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Structural manipulation and tailoring of dielectric properties in SrTi(1−x)Fe(x)Ta(x)O(3) perovskites: Design of new lead free relaxors

We report composition dependent structure evolution from SrTiO(3) to SrFe(0.5)Ta(0.5)O(3) by powder X-ray and neutron diffraction studies of SrTi(1−2x)Fe(x)Ta(x)O(3) (0.00 ≤ × ≤ 0.50) compositions. Structural studies reveal cubic (Pm3m) perovskite-type structure of the parent SrTiO(3) for x up to 0....

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Detalles Bibliográficos
Autores principales: Shukla, R., Patwe, S. J., Deshpande, S. K., Achary, S. N., Krishna, P. S. R., Shinde, A. B., Gopalakrishnan, J., Tyagi, A. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981879/
https://www.ncbi.nlm.nih.gov/pubmed/27514668
http://dx.doi.org/10.1038/srep23400
Descripción
Sumario:We report composition dependent structure evolution from SrTiO(3) to SrFe(0.5)Ta(0.5)O(3) by powder X-ray and neutron diffraction studies of SrTi(1−2x)Fe(x)Ta(x)O(3) (0.00 ≤ × ≤ 0.50) compositions. Structural studies reveal cubic (Pm3m) perovskite-type structure of the parent SrTiO(3) for x up to 0.075 and cation disordered orthorhombic (Pbnm) perovskite-type structure for x ≥ 0.33. A biphasic region consisting of a mixture of cubic and orthorhombic structures is found in the range for 0.10 ≤ × ≤ 0.25. Dielectric studies reveal transformation from a normal dielectric to relaxor like properties with increasing Fe(3+) and Ta(5+) concentration. Dielectric response is maximum at x = 0.33 in the series. The results establish a protocol for designing new lead-free relaxor materials based on the co-substitution of Fe(3+) and Ta(5+) for Ti(4+) in SrTiO(3). A complex interplay of strain effects arising from distribution of cations at the octahedral sites of the perovskite structure controls the dielectric properties.