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BiFeO3–BaTiO3 (BF–BT) ceramics exhibit great potential for diverse applications in high temperature piezoelectric transducers, temperature-stable dielectrics and pulsed-power capacitors. Further optimization of functional properties for different types of applications can be achieved by modification of processing parameters or chemical composition. In the present work, the influence of pentavalent niobium substitution for trivalent ferric ions on the structure, microstructure and dielectric properties of 0.7BF–0.3BT ceramics was investigated systematically. Doping with niobium led to incremental reductions in grain size (from 7.0 to 1.3 µm) and suppression of long-range ferroelectric ordering. It was found that core-shell type microstructural features became more prominent as the Nb concentration increased, which were correlated with the formation of distinct peaks in the dielectric permittivity–temperature relationship, at ~470 and 600 °C, which were attributed to the BT-rich shell and BF-rich core regions, respectively. Nb-doping of BF–BT ceramics yielded reduced electronic conductivity and dielectric loss, improved electrical breakdown strength and enhanced dielectric energy storage characteristics. These effects are attributed to the charge compensation of pentavalent Nb donor defects by bismuth vacancies, which suppresses the formation of oxygen vacancies and the associated electron hole conduction mechanism. The relatively high recoverable energy density (Wrec = 2.01 J cm−3) and energy storage efficiency (η = 68%) of the 0.7BiFeO3–0.3BaTiO3 binary system were achieved at 75 °C under an electric field of 15 kV mm−1. This material demonstrates the greatest potential for applications in energy storage capacitors and temperature-stable dielectrics. [ABSTRACT FROM AUTHOR]

• Domain switching and lattice strain in polycrystalline K 0.5 Bi 0.5 TiO 3 -BiFeO 3 -PbTiO 3 is evaluated by in-situ high energy synchrotron XRD. • The tetragonal {200} grain family exhibited the highest effective lattice strain up to 8.2 × 10−3 at an electric field of 5 kV/mm. • A partial phase transformation from tetragonal to rhombohedral occurred at high electric field levels, with an average strain of −1.54 × 10−3. • Relaxation of intergranular stress gives rise to enhanced domain switching in KBT-BF-PT ceramics. • The observed self-adapting mechanism could also be exploited in other high performance, high temperature piezoelectric ceramics. We report an in-situ synchrotron X-ray diffraction study of K 0.5 Bi 0.5 TiO 3 -BiFeO 3 -PbTiO 3 ceramics, which exhibit a T c of around 450 °C. The electromechanical actuation mechanisms comprise contributions from coexisting tetragonal and rhombohedral phases. The tetragonal {200} grain family exhibited the highest effective lattice strain, up to 8.2 × 10−3 at 5 kV/mm. Strong strain anisotropy in the tetragonal phase and field-induced intergranular stresses facilitate a partial transformation from tetragonal (high strain anisotropy) to rhombohedral (low strain anisotropy) at high electric field levels, with an average linear transformation strain of -1.54 × 10-3. The domain switching behavior was effectively enhanced in both tetragonal and rhombohedral phases after the phase transformation, due to the release of intergranular stress. This observed self-adapting mechanism in tuning intergranular stress through partial phase switching in the morphotropic KBT-BF-PT composition with large lattice distortion could also be exploited in other perovskite systems in order to achieve high performance high temperature piezoelectric ceramics. [ABSTRACT FROM AUTHOR]