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Borophene-graphene heterostructures

Integration of dissimilar two-dimensional (2D) materials is essential for nanoelectronic applications. Compared to vertical stacking, covalent lateral stitching requires bottom-up synthesis, resulting in rare realizations of 2D lateral heterostructures. Because of its polymorphism and diverse bondin...

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Detalles Bibliográficos
Autores principales: Liu, Xiaolong, Hersam, Mark C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788864/
https://www.ncbi.nlm.nih.gov/pubmed/31646179
http://dx.doi.org/10.1126/sciadv.aax6444
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author Liu, Xiaolong
Hersam, Mark C.
author_facet Liu, Xiaolong
Hersam, Mark C.
author_sort Liu, Xiaolong
collection PubMed
description Integration of dissimilar two-dimensional (2D) materials is essential for nanoelectronic applications. Compared to vertical stacking, covalent lateral stitching requires bottom-up synthesis, resulting in rare realizations of 2D lateral heterostructures. Because of its polymorphism and diverse bonding geometries, borophene is a promising candidate for 2D heterostructures, although suitable synthesis conditions have not yet been demonstrated. Here, we report lateral and vertical integration of borophene with graphene. Topographic and spatially resolved spectroscopic measurements reveal nearly atomically sharp lateral interfaces despite imperfect crystallographic lattice and symmetry matching. In addition, boron intercalation under graphene results in rotationally commensurate vertical heterostructures. The rich bonding configurations of boron suggest that borophene can be integrated into a diverse range of 2D heterostructures.
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spelling pubmed-67888642019-10-23 Borophene-graphene heterostructures Liu, Xiaolong Hersam, Mark C. Sci Adv Research Articles Integration of dissimilar two-dimensional (2D) materials is essential for nanoelectronic applications. Compared to vertical stacking, covalent lateral stitching requires bottom-up synthesis, resulting in rare realizations of 2D lateral heterostructures. Because of its polymorphism and diverse bonding geometries, borophene is a promising candidate for 2D heterostructures, although suitable synthesis conditions have not yet been demonstrated. Here, we report lateral and vertical integration of borophene with graphene. Topographic and spatially resolved spectroscopic measurements reveal nearly atomically sharp lateral interfaces despite imperfect crystallographic lattice and symmetry matching. In addition, boron intercalation under graphene results in rotationally commensurate vertical heterostructures. The rich bonding configurations of boron suggest that borophene can be integrated into a diverse range of 2D heterostructures. American Association for the Advancement of Science 2019-10-11 /pmc/articles/PMC6788864/ /pubmed/31646179 http://dx.doi.org/10.1126/sciadv.aax6444 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Liu, Xiaolong
Hersam, Mark C.
Borophene-graphene heterostructures
title Borophene-graphene heterostructures
title_full Borophene-graphene heterostructures
title_fullStr Borophene-graphene heterostructures
title_full_unstemmed Borophene-graphene heterostructures
title_short Borophene-graphene heterostructures
title_sort borophene-graphene heterostructures
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788864/
https://www.ncbi.nlm.nih.gov/pubmed/31646179
http://dx.doi.org/10.1126/sciadv.aax6444
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