Effect of chemisorbed CO on MoOx-Pt/C electrode on the kinetics of hydrogen oxidation reaction

被引:20
作者
Elezovic, N. R. [2 ]
Gajic-Krstajic, Lj M. [3 ]
Vracar, Lj M. [1 ]
Krstajic, N. V. [1 ]
机构
[1] Univ Belgrade, Fac Technol & Met, Belgrade 11000, Serbia
[2] Inst Multidisciplinary Res, Belgrade, Serbia
[3] Inst Tech Sci SASA, Belgrade, Serbia
关键词
Hydrogen oxidation; CO adsorption; RDE; Kinetic equation; Mechanism; MEMBRANE FUEL-CELLS; H-2/CO MIXTURES; METHANOL; ELECTROOXIDATION; TOLERANCE; ALLOY; PLATINUM; ELECTROCATALYSTS; CATALYSTS; RU;
D O I
10.1016/j.ijhydene.2010.09.004
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The influence of poisoning of MoOx-Pt catalyst by CO on the kinetics of H-2 oxidation reaction (HOR) at MoOx-Pt electrode in 0 5 mol dm(-3) HClO4 saturated with H-2 containing 100 ppm CO was examined on rotating disc electrode (RIDE) at 25 C MoOx-Pt nano catalyst prepared by the polyole method combined with MoOx post deposition was supported on commercial carbon black Vulcan XC 72 The MoOx-Pt/C catalyst was characterized by TEM technique The catalyst composition is very similar to the nominal one and post deposited MoOx species block only a small fraction of the active Pt particle surface area MoOx deposition on the carbon support can be ruled out from the EDAX results and from the low mobility of these oxides under used conditions Based on Tafel-Heyrovsky-Volmer mechanism the corresponding kinetic equations from a dual pathway model were derived to describe oxidation current potential behavior on RIDE over entire potential range at venous CO coverages The polarization RIDE curves were fitted with derived polarization equations according to the proposed model The fitting showed that the HOR proceeded most likely via the Tafel-Volmer (TV) pathway A very high electrocatalytic activity observed at MoOx-Pt catalyst for the hydrogen oxidation reaction in the presence of 100 ppm CO is achieved through chemical surface reaction of adsorbed CO with Mo surface oxides (C) 2010 Professor T Nejat Veziroglu Published by Elsevier Ltd All rights reserved
引用
收藏
页码:12878 / 12887
页数:10
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