Catalysts for direct formic acid fuel cells

被引:508
|
作者
Rice, C
Ha, S
Masel, RI
Wieckowski, A
机构
[1] Univ Illinois, Dept Chem Engn, Roger Adams Lab, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
关键词
formic acid; catalyst; fuel cell;
D O I
10.1016/S0378-7753(03)00026-0
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
Previous work has demonstrated that formic acid fuel cells show interesting properties for micro power generation. In this paper the effects of the anode catalyst composition on fuel cell performance is investigated. In particular, the performance of Pt, Pt/Pd and Pt/Ru catalysts for direct formic acid fuel cells is investigated and their effect on cell power density output at 30 degreesC are compared. It is found that the open cell potential varies significantly with the catalyst composition. The Pt/Pd catalyst shows an open cell potential of 0.91 V compared to 0.71 V with pure platinum and 0.59 V with Pt/Ru. The current at a cell potential of 0.5 V is 62 mA/cM with Pt/Pd compared to 33 mA/cm with pure platinum and 38 mA/cm(2) with Pt/Ru. Interestingly, the Pt/Ru catalyst gives the most power at low voltage 70 mW/cm(2) at 0.26 V, compared to 43 mW/cm(2) for pure platinum and 41 mW/cm(2) for Pt/Pd. All of the catalysts showed stable operation during several hour tests. Analysis of the data indicates that the addition of palladium enhances the rate of formic acid electrooxidation via a direct reaction mechanism, while ruthenium additions suppress the direct pathway and enhance electrooxidation via a reactive CO intermediate. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:229 / 235
页数:7
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