Dielectric capacitors possessing the inherent superiorities
of
high power density and ultrafast charge–discharge speed make
their utilization in energy-storage devices extremely propitious,
although the relatively low recoverable energy-storage density (W
rec) may impede their applications. In this
work, unlike the mainstream approach of destroying long-range ferroelectric/antiferroelectric
order and inducing relaxor properties to achieve a high W
rec value, we have selected end members with a high polarization
gene to promote the polarization behavior of the typical relaxor Sr0.7Bi0.2TiO3. Therefore, an ultrahigh W
rec ∼ 8 J/cm3 and a superior
efficiency (η) ∼ 91% are accomplished in the 0.98[0.56(Sr0.7Bi0.2)TiO3-0.44(Bi0.5Na0.5)TiO3]-0.02 Bi(Mg0.5Ti0.5)O3 sample. The achieved W
rec value is record high in Sr0.7Bi0.2TiO3-based systems as far as we know. The polarization-enhancement
behavior can be explained by the phase field simulation results, phase
content variance in X-ray diffraction Rietveld refinement, hardening
trend in Raman spectroscopy, domain morphology, and local symmetry
in transmission electron microscope analysis. Meanwhile, the ceramic
possesses excellent thermal stability (ΔW
rec < 12.7% and Δη < 10.4%, −50–200
°C), frequency (ΔW
rec <
2.69% and Δη < 2.06%, 0.5–500 Hz), and fatigue-resistant
stability (ΔW
rec < 0.08% and
Δη < 0.2%, up to 1 × 105 cycles). Accordingly,
this work proposes a design idea to tailor the polarization behavior
and energy-storage properties of typical relaxors.
Dielectric capacitors, as one of the important electronic devices, are widely used in various fields. However, most ferroelectric capacitors with high energy storage density require excessively high electric fields. In this work, we have prepared 0.9(Bi0.5Na0.5)0.7Sr0.3TiO3-0.1 Bi(Mg2/3Nb1/3)O3 relaxor ferroelectric ceramics with different BaZrO3 doping levels. A high energy storage ( Wr) of 4.07 J/cm3 and efficiency ( η) of 91% are simultaneously obtained in 0.94[0.9(Bi0.5Na0.5)0.7Sr0.3TiO3-0.1 Bi(Mg2/3Nb1/3)O3]-0.06BaZrO3 ceramic under a medium electric field of 260 kV/cm. Additionally, the ceramic also exhibits excellent temperature and frequency stability. Furthermore, the phase field simulation is used to simulate the evolution of domain structure and hysteresis loops of the ceramics with different doping levels. The results of phase field simulation explicitly explain the influence of different relaxation degrees on energy storage density and efficiency of the ceramics. We believe that the ceramic prepared in this work is one of the most promising candidate materials for some miniaturized energy storage devices operating under low or medium electric fields.
High-precision piezo actuators necessitate dielectrics with high electrostrain performance with low hysteresis. Polarity-modulated (Sr 0.7 Bi 0.2□0.1 )-TiO 3 -based ceramics exhibit extraordinarily discrete multiphase coexistence regions: (i) the relaxor phase coexistence (RPC) region with local weakly polar tetragonal (T) and pseudocubic (Pc) short-range polar nanodomains and (ii) the ferroelectric phase coexistence (FPC) region with T long-range domains and Pc nanodomains. The RPC composition features a specially high and pure electrostrain performance with nearzero hysteresis (S ∼ 0.185%, Q 33 ∼ 0.038 m 4 •C −2 ), which is double those of conventional Pb(Mg 1/3 Nb 2/3 )O 3 -based ceramics. Particular interest is paid to the RPC and FPC with multiscale characterization to unravel local structure−performance relationships. Guided by piezoelectric force microscopy, scanning transmission electron microscopy, and phase-field simulations, the RPC composition with multiphase low-angle weakly polar nanodomains shows local structural heterogeneity and contributes to a flat local free energy profile and thus to nanodomain switching and superior electrostrain performance, in contrast to the FPC composition with a macroscopic domain that shows stark hysteresis. This work provides a paradigm to design high-precision actuator materials with large electrostrain and ultralow hysteresis, extending our knowledge of multiphase coexistence species in ferroelectrics.
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