Issue 40, 2024

Fluorine-rich deep eutectic electrolytes enabling robust interphases and nonflammability of high-voltage lithium metal batteries

Abstract

High-voltage Li metal batteries (LMBs) are characterized by superior energy density compared to state-of-the-art Li-ion batteries, but it is an essential challenge to develop electrolytes that can be stably and safely cycled with both reactive Li metal anodes and high-voltage cathodes. Herein, we report a nonflammable deep eutectic electrolyte (DEE) consisting of 3-cyano-6-trifluoromethylpyridine (CTFP) and lithium bis(trifluoromethane)sulfonimide. Systematic investigations verify that the dual-site coordination with Li+ by pyridine-nitrogen and cyanide-nitrogen in CTFP induces a deep-eutectic effect, yielding room-temperature liquid electrolytes with a high ionic conductivity (1.36 × 10−4 S cm−1) and Li+ migration number (0.81). A series of derivative DEEs are studied to demonstrate that –CF3 groups in CTFP account for not only the lowered highest occupied molecular orbital (HOMO) energy level and therefore improved oxidation potential (∼4.84 V vs. Li/Li+), but also robust LiF-rich interphases on both anode and cathode sides. Finally, the optimized DEE exhibits compatibility with various LMB cathodes (LiFePO4, LiMn2O4, and LiNi0.8Co0.1Mn0.1O2), among which the 4.5 V-class LiNi0.8Co0.1Mn0.1O2 LMB achieves an initial capacity of 205.5 mA h g−1 at 0.1C and stable cycling over 200 cycles at 0.5C. Our findings provide a practical electrolyte and insightful general principles for electrolyte designs of LMBs.

Graphical abstract: Fluorine-rich deep eutectic electrolytes enabling robust interphases and nonflammability of high-voltage lithium metal batteries

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Article information

Article type
Paper
Submitted
22 6 2024
Accepted
08 9 2024
First published
09 9 2024

J. Mater. Chem. A, 2024,12, 27269-27279

Fluorine-rich deep eutectic electrolytes enabling robust interphases and nonflammability of high-voltage lithium metal batteries

J. Yang, M. Sun, R. Li, L. Yin, B. Huang and X. Pu, J. Mater. Chem. A, 2024, 12, 27269 DOI: 10.1039/D4TA04316B

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