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dc.contributor.authorCao, Chencheng
dc.contributor.authorZhong, Yijun
dc.contributor.authorChandula Wasalathilake, Kimal
dc.contributor.authorTadé, Moses O.
dc.contributor.authorXu, Xiaomin
dc.contributor.authorRabiee, H.
dc.contributor.authorRoknuzzaman, M.
dc.contributor.authorRahman, R.
dc.contributor.authorShao, Zongping
dc.date.accessioned2023-02-21T09:41:05Z
dc.date.available2023-02-21T09:41:05Z
dc.date.issued2022
dc.identifier.citationCao, C. and Zhong, Y. and Chandula Wasalathilake, K. and Tadé, M.O. and Xu, X. and Rabiee, H. and Roknuzzaman, M. et al. 2022. A low resistance and stable lithium-garnet electrolyte interface enabled by a multifunctional anode additive for solid-state lithium batteries. Journal of Materials Chemistry A. 10 (5): pp. 2519-2527.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/90619
dc.identifier.doi10.1039/d1ta07804f
dc.description.abstract

Solid-state batteries (SSBs) have attracted considerable attention due to their high intrinsic stability and theoretical energy density. As the core part, garnet electrolyte has been extensively investigated due to its high lithium-ion conductivity, wide electrochemical potential window, and easy synthesis. However, the poor and electrochemically unstable interfacial contact between the electrolyte and lithium anode greatly impedes the practical use of garnet based SSBs. Here, we report that such an interface challenge can be perfectly tackled by introducing multifunctional Li0.3La0.5TiO3 (LLTO) as an additive into the lithium anode. The limited reaction between the LLTO and lithium effectively changes the physical properties of the lithium anode, making it perfectly compatible with the garnet surface, and consequently significantly decreasing the interfacial resistance from 200 to only 48 Ω cm2 and greatly improving the interface stability and avoiding dendrite formation. Interestingly, LLTO provides additional lithium storage, and the close interface contact and the high lithium-ion conductivity of LLTO ensure high rate performance. Consequently, the symmetrical cell runs stably at 0.1 mA cm-2 for 400 h without obvious degradation. The SSB assembled with the LiFePO4 cathode and Li-LLTO composite anode demonstrates a specific capacity of 147 mA h g-1 and remarkable cycling stability with only 10% capacity decay over 700 cycles at 1C. This journal is

dc.languageEnglish
dc.publisherROYAL SOC CHEMISTRY
dc.relation.sponsoredbyhttp://purl.org/au-research/grants/arc/DP200103315
dc.relation.sponsoredbyhttp://purl.org/au-research/grants/arc/DP200103332
dc.subjectScience & Technology
dc.subjectPhysical Sciences
dc.subjectTechnology
dc.subjectChemistry, Physical
dc.subjectEnergy & Fuels
dc.subjectMaterials Science, Multidisciplinary
dc.subjectChemistry
dc.subjectMaterials Science
dc.subjectNEUTRON-DIFFRACTION
dc.subjectCHALLENGES
dc.subjectINTERPHASE
dc.subjectCONDUCTION
dc.subjectMEMBRANE
dc.subjectDESIGN
dc.titleA low resistance and stable lithium-garnet electrolyte interface enabled by a multifunctional anode additive for solid-state lithium batteries
dc.typeJournal Article
dcterms.source.volume10
dcterms.source.number5
dcterms.source.startPage2519
dcterms.source.endPage2527
dcterms.source.issn2050-7488
dcterms.source.titleJournal of Materials Chemistry A
dc.date.updated2023-02-21T09:41:04Z
curtin.departmentWASM: Minerals, Energy and Chemical Engineering
curtin.accessStatusFulltext not available
curtin.facultyFaculty of Science and Engineering
curtin.contributor.orcidShao, Zongping [0000-0002-4538-4218]
curtin.contributor.orcidZhong, Yijun [0000-0003-4112-7115]
curtin.contributor.orcidXu, Xiaomin [0000-0002-0067-3331]
curtin.contributor.researcheridShao, Zongping [B-5250-2013]
curtin.contributor.researcheridZhong, Yijun [H-1647-2013]
curtin.contributor.researcheridXu, Xiaomin [E-5439-2014]
dcterms.source.eissn2050-7496
curtin.contributor.scopusauthoridShao, Zongping [55904502000] [57200900274]
curtin.contributor.scopusauthoridXu, Xiaomin [57060970200]


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