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Hollow organic capsules assemble into cellular semiconductors

Author

Listed:
  • Boyuan Zhang

    (Columbia University)

  • Raúl Hernández Sánchez

    (Columbia University
    Columbia University)

  • Yu Zhong

    (Columbia University)

  • Melissa Ball

    (Columbia University)

  • Maxwell W. Terban

    (Columbia University)

  • Daniel Paley

    (Columbia University)

  • Simon J. L. Billinge

    (Columbia University
    Brookhaven National Laboratory)

  • Fay Ng

    (Columbia University)

  • Michael L. Steigerwald

    (Columbia University)

  • Colin Nuckolls

    (Columbia University
    Wuhan University of Science and Technology)

Abstract

Self-assembly of electroactive molecules is a promising route to new types of functional semiconductors. Here we report a capsule-shaped molecule that assembles itself into a cellular semiconducting material. The interior space of the capsule with a volume of ~415 Å3 is a nanoenvironment that can accommodate a guest. To self-assemble these capsules into electronic materials, we functionalize the thiophene rings with bromines, which encode self-assembly into two-dimensional layers held together through halogen bonding interactions. In the solid state and in films, these two-dimensional layers assemble into the three-dimensional crystalline structure. This hollow material is able to form the active layer in field effect transistor devices. We find that the current of these devices has strong response to the guest’s interaction within the hollow spaces in the film. These devices are remarkable in their ability to distinguish, through their electrical response, between small differences in the guest.

Suggested Citation

  • Boyuan Zhang & Raúl Hernández Sánchez & Yu Zhong & Melissa Ball & Maxwell W. Terban & Daniel Paley & Simon J. L. Billinge & Fay Ng & Michael L. Steigerwald & Colin Nuckolls, 2018. "Hollow organic capsules assemble into cellular semiconductors," Nature Communications, Nature, vol. 9(1), pages 1-6, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-04246-0
    DOI: 10.1038/s41467-018-04246-0
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