二硫化钼
塔菲尔方程
硫黄
钼
电化学
催化作用
材料科学
惰性
电催化剂
纳米尺度
电解质
化学工程
无机化学
纳米技术
化学
冶金
电极
有机化学
物理化学
工程类
作者
Chaoqun Gu,Tong Sun,Zhenyu Wang,Sisi Jiang,Zonghua Wang
标识
DOI:10.1002/smtd.202201529
摘要
Molybdenum disulfide (MoS2 ) is considered as one of the most promising non-noble-metal catalysts for hydrogen evolution reaction (HER). To achieve practical application, introducing sulfur (S) vacancies on the inert basal plane of MoS2 is a widely accepted strategy to improve its HER activity. However, probing active sites at the nanoscale and quantitatively analyzing the related electrocatalytic activity in electrolyte aqueous solution are still great challenges. In this work, utilizing high-resolution scanning electrochemical microscopy, optimized electrodes and newly designed thermal drift calibration software, the HER activity of the S vacancies on an MoS2 inert surface is in situ imaged with less than 20-nm-radius sensitivity and the HER kinetic data for S vacancies, including Tafel plot and onset potential, are quantitatively measured. Additionally, the stability of S vacancies over the wide range of pH 0-13 is investigated. This study provides a viable strategy for obtaining the catalytic kinetics of nanoscale active sites on structurally complex electrocatalysts and evaluating the stability of defects in different environments for 2D material-based catalysts.
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