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dc.contributor.authorEscribano López, Purificación
dc.contributor.authorPlanelles Aragó, José
dc.contributor.authorCordoncillo, Eloisa
dc.contributor.authorFerreira, Rute A. S.
dc.contributor.authorCarlos, Luís D.
dc.date.accessioned2012-10-22T13:47:25Z
dc.date.available2012-10-22T13:47:25Z
dc.date.issued2011
dc.identifier.issn0959-9428
dc.identifier.urihttp://hdl.handle.net/10234/49615
dc.description.abstractEu3+-Doped CdS hexagonal nanocrystals (NCs), with an average size of 4 nm, have been prepared through a simple methodology based on the direct precipitation of CdS NCs using 1-thioglycerol as a capping molecule. Steady-state and time-resolved photoluminescence studies (14–300 K) reveal an effective CdS NCs-to-Eu3+ energy transfer process involving surface localized states and mediated by a thermally activated exchange mechanism. Furthermore, the analysis of the optical data also points out the presence of two distinct Eu3+ local coordination sites with different relaxation kinetics and attributed to lattice-bound and surface-bound centres. The 5D0 lifetime values are longer than those reported previously for sol–gel derived Eu3+-doped CdS NCs.ca_CA
dc.language.isoengca_CA
dc.publisherRSCca_CA
dc.relation.isPartOfJournal of Materials Chemistry Issue 4, 2011ca_CA
dc.rights© The Royal Society of Chemistry 2011ca_CA
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/*
dc.titleSynthesis, characterization and optical studies on lanthanide-doped CdS quantum dots: new insights on CdS → lanthanide energy transfer mechanismsca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.1039/C0JM03188G
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccessca_CA
dc.relation.publisherVersionhttp://pubs.rsc.org/en/content/articlelanding/2011/jm/c0jm03188g#!divAbstractca_CA


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