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

被引:160
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
相关论文
共 90 条
[1]   Electrocatalysts for fuel cells [J].
Acres, GJK ;
Frost, JC ;
Hards, GA ;
Potter, RJ ;
Ralph, TR ;
Thompsett, D ;
Burstein, GT ;
Hutchings, GJ .
CATALYSIS TODAY, 1997, 38 (04) :393-400
[2]   Enhancement of the performance and reliability of CO poisoned PEM fuel cells [J].
Adams, WA ;
Blair, J ;
Bullock, KR ;
Gardner, CL .
JOURNAL OF POWER SOURCES, 2005, 145 (01) :55-61
[3]  
[Anonymous], FUEL CELLS B
[4]  
Arico AS, 1996, J APPL ELECTROCHEM, V26, P959, DOI 10.1007/BF00242049
[5]   Evaluation of the water-gas shift and CO methanation processes for purification of reformate gases and the coupling to a PEM fuel cell system [J].
Batista, MS ;
Santiago, EI ;
Assaf, EM ;
Ticianelli, EA .
JOURNAL OF POWER SOURCES, 2005, 145 (01) :50-54
[6]   High efficiency steam reforming of ethanol by cobalt-based catalysts [J].
Batista, MS ;
Santos, RKS ;
Assaf, EM ;
Assaf, JM ;
Ticianelli, EA .
JOURNAL OF POWER SOURCES, 2004, 134 (01) :27-32
[7]  
Bellows RJ, 1998, ELECTROCHEM SOLID ST, V1, P69, DOI 10.1149/1.1390639
[8]  
BENICEWICZ BC, 2003, ACS POL CHEM WORKSH
[9]   Alternative supports for the preparation of catalysts for low-temperature fuel cells: the use of carbon nanotubes [J].
Carmo, M ;
Paganin, VA ;
Rosolen, JM ;
Gonzalez, ER .
JOURNAL OF POWER SOURCES, 2005, 142 (1-2) :169-176
[10]   CO selective oxidation in a microchannel reactor for PEM fuel cell [J].
Chen, GW ;
Yuan, Q ;
Li, HQ ;
Li, SL .
CHEMICAL ENGINEERING JOURNAL, 2004, 101 (1-3) :101-106