Surface reconstruction of heterostructures in alkaline medium towards enhanced electrocatalytic hydrogen evolution

Constructing heterostructures has proved to be a successful strategy to fabricate electrocatalysts with high efficiency for water splitting. However, the structure evolution in alkaline hydrogen evolution reaction lacks investigation and the specific active center remains disputable. Herein, we take...

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Bibliographic Details
Published in:Rare metals Vol. 43; no. 6; pp. 2636 - 2647
Main Authors: Yang, Ming-Yang, Yuan, Ji, Fu, Xue-Lian, Chen, Jing-Jing, Hu, Jing, Lu, Zhou-Guang, Liu, Chen
Format: Journal Article
Language:English
Published: Beijing Nonferrous Metals Society of China 01-06-2024
Springer Nature B.V
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Summary:Constructing heterostructures has proved to be a successful strategy to fabricate electrocatalysts with high efficiency for water splitting. However, the structure evolution in alkaline hydrogen evolution reaction lacks investigation and the specific active center remains disputable. Herein, we take the well-designed Ni 3 S 2 @VO 2 heterostructures as a model to investigate the electrocatalytic activity and the surface reconstruction process of heterostructure catalysts in alkaline electrolyte. The Ni 3 S 2 @VO 2 heterostructures, with Ni 3 S 2 nanorods as the core and VO 2 nanoflakes as the shell, coupled with the high conductive Ni 3 S 2 , the hydrophilic VO 2 and modulated electronic structures at the interfaces, exhibited prominent activity and superior stability at various current densities. Further, the ex-situ characterizations confirmed that the surface reconstruction from Ni 3 S 2 @VO 2 into Ni 3 S 2 @amorphous-Ni(OH) 2 in alkaline media could optimize the water dissociation barrier and exposed large active area, thereby contributing to improved electrocatalytic performance. Our study not only introduces novel high-performance electrocatalysts for hydrogen evolution reaction (HER), but also provides a new avenue for re-examining hetero-structural catalysts in alkaline solutions. Graphical abstract
ISSN:1001-0521
1867-7185
DOI:10.1007/s12598-024-02625-9