Modulating the Oxygen Evolution Reaction of Single-Crystal Cobalt Carbonate Hydroxide via Surface Fe Doping and Facet Dependence

The oxygen evolution reaction (OER) is a critical half-reaction in water splitting and metal-air cells. The sensitivity of the OER to the composition and structure of the electrocatalyst presents a significant challenge in elucidating the structure-property relationship. In this study, highly stable single-crystal cobalt carbonate hydroxide [Co<sub>2</sub>(OH)<sub>2</sub>CO<sub>3</sub>, CoCH] was used as a model to investigate the correlations among structure, composition, and reactivity. Single-crystal CoCH nanowires (denoted as CoCH NWs) and Fe-doped CoCH nanowires (denoted as Fe-CoCH NWs) with an exposed (210) facet and Fe-doped CoCH nanosheets (denoted as Fe-CoCH NSs) with an exposed (2-13) facet were synthesized using electrochemical and one-step hydrothermal strategies, respectively. Their OER activity decreased in the following order: Fe-CoCH NWs > Fe-CoCH NSs > CoCH NWs. Theoretical investigation suggested that the doped Fe sites serve as active sites, and the crystal-facet dependence can finely adjust the 3d configuration of Fe sites, resulting in the optimal adsorption strengths and energy barriers for potential-determining steps on the (210) facet of CoCH. This renders the as-prepared Fe-CoCH NWs as some of the most promising Co-based OER catalysts.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2025-01-22
DOI
https://doi.org/10.1021/acs.jpclett.4c03018
Citations
5
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
1.82

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article

Modulating the Oxygen Evolution Reaction of Single-Crystal Cobalt Carbonate Hydroxide via Surface Fe Doping and Facet Dependence

Shenghua Ye, Lirong Zheng, Wenda Chen, Xueqing Yan et al.
5 citations
The Journal of Physical Chemistry Letters
Electrocatalysts for Energy Conversion
1.82
article

Modulating the Oxygen Evolution Reaction of Single-Crystal Cobalt Carbonate Hydroxide via Surface Fe Doping and Facet Dependence

Shenghua Ye, Lirong Zheng, Wenda Chen, Xueqing Yan, Xiaoping Ouyang, Yuanguo Xu, Qianling Zhang, Yongliang Li, Weibin Chen, D. Xiao, Shuyuan Wu, Xiangzhong Ren, Zhi‐Jun Ou, Jianhong Liu, Jie Zhang
article en
5 citations

Abstract

The oxygen evolution reaction (OER) is a critical half-reaction in water splitting and metal-air cells. The sensitivity of the OER to the composition and structure of the electrocatalyst presents a significant challenge in elucidating the structure-property relationship. In this study, highly stable single-crystal cobalt carbonate hydroxide [Co<sub>2</sub>(OH)<sub>2</sub>CO<sub>3</sub>, CoCH] was used as a model to investigate the correlations among structure, composition, and reactivity. Single-crystal CoCH nanowires (denoted as CoCH NWs) and Fe-doped CoCH nanowires (denoted as Fe-CoCH NWs) with an exposed (210) facet and Fe-doped CoCH nanosheets (denoted as Fe-CoCH NSs) with an exposed (2-13) facet were synthesized using electrochemical and one-step hydrothermal strategies, respectively. Their OER activity decreased in the following order: Fe-CoCH NWs > Fe-CoCH NSs > CoCH NWs. Theoretical investigation suggested that the doped Fe sites serve as active sites, and the crystal-facet dependence can finely adjust the 3d configuration of Fe sites, resulting in the optimal adsorption strengths and energy barriers for potential-determining steps on the (210) facet of CoCH. This renders the as-prepared Fe-CoCH NWs as some of the most promising Co-based OER catalysts.

The Journal of Physical Chemistry LettersVol. 16(4)
Shenzhen University (CN), Chinese Academy of Sciences (CN), Peking University (CN), Institute of High Energy Physics (CN), State Key Laboratory of Nuclear Physics and Technology, Xiangtan University (CN)
Science and Technology Foundation of Shenzhen City, National Natural Science Foundation of China, Natural Science Foundation of Guangdong Province, Shenzhen University, Department of Education of Guangdong Province, Shenzhen Technical Project
Openalex Percentile: Top 16%
Electrocatalysts for Energy Conversion
1.82
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