4.8 Article

Boosting and Balancing Electron and Hole Mobility in Single- and Bilayer WSe2 Devices via Tailored Molecular Functionalization

期刊

ACS NANO
卷 13, 期 10, 页码 11613-11622

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.9b05423

关键词

WSe2; molecular functionalization; self-assembled monolayers; ambipolar FETs; 2D materials

资金

  1. European Commission [GA-785219, GA-748971, GA-2014-628563]
  2. Agence Nationale de la Recherche [ANR-10-LABX-0026 CSC, ANR-11-LABX-0058 NIE, ANR-10-120 IDEX-0002-02]
  3. International Center for Frontier Research in Chemistry (icFRC)
  4. Chinese Scholarship Council
  5. CARITRO Foundation (project MILA), Trento (Italy) [2017.0369]
  6. Natural Sciences and Engineering Research Council of Canada (NSERC)
  7. Fonds de recherche du Quebec - Nature et Technologies (FRQNT)

向作者/读者索取更多资源

WSe2 is a layered ambipolar semiconductor enabling hole and electron transport, which renders it a suitable active component for logic circuitry. However, solid-state devices based on single- and bilayer WSe2 typically exhibit unipolar transport and poor electrical performance when conventional SiO2 dielectric and Au electrodes are used. Here, we show that silane-containing functional molecules form ordered monolayers on the top of the WSe2 surface, thereby boosting its electrical performance in single- and bilayer field-effect transistors. In particular, by employing SiO2 dielectric substrates and top Au electrodes, we measure unipolar mobility as high as mu(h) = 150 cm(2) V-1 s(-1) and mu(e) = 17.9 cm(2) V(-1 )s(-1) in WSe2 single-layer devices when ad hoc molecular monolayers are chosen. Additionally, by asymmetric double-side functionalization with two different molecules, we provide opposite polarity to the top and bottom layer of bilayer WSe2, demonstrating nearly balanced ambipolarity at the bilayer limit. Our results indicate that the controlled functionalization of the two sides of the WSe2 mono- and bilayer flakes with highly ordered molecular monolayers offers the possibility to simultaneously achieve energy level engineering and defect functionalization, representing a path toward deterministic control over charge transport in 2D materials.

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