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hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorCROGUENNEC, Laurence
hal.structure.identifierInstitut Laue-Langevin [ILL]
dc.contributor.authorSUARD, Emmanuelle
hal.structure.identifierCentre National d'Études Spatiales [Toulouse] [CNES]
dc.contributor.authorWILLMANN, Patrick
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.abstractEnLiNi1-yTiyO2 (y ≤ 0.15) layered oxides were synthesized at high temperature by solid-state reactions. Rietveld refinements of their X-ray and neutron diffraction patterns showed that these phases were characterized by an α-NaFeO2-type structure with the following cationic distribution: (Li1-zNi2+z)3b(Ti4+tNi2+t+zNi3+1-z-2t)3aO2 [t = y(1 + z)]. The amount of Ni2+ ions in the lithium site increases with y. A magnetic study confirmed the presence of paramagnetic ions in the interslab space and, therefore, the cationic distribution. These materials used as positive electrode in lithium batteries show reversible behavior. A large decrease of the capacity is observed with increasing y, because of the presence of extra nickel ions in the lithium sites. For the "LixNi0.95Ti0.05O2" composition, 144 mA h/g are obtained in discharge at the 14th cycle at the C/20 rate. The "LixNi1-yTiyO2" phases were characterized for y = 0.05 and 0.10: the simultaneous presence of titanium ions in the slab and of a significant amount of extra nickel ions in the lithium sites prevents phase transitions upon cycling.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enLayered compounds
dc.subject.enInorganic compounds
dc.subject.enChemical synthesis
dc.subject.enHigh temperature
dc.subject.enSolid state reactions
dc.subject.enX-ray diffractions
dc.subject.enNeutron diffraction
dc.title.enStructural and electrochemical characterization of the LiNi1-yTiyO2 electrode materials obtained by direct solid-state reactions
dc.typeArticle de revue
dc.identifier.doi10.1021/cm011265v
dc.subject.halChimie/Matériaux
bordeaux.journalChemistry of Materials
bordeaux.page2149-2157
bordeaux.volume14
bordeaux.issue5
bordeaux.peerReviewedoui
hal.identifierhal-00733619
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00733619v1
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