Abstract
Synthetic two-dimensional (2D) materials have no bulk counterparts and typically exist as single atomic layers due to substrate-stabilized growth. Multilayer formation, although broadly sought for structure and property tuning, has not yet been achieved in the case of synthetic 2D boron: that is, borophene1,2. Here, we experimentally demonstrate the synthesis of an atomically well-defined borophene polymorph beyond the single-atomic-layer (SL) limit. The structure of this bilayer (BL) borophene is consistent with two covalently bonded α-phase layers (termed BL-α borophene) as evidenced from bond-resolved scanning tunnelling microscopy, non-contact atomic force microscopy and density functional theory calculations. While the electronic density of states near the Fermi level of BL-α borophene is similar to SL borophene polymorphs, field-emission resonance spectroscopy reveals distinct interfacial charge transfer doping and a heightened local work function exceeding 5 eV. The extension of borophene polymorphs beyond the SL limit significantly expands the phase space for boron-based nanomaterials.
Original language | English (US) |
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Pages (from-to) | 35-40 |
Number of pages | 6 |
Journal | Nature materials |
Volume | 21 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2022 |
Funding
X.L., Q.L., M.S.R. and M.C.H. acknowledge support from the Office of Naval Research (ONR N00014\u221217-1-2993) and the National Science Foundation Materials Research Science and Engineering Center (NSF DMR-1720139). Q.R. and B.I.Y. acknowledge support from the Electronics Division of the US Army Research Office (W911NF-16-1-0255) and the Robert Welch Foundation (C-1590).
ASJC Scopus subject areas
- General Chemistry
- General Materials Science
- Condensed Matter Physics
- Mechanics of Materials
- Mechanical Engineering