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dc.contributor.authorDe Oliveira, Rafael Furlan
dc.contributor.authorMerces, Leandro
dc.contributor.authorMarques, Felipe
dc.contributor.authorTeixeira-Neto, Érico
dc.contributor.authorDe Camargo, Davi Henrique Starnini [UNESP]
dc.contributor.authorBufon, Carlos César Bof
dc.date.accessioned2018-12-11T16:53:34Z
dc.date.available2018-12-11T16:53:34Z
dc.date.issued2018-06-14
dc.identifierhttp://dx.doi.org/10.1021/acs.jpcc.8b00233
dc.identifier.citationJournal of Physical Chemistry C, v. 122, n. 23, p. 12131-12139, 2018.
dc.identifier.issn1932-7455
dc.identifier.issn1932-7447
dc.identifier.urihttp://hdl.handle.net/11449/171063
dc.description.abstractThe controllable transfer of a single electron in devices (SEDs) is one of the viable trends for a new generation of technology. However, novel applications demand innovative strategies to fabricate and evaluate SEDs. Here, we report a hybrid organic/inorganic SED that combines an ensemble of physisorbed, semiconducting molecular layers (SMLs) and Au nanoclusters embedded in the transport channel by in situ, field-induced metal migration. The SED is fabricated using an integrative platform based on rolled-up nanomembranes (rNMs) to connect ultrathin SMLs from the top, forming large-area tunnel junctions. The combination of high electric fields (1-4 MV/cm), electrode point contacts, low temperatures (10 K), and ultrathin molecular layers (<10 nm) lead to field-induced migration of Au electrode nanoparticles inward the SML of the junction channel. This phenomenon can be either observed in the as-prepared rNM junctions or intentionally induced by the application of high electric fields (>1 MV/cm). The propelled electrode particles become trapped in the soft molecular material, acting as Coulomb islands positioned in between a double-barrier tunnel junction. As a result, the hybrid organic/inorganic rNM junctions present single-charge effects, namely Coulomb blockade and Coulomb staircase. Such an in situ, field-induced metal migration process opens possibilities to create novel and complex SEDs by using different molecular materials. From another perspective, the reported metal diffusion in such nanoscale junctions deserves attention as it can occasionally mask molecule-dependent responses.en
dc.format.extent12131-12139
dc.language.isoeng
dc.relation.ispartofJournal of Physical Chemistry C
dc.sourceScopus
dc.titleSingle-Electron Charging Effects in Hybrid Organic/Inorganic Nanomembrane-Based Junctionsen
dc.typeArtigo
dc.contributor.institutionBrazilian Center for Research in Energy and Materials (CNPEM)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.description.affiliationBrazilian Nanotechnology National Laboratory (LNNano) Brazilian Center for Research in Energy and Materials (CNPEM)
dc.description.affiliationInstitute of Physics Gleb Wataghin (IFGW) University of Campinas (UNICAMP)
dc.description.affiliationDepartment of Materials Engineering University of São Paulo (USP)
dc.description.affiliationDepartment of Physical Chemistry Institute of Chemistry (IQ) University of Campinas (UNICAMP)
dc.description.affiliationPostgraduate Program in Materials Science and Technology (POSMAT) São Paulo State University (UNESP)
dc.description.affiliationUnespPostgraduate Program in Materials Science and Technology (POSMAT) São Paulo State University (UNESP)
dc.identifier.doi10.1021/acs.jpcc.8b00233
dc.rights.accessRightsAcesso restrito
dc.identifier.scopus2-s2.0-85047755286
unesp.author.orcid0000-0001-8980-3587[1]
unesp.author.orcid0000-0002-6202-9824[2]
dc.relation.ispartofsjr2,135
dc.relation.ispartofsjr2,135
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