Department Of Physics

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    Enhanced Curie temperature and superior temperature stability by site selected doping in BCZT based lead-free ceramics
    (Elsevier Ltd, 2022-01-31T00:00:00) Kumari, Sapna; Kumar, Amit; Kumar, Aman; Kumar, V.; Thakur, Vikas N.; Kumar, Ashok; Goyal, P.K.; Gaur, Anurag; Arya, Anil; Sharma, A.L.
    In this work, Bi3+ doped Ba0.98-3x/2BixCa0.02Zr0.02Ti0.976Cu0.008O3 [0 ? x ? 0.03] lead free ceramics, to be employed for structural, dielectric and ferroelectric studies, have been synthesized via conventional solid state reaction method. Rietveld refinement of the X-ray diffraction (XRD) data evidences the existence of a pure perovskite phase with tetragonal symmetry for all ceramics. The Scanning Electron Microscopy (SEM) reveals that the grain size, which is 16.14 ?m for x = 0 reduced to 2.11 ?m for x = 0.03. Dielectric studies demonstrate excellent dielectric behavior with high Curie temperature (TC ?159 �C), high dielectric constant (?r ?834, ?max ? 3146), and a low dielectric loss (tan? ? 0.019), for an optimum value of x = 0.02. The analysis of temperature coefficient of the dielectric permittivity indicates the applicability of these materials in multilayer ceramic capacitors. Impedance studies, conducted to understand the underlying physical mechanisms, are found to be in good agreement with the results of structural and dielectric studies. Furthermore, the ferroelectric measurement confirms the ferroelectric nature for all samples with an energy storage efficiency (?) of ?42% for x = 0.02 composition. � 2022 Elsevier Ltd and Techna Group S.r.l.
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    Selection of best composition of Na+ ion conducting PEO-PEI blend solid polymer electrolyte based on structural, electrical, and dielectric spectroscopic analysis
    (Springer, 2020) Pritam, Arya A; Sharma, A.L.
    In this paper, we report the investigation on structural, electrical, dielectric properties, and ion dynamics of novel blend polymer electrolyte matrix (PEO-PEI) complexed with sodium hexafluorophosphate salt. All the solid polymer electrolyte films have been synthesized via solution cast method. The SPE films were characterized by the X-ray diffraction, field emission scanning electron microscope, impedance-dielectric spectroscopy, and thermogravimetric analysis. The morphology of the SPE alters with salt addition and confirms the blend polymer complex formation. The FTIR analysis evidenced the complex formation, and increase in the fraction of free ions is achieved. The ionic conductivity exhibits a maximum at the stoichiometric ratio O/Na = 10 and follows the Arrhenius behavior. The fraction of free ions is maximum for the SPE film with the highest ionic conductivity. The optimum electrolyte possesses a voltage stability window of about 4�V, excellent thermal stability up to 380��C, and high ionic transference number (~ 1). The complex permittivity and conductivity have been simulated in whole frequency window to extract relaxation time and dielectric strength. The dielectric constant and relaxation time exhibited sequentially a maximum and minimum for the SPE film with the highest ionic conductivity. The loss tangent peak shifts toward high frequency with addition of salt, and it infers the faster ion dynamics in the polymer matrix. Then the ion transport parameters number density of charge carriers (n), ion mobility (?), and diffusion coefficient (D) have been obtained by three methods (FTIR, impedance spectroscopy, and loss tangent method) and are in absolute correlation with the impedance results. An ion transport mechanism has been proposed based on experimental findings. � 2019, Springer-Verlag GmbH Germany, part of Springer Nature.
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    Structural, electrical properties and dielectric relaxations in Na+-ion-conducting solid polymer electrolyte
    (Institute of Physics Publishing, 2018) Arya, A.; Sharma, A.L.
    In this paper, we have studied the structural, microstructural, electrical, dielectric properties and ion dynamics of a sodium-ion-conducting solid polymer electrolyte film comprising PEO8-NaPF6+ x wt. % succinonitrile. The structural and surface morphology properties have been investigated, respectively using x-ray diffraction and field emission scanning electron microscopy. The complex formation was examined using Fourier transform infrared spectroscopy, and the fraction of free anions/ion pairs obtained via deconvolution. The complex dielectric permittivity and loss tangent has been analyzed across the whole frequency window, and enables us to estimate the DC conductivity, dielectric strength, double layer capacitance and relaxation time. The presence of relaxing dipoles was determined by the addition of succinonitrile (wt./wt.) and the peak shift towards high frequency indicates the decrease of relaxation time. Further, relations among various relaxation times () have been elucidated. The complex conductivity has been examined across the whole frequency window; it obeys the Universal Power Law, and displays strong dependency on succinonitrile content. The sigma representation () was introduced in order to explore the ion dynamics by highlighting the dispersion region in the Cole-Cole plot () in the lower frequency window; increase in the semicircle radius indicates a decrease of relaxation time. This observation is accompanied by enhancement in ionic conductivity and faster ion transport. A convincing, logical scheme to justify the experimental data has been proposed. ? 2018 IOP Publishing Ltd.