4.8 Article

Three-Electrode Study of Electrochemical Ionomer Degradation Relevant to Anion-Exchange-Membrane Water Electrolyzers

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 14, Issue 16, Pages 18261-18274

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c22472

Keywords

anion-exchange-membrane water electrolysis; ionomer; supporting electrolyte; XPS; electrochemical degradation

Funding

  1. U.S. Department of Energy's Office of Energy Efficiency and Renewable Energy (EERE) under the Fuel Cell Technologies Office (FCTO) [DE-EE0008841]
  2. W.M. Keck Foundation
  3. M.J. Murdock Charitable Trust
  4. ONAMI
  5. Air Force Research Laboratory [FA8650-05-1-5041]
  6. NSF [0923577, 0421086]
  7. University of Oregon

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Anion-exchange-membrane water electrolyzers show promise for low-cost operation, but more research is needed to understand degradation and failure modes. Supporting electrolytes can improve performance and durability, but the interactions between anions and the ionomer membrane remain poorly understood.
Among existing water electrolysis (WE) technologies, anion-exchange-membrane water electrolyzers (AEMWEs) show promise for low-cost operation enabled by the basic solid-polymer electrolyte used to conduct hydroxide ions. The basic environment within the electrolyzer, in principle, allows the use of non-platinum-group metal catalysts and less-expensive cell components compared to acidic-membrane systems. Nevertheless, AEMWEs are still underdeveloped, and the degradation and failure modes are not well understood. To improve performance and durability, supporting electrolytes such as KOH and K2CO3 are often added to the water feed. The effect of the anion interactions with the ionomer membrane (particularly other than OH-), however, remains poorly understood. We studied three commercial anion-exchange ionomers (Aemion, Sustainion, and PiperION) during oxygen evolution (OER) at oxidizing potentials in several supporting electrolytes and characterized their chemical stability with surface-sensitive techniques. We analyzed factors including the ionomer conductivity, redox potential, and pH tolerance to determine what governs ionomer stability during OER. Specifically, we discovered that the oxidation of Aemion at the electrode surface is favored in the presence of CO32-/HCO3- anions perhaps due to the poor conductivity of that ionomer in the carbonate/bicarbonate form. Sustainion tends to lose its charge-carrying groups as a result of electrochemical degradation favored in basic electrolytes. PiperION seems to be similarly negatively affected by a pH drop and low carbonate/bicarbonate conductivity under the applied oxidizing potential. The insight into the interactions of the supporting electrolyte anions with the ionomer/membrane helps shed light on some of the degradation pathways possible inside of the AEMWE and enables the informed design of materials for water electrolysis.

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