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dc.contributor.authorBotelho, Gleice
dc.contributor.authorSczancoski, Júlio César
dc.contributor.authorAndres, Juan
dc.contributor.authorGracia, Lourdes
dc.contributor.authorLongo, Elson
dc.date.accessioned2016-04-22T07:22:24Z
dc.date.available2016-04-22T07:22:24Z
dc.date.issued2015-02
dc.identifier.citationBotelho, G., et al. "Experimental and Theoretical Study on the Structure, Optical Properties, and Growth of Metallic Silver Nanostructures in Ag3PO4." The Journal of Physical Chemistry C 119.11 (2015): 6293-6306.ca_CA
dc.identifier.urihttp://hdl.handle.net/10234/158917
dc.description.abstractTheoretical and experimental studies were performed on the structure, optical properties, and growth of silver nanostructures in silver phosphate (Ag3PO4). This material was synthesized by the coprecipitation method and processed in a microwave-assisted hydrothermal system at 150 °C for different times. The structural behavior was analyzed by means of X-ray diffraction, Rietveld refinement, and Raman spectroscopy. Field emission gun scanning electron microscopy as well as transmission electron microscopy revealed the presence of irregular spherical-like Ag3PO4 microparticles; metallic silver nanostructures were found on their surfaces. The growth processes of Ag nanostructures when irradiated with an electron beam were explained by theoretical calculations. First-principles calculations, within a quantum theory of atoms in molecules framework, have been carried out to provide deeper insight and understanding of the observed nucleation and early evolution of Ag nanoparticles on Ag3PO4 crystals, driven by an accelerated electron beam from an electronic microscope under high vacuum. The Ag nucleation and formation is a result of structural and electronic changes of the AgO4 tetrahedral cluster as a constituent building block of Ag3PO4, consistent with Ag metallic formation. The optical properties were investigated by ultraviolet–visible spectroscopy and photoluminescence (PL) measurements at room temperature. PL properties of this phosphate were explained by the recombination phenomenon of electron–hole pairs via cluster-to-cluster charge transfer.ca_CA
dc.description.sponsorShipThe authors are grateful to Prometeo/2009/053 (Generalitat Valenciana), Ministerio de Economia y Competitividad (Spain), CTQ2012-36253-C03-02, Spanish Brazilian program (PHB2009-0065-PC), CAPES (203038 009607/2013-56), INCTMN (2008/57872-1), FAPESP (2012/14004-5; 2013/ 07296-2), CNPq (147001/2013-7; 573636/2008-7) for fi nancially supporting this research. We also acknowledge the Servei Informa tica, Universitat Jaume I, for the generous allotment of computer time.ca_CA
dc.format.extent13 p.ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherAmerican Chemical Societyca_CA
dc.relation.isPartOfJ. Phys. Chem. C, 2015, 119 (11)ca_CA
dc.rightsCopyright © 2015 American Chemical Societyca_CA
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/*
dc.subjectNanostructuresca_CA
dc.subjectOptical propertiesca_CA
dc.subjectSilverca_CA
dc.titleExperimental and Theoretical Study on the Structure, Optical Properties, and Growth of Metallic Silver Nanostructures in Ag3PO4ca_CA
dc.title.alternativeExperimental and Theoretical Study on the Structure, Optical Properties, and Growth of Metallic Silver Nanostructures in Ag3PO4ca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.1021/jp512111v
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccessca_CA
dc.relation.publisherVersionhttp://pubs.acs.org/doi/abs/10.1021/jp512111vca_CA
dc.type.versioninfo:eu-repo/semantics/publishedVersionca_CA


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