Visualizing the structural evolution of individual active sites in MoS2 during electrocatalytic hydrogen evolution reaction

被引:47
作者
Huang, Teng-Xiang [1 ]
Cong, Xin [2 ]
Wu, Si-Si [1 ]
Wu, Jiang-Bin [2 ]
Bao, Yi-Fan [1 ]
Cao, Mao-Feng [1 ]
Wu, Liwen [1 ]
Lin, Miao-Ling [2 ]
Wang, Xiang [1 ,3 ]
Tan, Ping-Heng [2 ,4 ,5 ]
Ren, Bin [1 ,3 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Collaborat Innovat Ctr Chem Energy Mat iChEM, Dept Chem,State Key Lab Phys Chem Solid Surfaces,M, Xiamen, Peoples R China
[2] Chinese Acad Sci, Inst Semicond, State Key Lab Superlatt & Microstruct, Beijing, Peoples R China
[3] Innovat Lab Sci & Technol Energy Mat Fujian Prov I, Xiamen, Peoples R China
[4] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing, Peoples R China
[5] Univ Chinese Acad Sci, CAS Ctr Excellence Topol Quantum Computat, Beijing, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
TRANSITION-METAL DICHALCOGENIDES; IDENTIFICATION; MONOLAYER; SURFACE; TIP; CATALYST;
D O I
10.1038/s41929-024-01148-x
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Understanding the structural evolution of individual active sites during a reaction is a long-standing target in surface science and catalysis. It is still challenging to precisely characterize in situ the intrinsic nature and evolution of the active site because the active site is too small for characterization techniques to decipher the local properties. Here we used electrochemical tip-enhanced Raman spectroscopy to monitor the geometric and electronic evolution of individual active sites of MoS2 during the hydrogen evolution reaction. Reconstruction regions of 40 nm with varied lattice and electron density from the edge to the nearby basal plane were observed during the hydrogen evolution reaction. We further revealed the progressive generation of active sites during the activation process. The synergistic reconstruction around edge due to the lattice deformation reduces the activation energy barriers and promotes the electrocatalytic reaction. These discoveries offer insights into our understanding of the active site and its dynamics during electrocatalysis.
引用
收藏
页码:646 / 654
页数:9
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