4.6 Article

Investigation of Membrane Chemical Degradation as a Function of Catalyst Platinum Loading

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 168, Issue 6, Pages -

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/1945-7111/ac0221

Keywords

Fuel Cells; PEM; Membrane degradation; Ultra-low Pt

Funding

  1. LANL African American Partnership Program
  2. NNSA Minority Serving Institutes Program Managers

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Membrane chemical degradation significantly affects fuel cell durability, with factors such as ultra-low Pt electrode loadings and heterogeneous radical formation sites impacting degradation rate. Variations in catalyst layer thickness, ionomer to carbon ratio, and carbon support types also influence membrane degradation rates.
Membrane chemical degradation is one of many factors that can impact fuel cell durability. The fuel cell's lifetime heavily depends on the membrane and its ability to maintain chemical and mechanical integrity. Previous studies indicate that chemical degradation is due to the formation of hydroxyl radicals that attack the polymer structure resulting in membrane thinning, pinhole formation, and the release of fluoride and sulfate ions. Membrane durability was investigated using ultra-low Pt electrode loadings (<= 0.1 mg(Pt) cm(-2)). Accelerated stress testing (US-DOE protocols) demonstrated that the degradation rate was found to increase with higher Pt loadings. This is most likely due to more heterogeneous sites for radical formation due to hydrogen crossover to the cathode. We also explored membrane degradation rates while varying catalyst layer thickness, ionomer to carbon ratio, and types of carbon support. All of the aforementioned variables impact the membrane degradation rates.

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