and Kollár, Márton and Náfrádi, Bálint and Schiller, Andreas and Domanski, Konrad and Forró, Laszlo and Pavlović, Vera P. and Janaćković, Đorđe",
year = "2019",
abstract = "Highly ordered, anodically grown TiO 2 nanotubes on titanium supports were annealed in ammonia atmosphere in order to incorporate nitrogen doping (≤2 at.%) in the titanium oxide lattice. FESEM micrographs revealed nanotubes with an average outer diameter of 101.5 ± 1.5 nm and an average wall thickness of about 13 nm. Anatase crystals were formed inside the tubes after annealing in ammonia atmosphere for 30 min. With further annealing, rutile peaks appeared due to the thermal oxidation of the foil and rise as the duration of heat treatment was increased. The concentration and chemical nature of nitrogen in the nanotube arrays can be correlated to the optical response of dry-pressed heterojunctions of doped TiO 2 /CH 3 NH 3 PbI 3 single crystals. The N-TiO 2 /perovskite heterojunction with the highest amount of interstitial nitrogen exhibited an improved photocurrent, indicating the importance of the semiconductor doping-based heterojunction optimization strategies to deliver competitive levels of halide perovskite-based optoelectronic devices to be envisioned for urban infrastructures. © 2019",
publisher = "Elsevier",
journal = "Ceramics International",
title = "Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping",
pages = "10013-10020",
volume = "45",
number = "8",
doi = "10.1016/j.ceramint.2019.02.045",
url = "https://hdl.handle.net/21.15107/rcub_dais_5765"
}

Vujančević, J., Andričević, P., Bjelajac, A., Đokić, V., Popović, M., Rakočević, Z., Horváth, E., Kollár, M., Náfrádi, B., Schiller, A., Domanski, K., Forró, L., Pavlović, V. P.,& Janaćković, Đ.. (2019). Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping. in Ceramics International
Elsevier., 45(8), 10013-10020.
https://doi.org/10.1016/j.ceramint.2019.02.045
https://hdl.handle.net/21.15107/rcub_dais_5765

Vujančević J, Andričević P, Bjelajac A, Đokić V, Popović M, Rakočević Z, Horváth E, Kollár M, Náfrádi B, Schiller A, Domanski K, Forró L, Pavlović VP, Janaćković Đ. Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping. in Ceramics International. 2019;45(8):10013-10020.
doi:10.1016/j.ceramint.2019.02.045
https://hdl.handle.net/21.15107/rcub_dais_5765 .

Vujančević, Jelena, Andričević, Pavao, Bjelajac, Anđelika, Đokić, Veljko, Popović, Maja, Rakočević, Zlatko, Horváth, Endre, Kollár, Márton, Náfrádi, Bálint, Schiller, Andreas, Domanski, Konrad, Forró, Laszlo, Pavlović, Vera P., Janaćković, Đorđe, "Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping" in Ceramics International, 45, no. 8 (2019):10013-10020,
https://doi.org/10.1016/j.ceramint.2019.02.045 .,
https://hdl.handle.net/21.15107/rcub_dais_5765 .

TY  - DATA
AU  - Vujančević, Jelena
AU  - Andričević, Pavao
AU  - Bjelajac, Anđelika
AU  - Đokić, Veljko
AU  - Popović, Maja
AU  - Rakočević, Zlatko
AU  - Horváth, Endre
AU  - Kollár, Márton
AU  - Náfrádi, Bálint
AU  - Schiller, Andreas
AU  - Domanski, Konrad
AU  - Forró, Laszlo
AU  - Pavlović, Vera P.
AU  - Janaćković, Đorđe
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/5969
AB  - Table S1. Reported methods for nitrogen doping of anodized TiO2 nanotube arrays; Figure S1. SEM images and statistical distributions of outer diameters obtained by analyzing SEM micrographs of 100 nanotubes; Table S2. Average morphology parameters for TiO2-undoped, TiO2-N30, TiO2-N60 and TiO2-N90 samples; Table S3. Average crystals size for TiO2-undoped, TiO2-N30, TiO2-N60 and TiO2-N90 samples; Figure S2. Deconvoluted XPS spectra of N 1s core level of Ti foil (black line-experimental, grey line-background, magenta line-envelope); Table S4. Peak positions and atomic percentages of N1s core levels for TiO2-undoped, TiO2-N30, TiO2-N60 and TiO2-N90 samples; Table S5. Positions and atomic percentages of Ti 2p3/2 and O1s core peaks for TiO2-undoped, TiO2-N30, TiO2-N60 and TiO2-N90 samples; Figure S3. The time evolution of the current during the preconditioning of the TiO2/perovskite sample at a bias voltage of 100 V for 75 sec. Dashed line is the logarithmic fit of the base line of the current time evolution; Figure S4. Ideality factor for TiO2-undoped, TiO2-N30, TiO2-N60 and TiO2-N90 samples
T2  - Ceramics International
T1  - Supporting information for the article: Vujančević, J., Andričević, P., Bjelajac, A., Đokić, V., Popović, M., Rakočević, Z., Horváth, E., Kollár, M., Náfrádi, B., Schiller, A., Domanski, K., Forró, L., Pavlović, V., Janaćković, Đ., 2019. Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping. Ceramics International 45, 10013–10020. https://doi.org/10.1016/j.ceramint.2019.02.045
UR  - https://hdl.handle.net/21.15107/rcub_dais_5969
ER  - 

@misc{
author = "Vujančević, Jelena and Andričević, Pavao and Bjelajac, Anđelika and Đokić, Veljko and Popović, Maja and Rakočević, Zlatko and Horváth, Endre and Kollár, Márton and Náfrádi, Bálint and Schiller, Andreas and Domanski, Konrad and Forró, Laszlo and Pavlović, Vera P. and Janaćković, Đorđe",
year = "2019",
abstract = "Table S1. Reported methods for nitrogen doping of anodized TiO2 nanotube arrays; Figure S1. SEM images and statistical distributions of outer diameters obtained by analyzing SEM micrographs of 100 nanotubes; Table S2. Average morphology parameters for TiO2-undoped, TiO2-N30, TiO2-N60 and TiO2-N90 samples; Table S3. Average crystals size for TiO2-undoped, TiO2-N30, TiO2-N60 and TiO2-N90 samples; Figure S2. Deconvoluted XPS spectra of N 1s core level of Ti foil (black line-experimental, grey line-background, magenta line-envelope); Table S4. Peak positions and atomic percentages of N1s core levels for TiO2-undoped, TiO2-N30, TiO2-N60 and TiO2-N90 samples; Table S5. Positions and atomic percentages of Ti 2p3/2 and O1s core peaks for TiO2-undoped, TiO2-N30, TiO2-N60 and TiO2-N90 samples; Figure S3. The time evolution of the current during the preconditioning of the TiO2/perovskite sample at a bias voltage of 100 V for 75 sec. Dashed line is the logarithmic fit of the base line of the current time evolution; Figure S4. Ideality factor for TiO2-undoped, TiO2-N30, TiO2-N60 and TiO2-N90 samples",
journal = "Ceramics International",
title = "Supporting information for the article: Vujančević, J., Andričević, P., Bjelajac, A., Đokić, V., Popović, M., Rakočević, Z., Horváth, E., Kollár, M., Náfrádi, B., Schiller, A., Domanski, K., Forró, L., Pavlović, V., Janaćković, Đ., 2019. Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping. Ceramics International 45, 10013–10020. https://doi.org/10.1016/j.ceramint.2019.02.045",
url = "https://hdl.handle.net/21.15107/rcub_dais_5969"
}

Vujančević, J., Andričević, P., Bjelajac, A., Đokić, V., Popović, M., Rakočević, Z., Horváth, E., Kollár, M., Náfrádi, B., Schiller, A., Domanski, K., Forró, L., Pavlović, V. P.,& Janaćković, Đ.. (2019). Supporting information for the article: Vujančević, J., Andričević, P., Bjelajac, A., Đokić, V., Popović, M., Rakočević, Z., Horváth, E., Kollár, M., Náfrádi, B., Schiller, A., Domanski, K., Forró, L., Pavlović, V., Janaćković, Đ., 2019. Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping. Ceramics International 45, 10013–10020. https://doi.org/10.1016/j.ceramint.2019.02.045. in Ceramics International.
https://hdl.handle.net/21.15107/rcub_dais_5969

Vujančević J, Andričević P, Bjelajac A, Đokić V, Popović M, Rakočević Z, Horváth E, Kollár M, Náfrádi B, Schiller A, Domanski K, Forró L, Pavlović VP, Janaćković Đ. Supporting information for the article: Vujančević, J., Andričević, P., Bjelajac, A., Đokić, V., Popović, M., Rakočević, Z., Horváth, E., Kollár, M., Náfrádi, B., Schiller, A., Domanski, K., Forró, L., Pavlović, V., Janaćković, Đ., 2019. Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping. Ceramics International 45, 10013–10020. https://doi.org/10.1016/j.ceramint.2019.02.045. in Ceramics International. 2019;.
https://hdl.handle.net/21.15107/rcub_dais_5969 .

Vujančević, Jelena, Andričević, Pavao, Bjelajac, Anđelika, Đokić, Veljko, Popović, Maja, Rakočević, Zlatko, Horváth, Endre, Kollár, Márton, Náfrádi, Bálint, Schiller, Andreas, Domanski, Konrad, Forró, Laszlo, Pavlović, Vera P., Janaćković, Đorđe, "Supporting information for the article: Vujančević, J., Andričević, P., Bjelajac, A., Đokić, V., Popović, M., Rakočević, Z., Horváth, E., Kollár, M., Náfrádi, B., Schiller, A., Domanski, K., Forró, L., Pavlović, V., Janaćković, Đ., 2019. Dry-pressed anodized titania nanotube/CH3NH3PbI3 single crystal heterojunctions: The beneficial role of N doping. Ceramics International 45, 10013–10020. https://doi.org/10.1016/j.ceramint.2019.02.045" in Ceramics International (2019),
https://hdl.handle.net/21.15107/rcub_dais_5969 .