Mechanism of Catalyst Degradation in Proton Exchange Membrane Fuel Cells
Open accessAbstract
A mechanism of catalyst particle growth in proton exchange membrane fuel cells (PEMFCs) by Ostwald ripening is presented. Particle growth occurs as a coupled process involving platinum ion transport through aqueous liquid and/or ionomer, and electron transport through a carbon support. The dominating factor in degradation of a catalyst supported on carbon is the presence of platinum ions in solution (in liquid and/or in ionomer). Experiments were conducted on commercial PEMFC electrodes in three liquids, solution, dilute acid solution, and deionized water. Pt particle size grew from to after in solution. By contrast, no detectable growth occurred in dilute acid or in deionized water. This demonstrates that the higher the Pt ion concentration, the faster the kinetics. The role of electronic conduction through support was verified by conducting experiments in solution on Pt supported on an electronically insulating material, namely alumina. While significant growth occurred in Pt supported on carbon, no detectable growth occurred in Pt supported on alumina. This observation is in complete accord with the model, and demonstrates the role of electronic transport on degradation. That is, when supported on alumina, lack of an electronically conducting path suppresses degradation even with present in solution.
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- Authors
- Virkar, A. V., & Zhou, Y.
- Affiliations
- University of Utah (US)
- Venue
- Journal of The Electrochemical Society
- Publisher
- The Electrochemical Society
- Published
- 2007
- Volume
- 154
- Issue
- 6
- Pages
- B540
- ISSN
- 0013-4651 (ISSN-L)
- OpenAlex
- W1991015819
- Cited by
- 133
- References
- 18
- Citations by year
- 2026: 5 · 2025: 3 · 2024: 6 · 2023: 6 · 2022: 5 · 2021: 4 · 2020: 8 · 2019: 5 · 2018: 12 · 2017: 9 · 2016: 6 · 2015: 7 · 2014: 8 · 2013: 7 · 2012: 10
- FWCI
- 6.30
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of The Electrochemical Society (publishedVersion)
- Funders
- U.S. Department of Energy (DE‐FG02‐, FG0203ER46086)
- University of Utah
- Topics
- Physical Sciences › Engineering › Electrical and Electronic Engineering › Fuel Cells and Related Materials
- Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Electrocatalysts for Energy Conversion
- Physical Sciences › Materials Science › Materials Chemistry › Catalytic Processes in Materials Science
- Keywords
- catalyst deactivation, Ostwald ripening, proton exchange membrane fuel cells, ionomers, carbon support, electronic conduction, Pt/Al2O3 catalyst, fuel cell electrodes
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