Electronic tuning of RuO₂ polarizes metal–oxygen redox for proton exchange membrane water electrolysis

The metal-oxygen redox behavior governs the performance of transition metal oxides in many electrochemical reactions, especially for RuO<sub>2</sub> with the activity-stability paradox in the anode oxygen evolution reaction of proton exchange membrane water electrolyzers. Herein, we modulate the electronic structure of RuO<sub>2</sub> near the Fermi level to promote reversible Ru redox while suppressing the oxidative release of lattice oxygen. As a result, the RuO<sub>2</sub> integrated with electron-rich p-block metals Sb achieves an overpotential of 220 mV and long-term operational stability of 1200 h at 10 mA cm<sup>-2</sup>. The assembled proton exchange membrane water electrolyzers can operate steadily over 100 h at 100, 500, and 1000 mA cm<sup>-2</sup>. Further advanced in-situ characterizations reveal the more reversible and milder Ru redox and the passivated lattice oxygen reactivity, which suppresses drastic structural changes of RuO<sub>2</sub> during the oxygen evolution reaction. This work highlights the importance of engineering metal-oxygen redox behavior and provides insights for designing high-performance catalysts for energy conversion and storage devices.

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Publication Details

Journal
Nature Communications
Published
2025-09-30
DOI
https://doi.org/10.1038/s41467-025-63721-7
Citations
4
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
1.45

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article

Electronic tuning of RuO₂ polarizes metal–oxygen redox for proton exchange membrane water electrolysis

Dayin He, Huang Zhou, Jie Xu, Yuen Shing Wu et al.
4 citations
Nature Communications
Electrocatalysts for Energy Conversion
1.45
article

Electronic tuning of RuO₂ polarizes metal–oxygen redox for proton exchange membrane water electrolysis

Dayin He, Huang Zhou, Jie Xu, Yuen Shing Wu, Xingen Lin, Xusheng Zheng, Junmin Li, Wei‐Xue Li, Sulei Hu, Xianhui Ma, Xin Wang, Jie Zheng, Ge Yu, Peigen Liu, Zhixuan Chen, Xuyan Zhao, Ze Lin, Zihan Wang
article en
4 citations

Abstract

The metal-oxygen redox behavior governs the performance of transition metal oxides in many electrochemical reactions, especially for RuO<sub>2</sub> with the activity-stability paradox in the anode oxygen evolution reaction of proton exchange membrane water electrolyzers. Herein, we modulate the electronic structure of RuO<sub>2</sub> near the Fermi level to promote reversible Ru redox while suppressing the oxidative release of lattice oxygen. As a result, the RuO<sub>2</sub> integrated with electron-rich p-block metals Sb achieves an overpotential of 220 mV and long-term operational stability of 1200 h at 10 mA cm<sup>-2</sup>. The assembled proton exchange membrane water electrolyzers can operate steadily over 100 h at 100, 500, and 1000 mA cm<sup>-2</sup>. Further advanced in-situ characterizations reveal the more reversible and milder Ru redox and the passivated lattice oxygen reactivity, which suppresses drastic structural changes of RuO<sub>2</sub> during the oxygen evolution reaction. This work highlights the importance of engineering metal-oxygen redox behavior and provides insights for designing high-performance catalysts for energy conversion and storage devices.

Nature CommunicationsVol. 16(1)
Tongji University (CN), University of Science and Technology of China (CN), Anhui University (CN), Wenzhou University (CN), Hefei National Center for Physical Sciences at Nanoscale (CN), National Synchrotron Radiation Laboratory (CN)
Salt Science Research Foundation, National Natural Science Foundation of China, Chinese Academy of Sciences, University of Science and Technology of China, National Synchrotron Radiation Laboratory, Natural Science Foundation of Anhui Province, Youth Innovation Promotion Association, Beijing Synchrotron Radiation Facility
Openalex Percentile: Top 17%
Electrocatalysts for Energy Conversion
1.45
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