Impact of Carbon Support Structure on the Durability of PtCo Electrocatalysts
Autor: | R. Mukundan, Deborah J. Myers, Nancy Kariuki, David A. Langlois, Michael J. Zachman, Sergio Herrera, Haoran Yu, Rodney L. Borup, T. E. O’Brien, David A. Cullen |
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Rok vydání: | 2021 |
Předmět: |
Materials science
chemistry Chemical engineering Renewable Energy Sustainability and the Environment technology industry and agriculture Materials Chemistry Electrochemistry chemistry.chemical_element Condensed Matter Physics Carbon Durability Surfaces Coatings and Films Electronic Optical and Magnetic Materials |
Zdroj: | Journal of The Electrochemical Society. 168:054517 |
ISSN: | 1945-7111 0013-4651 |
DOI: | 10.1149/1945-7111/abfe46 |
Popis: | 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. |
Databáze: | OpenAIRE |
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