Shuo Chen
;
Kaiqin Yue
;
Jiawei Shi
;
Zhicheng Zheng
;
Yuanqing He
;
Hao Wan
;
Gen Chen
;
Ning Zhang
;
Xiaohe Liu
;
Renzhi Ma
説明:
(abstract)Most nonoxide catalysts based on transition metal elements will inevitably change their primitive phases under anodicoxidation conditions in alkaline media. Establishing a relationship between the bulk phase and surface evolution is imperative toreveal the intrinsic catalytic active sites. In this work, it is demonstrated that the introduction of Fe facilitates the phase transition oforthorhombic CoSe2 into its cubic counterpart and then accelerates the Co−Fe hydroxide layer generation on the surface duringelectrocatalytic oxygen evolution reaction (OER). As a result, the Fe-doped cubic CoSe2 catalyst exhibits a significantly enhancedactivity with a considerable overpotential decrease of 79.9 and 66.9 mV to deliver 10 mA·cm−2 accompanied by a Tafel slope of 48.0mV·dec−1 toward OER when compared to orthorhombic CoSe2 and Fe-doped orthorhombic CoSe2, respectively. Density functionaltheory (DFT) calculations reveal that the introduction of Fe on the surface hydroxide layers will tune electron density around Coatoms and raise the d-band center. These findings will provide deep insights into the surface reconstitution of the OER electrocatalysts based on transition metal elements.
権利情報:
キーワード: Oxygen evolution reaction, Electrocatalysis
刊行年月日: 2024-04-22
出版者: American Chemical Society (ACS)
掲載誌:
研究助成金:
原稿種別: 著者最終稿 (Accepted manuscript)
MDR DOI: https://doi.org/10.48505/nims.4540
公開URL: https://doi.org/10.1021/acs.inorgchem.4c00568
関連資料:
その他の識別子:
連絡先:
更新時刻: 2025-04-14 16:30:42 +0900
MDRでの公開時刻: 2025-04-14 14:56:25 +0900
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Chen_ACS-Manuscript-Accepted.pdf
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サイズ | 2.91MB | 詳細 |