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      Self-assembly of electronically abrupt borophene/organic lateral heterostructures

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          Abstract

          Integrating borophene with organic molecules results in electronically abrupt self-assembled lateral heterostructures.

          Abstract

          Two-dimensional boron sheets (that is, borophene) have recently been realized experimentally and found to have promising electronic properties. Because electronic devices and systems require the integration of multiple materials with well-defined interfaces, it is of high interest to identify chemical methods for forming atomically abrupt heterostructures between borophene and electronically distinct materials. Toward this end, we demonstrate the self-assembly of lateral heterostructures between borophene and perylene-3,4,9,10-tetracarboxylic dianhydride (PTCDA). These lateral heterostructures spontaneously form upon deposition of PTCDA onto submonolayer borophene on Ag(111) substrates as a result of the higher adsorption enthalpy of PTCDA on Ag(111) and lateral hydrogen bonding among PTCDA molecules, as demonstrated by molecular dynamics simulations. In situ x-ray photoelectron spectroscopy confirms the weak chemical interaction between borophene and PTCDA, while molecular-resolution ultrahigh-vacuum scanning tunneling microscopy and spectroscopy reveal an electronically abrupt interface at the borophene/PTCDA lateral heterostructure interface. As the first demonstration of a borophene-based heterostructure, this work will inform emerging efforts to integrate borophene into nanoelectronic applications.

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          Most cited references24

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          Lateral epitaxial growth of two-dimensional layered semiconductor heterojunctions.

          Two-dimensional layered semiconductors such as MoS₂ and WSe₂ have attracted considerable interest in recent times. Exploring the full potential of these layered materials requires precise spatial modulation of their chemical composition and electronic properties to create well-defined heterostructures. Here, we report the growth of compositionally modulated MoS₂-MoSe₂ and WS₂-WSe₂ lateral heterostructures by in situ modulation of the vapour-phase reactants during growth of these two-dimensional crystals. Raman and photoluminescence mapping studies demonstrate that the resulting heterostructure nanosheets exhibit clear structural and optical modulation. Transmission electron microscopy and elemental mapping studies reveal a single crystalline structure with opposite modulation of sulphur and selenium distributions across the heterostructure interface. Electrical transport studies demonstrate that the WSe₂-WS₂ heterojunctions form lateral p-n diodes and photodiodes, and can be used to create complementary inverters with high voltage gain. Our study is an important advance in the development of layered semiconductor heterostructures, an essential step towards achieving functional electronics and optoelectronics.
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            NANOELECTRONICS. Epitaxial growth of a monolayer WSe2-MoS2 lateral p-n junction with an atomically sharp interface.

            Two-dimensional transition metal dichalcogenides (TMDCs) such as molybdenum sulfide MoS2 and tungsten sulfide WSe2 have potential applications in electronics because they exhibit high on-off current ratios and distinctive electro-optical properties. Spatially connected TMDC lateral heterojunctions are key components for constructing monolayer p-n rectifying diodes, light-emitting diodes, photovoltaic devices, and bipolar junction transistors. However, such structures are not readily prepared via the layer-stacking techniques, and direct growth favors the thermodynamically preferred TMDC alloys. We report the two-step epitaxial growth of lateral WSe2-MoS2 heterojunction, where the edge of WSe2 induces the epitaxial MoS2 growth despite a large lattice mismatch. The epitaxial growth process offers a controllable method to obtain lateral heterojunction with an atomically sharp interface.
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              Experimental realization of two-dimensional boron sheets

              A variety of two-dimensional materials have been reported in recent years, yet single-element systems such as graphene and black phosphorus have remained rare. Boron analogues have been predicted, as boron atoms possess a short covalent radius and the flexibility to adopt sp(2) hybridization, features that favour the formation of two-dimensional allotropes, and one example of such a borophene material has been reported recently. Here, we present a parallel experimental work showing that two-dimensional boron sheets can be grown epitaxially on a Ag(111) substrate. Two types of boron sheet, a β12 sheet and a χ3 sheet, both exhibiting a triangular lattice but with different arrangements of periodic holes, are observed by scanning tunnelling microscopy. Density functional theory simulations agree well with experiments, and indicate that both sheets are planar without obvious vertical undulations. The boron sheets are quite inert to oxidization and interact only weakly with their substrate. We envisage that such boron sheets may find applications in electronic devices in the future.
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                Author and article information

                Journal
                Sci Adv
                Sci Adv
                SciAdv
                advances
                Science Advances
                American Association for the Advancement of Science
                2375-2548
                February 2017
                22 February 2017
                : 3
                : 2
                : e1602356
                Affiliations
                [1 ]Applied Physics Graduate Program, Northwestern University, Evanston, IL 60208, USA.
                [2 ]Department of Materials Science and Engineering, Northwestern University, Evanston, IL 60208, USA.
                [3 ]Center for Nanoscale Materials, Argonne National Laboratory, Argonne, IL 60439, USA.
                [4 ]Department of Engineering Sciences and Applied Mathematics, Northwestern University, Evanston, IL 60208, USA.
                [5 ]Department of Physics and Astronomy, Northwestern University, Evanston, IL 60208, USA.
                [6 ]Department of Chemistry, Northwestern University, Evanston, IL 60208, USA.
                [7 ]Department of Electrical Engineering and Computer Science, Northwestern University, Evanston, IL 60208, USA.
                Author notes
                [* ]Corresponding author. Email: m-hersam@ 123456northwestern.edu
                Author information
                http://orcid.org/0000-0002-6186-5257
                http://orcid.org/0000-0001-5991-1894
                http://orcid.org/0000-0002-9358-5743
                http://orcid.org/0000-0003-4788-1506
                http://orcid.org/0000-0003-2364-1866
                Article
                1602356
                10.1126/sciadv.1602356
                5321450
                b056263f-420e-490b-9099-43be33edbf77
                Copyright © 2017, The Authors

                This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license, 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.

                History
                : 25 September 2016
                : 09 January 2017
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000006, Office of Naval Research;
                Award ID: ID0EGYAI14022
                Award ID: N00014-14-1-0669
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000078, Division of Materials Research;
                Award ID: ID0EA5AI14023
                Award ID: DMR-1121262
                Award Recipient :
                Categories
                Research Article
                Research Articles
                SciAdv r-articles
                Chemistry
                Custom metadata
                Judith Urtula

                boron,two-dimensional,borophene,ptcda,organic,heterostructure,self-assembly,scanning tunneling microscopy,x-ray photoelectron spectroscopy,molecular dynamics

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