A comparative study on electrical conduction properties of Sr-substituted Ba1−x Sr x Zr0.1Ti0.9O3 (x=0.00–0.15) ceramics

A comparative study on electrical conduction properties of Sr-substituted Ba1−x Sr x... The lead-free polycrystalline Sr-substituted Ba1 − x Sr x Zr0.1Ti0.9O3 (BSZT) (x = 0.00–0.15) ceramics are synthesized by the high-temperature conventional solid-state reaction method. The Rietveld refinement of the X-ray diffraction pattern confirms the co-existence of tetragonal and cubic phase in the sample at x = 0.10, which is also confirmed from Raman spectroscopy. The surface micrographs show the formation of grains with well-defined grain boundaries and the significant enhancement in granular size with increasing Sr content. Moreover, the domain structure with “lamellar” and watermark characters is clearly observed for all the concentrations. The complex impedance analysis shows a significant increment in the net impedance of BSZT samples for the composition, x = 0.10. Exceptionally high value of impedance is attributed to the co-existence of two competing phases in the microscopic level. An enhancement in the impedance value is a consequence of reduction in the electrical conductivity of the sample. The modulus analysis confirms the presence of non-Debye-type relaxation in the material. The frequency gap (Δf) between the normalized master curve Z″/Z″m and M″/M″m decreases with increasing Sr concentration, which indicates a reduction in the polarization in BSZT samples. This result is well consistent with the results obtained from the complex impedance analysis. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Ionics Springer Journals

A comparative study on electrical conduction properties of Sr-substituted Ba1−x Sr x Zr0.1Ti0.9O3 (x=0.00–0.15) ceramics

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Publisher
Springer Berlin Heidelberg
Copyright
Copyright © 2017 by Springer-Verlag Berlin Heidelberg
Subject
Chemistry; Electrochemistry; Renewable and Green Energy; Optical and Electronic Materials; Condensed Matter Physics; Energy Storage
ISSN
0947-7047
eISSN
1862-0760
D.O.I.
10.1007/s11581-017-2085-y
Publisher site
See Article on Publisher Site

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