Jie Dai, Zihan Shen, Yu Chen, Mengran Li, Vanessa K. Peterson, Jiayi Tang, Xixi Wang, Yu Li, Daqin Guan, Chuan Zhou, Hainan Sun, Zhiwei Hu, Wei-Hsiang Huang, Chih-Wen Pao, Chien-Te Chen, Yinlong Zhu^*, Wei Zhou, Zongping Shao^*

Abstract

Proton exchange membrane water electrolyzers powered by sustainable energy represent a cutting-edge technology for renewable hydrogen generation, while slow anodic oxygen evolution reaction (OER) kinetics still remains a formidable obstacle that necessitates basic comprehension for facilitating electrocatalysts’ design. Here, we report a low-iridium complex oxide La1.2Sr2.7IrO7.33 with a unique hexagonal structure consisting of isolated Ir(V)O6 octahedra and true peroxide O22– groups as a highly active and stable OER electrocatalyst under acidic conditions. Remarkably, La1.2Sr2.7IrO7.33, containing 59 wt % less iridium relative to the benchmark IrO2, shows about an order of magnitude higher mass activity, 6-folds higher intrinsic activity than the latter, and also surpasses the state-of-the-art Ir-based oxides ever reported. Combined electrochemical, spectroscopic, and density functional theory investigations reveal that La1.2Sr2.7IrO7.33 follows the peroxide-ion participation mechanism under the OER condition, where the inherent peroxide ions with accessible nonbonded oxygen states are responsible for the high OER activity. This discovery offers an innovative strategy for designing advanced catalysts for various catalytic applications.

DOI: https://doi.org/10.1021/jacs.4c11477