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Phase structure, microstructure, electrical and energy storage properties of SBNLT lead free ceramics with Zr4+ substituted into B-sites

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Abstract

Lead-free (Sr0.3Bi0.35Na0.335Li0.015) (Ti1−xZrx) O3 ceramics (SBNLT1−xZrx) with x = 0–0.04 were prepared via the solid-state combustion technique using glycine as the fuel. The influence of Zr content on the phase structure, microstructure, electrical properties, and energy storage properties of the SBNLT1−xZrx ceramics was examined. The presence of a pure perovskite phase was shown by X-ray diffraction (XRD) patterns, with the coexistence of rhombohedral and tetragonal phases in all samples, as certified by the Rietveld refinement method. Scanning electron microscopy (SEM) was utilized to observe the morphology of the SBNLT1−xZrx ceramics, which revealed cube shaped grains with anisotropic growth. Average grain size increased from 2.01 to 2.49 µm when x increased from 0 to 0.01 and then reduced with further increases in Zr content. The maximum dielectric constant dropped from 4667 to 2990 when x increased from 0 to 0.04, caused by a shift from the morphotropic phase boundary (MPB). The maximum polarization (Pmax) of 29.18 µC/cm2, energy storage density (Wtotal) of 0.851 J/cm3 and recoverable energy storage (Wrec) of 0.609 J/cm3 were achieved when x = 0.02.

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Acknowledgements

This research was financially supported by Naresuan University and the National Science, Research, and Innovation Fund (NSRF) (R2566B067). This work was partially supported by Global and Frontier Research University Fund, Naresuan University; Grant No. R2567C001. The authors are grateful to the Department of Physics, Faculty of Science, Naresuan University for their supporting facilities. Thanks, are also given to Asst. Prof. Dr. Kyle V. Lopin for his assistance in editing the manuscript.

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Sinkruason, T., Luangpangai, A., Julphunthong, P. et al. Phase structure, microstructure, electrical and energy storage properties of SBNLT lead free ceramics with Zr4+ substituted into B-sites. J. Korean Ceram. Soc. (2024). https://doi.org/10.1007/s43207-024-00400-1

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