期刊
ACS APPLIED ENERGY MATERIALS
卷 -, 期 -, 页码 -出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsaem.3c01599
关键词
Molybdenum disulfide; Metal phosphide; Hybridstructure; Hydrogen evolution reaction; Wide pHconditions
In this study, a simple strategy was used to establish an effective synergy between CoP, Ni2P, and MoS2 nanosheets, resulting in a self-supporting electrode with abundant catalytic active sites and optimized electronic structure, leading to improved catalytic performance, especially under neutral conditions.
Structural engineering of the molybdenum disulfide (MoS2) retains its importance for the application of the hydrogen evolution reaction (HER) in a full pH range. However, the catalytic performance of reported MoS2-based materials, especially in neutral conditions, is unsatisfactory. Herein, an effective synergy between CoP, Ni2P, and MoS2 nanosheets is established via a simple strategy, which constructs a self-supporting (CoP/Ni2P/MoS2-CC) electrode endowed with abundant catalytic active sites, optimal electronic structure, and improved charge transfer capability. The optimized CoP/Ni2P/MoS2-CC sample shows low overpotentials of 335, 119, and 211 mV at 100 mA cm(-2) in neutral, alkaline, and acidic electrolytes with small Tafel slopes of 63, 62, and 82 mV dec(-1), respectively. Remarkably, the catalytic performance in neutral medium is superior to that of most of the reported MoS2-based hybrid electrocatalysts. Our work proves a facile and feasible strategy to promote the pH-universal catalytic activities of MoS2-based heterogeneous structures for hydrogen production.
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