Abstract

A stable BiI3 monosheet has been grown for the first time on the (0001) surface of the topological insulator Bi2Se3 as confirmed by scanning tunnelling microscopy, surface X-ray diffraction, and X-ray photoemision spectroscopy. BiI3 is deposited by molecular beam epitaxy from the crystalline BiTeI precursor that undergoes decomposition sublimation. The key fragment of the bulk BiI3 structure, {{rm{a}}}_{infty }^{2}[I—Bi—I] layer of edge-sharing BiI6 octahedra, is preserved in the ultra-thin film limit, but exhibits large atomic relaxations. The stacking sequence of the trilayers and alternations of the Bi—I distances in the monosheet are the same as in the bulk BiI3 structure. Momentum resolved photoemission spectroscopy indicates a direct band gap of 1.2 eV. The Dirac surface state is completely destroyed and a new flat band appears in the band gap of the BiI3 film that could be interpreted as an interface state.

Highlights

  • Two-dimensional (2D) metal halides have been of interest since a long time for their intriguing and tunable properties

  • A stoichiometrically almost exact BiI3 film is deposited by decomposition sublimation of BiTeI, as corroborated by X-ray photoemission spectroscopy (XPS), scanning tunnelling microscopy (STM) and surface X-ray diffraction (SXRD)

  • BiI3 was molecular beam epitaxy (MBE)-deposited onto the substrate that was kept at room temperature

Read more

Summary

Introduction

Two-dimensional (2D) metal halides have been of interest since a long time for their intriguing and tunable properties. We establish a different approach by depositing a monosheet of BiI3 on the (0001) surface of the topological insulator (TI) Bi2Se3 by using molecular beam epitaxy (MBE) from a Knudsen cell filled with presynthesized BiTeI single crystals heated to 380 °C. A stoichiometrically almost exact BiI3 film is deposited by decomposition sublimation of BiTeI, as corroborated by X-ray photoemission spectroscopy (XPS), scanning tunnelling microscopy (STM) and surface X-ray diffraction (SXRD).

Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.