| Literature DB >> 28926230 |
Hiroaki Nishino, Takeshi Fujita1, Nguyen Thanh Cuong2, Satoshi Tominaka3, Masahiro Miyauchi4, Soshi Iimura5, Akihiko Hirata1,6, Naoto Umezawa3, Susumu Okada, Eiji Nishibori7, Asahi Fujino, Tomohiro Fujimori, Shin-Ichi Ito, Junji Nakamura7, Hideo Hosono5,8, Takahiro Kondo7,8.
Abstract
Two-dimensional (2D) materials are promising for applications in a wide range of fields because of their unique properties. Hydrogen boride sheets, a new 2D material recently predicted from theory, exhibit intriguing electronic and mechanical properties as well as hydrogen storage capacity. Here, we report the experimental realization of 2D hydrogen boride sheets with an empirical formula of H1B1, produced by exfoliation and complete ion-exchange between protons and magnesium cations in magnesium diboride (MgB2) with an average yield of 42.3% at room temperature. The sheets feature an sp2-bonded boron planar structure without any long-range order. A hexagonal boron network with bridge hydrogens is suggested as the possible local structure, where the absence of long-range order was ascribed to the presence of three different anisotropic domains originating from the 2-fold symmetry of the hydrogen positions against the 6-fold symmetry of the boron networks, based on X-ray diffraction, X-ray atomic pair distribution functions, electron diffraction, transmission electron microscopy, photo absorption, core-level binding energy data, infrared absorption, electron energy loss spectroscopy, and density functional theory calculations. The established cation-exchange method for metal diboride opens new avenues for the mass production of several types of boron-based 2D materials by countercation selection and functionalization.Entities:
Year: 2017 PMID: 28926230 DOI: 10.1021/jacs.7b06153
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419