NiVO3 fused oxide nanoparticles - an electrochemically stable intercalation anode material for lithium ion batteries

dc.check.date2019-08-28
dc.check.infoAccess to this article is restricted until 12 months after publication by request of the publisher.en
dc.contributor.authorMcNulty, David
dc.contributor.authorCollins, Gillian
dc.contributor.authorO'Dwyer, Colm
dc.contributor.funderScience Foundation Irelanden
dc.date.accessioned2018-09-11T11:14:08Z
dc.date.available2018-09-11T11:14:08Z
dc.date.issued2018-08-28
dc.date.updated2018-09-06T08:27:19Z
dc.description.abstractFor oxides, especially as lithium-ion battery anodes, it is important to engineer the material not only to improve kinetics of reversible lithiation efficiency, but to avoid capacity and voltage fading, and side reactions, from conversion modes processes that can sometimes occur in tandem with intercalation. We report the first electrochemical evaluation of NiVO3 as an intercalation anode material for Li-ion batteries, which offers a high capacity with negligible fading without conversion mode side reactions. Binary metal oxide NiVO3 fused oxide nanoparticles (Ni-FONPs) are formed via thermal reduction of Ni-doped vanadium oxide nanotubes (Ni-VONTs). The electrochemical performance of Ni-FONPs is contrasted with a composite of Fe2O3 and V2O3 (Fe-FONPs) with a similar morphology, made using a similar process form Fe-doped VONTs. Galvanostatic cycling reveals that the binary metal oxide Ni-FONPs exhibit superior electrochemical performance compared to the Fe-FONPs by avoiding segregation into two oxides that ordinarily cycle as conversion mode material. The new anode material, Ni-FONPs, demonstrates state-of-the-art specific capacity retention (78% from the 2nd to the 500th cycle) and significantly long cycle life (500 cycles) when cycled using a specific current of 200 mA/g in a conductive additive and binder-free formulation. Limiting the lower voltage to ~ 0.2V avoid separate oxides of Ni and V, which independently, are detrimental to cycle life and capacity retention. Systematic analysis of differential capacity obtained from galvanostatic voltage profiles over 500 cycles offers a detailed insight into the charge storage mechanism and electrochemical behaviour for this stable NiVO3 anode material.en
dc.description.statusPeer revieweden
dc.description.versionAccepted Versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationMcNulty, D., Collins, G. and O'Dwyer, C. (2018) 'NiVO3 fused oxide nanoparticles - an electrochemically stable intercalation anode material for lithium ion batteries', Journal of Materials Chemistry A. doi:10.1039/C8TA05327Hen
dc.identifier.doi10.1039/C8TA05327H
dc.identifier.issn2050-7488
dc.identifier.issn2050-7496
dc.identifier.journaltitleJournal of Materials Chemistry Aen
dc.identifier.urihttps://hdl.handle.net/10468/6747
dc.language.isoenen
dc.publisherRoyal Society of Chemistryen
dc.relation.projectinfo:eu-repo/grantAgreement/SFI/SFI Technology and Innovation Development Award (TIDA)/13/TIDA/E2761/IE/LiONSKIN - Moldable Li-ion battery outer skin for electronic devices/en
dc.relation.projectinfo:eu-repo/grantAgreement/SFI/SFI Technology and Innovation Development Award (TIDA)/15/TIDA/2893/IE/Advanced Battery Materials for High Volumetric Energy Density Li-ion Batteries for Remote Off-Grid Power/en
dc.relation.projectinfo:eu-repo/grantAgreement/SFI/SFI Investigator Programme/14/IA/2581/IE/Diffractive optics and photonic probes for efficient mouldable 3D printed battery skin materials for portable electronic devices/en
dc.rights© 2018, the Authors. Published by the Royal Society of Chemistry. All rights reserved. This is the Accepted Manuscript of an article published in Journal of Materials Chemistry A on 28th August, 2018, available online: https://dx.doi.org/10.1039/C8TA05327Hen
dc.subjectOxideen
dc.subjectReversible lithiation efficiencyen
dc.subjectIntercalationen
dc.subjectNiVO3en
dc.titleNiVO3 fused oxide nanoparticles - an electrochemically stable intercalation anode material for lithium ion batteriesen
dc.typeArticle (peer-reviewed)en
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