Abstract

Poly(ethylene oxide) (PEO)-based solid polymer electrolytes (SPEs) are among the most promising materials for solid-state lithium metal batteries (LMBs) due to their inherent safety advantages; however, they suffer from insufficient room-temperature ionic conductivity (up to 10-6 S cm-1) and limited oxidation stability (<4 V). In this study, a novel "polymer-in-high-concentrated ionic liquid (IL)" (PiHCIL) electrolyte composed of PEO, N-propyl-N-methylpyrrolidinium bis(fluorosulfonyl) imide (C3mpyrFSI) IL, and LiFSI is designed. The EO/[Li/IL] ratio has been widely varied, and physical and electrochemical properties have been explored. The Li-coordination and solvation structure has been explored through Fourier-transform infrared spectroscopy and solid-state magic-angle spinning nuclear magnetic resonance. The newly designed electrolyte provides a promisingly high oxidative stability of 5.1 V and offers high ambient temperature ionic conductivity of 5.6 × 10-4 S cm-1 at 30 °C. Li|Li symmetric cell cycling shows very stable and reversible cycling of Li metal over 100 cycles and a smooth dendrite-free deposition morphology. All-solid-state cells using a composite lithium iron phosphate cathode exhibit promising cycling with 99.2% capacity retention at a C/5 rate over 100 cycles. Therefore, the novel approach of PiHCIL enables a new pathway to design high-performing SPEs for high-energy-density all-solid-state LMBs.

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