In situ preparation of crosslinked polymer electrolytes for lithium ion batteries

dc.bibliographicCitation.firstPage1707eng
dc.bibliographicCitation.issue8eng
dc.bibliographicCitation.journalTitlePolymerseng
dc.bibliographicCitation.volume12eng
dc.contributor.authorRöchow, Eike T.
dc.contributor.authorCoeler, Matthias
dc.contributor.authorPospiech, Doris
dc.contributor.authorKobsch, Oliver
dc.contributor.authorMechtaeva, Elizaveta
dc.contributor.authorVogel, Roland
dc.contributor.authorVoit, Brigitte
dc.contributor.authorNikolowski, Kristian
dc.contributor.authorWolter, Mareike
dc.date.accessioned2021-12-14T08:15:08Z
dc.date.available2021-12-14T08:15:08Z
dc.date.issued2020
dc.description.abstractSolid polymer electrolytes for bipolar lithium ion batteries requiring electrochemical stability of 4.5 V vs. Li/Li+ are presented. Thus, imidazolium-containing poly(ionic liquid) (PIL) networks were prepared by crosslinking UV-photopolymerization in an in situ approach (i.e., to allow preparation directly on the electrodes used). The crosslinks in the network improve the mechanical stability of the samples, as indicated by the free-standing nature of the materials and temperature-dependent rheology measurements. The averaged mesh size calculated from rheologoical measurements varied between 1.66 nm with 10 mol% crosslinker and 4.35 nm without crosslinker. The chemical structure of the ionic liquid (IL) monomers in the network was varied to achieve the highest possible ionic conductivity. The systematic variation in three series with a number of new IL monomers offers a direct comparison of samples obtained under comparable conditions. The ionic conductivity of generation II and III PIL networks was improved by three orders of magnitude, to the range of 7.1 × 10−6 S·cm−1 at 20 °C and 2.3 × 10−4 S·cm−1 at 80 °C, compared to known poly(vinylimidazolium·TFSI) materials (generation I). The transition from linear homopolymers to networks reduces the ionic conductivity by about one order of magnitude, but allows free-standing films instead of sticky materials. The PIL networks have a much higher voltage stability than PEO with the same amount and type of conducting salt, lithium bis(trifluoromethane sulfonyl)imide (LiTFSI). GII-PIL networks are electrochemically stable up to a potential of 4.7 V vs. Li/Li+, which is crucial for a potential application as a solid electrolyte. Cycling (cyclovoltammetry and lithium plating-stripping) experiments revealed that it is possible to conduct lithium ions through the GII-polymer networks at low currents. We concluded that the synthesized PIL networks represent suitable candidates for solid-state electrolytes in lithium ion batteries or solid-state batteries.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/7721
dc.identifier.urihttps://doi.org/10.34657/6768
dc.language.isoengeng
dc.publisherBasel : MDPIeng
dc.relation.doihttps://doi.org/10.3390/POLYM12081707
dc.relation.essn2073-4360
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subject.ddc540eng
dc.subject.otherElectrochemical stabilityeng
dc.subject.otherIonic conductivityeng
dc.subject.otherLithium ion batteryeng
dc.subject.otherPhotopolymerizationeng
dc.subject.otherPolymer electrolyteeng
dc.subject.otherPolymeric ionic liquideng
dc.titleIn situ preparation of crosslinked polymer electrolytes for lithium ion batterieseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIPFeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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