X射线光电子能谱
异质结
扫描隧道显微镜
拉曼光谱
剥脱关节
图层(电子)
单层
材料科学
半导体
纳米技术
光谱学
量子隧道
开尔文探针力显微镜
光电子学
化学物理
石墨烯
原子力显微镜
化学工程
化学
光学
量子力学
物理
工程类
作者
Fanglue Wu,Zhuotong Liu,Nathaniel Hawthorne,Michael Chandross,Quentarius Moore,Nicolas Argibay,John F. Curry,James D. Batteas
出处
期刊:ACS Nano
[American Chemical Society]
日期:2020-11-30
卷期号:14 (12): 16939-16950
被引量:40
标识
DOI:10.1021/acsnano.0c06014
摘要
Heterojunctions of semiconductors and metals are the fundamental building blocks of modern electronics. Coherent heterostructures between dissimilar materials can be achieved by composition, doping, or heteroepitaxy of chemically different elements. Here, we report the formation of coherent single-layer 1H-1T MoS2 heterostructures by mechanical exfoliation on Au(111), which are chemically homogeneous with matched lattices but show electronically distinct semiconducting (1H phase) and metallic (1T phase) character, with the formation of these heterojunctions attributed to a combination of lattice strain and charge transfer. The exfoliation approach employed is free of tape residues usually found in many exfoliation methods and yields single-layer MoS2 with millimeter (mm) size on the Au surface. Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), scanning tunneling microscopy (STM), and scanning tunneling spectroscopy (STS) have collectively been employed to elucidate the structural and electronic properties of MoS2 monolayers on Au substrates. Bubbles in the MoS2 formed by the trapping of ambient adsorbates beneath the single layer during deposition, have also been observed and characterized. Our work here provides a basis to produce two-dimensional heterostructures which represent potential candidates for future electronic devices.
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