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    Structural, dielectric and ferroelectric properties of Cu2+- and Cu2+/Bi3+-doped BCZT lead-free ceramics: a comparative study
    (Springer, 2021-05-29T00:00:00) Kumari, Sapna; Kumar, Amit; Kumar, V.; Dubey, S.K.; Goyal, P.K.; Kumar, Suresh; Sharma, A.L.; Arya, Anil
    Perovskite-type Ba0.98Ca0.02Zr0.02Ti0.98O3 (BCZT), Ba0.98Ca0.02Zr0.02Ti0.976Cu0.008O3 (BCZTC) and Ba0.9725Bi0.005Ca0.02Zr0.02Ti0.976Cu0.008O3 (BCZTCB) lead-free ceramics were synthesised via solid-state reaction method at a sintering temperature of 1380��C. Effects of CuO and Bi2O3/CuO doping on structural, microstructural, dielectric and ferroelectric properties were investigated systematically. X-ray diffraction technique confirmed the existence of pure perovskite phase with the tetragonal structure in pure and in the doped BCZT ceramics at room temperature. The dielectric analysis demonstrated two anomalies around 24��C and 126��C for BCZT, which were identified as orthorhombic to tetragonal (TO-T) and tetragonal to cubic (TC) phase transition temperature, respectively. The TO-T temperature shifted to below 16��C, while the TC increased to 132��C for the BCZTCB sample. The physical mechanisms of the conduction processes were investigated through impedance spectroscopy, and the values of resistance, conductivity and activation energies associated with the grain and grain boundaries were evaluated. The activation energy was determined to be higher for doped samples than for pure BCZT. Further, the dopant-dependent ferroelectric nature of the ceramic samples was evidenced by the analysis of characteristic hysteresis loop, and a value of remnant polarization (Pr = 4.59�?C/cm2) was obtained for the BCZTCB ceramic sample. Furthermore, the d33 value, which was 54 pC/N for pure BCZT, was determined to be 140 pC/N and 64 pC/N for BCZTC and BCZTCB, respectively. � 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
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    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