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Fluorine-Substituted Lithium Chloride Solid Electrolytes for High-Voltage All-Solid-State Lithium-Ion Batteries AITranslate

Korea Institute of Science and Technology; Korea University of Science and Technology; Lawrence Livermore National Laboratory; Lawrence Livermore National Laboratory; Korea Institute of Science and Technology; Korea University of Science and Technology
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Publisher: ACS
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Abstract AITranslate

Lithium ternary halides are promising solid electrolytes, owing to their high ionic conductivity and reasonably high oxidative and chemical stability. Recently, fluorine substitution in Li3MCl6 has been suggested as a promising approach for further enhancing oxidation stability. Accordingly, this study outlines a material design strategy for F-substituted Li3MCl6 through systematic theoretical analyses. Calculations reveal that the mixing limit of F in Li3MCl6–xFx is in the range of 0.5–1.5, and the resulting Li3MCl6–xFx phases can retain ionic conductivity above 1 mS/cm up to x = 1.0. The calculations also predict that the formation of F-containing passivating phases could increase the oxidation potential for Li3MCl5F to ∼6.3 V. The proposed material design strategy is validated through the synthesis of Li3YCl5F, which is confirmed to show both high ionic conductivity and enhanced oxidation stability. The design guidelines presented herein can accelerate the potential use of halide-based electrolyte chemistries in high-voltage all-solid-state batteries.

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DOI:https://doi.org/10.1021/acsenergylett.3c02307

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Citation Information:

Lithium ternary halides are promising solid electrolytes, owing to their high ionic conductivity and reasonably high oxidative and chemical stability. Recently, fluorine substitution in Li3MCl6 has been suggested as a promising approach for further enhancing oxidation stability. Accordingly, this study outlines a material design strategy for F-substituted Li3MCl6 through systematic theoretical analyses. Calculations reveal that the mixing limit of F in Li3MCl6–xFx is in the range of 0.5–1.5, and the resulting Li3MCl6–xFx phases can retain ionic conductivity above 1 mS/cm up to x = 1.0. The calculations also predict that the formation of F-containing passivating phases could increase the oxidation potential for Li3MCl5F to ∼6.3 V. The proposed material design strategy is validated through the synthesis of Li3YCl5F, which is confirmed to show both high ionic conductivity and enhanced oxidation stability. The design guidelines presented herein can accelerate the potential use of halide-based electrolyte chemistries in high-voltage all-solid-state batteries.

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GB/T 7714-2015 [1] Sooyeon Kim, Yongheum Lee, Kwangnam Kim, et al. ACS Energy Letters, 2024(9). DOI:10.1021/acsenergylett.3c02307.
MLA [1] Sooyeon Kim, et al., ACS Energy Letters, no. 9, 2024, https://doi.org/10.1021/acsenergylett.3c02307.
APA [1] Sooyeon Kim, Yongheum Lee, Kwangnam Kim, Brandon C. Wood, Sang Soo Han, & Seungho Yu. (2024). ACS Energy Letters(9). https://doi.org/10.1021/acsenergylett.3c02307
IEEE [1] Sooyeon Kim, Yongheum Lee, Kwangnam Kim, Brandon C. Wood, Sang Soo Han, and Seungho Yu, ACS Energy Letters, no. 9, 2024, doi: 10.1021/acsenergylett.3c02307.