Affiliation:
1. College of Materials Science and Engineering Sichuan University Chengdu 610065 China
2. Key Laboratory of Flexible Electronics (KLOFE) & Institute of Advanced Materials (IAM) Nanjing Tech University Nanjing 211816 China
3. Center of Engineering Experimental Teaching School of Chemical Engineering Sichuan University Chengdu 610065 China
Abstract
AbstractThe exposure of active edge sites of transition metal dichalcogenide (TMD) in TMD‐based heterostructures is essential to enhance the catalytic activity toward electrochemical catalytic hydrogen evolution (HER). The construction of TMD‐based edge‐epitaxial heterostructures can maximally expose the active edge sites. However, owing to the 2D crystal structures, it remains a great challenge to vertically align layered TMDs on non‐layered metal chalcogenides. Herein, the synthesis of Cu2‐xSe‐MoSe2 edge‐epitaxial heterostructure is reported by a facile one‐pot wet‐chemical method. A high density of MoSe2 nanosheets grown vertically to the <111>Cu2‐xSe on the surface of Cu2‐xSe nanocrystals is observed. Such edge‐epitaxial configuration allows the exposure of abundant active edge sites of MoSe2 and enhances the changer transfer between MoSe2 and Cu2‐xSe. As a result, the obtained Cu2‐xSe‐MoSe2 epitaxial heterostructures show excellent HER performance as compared to that of Cu2‐xSe@1T/2H‐MoSe2 core@shell heterostructure with similar size. This work not only offers a novel approach for designing efficient electrochemical catalysis but also enriches the diversity of TMD‐based heterostructures, holding promise for various applications in the future.
Funder
National Natural Science Foundation of China
Fundamental Research Funds for the Central Universities
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry
Cited by
2 articles.
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