Composite polymer electrolytes consisting of at least 35 mol% poly(vinylidene fluoride) (PVdF) and mixtures of propylene carbonate (PC) and dimethyl formamide (DMF), lithium salts (LiAsF6, LiN(CF3SO2)(2), or LiC(CF3SO2)(3), and small amounts (similar to 5 mol%) of plasticizer, either diethylphthalate (DEP) or dibutylphthalate (DBP), were investigated by differential scanning calorimetry, complex impedance analysis and Li-7 NMR spectroscopy. Despite the composite nature of these materials, they all exhibit a single glass transition temperature (T-g). Significant variations of T-g with the two different plasticizers were noted. The sample containing the LiC(CF3SO2)(3) salt has the highest electrical conductivity of the series, similar to 3X10(-4) S/cm at 25 degrees C. Time-dependent impedance measurements utilizing cells with lithium electrodes revealed the growth of a passivating interface layer comparable to those observed with other polymer electrolytes. The onset of NMR motional line-narrowing is correlated with T-g for all samples prepared with DBP, as is known to occur in ’single component’ polyether-based electrolytes. However the onset of narrowing for the samples containing DEP occurs about 30 K above T-g. Lithium-7 spin-lattice relaxation measurements exhibit non-exponential recovery profiles below T-g, with about similar to 15% of the Li species relax differently than the majority. Activation energies extracted from 7LiT(1) data show that localized Li motion is significantly impeded in the DEP-containing samples, relative to those prepared with DBP.