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Enhancing Ionic Conductivity by in Situ Formation of Li7SiPS8/Argyrodite Hybrid Solid Electrolytes

Solid electrolytes (SEs) with high ionic conductivities are prerequisites to establish solid state batteries on a broad basis. Here we report a novel approach to thiophosphate SEs with improved ionic conductivities based on the in situ formation of LGPS-type tetra-Li7SiPS8/lithium argyrodite Li6PS5X...

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Bibliographic Details
Published in:Chemistry of materials 2022-09, Vol.34 (17), p.7666-7677
Main Authors: Calaminus, Robert, Harm, Sascha, Fabini, Douglas H., Balzat, Lucas G., Hatz, Anna-Katharina, Duppel, Viola, Moudrakovski, Igor, Lotsch, Bettina V.
Format: Article
Language:English
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Summary:Solid electrolytes (SEs) with high ionic conductivities are prerequisites to establish solid state batteries on a broad basis. Here we report a novel approach to thiophosphate SEs with improved ionic conductivities based on the in situ formation of LGPS-type tetra-Li7SiPS8/lithium argyrodite Li6PS5X (X= Cl, Br, I) hybrid SEs. Quantitative phase analysis reveals the formation of halogen-poor argyrodites Li6+y PS5+y X1–y next to the tetra-Li7SiPS8 majority phase and an amorphous side phase. EIS measurements indicate ionic conductivities of up to 7 mS cm–1, which exceed those of the parent tetra-Li7SiPS8 and Li6PS5X (X = Cl, Br, I) phases as well as those of simple physical mixtures whose conductivities are well described by the effective medium approximation. In contrast to previous reports, no evidence for halide substitution of the PS4 3– anions in tetra-Li7SiPS8 was found. Instead, the observed increase in ionic conductivity along with reduced grain boundary resistance is attributed to the directed growth of the tetra-Li7SiPS8 majority phase in the presence of an argyrodite side phase. As a result, a substantially increased isotropic Li diffusion radius is observed by PFG NMR, consistent with both more bulk-like Li transport within secondary particles and with reduced grain boundary resistance through more benign argyrodite interphases as compared to pristine tetra-Li7SiPS8. The microstructural changes induced by hybridization thus provide access to the bulk properties of tetra-Li7SiPS8.
ISSN:0897-4756
1520-5002
DOI:10.1021/acs.chemmater.2c00346