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二维二硫化钼上硫空位的高分辨率电化学成像

High Resolution Electrochemical Imaging for Sulfur Vacancies on 2D Molybdenum Disulfide.

作者信息

Gu Chaoqun, Sun Tong, Wang Zhenyu, Jiang Sisi, Wang Zonghua

机构信息

College of Chemistry and Chemical Engineering, Shandong Sino-Japanese Center for Collaborative Research of Carbon Nanomaterials, Instrumental Analysis Center of Qingdao University, Qingdao University, Qingdao, 266071, P. R. China.

出版信息

Small Methods. 2023 Mar;7(3):e2201529. doi: 10.1002/smtd.202201529. Epub 2023 Jan 22.

Abstract

Molybdenum disulfide (MoS ) 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 MoS 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 MoS 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.

摘要

二硫化钼(MoS₂)被认为是析氢反应(HER)最具前景的非贵金属催化剂之一。为实现实际应用,在MoS₂的惰性基面引入硫(S)空位是一种被广泛认可的提高其HER活性的策略。然而,在纳米尺度探测活性位点并在电解质水溶液中定量分析相关电催化活性仍是巨大挑战。在这项工作中,利用高分辨率扫描电化学显微镜、优化电极和新设计的热漂移校准软件,以小于20纳米半径的灵敏度原位成像MoS₂惰性表面上S空位的HER活性,并定量测量S空位的HER动力学数据,包括塔菲尔曲线和起始电位。此外,还研究了S空位在pH值0至13宽范围内的稳定性。该研究为获取结构复杂的电催化剂上纳米级活性位点的催化动力学以及评估二维材料基催化剂在不同环境中缺陷的稳定性提供了可行策略。

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