塔菲尔方程
二硫化钼
电催化剂
磷化物
催化作用
制氢
钼
材料科学
电解质
镍
化学工程
钴
氢
无机化学
电化学
化学
电极
冶金
物理化学
有机化学
工程类
作者
Xiaoxiao Cheng,Yun Tong
标识
DOI:10.1021/acsaem.3c01599
摘要
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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