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锂离子电池局部高浓度氟化电解质的离子电导率与溶剂化结构之间的关系

The Relationship between Ionic Conductivity and Solvation Structures of Localized High-Concentration Fluorinated Electrolytes for Lithium-Ion Batteries.

作者信息

Hossain Md Jamil, Wu Qisheng, Marin Bernardez Edelmy J, Quilty Calvin D, Marschilok Amy C, Takeuchi Esther S, Bock David C, Takeuchi Kenneth J, Qi Yue

机构信息

School of Engineering, Brown University, Providence, Rhode Island 02912, United States.

Department of Chemistry, Stony Brook University, Stony Brook, New York 11794, United States.

出版信息

J Phys Chem Lett. 2023 Aug 31;14(34):7718-7731. doi: 10.1021/acs.jpclett.3c01453. Epub 2023 Aug 22.

Abstract

Localized high-concentration electrolytes (LHCEs) combine a diluent with a high-concentration electrolyte, offering promising properties. The ions, solvent, and diluent interact to form complex heterogeneous liquid structures, where high salt concentration clusters are embedded in the diluent. Optimizing LHCEs for desired electrolyte properties like high ionic conductivity, low viscosity, and effective solid electrolyte interphase (SEI) formation ability within the vast chemical and compositional design space requires deeper understanding and theoretical guidance. We investigated the structures and conductivities of LHCEs based on a fluorinated solvent with two different diluents at varying concentrations. 2,2,3,3-Tetrafluoropropyl trifluoroacetate (TFPTFA) enters the solvation cluster due to its stronger Li-ion interactions, whereas 1,1,2,2-tetrafluoroethyl 2,2,2-trifluoroethyl ether (TFETFE) enters only at extremely high diluent concentrations. The ionic conductivity increases with decreasing diluent concentrations, with a slope change during cluster percolation. Overall, TFETFE demonstrates higher effectiveness than TFPTFA, forming higher local salt concentration clusters and resulting in higher ionic conductivity.

摘要

局部高浓度电解质(LHCEs)将稀释剂与高浓度电解质相结合,具有良好的性能。离子、溶剂和稀释剂相互作用形成复杂的非均相液体结构,其中高盐浓度簇嵌入在稀释剂中。在广阔的化学和成分设计空间内,为实现高离子电导率、低粘度和有效的固体电解质界面(SEI)形成能力等所需电解质性能而优化LHCEs,需要更深入的理解和理论指导。我们研究了基于含两种不同稀释剂的氟化溶剂、不同浓度的LHCEs的结构和电导率。2,2,3,3-四氟丙基三氟乙酸酯(TFPTFA)因其与锂离子的相互作用更强而进入溶剂化簇,而1,1,2,2-四氟乙基2,2,2-三氟乙基醚(TFETFE)仅在极高的稀释剂浓度下才会进入。离子电导率随稀释剂浓度降低而增加,在簇渗滤过程中斜率发生变化。总体而言,TFETFE比TFPTFA表现出更高的效能,形成更高的局部盐浓度簇并导致更高的离子电导率。

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