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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/67212
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dc.contributor.authorPontes, F. M.-
dc.contributor.authorLeal, S. H.-
dc.contributor.authorPizani, P. S.-
dc.contributor.authorSantos, M. R M C-
dc.contributor.authorLeite, E. R.-
dc.contributor.authorLongo, Elson-
dc.contributor.authorLanciotti, F.-
dc.contributor.authorBoschi, T. M.-
dc.contributor.authorVarela, José Arana-
dc.date.accessioned2014-05-27T11:20:37Z-
dc.date.accessioned2016-10-25T18:18:28Z-
dc.date.available2014-05-27T11:20:37Z-
dc.date.available2016-10-25T18:18:28Z-
dc.date.issued2003-03-01-
dc.identifierhttp://dx.doi.org/10.1557/JMR.2003.0087-
dc.identifier.citationJournal of Materials Research, v. 18, n. 3, p. 659-663, 2003.-
dc.identifier.issn0884-2914-
dc.identifier.urihttp://hdl.handle.net/11449/67212-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/67212-
dc.description.abstractStrontium-modified lead titanate thin films with composition Pb1-xSrxTiO3 were grown on Pt/Ti/SiO2/Si substrates using the polymeric precursor method. The structural phase evolution as a function of the Sr contents was studied using micro-Raman scattering, specular reflectance infrared Fourier transform spectroscopy, and x-ray diffraction. The results showed a gradual change from tetragonal to cubic structure, the transition occurring at about x = 0.58. The infrared reflectance spectra showed that the frequency of several peaks decreases as the strontium concentration increases. These features are correlated with a decrease in the tetragonal distortion of the TiO6 octahedra as the strontium concentration increases.en
dc.format.extent659-663-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectDoping (additives)-
dc.subjectFourier transform infrared spectroscopy-
dc.subjectLead compounds-
dc.subjectRaman scattering-
dc.subjectStrontium-
dc.subjectX ray diffraction analysis-
dc.subjectSoft chemical techniques-
dc.subjectThin films-
dc.titleStructural phase evolution of strontium-doped lead titanate thin films prepared by the soft chemical techniqueen
dc.typeoutro-
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)-
dc.contributor.institutionUniversidade Federal do Piauí (UFPI)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationLab. Interdisc. Eletroquim./Ceram. Ctro. Multidisc. Para D.M.C. Univ. Federal de Sao Carlos (UFSCar), Via Washington, Km 235, CP-676, CEP-13565-905, Sao Carlos, S.P.-
dc.description.affiliationCentro de Ciencias da Natureza (CCN) Departamento de Química Universidade Federal do Piaui (UFPI), Teresina, PI-
dc.description.affiliationDepartamento de Física Univ. Federal de Sao Carlos (UFSCar), Via Washington, Km 235, CEP-13565-905, Sao Carlos, S.P.-
dc.description.affiliationInstituto de Química Univ. Estadual Paulista (UNESP), Araraquara, S.P.-
dc.description.affiliationUnespInstituto de Química Univ. Estadual Paulista (UNESP), Araraquara, S.P.-
dc.identifier.doi10.1557/JMR.2003.0087-
dc.identifier.wosWOS:000181411200019-
dc.rights.accessRightsAcesso restrito-
dc.identifier.file2-s2.0-0038676283.pdf-
dc.relation.ispartofJournal of Materials Research-
dc.identifier.scopus2-s2.0-0038676283-
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