Solid-state lithium battery with garnet Li7La3Zr2O12 nanofibers composite polymer electrolytes

In recent years, solid-state lithium-ion batteries with high safety and excellent performance have become a research hotspot. Garnet Li7La3Zr2O12 (LLZO) has been widely used in lithium-ion batteries because of its high ionic conductivity, wide electrochemical window, excellent thermal performance, a...

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Veröffentlicht in:Solid state ionics 2022-05, Vol.378, p.115897, Article 115897
Hauptverfasser: Wang, Yifei, Liu, Tao, Liu, Chuwei, Liu, Guoqiang, Yu, Jingkun, Zou, Qingjie
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Sprache:eng
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Zusammenfassung:In recent years, solid-state lithium-ion batteries with high safety and excellent performance have become a research hotspot. Garnet Li7La3Zr2O12 (LLZO) has been widely used in lithium-ion batteries because of its high ionic conductivity, wide electrochemical window, excellent thermal performance, and promising stability. In this study, Ga-LLZO was prepared by the electrospinning method and combined with PVDF-HFP to prepare a composite polymer electrolyte. The addition of 15 wt% Ga-LLZO nanofibers in the electrolyte improved the ionic conductivity, reaching 8.92 × 10−4 S·cm−1 at room temperature. The electrochemical window for PVDF-HFP/LiTFSI/Ga-LLZO composite polymer electrolyte was 5.2 V vs Li/Li+. In addition, LiFePO4|PVDF-HFP/LiTFSI/Ga-LLZO|Li exhibited good cycling performance and rate capability. High-performance composite electrolyte films of ceramic nanofiber Ga-LLZO and polymer were successfully prepared for high-performance solid-state lithium batteries. •Ga-LLZO nanofibers were combined with polymer PVDF-HFP, which exhibited higher lithium ion conductivity, reaching 8.94 × 10−4 S·cm−1 at room temperature.•The electrochemical window for PVDF-HFP/LiTFSI/Ga-LLZO composite polymer electrolyte was 5.2 V vs Li/Li+.•High-performance composite electrolyte films of ceramic nanofiber Ga-LLZO and polymer were successfully prepared for high-performance solid-state lithium batteries.
ISSN:0167-2738
1872-7689
DOI:10.1016/j.ssi.2022.115897