Truly solid polymer electrolyte membranes are designed by thermally induced free radical polymerisation. The overall membrane architecture is built on a semi-interpenetrating polymer network (s-IPN) structure, where a di-methacrylate oligomer is cross-linked (in situ) in the presence of a long thermoplastic linear PEO chain and a supporting lithium salt to obtain a freestanding, flexible and non-tacky film. In the envisaged systems, the di-methacrylate functions as a soft cross-linker, thus avoiding physico-mechanical deformation of the s-IPNs at elevated temperature, without hampering the ionic conductivity. s-IPNs exhibit remarkable stability towards lithium metal and no traces of impurity are detected while testing their oxidation stability (4.7 V vs. Li/Li+) towards anodic potential. The newly elaborated system is also successfully tested at moderately high temperature in Li metal cells in which LiFePO4/C is used as the cathode active material, showing excellent indications of safe and highly durable electrolyte separator (i.e.; 2000 cycles at reasonably high 1C rate). © 2015 Elsevier B.V.

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