High-Order Commensurate Zwitterionic Quinonoid Phase Induces a Nanoscale Dipole Lattice on Graphene

datacite.alternateIdentifier.citationJOURNAL OF PHYSICAL CHEMISTRY C,Vol.128,9712-9721,2024
datacite.alternateIdentifier.doi10.1021/acs.jpcc.4c01695
datacite.creatorNassar, Gaelle
datacite.creatorCortes Arriagada, Diego
datacite.creatorSanhueza Vega, Luis
datacite.creatorLandois, Perine
datacite.creatorPaillet, Matthieu
datacite.creatorHrich, Haitham
datacite.creatorContreras, Sylvie
datacite.creatorSiri, Olivier
datacite.creatorPascal, Simon
datacite.creatorMasson, Laurence
datacite.creatorBecker, Conrad
datacite.creatorRanguis, Alain
datacite.creatorParret, Romain
datacite.creatorCanard, Gabriel
datacite.creatorLeoni, Thomas
datacite.date2024
datacite.titleHigh-Order Commensurate Zwitterionic Quinonoid Phase Induces a Nanoscale Dipole Lattice on Graphene
dc.date.accessioned2024-09-10T18:47:13Z
dc.date.available2024-09-10T18:47:13Z
dc.description.abstractSince the introduction of hybrid van der Waals heterostructures (h-vdWHs) for device architecture development, many vertically staked organic two-dimensional materials have been investigated in order to control transport properties. This article introduces a novel h-vdWH that achieves periodic interaction by the development of a superlattice. We describe a complete investigation of the diphenyl-functionalized p-benzoquinonemonoimine zwitterion on highly oriented pyrolytic graphite and monolayer graphene using high-resolution scanning tunneling microscopy images and numerical simulations. The molecular phase on both substrates exhibits a structurally identical antiparallel dipole alignment in a head-to-tail dimer configuration. Density functional theory calculations reveal that this molecular adsorption induces a local dipole at the graphene interface due to the rearrangement of the electron density distribution.
dc.identifier.urihttps://repositoriodigital.uct.cl/handle/10925/6000
dc.language.isoen
dc.publisherAMER CHEMICAL SOC
dc.sourceJOURNAL OF PHYSICAL CHEMISTRY C
oaire.resourceTypeWOS
oaire.resourceType.enArticle
uct.indizacionSCI
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