The origin of photoluminescence in amorphous lead titanate

dc.contributor.authorLeite, E. R.
dc.contributor.authorParis, E. C.
dc.contributor.authorPontes, F. M.
dc.contributor.authorPaskocimas, C. A.
dc.contributor.authorLongo, Elson [UNESP]
dc.contributor.authorSensato, F.
dc.contributor.authorPinheiro, C. D.
dc.contributor.authorVarela, José Arana [UNESP]
dc.contributor.authorPizani, P. S.
dc.contributor.authorCampos, CEM
dc.contributor.authorLanciotti, F.
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.contributor.institutionUniversidade Federal da Paraíba (UFPB)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:20:38Z
dc.date.available2014-05-20T15:20:38Z
dc.date.issued2003-03-15
dc.description.abstractWe discuss the nature of visible photoluminescence at room temperature in amorphous lead titanate in the light of the results of recent experimental and theoretical calculations. Experimental results obtained by XANES and EXAFS revealed that amorphous lead titanate is composed of a Ti-O network having fivefold Ti coordination and NBO-type (non-bridging oxygen) defects. These defects can modify the electronic structure of amorphous compounds. Our calculation of the electronic structure involved the use of first-principle molecular calculations to simulate the variation of the electronic structure in the lead titanate crystalline phase, which is known to have a direct band gap, and we also made an in-depth examination of amorphous lead titanate. The results of our theoretical calculations of amorphous lead titanate indicate that the formation of fivefold coordination in the amorphous system may introduce delocalized electronic levels in the HOMO ( highest occupied molecular orbital) and the LUMO ( lowest unoccupied molecular orbital). A comparison of the experimental and theoretical results of amorphous compounds suggests the possibility of a radiative recombination (electron-hole pairs), which may be responsible for the emission of photoluminescence. (C) 2003 Kluwer Academic Publishers.en
dc.description.affiliationUFSCar, Dept Chem, CMDMC, LIEC, BR-13565905 Sao Carlos, SP, Brazil
dc.description.affiliationUFPB, CFP, DCEN, Cajazeiras, PB, Brazil
dc.description.affiliationUNESP, Inst Chem, Araraquara, SP, Brazil
dc.description.affiliationUFSCar, Dept Phys, BR-13565905 Sao Carlos, SP, Brazil
dc.description.affiliationUnespUNESP, Inst Chem, Araraquara, SP, Brazil
dc.format.extent1175-1178
dc.identifierhttp://dx.doi.org/10.1023/A:1022837132220
dc.identifier.citationJournal of Materials Science. Dordrecht: Kluwer Academic Publ, v. 38, n. 6, p. 1175-1178, 2003.
dc.identifier.doi10.1023/A:1022837132220
dc.identifier.issn0022-2461
dc.identifier.urihttp://hdl.handle.net/11449/31896
dc.identifier.wosWOS:000181626100010
dc.language.isoeng
dc.publisherKluwer Academic Publ
dc.relation.ispartofJournal of Materials Science
dc.relation.ispartofjcr2.993
dc.relation.ispartofsjr0,807
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.titleThe origin of photoluminescence in amorphous lead titanateen
dc.typeArtigo
dcterms.licensehttp://www.springer.com/open+access/authors+rights
dcterms.rightsHolderKluwer Academic Publ
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Química, Araraquarapt

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