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hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorKIM, Ka-Young
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorDURAND, A.
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorHEINTZ, Jean-Marc
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorVEILLERE, Amélie
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorJUBERA, Veronique
dc.date.issued2016-03
dc.identifier.issn0022-4596
dc.description.abstractEnA Eu3+ doped Y3NbO7 niobate powder was synthetized using a polymerizable complex route. It gave rise to nanometric particles that crystallized in the fluorine structure, corresponding to the Y3NbO7 phase. The thermal evolution of this powder was followed up to 1600 °C, using X-ray diffraction and optical characterizations. The fluorine structure was maintained in the whole temperature range. However, spectral evolution of the samples calcined above 900 °C showed a more complex situation. Emission spectra of powders heat treated at different temperatures showed an evolution of the emission lines that can be attributed first to a better crystallization of the niobate phase and second to its partial decomposition in favor of the formation of YNbO4 and Y2O3. Although the Y3NbO7 phase appeared stable up to 1650 °C, from X-ray diffraction analysis, spectral analysis showed that the local environment of the doping element is modified from 1100 °C.
dc.description.sponsorshipInitiative d'excellence de l'Université de Bordeaux - ANR-10-IDEX-0003
dc.language.isoen
dc.publisherElsevier
dc.subject.enLuminescence
dc.subject.enSolid solution
dc.title.enSpectral evolution of Eu3+ doped Y3NbO7 niobate induced by temperature
dc.typeArticle de revue
dc.identifier.doi10.1016/j.jssc.2015.12.023
dc.subject.halChimie/Matériaux
bordeaux.journalJournal of Solid State Chemistry
bordeaux.page169-174
bordeaux.volume235
bordeaux.peerReviewedoui
hal.identifierhal-01253808
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01253808v1
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