Designing Polymer‐in‐Salt Electrolyte and Fully Infiltrated 3D Electrode for Integrated Solid‐State Lithium Batteries
Solid‐state lithium batteries (SSLBs) are promising owing to enhanced safety and high energy density but plagued by the relatively low ionic conductivity of solid‐state electrolytes and large electrolyte–electrode interfacial resistance. Herein, we design a poly(vinylidene fluoride‐co‐hexafluoroprop...
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Veröffentlicht in: | Angewandte Chemie International Edition 2021-06, Vol.60 (23), p.12931-12940 |
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Sprache: | eng |
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Zusammenfassung: | Solid‐state lithium batteries (SSLBs) are promising owing to enhanced safety and high energy density but plagued by the relatively low ionic conductivity of solid‐state electrolytes and large electrolyte–electrode interfacial resistance. Herein, we design a poly(vinylidene fluoride‐co‐hexafluoropropylene) (PVDF‐HFP)‐based polymer‐in‐salt solid electrolyte (PISSE) with high room‐temperature ionic conductivity (1.24×10−4 S cm−1) and construct a model integrated TiO2/Li SSLB with 3D fully infiltration of solid electrolyte. With forming aggregated ion clusters, unique ionic channels are generated in the PISSE, providing much faster Li+ transport than common polymer electrolytes. The integrated device achieves maximized interfacial contact and electrochemical and mechanical stability, with performance close to liquid electrolyte. A pouch cell made of 2 SSLB units in series shows high voltage plateau (3.7 V) and volumetric energy density comparable to many commercial thin‐film batteries.
A PVDF‐HFP‐based polymer‐in‐salt solid electrolyte (PISSE) with high ionic conductivity at room temperature and a solid‐state lithium battery (SSLB) with 3D fully infiltration of PISSE is developed. The integrated device achieves maximized interfacial contact and electrochemical and mechanical stability, presenting high performance close to that with liquid electrolyte. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.202101537 |