二硫化钼
单层
成核
外延
双层
材料科学
蓝宝石
光电子学
纳米技术
化学物理
化学
图层(电子)
膜
光学
复合材料
有机化学
激光器
物理
生物化学
作者
Lei Liu,Taotao Li,Liang Ma,Weisheng Li,Si Gao,Wenjie Sun,Ruikang Dong,Xilu Zou,Dongxu Fan,Liangwei Shao,Chenyi Gu,Ningxuan Dai,Zhihao Yu,Xiaoqing Chen,Xuecou Tu,Yuefeng Nie,Peng Wang,Jinlan Wang,Yi Shi,Xinran Wang
出处
期刊:Nature
[Nature Portfolio]
日期:2022-05-04
卷期号:605 (7908): 69-75
被引量:307
标识
DOI:10.1038/s41586-022-04523-5
摘要
Two-dimensional transition-metal dichalcogenides (TMDs) are of interest for beyond-silicon electronics1,2. It has been suggested that bilayer TMDs, which combine good electrostatic control, smaller bandgap and higher mobility than monolayers, could potentially provide improvements in the energy-delay product of transistors3-5. However, despite advances in the growth of monolayer TMDs6-14, the controlled epitaxial growth of multilayers remains a challenge15. Here we report the uniform nucleation (>99%) of bilayer molybdenum disulfide (MoS2) on c-plane sapphire. In particular, we engineer the atomic terrace height on c-plane sapphire to enable an edge-nucleation mechanism and the coalescence of MoS2 domains into continuous, centimetre-scale films. Fabricated field-effect transistor (FET) devices based on bilayer MoS2 channels show substantial improvements in mobility (up to 122.6 cm2 V-1 s-1) and variation compared with FETs based on monolayer films. Furthermore, short-channel FETs exhibit an on-state current of 1.27 mA μm-1, which exceeds the 2028 roadmap target for high-performance FETs16.
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