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    A low resistance and stable lithium-garnet electrolyte interface enabled by a multifunctional anode additive for solid-state lithium batteries

    Access Status
    Fulltext not available
    Authors
    Cao, Chencheng
    Zhong, Yijun
    Chandula Wasalathilake, Kimal
    Tadé, Moses O.
    Xu, Xiaomin
    Rabiee, H.
    Roknuzzaman, M.
    Rahman, R.
    Shao, Zongping
    Date
    2022
    Type
    Journal Article
    
    Metadata
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    Citation
    Cao, 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.
    Source Title
    Journal of Materials Chemistry A
    DOI
    10.1039/d1ta07804f
    ISSN
    2050-7488
    Faculty
    Faculty of Science and Engineering
    School
    WASM: Minerals, Energy and Chemical Engineering
    Funding and Sponsorship
    http://purl.org/au-research/grants/arc/DP200103315
    http://purl.org/au-research/grants/arc/DP200103332
    URI
    http://hdl.handle.net/20.500.11937/90619
    Collection
    • Curtin Research Publications
    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

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