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hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorBLANGERO, Maxime
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorCARLIER-LARREGARAY, Dany
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorPOLLET, Michaël
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorDARRIET, Jacques
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorDELMAS, Claude
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorDOUMERC, Jean-Pierre
dc.date.issued2008
dc.identifier.issn1098-0121
dc.description.abstractEnThe high temperature phase transition in the three-layered P[prime]3-NaxCoO2 (x~0.62) has been investigated by means of heat capacity measurement, x-ray diffraction, and 23Na magic angle spinning (MAS)–NMR spectroscopy in the 300–550 K range. The phase transition occurs nearby TS=350 K. Below TS, the unit cell is monoclinic (space group C2/m). Above TS, the monoclinic cell is reversibly converted into a rhombohedral cell (space group R3m). The crystallographic change mainly manifests into Na rearrangement in the interslab from a low symmetry position to a higher symmetry position. A global picture for both systems of the (x,y,z) off-center position of Na could be understood as a balance between on-site Na+-Co3+/4+ electrostatic repulsions (z shift) and in-plane Na+-Na+ electrostatic repulsions (xy shift). We suggest that Na+ interlayer redistribution is the driving force of the phase transition. 23Na MAS-NMR spectroscopy has been used to investigate changes in the environment and in the distribution of the sodium cations occurring by raising the temperature. The gradual suppression of the second-order quadrupolar interactions and the resulting new resonance is consistent with the sodium site exchange mechanism. Changes in the resistivity at TS suggest a strong coupling between the Na+ and CoO2 layers.
dc.language.isoen
dc.publisherAmerican Physical Society
dc.subject.enPhase transition
dc.subject.enInorganic compounds
dc.subject.enHigh temperature
dc.subject.enSodium cobaltite
dc.subject.enMAS–NMR spectroscopy
dc.title.enHigh-temperature phase transition in the three-layered sodium cobaltite Pf3-NaxCoO2 (x~0.62)
dc.typeArticle de revue
dc.identifier.doi10.1103/PhysRevB.77.184116
dc.subject.halChimie/Matériaux
bordeaux.journalPhysical Review B: Condensed Matter and Materials Physics (1998-2015)
bordeaux.page184116 (8 p.)
bordeaux.volume77
bordeaux.issue18
bordeaux.peerReviewedoui
hal.identifierhal-00286556
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00286556v1
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