Rapid wafer-scale fabrication with layer-by-layer thickness control of atomically thin MoS2 films using gas-phase chemical vapor deposition

被引:35
|
作者
Shinde, Nitin Babu [1 ]
Francis, Bellarmine [2 ]
Rao, M. S. Ramachandra [2 ]
Ryu, Beo Deul [3 ]
Chandramohan, S. [1 ]
Eswaran, Senthil Kumar [1 ,4 ]
机构
[1] SRM Inst Sci & Technol SRMIST, Dept Phys & Nanotechnol, 2D Mat Lab 2DML, Chennai 603203, Tamil Nadu, India
[2] IIT Madras, Dept Phys, NFMTC, Chennai 600036, Tamil Nadu, India
[3] Chonbuk Natl Univ, Sch Semicond & Chem Engn, Semicond Phys Res Ctr, Jeonju 561756, South Korea
[4] SRM Inst Sci & Technol SRMIST, Nanotechnol Res Ctr, Chennai 603203, Tamil Nadu, India
来源
APL MATERIALS | 2019年 / 7卷 / 08期
关键词
MONOLAYER MOS2; VALLEY POLARIZATION; GROWTH; PHOTOLUMINESCENCE; HETEROSTRUCTURES; OPTOELECTRONICS; EVOLUTION; UNIFORM; MOO3;
D O I
10.1063/1.5095451
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Design and development of the growth-process for the production of wafer-scale spatially homogeneous thickness controlled atomically thin transition metal dichalcogenides (TMDs) is one of the key challenges to realize modern electronic devices. Here, we demonstrate rapid and scalable synthesis of MoS2 films with precise thickness control via gas-phase chemical vapor deposition approach. We show that a monolayer MoS2 can be synthesized over a 2-in. sapphire wafer in a growth time as low as 4 min. With a linear growth rate of 1-layer per 4 min, MoS2 films with thicknesses varying from 1- to 5-layers with monolayer precision are produced. We propose that, in addition to Raman spectroscopy, the energy splitting of exciton bands in optical-absorbance spectra may be another choice for layer thickness identification. With suitable precursor selection, our approach can facilitate the rapid synthesis of spatially homogeneous atomically thin TMDs on a large scale. (C) 2019 Author(s).
引用
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页数:8
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