Abstract

In the broad application of tunable devices, the temperature stability of the dielectric tunable performance of ceramics should be considered. In this work, (1- x )Ba(Zr 0.36 Ti 0.64 )O 3 – x (Ba 0.82 Ca 0.18 )TiO 3 (BZ 0.36 T– x BC 0.18 T) ceramics, where x = 0.3–0.7, were prepared by the solid-state high-temperature method. The combined effects of Ca 2+ and Zr 4+ ions on the microstructure of BZ 0.36 T– x BC 0.18 T ceramics were observed. The crystal structure was analyzed through X-ray diffraction, showing a pure perovskite ABO 3 -type structure, indicating the formation of a BCZT solid solution. High dielectric tunability ( n r > 85% at < 10 kV/cm) under a low DC bias field is achieved in BZ 0.36 T–0.5BC 0.18 T and BZ 0.36 T–0.6BC 0.18 T, especially the maximum value of n r ∼87.51% at 7.68 kV/cm obtained for BZ 0.36 T–0.6BC 0.18 T. High tunability under a low DC bias field may be related to not only the extrinsic contribution (dipole reorientation, domain-wall motion) but also the intrinsic contribution (lattice phonon or anharmonic interactions of B-site ions). The maximum FOM value of ∼847 is achieved in BZ 0.36 T–0.5BC 0.18 T, which is related to the high n r ∼74.57% and lower tan δ ∼8.8 × 10 −4 at 400 V, demonstrating its excellent performance for tunable device applications. Furthermore, the FOM – T curve of BZ 0.36 T–0.3BC 0.18 T ceramics in the range of 126–269 is flatter than other compositions in the temperature range of −20°C-100 °C, showing an improved dielectric tunable performance with better temperature stability. The improved temperature stability of BZ 0.36 T–0.3BC 0.18 T may contribute to the enhancement of the diffuse phase transition (DPT) degree, which results in a flattened phase transition region. These results suggest that BZ 0.36 T–0.3BC 0.18 T is competitive candidate for temperature-stable tunable device applications, and the compositional tailored DPT can be expected to be a feasible means to improve the temperature stability of dielectric tunable performance.

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