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dc.contributor.authorØstli, Elise Ramleth
dc.contributor.authorEbadi, Mahsa
dc.contributor.authorTesfamhret, Yonas
dc.contributor.authorMahmoodinia, Mehdi
dc.contributor.authorLacey, Matthew
dc.contributor.authorBrandell, Daniel
dc.contributor.authorSvensson, Ann Mari
dc.contributor.authorSelbach, Sverre Magnus
dc.contributor.authorWagner, Nils Peter
dc.date.accessioned2023-03-03T10:18:25Z
dc.date.available2023-03-03T10:18:25Z
dc.date.created2022-06-03T14:40:54Z
dc.date.issued2022
dc.identifier.issn1864-5631
dc.identifier.urihttps://hdl.handle.net/11250/3055705
dc.description.abstractTiO2-coating of LiNi0.5-xMn1.5+xO4 (LNMO) by atomic layer deposition (ALD) has been studied as a strategy to stabilize the cathode/electrolyte interface and mitigate transition metal (TM) ion dissolution. The TiO2 coatings were found to be uniform, with thicknesses estimated to 0.2, 0.3, and 0.6 nm for the LNMO powders exposed to 5, 10, and 20 ALD cycles, respectively. While electrochemical characterization in half-cells revealed little to no improvement in the capacity retention neither at 20 nor at 50 °C, improved capacity retention and coulombic efficiencies were demonstrated for the TiO2-coated LNMO in LNMO||graphite full-cells at 20 °C. This improvement in cycling stability could partly be attributed to thinner cathode electrolyte interphase on the TiO2-coated samples. Additionally, energy-dispersive X-ray spectroscopy revealed a thinner solid electrolyte interphase on the graphite electrode cycled against TiO2-coated LNMO, indicating retardation of TM dissolution by the TiO2-coating.en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.titleOn the Durability of Protective Titania Coatings on High-Voltage Spinel Cathodesen_US
dc.title.alternativeOn the Durability of Protective Titania Coatings on High-Voltage Spinel Cathodesen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.volume15en_US
dc.source.journalChemSusChemen_US
dc.source.issue12en_US
dc.identifier.doi10.1002/cssc.202200324
dc.identifier.cristin2029414
dc.relation.projectNorges forskningsråd: 245963/F50en_US
dc.relation.projectNorges forskningsråd: 197405en_US
dc.relation.projectNorges forskningsråd: 257653en_US
cristin.ispublishedtrue
cristin.fulltextpreprint
cristin.qualitycode1


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
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