Kinetics of the hydrogen oxidation on pt modified MoOx nano-sized catalyst in the presence of carbon monoxide
Authors
Krstajić, NedeljkoElezović, Nevenka R.
Vračar, Ljiljana
Gajić Krstajić, Ljiljana

Radmilović, Velimir R.

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Due to the importance of the HOR in fuel-cells technology, various Pt-based catalysts have been examined from the viewpoint of immunity of the electrocatalysis of the HOR from CO-poisoning of the anode catalysts. An appreciable improvement of the CO tolerance has been found at Pt with adatoms such as Ru, Sn [1,2], Pt-M (M=Ru, Rh, Os, W Sn) [3-5] based alloys, and Pt with oxides (RuOxHy) [6]. In the present work, the electrocatalytic of home made highly dispersed nano-sized MoOx-Pt/C catalysts prepared by the polyole method combined by MoOx post-deposition was investigated in the presence of CO, in 0.5 moldm-3 HClO4 solution. The partial pressure of CO in CO/H2 gas mixture was 100 ppm. Carbon monoxide was adsorbed on the RDE for various time interval with keeping the potential at 0.05 V (RHE). The coverage of CO was determined by applying the first potential sweep (from 0.04 to 1.20 V), in N2 saturated solution at potential scan rate of 0.1 Vs-1 and compared it with the sweep on the cle...an electrode, by measuring the decrease in the hydrogen desorption charge, ΔQH. MoOx(20%)Pt/C catalyst exhibits an excellent CO tolerance, as it was found that the reduction in kinetic current, Ik, is negligible even at ΘCO = 0.46. It was found for this catalyst too, that the CO adsorption rate was much slower than that of Pt and the Pt sites for HOR were not so rigidly blocked by adsorbed CO partially due to its enhanced mobility, resulting from their modified electronic structure of surface Pt sites. Voltammetric studies suggest that an excellent CO tolerance of this catalyst could be also result of the oxidation of adsorbed CO to CO2 by oxophilic MoOx species at low overpotentials by a redox-mediated mechanism.
Keywords:
Pt-based catalysts / electrocatalysis / carbon monoxide / platinum / hydrogen oxidationSource:
Programme and The Book of Abstracts / Eleventh Annual Conference YUCOMAT 2009, Herceg Novi, August 31 – September 4, 2009, 2009, 85-85Publisher:
- Belgrade : Institute of Technical Sciences of SASA
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Related info:
- Referenced by
https://hdl.handle.net/21.15107/rcub_dais_266
Institution/Community
Институт техничких наука САНУ / Institute of Technical Sciences of SASATY - CONF AU - Krstajić, Nedeljko AU - Elezović, Nevenka R. AU - Vračar, Ljiljana AU - Gajić Krstajić, Ljiljana AU - Radmilović, Velimir R. PY - 2009 UR - https://dais.sanu.ac.rs/123456789/4956 AB - Due to the importance of the HOR in fuel-cells technology, various Pt-based catalysts have been examined from the viewpoint of immunity of the electrocatalysis of the HOR from CO-poisoning of the anode catalysts. An appreciable improvement of the CO tolerance has been found at Pt with adatoms such as Ru, Sn [1,2], Pt-M (M=Ru, Rh, Os, W Sn) [3-5] based alloys, and Pt with oxides (RuOxHy) [6]. In the present work, the electrocatalytic of home made highly dispersed nano-sized MoOx-Pt/C catalysts prepared by the polyole method combined by MoOx post-deposition was investigated in the presence of CO, in 0.5 moldm-3 HClO4 solution. The partial pressure of CO in CO/H2 gas mixture was 100 ppm. Carbon monoxide was adsorbed on the RDE for various time interval with keeping the potential at 0.05 V (RHE). The coverage of CO was determined by applying the first potential sweep (from 0.04 to 1.20 V), in N2 saturated solution at potential scan rate of 0.1 Vs-1 and compared it with the sweep on the clean electrode, by measuring the decrease in the hydrogen desorption charge, ΔQH. MoOx(20%)Pt/C catalyst exhibits an excellent CO tolerance, as it was found that the reduction in kinetic current, Ik, is negligible even at ΘCO = 0.46. It was found for this catalyst too, that the CO adsorption rate was much slower than that of Pt and the Pt sites for HOR were not so rigidly blocked by adsorbed CO partially due to its enhanced mobility, resulting from their modified electronic structure of surface Pt sites. Voltammetric studies suggest that an excellent CO tolerance of this catalyst could be also result of the oxidation of adsorbed CO to CO2 by oxophilic MoOx species at low overpotentials by a redox-mediated mechanism. PB - Belgrade : Institute of Technical Sciences of SASA C3 - Programme and The Book of Abstracts / Eleventh Annual Conference YUCOMAT 2009, Herceg Novi, August 31 – September 4, 2009 T1 - Kinetics of the hydrogen oxidation on pt modified MoOx nano-sized catalyst in the presence of carbon monoxide SP - 85 EP - 85 UR - https://hdl.handle.net/21.15107/rcub_dais_4956 ER -
@conference{ author = "Krstajić, Nedeljko and Elezović, Nevenka R. and Vračar, Ljiljana and Gajić Krstajić, Ljiljana and Radmilović, Velimir R.", year = "2009", abstract = "Due to the importance of the HOR in fuel-cells technology, various Pt-based catalysts have been examined from the viewpoint of immunity of the electrocatalysis of the HOR from CO-poisoning of the anode catalysts. An appreciable improvement of the CO tolerance has been found at Pt with adatoms such as Ru, Sn [1,2], Pt-M (M=Ru, Rh, Os, W Sn) [3-5] based alloys, and Pt with oxides (RuOxHy) [6]. In the present work, the electrocatalytic of home made highly dispersed nano-sized MoOx-Pt/C catalysts prepared by the polyole method combined by MoOx post-deposition was investigated in the presence of CO, in 0.5 moldm-3 HClO4 solution. The partial pressure of CO in CO/H2 gas mixture was 100 ppm. Carbon monoxide was adsorbed on the RDE for various time interval with keeping the potential at 0.05 V (RHE). The coverage of CO was determined by applying the first potential sweep (from 0.04 to 1.20 V), in N2 saturated solution at potential scan rate of 0.1 Vs-1 and compared it with the sweep on the clean electrode, by measuring the decrease in the hydrogen desorption charge, ΔQH. MoOx(20%)Pt/C catalyst exhibits an excellent CO tolerance, as it was found that the reduction in kinetic current, Ik, is negligible even at ΘCO = 0.46. It was found for this catalyst too, that the CO adsorption rate was much slower than that of Pt and the Pt sites for HOR were not so rigidly blocked by adsorbed CO partially due to its enhanced mobility, resulting from their modified electronic structure of surface Pt sites. Voltammetric studies suggest that an excellent CO tolerance of this catalyst could be also result of the oxidation of adsorbed CO to CO2 by oxophilic MoOx species at low overpotentials by a redox-mediated mechanism.", publisher = "Belgrade : Institute of Technical Sciences of SASA", journal = "Programme and The Book of Abstracts / Eleventh Annual Conference YUCOMAT 2009, Herceg Novi, August 31 – September 4, 2009", title = "Kinetics of the hydrogen oxidation on pt modified MoOx nano-sized catalyst in the presence of carbon monoxide", pages = "85-85", url = "https://hdl.handle.net/21.15107/rcub_dais_4956" }
Krstajić, N., Elezović, N. R., Vračar, L., Gajić Krstajić, L.,& Radmilović, V. R.. (2009). Kinetics of the hydrogen oxidation on pt modified MoOx nano-sized catalyst in the presence of carbon monoxide. in Programme and The Book of Abstracts / Eleventh Annual Conference YUCOMAT 2009, Herceg Novi, August 31 – September 4, 2009 Belgrade : Institute of Technical Sciences of SASA., 85-85. https://hdl.handle.net/21.15107/rcub_dais_4956
Krstajić N, Elezović NR, Vračar L, Gajić Krstajić L, Radmilović VR. Kinetics of the hydrogen oxidation on pt modified MoOx nano-sized catalyst in the presence of carbon monoxide. in Programme and The Book of Abstracts / Eleventh Annual Conference YUCOMAT 2009, Herceg Novi, August 31 – September 4, 2009. 2009;:85-85. https://hdl.handle.net/21.15107/rcub_dais_4956 .
Krstajić, Nedeljko, Elezović, Nevenka R., Vračar, Ljiljana, Gajić Krstajić, Ljiljana, Radmilović, Velimir R., "Kinetics of the hydrogen oxidation on pt modified MoOx nano-sized catalyst in the presence of carbon monoxide" in Programme and The Book of Abstracts / Eleventh Annual Conference YUCOMAT 2009, Herceg Novi, August 31 – September 4, 2009 (2009):85-85, https://hdl.handle.net/21.15107/rcub_dais_4956 .