TY  - JOUR
AU  - Popović, Maja
AU  - Novaković, Mirjana
AU  - Vaňa, Dušan
AU  - Ronning, Carsten
AU  - Jugović, Dragana
AU  - Rajić, Vladimir
AU  - Noga, Pavol
PY  - 2023
UR  - https://dais.sanu.ac.rs/123456789/14289
AB  - Titanium nitride (TiN) is an attractive alternative for modern and future photonic applications, as its optical properties can be engineered over a wide spectral range. In this study, we have used sequential implantation of gold and silver ions with varying ion fluence, as well as subsequent annealing, in order to modify the optical and plasmonic properties of TiN thin films and correlated this to their structural properties. Our investigations show that the columnar structure of the TiN films is partially destroyed upon implantation, but metallic Au and Ag nanoparticles are formed. The irradiation further induces a reduction of the lattice constant as well as changes the TiN stoichiometry and grain size. From the optical point of view, the implanted films possess less metallicity with increasing Ag fluence and losses several times lower than the as-deposited film, which can be correlated with the deficiency of nitrogen and additional defects. Subsequent annealing partially recovered the destroyed columnar structure, and the films become more metallic where the optical losses are much smaller in comparison to the as-implanted situation, being comparable to those of pure Au and Ag. In this way, by varying the implantation fluence of silver ions properly while keeping the gold fluence constant, we were able to optimize experimental parameters in such a way to ensure the formation of TiN with desirable optical performances.
PB  - Elsevier BV
T2  - Optical Materials
T1  - Structure-dependent optical properties of Au/Ag irradiated TiN thin films
SP  - 113684
VL  - 138
DO  - 10.1016/j.optmat.2023.113684
UR  - https://hdl.handle.net/21.15107/rcub_dais_14289
ER  - 

@article{
author = "Popović, Maja and Novaković, Mirjana and Vaňa, Dušan and Ronning, Carsten and Jugović, Dragana and Rajić, Vladimir and Noga, Pavol",
year = "2023",
abstract = "Titanium nitride (TiN) is an attractive alternative for modern and future photonic applications, as its optical properties can be engineered over a wide spectral range. In this study, we have used sequential implantation of gold and silver ions with varying ion fluence, as well as subsequent annealing, in order to modify the optical and plasmonic properties of TiN thin films and correlated this to their structural properties. Our investigations show that the columnar structure of the TiN films is partially destroyed upon implantation, but metallic Au and Ag nanoparticles are formed. The irradiation further induces a reduction of the lattice constant as well as changes the TiN stoichiometry and grain size. From the optical point of view, the implanted films possess less metallicity with increasing Ag fluence and losses several times lower than the as-deposited film, which can be correlated with the deficiency of nitrogen and additional defects. Subsequent annealing partially recovered the destroyed columnar structure, and the films become more metallic where the optical losses are much smaller in comparison to the as-implanted situation, being comparable to those of pure Au and Ag. In this way, by varying the implantation fluence of silver ions properly while keeping the gold fluence constant, we were able to optimize experimental parameters in such a way to ensure the formation of TiN with desirable optical performances.",
publisher = "Elsevier BV",
journal = "Optical Materials",
title = "Structure-dependent optical properties of Au/Ag irradiated TiN thin films",
pages = "113684",
volume = "138",
doi = "10.1016/j.optmat.2023.113684",
url = "https://hdl.handle.net/21.15107/rcub_dais_14289"
}

Popović, M., Novaković, M., Vaňa, D., Ronning, C., Jugović, D., Rajić, V.,& Noga, P.. (2023). Structure-dependent optical properties of Au/Ag irradiated TiN thin films. in Optical Materials
Elsevier BV., 138, 113684.
https://doi.org/10.1016/j.optmat.2023.113684
https://hdl.handle.net/21.15107/rcub_dais_14289

Popović M, Novaković M, Vaňa D, Ronning C, Jugović D, Rajić V, Noga P. Structure-dependent optical properties of Au/Ag irradiated TiN thin films. in Optical Materials. 2023;138:113684.
doi:10.1016/j.optmat.2023.113684
https://hdl.handle.net/21.15107/rcub_dais_14289 .

Popović, Maja, Novaković, Mirjana, Vaňa, Dušan, Ronning, Carsten, Jugović, Dragana, Rajić, Vladimir, Noga, Pavol, "Structure-dependent optical properties of Au/Ag irradiated TiN thin films" in Optical Materials, 138 (2023):113684,
https://doi.org/10.1016/j.optmat.2023.113684 .,
https://hdl.handle.net/21.15107/rcub_dais_14289 .

TY  - JOUR
AU  - Rajić, Vladimir
AU  - Stojković Simatović, Ivana
AU  - Veselinović, Ljiljana
AU  - Belošević Čavor, Jelena
AU  - Novaković, Mirjana
AU  - Popović, Maja
AU  - Škapin, Srečo Davor
AU  - Mojović, Miloš
AU  - Stojadinović, Stevan
AU  - Rac, Vladislav
AU  - Janković Častvan, Ivona
AU  - Marković, Smilja
PY  - 2020
UR  - https://pubs.rsc.org/en/content/articlelanding/2020/cp/d0cp03377d
UR  - https://dais.sanu.ac.rs/123456789/9543
AB  - Eco-friendly and rapid microwave processing of a precipitate was used to produce Fe-doped zinc oxide (Zn1−xFexO, x = 0, 0.05, 0.1, 0.15 and 0.20; ZnO:Fe) nanoparticles, which were tested as catalysts toward the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in a moderately alkaline solution. The phase composition, crystal structure, morphology, textural properties, surface chemistry, optical properties and band structure were examined to comprehend the influence of Zn2+ partial substitution with Fe3+ on the catalytic activity of ZnO:Fe. Linear sweep voltammetry showed an improved catalytic activity of ZnO:5Fe toward the ORR, compared to pure ZnO, while with increased amounts of the Fe-dopant the activity decreased. The improvement was suggested by a more positive onset potential (0.394 V vs. RHE), current density (0.231 mA cm−2 at 0.150 V vs. RHE), and faster kinetics (Tafel slope, b = 248 mV dec−1), and it may be due to the synergistic effect of (1) a sufficient amount of surface oxygen vacancies, and (2) a certain amount of plate-like particles composed of crystallites with well developed (0001) and (000) facets. Quite the contrary, the OER study showed that the introduction of Fe3+ ions into the ZnO crystal structure resulted in enhanced catalytic activity of all ZnO:Fe samples, compared to pure ZnO, probably due to the modified binding energy and an optimized band structure. With the maximal current density of 1.066 mA cm−2 at 2.216 V vs. RHE, an onset potential of 1.856 V vs. RHE, and the smallest potential difference between the OER and ORR (ΔE = 1.58 V), ZnO:10Fe may be considered a promising bifunctional catalyst toward the OER/ORR in moderately alkaline solution. This study demonstrates that the electrocatalytic activity of ZnO:Fe strongly depends on the defect chemistry and consequently the band structure. Along with providing fundamental insight into the electrocatalytic activity of ZnO:Fe, the study also indicates an optimal stoichiometry for enhanced bifunctional activity toward the OER/ORR, compared to pure ZnO.
PB  - Royal Society of Chemistry
T2  - Physical Chemistry Chemical Physics
T1  - Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry
SP  - 22078
EP  - 22095
VL  - 22
IS  - 38
DO  - 10.1039/D0CP03377D
UR  - https://hdl.handle.net/21.15107/rcub_dais_9543
ER  - 

@article{
author = "Rajić, Vladimir and Stojković Simatović, Ivana and Veselinović, Ljiljana and Belošević Čavor, Jelena and Novaković, Mirjana and Popović, Maja and Škapin, Srečo Davor and Mojović, Miloš and Stojadinović, Stevan and Rac, Vladislav and Janković Častvan, Ivona and Marković, Smilja",
year = "2020",
abstract = "Eco-friendly and rapid microwave processing of a precipitate was used to produce Fe-doped zinc oxide (Zn1−xFexO, x = 0, 0.05, 0.1, 0.15 and 0.20; ZnO:Fe) nanoparticles, which were tested as catalysts toward the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in a moderately alkaline solution. The phase composition, crystal structure, morphology, textural properties, surface chemistry, optical properties and band structure were examined to comprehend the influence of Zn2+ partial substitution with Fe3+ on the catalytic activity of ZnO:Fe. Linear sweep voltammetry showed an improved catalytic activity of ZnO:5Fe toward the ORR, compared to pure ZnO, while with increased amounts of the Fe-dopant the activity decreased. The improvement was suggested by a more positive onset potential (0.394 V vs. RHE), current density (0.231 mA cm−2 at 0.150 V vs. RHE), and faster kinetics (Tafel slope, b = 248 mV dec−1), and it may be due to the synergistic effect of (1) a sufficient amount of surface oxygen vacancies, and (2) a certain amount of plate-like particles composed of crystallites with well developed (0001) and (000) facets. Quite the contrary, the OER study showed that the introduction of Fe3+ ions into the ZnO crystal structure resulted in enhanced catalytic activity of all ZnO:Fe samples, compared to pure ZnO, probably due to the modified binding energy and an optimized band structure. With the maximal current density of 1.066 mA cm−2 at 2.216 V vs. RHE, an onset potential of 1.856 V vs. RHE, and the smallest potential difference between the OER and ORR (ΔE = 1.58 V), ZnO:10Fe may be considered a promising bifunctional catalyst toward the OER/ORR in moderately alkaline solution. This study demonstrates that the electrocatalytic activity of ZnO:Fe strongly depends on the defect chemistry and consequently the band structure. Along with providing fundamental insight into the electrocatalytic activity of ZnO:Fe, the study also indicates an optimal stoichiometry for enhanced bifunctional activity toward the OER/ORR, compared to pure ZnO.",
publisher = "Royal Society of Chemistry",
journal = "Physical Chemistry Chemical Physics",
title = "Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry",
pages = "22078-22095",
volume = "22",
number = "38",
doi = "10.1039/D0CP03377D",
url = "https://hdl.handle.net/21.15107/rcub_dais_9543"
}

Rajić, V., Stojković Simatović, I., Veselinović, L., Belošević Čavor, J., Novaković, M., Popović, M., Škapin, S. D., Mojović, M., Stojadinović, S., Rac, V., Janković Častvan, I.,& Marković, S.. (2020). Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry. in Physical Chemistry Chemical Physics
Royal Society of Chemistry., 22(38), 22078-22095.
https://doi.org/10.1039/D0CP03377D
https://hdl.handle.net/21.15107/rcub_dais_9543

Rajić V, Stojković Simatović I, Veselinović L, Belošević Čavor J, Novaković M, Popović M, Škapin SD, Mojović M, Stojadinović S, Rac V, Janković Častvan I, Marković S. Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry. in Physical Chemistry Chemical Physics. 2020;22(38):22078-22095.
doi:10.1039/D0CP03377D
https://hdl.handle.net/21.15107/rcub_dais_9543 .

Rajić, Vladimir, Stojković Simatović, Ivana, Veselinović, Ljiljana, Belošević Čavor, Jelena, Novaković, Mirjana, Popović, Maja, Škapin, Srečo Davor, Mojović, Miloš, Stojadinović, Stevan, Rac, Vladislav, Janković Častvan, Ivona, Marković, Smilja, "Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry" in Physical Chemistry Chemical Physics, 22, no. 38 (2020):22078-22095,
https://doi.org/10.1039/D0CP03377D .,
https://hdl.handle.net/21.15107/rcub_dais_9543 .

TY  - JOUR
AU  - Rajić, Vladimir
AU  - Stojković Simatović, Ivana
AU  - Veselinović, Ljiljana
AU  - Belošević Čavor, Jelena
AU  - Novaković, Mirjana
AU  - Popović, Maja
AU  - Škapin, Srečo Davor
AU  - Mojović, Miloš
AU  - Stojadinović, Stevan
AU  - Rac, Vladislav
AU  - Janković Častvan, Ivona
AU  - Marković, Smilja
PY  - 2020
UR  - https://pubs.rsc.org/en/content/articlelanding/2020/cp/d0cp03377d
UR  - https://dais.sanu.ac.rs/123456789/9544
AB  - Eco-friendly and rapid microwave processing of a precipitate was used to produce Fe-doped zinc oxide (Zn1−xFexO, x = 0, 0.05, 0.1, 0.15 and 0.20; ZnO:Fe) nanoparticles, which were tested as catalysts toward the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in a moderately alkaline solution. The phase composition, crystal structure, morphology, textural properties, surface chemistry, optical properties and band structure were examined to comprehend the influence of Zn2+ partial substitution with Fe3+ on the catalytic activity of ZnO:Fe. Linear sweep voltammetry showed an improved catalytic activity of ZnO:5Fe toward the ORR, compared to pure ZnO, while with increased amounts of the Fe-dopant the activity decreased. The improvement was suggested by a more positive onset potential (0.394 V vs. RHE), current density (0.231 mA cm−2 at 0.150 V vs. RHE), and faster kinetics (Tafel slope, b = 248 mV dec−1), and it may be due to the synergistic effect of (1) a sufficient amount of surface oxygen vacancies, and (2) a certain amount of plate-like particles composed of crystallites with well developed (0001) and (000) facets. Quite the contrary, the OER study showed that the introduction of Fe3+ ions into the ZnO crystal structure resulted in enhanced catalytic activity of all ZnO:Fe samples, compared to pure ZnO, probably due to the modified binding energy and an optimized band structure. With the maximal current density of 1.066 mA cm−2 at 2.216 V vs. RHE, an onset potential of 1.856 V vs. RHE, and the smallest potential difference between the OER and ORR (ΔE = 1.58 V), ZnO:10Fe may be considered a promising bifunctional catalyst toward the OER/ORR in moderately alkaline solution. This study demonstrates that the electrocatalytic activity of ZnO:Fe strongly depends on the defect chemistry and consequently the band structure. Along with providing fundamental insight into the electrocatalytic activity of ZnO:Fe, the study also indicates an optimal stoichiometry for enhanced bifunctional activity toward the OER/ORR, compared to pure ZnO.
PB  - Royal Society of Chemistry
T2  - Physical Chemistry Chemical Physics
T1  - Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry
SP  - 22078
EP  - 22095
VL  - 22
IS  - 38
DO  - 10.1039/D0CP03377D
UR  - https://hdl.handle.net/21.15107/rcub_dais_9544
ER  - 

@article{
author = "Rajić, Vladimir and Stojković Simatović, Ivana and Veselinović, Ljiljana and Belošević Čavor, Jelena and Novaković, Mirjana and Popović, Maja and Škapin, Srečo Davor and Mojović, Miloš and Stojadinović, Stevan and Rac, Vladislav and Janković Častvan, Ivona and Marković, Smilja",
year = "2020",
abstract = "Eco-friendly and rapid microwave processing of a precipitate was used to produce Fe-doped zinc oxide (Zn1−xFexO, x = 0, 0.05, 0.1, 0.15 and 0.20; ZnO:Fe) nanoparticles, which were tested as catalysts toward the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in a moderately alkaline solution. The phase composition, crystal structure, morphology, textural properties, surface chemistry, optical properties and band structure were examined to comprehend the influence of Zn2+ partial substitution with Fe3+ on the catalytic activity of ZnO:Fe. Linear sweep voltammetry showed an improved catalytic activity of ZnO:5Fe toward the ORR, compared to pure ZnO, while with increased amounts of the Fe-dopant the activity decreased. The improvement was suggested by a more positive onset potential (0.394 V vs. RHE), current density (0.231 mA cm−2 at 0.150 V vs. RHE), and faster kinetics (Tafel slope, b = 248 mV dec−1), and it may be due to the synergistic effect of (1) a sufficient amount of surface oxygen vacancies, and (2) a certain amount of plate-like particles composed of crystallites with well developed (0001) and (000) facets. Quite the contrary, the OER study showed that the introduction of Fe3+ ions into the ZnO crystal structure resulted in enhanced catalytic activity of all ZnO:Fe samples, compared to pure ZnO, probably due to the modified binding energy and an optimized band structure. With the maximal current density of 1.066 mA cm−2 at 2.216 V vs. RHE, an onset potential of 1.856 V vs. RHE, and the smallest potential difference between the OER and ORR (ΔE = 1.58 V), ZnO:10Fe may be considered a promising bifunctional catalyst toward the OER/ORR in moderately alkaline solution. This study demonstrates that the electrocatalytic activity of ZnO:Fe strongly depends on the defect chemistry and consequently the band structure. Along with providing fundamental insight into the electrocatalytic activity of ZnO:Fe, the study also indicates an optimal stoichiometry for enhanced bifunctional activity toward the OER/ORR, compared to pure ZnO.",
publisher = "Royal Society of Chemistry",
journal = "Physical Chemistry Chemical Physics",
title = "Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry",
pages = "22078-22095",
volume = "22",
number = "38",
doi = "10.1039/D0CP03377D",
url = "https://hdl.handle.net/21.15107/rcub_dais_9544"
}

Rajić, V., Stojković Simatović, I., Veselinović, L., Belošević Čavor, J., Novaković, M., Popović, M., Škapin, S. D., Mojović, M., Stojadinović, S., Rac, V., Janković Častvan, I.,& Marković, S.. (2020). Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry. in Physical Chemistry Chemical Physics
Royal Society of Chemistry., 22(38), 22078-22095.
https://doi.org/10.1039/D0CP03377D
https://hdl.handle.net/21.15107/rcub_dais_9544

Rajić V, Stojković Simatović I, Veselinović L, Belošević Čavor J, Novaković M, Popović M, Škapin SD, Mojović M, Stojadinović S, Rac V, Janković Častvan I, Marković S. Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry. in Physical Chemistry Chemical Physics. 2020;22(38):22078-22095.
doi:10.1039/D0CP03377D
https://hdl.handle.net/21.15107/rcub_dais_9544 .

Rajić, Vladimir, Stojković Simatović, Ivana, Veselinović, Ljiljana, Belošević Čavor, Jelena, Novaković, Mirjana, Popović, Maja, Škapin, Srečo Davor, Mojović, Miloš, Stojadinović, Stevan, Rac, Vladislav, Janković Častvan, Ivona, Marković, Smilja, "Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry" in Physical Chemistry Chemical Physics, 22, no. 38 (2020):22078-22095,
https://doi.org/10.1039/D0CP03377D .,
https://hdl.handle.net/21.15107/rcub_dais_9544 .

TY  - CONF
AU  - Rakočević, Lazar
AU  - Potočnik, Jelena
AU  - Novaković, Mirjana
AU  - Jugović, Dragana
AU  - Stojković Simatović, Ivana
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/6972
AB  - The lithium-ion batteries are the most commonly used for energy storage in portable devices. Since lithium is relatively rare on earth but rapidly consumed, it is necessary to find an adequate replacement. Owing to the similar chemical properties of sodium and lithium, but much higher availability, sodium ion batteries are one of the best candidates to replace lithium-ion batteries. A variety of materials such as manganese oxide, vanadium oxide or phosphate can be used as an electrode material (anode and cathode) in sodium ion batteries due to the high ability of intercalation of sodium. In this work, NaxMnO2 powder was synthesized by glycine nitrate method. The precursor powder was annealed for four hours at different temperatures: 800, 850, 900 and 950 °C. The characterization of the obtained materials was carried out using following methods: X-ray diffraction (XRD), scanning electron spectroscopy with energy dispersive X-ray spectroscopy (SEM/EDS) and transmission electron spectroscopy with energy dispersive Xray spectroscopy (TEM/EDS). Electrochemical properties were studied using cyclic voltammetry and chronopotentiometry in an aqueous solution of NaNO3. The layer structured Na0.7MnO2.05 with sheet-like morphology and Na0.4MnO2 with 3-D tunnel structure and rod-like morphology was obtained at 800 oC and 900 oC respectively. Na0.44MnO2 with rod-like morphology was annealed at 900 and 950 oC. 3D-tunnel structure Na0.44MnO2 obtained at 900 oC showed the best electrochemical behaviour in aqueous NaNO3 solution.
PB  - Belgrade : Institute of Technical Sciences of SASA
C3  - Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia
T1  - Synthesis temperature influence on the structure, morphology and electrochemical performance of NaxMnO2 as cathode materials for sodium-ion rechearchable batteries
SP  - 59
EP  - 59
UR  - https://hdl.handle.net/21.15107/rcub_dais_6972
ER  - 

@conference{
author = "Rakočević, Lazar and Potočnik, Jelena and Novaković, Mirjana and Jugović, Dragana and Stojković Simatović, Ivana",
year = "2019",
abstract = "The lithium-ion batteries are the most commonly used for energy storage in portable devices. Since lithium is relatively rare on earth but rapidly consumed, it is necessary to find an adequate replacement. Owing to the similar chemical properties of sodium and lithium, but much higher availability, sodium ion batteries are one of the best candidates to replace lithium-ion batteries. A variety of materials such as manganese oxide, vanadium oxide or phosphate can be used as an electrode material (anode and cathode) in sodium ion batteries due to the high ability of intercalation of sodium. In this work, NaxMnO2 powder was synthesized by glycine nitrate method. The precursor powder was annealed for four hours at different temperatures: 800, 850, 900 and 950 °C. The characterization of the obtained materials was carried out using following methods: X-ray diffraction (XRD), scanning electron spectroscopy with energy dispersive X-ray spectroscopy (SEM/EDS) and transmission electron spectroscopy with energy dispersive Xray spectroscopy (TEM/EDS). Electrochemical properties were studied using cyclic voltammetry and chronopotentiometry in an aqueous solution of NaNO3. The layer structured Na0.7MnO2.05 with sheet-like morphology and Na0.4MnO2 with 3-D tunnel structure and rod-like morphology was obtained at 800 oC and 900 oC respectively. Na0.44MnO2 with rod-like morphology was annealed at 900 and 950 oC. 3D-tunnel structure Na0.44MnO2 obtained at 900 oC showed the best electrochemical behaviour in aqueous NaNO3 solution.",
publisher = "Belgrade : Institute of Technical Sciences of SASA",
journal = "Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia",
title = "Synthesis temperature influence on the structure, morphology and electrochemical performance of NaxMnO2 as cathode materials for sodium-ion rechearchable batteries",
pages = "59-59",
url = "https://hdl.handle.net/21.15107/rcub_dais_6972"
}

Rakočević, L., Potočnik, J., Novaković, M., Jugović, D.,& Stojković Simatović, I.. (2019). Synthesis temperature influence on the structure, morphology and electrochemical performance of NaxMnO2 as cathode materials for sodium-ion rechearchable batteries. in Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia
Belgrade : Institute of Technical Sciences of SASA., 59-59.
https://hdl.handle.net/21.15107/rcub_dais_6972

Rakočević L, Potočnik J, Novaković M, Jugović D, Stojković Simatović I. Synthesis temperature influence on the structure, morphology and electrochemical performance of NaxMnO2 as cathode materials for sodium-ion rechearchable batteries. in Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia. 2019;:59-59.
https://hdl.handle.net/21.15107/rcub_dais_6972 .

Rakočević, Lazar, Potočnik, Jelena, Novaković, Mirjana, Jugović, Dragana, Stojković Simatović, Ivana, "Synthesis temperature influence on the structure, morphology and electrochemical performance of NaxMnO2 as cathode materials for sodium-ion rechearchable batteries" in Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia (2019):59-59,
https://hdl.handle.net/21.15107/rcub_dais_6972 .

TY  - CONF
AU  - Marković, Smilja
AU  - Rajić, Vladimir B.
AU  - Stojković Simatović, Ivana
AU  - Veselinović, Ljiljana
AU  - Belošević Čavor, Jelena
AU  - Ivanovski, Valentin N.
AU  - Novaković, Mirjana
AU  - Škapin, Srečo Davor
AU  - Stojadinović, Stevan
AU  - Rac, Vladislav
AU  - Uskoković, Dragan
PY  - 2019
UR  - https://dais.sanu.ac.rs/123456789/6677
AB  - Even has been under study since 1935, zinc oxide (ZnO) based materials still attract a huge scientific attention. Owing to a wide band gap energy (3.37 eV at room temperature) and a large exciton binding energy (60 meV) ZnO has a variety of application, e.g. in electronics, optoelectronics, spintronics and photocatalysis. Besides, it has been shown that zinc oxide-based materials have a great potential as photoelectrocatalysts in the processes of water splitting, yielding an increased both photocurrent density and photoconversion efficiency. However, with a band gap energy of 3.37 eV, ZnO is restricted to absorb UV light only. This restriction can be overcome by modifying optical properties of zinc oxide particles. During the years different approaches have been applied to modify the visible light photocatalytic activity of ZnO materials, for example: (1) metal and nonmetal ion doping, (2) hydrogenation, (3) the incorporation of crystalline defects in the form of vacancies and interstitials, (4) the modification of particles morphology and surface topology, etc.
In this study we employed 3d metal ion substitution to improve visible light-driven photoactivity of zinc oxide particles. We investigated the influence of Fe concentration in Zn1-xFeyO(1-x+1.5y) nanoparticles on crystal structure, textural, optical and photoelectrocatalytic properties. Zn1-xFeyO(1-x+1.5y) nanoparticles with nominally 5, 10, 15 and 20 at.% of Fe ions were synthesized by microwave processing of a precipitate. The crystal structure and phase purity of the samples were investigated by X-ray diffraction, Raman and ATR-FTIR spectroscopy. Mössbauer spectroscopy was carried out to clarify the valence state of the iron ions in the ZnO crystal structure. Effects of the iron ions concentration on particles morphology and texture properties were observed with field emission scanning electron microscopy (FE–SEM), transmission electron microscopy (TEM) with elemental mapping, and nitrogen adsorption–desorption isotherm, respectively. The optical properties were studied using UV–Vis diffuse reflectance and photoluminescence (PL) spectroscopy. Photoelectrochemical activity of the Zn1-xFeyO(1-x+1.5y) samples as anode material was evaluated by linear sweep voltammetry in Na2SO4 electrolyte; the oxygen evolution kinetics were determined and compared. In addition, a series of first principles calculations were performed to address the influence of the iron concentration on the electronic structure of Zn1-xFeyO(1-x+1.5y) samples.
PB  - Belgrade : Materials Research Society of Serbia
C3  - Programme and The Book of abstracts / Twenty-first Annual Conference YUCOMAT 2019 & Eleventh World Round Table Conference on Sintering WRTCS 2019, Herceg Novi, Montenegro, September 2-6, 2019
T1  - Point defect-enhanced optical and photoelectrochemical water splitting activity of nanostructured Zn1-xFeyO(1-x+1.5y)
SP  - 54
EP  - 54
UR  - https://hdl.handle.net/21.15107/rcub_dais_6677
ER  - 

@conference{
author = "Marković, Smilja and Rajić, Vladimir B. and Stojković Simatović, Ivana and Veselinović, Ljiljana and Belošević Čavor, Jelena and Ivanovski, Valentin N. and Novaković, Mirjana and Škapin, Srečo Davor and Stojadinović, Stevan and Rac, Vladislav and Uskoković, Dragan",
year = "2019",
abstract = "Even has been under study since 1935, zinc oxide (ZnO) based materials still attract a huge scientific attention. Owing to a wide band gap energy (3.37 eV at room temperature) and a large exciton binding energy (60 meV) ZnO has a variety of application, e.g. in electronics, optoelectronics, spintronics and photocatalysis. Besides, it has been shown that zinc oxide-based materials have a great potential as photoelectrocatalysts in the processes of water splitting, yielding an increased both photocurrent density and photoconversion efficiency. However, with a band gap energy of 3.37 eV, ZnO is restricted to absorb UV light only. This restriction can be overcome by modifying optical properties of zinc oxide particles. During the years different approaches have been applied to modify the visible light photocatalytic activity of ZnO materials, for example: (1) metal and nonmetal ion doping, (2) hydrogenation, (3) the incorporation of crystalline defects in the form of vacancies and interstitials, (4) the modification of particles morphology and surface topology, etc.
In this study we employed 3d metal ion substitution to improve visible light-driven photoactivity of zinc oxide particles. We investigated the influence of Fe concentration in Zn1-xFeyO(1-x+1.5y) nanoparticles on crystal structure, textural, optical and photoelectrocatalytic properties. Zn1-xFeyO(1-x+1.5y) nanoparticles with nominally 5, 10, 15 and 20 at.% of Fe ions were synthesized by microwave processing of a precipitate. The crystal structure and phase purity of the samples were investigated by X-ray diffraction, Raman and ATR-FTIR spectroscopy. Mössbauer spectroscopy was carried out to clarify the valence state of the iron ions in the ZnO crystal structure. Effects of the iron ions concentration on particles morphology and texture properties were observed with field emission scanning electron microscopy (FE–SEM), transmission electron microscopy (TEM) with elemental mapping, and nitrogen adsorption–desorption isotherm, respectively. The optical properties were studied using UV–Vis diffuse reflectance and photoluminescence (PL) spectroscopy. Photoelectrochemical activity of the Zn1-xFeyO(1-x+1.5y) samples as anode material was evaluated by linear sweep voltammetry in Na2SO4 electrolyte; the oxygen evolution kinetics were determined and compared. In addition, a series of first principles calculations were performed to address the influence of the iron concentration on the electronic structure of Zn1-xFeyO(1-x+1.5y) samples.",
publisher = "Belgrade : Materials Research Society of Serbia",
journal = "Programme and The Book of abstracts / Twenty-first Annual Conference YUCOMAT 2019 & Eleventh World Round Table Conference on Sintering WRTCS 2019, Herceg Novi, Montenegro, September 2-6, 2019",
title = "Point defect-enhanced optical and photoelectrochemical water splitting activity of nanostructured Zn1-xFeyO(1-x+1.5y)",
pages = "54-54",
url = "https://hdl.handle.net/21.15107/rcub_dais_6677"
}

Marković, S., Rajić, V. B., Stojković Simatović, I., Veselinović, L., Belošević Čavor, J., Ivanovski, V. N., Novaković, M., Škapin, S. D., Stojadinović, S., Rac, V.,& Uskoković, D.. (2019). Point defect-enhanced optical and photoelectrochemical water splitting activity of nanostructured Zn1-xFeyO(1-x+1.5y). in Programme and The Book of abstracts / Twenty-first Annual Conference YUCOMAT 2019 & Eleventh World Round Table Conference on Sintering WRTCS 2019, Herceg Novi, Montenegro, September 2-6, 2019
Belgrade : Materials Research Society of Serbia., 54-54.
https://hdl.handle.net/21.15107/rcub_dais_6677

Marković S, Rajić VB, Stojković Simatović I, Veselinović L, Belošević Čavor J, Ivanovski VN, Novaković M, Škapin SD, Stojadinović S, Rac V, Uskoković D. Point defect-enhanced optical and photoelectrochemical water splitting activity of nanostructured Zn1-xFeyO(1-x+1.5y). in Programme and The Book of abstracts / Twenty-first Annual Conference YUCOMAT 2019 & Eleventh World Round Table Conference on Sintering WRTCS 2019, Herceg Novi, Montenegro, September 2-6, 2019. 2019;:54-54.
https://hdl.handle.net/21.15107/rcub_dais_6677 .

Marković, Smilja, Rajić, Vladimir B., Stojković Simatović, Ivana, Veselinović, Ljiljana, Belošević Čavor, Jelena, Ivanovski, Valentin N., Novaković, Mirjana, Škapin, Srečo Davor, Stojadinović, Stevan, Rac, Vladislav, Uskoković, Dragan, "Point defect-enhanced optical and photoelectrochemical water splitting activity of nanostructured Zn1-xFeyO(1-x+1.5y)" in Programme and The Book of abstracts / Twenty-first Annual Conference YUCOMAT 2019 & Eleventh World Round Table Conference on Sintering WRTCS 2019, Herceg Novi, Montenegro, September 2-6, 2019 (2019):54-54,
https://hdl.handle.net/21.15107/rcub_dais_6677 .

TY  - CONF
AU  - Rakočević, Lazar
AU  - Novaković, Mirjana
AU  - Potočnik, Jelena
AU  - Jugović, Dragana
AU  - Stojković Simatović, Ivana
PY  - 2018
UR  - https://dais.sanu.ac.rs/123456789/4726
AB  - The application of rechargeable batteries is growing significantly and there is a need for developing cheaper batteries with good performances. Sodium-ion batteries could be a viable option due to higher abundance of sodium against lithium mineral resources, its low price and similar principles intercalate Na+ ions as Li+ ions in lithium-ion batteries. Different materials as manganese oxides and vanadium oxide are used as electrode materials in sodium batteries. Na0.44MnO2 was regarded as one of the most promising cathode materials for sodium-ion batteries due to its high specific capacity and good cyclability. In this work, Na0.4MnO2 was synthesized using glycine-nitrate method (GNM). The structure of synthesized powder was characterized by X-Ray Diffraction (XRD), while the particles morphology was examined by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The elemental mapping was performed by energy-dispersive Xray spectroscopy (EDS). XRD results showed that the phase structure of Na0.4MnO2 was orthorhombic with tunnel structure. TEM and SEM micrographs of obtained powder material showed uniformed rod-like shape particles with the average lengths and widths of 300 nm and 80 nm, respectively and EDS analysis confirmed that the sample contains Na, Mn, and O in an appropriate ration. The electrochemical behavior of Na0.4MnO2 was investigated by cyclic voltammetry (CV) in a saturated aqueous solution of NaNO3 at scan rates from 20 to 400 mV•s-1. The initial discharge capacity of Na0.4MnO2 in NaNO3 solution was 50 mA•h•g- 1, while after 15 cycles its value increased for 9%. while the efficiency (the ratio of the capacity charge and discharge) was amounting to ~ 95%. This indicates that material synthesized by GNM can be used as cathode material in aqueous sodium-ion batteries
PB  - Belgrade : Institute of Technical Sciences of SASA
C3  - Program and the Book of Abstracts / Seventeenth Young Researchers' Conference Materials Sciences and Engineering, December 5-7, 2018, Belgrade, Serbia
T1  - Synthesis and characterization of Na0.4MnO2 as cathode material for aqueous sodium-ion batteries
SP  - 48
EP  - 48
UR  - https://hdl.handle.net/21.15107/rcub_dais_4726
ER  - 

@conference{
author = "Rakočević, Lazar and Novaković, Mirjana and Potočnik, Jelena and Jugović, Dragana and Stojković Simatović, Ivana",
year = "2018",
abstract = "The application of rechargeable batteries is growing significantly and there is a need for developing cheaper batteries with good performances. Sodium-ion batteries could be a viable option due to higher abundance of sodium against lithium mineral resources, its low price and similar principles intercalate Na+ ions as Li+ ions in lithium-ion batteries. Different materials as manganese oxides and vanadium oxide are used as electrode materials in sodium batteries. Na0.44MnO2 was regarded as one of the most promising cathode materials for sodium-ion batteries due to its high specific capacity and good cyclability. In this work, Na0.4MnO2 was synthesized using glycine-nitrate method (GNM). The structure of synthesized powder was characterized by X-Ray Diffraction (XRD), while the particles morphology was examined by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The elemental mapping was performed by energy-dispersive Xray spectroscopy (EDS). XRD results showed that the phase structure of Na0.4MnO2 was orthorhombic with tunnel structure. TEM and SEM micrographs of obtained powder material showed uniformed rod-like shape particles with the average lengths and widths of 300 nm and 80 nm, respectively and EDS analysis confirmed that the sample contains Na, Mn, and O in an appropriate ration. The electrochemical behavior of Na0.4MnO2 was investigated by cyclic voltammetry (CV) in a saturated aqueous solution of NaNO3 at scan rates from 20 to 400 mV•s-1. The initial discharge capacity of Na0.4MnO2 in NaNO3 solution was 50 mA•h•g- 1, while after 15 cycles its value increased for 9%. while the efficiency (the ratio of the capacity charge and discharge) was amounting to ~ 95%. This indicates that material synthesized by GNM can be used as cathode material in aqueous sodium-ion batteries",
publisher = "Belgrade : Institute of Technical Sciences of SASA",
journal = "Program and the Book of Abstracts / Seventeenth Young Researchers' Conference Materials Sciences and Engineering, December 5-7, 2018, Belgrade, Serbia",
title = "Synthesis and characterization of Na0.4MnO2 as cathode material for aqueous sodium-ion batteries",
pages = "48-48",
url = "https://hdl.handle.net/21.15107/rcub_dais_4726"
}

Rakočević, L., Novaković, M., Potočnik, J., Jugović, D.,& Stojković Simatović, I.. (2018). Synthesis and characterization of Na0.4MnO2 as cathode material for aqueous sodium-ion batteries. in Program and the Book of Abstracts / Seventeenth Young Researchers' Conference Materials Sciences and Engineering, December 5-7, 2018, Belgrade, Serbia
Belgrade : Institute of Technical Sciences of SASA., 48-48.
https://hdl.handle.net/21.15107/rcub_dais_4726

Rakočević L, Novaković M, Potočnik J, Jugović D, Stojković Simatović I. Synthesis and characterization of Na0.4MnO2 as cathode material for aqueous sodium-ion batteries. in Program and the Book of Abstracts / Seventeenth Young Researchers' Conference Materials Sciences and Engineering, December 5-7, 2018, Belgrade, Serbia. 2018;:48-48.
https://hdl.handle.net/21.15107/rcub_dais_4726 .

Rakočević, Lazar, Novaković, Mirjana, Potočnik, Jelena, Jugović, Dragana, Stojković Simatović, Ivana, "Synthesis and characterization of Na0.4MnO2 as cathode material for aqueous sodium-ion batteries" in Program and the Book of Abstracts / Seventeenth Young Researchers' Conference Materials Sciences and Engineering, December 5-7, 2018, Belgrade, Serbia (2018):48-48,
https://hdl.handle.net/21.15107/rcub_dais_4726 .

TY  - CONF
AU  - Rakočević, Lazar
AU  - Novaković, Mirjana
AU  - Potočnik, Jelena
AU  - Jugović, Dragana
AU  - Stojković Simatović, Ivana
PY  - 2018
UR  - https://dais.sanu.ac.rs/123456789/3628
AB  - Due to the increasing use of batteries in everyday life and in industry, there is a need for developing cheaper batteries than the widely used lithium ion batteries. Lower price and higher abundance of sodium compared to lithium mineral resources intensified the development of Na-ion batteries. Aqueous lithium/ sodium rechargeable batteries have attracted considerable attention for energy storage because they do not contain flammable organic electrolytes as commercial batteries do, the ionic conductivity of the aqueous electrolyte is about two orders of magnitude higher than in non-aqueous electrolyte and the electrolyte salt and solvent are cheaper. Various materials such as manganese oxides, vanadium oxide and phosphates have been used as electrode materials (cathodic and anodic) in sodium batteries due to high sodium intercalation ability in both, organic and aqueous electrolytes. The most frequently used type of manganese oxides are Li–Mn–O or Na–Mn–O systems due to their tunnel or layered crystal structures which facilitate the lithium/sodium intercalation-deintercalation. In this work, a glycine-nitrate method (GNM) was applied for the synthesis of cathode material Na0.4MnO2.
PB  - Belgrade : Serbian Academy of Sciences and Arts
C3  - Program and Book of Abstracts / First International Conference on Electron Microscopy of Nanostructures ELMINA 2018, August 27-29, 2018, Belgrade, Serbia
T1  - Synthesis and Characterization of Na0.4MnO2 as a Positive Electrode Material for an Aqueous Electrolyte Sodium-ion Energy Storage Device
SP  - 154
EP  - 156
UR  - https://hdl.handle.net/21.15107/rcub_dais_3628
ER  - 

@conference{
author = "Rakočević, Lazar and Novaković, Mirjana and Potočnik, Jelena and Jugović, Dragana and Stojković Simatović, Ivana",
year = "2018",
abstract = "Due to the increasing use of batteries in everyday life and in industry, there is a need for developing cheaper batteries than the widely used lithium ion batteries. Lower price and higher abundance of sodium compared to lithium mineral resources intensified the development of Na-ion batteries. Aqueous lithium/ sodium rechargeable batteries have attracted considerable attention for energy storage because they do not contain flammable organic electrolytes as commercial batteries do, the ionic conductivity of the aqueous electrolyte is about two orders of magnitude higher than in non-aqueous electrolyte and the electrolyte salt and solvent are cheaper. Various materials such as manganese oxides, vanadium oxide and phosphates have been used as electrode materials (cathodic and anodic) in sodium batteries due to high sodium intercalation ability in both, organic and aqueous electrolytes. The most frequently used type of manganese oxides are Li–Mn–O or Na–Mn–O systems due to their tunnel or layered crystal structures which facilitate the lithium/sodium intercalation-deintercalation. In this work, a glycine-nitrate method (GNM) was applied for the synthesis of cathode material Na0.4MnO2.",
publisher = "Belgrade : Serbian Academy of Sciences and Arts",
journal = "Program and Book of Abstracts / First International Conference on Electron Microscopy of Nanostructures ELMINA 2018, August 27-29, 2018, Belgrade, Serbia",
title = "Synthesis and Characterization of Na0.4MnO2 as a Positive Electrode Material for an Aqueous Electrolyte Sodium-ion Energy Storage Device",
pages = "154-156",
url = "https://hdl.handle.net/21.15107/rcub_dais_3628"
}

Rakočević, L., Novaković, M., Potočnik, J., Jugović, D.,& Stojković Simatović, I.. (2018). Synthesis and Characterization of Na0.4MnO2 as a Positive Electrode Material for an Aqueous Electrolyte Sodium-ion Energy Storage Device. in Program and Book of Abstracts / First International Conference on Electron Microscopy of Nanostructures ELMINA 2018, August 27-29, 2018, Belgrade, Serbia
Belgrade : Serbian Academy of Sciences and Arts., 154-156.
https://hdl.handle.net/21.15107/rcub_dais_3628

Rakočević L, Novaković M, Potočnik J, Jugović D, Stojković Simatović I. Synthesis and Characterization of Na0.4MnO2 as a Positive Electrode Material for an Aqueous Electrolyte Sodium-ion Energy Storage Device. in Program and Book of Abstracts / First International Conference on Electron Microscopy of Nanostructures ELMINA 2018, August 27-29, 2018, Belgrade, Serbia. 2018;:154-156.
https://hdl.handle.net/21.15107/rcub_dais_3628 .

Rakočević, Lazar, Novaković, Mirjana, Potočnik, Jelena, Jugović, Dragana, Stojković Simatović, Ivana, "Synthesis and Characterization of Na0.4MnO2 as a Positive Electrode Material for an Aqueous Electrolyte Sodium-ion Energy Storage Device" in Program and Book of Abstracts / First International Conference on Electron Microscopy of Nanostructures ELMINA 2018, August 27-29, 2018, Belgrade, Serbia (2018):154-156,
https://hdl.handle.net/21.15107/rcub_dais_3628 .