Effects of short-side-chain perfluorosulfonic acid ionomers as binders on the performance of low Pt loading fuel cell cathodes

被引:102
作者
Park, Young-Chul [1 ]
Kakinuma, Katsuyoshi [1 ]
Uchida, Hiroyuki [2 ]
Watanabe, Masahiro [1 ]
Uchida, Makoto [1 ]
机构
[1] Univ Yamanashi, Fuel Cell Nanomat Ctr, Kofu, Yamanashi 4000021, Japan
[2] Univ Yamanashi, Clean Energy Res Ctr, Kofu, Yamanashi 4008511, Japan
关键词
Short-side-chain perfluorosulfonic acid ionomer; Low Pt loading; Cathode catalyst layer; Polymer electrolyte fuel cells; GAS-DIFFUSION ELECTRODES; CATALYST LAYERS; MEMBRANES; PROTON; DEPENDENCE; TRANSPORT; PLATINUM; WATER;
D O I
10.1016/j.jpowsour.2014.10.149
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
We investigated the effects of short-side-chain (SSC) perfiuorosulfonic acid ionomers on the electrochemical properties, fuel cell performance and ionomer distribution of a highly dispersed Pt/GCB catalyst with a low Pt loading, 0.05 mg cm(-2). The SSC ionomers in the cathode catalyst layers (CLs) resulted in an improvement of the Pt utilization (U-pt) and Pt effectiveness (Ef(pt)) values compared with those for the conventional long-side-chain (LSC) ionomer. Furthermore, the SSC ionomers with high ion exchange capacity (IEC), e.g., SSC-1.43 and SSC-1.80 ionomers, exhibited significantly enhanced cell performance under low to medium relative humidity (RH) conditions. This result is ascribed to the higher proton conductivity of the SSC ionomers and more effective trapping of water that is produced during the oxygen reduction reaction (ORR) than those of the [SC ionomer. It was also found that the SSC ionomers showed better continuity and uniformity on the Pt and carbon particles than the LSC ionomer, which might have led to improvement of both the mass transport and the proton-conducting network in the CLs. The application of the SSC ionomers as binders demonstrated an increase of the performance at the low Pt loading fuel cell cathode over a wide range of humidity. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:384 / 391
页数:8
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