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Complexes of amorphous tetraglyme (G4) and lithium bis(trifluoromethylsulfonyl)imide (LiTFSI) or lithium bis(perfluoroethylsulfonyl)imide (LiBETI) were prepared as pol(yethylene) oxide-type electrolytes. Addition of equimolar amounts of LiTFSI and tetraglyme results in a room temperature ionic liquid with the general formula Li(G4)TFSI. Differential scanning calorimetry analysis of Li(G4)TFSI reveals that it has a and the complex remains amorphous over a wide temperature range (−100 to 200°C), and has a very low vapor pressure for tetraglyme at room temperature. The corresponding BETI complex, Li(G4)BETI, crystallizes upon cooling and displays a Room temperature conductivities (25°C) of Li(G4)TFSI and Li(G4)BETI were 1.13 and 0.63 mS/cm, respectively. Composite polymer electrolytes were prepared by addition of the complexes to polycations possessing TFSI or BETI anions. The composites afforded thin flexible membranes at polymer concentrations ⩾50 mol % polymer with room temperature conductivities greater than S/cm. In general, increased concentrations of BETI anions in these materials resulted in increased mechanical stability but decreased ionic mobility. The complexes and composite polymer electrolytes displayed excellent anodic stability up to +4.5 V (vs. and exhibited breakdown voltages ⩾+5.5 V (vs. on stainless steel electrodes. © 2004 The Electrochemical Society. All rights reserved.
Pappenfus et al. (2004) studied this question.