Journal
JOURNAL OF ENERGY CHEMISTRY
Volume 62, Issue -, Pages 516-522Publisher
ELSEVIER
DOI: 10.1016/j.jechem.2021.04.010
Keywords
MoS2; Topological insulator; Hydrogen evolution; Surface states; Electron transfer
Funding
- European Research Council (ERC) [291472]
- ERC Advanced Grant [742068]
- National Natural Science Foundation of China [12074038]
- Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [314790414]
- European Research Council (ERC) [742068] Funding Source: European Research Council (ERC)
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2H-MoS2 is a promising non-noble metal electrocatalyst, but its performance is limited by the chemically inert basal plane; coupling with Bi2Te3 topological insulator films can enhance HER activities; theoretical investigations suggest that the charge redistribution at the interface and activation of topological surface states play a key role in enhancing catalytic activity.
2H-MoS2 is a well-studied and promising non-noble metal electrocatalyst for heterogeneous reactions, such as the hydrogen evolution reaction (HER). The performance is largely limited by the chemically inert basal plane, which is unfavorable for surface adsorption and reactions. Herein, we report a facile method to boost the HER activities of 2H-MoS2 by coupling with epitaxial Bi2Te3 topological insulator films. The as-obtained MoS2/ Bi2Te3/SrTiO3 catalyst exhibits prominent HER catalytic activities compared to that of pure MoS2 structures, with a 189 mV decrease in the overpotential required to reach a current density of 10 mA cm(-2) and a low Tafel slope of 58 mV dec(-1). Theoretical investigations suggest that the enhanced catalytic activity originates from the charge redistribution at the interface between the Bi(2)Te(3)topological insulator films and the MoS2 layer. The delocalized sp-derived topological surface states could denote electrons to the MoS2 layer and activate the basal plane for hydrogen adsorption. This study demonstrates the potential of manipulating topological surface states to design high-performance electrocatalysts. (C) 2021 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press.
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