Breathing mode in Nd-CoOx for active and stable proton exchange membrane water electrolysis

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 Co<sub>3</sub>O<sub>4</sub>-based catalyst with oxygen vacancies and Nd-insertion (Nd-CoO<sub>x</sub>). This catalyst achieves a low overpotential of 317 mV at 10 mA cm<sup>-2</sup> for acidic oxygen evolution reaction and remains stable over 800 h. The oxygen vacancies in Nd-CoO<sub>x</sub> 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-CoO<sub>x</sub> delivers good performance in water electrolysis to achieve 200 mA cm<sup>-2</sup> at a low cell voltage of 1.69 V with low degradation over 100 h, and can reach 1 and 2 A cm<sup>-2</sup> at 1.93 V and 2.12 V, respectively.

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Publication Details

Journal
Nature Communications
Published
2025-12-09
DOI
https://doi.org/10.1038/s41467-025-66408-1
Citations
2
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.73

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article

Breathing mode in Nd-CoOx for active and stable proton exchange membrane water electrolysis

Jun Bo Zhong, Kun Feng, Xueqiang Fan, Haiping Lin et al.
2 citations
Nature Communications
Electrocatalysts for Energy Conversion
0.73
article

Breathing mode in Nd-CoOx for active and stable proton exchange membrane water electrolysis

Jun Bo Zhong, Kun Feng, Xueqiang Fan, Haiping Lin, Cheng Lu, Shuo Li, Jianhua Wang, Bai Xu, Jiabin Xu, Yong Feng
article en
2 citations

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 Co<sub>3</sub>O<sub>4</sub>-based catalyst with oxygen vacancies and Nd-insertion (Nd-CoO<sub>x</sub>). This catalyst achieves a low overpotential of 317 mV at 10 mA cm<sup>-2</sup> for acidic oxygen evolution reaction and remains stable over 800 h. The oxygen vacancies in Nd-CoO<sub>x</sub> 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-CoO<sub>x</sub> delivers good performance in water electrolysis to achieve 200 mA cm<sup>-2</sup> at a low cell voltage of 1.69 V with low degradation over 100 h, and can reach 1 and 2 A cm<sup>-2</sup> at 1.93 V and 2.12 V, respectively.

Nature CommunicationsVol. 16(1)
Western University (CA), Peking University (CN), Soochow University (CN), Shaanxi Normal University (CN)
Salt Science Research Foundation, National Natural Science Foundation of China, China Postdoctoral Science Foundation, Priority Academic Program Development of Jiangsu Higher Education Institutions, National Synchrotron Radiation Laboratory, Higher Education Discipline Innovation Project
Openalex Percentile: Top 27%
Electrocatalysts for Energy Conversion
0.73
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