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hal.structure.identifierDepartment of Chemistry
dc.contributor.authorPRITUZHALOV, V. A.
hal.structure.identifierDepartment of Chemistry
dc.contributor.authorARDASHNIKOVA, E. I.
hal.structure.identifierDepartment of Chemistry
dc.contributor.authorVINOGRADOV, A. A.
hal.structure.identifierDepartment of Chemistry
dc.contributor.authorDOLGIKH, V. A.
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorVIDEAU, Jean-Jacques
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorFARGIN, Evelyne
hal.structure.identifierElectron Microscopy for Materials Science [EMAT]
dc.contributor.authorABAKUMOV, A. M.
hal.structure.identifierElectron Microscopy for Materials Science [EMAT]
dc.contributor.authorTARAKINA, N. V.
hal.structure.identifierElectron Microscopy for Materials Science [EMAT]
dc.contributor.authorVAN TENDELOO, Gustaaf
dc.date.issued2011
dc.identifier.issn0022-1139
dc.description.abstractEnThe anion-excess fluorite-like solid solutions with general composition Bi<sub>1−<i>x</i></sub>Te<sub><i>x</i></sub>(O,F)<sub>2+<i>δ</i></sub> (<i>x</i> > 0.5) have been synthesized by a solid state reaction of TeO<sub>2</sub>, BiF<sub>3</sub> and Bi<sub>2</sub>O<sub>3</sub> at 873 K with following quenching. The homogeneity areas and polymorphism of the I ↔ IV Bi<sub>1−<i>x</i></sub>Te<sub><i>x</i></sub>(O,F)<sub>2+<i>δ</i></sub> phases were investigated. The crystal structure of the low temperature IV-Bi<sub>1−<i>x</i></sub>Te<sub><i>x</i></sub>(O,F)<sub>2+<i>δ</i></sub> phase has been solved using electron diffraction and X-ray powder diffraction (<i>a</i> = 11.53051(9) Å, S.G. <i>Ia</i>-3, <i>R</i><sub>I</sub> = 0.046, <i>R</i><sub>P</sub> = 0.041). Glass formation area in the Bi<sub>2</sub>O<sub>3</sub>-BiF<sub>3</sub>-TeO<sub>2</sub> (10% TiO<sub>2</sub>) system was investigated. IVBi<sub>1−<i>x</i></sub>Te<sub><i>x</i></sub>(O,F)<sub>2+<i>δ</i></sub> phase starts to crystallize at short-time (0.5-3 h) annealing of oxyfluoride glasses at temperatures above <i>T</i><sub>g</sub> (600-615 K). The ionic conductivity of the crystalline Bi<sub>1−<i>x</i></sub>Te<sub><i>x</i></sub>(O,F)<sub>2+<i>δ</i></sub> phase and corresponding glass-ceramics was investigated. Activation energy of conductivity <i>E</i><sub>a</sub> = 0.41(2) eV for the IV-Bi<sub>1−<i>x</i></sub>Te<sub><i>x</i></sub>(O,F)<sub>2+<i>δ</i></sub> crystalline samples and <i>E</i><sub>a</sub> = 0.73 eV for the glass-ceramic samples were obtained. Investigation of the oxyfluoride samples with a constant cation ratio demonstrates essential influence of excess fluorine anions on the ionic conductivity.
dc.language.isoen
dc.publisherElsevier
dc.title.enNew anion-conducting solid solutions Bi<sub>1−<i>x</i></sub>Te<sub><i>x</i></sub>(O,F)<sub>2+<i>δ</i></sub> (<i>x</i> > 0.5) and glass-ceramic material on their base
dc.typeArticle de revue
dc.identifier.doi10.1016/j.jfluchem.2011.06.042
dc.subject.halChimie/Matériaux
bordeaux.journalJournal of Fluorine Chemistry
bordeaux.page1110-1116
bordeaux.volume132
bordeaux.issue12
bordeaux.peerReviewedoui
hal.identifierhal-00635928
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00635928v1
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