LAUSR

A plastic crystalline electrolyte (PCE) consisting of 0.4 mol/L lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) in succinonitrile (SN) was blended with poly(ethylene oxide) (PEO), poly(vinylpyrrolidone) (PVP), poly(ethylene carbonate) (PEC), and polyacrylonitrile (PAN). The influences of the regarding polymers on thermomechanical properties of the PCE were studied systematically, utilizing differential scanning calorimetry, thermogravimetric analysis, and oscillation experiments. Depending on the chosen polymer, the melting temperature and overall crystallinity of the PCE were increased. For PCEs containing PEO and PVP, overall crystallinity was enhanced the most resulting in lamellae-like superstructures, identified by light microscopy images. Furthermore, the onset for the sublimation process of SN was shifted to higher temperatures, and the mechanical strength was increased by the presence of some polymers, with exception of PEC. Electrochemical characterization, including electrochemical impedance spectroscopy and linear sweep voltammetry, revealed ionic conductivities of 10–4 S/cm at room temperature for PCE with PAN and extended electrochemical stability windows of ≥4.5 V vs lithiated graphite for PCE with PEO. By correlating the thermomechanical and electrochemical properties, some structure-property relationships were drawn, pointing out great potential for specific tailoring of PCEs by polymer additives. The synergistic effect of increasing both, mechanical stability and ionic conductivity, made the PCE + PAN composition especially attractive for a possible application in batteries.