dc.contributorUniversidade Federal de São Carlos (UFSCar)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:21:05Z
dc.date.available2014-05-20T15:21:05Z
dc.date.created2014-05-20T15:21:05Z
dc.date.issued2006-12-01
dc.identifierJournal of Solid State Chemistry. San Diego: Academic Press Inc. Elsevier B.V., v. 179, n. 12, p. 3997-4002, 2006.
dc.identifier0022-4596
dc.identifierhttp://hdl.handle.net/11449/32260
dc.identifier10.1016/j.jssc.2006.09.010
dc.identifierWOS:000242787500051
dc.description.abstractPhotoluminescent disordered ZrTiO4 powders were obtained by the polymeric precursor soft-chemical method. This oxide system (ordered and disordered) was characterized by photoluminescence, Raman spectroscopy, X-ray diffraction, differential scanning calorimetry and UV vis absorption experiments. The UV absorption tail formation in the disordered oxides was related to the diminution of optical band gap. In the disordered phase, this oxide displayed broad band photoluminescence caused by change in coordination number of titanium and zirconium with oxygen atoms. The gap decreased from 3.09 eV in crystalline oxide to 2.16 eV in disordered oxide. The crystalline oxide presented an orthorhombic alpha-PbO2-type structure in which Zr4+ and Ti4+ were randomly distributed in octahedral coordination polyhedra with oxygen atoms. The amorphous-crystalline transition occurred at almost 700 degrees C, at which point the photoluminescence vanished. The Raman peak at close to 80-200 cm(-1) indicated the presence of locally ordered Ti-O-n and Zr-O-n polyhedra in disordered photoluminescent oxides. (c) 2006 Elsevier B.V. All rights reserved.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationJournal of Solid State Chemistry
dc.relation2.179
dc.relation0,632
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectZrTiO4
dc.subjectphoto luminescence
dc.subjectpolymeric precursor method
dc.subjectorder-disorder level
dc.titlePhoto luminescence: A probe for short, medium and long-range self-organization order in ZrTiO4 oxide
dc.typeArtículos de revistas


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