Abstract
New solid polymer blend electrolyte films based on biodegradable polymer blend comprising of polyvinyl alcohol (PVA) and poly (N-vinyl pyrrolidone) (PVP) doped with different wt% of lithium carbonate (Li2CO3) salt have been prepared by solution casting method. The resulting PVA/PVP/Li2CO3 polymer blend electrolyte films have been characterized by various analytical techniques such as FTIR, UV–vis, XRD, TGA, polarized optical microscopy and scanning electron microscopy. The FTIR and XRD analysis confirmed the complex formation between PVA/PVP blend and Li2CO3 salt. The ionic conductivity and the dielectric properties of PVA/PVP/Li2CO3 polymer blend electrolyte films were investigated using an impedance spectroscopy. It was observed that the ionic conductivity of PVA/PVP/Li2CO3 electrolyte system increases as a function of Li2CO3 concentration. The highest ionic conductivity was found to be 1.15 × 10−5 S cm−1 for polymer blend electrolyte with 20 wt% Li2CO3 content. On the other hand, the dielectric results revealed the non-Debye type of behaviour. The dielectric constant values indicate a strong dielectric dispersion in the studied frequency range which increases as the Li2CO3 content increases. The dielectric constant as high as 1200 (ε = 1201.57, 50 Hz, 150 °C) and the dielectric loss well below 4 (tan δ = 3.94, 50 Hz, 150 °C) were obtained for polymer blend electrolytes with 25 wt% Li2CO3 salt. Thus, the results obtained in the present study suggest that the PVA/PVP/Li2CO3 polymer blend electrolyte system seems to be a promising candidate for solid state battery applications.
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Kalim Deshmukh is grateful to the management of B. S. Abdur Rahman University, Chennai-600048, TN, India for providing Junior Research Fellowship (JRF) to carry out this research work.
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Deshmukh, K., Ahamed, M.B., Polu, A.R. et al. Impedance spectroscopy, ionic conductivity and dielectric studies of new Li+ ion conducting polymer blend electrolytes based on biodegradable polymers for solid state battery applications. J Mater Sci: Mater Electron 27, 11410–11424 (2016). https://doi.org/10.1007/s10854-016-5267-x
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DOI: https://doi.org/10.1007/s10854-016-5267-x