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BST solid solutions, temperature evolution of the ferroelectric transitions

Solid solutions Ba 1 − x Sr x TiO 3 (BST) are of high technological importance, particularly in microwave domain. Barium titanate has “naturally” three transitions, between four stable ferroelectric phases: (C) cubic, (T) tetragonal, (O) orthorhombic, (R) rhombohedral. Jaffe et al . [B. Jaffe, W.R....

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Published in:Applied surface science 2006-10, Vol.253 (1), p.354-357
Main Authors: Alexandru, H.V., Berbecaru, C., Ioachim, A., Nedelcu, L., Dutu, A.
Format: Article
Language:English
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Summary:Solid solutions Ba 1 − x Sr x TiO 3 (BST) are of high technological importance, particularly in microwave domain. Barium titanate has “naturally” three transitions, between four stable ferroelectric phases: (C) cubic, (T) tetragonal, (O) orthorhombic, (R) rhombohedral. Jaffe et al . [B. Jaffe, W.R. Cook, H. Jaffe, Piezoelectric Ceramics, Academic Press, 1971] has given the dependence of the transition temperatures up to 30% of Sr content. We have extrapolated these temperatures and we have found that some phases might disappear at higher Sr concentrations. A family of solid solutions with x = 25, 50, 75, 90% was prepared by standard solid-state reaction and sintered at 1230 and 1260 °C, respectively. The permitivities and the dielectric losses were measured with a self-acting bridge (1 kHz), on a large temperature range (±200 °C). The composition x = 25% shows three peak values of permittivity as expected, while the composition x = 50%, only two peak values, corresponding to phase transitions cubic–tetragonal–rhombohedral, phase orthorhombic being excluded. Compositions with x ≥ 63%, Sr shows only one peak value corresponding to a genuine transition cubic–rhombohedral. The cubic transition to several lower phases shows almost a linear decrease of the Curie point with the increase of Sr fraction. For Sr concentration x ≥ 80%, the Curie point appears to fall more rapidly than linear. To our best knowledge, there is for the first time, this effect is reported.
ISSN:0169-4332
1873-5584
DOI:10.1016/j.apsusc.2006.06.011