Investigation of Pt, Pt3Co, and Pt3Co/Mo Cathodes for the ORR in a Microfluidic H2/O2 Fuel Cell

被引:22
|
作者
Brushett, Fikile R. [1 ]
Duong, Hung T. [2 ]
Ng, Jia Wei [1 ]
Behrens, Rachel L. [2 ]
Wieckowski, Andrzej [2 ]
Kenis, Paul J. A. [1 ]
机构
[1] Univ Illinois, Dept Chem & Biomol Engn, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
基金
美国国家科学基金会;
关键词
OXYGEN REDUCTION REACTION; POLYMER ELECTROLYTE MEMBRANE; BINDING-ENERGY; PART II; CATALYSTS; DURABILITY; STABILITY; ELECTROCATALYSTS; ALLOYS; CO;
D O I
10.1149/1.3368721
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We report on the performance and durability of four Pt-based cathode catalysts in a microfluidic H-2/O-2 fuel cell: commercial unsupported Pt and Pt3Co as well as in-house acid-treated Pt3Co (Pt3Co-at )and Pt3Co/Mo. Commercial Pt3Co was used as the starting material for both Pt3Co-at and Pt3Co/Mo. The composition of the resulting catalysts was confirmed via X-ray photoelectron spectroscopy analysis. In situ cathode studies were performed using an acidic microfluidic H-2/O-2 fuel cell with an analytical platform. The electrolyte flow rate was optimized to minimize the effects of water management such that fuel cell performance is kinetically limited by the oxygen reduction reaction (ORR). In addition, electrolyte concentration was separately varied to determine cathode performance as a function of acidic pH. All four catalysts demonstrated good short-term activity and stability under fuel cell operating conditions in harsh acidic environments, with the Pt3Co/Mo alloy exhibiting the highest activity. Furthermore, both modified catalysts, Pt3Co/Mo and Pt3Co-at, exhibited superior durability compared to commercially available Pt3Co and Pt in the accelerated cathode aging studies performed within the microfluidic fuel cell via potential cycling. In situ impedance analysis of the Pt3Co/Mo cathode revealed enhanced catalyst stability and electrode durability as the cause of the dramatic improvements in long-term performance. (C) 2010 The Electrochemical Society. [DOI: 10.1149/1.3368721] All rights reserved.
引用
收藏
页码:B837 / B845
页数:9
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