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Thickness sorting of two-dimensional transition metal dichalcogenides via copolymer-assisted density gradient ultracentrifugation

Author

Listed:
  • Joohoon Kang

    (Northwestern University)

  • Jung-Woo T. Seo

    (Northwestern University)

  • Diego Alducin

    (University of Texas at San Antonio)

  • Arturo Ponce

    (University of Texas at San Antonio)

  • Miguel Jose Yacaman

    (University of Texas at San Antonio)

  • Mark C. Hersam

    (Northwestern University
    Northwestern University
    Northwestern University)

Abstract

Two-dimensional transition metal dichalcogenides have emerged as leading successors to graphene due to their diverse properties, which depend sensitively on sample thickness. Although solution-based exfoliation methods hold promise for scalable production of these materials, existing techniques introduce irreversible structural defects and/or lack sufficient control over the sample thickness. In contrast, previous work on carbon nanotubes and graphene has shown that isopycnic density gradient ultracentrifugation can produce structurally and electronically monodisperse nanomaterial populations. However, this approach cannot be directly applied to transition metal dichalcogenides due to their high intrinsic buoyant densities when encapsulated with ionic small molecule surfactants. Here, we overcome this limitation and thus demonstrate thickness sorting of pristine molybdenum disulfide (MoS2) by employing a block copolymer dispersant composed of a central hydrophobic unit flanked by hydrophilic chains that effectively reduces the overall buoyant density in aqueous solution. The resulting solution-processed monolayer MoS2 samples exhibit strong photoluminescence without further chemical treatment.

Suggested Citation

  • Joohoon Kang & Jung-Woo T. Seo & Diego Alducin & Arturo Ponce & Miguel Jose Yacaman & Mark C. Hersam, 2014. "Thickness sorting of two-dimensional transition metal dichalcogenides via copolymer-assisted density gradient ultracentrifugation," Nature Communications, Nature, vol. 5(1), pages 1-7, December.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms6478
    DOI: 10.1038/ncomms6478
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