Tracking single adatoms in liquid in a transmission electron microscope

被引:60
作者
Clark, Nick [1 ,2 ]
Kelly, Daniel J. [1 ,2 ]
Zhou, Mingwei [2 ,3 ]
Zou, Yi-Chao [1 ,2 ,4 ]
Myung, Chang Woo [5 ]
Hopkinson, David G. [1 ,2 ]
Schran, Christoph [5 ]
Michaelides, Angelos [5 ]
Gorbachev, Roman [2 ,3 ]
Haigh, Sarah J. [1 ,2 ]
机构
[1] Univ Manchester, Dept Mat, Manchester, Lancs, England
[2] Univ Manchester, Natl Graphene Inst, Manchester, Lancs, England
[3] Univ Manchester, Dept Phys & Astron, Manchester, Lancs, England
[4] Sun Yat Sen Univ, Sch Mat Sci & Engn, Guangzhou, Peoples R China
[5] Univ Cambridge, Yusuf Hamied Dept Chem, Cambridge, England
基金
英国工程与自然科学研究理事会; 欧洲研究理事会; 中国国家自然科学基金;
关键词
IN-SITU; GRAPHENE; RESOLUTION; MONOLAYER; CHEMISTRY; GROWTH;
D O I
10.1038/s41586-022-05130-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Single atoms or ions on surfaces affect processes from nucleation(1) to electrochemical reactions(2) and heterogeneous catalysis(3). Transmission electron microscopy is a leading approach for visualizing single atoms on a variety of substrates(4,5). It conventionally requires high vacuum conditions, but has been developed for in situ imaging in liquid and gaseous environments(6,7) with a combined spatial and temporal resolution that is unmatched by any other method-notwithstanding concerns about electron-beam effects on samples. When imaging in liquid using commercial technologies, electron scattering in the windows enclosing the sample and in the liquid generally limitsthe achievable resolution to a few nanometres(6,8,9). Graphene liquid cells, on the other hand, have enabled atomic-resolution imaging of metal nanoparticles in liquids(10). Here we show that a double graphene liquid cell, consisting of a central molybdenum disulfide monolayer separated by hexagonal boron nitride spacers from the two enclosinggraphene windows, makes it possible to monitor, with atomic resolution, the dynamics of platinum adatoms on the monolayer in an aqueous salt solution. By imaging more than 70,000 single adatom adsorption sites, we compare the site preference and dynamic motion ofthe adatoms in both a fully hydrated and a vacuum state. We find a modified adsorption site distribution and higher diffusivities for the adatoms in the liquid phase compared with those in vacuum. This approach pavesthe way for in situ liquid-phase imaging of chemical processes with single-atom precision.
引用
收藏
页码:942 / +
页数:20
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