4.8 Article

Multicomponent Covalent Chemical Patterning of Graphene

Journal

ACS NANO
Volume 15, Issue 6, Pages 10618-10627

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.1c03373

Keywords

graphene; covalent patterning; multifunctional surfaces; Raman spectroscopy; chemical patterning

Funding

  1. Fund of Scientific Research Flanders (FWO)
  2. KU Leuven - Internal Funds [C14/19/079]
  3. FWO [EOS 30489208]
  4. KU Leuven [C14/18/061]
  5. Research Foundation Flanders [G0A1219N]
  6. European Union's European Fund for Regional Development, Flanders Innovation AMP
  7. Entrepreneurship
  8. Province of West-Flanders (Accelerate3 project, Interreg Vlaanderen-Nederland program)
  9. PDM fellowship from KU Leuven

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This study demonstrates spatially controlled, multifunctional covalent chemical patterning of single layer graphene, with the ability to attach three different functional groups to the basal plane in dense, well-defined patterns. The method combines lithography and a self-limiting variant of diazonium chemistry, allowing for precise control over the layer thickness of the covalent films down to 1 nm. This research lays a solid foundation for the fabrication of chemically patterned multifunctional graphene interfaces for device applications.
The chemical patterning of graphene is being pursued tenaciously due to exciting possibilities in electronics, catalysis, sensing, and photonics. Despite the intense efforts, spatially controlled, multifunctional covalent patterning of graphene has not been achieved. The lack of control originates from the inherently poor reactivity of the basal plane of graphene, which necessitates the use of harsh chemistries. Here, we demonstrate spatially resolved multicomponent covalent chemical patterning of single layer graphene using a facile and efficient method. Three different functional groups could be covalently attached to the basal plane in dense, well-defined patterns using a combination of lithography and a self-limiting variant of diazonium chemistry requiring no need for graphene activation. The layer thickness of the covalent films could be controlled down to 1 nm. This work provides a solid foundation for the fabrication of chemically patterned multifunctional graphene interfaces for device applications.

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