Mesoporous Single-Crystalline Particles as Robust and Efficient Acidic Oxygen Evolution Catalysts
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Updated: May 15, 2025

Synthesis of Platinum-nickel Nanowires and Optimization for Oxygen Reduction Performance
Published on: April 27, 2018
Yong Wang1,2, Yunpu Qin1, Sijia Liu1
1Institute for Advanced Materials and Technology, University of Science and Technology Beijing, Beijing 100083, China.
Abstract:
The scarcity of iridium (Ir) limits its widespread use in acidic oxygen evolution reaction (OER). Herein, mesoporous single-crystalline spinel Co3O4 with atomically dispersed low-valence-state Ir has been developed to enable Ir's efficient and stable utilization. The surface Pourbaix diagram suggests that under acidic OER conditions, O* fully covers both Co3O4(111) and (110) surfaces, passivating Co sites but enhancing Co3O4's structural stability, a benefit further improved by Ir doping. Mesopores offer numerous loading sites for Ir single atoms (13.8 wt %), which activate the originally O*-passivated Co3O4(111) surface by creating high-intrinsic-activity Co-Ir bridge sites; meanwhile, Ir and Co leaching rates are reduced to about 1/4 and 1/5, respectively, compared to conventional Ir/Co3O4 catalysts. Our catalyst exhibits a low η10 of 248 mV for over 100 h, showcasing its potential in water electrolysis.
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