Lithium ion conducting polymer blend electrolyte films based on poly(vinyl alcohol) (PVA) and poly(vinyl pyrrolidone) (PVP) with different Mwt% of lithium nitrate (LiNO 3) salt, using a solution cast technique, have been prepared. The polymer blend electrolyte has been characterized by XRD, FTIR, DSC and impedance analyses. The XRD study reveals the amorphous nature of the polymer electrolyte. The FTIR study confirms the complex formation between the polymer and salt. The shifts in T g values of 70 PVA-30 PVP blend and 70 PVA-30 PVP with different Mwt% of LiNO 3 electrolytes shown by DSC thermograms indicate an interaction between the polymer and the salt. The dependence of T g and conductivity upon salt concentration has been discussed. The ion conductivity of the prepared polymer electrolyte has been found by a.c. impedance spectroscopic analysis. The PVA-PVP blend system with a composition of 70 wt% PVA: 30 wt% PVP exhibits the highest conductivity of 1•58 × 10 −6 Scm −1 at room temperature. Polymer samples of 70 wt% PVA-30 wt% PVP blend with different molecular weight percentage of lithium nitrate with DMSO as solvent have been prepared and studied. High conductivity of 6•828 × 10 −4 Scm −1 has been observed for the composition of 70 PVA:30 PVP:25 Mwt% of LiNO 3 with low activation energy 0•2673 eV. The conductivity is found to increase with increase in temperature. The temperature dependent conductivity of the polymer electrolyte follows the Arrhenius relationship which shows hopping of ions in the polymer matrix. The relaxation parameters (ω) and (τ) of the complexes have been calculated by using loss tangent spectra. The mechanical properties of polymer blend electrolyte such as tensile strength, elongation and degree of swelling have been measured and the results are presented.
This work aims at developing and characterizing a proton conducting polymer electrolyte based on Poly(N-vinyl pyrrolidone) (PVP) doped with ammonium bromide (NH 4 Br). Proton conducting polymer electrolytes based on PVP doped NH 4 Br in different molar ratios have been prepared by solution casting technique using distilled water as solvent. The XRD pattern confirms the dissociation of salt. The FTIR analysis confirms the complex formation between the polymer and the salt. The conductivity analysis shows that the polymer electrolyte with 25 mol % NH 4 Br has the highest conductivity equal to 1.06 Â 10 À3 S cm À1 at room temperature. Also it has been observed that the activation energy evaluated from the Arrhenius plot is low (0.50 eV) for 25 mol % NH 4 Br doped polymer electrolyte. The influence of salt concentration on dc conductivity and activation energy of the polymer electrolyte has been discussed.
Solid polymer electrolyte membranes consisting of polyacrylonitrile (PAN) as a host polymer, ammonium nitrate (NH4NO3) as a complexing salt, and propylene carbonate (PC) as a plasticizer were prepared by a solution casting technique. An increase in the amorphous nature of the polymer electrolytes was confirmed by X‐ray diffraction analysis. A shift in the glass‐transition temperature of the PAN/NH4NO3/PC electrolytes was observed in the differential scanning calorimetry thermograms; this indicated interactions between the polymer and the salt. The impedance spectroscopy technique was used to study the mode of ion conduction in the plasticized polymer electrolyte. The highest ionic conductivity was found to be 7.48 × 10−3 S/cm at 303 K for 80 mol % PAN, 20 mol % NH4NO3, and 0.02 mol % PC. The activation energy of the plasticized polymer electrolyte (80 mol % PAN/20 mol % NH4NO3/0.02 mol % PC) was found to be 0.08 eV; this was considerably lower than that of the film without the plasticizers. The dielectric behavior of the electrolyte is discussed in this article. A literature survey indicated that the synthesis and characterization of ammonium‐salt‐doped, proton‐conducting polymer electrolytes based on PAN has been rare. The use of the best composition membrane (80 mol % PAN/20 mol % NH4NO3/0.02 mol % PC) proton battery was constructed and evaluated. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41743.
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