Baselining Activity and Stability of ORR Catalysts and Electrodes for Proton Exchange Membrane Fuel Cells for Heavy-Duty Applications

质子交换膜燃料电池 催化作用 电极 电化学 阴极 膜电极组件 浸出(土壤学) 材料科学 化学 铂金 碳纤维 合金 活性炭 化学工程 复合材料 电解质 有机化学 物理化学 土壤水分 土壤科学 吸附 工程类 复合数 生物化学 环境科学
作者
X. Wang,Leiming Hu,Kenneth C. Neyerlin,Rajesh K Ahluwalia
出处
期刊:Journal of The Electrochemical Society [Institute of Physics]
卷期号:170 (2): 024503-024503
标识
DOI:10.1149/1945-7111/acb847
摘要

Activity and stability of electrodes with Pt and PtCo alloy catalysts supported on high surface area carbon, hereafter to as a-Pt/C and d-PtCo/C, were evaluated for heavy-duty applications. Both catalysts had nearly identical Pt loading (50-wt% Pt on carbon and 0.25 mg Pt cm −2 ) and had undergone thermal treatment to stabilize them by growing the average particle size to 4–5 nm. Both were subjected to 90,000 (90 k) standard accelerated stress tests (AST) cycles consisting of 0.6–0.95 V square wave potentials, 3-s hold at upper and lower potential limits in H 2 /N 2 at 1.5 atm, 80 °C and 100% RH. Test protocols were developed to monitor the performance losses and characterize them in terms of activity for the oxygen reduction reaction (ORR), oxygen transport in the electrode and proton transport in the membrane and cathode catalyst layer. Despite the nearly double initial ORR activity, the PtCo/C electrode degraded faster due to the leaching of Co from the catalyst that had started even before the imposition of the AST potential cycles. Commensurate with Co leaching, Co poisoning of ionomer is responsible for the inferior performance of d-PtCo/C electrode at high current densities both before and after AST.
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