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Title: Effect of (Sr{sub 0.7}Ca{sub 0.3})TiO{sub 3}-substitution on structure, dielectric, ferroelectric, and magnetic properties of BiFeO{sub 3} ceramics

Journal Article · · Journal of Applied Physics
DOI:https://doi.org/10.1063/1.4952713· OSTI ID:22596714

Bi{sub 1−x}(Sr{sub 0.7}Ca{sub 0.3}){sub x}Fe{sub 1−x}Ti{sub x}O{sub 3} ceramics were prepared by a standard solid state reaction process, and the influence of Sr/Ca ratio on structure and properties for Bi{sub 1−x}(Sr,Ca){sub x}Fe{sub 1−x}Ti{sub x}O{sub 3} system was discussed by comparing with Sr{sub 0.5}Ca{sub 0.5}TiO{sub 3}-modified BiFeO{sub 3} ceramics. Rietveld analysis of X-ray diffraction data revealed that the crystal structure changed from rhombohedral R3c (x ≤ 0.4) to orthorhombic Pnma (x = 0.6) with Sr{sub 0.7}Ca{sub 0.3}TiO{sub 3} substitution, and biphasic structure (R3c + Pnma) was determined at x = 0.5, while that for Bi{sub 1−x}(Sr{sub 0.5}Ca{sub 0.5}){sub x}Fe{sub 1−x}Ti{sub x}O{sub 3} system was at x = 0.4. This indicated that the morphotropic phase boundary in Bi{sub 1−x}(Sr,Ca){sub x}Fe{sub 1−x}Ti{sub x}O{sub 3} system shifted toward (Sr,Ca)TiO{sub 3} side with increasing Sr/Ca ratio. The Raman spectrometric analysis and selected area electron diffraction analysis also confirmed this transition. The dielectric relaxation could be well fitted by Arrhenius law, and the different activation energies were attributed to the different origins of the dielectric relaxations with increasing temperature. The current density-field (J-E) curves indicated that the leakage current was reduced to about five orders of magnitude with Sr{sub 0.7}Ca{sub 0.3}TiO{sub 3} substitution. The P-E hysteresis loops obtained by three different methods indicated the enhanced ferroelectricity at x = 0.4, and it could be attributed to the decrement of leakage current. Meanwhile, the magnetization was enhanced with Sr{sub 0.7}Ca{sub 0.3}TiO{sub 3} substitution, and the maximum remanent magnetization was determined at x = 0.2. The enhanced magnetization originated from the partial substitution of Fe{sup 3+} by Ti{sup 4+}.

OSTI ID:
22596714
Journal Information:
Journal of Applied Physics, Vol. 119, Issue 20; Other Information: (c) 2016 Author(s); Country of input: International Atomic Energy Agency (IAEA); ISSN 0021-8979
Country of Publication:
United States
Language:
English