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具有碲原子随机局部位移的单层三元碲化物的相控合成

Phase-Controlled Synthesis of Monolayer Ternary Telluride with a Random Local Displacement of Tellurium Atoms.

作者信息

Tang Bijun, Zhou Jiadong, Sun Pingping, Wang Xiaowei, Bai Lichun, Dan Jiadong, Yang Jiefu, Zhou Kun, Zhao Xiaoxu, Pennycook Stephen J, Liu Zheng

机构信息

School of Materials Science and Engineering, Nanyang Technological University, Singapore, 639798, Singapore.

School of Mechanical and Aerospace Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore, 639798, Singapore.

出版信息

Adv Mater. 2019 Jun;31(23):e1900862. doi: 10.1002/adma.201900862. Epub 2019 Apr 17.

DOI:10.1002/adma.201900862
PMID:30997722
Abstract

Alloying 2D transition metal dichalcogenides has opened up new opportunities for bandgap engineering and phase control. Developing a simple and scalable synthetic route is therefore essential to explore the full potential of these alloys with tunable optical and electrical properties. Here, the direct synthesis of monolayer WTe S alloys via one-step chemical vapor deposition (CVD) is demonstrated. The WTe S alloys exhibit two distinct phases (1H semiconducting and 1T ' metallic) under different chemical compositions, which can be controlled by the ratio of chalcogen precursors as well as the H flow rate. Atomic-resolution scanning transmission electron microscopy-annular dark field (STEM-ADF) imaging reveals the atomic structure of as-formed 1H and 1T ' alloys. Unlike the commonly observed displacement of metal atoms in the 1T ' phase, local displacement of Te atoms from original 1H lattice sites is discovered by combined STEM-ADF imaging and ab initio molecular dynamics calculations. The structure distortion provides new insights into the structure formation of alloys. This generic synthetic approach is also demonstrated for other telluride-based ternary monolayers such as WTe Se single crystals.

摘要

对二维过渡金属二硫属化物进行合金化处理为带隙工程和相控带来了新机遇。因此,开发一种简单且可扩展的合成路线对于探索这些具有可调光学和电学性质的合金的全部潜力至关重要。在此,展示了通过一步化学气相沉积(CVD)直接合成单层WTeS合金。WTeS合金在不同化学组成下呈现出两种不同的相(1H半导体相和1T'金属相),这可以通过硫属前驱体的比例以及氢气流速来控制。原子分辨率扫描透射电子显微镜 - 环形暗场(STEM - ADF)成像揭示了所形成的1H和1T'合金的原子结构。与在1T'相中通常观察到的金属原子位移不同,通过结合STEM - ADF成像和从头算分子动力学计算发现,Te原子从原始1H晶格位置发生了局部位移。这种结构畸变对合金的结构形成提供了新的见解。这种通用的合成方法也适用于其他基于碲化物的三元单层,如WTeSe单晶。

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