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hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorLEVASSEUR, Stéphane
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorMÉNÉTRIER, Michel
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorDELMAS, Claude
dc.date.issued2002
dc.identifier.issn0897-4756
dc.description.abstractEnHT-Lix0Co1-yMgyO2 (where x0 is the Li/(Co + Mg) ratio; x0 = 0.98, 1.0, 1.10; y = 0.0, 0.03, 0.06, and 0.10) materials were synthesized via a solid-state reaction. These samples were characterized by X-ray diffraction, 7Li MAS NMR spectroscopy, and electrical properties measurements. The XRD study showed that pure phases are obtained for 0.0 ≤ y < 0.10 and x0 ≥ 1.0. 7Li MAS NMR spectra of the Mg-doped phases exhibit two types of new signals at 55 ppm and 325, 7, −9, and − 27 ppm in addition to the signal at 0 ppm resulting from the presence of diamagnetic CoIII ions. On the basis of our general knowledge of Li NMR in layered oxides with electron spins, we suggest that Mg doping in LiCoO2 always leads to the simultaneous presence of CoIV ions (sharing an itinerant electron hole with neighboring CoIII ions) and, to a smaller extent, of intermediate spin Co3+(IS) ions trapped in a square-based pyramidal environment because of an oxygen vacancy. This feature is further enhanced by lithium overstoichiometry.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enLithium
dc.subject.enInorganic compounds
dc.subject.enChemical synthesis
dc.subject.enSolid state reaction
dc.subject.enX-ray diffraction
dc.subject.enNMR
dc.title.enOn the dual effect of Mg doping in LiCoO2 and Li1+dCoO2 : structural, electronic properties, and 7Li MAS NMR studies
dc.typeArticle de revue
dc.identifier.doi10.1021/cm021107j
dc.subject.halChimie/Matériaux
bordeaux.journalChemistry of Materials
bordeaux.page3584-3590
bordeaux.volume14
bordeaux.issue8
bordeaux.peerReviewedoui
hal.identifierhal-00733645
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00733645v1
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