Self-Coordinating Electronic Metal–Support Interaction Stabilizes Ultralow-Loading Ir Single Atoms for Durable Acidic Oxygen Evolution

Engineering electronic metal–support interactions (EMSI) enables scalable proton exchange membrane water electrolysis (PEMWE) at ultralow Ir loadings by buffering Ir against overoxidation and dissolution under acidic oxygen evolution conditions (OER). However, a seemingly disparate interpretation has persisted: high-valent Ir is often associated with optimal intermediate adsorption, whereas low-valent Ir correlates with improved corrosion resistance, suggesting that static EMSI fails to rationalize the activity-stability trade-off. Here, we construct an atomically dispersed Ir–O–Co interface by anchoring isolated Ir single atoms on spinel Co 3 O 4, providing a new perspective on a dynamic charge-compensation mechanism: at low bias, the Ir site is progressively oxidized to enhance water activation and intermediate turnover; at high bias, the Co 3 O 4 compensates charge back to the Ir site, thereby suppressing overoxidation-driven dissolution. Such self-coordinating EMSI breaks the conventional activity-stability trade-off in acidic OER. In an integrated PEM electrolyzer, the Ir single-atom catalyst sustains operation for >1500 h at 1.0 A cm –2 with an ultralow Ir loading of 0.1 mg cm –2, highlighting the importance of self-coordinating EMSI for durable, precious-metal-minimized PEMWE anodes.

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Journal
Journal of the American Chemical Society
Published
2026-06-17
DOI
https://doi.org/10.1021/jacs.6c03983
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.00

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article

Self-Coordinating Electronic Metal–Support Interaction Stabilizes Ultralow-Loading Ir Single Atoms for Durable Acidic Oxygen Evolution

W Z Chen, Fei Song, Yupeng Zhu, Jin‐Xia Lin et al.
Journal of the American Chemical Society
Electrocatalysts for Energy Conversion
article

Self-Coordinating Electronic Metal–Support Interaction Stabilizes Ultralow-Loading Ir Single Atoms for Durable Acidic Oxygen Evolution

W Z Chen, Fei Song, Yupeng Zhu, Jin‐Xia Lin, Rui Jiang, Ganwen Chen, Ruihan Gong, Hua Bing Tao, Xiang Chen, Bailin Tian, Yu Yu, Yishui Ding, Gao Y, Chenrui Ji, Hongqiang Jin
article en

Abstract

Engineering electronic metal–support interactions (EMSI) enables scalable proton exchange membrane water electrolysis (PEMWE) at ultralow Ir loadings by buffering Ir against overoxidation and dissolution under acidic oxygen evolution conditions (OER). However, a seemingly disparate interpretation has persisted: high-valent Ir is often associated with optimal intermediate adsorption, whereas low-valent Ir correlates with improved corrosion resistance, suggesting that static EMSI fails to rationalize the activity-stability trade-off. Here, we construct an atomically dispersed Ir–O–Co interface by anchoring isolated Ir single atoms on spinel Co 3 O 4, providing a new perspective on a dynamic charge-compensation mechanism: at low bias, the Ir site is progressively oxidized to enhance water activation and intermediate turnover; at high bias, the Co 3 O 4 compensates charge back to the Ir site, thereby suppressing overoxidation-driven dissolution. Such self-coordinating EMSI breaks the conventional activity-stability trade-off in acidic OER. In an integrated PEM electrolyzer, the Ir single-atom catalyst sustains operation for >1500 h at 1.0 A cm –2 with an ultralow Ir loading of 0.1 mg cm –2, highlighting the importance of self-coordinating EMSI for durable, precious-metal-minimized PEMWE anodes.

Journal of the American Chemical Society
Anhui University (CN), National University of Singapore (SG), Xiamen University (CN), Beijing Jiaotong University (CN), Anhui Science and Technology University (CN), Shanghai Advanced Research Institute (CN), Collaborative Innovation Center of Chemistry for Energy Materials (CN), Shanghai Synchrotron Radiation Facility, Anhui University of Technology (CN), Tsinghua University (CN)
Xiamen Municipal Bureau of Science and Technology, National Research Foundation Singapore, National Natural Science Foundation of China, Ministry of Education of the People's Republic of China, National Key Research and Development Program of China
Openalex Percentile: Top 20%
Electrocatalysts for Energy Conversion
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