IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v7y2016i1d10.1038_ncomms10657.html
   My bibliography  Save this article

Monolayer-to-bilayer transformation of silicenes and their structural analysis

Author

Listed:
  • Ritsuko Yaokawa

    (TOYOTA Central R&D Labs, Inc.)

  • Tetsu Ohsuna

    (TOYOTA Central R&D Labs, Inc.)

  • Tetsuya Morishita

    (CD-FMat, National Institute of Advanced Industrial Science and Technology (AIST))

  • Yuichiro Hayasaka

    (The Electron Microscopy Center, Tohoku University)

  • Michelle J. S. Spencer

    (School of Science, RMIT University)

  • Hideyuki Nakano

    (TOYOTA Central R&D Labs, Inc.
    JST Presto)

Abstract

Silicene, a two-dimensional honeycomb network of silicon atoms like graphene, holds great potential as a key material in the next generation of electronics; however, its use in more demanding applications is prevented because of its instability under ambient conditions. Here we report three types of bilayer silicenes that form after treating calcium-intercalated monolayer silicene (CaSi2) with a BF4− -based ionic liquid. The bilayer silicenes that are obtained are sandwiched between planar crystals of CaF2 and/or CaSi2, with one of the bilayer silicenes being a new allotrope of silicon, containing four-, five- and six-membered sp3 silicon rings. The number of unsaturated silicon bonds in the structure is reduced compared with monolayer silicene. Additionally, the bandgap opens to 1.08 eV and is indirect; this is in contrast to monolayer silicene which is a zero-gap semiconductor.

Suggested Citation

  • Ritsuko Yaokawa & Tetsu Ohsuna & Tetsuya Morishita & Yuichiro Hayasaka & Michelle J. S. Spencer & Hideyuki Nakano, 2016. "Monolayer-to-bilayer transformation of silicenes and their structural analysis," Nature Communications, Nature, vol. 7(1), pages 1-6, April.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10657
    DOI: 10.1038/ncomms10657
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms10657
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms10657?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10657. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.