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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/111716
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dc.contributor.authorPerrella, Rafael V.-
dc.contributor.authorSantos, Daniela P. dos-
dc.contributor.authorPoirier, Gael Y.-
dc.contributor.authorGoes, Marcio S.-
dc.contributor.authorRibeiro, Sidney Jose L.-
dc.contributor.authorSchiavon, Marco A.-
dc.contributor.authorFerrari, Jefferson L.-
dc.date.accessioned2014-12-03T13:08:55Z-
dc.date.accessioned2016-10-25T20:09:33Z-
dc.date.available2014-12-03T13:08:55Z-
dc.date.available2016-10-25T20:09:33Z-
dc.date.issued2014-05-01-
dc.identifierhttp://dx.doi.org/10.1016/j.jlumin.2014.01.052-
dc.identifier.citationJournal Of Luminescence. Amsterdam: Elsevier Science Bv, v. 149, p. 333-340, 2014.-
dc.identifier.issn0022-2313-
dc.identifier.urihttp://hdl.handle.net/11449/111716-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/111716-
dc.description.abstractThe relentless pursuit for materials containing rare earth ions with photoluminescent properties has led to several studies with applications in the development of new technologies. The main focus of this work is the preparation of Er3+-doped polycrystalline Y2O3 with photoluminescent properties using PEG as an organic precursor and heat-treated at different temperatures. The methodology used in this synthesis is highly attractive due to its high feasibility for improved technology and low cost for preparing materials. The behavior of the viscous resin has been evaluated and the final compounds exhibited the formation of a cubic polycrystalline phase, which is able to support variations in Er3+ doping concentrations up to 10 mol%, without significant changes in the polycrystalline parameters. The values of the nanocrystallite size calculated by Scherrer's equation showed direct dependence on the heat-treatment temperature as well as the Er3+ concentration. Intense emission in the visible region under excitation at 980 nm was attributed to an upconversion phenomenon assigned to the intraconfigurational f-f transitions of Er3+ ions. The upconversion mechanism was investigated and it was demonstrated that the higher intense emission in the red region in comparison to the emission in the green region is related to the crystallite size. The studies about the intensity showed the dependence of upconversion emission of power source, indicating that two-photon are responsible for the green and red photoluminescence. These polycrystalline materials exhibit properties that make them promising for use in solar energy systems, C-telecom band or solid-state laser devices. (C) 2014 Elsevier B.V. All rights reserved.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)-
dc.format.extent333-340-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectUpconversionen
dc.subjectPhotoluminescenceen
dc.subjectCrystalline structureen
dc.subjectRare earthsen
dc.titleEr3+-doped Y2O3 obtained by polymeric precursor: Synthesis, structure and upconversion emission propertiesen
dc.typeoutro-
dc.contributor.institutionUniversidade Federal de São João del-Rei (UFSJ)-
dc.contributor.institutionUniversidade Federal de Alfenas (UNIFAL)-
dc.contributor.institutionUniv Fed Integracao Latino Amer UNILA-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv Fed Sao Joao del Rei, Dept Ciencias Nat, GPQM, BR-36301160 Sao Joao Del Rei, MG, Brazil-
dc.description.affiliationUniv Fed Alfenas, Inst Ciencia & Tecnol, BR-37715400 Pocos De Caldas, MG, Brazil-
dc.description.affiliationUniv Fed Integracao Latino Amer UNILA, BR-85867970 Foz Do Iguacu, PR, Brazil-
dc.description.affiliationUNESP, Inst Quim, BR-14800970 Araraquara, SP, Brazil-
dc.description.affiliationUnespUNESP, Inst Quim, BR-14800970 Araraquara, SP, Brazil-
dc.description.sponsorshipIdFAPEMIG: REDE-113/10-
dc.identifier.doi10.1016/j.jlumin.2014.01.052-
dc.identifier.wosWOS:000333788900053-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Luminescence-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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