催化作用
阴极
材料科学
质子交换膜燃料电池
降级(电信)
电化学
相对湿度
溶解
耐久性
化学工程
合金
电极
冶金
复合材料
化学
电气工程
工程类
物理化学
物理
热力学
生物化学
作者
Nagappan Ramaswamy,Swami Kumaraguru,Ratandeep S. Kukreja,Daniel Groom,Karalee Jarvis,Paulo J. Ferreira
标识
DOI:10.1149/1945-7111/ac4374
摘要
Maintaining the high performance of proton-exchange membrane fuel cells (PEMFC) over the course of its lifetime is a key enabling factor for its successful commercialization as a primary power source in zero-emission transportation applications. In this context, it is important to mitigate the degradation of PtCo-alloy based cathode catalysts used for oxygen reduction reaction (ORR). PtCo-alloy catalysts exhibit high activity at beginning-of-life (BOL) which tends to decrease during operation due to loss of electrochemical surface area (ECSA) and dissolution-contamination related effects of the Co-alloying component. Here, we demonstrate the use of relative humidity (RH) of the inlet gases as a controllable parameter to mitigate the degradation of PtCo-alloy catalyst degradation. We employ a catalyst-specific voltage cycling accelerated stress test (AST) durability protocol as a function of inlet RH to degrade PtCo catalysts. A series of in situ electrochemical diagnostics and ex situ characterizations have been carried out to investigate the catalyst layer characteristics at end-of-test (EOT). Our results show that at sub-saturated conditions of durability protocol operation, PtCo catalyst sustains higher EOT H 2 /air performance due to better retention of ECSA and smaller impact of Co 2+ dissolution/contamination.
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