Vertically Aligned MoS2 with In-Plane Selectively Cleaved Mo–S Bond for Hydrogen Production
Author(s) -
Yang Li,
Shouwei Zuo,
Qiaohong Li,
Xin Wu,
Jing Zhang,
Huabin Zhang,
Jian Zhang
Publication year - 2021
Publication title -
nano letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.853
H-Index - 488
eISSN - 1530-6992
pISSN - 1530-6984
DOI - 10.1021/acs.nanolett.0c04978
Subject(s) - vacancy defect , basal plane , hydrogen bond , materials science , adsorption , catalysis , desorption , transition metal , crystallography , hydrogen , plane (geometry) , chemical physics , chemistry , nanotechnology , molecule , geometry , organic chemistry , mathematics
Perturbing the periodic electronic structure of the MoS 2 basal plane via vacancy engineering offers an opportunity to explore its intrinsic activity. A significant challenge is the design of vacancy states, which include its type, distribution, and accessibility. Here, well-dispersed and vertically aligned MoS 2 nanosheets with an in-plane selectively cleaved Mo-S bond on a carbon matrix (c-MoS 2 -C) have been prepared by a self-engaged strategy, which synergistically realizes uniform vacancy manufacturing and three-dimensional (3D) self-assembly of the defective MoS 2 nanosheets. X-ray adsorption spectroscopy investigation confirms that the cleaved MoS 2 basal plane generates newly active edge sites, where the Mo centers feature unsaturated coordination geometry. Theoretical calculations reveal that the exposed interior edge Mo sites represent new active centers for hydrogen adsorption/desorption. As expected, the synthesized c-MoS 2 -C exhibits markedly enhanced hydrogen evolution activity and superior stability. This in-plane activation strategy could be extended to other types of transition-metal dichalcogenides and catalytic reaction systems.
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