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While iridium-based perovskites have been identified as promising candidates for the oxygen evolution reaction (OER) in proton exchange membrane (PEM) electrolyzer applications, an improved fundamental understanding of these highly dynamic materials under reaction conditions is needed to inform more robust future catalyst design. Herein, we study the highly active SrIr0.8Zn0.2O3 perovskite for the OER in acid by employing electrochemical experiments with in situ and ex situ characterization techniques to understand the dynamic nature of this material at both short and long time scales. We observe initial intrinsic OER activity improvement with electrochemical cycling as well as an initial increase of Ir oxidation state under OER conditions via in situ X-ray absorption spectroscopy. We discover that the SrIr0.8Zn0.2O3 perovskite experiences an OER-induced metal to insulator transition (MIT) with extensive electrochemical cycling, caused by surface reorganization and changes to the material crystallinity that occur with exposure to an acidic and oxidizing environment. Our novel identification of an OER-induced MIT for iridate perovskites reveals an additional stability concern for iridate catalysts which are known to experience material dissolution challenges; this work ultimately aims to inform future catalyst material design for PEM water electrolysis applications.
Edgington et al. (Wed,) studied this question.