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hal.structure.identifierRéseau sur le stockage électrochimique de l'énergie [RS2E]
hal.structure.identifierLaboratoire réactivité et chimie des solides - UMR CNRS 7314 UPJV [LRCS]
dc.contributor.authorMASQUELIER, Christian
hal.structure.identifierRéseau sur le stockage électrochimique de l'énergie [RS2E]
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorCROGUENNEC, Laurence
dc.date.issued2013
dc.identifier.issn0009-2665
dc.description.abstractEnFor more than 20 years, most of the technological achievements for the realization of positive electrodes for practical rechargeable Li battery systems have been devoted to transition metal oxides such as LixMO2 (M = Co, Ni, Mn), LixMn2O4, LixV2O5, or LixV3O8. The first two classes of materials built on close-packed oxygen stacking adopt bidimensional and tridimensional crystal structures, respectively (Figure 1), from which lithium ions may be easily intercalated or extracted in a reversible manner. These oxides are reasonably good ionic and electronic conductors, and lithium insertion/extraction proceeds while operating on the M4+/M3+ redox couple, located between 4 and 5 V versus Li+/Li...
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.title.enPolyanionic (Phosphates, Silicates, Sulfates) Frameworks as Electrode Materials for Rechargeable Li (or Na) Batteries
dc.typeArticle de revue
dc.identifier.doi10.1021/cr3001862
dc.subject.halChimie/Cristallographie
bordeaux.journalChemical Reviews
bordeaux.page6552-6591
bordeaux.volume113
bordeaux.issue8
bordeaux.peerReviewedoui
hal.identifierhal-00834789
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00834789v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Chemical%20Reviews&rft.date=2013&rft.volume=113&rft.issue=8&rft.spage=6552-6591&rft.epage=6552-6591&rft.eissn=0009-2665&rft.issn=0009-2665&rft.au=MASQUELIER,%20Christian&CROGUENNEC,%20Laurence&rft.genre=article


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