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Authordc.contributor.authorO’Dwyer, Colm 
Authordc.contributor.authorLavayen, Vladimir es_CL
Authordc.contributor.authorSanta Ana, María Angélica es_CL
Authordc.contributor.authorBenavente Espinosa, Eglantina es_CL
Authordc.contributor.authorGonzález Moraga, Guillermo es_CL
Authordc.contributor.authorSotomayor Torres, Clivia es_CL
Admission datedc.date.accessioned2012-11-21T20:26:36Z
Available datedc.date.available2012-11-21T20:26:36Z
Publication datedc.date.issued2007-08-06
Cita de ítemdc.identifier.citationResearch Letters in Physical Chemistry, Article ID 32528, 5 pages, 2007.es_CL
Identifierdc.identifier.issn1155-2007
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/119608
Abstractdc.description.abstractWe report on unique high-volume low-dimensional V2O5-based turbostratic nanostructures, prepared using sol-gel synthetic methods from V2O5 · nH2O xerogels. Electrochemical intercalation of Li+ to form Li0.65V2O5 resulted in a maximum measured charge capacity of 1225 mAhg−1 as the β-LixV2O5 phase. Conductivities of the order of 10−3 S cm−1 were found on compressednanotube parallelepipedal samples, which exhibit an anisotropy factor of 70 at room temperature by preferential alignment of the nanotubes. The improved electrochemical properties observed in novel vanadium oxide nanostructured arrays are attributed to the increased volumetric density for ion intercalation, shorter diffusion paths to the intercalation sites, and a high degree of crystallinity of the individual nanotubular host structures.es_CL
Patrocinadordc.description.sponsorshipThe support of the Science Foundation Ireland (SFI) under investigator award 02/IN.1/172, the Network of Excellence PhOREMOST, the University of Chile, the Universidad Tecnol ´ ogica Metropolitana, and FONDECyT Grants 1050344, 1030102, 7050081, 1050788 are gratefully acknowledged.es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherHindawi Publishing Corporationes_CL
Títulodc.titleAnisotropic Vanadium Oxide Nanostructured Host Matrices for Lithium Ion Intercalationes_CL
Document typedc.typeArtículo de revista


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