Tripkovic, A. V.

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  • Tripkovic, A. V. (1)
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Formic acid oxidation on Pt-Au nanoparticles: Relation between the catalyst activity and the poisoning rate

Obradović, Maja D.; Rogan, Jelena R.; Babić, Biljana M.; Tripkovic, A. V.; Gautam, A. R. S.; Radmilovíć, Velimir R.; Gojković, Snežana Lj.

(2012)

TY  - JOUR
AU  - Obradović, Maja D.
AU  - Rogan, Jelena R.
AU  - Babić, Biljana M.
AU  - Tripkovic, A. V.
AU  - Gautam, A. R. S.
AU  - Radmilovíć, Velimir R.
AU  - Gojković, Snežana Lj.
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4583
AB  - Pt-Au nanoparticles supported on high area carbon were prepared by simultaneous reduction of Au and Pt precursors and by reduction of Pt precursor on already prepared Au nanoparticles. The first method produced a solid solution of Pt in Au containing similar to 5% Pt with the remaining Pt on the nanoparticles surface. For the Pt:Au precursor ratio of 1:4 and 1:9, the surface ratio was found to be 0.70:0.30 and 0.55:0.45, respectively. By the second method with the Pt:Au precursors ratio of 1:12, the surface ratio was 0.30:0.70. The voltammetric peaks of Pt-oxide reduction and CO(ads) oxidation demonstrated electronic modification of Pt by Au in all catalysts. With decreasing Pt:Au surface ratio the activity for HCOOH oxidation increases and surface coverage by CO(ads) decreases. The highest activity under potentiodynamic and quasi steady-state conditions without poisoning by CO(ads) was observed for the catalyst with the lowest Pt:Au surface ratio. Chronoamperometic test showed that its high catalytic activity is associated with a high deactivation rate. It was postulated that too strong adsorption of a reactive or non-reactive intermediate caused by electron modification of Pt by underlying Au, is responsible for the deactivation. This result stresses that high Pt dispersion, necessary for promotion of the dehydrogenation path in HCOOH oxidation, can produce too strong adsorption of intermediates causing deactivation of the catalyst. (C) 2011 Elsevier B.V. All rights reserved.
T2  - Journal of Power Sources
T1  - Formic acid oxidation on Pt-Au nanoparticles: Relation between the catalyst activity and the poisoning rate
VL  - 197
SP  - 72
EP  - 79
DO  - 10.1016/j.jpowsour.2011.09.043
ER  - 
@article{
author = "Obradović, Maja D. and Rogan, Jelena R. and Babić, Biljana M. and Tripkovic, A. V. and Gautam, A. R. S. and Radmilovíć, Velimir R. and Gojković, Snežana Lj.",
year = "2012",
abstract = "Pt-Au nanoparticles supported on high area carbon were prepared by simultaneous reduction of Au and Pt precursors and by reduction of Pt precursor on already prepared Au nanoparticles. The first method produced a solid solution of Pt in Au containing similar to 5% Pt with the remaining Pt on the nanoparticles surface. For the Pt:Au precursor ratio of 1:4 and 1:9, the surface ratio was found to be 0.70:0.30 and 0.55:0.45, respectively. By the second method with the Pt:Au precursors ratio of 1:12, the surface ratio was 0.30:0.70. The voltammetric peaks of Pt-oxide reduction and CO(ads) oxidation demonstrated electronic modification of Pt by Au in all catalysts. With decreasing Pt:Au surface ratio the activity for HCOOH oxidation increases and surface coverage by CO(ads) decreases. The highest activity under potentiodynamic and quasi steady-state conditions without poisoning by CO(ads) was observed for the catalyst with the lowest Pt:Au surface ratio. Chronoamperometic test showed that its high catalytic activity is associated with a high deactivation rate. It was postulated that too strong adsorption of a reactive or non-reactive intermediate caused by electron modification of Pt by underlying Au, is responsible for the deactivation. This result stresses that high Pt dispersion, necessary for promotion of the dehydrogenation path in HCOOH oxidation, can produce too strong adsorption of intermediates causing deactivation of the catalyst. (C) 2011 Elsevier B.V. All rights reserved.",
journal = "Journal of Power Sources",
title = "Formic acid oxidation on Pt-Au nanoparticles: Relation between the catalyst activity and the poisoning rate",
volume = "197",
pages = "72-79",
doi = "10.1016/j.jpowsour.2011.09.043"
}
Obradović, M. D., Rogan, J. R., Babić, B. M., Tripkovic, A. V., Gautam, A. R. S., Radmilovíć, V. R.,& Gojković, S. Lj.. (2012). Formic acid oxidation on Pt-Au nanoparticles: Relation between the catalyst activity and the poisoning rate. in Journal of Power Sources, 197, 72-79.
https://doi.org/10.1016/j.jpowsour.2011.09.043
Obradović MD, Rogan JR, Babić BM, Tripkovic AV, Gautam ARS, Radmilovíć VR, Gojković SL. Formic acid oxidation on Pt-Au nanoparticles: Relation between the catalyst activity and the poisoning rate. in Journal of Power Sources. 2012;197:72-79.
doi:10.1016/j.jpowsour.2011.09.043 .
Obradović, Maja D., Rogan, Jelena R., Babić, Biljana M., Tripkovic, A. V., Gautam, A. R. S., Radmilovíć, Velimir R., Gojković, Snežana Lj., "Formic acid oxidation on Pt-Au nanoparticles: Relation between the catalyst activity and the poisoning rate" in Journal of Power Sources, 197 (2012):72-79,
https://doi.org/10.1016/j.jpowsour.2011.09.043 . .
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