Surface-reconstructed oxygen-vacancy-rich amorphous-crystalline Ni(Co) heterostructure for boosted oxygen evolution reaction

被引:1
作者
Liu, Xue-jian [1 ,2 ]
Chen, Zhi-gang [2 ]
Zhu, Cheng-feng [1 ,2 ]
Yang, Guang [1 ,2 ]
Weng, Xue-fei [2 ]
Cui, Yi [2 ]
机构
[1] Univ Sci & Technol China, Sch Nanotech & Nanob, Hefei 230026, Peoples R China
[2] Chinese Acad Sci, Suzhou Inst Nanotech & Nanobion, Vacuum Interconnected Nanotech Workstn, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemical deposition; Surface reconstruction; Ternary metallic heterostructure; Oxygen vacancy; Oxygen evolution reaction; TEMPLATE-FREE SYNTHESIS; HIGHLY-EFFICIENT; METAL PHOSPHIDE; ELECTROCATALYST; PERFORMANCE; CATALYSTS; CO3O4; ELECTRODEPOSITION; MORPHOLOGY; GROWTH;
D O I
10.1063/1674-0068/cjcp2202031
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
The design of low-cost and robust electrocatalysts with rich active sites remains challenging for improving the efficiency of water oxidation. Herein, ternary Ni-Co-Mo oxide films were uniformly synthesized on Cu foil via simple electrochemical deposition method. After surface reconstruction, the robust amorphous-crystalline amorphous-crystalline Ni(Co) heterostructure with rich oxygen vacancies were achieved. Accordingly, the as-obtained surface-reconstructed heterostructure catalysts exhibited a superior oxygen evolution reaction activity with overpotential as low as 308 mV at 20 mA/cm(2) and a small Tafel slope of 90 mV/dec. Moreover, a negligible activity degradation was observed for the heterostructure catalyst via continuously catalyzing OER process over 24 h, highlighting the structural robustness of the self-reconstructed Ni-Co-Mo catalyst for practical electrocatalytic applications.
引用
收藏
页码:460 / 468
页数:9
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