4.6 Article

Durability of Polymer Electrolyte Membrane Fuel Cells Operated at Subfreezing Temperatures

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 163, Issue 13, Pages F1317-F1329

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/2.0191613jes

Keywords

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Funding

  1. Fuel Cell Technologies Office, Energy Efficiency and Renewable Energy, U.S. Department of Energy
  2. U.S. Department of Commerce
  3. NIST Ionizing Radiation Division
  4. Director's Office of NIST
  5. NIST Center for Neutron Research
  6. U.S. Department of Energy [DE-AI01-01EE50660]

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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 degrees C vs. -20 degrees C vs. -30 degrees 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 (approximate to-20 degrees C) and high current densities (0.04 A cm(-2)). Significant ice formation was also observed in the GDLs at higher subfreezing temperatures (approximate to-10 degrees 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 degrees C and -30 degrees C). (C) The Author(s) 2016. Published by ECS. All rights reserved.

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