Emergence of electrochemical catalytic activity via an electrochemical-probe on defective transition metal dichalcogenide nanosheets

APL Energy Pub Date : 2024-02-27 DOI:10.1063/5.0175653
A. Kumatani, H. Ogawa, T. Endo, J. Lustikova, H. Ida, Y. Takahashi, Y. Miyata, Y. Ikuhara, H. Shiku, Y. Wakayama
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Abstract

Two-dimensional transition metal dichalcogenides (2D TMDs) have shown exceptional electrochemical catalytic activity for the efficient generation of hydrogen through electrochemical water splitting. In the case of molybdenum disulfide (MoS2), a prominent member of 2D TMDs, the electrochemically active sites primarily reside at the edges, while the basal plane, which constitutes the majority of the MoS2 structure, remains relatively inactive. In this study, we aimed to activate the inert sites of the basal plane with some defective structure for hydrogen evolution reaction (HER) by employing an electrochemical-probe in combination with voltage sweeping. The initiation of HER at these previously inactive sites was visualized and confirmed using scanning electrochemical cell microscopy (SECCM). Our findings reveal that the enhanced HER activity originates from surface defects induced by the probing process.
通过电化学探针在有缺陷的过渡金属二卤化物纳米片上发现电化学催化活性
二维过渡金属二掺杂物(2D TMDs)在通过电化学水分离高效制氢方面表现出了卓越的电化学催化活性。二硫化钼(MoS2)是二维 TMD 的重要成员,其电化学活性位点主要位于边缘,而构成 MoS2 结构大部分的基底面则相对不活跃。在本研究中,我们旨在通过电化学探针结合电压扫描,激活基底面上具有某些结构缺陷的惰性位点,使其发生氢进化反应(HER)。使用扫描电化学细胞显微镜(SECCM)观察并确认了在这些先前不活跃的位点上启动氢进化反应的过程。我们的研究结果表明,HER 活性的增强源于探测过程诱发的表面缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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