On the impact of water activity on reversal tolerant fuel cell anode performance and durability

被引:86
|
作者
Hong, Bo Ki [1 ,2 ]
Mandal, Pratiti [1 ]
Oh, Jong-Gil [2 ]
Litster, Shawn [1 ]
机构
[1] Carnegie Mellon Univ, Dept Mech Engn, Scott Hall,Room 5107,5000 Forbes Ave, Pittsburgh, PA 15213 USA
[2] Hyundai Motor Co, Fuel Cell Engn Design Team, Yongin 446716, Gyeonggi Do, South Korea
基金
美国安德鲁·梅隆基金会;
关键词
Fuel starvation; Cell reversal; Reversal tolerant anode; Oxygen evolution reaction; Water electrolysis; Carbon corrosion; PROTON-EXCHANGE MEMBRANE; RAY COMPUTED-TOMOGRAPHY; CARBON CORROSION; RELATIVE-HUMIDITY; LOW-TEMPERATURE; DEGRADATION; STARVATION; CATALYST; HETEROGENEITIES; MECHANISMS;
D O I
10.1016/j.jpowsour.2016.07.002
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
Durability of polymer electrolyte fuel cells in automotive applications can be severely affected by hydrogen starvation arising due to transients during the drive-cycle. It causes individual cell voltage reversal, yielding water electrolysis and carbon corrosion reactions at the anode, ultimately leading to catastrophic cell failure. A popular material-based mitigation strategy is to employ a reversal tolerant anode (RTA) that includes oxygen evolution reaction (OER) catalyst (e.g., IrO2) to promote water electrolysis over carbon corrosion. Here we report that RTA performance surprisingly drops under not only water-deficient but also water-excess conditions. This presents a significant technical challenge since the most common triggers for cell reversal involve excess liquid water. Our findings from detailed electro-chemical diagnostics and nano-scale X-ray computed tomography provide insight into how automotive fuel cells can overcome critical vulnerabilities using material-based solutions. Our work also highlights the need for improved materials, electrode designs, and operation strategies for robust RTAs. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:280 / 288
页数:9
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