Impact of the Chlorination of Lithium Argyrodites on the Electrolyte/Cathode Interface in Solid-State Batteries

dc.contributor.authorZuo, Tong-Tong
dc.contributor.authorWalther, Felix
dc.contributor.authorTeo, Jun Hao
dc.contributor.authorRueß, Raffael
dc.contributor.authorWang, Yubo
dc.contributor.authorRohnke, Marcus
dc.contributor.authorSchröder, Daniel
dc.contributor.authorNazar, Linda F.
dc.contributor.authorJanek, Jürgen
dc.date.accessioned2023-12-07T14:22:22Z
dc.date.available2023-12-07T14:22:22Z
dc.date.issued2023
dc.description.abstractLithium argyrodite-type electrolytes are regarded as promising electrolytes due to their high ionic conductivity and good processability. Chemical modifications to increase ionic conductivity have already been demonstrated, but the influence of these modifications on interfacial stability remains so far unknown. In this work, we study Li6PS5Cl and Li5.5PS4.5Cl1.5 to investigate the influence of halogenation on the electrochemical decomposition of the solid electrolyte and the chemical degradation mechanism at the cathode interface in depth. Electrochemical measurements, gas analysis and time-of-flight secondary ion mass spectrometry indicate that the Li5.5PS4.5Cl1.5 shows pronounced electrochemical decomposition at lower potentials. The chemical reaction at higher voltages leads to more gaseous degradation products, but a lower fraction of solid oxygenated phosphorous and sulfur species. This in turn leads to a decreased interfacial resistance and thus a higher cell performance.
dc.identifier.urihttps://jlupub.ub.uni-giessen.de//handle/jlupub/18784
dc.identifier.urihttp://dx.doi.org/10.22029/jlupub-18148
dc.language.isoen
dc.rightsNamensnennung - Nicht kommerziell - Keine Bearbeitungen 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddcddc:540
dc.titleImpact of the Chlorination of Lithium Argyrodites on the Electrolyte/Cathode Interface in Solid-State Batteries
dc.typearticle
local.affiliationFB 08 - Biologie und Chemie
local.source.articlenumbere202213228
local.source.journaltitleAngewandte Chemie. International edition
local.source.urihttps://doi.org/10.1002/anie.202213228
local.source.volume62

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