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dc.contributor.authorBoyano, I.-
dc.contributor.authorBengoechea, M.-
dc.contributor.authorMeatza, I. de-
dc.contributor.authorMiguel, O.-
dc.contributor.authorCantero, I.-
dc.contributor.authorOchoteco, E.-
dc.contributor.authorRodríguez, J.-
dc.contributor.authorLira-Cantú, Mónica-
dc.contributor.authorGómez-Romero, P.-
dc.date.accessioned2009-08-04T07:12:02Z-
dc.date.available2009-08-04T07:12:02Z-
dc.date.issued2007-04-15-
dc.identifier.citationJournal Power Sources166(2): 471-477 (2007)en_US
dc.identifier.issn0378-7753-
dc.identifier.urihttp://hdl.handle.net/10261/15625-
dc.description.abstractWith the aim of improving the electrochemical properties of this candidate cathodic material for lithium ion batteries, a vanadium oxide (V2O5) and polypyrrole (Ppy) hybrid was prepared using pyridinesulfonic acid (PSA) as additive. The hybrid synthesis has been carried out in the literature by chemical polymerization of pyrrole in the host inorganic matrix, using the V2O5 dispersed in an acidic solution as an oxidizing agent. In this work the hybrid has been synthesised with PSA giving good results compared to other samples of the pristine V2O5 and to the Ppy/V2O5 hybrid without additive. An improvement of about 20% in the charge storage capacity has been achieved. The reasons for this improvement are discussed and analyzed using different experimental techniques. The hybrid material has the added advantage of an improved performance without the addition of any binder or conducting element as a cathode in a lithium ion battery.en_US
dc.description.sponsorshipWe thank the Spanish Ministry for Science and Technology (MAT2002-04529-C03) for financial support.en_US
dc.format.extent579917 bytes-
dc.format.mimetypeimage/jpeg-
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsclosedAccessen_US
dc.subjectBatteriesen_US
dc.subjectLi-ionen_US
dc.subjectV2O5en_US
dc.subjectConducting polymersen_US
dc.subjectHybrid materialsen_US
dc.titleImprovement in the Ppy/V2O5 hybrid as a cathode material for Li ion batteries using PSA as an organic additiveen_US
dc.typeartículoen_US
dc.identifier.doi10.1016/j.jpowsour.2006.12.106-
dc.description.peerreviewedPeer revieweden_US
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.jpowsour.2006.12.106en_US
dc.contributor.funderMinisterio de Ciencia y Tecnología (España)-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100006280es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
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