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The study investigates the degradation of high temperature PEM fuel cells under accelerated potential cycling conditions, with three different cathode flow field designs showing varying performance degradation.

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Abstract

Abstract Degradation of phosphoric acid doped polybenzimidazole membrane based fuel cells under accelerated potential cycling conditions is investigated in current study. Three unit cells with identical high temperature membrane electrode assembly were assembled with three different cathode flow field designs. The fuel cell is cycled between 0.5 V and 0.9 V with 3 min dwelling time for each voltage set point. Performance degradation mechanisms associated with differences in cathode flow design are identified. The fuel cell with multiple serpentine design is operated for a maximum of 4,821 potential cycles with only 38.6% of initial performance remaining at the end‐of‐test (EoT), whereas straight and parallel design operated for only 3,188 cycles. The electrochemical characterization studies reveal the cause of observed performance losses from polarization curves. Irrespective of the design type used there are very high activation losses observed which accelerated with accelerated stress tests (AST) testing. The impedance studies reveal high charge transfer resistance related to increased platinum crystal growth on cathode and reduced electrochemical surface area (ECSA) of catalyst. Overall the AST results in irreversible performance loss and severe degradation of the cathode catalyst support and catalyst itself.

Key findings

  • The fuel cell with multiple serpentine design operated for 4,821 cycles with 38.6% of initial performance remaining.
  • Straight and parallel designs operated for 3,188 cycles with unknown performance remaining.
  • High activation losses and charge transfer resistance were observed, accelerated by accelerated stress tests (AST) testing.

Keywords

Proton exchange membrane fuel cellCathodeMembrane electrode assemblyPolarization (electrochemistry)ElectrochemistryElectrode

Identifiers

Journal
Fuel Cells
Year
2019