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Persistent URL http://purl.org/net/epubs/work/47766963
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Record Id 47766963
Title Structure and dielectric properties of double A-site doped bismuth sodium titanate relaxor ferroelectrics for high power energy storage applications
Contributors
Abstract The structural and dielectric properties of barium/strontium substituted Bi0.5Na0.5TiO3 were examined in compositions of general formula (Ba0.4Sr0.6TiO3)x(Bi0.5Na0.5TiO3)1-x. An average classic cubic perovskite structure is maintained from x = 0.5 to 1.0. The temperature dependence of dielectric properties of studied compositions shows relaxor ferroelectric behaviour attributed to the existence of polar nano-regions. Ferroelectric measurements under variable temperature demonstrated two transitions from normal ferroelectric to relaxor-ferroelectric and relaxor-ferroelectric to paraelectric, at the dipole freezing temperature, Tf, and temperature of maximum permittivity, Tm, respectively. The obtained value of Tf coincides with the onset of linear thermal expansion of the cubic unit cell parameter obtained from high resolution powder neutron diffraction data. Careful analysis of the neutron diffraction data revealed no significant change in the average cubic structure from -263 to 150 C. However, changes in the Gaussian variance component of the neutron peak shape, reveal three distinct regions with transitions at about -100 and 100 C corresponding to the beginning and end of the dielectric dispersion seen in the permittivity and loss spectra. This variation in the Gaussian variance parameter is attributed to the activity of the polar nano-regions. The composition (Ba0.4Sr0.6)0.5(Bi0.5Na0.5)0.5TiO3 was found to exhibit the maximum recoverable energy storage density, with a value of 1.618 J cm-3 and 76.9% storage efficiency at a field of 17 kV mm-1.
Organisation ISIS , ISIS-HRPD , STFC
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Funding Information
Related Research Object(s): 10.5286/ISIS.E.82367191
Language English (EN)
Type Details URI(s) Local file(s) Year
Journal Article J Mater Chem A 8, no. 45 (2020): 23965-23973. doi:10.1039/D0TA07772K 2020