Afficher la notice abrégée

hal.structure.identifierInstitut Charles Gerhardt Montpellier - Institut de Chimie Moléculaire et des Matériaux de Montpellier [ICGM ICMMM]
dc.contributor.authorBOYANOV, Simeon
hal.structure.identifierInstitut Charles Gerhardt Montpellier - Institut de Chimie Moléculaire et des Matériaux de Montpellier [ICGM ICMMM]
dc.contributor.authorBERNARDI, J.
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorBEKAERT, Emilie
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorMÉNÉTRIER, Michel
hal.structure.identifierInstitut Charles Gerhardt Montpellier - Institut de Chimie Moléculaire et des Matériaux de Montpellier [ICGM ICMMM]
dc.contributor.authorDOUBLET, Marie-Liesse
hal.structure.identifierInstitut Charles Gerhardt Montpellier - Institut de Chimie Moléculaire et des Matériaux de Montpellier [ICGM ICMMM]
dc.contributor.authorMONCONDUIT, Laure
dc.date.issued2009
dc.identifier.issn0897-4756
dc.description.abstractEnThe Li reactivity of NiP<sub>2</sub> is investigated by means of electrochemical tests, in situ XRD, and <sup>31</sup>P NMR characterizations as well as first principles DFT calculations. A two-step insertion/conversion reaction is shown to transform the NiP<sub>2</sub> starting electrode into an intermediate Li<sub>2</sub>NiP<sub>2</sub> single phase and then to convert into the Li<sub>3</sub>P/Ni° nanocomposite. The ternary phase is fully characterized and is shown to be structurally very close to the starting NiP<sub>2</sub> regarding the Ni ions environment. This demonstrates that its formation results from a P-redox insertion mechanism associated with a very good reversibility. However, its nucleation upon delithiation from the fully converted Li<sub>3</sub>P/Ni composite is shown to be kinetically limited (poor structural relationship) which strongly suggests that restricted lithiation is required for best cycleability of the NiP<sub>2</sub>/Li cell.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enLithium
dc.subject.enReactivity
dc.subject.enNiP<sub>2</sub>
dc.subject.enElectrochemistry
dc.subject.enXRD
dc.subject.en<sup>31</sup> P Nuclear magnetic resonance
dc.subject.enDFT
dc.title.enP-redox mechanism at the origin of the high lithium storage in NiP2-based batteries
dc.typeArticle de revue
dc.identifier.doi10.1021/cm802393z
dc.subject.halChimie/Matériaux
bordeaux.journalChemistry of Materials
bordeaux.page298-308
bordeaux.volume21
bordeaux.issue2
bordeaux.peerReviewedoui
hal.identifierhal-00355776
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00355776v1
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=Chemistry%20of%20Materials&amp;rft.date=2009&amp;rft.volume=21&amp;rft.issue=2&amp;rft.spage=298-308&amp;rft.epage=298-308&amp;rft.eissn=0897-4756&amp;rft.issn=0897-4756&amp;rft.au=BOYANOV,%20Simeon&amp;BERNARDI,%20J.&amp;BEKAERT,%20Emilie&amp;M%C3%89N%C3%89TRIER,%20Michel&amp;DOUBLET,%20Marie-Liesse&amp;rft.genre=article


Fichier(s) constituant ce document

FichiersTailleFormatVue

Il n'y a pas de fichiers associés à ce document.

Ce document figure dans la(les) collection(s) suivante(s)

Afficher la notice abrégée