Durability of polymer electrolyte membrane fuel cells operated at subfreezing temperatures

Natalia Macauley, Roger W. Lujan, Dusan Spernjak, Daniel S. Hussey, David L. Jacobson, Karren More, Rodney L. Borup, Rangachary Mukundan

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

The structure, composition, and interfaces of membrane electrode assemblies (MEA) and gas-diffusion layers (GDLs) have a significant effect on the performance of single-proton-exchange-membrane (PEM) fuel cells operated isothermally at subfreezing temperatures. During isothermal constant-current operation at subfreezing temperatures, water forming at the cathode initially hydrates the membrane, then forms ice in the catalyst layer and/or GDL. This ice formation results in a gradual decay in voltage. High-frequency resistance initially decreases due to an increase in membrane water content and then increases over time as the contact resistance increases. The water/ice holding capacity of a fuel cell decreases with decreasing subfreezing temperature (-10�C vs. -20�C vs. -30�C) and increasing current density (0.02 A cm-2 vs. 0.04 A cm-2). Ice formation monitored using in-situ high-resolution neutron radiography indicated that the ice was concentrated near the cathode catalyst layer at low operating temperatures (≈-20�C) and high current densities (0.04 A cm-2). Significant ice formation was also observed in the GDLs at higher subfreezing temperatures (≈-10�C) and lower current densities (0.02 A cm-2). These results are in good agreement with the long-term durability observations that show more severe degradation at lower temperatures (-20�C and -30�C).

Original languageEnglish
Pages (from-to)F1317-F1329
JournalJournal of the Electrochemical Society
Volume163
Issue number13
DOIs
StatePublished - 2016

Funding

This work was supported by the Fuel Cell Technologies Office, Energy Efficiency and Renewable Energy, U.S. Department of Energy. The authors from Los Alamos thank the Technology Development Managers, Dr. Dimitrios Papageorgopoulos and Dr. Nancy Garland for supporting this effort. This work was also supported by the U.S. Department of Commerce, the NIST Ionizing Radiation Division, the Director's Office of NIST, the NIST Center for Neutron Research, and the U.S. Department of Energy through interagency agreement no. DE-AI01-01EE50660. Microscopy was performed as part of a user project at ORNL's Center for Nanophase Materials Sciences (CNMS), which is a U.S. Department of Energy, Office of Science User Facility.

FundersFunder number
U.S. Department of Energy
National Institute of Standards and Technology
U.S. Department of Commerce
Office of Science
Office of Energy Efficiency and Renewable Energy
NIST Center for Neutron ResearchDE-AI01-01EE50660
Fuel Cell Technologies Office

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