Impact of Carbon Support Structure on the Durability of PtCo Electrocatalysts

质子交换膜燃料电池 材料科学 催化作用 化学工程 溶解 铂金 电解质 电化学 浸出(土壤学) 多孔性 过渡金属 碳纤维 阴极 电极 冶金 复合材料 化学 物理化学 土壤科学 土壤水分 工程类 复合数 生物化学 环境科学
作者
Thomas O’Brien,Sergio Herrera,David A. Langlois,Nancy N. Kariuki,Haoran Yu,Michael J. Zachman,Deborah J. Myers,David A. Cullen,Rodney L. Borup,Rangachary Mukundan
出处
期刊:Journal of The Electrochemical Society [Institute of Physics]
卷期号:168 (5): 054517-054517 被引量:12
标识
DOI:10.1149/1945-7111/abfe46
摘要

High performing, low-Pt content fuel cell membrane electrode assemblies (MEAs) are critical to the economic viability of proton exchange membrane fuel cells (PEMFCs) for the transportation industry. Considerable research has been conducted to reduce the Pt content in fuel cells, leading to the development of transition metal alloys, such as Platinum-Cobalt (PtCo). The degree of degradation of PtCo catalysts can be impacted by not only the composition and morphology of the catalyst particle itself, but also its interactions with the carbon support. In this study several low-PtCo MEAs were fabricated, with various combinations of porous and solid carbon cathode catalyst supports. The MEAs were subjected to an accelerated stress test (AST), and the catalyst degradation characterized using electrochemical, X-ray scattering, and electron microscopy techniques. Porous supports retain more of their electrochemically-active surface area (ECSA) and demonstrate higher performance after the AST. This is believed to be due to the ability of the porous supports to trap the metal particles within the pores, slowing their dissolution/precipitation, and agglomeration. However porous supports also exhibit greater increases in transport resistance probably associated with enhanced Co leaching under the AST conditions.

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