Role of Hydration in Uncovering the OER Activity of Amorphous Iridium Oxide Electrocatalysts

作者：Connor Sherwin, Verónica Celorrio, Alessandro Difilippo, Katie Rigg, Mark Clapp, Armando Ibraliu, Luke Luisman, Thomas Wakelin, Amber Watson, Nikolay Zhelev, Lucy K. McLeod, Christopher M. Zalitis, Andrea E. Russell · 发表于：ACS Catalysis · 年份：2025 · DOI：10.1021/acscatal.5c05765 · 被引用次数：2 · 研究领域：Electrocatalysts for Energy Conversion、CO2 Reduction Techniques and Catalysts、Advanced Electron Microscopy Techniques and Applications

High Resolution Image Download MS PowerPoint Slide Understanding the structural properties of iridium oxide electrocatalysts under operational conditions is critical for elucidating the structure–property relationships that enhance the catalytic activity for the oxygen evolution reaction. In this study, in situ X-ray absorption spectroscopy under realistic conditions was employed to investigate the potentiodynamic and time-resolved structural evolution of a commercial iridium oxide, alongside its fully hydrated and crystalline counterparts. Our findings reveal two distinct electrochemical regimes, a low potential plateau associated with a nonconductive Ir 3+ state and a linear region where small potential variations induce reversible oxidation state and structural transformations. The structural changes were found to occur reversibly on the commercial material even after prolonged exposure to OER potentials. Notably, the hydrated IrO x exhibits extremely high OER activity, surpassing the commercial material by nearly an order of magnitude, yet it suffers from significant instability. In contrast, the crystalline IrO 2 demonstrates poor activity as its catalytic performance appears to be confined to the surface. These findings highlight the critical role of hydration in modulating both activity and stability, offering valuable insights for the rational design of next generation iridium based OER catalysts.