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Enhanced Multiferroic and Magnetocapacitive Properties of (1 − x) Ba0.7 Ca0.3 TiO3- x BiFeO3 Ceramics.
- Source :
-
Journal of the American Ceramic Society . Mar2014, Vol. 97 Issue 3, p816-825. 10p. - Publication Year :
- 2014
-
Abstract
- The structures, Curie temperature, dielectric relaxor behaviors, ferroelectricity, ferromagnetism, and magnetocapacitance of the (1− x) Ba0.70 Ca0.30 TiO3- x BiFeO3 [(1− x) BCT- x BF, x = 0-0.90] solid solutions have been systematically investigated. The ceramics have coexisted tetragonal (T) and orthorhombic (O) phases when x ≤ 0.06, coexisted pseudocubic (PC) and O phases when x = 0.065, coexisted cubic and O phases when 0.07 ≤ x ≤ 0.12, PC phase when 0.21 ≤ x ≤ 0.42, coexisted T and rhombohedral (R) phases when 0.52 ≤ x ≤ 0.70, and R phase when x ≥ 0.75. Significantly, composition-dependent microstructures and Curie temperature are observed, the average grain size increases from 1.9 μm for x = 0, reaches 12.0 μm for x = 0.67, and then decreases to 1.3 μm for x = 0.90. At room temperature, the ceramics with x = 0.42-0.70 show piezoelectric properties and multiferroic behaviors, characterized by the polarization-electric field, polarization current intensity-electric field, and magnetization-magnetic field curves, the composition with x = 0.67 has maximum polarization, remnant polarization, maximum magnetization, and remnant magnetization of 15.0 μC/cm2, 9.1 μC/cm2, 0.33 emu/g, and 0.14 emu/g, respectively. In addition, the magnetocapacitance is evidenced by the increased relative dielectric constant with increasing the applied magnetic field ( H). With Δ H = 8 kOe, the composition with x = 0.67 shows the largest values of (εr( H) − εr(0))/εr(0) = 2.96% at room temperature. The structure-property relationship is discussed intensively. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00027820
- Volume :
- 97
- Issue :
- 3
- Database :
- Academic Search Index
- Journal :
- Journal of the American Ceramic Society
- Publication Type :
- Academic Journal
- Accession number :
- 94777086
- Full Text :
- https://doi.org/10.1111/jace.12702