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dc.contributor.authorSanctis, AD
dc.contributor.authorMehew, JD
dc.contributor.authorAlkhalifa, S
dc.contributor.authorWithers, F
dc.contributor.authorCraciun, MF
dc.contributor.authorRusso, S
dc.date.accessioned2018-12-04T10:23:05Z
dc.date.issued2018-11-26
dc.description.abstractThe observation of novel physical phenomena such as Hofstadter’s butterfly, topological currents, and unconventional superconductivity in graphene has been enabled by the replacement of SiO2 with hexagonal boron nitride (hBN) as a substrate and by the ability to form superlattices in graphene/hBN heterostructures. These devices are commonly made by etching the graphene into a Hall-bar shape with metal contacts. The deposition of metal electrodes, the design, and specific configuration of contacts can have profound effects on the electronic properties of the devices possibly even affecting the alignment of graphene/hBN superlattices. In this work, we probe the strain configuration of graphene on hBN in contact with two types of metal contacts, two-dimensional (2D) top-contacts and one-dimensional edge-contacts. We show that top-contacts induce strain in the graphene layer along two opposing leads, leading to a complex strain pattern across the device channel. Edge-contacts, on the contrary, do not show such strain pattern. A finite-elements modeling simulation is used to confirm that the observed strain pattern is generated by the mechanical action of the metal contacts clamped to the graphene. Thermal annealing is shown to reduce the overall doping while increasing the overall strain, indicating an increased interaction between graphene and hBN. Surprisingly, we find that the two contact configurations lead to different twist-angles in graphene/hBN superlattices, which converge to the same value after thermal annealing. This observation confirms the self-locking mechanism of graphene/hBN superlattices also in the presence of strain gradients. Our experiments may have profound implications in the development of future electronic devices based on heterostructures and provide a new mechanism to induce complex strain patterns in 2D materials.en_GB
dc.description.sponsorshipEngineering and Physical Sciences Research Council (EPSRC)en_GB
dc.description.sponsorshipRoyal Societyen_GB
dc.description.sponsorshipNewton Funden_GB
dc.description.sponsorshipLeverhulme Trusten_GB
dc.description.sponsorshipHigher Committee for Education Development in Iraq (HCED)en_GB
dc.description.sponsorshipRoyal Academy of Engineeringen_GB
dc.identifier.citationVol. 18 (12), pp. 7919-7926en_GB
dc.identifier.doi10.1021/acs.nanolett.8b03854
dc.identifier.grantnumberEP/M002438/1en_GB
dc.identifier.grantnumberEP/M001024/1en_GB
dc.identifier.grantnumberEPK017160/1en_GB
dc.identifier.grantnumberEP/K031538/1en_GB
dc.identifier.grantnumberEP/J000396/1en_GB
dc.identifier.grantnumberEP/L015331/ 1en_GB
dc.identifier.urihttp://hdl.handle.net/10871/34978
dc.language.isoenen_GB
dc.publisherAmerican Chemical Societyen_GB
dc.rights© 2018 American Chemical Society. This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.en_GB
dc.titleStrain-engineering of twist-angle in graphene/hBN superlattice devicesen_GB
dc.typeArticleen_GB
dc.date.available2018-12-04T10:23:05Z
dc.descriptionThis is the author accepted manuscript. The final version is available on open access from American Chemical Society via the DOI in this recorden_GB
dc.identifier.journalNano Lettersen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2018-11-26
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2018-10-26
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2018-12-04T10:18:43Z
refterms.versionFCDAM
refterms.dateFOA2019-02-18T11:13:14Z


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© 2018 American Chemical Society. This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
Except where otherwise noted, this item's licence is described as © 2018 American Chemical Society. This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.