Dual-Site Cobalt-Doped RuO <sub>2</sub> /TiO <sub>2</sub> Electrocatalyst Enables Stable and Cost-Efficient Acidic Oxygen Evolution for PEM Water Electrolysis

Developing efficient, cost-effective, and durable electrocatalysts for proton exchange membrane water electrolysis (PEMWE) remains a significant challenge, requiring the stabilization and enhancement of catalyst activity under harsh conditions. Here, we present cobalt-doped ruthenium dioxide (Co<sub>0.3</sub>Ru<sub>0.7</sub>O<sub>2</sub>) on TiO<sub>2</sub> as an electrocatalyst toward an acidic oxygen evolution reaction. The Co<sub>0.3</sub>Ru<sub>0.7</sub>O<sub>2</sub>-TiO<sub>2</sub> achieves an impressive overpotential of 322 mV at 1 A cm<sup>-2</sup> and demonstrates stable operation for over 1000 h at 500 mA cm<sup>-2</sup> in a PEMWE device. Comprehensive experimental and theoretical calculation results demonstrate that the doping of Co atoms into the rutile RuO<sub>2</sub> lattice optimizes the geometric configuration. Moreover, the lattice-matched interface between Co<sub>0.3</sub>Ru<sub>0.7</sub>O<sub>2</sub> and TiO<sub>2</sub> promotes interfacial electron redistribution and stabilizes active centers under oxidative conditions. This facilitates a dual-site fully parallel oxidation (DFO) pathway in which intermediates are synchronously adsorbed and desorbed at Ru and Co sites, enabling direct <i>O-O</i> coupling. This work highlights the synergistic effect of the Ru-Co dual sites and TiO<sub>2</sub> support in establishing a stable, self-regulating electronic environment that drives efficient intermediate transformation via the DFO mechanism.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-09-24
DOI
https://doi.org/10.1021/jacs.5c14137
Citations
20
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
7.27
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article

Dual-Site Cobalt-Doped RuO 2 /TiO 2 Electrocatalyst Enables Stable and Cost-Efficient Acidic Oxygen Evolution for PEM Water Electrolysis

Ke Xu, Yong Han, Zhangquan Peng, Chenyu Yang et al.
20 citations
Journal of the American Chemical Society
Electrocatalysts for Energy Conversion
7.27
article

Dual-Site Cobalt-Doped RuO 2 /TiO 2 Electrocatalyst Enables Stable and Cost-Efficient Acidic Oxygen Evolution for PEM Water Electrolysis

Ke Xu, Yong Han, Zhangquan Peng, Chenyu Yang, Jinxuan Liu, Xueliang Mu, Shu Zhu, Edmund C. M. Tse, Yuanyuan Zhao, Zhiwei Zhao, Fei Li, Qing Li, Qinghua Liu, Wei Liu, Liang Frank Wang, Jian‐Feng Li, Zhi Liu, Jing Liang, Junfeng Gao
article en
20 citations

Abstract

Developing efficient, cost-effective, and durable electrocatalysts for proton exchange membrane water electrolysis (PEMWE) remains a significant challenge, requiring the stabilization and enhancement of catalyst activity under harsh conditions. Here, we present cobalt-doped ruthenium dioxide (Co<sub>0.3</sub>Ru<sub>0.7</sub>O<sub>2</sub>) on TiO<sub>2</sub> as an electrocatalyst toward an acidic oxygen evolution reaction. The Co<sub>0.3</sub>Ru<sub>0.7</sub>O<sub>2</sub>-TiO<sub>2</sub> achieves an impressive overpotential of 322 mV at 1 A cm<sup>-2</sup> and demonstrates stable operation for over 1000 h at 500 mA cm<sup>-2</sup> in a PEMWE device. Comprehensive experimental and theoretical calculation results demonstrate that the doping of Co atoms into the rutile RuO<sub>2</sub> lattice optimizes the geometric configuration. Moreover, the lattice-matched interface between Co<sub>0.3</sub>Ru<sub>0.7</sub>O<sub>2</sub> and TiO<sub>2</sub> promotes interfacial electron redistribution and stabilizes active centers under oxidative conditions. This facilitates a dual-site fully parallel oxidation (DFO) pathway in which intermediates are synchronously adsorbed and desorbed at Ru and Co sites, enabling direct <i>O-O</i> coupling. This work highlights the synergistic effect of the Ru-Co dual sites and TiO<sub>2</sub> support in establishing a stable, self-regulating electronic environment that drives efficient intermediate transformation via the DFO mechanism.

Journal of the American Chemical SocietyVol. 147(43)
University of Science and Technology of China (CN), China National Offshore Oil Corporation (China) (CN), Dalian Institute of Chemical Physics (CN), Xiamen University (CN), Chinese Academy of Sciences (CN), China University of Petroleum, Beijing (CN), Dalian University of Technology (CN), ShanghaiTech University (CN), China Resources (China) (CN), Dalian University (CN), Materials Modification (United States) (US), Suzhou Research Institute (CN), Division of Materials Science and Engineering (AU), Ministry of Education (ET), National Synchrotron Radiation Laboratory (CN), Lithium Power (United States) (US), Collaborative Innovation Center of Chemistry for Energy Materials (CN), Joint Research Centre (NL), State Key Laboratory of Materials Processing and Die & Mould Technology (CN), Huazhong University of Science and Technology (CN), University of Hong Kong (HK)
Openalex Percentile: Top 2%
Electrocatalysts for Energy Conversion
7.27
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