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Abstract Proton exchange membrane water electrolysers promise to usher in a new era of clean energy, but they remain a formidable obstacle in designing active and durable electrocatalysts for the acidic oxygen evolution reaction (OER). In this study, a protonated iridium oxide embedded with single‐atom dispersed ruthenium atoms (H 3.8 Ir 1− x Ru x O 4 ) that demonstrates exceptional activity and stability in acidic water oxidation is introduced. The single Ru dopants favorably induce localized oxygen vacancies in the Ir─O lattice, synergistically strengthening the adsorption of OOH* intermediates and enhancing the intrinsic OER activity. In addition, the preferential oxidation of Ru and the electronegativity of the oxygen vacancies significantly stabilize the Ir─O active sites, improving the OER stability. Consequently, the H 3.8 Ir 1─ x Ru x O 4 catalyst shows an overpotential of 255 mV at 10 mA cm −2 and displays exceptional catalytic endurance in acidic electrolytes, surpassing 1100 h, representing a remarkable one‐order‐of‐magnitude increase in stability compared to that of pristine H 3.8 IrO 4 . A proton exchange membrane electrolyser utilizing the H 3.8 Ir 1− x Ru x O 4 catalyst as an anode exhibits stable performance for more than 1280 h under a high current density of 2 A cm −2 .
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Jialin Tang
California State University, Fullerton
Xinyan Liu
University of Electronic Science and Technology of China
Xiaoxia Xiong
University of Electronic Science and Technology of China
Advanced Materials
University of Science and Technology of China
University of Electronic Science and Technology of China
Hefei National Center for Physical Sciences at Nanoscale
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Tang et al. (Thu,) studied this question.
synapsesocial.com/papers/68e5c0e5b6db643587558753 — DOI: https://doi.org/10.1002/adma.202407394