Abstract

Enhancing the interphase stability of polymer electrolytes with high-voltage cathodes is crucial for the development of high-energy-density lithium metal batteries (LMBs), especially in wearable devices area. Herein, lithium difluorophosphate (LiDFP) is incorporated into the solid polymer electrolyte of poly(ethylene oxide) (PEO) to enhance the formation of a robust cathode-electrolyte interphase (CEI) in high-voltage LiCoO2 LMBs. Through combining electrochemical measurements, spectroscopic techniques and theoretical calculations, the underlying modification mechanism is revealed. Due to its stronger anionic coordination with both polymer electrolyte chain and proton, and more oxidation-active resultant anion-coordinated polymer compared with lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), LiDFP suppresses the formation of the strong acid HTFSI deriving from the deprotonated process of the terminal O-H group thus avoiding the further oxidative attack to the polymeric framework. Furthermore, under the synergetic decomposition of HDFP intermediate, the polymer-derived radical helps to reconstruct a chemo-mechanically stable and Li-conductive CEI layer, which consists of abundant LiF/Li3PO4/LixPOyFz inorganic species distributed in lithiated organic macromolecules. The in-situ constructed CEI effectively passivates catalytic sites on LiCoO2 directly against PEO, resulting in well-maintained layered structure during high-voltage cycling. The proposed interphasial chemistry that regulates CEI formation provides directive knowledge of electrolyte optimization for high-voltage solid-state batteries.

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