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hal.structure.identifierInstitute of General and Inorganic Chemistry
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorSTOYANOVA, R.
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorCARLIER-LARREGARAY, Dany
hal.structure.identifierCentral Laboratory of Solar Energy and New Energy Sources [CL SENES]
dc.contributor.authorSENDOVA-VASSILEVA, M.
hal.structure.identifierInstitute of General and Inorganic Chemistry
dc.contributor.authorYONCHEVA, M.
hal.structure.identifierInstitute of General and Inorganic Chemistry
dc.contributor.authorZHECHEVA, E.
hal.structure.identifierInstitute of General and Inorganic Chemistry
hal.structure.identifierCentral Laboratory of Mineralogy and Crystallography
dc.contributor.authorNIHTIANOVA, D.
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorDELMAS, Claude
dc.date.issued2010
dc.identifier.issn0022-4596
dc.description.abstractEnSodium manganates with nominal composition Na<sub>2/3</sub>MnO<sub>2</sub> were prepared by solid state reaction between Na<sub>2</sub>CO<sub>3</sub> and MnCO<sub>3</sub> at 1000 °C. The composition and structure of Na<i><sub>x</sub></i>MnO<sub>2</sub> were controlled by the rate of cooling from the temperature of preparation. This is a consequence of the capability of Na<sub>2/3</sub>MnO<sub>2</sub> to accommodate over<i>-</i>stoichiometric Mn<sup>4+</sup> ions up to 12.5%. Structural characterization was carried out by XRD powder diffractions, TEM analysis and Raman spectroscopy. The composition and oxidation state of manganese were determined by chemical analysis and magnetic susceptibility measurements. The manganese distribution in the layers was analysed using electron paramagnetic resonance (EPR) spectroscopy. By quenching from 1000 °C, the orthorhombic distorted modification is stabilized. A phase separation into orthorhombic and hexagonal modifications takes place when Na<sub>2/3</sub>MnO<sub>2</sub> is slow cooled. The structure changes are concomitant with an increase in the oxidation state of Mn. The over<i>-</i>stoichiometric Mn<sup>4+</sup> ions are accommodated in the hexagonal modification by creation of vacancies in the MnO<sub>2</sub><i>-</i>layers.
dc.language.isoen
dc.publisherElsevier
dc.subject.enLayered oxides
dc.subject.enSodium manganates
dc.subject.enElectron paramagnetic resonance spectroscopy
dc.subject.enRaman spectroscopy
dc.title.enStabilization of over-stoichiometric Mn<sup>4+</sup> in layered Na<sub>2/3</sub>MnO<sub>2</sub>
dc.typeArticle de revue
dc.identifier.doi10.1016/j.jssc.2010.04.024
dc.subject.halChimie/Matériaux
bordeaux.journalJournal of Solid State Chemistry
bordeaux.page1372-1379
bordeaux.volume183
bordeaux.issue6
bordeaux.peerReviewedoui
hal.identifierhal-00494476
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00494476v1
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