Relaxor ferroelectric behaviour observed in (Ca0.5Sr0.5Ba0.5Pb0.5)Nb2O7 perovskite layered structure ceramics

Relaxor ferroelectric behaviour was observed in perovskite layered structure (PLS) (Ca_0.5Sr_0.5Ba_0.5Pb_0.5)Nb₂O₇ (CSBPN) ceramics engineered using the high entropy approach. The CSBPN ceramics were sintered at 1350 °C and are single-phase with an orthorhombic structure (Cmcm space group) at room temperature. Their relaxor ferroelectric behaviour is characterized by a broad and frequency-dependent permittivity maximum and a current peak around zero electric field in the hysteresis loop. The presence of polar nanoregions is supported by piezoresponse force microscopy images. The value of the relative permittivity ?′ = 130 at 1 kHz and room temperature is much larger than that for conventional PLS ceramics Sr₂Nb₂O₇ (?′ = 42) and Ca₂Nb₂O₇ (?′ = 38). This can be attributed to the presence of polar nanoregions and the lattice distortion effect in high entropy materials. The appealing dielectric and relaxor behaviour of CSBPN ceramics confirms the efficacy of the high entropy approach to obtain improved properties.     

Improvement of energy storage properties of NaNbO3-based ceramics through the cooperation of relaxation and oxygen vacancy defects

The development of materials with high energy storage plays a crucial role in solving energy consumption. Traditional dielectric ceramics have the disadvantages of low energy storage and low efficiency. The most effective solution is to reduce the dielectric loss and increase the breakdown strength. In this paper, (Na_0.73Bi_0.08Sm_0.01)(Nb_0.91Ta_0.09)O₃ relaxor ferroelectric ceramics were prepared, which achieved a high energy storage density of 1.66 J cm^?3, high efficiency (83.6%) at 214 kV/cm at room temperature. The addition of Bi₂O₃ makes the A site cations disordered, thereby generating random fields, breaking the long-range order, and forming polar nanodomains. That allows the ceramic to acquire relaxation properties, reducing the dielectric loss. The impedance analysis proves that the breakdown strength is related to the addition of Sm₂O₃. The addition of Sm reduces the oxygen vacancy defect concentration and inhibits the migration of carriers, thereby improving its breakdown strength. Through proper doping of Bi and Sm, the relaxation properties and breakdown field strength of the ceramics are enhanced to obtain excellent energy storage performance. This provides a new idea in terms of relaxation and oxygen vacancy defects for NaNbO₃-based energy storage ceramics.     

Giant strains of 0.70% achieved via a field-induced multiple phase transition in BNT-based relaxor antiferroelectric ceramics

Bismuth sodium titanate (BNT)-based lead-free ceramics have attracted a great deal of attention due to their large electrostrains. In this work, a remarkably symmetric strain of 0.7% together with excellent temperature (0.5–0.7% from 25 to 100 °C)/frequency (ΔS<4% from 1 to 20 Hz) stability was observed in the 0.91(Bi_0.5Na_0.5)TiO₃-0.06BaTiO₃-0.03NaNbO₃ (BNT-6BT-3NN) AFE P4bm ceramic through constructing R3c/P4mm/P4bm triple-phase coexistence phase boundary. Compared with other two compositions near double-phase coexistence ferroelectric (FE)-antiferroelectric (AFE) phase boundaries, the BNT-6BT-3NN ceramic exhibits a unique field-induced multiple phase transition from the initial AFE P4bm phase to the metastable FE P4mm phase and finally into the FE R3c phase. In-situ structural analysis evidenced a significantly enhanced lattice strain but a comparable strain value from domain switching in BNT-6BT-3NN compared with other compositions. The present study provides a novel strategy for designing high-performance large-strain ceramics in BNT-based relaxor AFE systems.     

Stronger B-site ionic disorder boosting enhanced dielectric energy-storage performance in BNT-based relaxor ferroelectric ceramics

Because of their possible applications in dielectric energy-storage capacitor devices, (Bi_0.5Na_0.5)TiO₃-based (BNT) relaxor ferroelectric (RFE) ceramics are feasible alternatives to lead-containing electroceramics. Good energy-storage performance (ESP), including high recoverable energy density (W_rec) and good energy discharge efficiency (η), is required to achieve device miniaturization and long device lifetimes. An advanced method was used to overcome the challenges of A-site ionic disordered RFE in achieving high inducible polarization and low hysteresis, with the former dictating a large W_rec and the latter dictating a high η. In this study, an ABO₃ perovskite-structured complex end-member Bi(Mg_2/3Nb_1/3)O₃ (BMN) was added to a 0.7Bi_0.5Na_0.4K_0.1TiO₃–0.3Ba_0.5Sr_0.5TiO₃ (0.7BNKT–0.3BST) matrix. The differences in the valence states and ionic radii of Mg²⁺, Ti⁴⁺, and Nb⁵⁺ increased the local electric field fluctuation, which contributed to the expanded dielectric relaxation properties. The combined substantial prevention of hysteresis and remanent polarization suggests high potential applicability for ESP. Finally, an enhancement in W_rec to 4.98 J/cm³ was achieved in 0.595BNKT–0.255BST–0.15BMN with an ultrahigh η of 97.3% in a medium-strength electric field of 300 kV/cm. The ESP also demonstrated good thermostability between 30 and 120 °C. Furthermore, the strategy used in this study to generate RFEs can serve as a guide for future research.