Department Of Physics
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Item Structural, microstructural and electrochemical properties of dispersed-type polymer nanocomposite films(Institute of Physics Publishing, 2018) Arya, A.; Sharma, A.L.Free-standing solid polymer nanocomposite (PEO-PVC) + LiPF6-TiO2 films have been prepared through a standard solution-cast technique. The improvement in structural, microstructural and electrochemical properties has been observed on the dispersion of nanofiller in polymer salt complex. X-ray diffraction studies clearly reflect the formation of complex formation, as no corresponding salt peak appeared in the diffractograms. The Fourier transform infrared analysis suggested clear and convincing evidence of polymer-ion, ion-ion and polymer-ion-nanofiller interaction. The highest ionic conductivity of the prepared solid polymer electrolyte (SPE) films is ?5 10-5 S cm-1 for 7 wt.% TiO2. The linear sweep voltammetry provides the electrochemical stability window of the prepared SPE films, about ?3.5 V. The ion transference number has been estimated, t ion = 0.99 through the DC polarization technique. Dielectric spectroscopic studies were performed to understand the ion transport process in polymer electrolytes. All solid polymer electrolytes possess good thermal stability up to 300 ?C. Differential scanning calorimetry analysis confirms the decrease of the melting temperature and signal of glass transition temperature with the addition of nanofiller, which indicates the decrease of crystallinity of the polymer matrix. An absolute correlation between diffusion coefficient (D), ion mobility (?), number density (n), double-layer capacitance (C dl), glass transition temperature, melting temperature (T m), free ion area (%) and conductivity (?) has been observed. A convincing model to study the role of nanofiller in a polymer salt complex has been proposed, which supports the experimental findings. The prepared polymer electrolyte system with significant ionic conductivity, high ionic transference number, and good thermal and voltage stability could be suggested as a potential candidate as electrolyte cum separator for the fabrication of a rechargeable lithium-ion battery system. ? 2018 IOP Publishing Ltd.Item Optimization of salt concentration and explanation of two peak percolation in blend solid polymer nanocomposite films(Springer New York LLC, 2018) Arya, A.; Sharma, A.L.The present paper is focused toward the preparation of the flexible and free-standing blend solid polymer electrolyte films based on PEO-PVP complexed with NaPF6 by the solution cast technique. The structural/morphological features of the synthesized polymer nanocomposite films have been investigated in detail using X-ray diffraction, Fourier transform infra-red spectroscopy, Field emission scanning electron microscope, and Atomic force microscopy techniques. The film PEO-PVP + NaPF6 ((Formula presented.)8) exhibits highest ionic conductivity ~ 5.92 ? 10?6 S cm?1 at 40 ?C and ~ 2.46 ? 10?4 S cm?1 at 100 ?C. The temperature-dependent conductivity shows an Arrhenius type behavior and activation energy decreases with the addition of salt. The high temperature (100 ?C) conductivity monitoring is done for the optimized PEO-PVP + NaPF6 ((Formula presented.)8) highly conductive system and the conductivity is still maintained stable up to 160 h (approx. 7 days). The thermal transitions parameters were measured by the differential scanning calorimetry (DSC) measurements. The prepared polymer electrolyte film displays the smoother surface on addition of salt and a thermal stability up to 300 ?C. The ion transference number (tion) for the highest conducting sample is found to be 0.997 and evidence that the present system is ion dominating with negligible electron contribution. Both linear sweep voltammetry and cyclic voltammetry supports the use of prepared polymer electrolyte with long-term cycle stability and thermal stability for the solid-state sodium ion batteries. Finally, a two peak percolation mechanism has been proposed on the basis of experimental findings. [Figure not available: see fulltext.] ? 2018 Springer-Verlag GmbH Germany, part of Springer Nature