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dc.contributor.authorKim, Eun Jeong
dc.contributor.authorMa, Le Anh
dc.contributor.authorPickup, David M.
dc.contributor.authorChadwick, Alan V.
dc.contributor.authorYounesi, Reza
dc.contributor.authorMaughan, Philip Adam
dc.contributor.authorIrvine, John T. S.
dc.contributor.authorArmstrong, Robert
dc.identifier.citationKim , E J , Ma , L A , Pickup , D M , Chadwick , A V , Younesi , R , Maughan , P A , Irvine , J T S & Armstrong , R 2020 , ' Vacancy enhanced oxygen redox reversibility in P3-type magnesium doped sodium manganese oxide Na 0.67 Mg 0.2 Mn 0.8 O 2 ' , ACS Applied Energy Materials , vol. In press .
dc.identifier.otherPURE: 270460440
dc.identifier.otherPURE UUID: efe84b7b-cd76-4c58-a029-7355d285b120
dc.identifier.otherORCID: /0000-0002-8394-3359/work/81405684
dc.identifier.otherORCID: /0000-0003-1937-0936/work/81405802
dc.identifier.otherWOS: 000595488500017
dc.identifier.otherScopus: 85098177726
dc.descriptionEJK would like to thank the Alistore ERI for the award of a studentship. This work was supported by the Faraday Institution (grant number FIRG018).en
dc.description.abstractLithium-rich layered oxides and sodium layered oxides represent attractive positive electrode materials exhibiting excess capacity delivered by additional oxygen redox activity. However, structural degradation in the bulk and detrimental reactions with the electrolyte on the surface often occur, leading to limited reversibility of oxygen redox processes. Here we present the properties of P3-type Na0.67Mg0.2Mn0.8O2 synthesized under both air and oxygen. Both materials exhibit stable cycling performance in the voltage range 1.8-3.8 V where the Mn3+/Mn4+ redox couple entirely dominates the electrochemical reaction. Oxygen redox activity is triggered for both compounds in the wider voltage window 1.8-4.3 V with typical large voltage hysteresis from non-bonding O 2p states generated by substituted Mg. Interestingly, for the compound prepared under oxygen, an additional reversible oxygen redox activity is shown with exceptionally small voltage hysteresis (20 mV). The presence of vacancies in the transition metal layers is shown to play a critical role not only in forming unpaired O 2p states independent of substituted elements but also in stabilising the P3 structure during charge with reduced structural transformation to the O’3 phase at the end of discharge. This study reveals the important role of vacancies in P3-type sodium layered oxides to increase energy density using both cationic and anionic redox processes.
dc.relation.ispartofACS Applied Energy Materialsen
dc.rightsCopyright © 2020 American Chemical Society. This work has been made available online in accordance with publisher policies or with permission. Permission for further reuse of this content should be sought from the publisher or the rights holder. This is the author created accepted manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at
dc.subjectSodium ion batteriesen
dc.subjectPositive electrode materialsen
dc.subjectP3 structureen
dc.subjectTransition metal vacanciesen
dc.subjectOxygen redoxen
dc.subjectQD Chemistryen
dc.titleVacancy enhanced oxygen redox reversibility in P3-type magnesium doped sodium manganese oxide Na0.67Mg0.2Mn0.8O2en
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews.School of Chemistryen
dc.contributor.institutionUniversity of St Andrews.Centre for Designer Quantum Materialsen
dc.contributor.institutionUniversity of St Andrews.EaSTCHEMen
dc.description.statusPeer revieweden

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