Electron-Beam-Induced Synthesis of Hexagonal 1H-MoSe2 from Square β-FeSe Decorated with Mo Adatoms
Author(s) -
John A. Brehm,
Junhao Lin,
Jiadong Zhou,
Hunter Sims,
Zheng Liu,
Sokrates T. Pantelides,
Kazu Suenaga
Publication year - 2018
Publication title -
nano letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.853
H-Index - 488
eISSN - 1530-6992
pISSN - 1530-6984
DOI - 10.1021/acs.nanolett.7b05457
Subject(s) - scanning transmission electron microscopy , materials science , hexagonal crystal system , nucleation , nanowire , transmission electron microscopy , electron diffraction , electron , crystallography , lattice (music) , cathode ray , electron microscope , diffraction , nanotechnology , optics , chemistry , physics , quantum mechanics , organic chemistry , acoustics
Two-dimensional (2D) materials have generated interest in the scientific community because of the advanced electronic applications they might offer. Powerful electron beam microscopes have been used not only to evaluate the structures of these materials but also to manipulate them by forming vacancies, nanofragments, and nanowires or joining nanoislands together. In this work, we show that the electron beam in a scanning transmission electron microscope (STEM) can be used in yet another way: to mediate the synthesis of 2D 1 H-MoSe 2 from Mo-decorated 2D β-FeSe and simultaneously image the process on the atomic scale. This is quite remarkable given the different crystal structures of the reactant (square lattice β-FeSe) and the product (hexagonal lattice 1 H-MoSe 2 ). The feasibility of the transformation was first explored by theoretical calculations that predicted that the reaction is exothermic. Furthermore, a theoretical reaction path to forming a stable 1 H-MoSe 2 nucleation kernel within pure β-FeSe was found, demonstrating that the pertinent energy barriers are smaller than the energy supplied by the STEM electron beam.
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