Spatial defects nanoengineering for bipolar conductivity in MoS2

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作者
Xiaorui Zheng
Annalisa Calò
Tengfei Cao
Xiangyu Liu
Zhujun Huang
Paul Masih Das
Marija Drndic
Edoardo Albisetti
Francesco Lavini
Tai-De Li
Vishal Narang
William P. King
John W. Harrold
Michele Vittadello
Carmela Aruta
Davood Shahrjerdi
Elisa Riedo
机构
[1] New York University,Tandon School of Engineering
[2] CUNY Graduate Center Advanced Science Research Center,CUNY Graduate Center
[3] Ph.D. Program in Physics and Chemistry,Department of Chemistry
[4] College of Staten Island (CUNY),Department of Physics and Astronomy
[5] University of Pennsylvania,Dipartimento di Fisica
[6] Politecnico di Milano,Department of Mechanical Science and Engineering
[7] University of Illinois,Department of Chemistry and Environmental Science
[8] Medgar Evers College of CUNY,National Research Council CNR
[9] 2010,SPIN
[10] University of Roma Tor Vergata,undefined
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摘要
Understanding the atomistic origin of defects in two-dimensional transition metal dichalcogenides, their impact on the electronic properties, and how to control them is critical for future electronics and optoelectronics. Here, we demonstrate the integration of thermochemical scanning probe lithography (tc-SPL) with a flow-through reactive gas cell to achieve nanoscale control of defects in monolayer MoS2. The tc-SPL produced defects can present either p- or n-type doping on demand, depending on the used gasses, allowing the realization of field effect transistors, and p-n junctions with precise sub-μm spatial control, and a rectification ratio of over 104. Doping and defects formation are elucidated by means of X-Ray photoelectron spectroscopy, scanning transmission electron microscopy, and density functional theory. We find that p-type doping in HCl/H2O atmosphere is related to the rearrangement of sulfur atoms, and the formation of protruding covalent S-S bonds on the surface. Alternatively, local heating MoS2 in N2 produces n-character.
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