Overview of the development of CO-tolerant anode electrocatalysts for proton-exchange membrane fuel cells

被引:157
作者
Wee, Jung-Ho [1 ]
Lee, Kwan-Young [1 ]
机构
[1] Korea Univ, Dept Biol & Chem Engn, Seoul 136701, South Korea
关键词
proton-exchange membrane fuel cell; carbon monoxide tolerance; hydrogen oxidation; platinum catalyst; Pt-Ru anode; selective carbon dioxide oxidation;
D O I
10.1016/j.jpowsour.2005.08.010
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
Poisoning of Pt anode electrocatalysts by carbon monoxide (CO) is deemed to be one of the most significant barriers to be overcome in the development of proton-exchange membrane fuel cell systems (PEMFCs). The use of CO-tolerant electrocatalysts serves as the most hopeful way to solve this problem. It is well established that Pt-based alloy systems of CO-tolerant electrocatalysts can substantially withstand the presence of CO in the fuel stream. Based on literature starting in 2000, a few efforts have still been conducted at developing a more CO-tolerant anode electrocatalyst than the traditional Pt/C or PtRu/C systems. This review introduces and discusses these efforts. Pt-based electrocatalysts, including PtSn/C, PtMo/C (atomic ratio = 5:1), PtRuMo/C (Mo = 10 wt.%), PtRu-HMoO3/C and PtRu/(C nanotubes), appear to be poisoned by CO at the same, or a lower, level than traditional Pt/C or PtRu/C electrocatalysts. Platinum-free electrocatalysts, such as PdAu/C, have proven to be less strongly poisoned by CO than PtRu/C counterparts at temperatures of 60 degrees C. A greater tolerance to CO can be achieved by modifying the structure of the electrocatalyst. This involves the use of a composite or double-layer that is designed to make the CO react with one of the electrocatalyst in advance while the main hydrogen reacts at another layer with a traditional Pt/C electrocatalyst. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:128 / 135
页数:8
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