dc.contributor.advisor | | |
dc.contributor.author | Serras, Paula | es_ES |
dc.contributor.author | Palomares, Verónica | es_ES |
dc.contributor.author | Alonso Masa, Javier | es_ES |
dc.contributor.author | Sharma, Neeraj | es_ES |
dc.contributor.author | López del Amo, Juan Miguel | es_ES |
dc.contributor.author | Kubiak, Pierre | es_ES |
dc.contributor.author | Fdez-Gubieda, María Luisa | es_ES |
dc.contributor.author | Rojo, Teófilo | es_ES |
dc.contributor.other | Universidad de Cantabria | es_ES |
dc.date.accessioned | 2024-01-12T10:05:46Z | |
dc.date.available | 2024-01-12T10:05:46Z | |
dc.date.issued | 2013-12-10 | es_ES |
dc.identifier.issn | 0897-4756 | es_ES |
dc.identifier.issn | 1520-5002 | es_ES |
dc.identifier.uri | https://hdl.handle.net/10902/31077 | |
dc.description.abstract | A mixed-valence V3+/V4+ composite material belonging to the Na3V2O2x(PO4)2F3-2x/C family is synthesized and the electrochemical Na extraction/insertion mechanism is determined using a combination of high-resolution synchrotron X-ray diffraction (XRD) data, X-ray absorption spectroscopy (XAS), 23Na and 19F solid state nuclear magnetic resonance (NMR), double titration (for the elucidation of the vanadium oxidation state), and electrochemical measurements. The vanadium oxidation state is found to be +3.8 for the as-prepared sample. Detailed analysis of the cathode structural evolution illustrated that the V4+/V5+ couple is active in this compound during electrochemical cycling between 2.8 V and 4.3 V. This study demonstrates how the sodium-ion extraction and insertion pathways in cathode materials can be followed (and verified) using several experimental techniques, especially when multiple potential oxidation states are present in the parent compound. | es_ES |
dc.description.sponsorship | This work was financially supported by the Ministerio de Educación y Ciencia (No. MAT2010-19442) and the Gobierno Vasco/Eusko Jaurlaritza (Etortek CICEnergigune-10, SAIOTEK-12-ENERGIBA and IT570-13). University of Basque Country is acknowledged for funding under Project No. UFI11/53. Access to synchrotron X-ray radiation facilities of ELETTRA, Trieste, Italy beamline XAFS (Project No. 20125173) is acknowledged. We thank Giuliana Aquilanti and Luca Olivi, from the XAFS beamline at ELETTRA, for their support, help, and expert advice on beamline operation. N.S. would like to thank AINSE, Ltd., for providing support through the research fellowship scheme. Part of this research was undertaken on the Powder Diffraction beamline at the Australian Synchrotron, Victoria, Australia. | |
dc.format.extent | 9 p. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | American Chemical Society | es_ES |
dc.rights | Alojado según Resolución CNEAI 5/12/23 (ANECA) | es_ES |
dc.rights | © 2013 American Chemical Society | |
dc.source | Chemistry of Materials, 2013, 25(24), 4917-4925 | es_ES |
dc.subject.other | Sodium ion batteries | |
dc.subject.other | Electrochemistry | |
dc.subject.other | Mixed valence sodium vanadium fluorophosphate | |
dc.subject.other | X-ray diffraction and X-ray absorption near edge structure | |
dc.title | Electrochemical Na extraction/insertion of Na3V2O2x(PO4)2F3-2x | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.relation.publisherVersion | https://doi.org/10.1021/cm403679b | es_ES |
dc.rights.accessRights | closedAccess | |
dc.identifier.DOI | 10.1021/cm403679b | es_ES |
dc.type.version | publishedVersion | es_ES |