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dc.contributor.authorSantos, Carla, I. M.es_ES
dc.contributor.authorMariz, Inês F. A.es_ES
dc.contributor.authorPinto, Sandra N.es_ES
dc.contributor.authorGonçalves, Giles_ES
dc.contributor.authorBdikin, Igores_ES
dc.contributor.authorMarques, Paula A.A.P.es_ES
dc.contributor.authorNeves, Maria da Graça P.M.S.es_ES
dc.contributor.authorMartinho, José M. G.es_ES
dc.contributor.authorMaçôas, Ermelinda M. S.es_ES
dc.date.accessioned2018-10-03T14:03:30Z-
dc.date.available2018-10-03T14:03:30Z-
dc.date.issued2018-07-14-
dc.identifier.citationNanoscale 10(26): 12505-12514 (2018)es_ES
dc.identifier.issn2040-3364-
dc.identifier.urihttp://hdl.handle.net/10261/170561-
dc.description.abstractCarbon nanodots (Cdots) are now emerging as promising nonlinear fluorophores for applications in biological environments. A thorough and systematic approach to the two-photon induced emission of Cdots that could provide design guidelines to control their nonlinear emission properties is still missing. In this work, we address the nonlinear optical spectroscopy of Cdots prepared by controlled chemical cutting of graphene oxide (GO). The two-photon absorption in the 700–1000 nm region and the corresponding emission spectrum are carefully investigated. The highest two-photon absorption cross-section estimated was 130 GM at 720 nm. This value is comparable with the one reported for graphene nanoribbons with push–pull architecture. The emission spectrum depends on the excitation mode. At the same excitation energy, nonlinear excitation results in excitation-wavelength independent emission, while upon linear excitation the emission is excitation-wavelength dependent. The biphotonic interaction seems to be selective towards sp2 clusters bearing electron donor and acceptor groups found in push–pull architectures. Both linear and nonlinear emission can be understood based on the existence of isolated sp2 clusters involved in π–π stacking interactions with clusters in adjacent layers.es_ES
dc.description.sponsorshipThe authors are grateful to Fundação para a Ciência e Tecnologia (FCT, Portugal), European Union, QREN, FEDER and COMPETE for funding the QOPNA, TEMA, and CQFM research unit (project Pest-C/QUI/UI0062/2013, UID/EMS/ 00481/2013 and UID/NAN/50024/2013). FCT is acknowledged for the Post-Doctoral grants of C. I. M. S., S. N. P and I. F. A. M., and for supporting the individual work contract of E. M., I. B. and P. A. A. P. M. within the Investigador FCT program (SFRH/BPD/105478/2014, SFRH/BPD/92409/2013, SFRH/BPD/ 75782/2011, IF/00759/2013, IF/00582/2015 and IF/00917/ 2013). G. G. gratefully acknowledges the funding by European Commission under individual fellowship Marie SklodowskaCurie (NANOTER, Grant Agreement 708351).es_ES
dc.language.isoenges_ES
dc.publisherRoyal Society of Chemistry (UK)es_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/708351es_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/SEV-2015-0496es_ES
dc.relation.isversionofPostprintes_ES
dc.rightsopenAccessen_EN
dc.subjectGraphene quantum dotses_ES
dc.subjectAromatic-hydrocarbonses_ES
dc.subjectFluorescencees_ES
dc.subjectOxidees_ES
dc.subjectNanodotses_ES
dc.subjectNitrogenes_ES
dc.subjectNanoparticleses_ES
dc.titleSelective two-photon absorption in carbon dots: a piece of the photoluminescence emission puzzlees_ES
dc.typeartículoes_ES
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1039/C8NR03365Jes_ES
dc.embargo.terms2019-07-14es_ES
dc.contributor.funderFundação para a Ciência e a Tecnologia (Portugal)es_ES
dc.contributor.funderEuropean Commissiones_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100001871es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.cerifentitytypePublications-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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item.languageiso639-1en-
item.openairetypeartículo-
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