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dc.contributor.authorSharma, N.
dc.contributor.authorTapia-Ruiz, N.
dc.contributor.authorSingh, G.
dc.contributor.authorArmstrong, Robert
dc.contributor.authorPramudita, J.C.
dc.contributor.authorBrand, H.E.A.
dc.contributor.authorBillaud, Juliette
dc.contributor.authorBruce, FRS, Peter
dc.contributor.authorRojo, T.
dc.date.accessioned2016-09-28T23:34:49Z
dc.date.available2016-09-28T23:34:49Z
dc.date.issued2015-10-27
dc.identifier233977421
dc.identifier4c0ff479-dd25-4829-b661-70d501fe63e6
dc.identifier84945538894
dc.identifier000363915000009
dc.identifier.citationSharma , N , Tapia-Ruiz , N , Singh , G , Armstrong , R , Pramudita , J C , Brand , H E A , Billaud , J , Bruce, FRS , P & Rojo , T 2015 , ' Rate dependent performance related to crystal structure evolution of Na 0.67 Mn 0.8 Mg 0.2 O 2 in a sodium-ion battery ' , Chemistry of Materials , vol. 27 , no. 20 , pp. 6976-6986 . https://doi.org/10.1021/acs.chemmater.5b02142en
dc.identifier.issn0897-4756
dc.identifier.otherORCID: /0000-0003-1937-0936/work/28123630
dc.identifier.urihttps://hdl.handle.net/10023/9571
dc.descriptionJ.C.P. would like thank UNSW/ANSTO for the PhD Scholarship. N.S. would like to thank AINSE Ltd for providing support through the research fellowship scheme. CIC Energigune work was financially supported by Ministerio de Economía y Competitividad (Proyecto I+D. Retos 2013), reference numbers ENE 2013-44330-R and FPDI-2013-17329, and the Gobierno Vasco/EuskoJaurlaritza (Etortek CICEnergigune 10, SAIOTEK-12 ENERGIBA and IT570-13). P.G.B. is indebted to the EPSRC, including the SUPERGEN programme, for financial support.en
dc.description.abstractSodium-ion batteries are considered as a favorable alternative to the widely used lithium-ion batteries for applications such as grid-scale energy storage. However, to meet the energy density and reliability that is necessary, electrodes that are structurally stable and well characterized during electrochemical cycling need to be developed. Here, we report on how the applied discharge current rate influences the structural evolution of Na0.67Mn0.8Mg0.2O2 electrode materials. A combination of ex situ and in situ X-ray diffraction (XRD) data were used to probe the structural transitions at the discharged state and during charge/discharge. Ex situ data shows a two-phase electrode at the discharged state comprised of phases that adopt Cmcm and P63/mmc symmetries at the 100 mA/g rate but a predominantly P63/mmc electrode at 200 and 400 mA/g rates. In situ synchrotron XRD data at 100 mA/g shows a solely P63/mmc electrode when 12 mA/g charge and 100 mA/g discharge is used even though ex situ XRD data shows the presence of both Cmcm and P63/mmc phases. The in situ data allows the Na site occupancy evolution to be determined as well as the rate of lattice expansion and contraction. Electrochemically, lower applied discharge currents, e.g., 100 mA/g, produce better capacity than higher applied currents, e.g., 400 mA/g, and this is related in part to the quantity of the Cmcm phase that is formed near the discharged state during a two-phase reaction (via ex situ measurements), with lower rates producing more of this Cmcm phase. Thus, producing more Cmcm phase allows access to higher capacities while higher rates show a lower utilization of the cathode during discharge as less (if any) Cmcm phase is formed. Therefore, this work shows how structural transitions can depend on the electrochemically applied current which has significant ramifications on how sodium-ion batteries, and batteries in general, are analyzed for performance during operation.
dc.format.extent11
dc.format.extent1342799
dc.language.isoeng
dc.relation.ispartofChemistry of Materialsen
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subjectSDG 7 - Affordable and Clean Energyen
dc.subject.lccQDen
dc.titleRate dependent performance related to crystal structure evolution of Na0.67Mn0.8Mg0.2O2 in a sodium-ion batteryen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doi10.1021/acs.chemmater.5b02142
dc.description.statusPeer revieweden
dc.date.embargoedUntil2016-09-28
dc.identifier.urlhttp://pubs.acs.org/doi/suppl/10.1021/acs.chemmater.5b02142en
dc.identifier.grantnumberEP/H019596/1en


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