Monte Carlo simulation on dielectric relaxation and dipole cluster state in relaxor ferroelectrics

The Ginzburg-Landau theory on ferroelectrics with random field induced by dipole defects is studied by using Monte Carlo simulation, in order to investigate the dipole configuration and the dielectric relaxation of relaxor ferro-electrics. With the increase of random field, the dipole configuration evolves from the long-range ferroelectric order into the coexistence of short-range dipole-clusters and less polarized matrix. The dipole-cluster phase above the transition temperature and superparaelectric fluctuations far below this temperature are identified for the relaxor ferroelectrics. We investigate the frequency dispersion and the time-domain spectrum of the dielectric relaxation, demonstrating the Vogel-Fulcher relationship and the multi-peaked time-domain distribution of the dielectric relaxation.

NUMERICAL ANALYSIS OF DIELECTRIC RESPONSE IN RELAXOR FERROELECTRICS

The dielectric response of complex perovskite relaxor ferrolectrics Pb(Mg1/3Nb2/3) O3 with respect to temperature and frequency was carefully measured. Using a normalized method of the 'universal' many-body theory, the relaxation process was analyzed around the temperature of dielectric absorption maximum. There is no structural phase transition near this temperature and the behavior is closely like that of a polar dipole medium. The functional relationship about frequency and temperature of dielectric pormittivity maximum was also fitted to discuss the dynamic behavior of polar microregion. It is confirmed that a new power exponential Arrhenius relation is better to characterize the relaxation behavior than the Vogel-Fulcher and Debye relations. Based on the polarization theory of polar dipoles, we analyzed the relaxation mechanism of ferroelectric microdomains of relaxor ferroelectrics, and get an ideal distribution function of relaxation time. Consequently, a simulated dielectric response dependence on temperature and frequencies can be expressed, which is well coincided with experiment results.

Large electrocaloric effect over a wide temperature span in lead-free bismuth sodium titanate-based relaxor ferroelectrics

For efficient solid-state refrigeration technologies based on electrocaloric effect(ECE),it is a great challenge of simultaneously obtaining a large adiabatic temperature change(DT)within a wide temperature span(Tspan)in lead-free ferroelectric ceramics.Here,we studied the electrocaloric effect(ECE)in(1-x)(Na_(0.5)Bi_(0.5))TiO_(3)-xCaTiO_(3)((1-x)NBT-xCT)and explored the combining effect of morphotropic phase boundary(MPB)and relaxor feature.The addition of CT not only constructs a MPB region with the coexistence of rhombohedral and orthorhombic phases,but also enhances the relaxor feature.The ECE peak appears around the freezing temperature(Tf),and shifts toward to lower temperature with the increasing CT amount.The directly measured ECE result shows that the ceramic of x=0.10,which is in the MPB region,has an optimal ECE property of DTmax=1.28 K@60℃under 60 kV/cm with a wide Tspan of 65C.The enhanced ECE originates from the electric-field-induced transition between more types of polar nanoregions and long-range ferroelectric macrodomains.For the composition with more relaxor feature in the MPB region,such as x?0.12,the ECE is relatively weak under low electric fields but it exhibits a sharp increment under a sufficiently high electric field.This work provides a guideline to develop the solidestate cooling devices for electronic components.

Abnormal phase transition and polarization mismatch phenomena in BaTiO_(3)-based relaxor ferroelectrics

Relaxor ferroelectrics have been extensively studied due to their outstanding dielectric,piezoelectric,energy storage,and electro-optical properties.Although various theories were proposed to elaborate on the relaxation phenomena,polar nanoregions formed by disruption of the long-range-order structures are considered to play a key role in relaxor ferroelectrics.Generally,relaxor ferro-electrics are formed by aliovalent substitution or isovalent substitution in normal ferroelectrics,or further combinations of solid solutions.Herein,one category of BaTiO_(3)-based relaxor ferroelectrics with abnormal phase transition and polarization mismatch phenomena is focused.Characteristic parameters of such BaTiO_(3)-based relaxor ferroelectrics,including the Curie temperature,polarization,and lattice parameter,show a typical“U”-shaped variation with compositions.The studied BaTiO_(3)-based relaxor ferroelectrics are mostly solid solutions of A-site coupling and B-site coupling ferroelectrics,exhibiting polarization mismatch in certain compositions[e.g.,0.9BaTiO_(3)-0.1BiScO_(3),0.8BaTiO_(3)-0.2Bi(Mg_(1/2)Ti_(1/2)O_(3),0.8BaTiO_(3)-0.2Bi(Mg_(2/3)Nb_(1/3)O_(3),0.5BaTiO_(3)-0.5Pb(Mg_(1/3)Nb_(2/3)O_(3),0.4BaTiO_(3)-0.6Pb(Zn_(1/3)Nb_(2/3)O_(30,etc.].Of particular interest is that excellent electrical properties can be achieved in the studied relaxor ferroelectrics.Therefore,polarization mismatch theory can also provide guidance for the design of new high-performance lead-free relaxor ferroelectrics.

DIELECTRIC RELAXATION IN RELAXOR FERROELECTRICS

In this review the dielectric properties of relaxor ferroelectrics are discussed and compared withthe properties of normal dielectrics and ferroelectrics. We try to draw a general picture ofdielectric relaxation starting from a textbook review of the underlying concepts and pay attentionto common behavior of relaxors rather than to the features observed in specific materials. We hopethat this general approach is beneficial to those physicists, chemists, material scientists and deviceengineers who deal with relaxors. Based on the analysis of dielectric properties, a comprehensivedefinition of relaxors is proposed: relaxors are defined as ferroelectrics in which the maximum inthe temperature dependence of static susceptibility occurs within the temperature range ofdielectric relaxation, but does not coincide with the temperature of singularity of relaxation timeor soft mode frequency.

Large Energy Capacitive High-Entropy Lead-Free Ferroelectrics

Advanced lead-free energy storage ceramics play an indispensable role in next-generation pulse power capacitors market.Here,an ultrahigh energy storage density of~13.8 J cm^(-3)and a large efficiency of~82.4%are achieved in high-entropy lead-free relaxor ferroelectrics by increasing configuration entropy,named high-entropy strategy,realizing nearly ten times growth of energy storage density compared with low-entropy material.Evolution of energy storage performance and domain structure with increasing configuration entropy is systematically revealed for the first time.The achievement of excellent energy storage properties should be attributed to the enhanced random field,decreased nanodomain size,strong multiple local distortions,and improved breakdown field.Furthermore,the excellent frequency and fatigue stability as well as charge/discharge properties with superior thermal stability are also realized.The significantly enhanced comprehensive energy storage performance by increasing configuration entropy demonstrates that high entropy is an effective but convenient strategy to design new high-performance dielectrics,promoting the development of advanced capacitors.

Order-Disorder Phase Transition and Dielectric Mechanism in Relaxor Ferroelectrics

An overview is presented on the order-disorder structural transitions and the dielectric mechanism in the complex-perovskite type relaxor ferroelectrics, i.e., the relaxors. Emphasis is put on the theoretical understanding of the structural transitions, the macroscopic dielectric properties, and the relationship between them. The influences of the composition, the temperature, and the atomic interactions on the order-disorder microstructures can be well understood in the cluster-variation-method calculations. The criterion drawn from theoretical analysis is successful in predicting the order-disorder structure of relaxors. Among various physical models about relaxors, the dipole glassy model that described the dielectric response as the thermally activated flips of the local spontaneous polarization under random interactions is discussed in details. The Monte Carlo simulation results of this model are consistent with the linear and nonlinear experiments of relaxors.

High energy storage capability of perovskite relaxor ferroelectrics via hierarchical optimization

Ultrafast charge/discharge process and ultrahigh power density enable dielectrics essential components in modern electrical and electronic devices, especially in pulse power systems. However, in recent years, the energy storage performances of present dielectrics are increasingly unable to satisfy the growing demand for miniaturization and integration, which stimulates further researches on dielectrics with higher energy density and efficiency.Among various inorganic dielectrics, perovskite relaxor ferroelectrics are recognized as promising candidates for energy storage applications, with high permittivity and relatively high efficiency. Here, we focus on recent progress and achievements on optimizing perovskite relaxor ferroelectrics toward better energy storage capability through hierarchical design. The principles and key parameters of dielectric energy storage, together with the definition of majority types of dielectrics, are introduced at first. Strategies within various scales include domain, grain size, orientation, and composite engineering are summarized. The existing challenges are presented and future prospects are proposed in the end, with the background of both academic explorations and industrial applications.

Large electrostrain in Bi_(1/2)Na_(1/2)TiO_(3)-based relaxor ferroelectrics:A case study of Bi_(1/2)Na_(1/2)TiO3-Bi_(1/2)K_(1/2)TiO_(3)-Bi(Ni_(2/3)Nb_(1/3))O_(3) ceramics

(1-x)(0.8Bi_(1/2)Na_(1/2)TiO3-0.2Bi_(1/2)K_(1/2)TiO3)-xBi(Ni_(2/3)Nb_(1/3))O3(BNKT-xBNN)solid solution ceramics were fabricated by high temperature solid-state reaction method.All the compositions possess relaxor ferroelectric features,among which the ergodic BNKT-0.02BNN exhibits large repeatable electrostrain value Suni¼0.51%at electric field of 65 kV/cm,with high piezoelectric stain coefficient d33*of 890 pm/V at 45 kV/cm,while the non-ergodic compositions present unrepeatable large strain response.Based on the electric field-composition phase diagram,the repeatability of strain response in ergodic compositions can be attributed to the reversible electric-field-induced phase transition.In addition,the effects of BNN contents on the macroscopic strain properties are explored by analyzing the existing states of the polar regions with corresponding thermal evolutions and electric-field-induced phase transitions.This research is expected to guide the design of lead free relaxor ferroelectric materials with desired electrostrain properties.

LARGE ELECTROCALORIC EFFECT IN RELAXOR FERROELECTRICS

Organic and inorganic relaxor ferroelectrics used for electrocaloric effect(ECE)applications areintroduced.Relaxor ferroelectrics offer several advantages for ECE devices,e.g.,infinite stateswithout applying electric field,field-induced large polarization,no-hysteresis ofheating and cooling,small-hysteresis polarization loss,room temperature phase transition,and broad temperaturerange.The ECE in relaxor ferroelectrics under a high electric field can be described using a theorysimilar to that for first-order phase transition materials.Large ECE was observed directly inhigh-energy electron irradiated poly(vinylidene fluoride-trifluoroethylene)(P(VDF-TrFE)68/32 mol%copolymers,P(VDF-TrFE-CFE)(CFE-chlorofluoroethylene)59.2/33.6/7.2 mol%terpolymers,P(vDF-TrFE-CFE)-P(VDF-CTFE)(CTFE-chlorotrifluoroethylene)95/5 wt%terpolymer blended films,and(PbLa)(ZrTi)O_(3)(PLZT)ceramic thin films.ECE reported inPb(Sc_(1/2)Ta_(1/2))O_(3)(PST),Pb(Mg_(1/3)Nb_(2/3))O_(3)-PbTiO_(3)(PMN-PT)thin films is also summarized.Finally,the perspective of ECE devices is llustrated.

Moderate Fields, Maximum Potential: Achieving High Records with Temperature‑Stable Energy Storage in Lead‑Free BNT‑Based Ceramics

The increasing awareness of environmental concerns has prompted a surge in the exploration of leadfree,high-power ceramic capacitors.Ongoing efforts to develop leadfree dielectric ceramics with exceptional energystorage performance(ESP)have predominantly relied on multicomponent composite strategies,often accomplished under ultrahigh electric fields.However,this approach poses challenges in insulation and system downsizing due to the necessary working voltage under such conditions.Despite extensive study,bulk ceramics of(Bi_(0.5)Na_(0.5))TiO_(3)(BNT),a prominent lead-free dielectric ceramic family,have seldom achieved a recoverable energy-storage(ES)density(Wrec)exceeding 7 J cm^(−3).This study introduces a novel approach to attain ceramic capacitors with high ESP under moderate electric fields by regulating permittivity based on a linear dielectric model,enhancing insulation quality,and engineering domain structures through chemical formula optimization.The incorporation of SrTiO_(3)(ST)into the BNT matrix is revealed to reduce the dielectric constant,while the addition of Bi(Mg_(2/3)Nb_(1/3))O_(3)(BMN)aids in maintaining polarization.Additionally,the study elucidates the methodology to achieve high ESP at moderate electric fields ranging from 300 to 500 kV cm^(−1).In our optimized composition,0.5(Bi_(0.5)Na_(0.4)K_(0.1))TiO_(3)–0.5(2/3ST-1/3BMN)(B-0.5SB)ceramics,we achieved a Wrec of 7.19 J cm^(−3) with an efficiency of 93.8%at 460 kV cm^(−1).Impressively,the B-0.5SB ceramics exhibit remarkable thermal stability between 30 and 140℃ under 365 kV cm^(−1),maintaining a Wrec exceeding 5 J cm^(−3).This study not only establishes the B-0.5SB ceramics as promising candidates for ES materials but also demonstrates the feasibility of optimizing ESP by modifying the dielectric constant under specific electric field conditions.Simultaneously,it provides valuable insights for the future design of ceramic capacitors with high ESP under constraints of limited electric field.

Excellent energy storage performance in Bi_(0.5)Na_(0.5)TiO_(3)-based lead-free high-entropy relaxor ferroelectrics via B-site modification

Next-generation advanced high/pulsed power capacitors urgently require dielectric materials with outstanding energy storage performance.Bi_(0.5)Na_(0.5)TiO_(3)-based lead-free materials exhibit high polarization,but the high remanent polarization and large polarization hysteresis limit their applications in dielectric capacitors.Herein,high-entropy perovskite relaxor ferroelectrics(Na_(0.2)Bi_(0.2)Ba_(0.2)Sr_(0.2)Ca_(0.2))(Ti1-x%Zrx%)O_(3)are designed by adding multiple ions in the A-site and replacing the B-site Ti^(4+)with a certain amount of Zr^(4+).The newly designed system showed high relaxor feature and slim polarization-electric(P-E)loops.Especially,improved relaxor feature and obviously delayed polarization saturation were found with the increasing of Zr^(4+).Of particular importance is that both high recoverable energy storage density of 6.6 J/cm^(3) and energy efficiency of 93.5%were achieved under 550 kV/cm for the ceramics of x=6,accompanying with excellent frequency stability,appreciable thermal stability,and prosperous discharge property.This work not only provides potential dielectric materials for energy storage applications,but also offers an effective strategy to obtain dielectric ceramics with ultrahigh comprehensive energy storage performance to meet the demanding requirements of advanced energy storage applications.

A novel lead-free relaxor with endotaxial nanostructures for capacitive energy storage

Dielectric capacitors with a fast charging/discharging rate,high power density,and long-term stability are essential components in modern electrical devices.However,miniaturizing and integrating capacitors face a persistent challenge in improving their energy density(W_(rec))to satisfy the specifications of advanced electronic systems and applications.In this work,leveraging phase-field simulations,we judiciously designed a novel lead-free relaxor ferroelectric material for enhanced energy storage performance,featuring flexible distributed weakly polar endotaxial nanostructures(ENs)embedded within a strongly polar fluctuation matrix.The matrix contributes to substantially enhanced polarization under an external electric field,and the randomly dispersed ENs effectively optimize breakdown phase proportion and provide a strong restoring force,which are advantageous in bolstering breakdown strength and minimizing hysteresis.Remarkably,this relaxor ferroelectric system incorporating ENs achieves an exceptionally high W_(rec)value of 10.3 J/cm^(3),accompanied by a large energy storage efficiency(η)of 85.4%.This work introduces a promising avenue for designing new relaxor materials capable of capacitive energy storage with exceptional performance characteristics.

Design of superior electrostriction in BaTiO_(3) -based lead-free relaxors via the formation of polarization nanoclusters

Electrostrictive materials have wide applications in modern high-precision electronic devices.Driven by growing environmental concerns,there is demand for lead-free materials with superior electrostriction behaviors.In this study,we demonstrate a record-high electrostrictive coefficient of~0.0712 m^(4) C^(-2) in perovskite ferroelectric ceramics,along with hysteresis-free strain as well as excellent frequency and thermal stabilities,in lead-free BaTiO_(3)-based ceramics through a polarization nanocluster design.By appro-priately introducing Li+and Bi^(3+)into the BaTiO 3 lattice matrix,the long-range ferroelectric ordering can be broken,and polarization nanoclusters can be formed,resulting in a relaxor state with concurrently suppressed polariza-tion and maintained electro-strain.A three-dimensional atomic model constructed using advanced neutron total-scattering data combined with the reverse Monte Carlo method indicates the existence of Bi and Li segregations at the subnanometer scale,which confirms the prediction made by density functional theory calculations.Such a short-range chemical order destroys the long-range ferroelectric order of the off-centered Ti polar displacements and leads to the embedding of Li+/Bi ^(3+)-rich polar nanoregions in the Ba^(2+)-rich polarization disorder matrix.Further,a completely reversible electric-field-induced lattice strain is observed,giving rise to pure electrostriction without hysteresis behavior.This work provides a novel strategy for developing lead-free relaxor ferroelectrics with high electrostriction performance.

BS_(0.5)BNT-based relaxor ferroelectric ceramic/glass-ceramic composites for energy storage

Relaxor ferroelectric ceramics have very high dielectric constant(e)but relatively low electrical breakdown strength(Eb),while glass-ceramics exhibit higher E,due to the more uniformly dispersed amorphous phases and submicrocrystals/nanocrystals inside.How to effectively combine the advantages of both relaxor ferroelectric ceramics and glass-ceramics is of great significance for the development of new dielectric materials with high energy storage performance.In this work,we firstly prepared BaO-SrO-Bi_(2)O_(3)-Na_(2)0-TiO_(2)-Al_(2)O_(3)-SiO_(2)(abbreviated as GS)glass powders,and then fabricated(Ba_(0.3)Sr_(0.7))_(0.5)(Bi_(0.5)Na_(0.5))_(0.5)TiO_(3)+x wt%GS ceramic composites(abbreviated as BSo.sBNT-xGS,x=0,2,6,10,14,16,and 18).Submicrocrystals/nanocrystals with a similar composition to BSo.sBNT were crystalized from the glass,ensuring the formation of uniform core-shell structure in BSo.sBNT-xGS relaxor ferroelectric ceramic/glass-ceramic composites.When the addition amount of GS was 14 wt%,the composite possessed both high&r(>3200 at 1 kHz)and high E,(~170 kV/cm)at room temperature,and their recoverable energy storage density and efficiency were Wrec=2.1 J/cm’and n=65.2%,respectively.The BSo.sBNT-14GS composite also had several attractive properties such as good temperature,frequency,cycle stability,and fast charge-discharge speed.This work provides insights into the relaxor ceramic/glass-ceramic composites for pulsed power capacitors and sheds light on the utilization of the hybrid systems.

The first 2D organic-inorganic hybrid relaxor-ferroelectric single crystal

Inorganic relaxor ferroelectric solid solution single crystals are spurring new generations of high performance electromechanical devices,including transducers,sensors,and actuators,due to their ultrahigh electric field induced strain,large piezoelectric constant,high electromechanical coupling factor and low dielectric loss.However,relaxor ferroelectric single crystals found in organic-inorganic hybrid perovskites are very limited,but achieving these superior properties in them will be of great significance in the design of modern functional materials.Fortunately,here the first two-dimensional(2D)organic-inorganic hybrid relaxor ferroelectric single crystal,[Br(CH_(2))_(3)NH_(3)]_(2)PbBr_(4)(BPA_(2)-PbBr_(4),BPA=3-bromopropylamine),achieves some of superior properties.Interestingly,BPA_(2)-PbBr_(4)reveals a successive relaxor ferroelectric-ferroelectric-paraelectric phase transitions accompanying by a large degree of relaxationΔT_(relax)=61 K and ultralow energy loss(tanδ<0.001).Meanwhile,it exhibits a superior second harmonic generation(SHG)effect with maximum value accounts for 95%of the standard KDP due to great deformation of structure(3.2302×10^(-4)).In addition,temperature dependent luminescence spectra(80-415 K)exhibit fluorescence and phosphorescence overlapping emission originated from inorganic and organic components with the nanosecond-scale short lifetime and the millisecond-scale long lifetime,respectively,and the color of the emitted light is continuously adjustable,which is the first to achieve luminescence and relaxor ferroelectricity compatibility.

High energy storage performance in AgNbO_(3) relaxor ferroelectric films induced by nanopillar structure

Inspired by the increasing demand for energy-storage capacitors in electrical and electronic systems, dielectrics with high energy-storage performance have attracted more and more attention. AgNbO_(3) -based lead-free ceramics serve as one of the most promising environmental-friendly candidates. However, their energy storage optimization is seriously limited by the low breakdown strength. Fortunately, thin film as a form of AgNbO3 materials can effectively improve the breakdown strength. In this work, AgNbO_(3)film with ∼550 nm in thickness was deposited on SrRuO_(3 )/(001)SrTiO_(3) using pulsed laser deposition. The AgNbO_(3) film reveals typical relaxor ferroelectric hysteresis loops due to the new nanopillar structure, which contributes to high breakdown strength of up to 1200 kV cm^(-1) . Benefiting from the high breakdown strength, a recoverable energy storage density of 10.3 J cm^(-3) and an energy efficiency of 72.2% are obtained in the AgNbO_(3) film, which demonstrates the promising prospect of AgNbO_(3) film for energy storage applications.

Elastic,dielectric,and piezoelectric characterization of 0.92Pb(Zn_(1/3) Nb_(2/3))O_3-0.08PbTiO_3 single crystal by Brillouin scattering

In this paper,a complete set of elastic,piezoelectric,and dielectric constants of high-quality tetragonal poled0.92Pb（Zn1/3Nb2/3）O3-0.08PbTiO3 single crystal grown by the modified flux method is determined using high-resolution Brillouin scattering.A comparison is made between the results obtained by a hybrid method combining ultrasonic and resonant techniques and the results obtained by the Brillouin scattering.The elastic,piezoelectric,and dielectric constants obtained by the two methods are similar.The Brillouin spectrum consists of one longitudinal and two transverse acoustic phonon modes,and the variations of the Brillouin shifts,the full widths at half maximum,and the scattering intensities of these modes with scattering angle 9 are investigated.In particular,the transverse acoustic phonon mode at the lowfrequency becomes markedly soft from 28.2 GHz to 18.4 GHz and broadens gradually with the increase of θ,while its intensity decreases gradually as compared with that of the original one.The possible origins of the results are discussed.

Boosting the piezoelectric property of relaxor ferroelectric single crystal via active manipulation of defect dipole polarization

To further enhance the property of piezoelectric materials is of great significance to improve the overall performance of electro-mechanical devices.Here in this work,we propose a thermal annealing and high temperature poling approach to achieve significantly enhanced piezoelectricity in Pb(In_(1/2)Nb_(1/2))O_(3)single bondPb(Mg_(1/3)Nb_(2/3))O_(3)single bondPbTiO_(3)(PIN-PMN-PT)crystals with a morphotropic phase boundary(MPB)composition.The main idea of our approach is to realize a more sufficiently polarized crystal via active manipulation of defects and orientation of defect polarization.Manipulation of defect dipoles by the high temperature poling is proved by the piezo-response force microscopy.Finally,a d_(33)of 3300 pC/N and a SE of 0.25%are obtained,nearly 60%higher than that of conventionally poled crystals.Moreover,such a boosting of piezoelectric property is obtained under a maintained Curie temperature.Our research not only reveals the active control of defect dipole via modified poling method in the PIN-PMN-PT crystal,but also provides a feasible strategy to further improve the property of piezoelectric materials.

Improved energy storage performance of bismuth sodium titanate-based lead-free relaxor ferroelectric ceramics via Bi-containing complex ions doping

Lead-free dielectric ceramics can be used to make quick charge-discharge capacitor devices due to their high power density.Their use in advanced electronic systems,however,has been hampered by their poor energy storage performance(ESP),which includes low energy storage efficiency and recoverable energy storage density(Wrec).In this work,we adopted a combinatorial optimization strategy to improve the ESP in(Bi_(0.5)Na_(0.5))TiO_(3)(BNT)-based relaxor ferroelectric ceramics.To begin,the Bi-containing complex ions Bi(Mg_(2/3)Nb_(1/3))O_(3)(BMN)were introduced into a BNT-based matrix in order to improve the diffuse phase transition,increase Bi-O bond coupling,avoid macro domain development,and limit polarization response hysteresis.Second,the viscous polymer process was employed to reduce sample thickness and porosity,resulting in an apparent increase in breakdown strength in(1-x)[0.7(Bi_(1/2)Na_(1/2))TiO_(3)]-0.3SrTiO_(3)-xBi(Mg_(2/3)Nb_(1/3))O_(3)(BS-xBMN)ceramics.Finally,in x=0.20 composition,an amazing Wrecof 5.62 J·cm^(-3)and an ultra-high efficiency of 91.4%were simultaneously achieved at a relatively low field of 330 kV·cm^(-1),together with remarkable temperature stability in the temperature range of 30-140℃(3.5 J·cm^(-3)±5%variation).This research presents a new lead-free dielectric material with superior ESP for use in pulsed power capacitors.