4.8 Article

Post-mortem analysis of a long-term tested proton exchange membrane fuel cell stack under low cathode humidification conditions

Journal

JOURNAL OF POWER SOURCES
Volume 253, Issue -, Pages 90-97

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jpowsour.2013.11.056

Keywords

Proton exchange membrane fuel cell; Stack; Durability; Degradation; Low humidity conditions; Post-mortem analysis

Funding

  1. Korea Institute of Energy Technology Evaluation and Planning (KETEP)
  2. Korean Ministry of Knowledge Economy [2011T100200280]
  3. Fundamental R&D Program for Core Technology of Materials
  4. Ministry of Knowledge Economy [10037289]
  5. Fusion Research Program for Green Technologies through the National Research Foundation of Korea (NRF) [2011-0004428]
  6. Korea Evaluation Institute of Industrial Technology (KEIT) [10037289] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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During continuous power operation for 2740 h, the major mechanisms and patterns of performance degradation in a polymer electrolyte membrane fuel cell (PEMFC) stack are investigated under low cathode humidification with simulated reformate fuel gases through the use of various physicochemical and electrochemical analysis tools. As operating time increases, the operating voltages and open-circuit voltages (OCVs) of the stack decrease with the large voltage distributions. In the post-mortem analysis of the stack, the delamination of the catalyst layer (CL) of unstable operating membrane electrode assemblies (MEAs) is significant near the cathode gas inlets. This observation is in agreement with the results of OCV, hydrogen crossover current, and anode off-gas measurements. This phenomenon may be due to the acceleration of carbon corrosion in the cathode during the frequent start-up and shut-down process, because the local cathode potential can reach more than 1.5 V in the air/fuel boundary. Additionally, the frequent membrane hydration and dehydration by the accumulation of excess water (through electrochemical reaction) and faster water evaporation (under dry-air cathode conditions and high operating temperatures) may accelerate the interface delamination between the membrane and cathode CL with a substantially uneven distribution of water. (C) 2013 Elsevier B.V. All rights reserved.

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