“…Following the first approach, further studies showedv ery promising resultsfor such electrolyte systems by using avariety of ILs and replacing the PEO matrix, for instance, with "inactive" PVdF-HFP, [240][241][242][243][244][245][246][247] poly(urethane acrylate), [248] cross-linked polymers, [248][249][250][251][252] polymer blends, [253,254] or polymerici onic liquids (PILs). [255][256][257][258][259] Concerning the utilization of "inactive" polymerm atrices, such as PVdF-HFP, the enhanced conductivity for ac ontrolled amount of added IL was assigned to the increased number of chargec arriers, as supported by the presence of strong electron-withdrawing functionalg roups,s uch as ÀCÀF( and their high dielectric constant, e = 8.4);t his leads to extendedl ithium salt dissolution, and thus, compensates for decreased ion mobility due to increased viscosity. [260] Nevertheless,d espite their highly favorable electrochemical and, in particular,s afety characteristics, such IL-SPE electrolyte systemss uffer two major issues:1 )a relatively low ionic conductivitya ta na mbient temperature of around 10 À4 Scm À1 , which is commonly not sufficientf or practical applications (ionic conductivities comparable to those of liquid,c arbonatebased electrolytes mayb ea chieved at 70 8C); [169,232] and 2) incompatibility with state-of-the-art cathode materials, which reversibly (de-)insertingl ithiumi ons at potentials highert han 4V ,f or instance, Li(Ni 1/3 Mn 1/3 Co 1/3 )O 2 , [261] limiting their utilization so far to active materials such as LiFePO 4 [258,[262][263][264] LiFe 1Àx Mn x PO 4 , [265] LiMnPO 4 , [266] or vanadium oxides [267,…”