Author
Listed:
- Yong Feng
(Soochow University, Institute of Functional Nano and Soft Materials Laboratory (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies)
- Jianhua Wang
(Chang’an District, School of Physics and Information Technology, Shaanxi Normal University)
- Kun Feng
(Soochow University, Institute of Functional Nano and Soft Materials Laboratory (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies)
- Bai Xu
(Soochow University, Institute of Functional Nano and Soft Materials Laboratory (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies)
- Jiabin Xu
(Soochow University, Institute of Functional Nano and Soft Materials Laboratory (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies
University of Western Ontario, Department of Chemistry)
- Shuo Li
(Soochow University, Institute of Functional Nano and Soft Materials Laboratory (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies)
- Cheng Lu
(Soochow University, Institute of Functional Nano and Soft Materials Laboratory (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies)
- Xing Fan
(Peking University, Center for Carbon-based Electronics and Key Laboratory for the Physics and Chemistry of Nanodevices, School of Electronics)
- Haiping Lin
(Chang’an District, School of Physics and Information Technology, Shaanxi Normal University)
- Jun Zhong
(Soochow University, Institute of Functional Nano and Soft Materials Laboratory (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies)
Abstract
Proton-exchange membrane water electrolysis in acidic solutions holds great promise for advancing the green-hydrogen economy but limited by using precious-metal catalysts. Here, we develop a low-cost Co3O4-based catalyst with oxygen vacancies and Nd-insertion (Nd-CoOx). This catalyst achieves a low overpotential of 317 mV at 10 mA cm−2 for acidic oxygen evolution reaction and remains stable over 800 h. The oxygen vacancies in Nd-CoOx enhance its catalytic activity, while Nd enables the long-term stability through a flexible “breathing mode” during oxygen evolution reaction, as revealed by in-situ methods such as X-ray absorption spectroscopy and Raman spectroscopy. The presence of Nd also improves the catalytic activity with the oxide path mechanism. This favorable strategy can be extended to other lanthanides. When used as the anode, Nd-CoOx delivers good performance in water electrolysis to achieve 200 mA cm−2 at a low cell voltage of 1.69 V with low degradation over 100 h, and can reach 1 and 2 A cm−2 at 1.93 V and 2.12 V, respectively.
Suggested Citation
Yong Feng & Jianhua Wang & Kun Feng & Bai Xu & Jiabin Xu & Shuo Li & Cheng Lu & Xing Fan & Haiping Lin & Jun Zhong, 2025.
"Breathing mode in Nd-CoOx for active and stable proton exchange membrane water electrolysis,"
Nature Communications, Nature, vol. 16(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-66408-1
DOI: 10.1038/s41467-025-66408-1
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