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dc.contributor.authorJohnson, L.
dc.contributor.authorLi, C.
dc.contributor.authorLiu, Z.
dc.contributor.authorChen, Y.
dc.contributor.authorFreunberger, S.A.
dc.contributor.authorAshok, P.C.
dc.contributor.authorPraveen, B.B.
dc.contributor.authorDholakia, K.
dc.contributor.authorTarascon, J.-M.
dc.contributor.authorBruce, P.G.
dc.date.accessioned2015-05-31T23:11:16Z
dc.date.available2015-05-31T23:11:16Z
dc.date.issued2014-12
dc.identifier.citationJohnson , L , Li , C , Liu , Z , Chen , Y , Freunberger , S A , Ashok , P C , Praveen , B B , Dholakia , K , Tarascon , J-M & Bruce , P G 2014 , ' The role of LiO 2 solubility in O 2 reduction in aprotic solvents and its consequences for Li-O 2 batteries ' Nature Chemistry , vol. 6 , no. 12 , pp. 1091-1099 . DOI: 10.1038/nchem.2101en
dc.identifier.issn1755-4330
dc.identifier.otherPURE: 159066793
dc.identifier.otherPURE UUID: b097b0fc-c024-4345-91c3-008fd7f6e508
dc.identifier.otherScopus: 84911463465
dc.identifier.urihttp://hdl.handle.net/10023/6719
dc.identifier.urihttp://www.nature.com/nchem/journal/v6/n12/full/nchem.2101.html#supplementary-informationen
dc.descriptionP.G.B. acknowledges financial support from the Engineering and Physical Sciences Research Council (including the SUPERGEN programme). S.A.F. acknowledges financial support from the Austrian Federal Ministry of Economy, Family and Youth and the Austrian National Foundation for Research, Technology and Development as well as the Austrian Science Fund (FWF): P26870-N19. K.D. thanks the UK EPSRC for funding and the European Union project FAMOS (FP7 ICT, contract no. 317744).en
dc.description.abstractWhen lithium–oxygen batteries discharge, ​O2 is reduced at the cathode to form solid ​Li2O2. Understanding the fundamental mechanism of ​O2 reduction in aprotic solvents is therefore essential to realizing their technological potential. Two different models have been proposed for ​Li2O2 formation, involving either solution or electrode surface routes. Here, we describe a single unified mechanism, which, unlike previous models, can explain ​O2 reduction across the whole range of solvents and for which the two previous models are limiting cases. We observe that the solvent influences ​O2 reduction through its effect on the solubility of LiO2, or, more precisely, the free energy of the reaction LiO2* ⇌ Li(sol)+ + O2−(sol) + ion pairs + higher aggregates (clusters). The unified mechanism shows that low-donor-number solvents are likely to lead to premature cell death, and that the future direction of research for lithium–oxygen batteries should focus on the search for new, stable, high-donor-number electrolytes, because they can support higher capacities and can better sustain discharge.en
dc.format.extent9en
dc.language.isoeng
dc.relation.ispartofNature Chemistryen
dc.rights© 2014 The Authors. NPG Terms of reuse of archived manuscipts applies http://www.nature.com/authors/policies/license.htmlen
dc.subjectQD Chemistryen
dc.subjectQC Physicsen
dc.subject.lccQDen
dc.subject.lccQCen
dc.titleThe role of LiO2 solubility in O2 reduction in aprotic solvents and its consequences for Li-O2 batteriesen
dc.typeJournal articleen
dc.description.versionPostprinten
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. School of Physics and Astronomyen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.identifier.doihttps://doi.org/10.1038/nchem.2101
dc.description.statusPeer revieweden
dc.date.embargoedUntil01-06-20


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