Gel composite electrolyte - an effective way to utilize ceramic fillers in lithium batteries

X. Chelsea Chen, Yiman Zhang, Laura C. Merrill, Charles Soulen, Michelle L. Lehmann, Jennifer L. Schaefer, Zhijia Du, Tomonori Saito, Nancy J. Dudney

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

Achieving synergy between ion-conducting polymers and ceramics in a composite electrolyte has been proven to be difficult as the complicated ceramic/polymer interface presents challenges to understand and control. In this work, we report a strategy to utilize discrete ceramic fillers to form a gel composite electrolyte with enhanced transport properties for lithium metal batteries. The matrix of the composite membrane is crosslinked poly(ethylene oxide) with bis(trifluoromethane)sulfonimide lithium salt (LiTFSI). The membrane is plasticized with tetraethylene glycol dimethyl ether (TEGDME). The incorporation of doped-lithium aluminum titanium phosphate particles (LICGC™) into the membrane greatly improves the membrane's cycling characteristics against the lithium electrode, exhibiting lower interfacial impedance, lower overpotential and higher rate capability. The underpinnings of the superior performance of the gel composite electrolyte are discussed in depth. LICGC™ can immobilize the TFSIanions in the polymer matrix and simultaneously promote Li+transport by increasing the plasticizer to Li+ratio. Further, the transport enhancement is achieved without sacrificing mechanical properties. The composite membrane shows significantly improved handleability and processability. This work sheds light on the design strategy for a safe electrolyte towards stable Li metal batteries.

Original languageEnglish
Pages (from-to)6555-6566
Number of pages12
JournalJournal of Materials Chemistry A
Volume9
Issue number10
DOIs
StatePublished - Mar 14 2021

Funding

This research was primarily sponsored by the U.S. Department of Energy (DOE), Office of Energy Efficiency and Renewable Energy for the Vehicle Technologies Office's Advanced Battery Materials Research Program (Tien Duong, Program Manager). The transference measurement (L. C. Merrill) was supported by an appointment to the Oak Ridge National Laboratory ASTRO Program, sponsored by the U.S. Department of Energy and administered by the Oak Ridge Institute for Science and Education. X. C. C. acknowledges Dr Christopher Nelson for help with full cell cycling data analysis.

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