A polymer electrolyte system has been developed using a biodegradable polymer namely poly-ε-caprolactone (PCL) in combination with zinc triflate [Zn(CF3SO3)2] in different weight percentages and characterized during this investigation. Free-standing thin films of varying compositions were prepared by solution casting technique. The successful doping of the polymer has been confirmed by means of Fourier transform infrared spectroscopy (FTIR) by analyzing the carbonyl (C=O) stretching region of the polymer. The maximum ionic conductivity obtained at room temperature (25°C) was found to be 8.8x10–6 S/cm in the case of PCL complexed with 25 wt% Zn(CF3SO3)2 which is five orders of magnitude higher than that of the pure polymer host material. The increase in amorphous phase with an increase in salt concentration of the prepared polymer electrolyte has also been confirmed from the concordant results obtained from X-ray diffraction (XRD), differential scanning calorimetry (DSC) and scanning electron microscopic (SEM) analyses. Furthermore, the electrochemical stability window of the prepared polymer electrolyte was found to be 3.7 V. An electrochemical cell has been fabricated based on Zn/MnO2 electrode couple as an application area and its discharge characteristics were evaluated

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Nanocomposite polymer electrolyte (NCPE) films of [75 wt % poly(ε‐caprolactone) : 25 wt % zinc triflate] + x wt % nanofiller Al2O3 (x = 1, 3, 5, 7) were prepared by solution cast technique. Such NCPE films were characterized using Fourier transform infrared and AC impedance spectroscopic techniques. Complexation of polymer with salt and nanofiller was revealed from FTIR analysis. On the other hand, an apparent increase in the number density of charge carriers upto 5 wt % loading of the nanofiller was also confirmed. Furthermore, AC impedance spectroscopic studies have shown that ionic conductivity increases with the addition of Al2O3 and reaches a maximum of 2.5 × 10−5 S cm−1 at room temperature for 5 wt % loading of nanofiller. The dielectric behavior of all the synthesized samples has also been analyzed and presented. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 40524.

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