Carbon supported PtBi catalysts for direct formic acid fuel cells

被引:37
|
作者
Yu, Xingwen [1 ]
Pickup, Peter G. [1 ]
机构
[1] Mem Univ Newfoundland, Dept Chem, St John, NF A1B 3X7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Direct formic acid fuel cell; Catalyst; Platinum; Bismuth; Decoration co-deposition; POISON FORMATION REACTION; ELECTROCATALYTIC ACTIVITY; ANODE CATALYST; INTERMETALLIC COMPOUNDS; PT(111) ELECTRODES; OXIDATION; PTPB; ELECTROOXIDATION; BI; NANOPARTICLES;
D O I
10.1016/j.electacta.2011.02.006
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Carbon supported PtBi bimetallic catalysts (PtBi/C) prepared by depositing Bi on a commercial Pt/C catalyst and by codeposition of Pt and Bi have been compared for formic acid oxidation in a multi-anode direct formic acid fuel cell. Both types of catalyst gave much higher cell performances than the Pt/C, with only low amounts of Bi (Pt to Bi mole ratios of 11:1 and 14:1, respectively) required for optimum performance. The high Pt to Bi ratio for the best codeposited catalyst indicates that the Bi was concentrated at the surface, and this is consistent with X-ray diffraction and X-ray photoelectron spectroscopy results. However, cyclic voltammetry revealed a strong electronic effect that is inconsistent with surface decoration. The effects of the Bi have been attributed to selective blocking of sites at which CO is formed. (C) 2011 Elsevier Ltd. All rights reserved.
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页码:4037 / 4043
页数:7
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