4.8 Article

Uniform doping of graphene close to the Dirac point by polymer-assisted assembly of molecular dopants

Journal

NATURE COMMUNICATIONS
Volume 9, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-018-06352-5

Keywords

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Funding

  1. Swedish Foundation for Strategic Research (SSF) [IS14-0053, GMT14-0077, RMA15-0024]
  2. Knut and Alice Wallenberg Foundation
  3. Chalmers Area of Advance NANO
  4. Swedish Research Council (VR) [2015-03758, 2016-048287]
  5. Swedish-Korean Basic Research Cooperative Program of the NRF [NRF-2017R1A2A1A18070721]
  6. European Union's Horizon 2020 research and innovation program [766714/HiTIMe]
  7. NSF & NIH/NIGMS via NSF award [DMR-1332208]
  8. Swedish Research Council [2015-03758] Funding Source: Swedish Research Council
  9. Swedish Foundation for Strategic Research (SSF) [IS14-0053] Funding Source: Swedish Foundation for Strategic Research (SSF)
  10. Vinnova [2015-03758] Funding Source: Vinnova

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Tuning the charge carrier density of two-dimensional (2D) materials by incorporating dopants into the crystal lattice is a challenging task. An attractive alternative is the surface transfer doping by adsorption of molecules on 2D crystals, which can lead to ordered molecular arrays. However, such systems, demonstrated in ultra-high vacuum conditions (UHV), are often unstable in ambient conditions. Here we show that air-stable doping of epitaxial graphene on SiC-achieved by spin-coating deposition of 2,3,5,6-tetrafluoro-tetracyano-quino-dimethane (F4TCNQ) incorporated in poly(methyl-methacrylate)-proceeds via the spontaneous accumulation of dopants at the graphene-polymer interface and by the formation of a charge-transfer complex that yields low-disorder, charge-neutral, large-area graphene with carrier mobilities similar to 70 000 cm(2) V-1 s(-1) at cryogenic temperatures. The assembly of dopants on 2D materials assisted by a polymer matrix, demonstrated by spincoating wafer-scale substrates in ambient conditions, opens up a scalable technological route toward expanding the functionality of 2D materials.

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