4.8 Article

One-Pot Selective Epitaxial Growth of Large WS2/MoS2 Lateral and Vertical Heterostructures

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 142, 期 38, 页码 16276-16284

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.0c05691

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资金

  1. National Natural Science Foundation of China [21971172, 21671141, 51971245]
  2. 973 Program-The National Basic Research Program of China Special Funds for the Chief Young Scientist [2015CB358600]
  3. Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions for Optical Engineering
  4. Jiangsu Collaborative Innovation Center of Photovoltaic Science and Engineering (Changzhou University)
  5. Beijing Natural Science Foundation of China-Haidian Special Project [L182065]
  6. Beijing Natural Science Foundation [2202046]

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Controllable nucleation sites play a key role in the selective growth of heterostructures. Here, we are the first to report a one-pot strategy to realize the confined and selective growth of large MoS2/WS2 lateral and vertical heterostructures. A hydroxide-assisted process is introduced to control the nucleation sites, thereby realizing the optional formation of lateral and vertical heterostructures. Time-of-flight secondary ion mass spectrometry verifies the critical role of hydroxide groups toward the controllable growth of these heterostructures. The size of the as-grown MoS2/WS2 lateral heterostructures can be as large as 1 mm, which is the largest lateral size reported thus far. The obtained MoS2/WS2 heterostructures have a high carrier mobility of similar to 58 cm(2) V-1 s(-1), and the maximum on/off current ratio is >10(8). This approach provides not only a pathway for the selective growth of large MoS2/WS2 lateral and vertical heterostructures but also a fundamental understanding of surface chemistry for controlling the selective growth of transition-metal dichalcogenide heterostructures.

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