Ultrafast Discharge Research Articles

Enhanced energy storage and mechanical properties in niobate-based glass-ceramics

The advancement of energy storage glass-ceramics, serving as quintessential elements within pulse power capacitors, is deemed essential for the progression of sophisticated electronic systems, attributable to their ultrafast discharge rate and elevated dielectric breakdown strength (DBS). In this study, the incorporation of 1.2 mol% Nd2O3 into SiO2-Na2O-K2O-BaO-Nb2O5-Nd2O3 (SNKBNN) glass-ceramics has significantly enhanced the material performance. Specifically, a high recoverable energy storage density (Wrec) of 2.06 J/cm3 can be achieved, alongside an ultrahigh efficiency (η) of 92.3 % under an electric field of 630 kV/cm. Additionally, this glass-ceramics also exhibit a high discharge energy density (Wd) of 0.97 J/cm3, an ultrafast discharge rate of 7 ns, and an exceptionally high hardness (Hv) of 10.51 GPa. Additionally, these glass-ceramics exhibit exceptional stability across a range of temperatures (25 to 150 ℃), frequencies (10 to 1000 Hz), and cycling durability (up to 104 cycles). The research has corroborated the structural interdependence between energy storage and mechanical properties, establishing a foundational understanding of their synergistic relationship. The synthesized glass-ceramics demonstrate significant potential for use in high-power dielectric capacitors.

Excellent energy-storage performance in BNT-BT lead-free ceramics through optimized electromechanical breakdown

Dielectric capacitors with high recoverable energy storage density (Wrec) are in urgent demand for clean energy technologies. However, their lower breakdown strength (Eb) strongly limits their energy storage performance. We, herein, propose a facile method to enhance Eb by enhancing mechanical strength via second phase modulation. The efficiency of this method is validated in the (1-x)(0.94Na0.5Bi0.5TiO3-0.06BaTiO3)-xSr(Ta0.5Sb0.5)O3 ((BNT-BT)-xSTS, x = 0.1, 0.15, 0.2, 0.25, and 0.3) ceramics. The introduction of Sr(Ta0.5Sb0.5)O3 (STS) increases the relaxor degree, refines grain size, and most importantly, creates a second phase of BiSb2O7, which hinders dislocation movement and improves mechanical strength. Our results show that the breakdown strength strongly depends on the mechanical strength. The highest hardness of 7.42 GPa accompanied by the largest Eb of 620 kV/cm was obtained in (BNT-BT)-0.25STS sample. The sample exhibits the best energy storage properties of a large Wrec = 8.3 J/cm3, a high efficiency of 82.3 %, and excellent temperature/frequency stability. Furthermore, the sample also exhibits good charge/discharge stability and ultra-fast transient discharge time (62.26 ns). This work provides a theoretical guidance for developing lead-free dielectrics with superior energy-storage performance.

Ultrahigh energy storage performance in BNT-based binary ceramic via relaxor design and grain engineering

Dielectric capacitors attract much attention for advanced electronic systems owing to their ultra-fast discharge rate and high power density. However, the low energy storage density (Wrec) and efficiency (η) severely limit their applications. Herein, Bi0.5Na0.5TiO3-K0.5Na0.5NbO3 binary ceramic is developed to obtain excellent energy storage performance with strong relaxor behavior, together with large polarization and distorted lattice calculated by first-principles calculations. The atomic-scale local structure analysis of 0.75Bi0.5Na0.5TiO3–0.25K0.5Na0.5NbO3 ceramic reveals distorted polarization distribution and small polar nanoregion related with the enhanced relaxation and low hysteresis. Finite element analysis demonstrates ultrafine grain and increased grain boundary density following hot-pressing sintering are crucial factors in significantly enhancing the breakdown strength (Eb). As a result, ultrahigh Wrec of 12.39 J/cm3 and η of 87.1 % are achieved at a superhigh Eb of 713 kV/cm. Encouragingly, excellent performance of temperature, frequency and fatigue stability at 400 kV/cm are obtained, and high power density of ∼ 306 MW/cm3 as well as fast discharge speed of ∼ 23.3 ns are also realized. This work proposes a simple binary design with strong relaxor behavior, and highlights the potential of grain engineering to achieve outstanding energy storage performance with great stability and excellent charge-discharge property for pulse power devices.

Excellent low-E energy storage and fluorescence temperature sensing features in Bi0.5Na0.5TiO3-based transparent ceramics

Transparent dielectric ceramics with ultrafast discharge rates and gigantic power densities are ideal candidates for transparent pulse capacitors (TPCs). However, the requirement of a high external electric field and inferior temperature stability hinder practical applications. (Bi0.5Na0.5)TiO3-based ceramics exhibit large polarization and two characteristic dielectric peaks, easy to obtain high energy-storage density under low electric fields (low-E) and maintain stable energy-storage performance (ESP) within a wide temperature range. However, their low optical transmittance (T%) limits their development into TPCs. In this work, to concurrently obtain high T% and excellent ESP and stability under low-E conditions, we propose a collaborative optimization strategy for determining the regulations of grain size, bandgap energy and domain structure. The results show that the pellucidity and energy-storage characteristics improve with decreasing grain and domain sizes. A relatively high T% of 45.6 % (at 710 nm) and recoverable energy-storage density (Wrec ∼ 3.46 J cm−3 at 197 kV cm−1) are obtained for the (1-x)[0.85(Bi0.5-3yNa0.5-yYb3yHoyTiO3)-0.15SrZrO3]-xBaHfO3 ceramics. Additionally, the dielectric temperature stability also results in splendid storage temperature stability (ΔWrec/Wrec < 3.1 % in the range of 0–200 °C). Importantly, codoping Ho/Yb in the ceramics induces excellent fluorescence temperature sensing feature. The multifunctional TPCs have application potential in the field of search and rescue signal transmission, providing ideas for developing novel optoelectronic devices.

Superior energy storage performance achieved in tungsten bronze SBCN-based ceramics through tape-casting

Simultaneously integrating outstanding energy storage density and good energy storage efficiency in advanced ferroelectrics is crucial to implementing the application of dielectrics in high-power pulse devices. In this work, (Sr0.5Ba0.5)2Ca0.5Nb5-xSbxO15 ceramics were designed and prepared by adopting the B sites substitution engineering together with combining strategies of tape-casting method and two-step sintering process. Benefiting from the refined grain size and high density, the breakdown field of (Sr0.5Ba0.5)2Ca0.5Nb4.8Sb0.2O15 (SBCNS0.2) was promoted to 400 kV/cm. By the substitution of Sb5+ in the B sites, the weaker interaction force of Sb-O bond in BO6 octahedral polar unit induced the occurrence of polar nanoregions (PNRs) at room temperature to strengthen the dielectric relaxation behavior. Then it is noteworthy that SBCNS0.2 ceramics simultaneously obtained excellent recoverable energy density (Wrec, 3.9 J/cm3), energy storage efficiency (η, 90.5 %), power density (PD, 156.0 MW/cm3), and current density (CD, 1356.7 A/cm2). In addition, the SBCNS0.2 ceramics exhibited an ultrafast discharge time (t0.9, 67 ns). These results reveal prospective potential of unfilled tungsten bronze SBCNS0.2 ceramics in power capacitor applications and provide an effective strategy for improving excellent energy storage properties from the perspective of preparation methods.

Superior dielectric energy storage performance of ultrafine-grained BNT-SBT solid-solution ceramics by solution combustion synthesis

The micrometer scale grain size and large remnant polarization of Bi0.5Na0.5TiO3 (BNT) ferroelectric ceramics severely constrain the breakdown strength and energy efficiency, respectively, restricting their energy storage application despite their large polarization. Hereby, superior energy storage performance is reported by a synergistic strategy of introducing Sr0.7Bi0.2TiO3 (SBT) relaxor ferroelectrics and a solution combustion synthesis (SCS) method. The BNT-SBT solid-solution ceramics are comparatively investigated by the two methods, conventional sintering (CS) and SCS. An ultrafine average grain size of ∼0.39 μm was obtained in the SCS-derived ceramic, and thus exhibits an ultra-high critical electric field of 548 kV/cm, and a high recoverable energy density of ∼5.69 J/cm3. Those key energy storage parameters are superior to those of the previous reported samples prepared by the CS method. Meanwhile, a high energy efficiency ∼90 %, a large power density of ∼130.44 MW/cm3 (at 320 kV/cm), and an ultrafast discharge time of ∼61.7 ns are also achieved. This study indicates that grain engineering combing with chemical design is an effective way to enhance the dielectric energy storage performance.

Ferroelectric and Relaxor-Ferroelectric Phases Coexisting Boosts Energy Storage Performance in (Bi0.5Na0.5)TiO3-Based Ceramics.

With the intensification of the energy crisis, it is urgent to vigorously develop new environment-friendly energy storage materials. In this work, coexisting ferroelectric and relaxor-ferroelectric phases at a nanoscale were constructed in Sr(Zn1/3Nb2/3)O3 (SZN)-modified (Bi0.5Na0.5)0.94Ba0.06TiO3 (BNBT) ceramics, simultaneously contributing to large polarization and breakdown electric field and giving rise to a superior energy storage performance. Herein, a high recoverable energy density (Wrec) of 5.0 J/cm3 with a conversion efficiency of 82% at 370 kV/cm, a practical discharged energy density (Wd) of 1.74 J/cm3 at 230 kV/cm, a large power density (PD) of 157.84 MW/cm3, and an ultrafast discharge speed (t0.9) of 40 ns were achieved in the 0.85BNBT-0.15SZN ceramics characterized by the coexistence of a rhombohedral-tetragonal phase (ferroelectric state) and a pseudo-cubic phase (relaxor-ferroelectric state). Furthermore, the 0.85BNBT-0.15SZN ceramics also exhibited excellent temperature stability (25-120 °C) and cycling stability (104 cycles) of their energy storage properties. These results demonstrate the great application potential of 0.85BNBT-0.15SZN ceramics in capacitive pulse energy storage devices.

Achieving enhanced energy storage performance and ultra-fast discharge time in tungsten–bronze ceramic

Achieving enhanced energy storage performance and ultra-fast discharge time in tungsten–bronze ceramic

Giant overall energy density performances via introducing aliovalent cations in BNT-based ferroelectric ceramics

The strategy of introducing aliovalent cations in the ferroelectric perovskites is the most promising for obtaining excellent overall energy storage density performances, simultaneously with good efficiency and thermal stability in dielectric ceramics for high pulse power technologies. Aliovalent cations could greatly enhance the short-range ferroelectric order (Polar nanoregions, PNRs), and local random field caused by vacancies, mismatch between size, electronic configuration, and other physical and chemical properties of aliovalent cations with the host perovskite. PNRs and local random field make the ceramic relaxor like with excellent overall energy storage density results such as total energy storage density (WT = 10.55 J/cm3, recoverable energy storage density Wrec = 7.82 J/cm3), power density (PD = 197 MW/cm3), current density (CD = 1312 A/cm2), and ultra-fast discharge rate (t = 24 ns) simultaneously with good working efficiency of 74 % by introducing 14 mol% of Bi(Zn1/3Nb2/3) aliovalent cations in the morphotropic phase boundary (MPB) (Bi0.47Na0.47)TiO3–0.06BaTiO3 composition. In addition, the same optimum sample also showed good thermal stability up to 240 °C, with <10–13 % variation in recoverable energy storage density and working efficiency respectively. The reason of excellent overall energy storage density, and their thermal stability in a broad temperature range might be due to short-range ferroelectric order, local random field, relaxor ferroelectric polymorphic phases, highly dense microstructure with small and uniform grains, as well as large band gape. Our study provides a good clue to obtain giant overall energy density results with good working efficiency and thermal stability in relaxor ferroelectric ceramics for high pulse power technology.

Pulsed THz radiation under ultrafast optical discharge of vacuum photodiode

In this paper, we first present an experimental demonstration of terahertz radiation pulse generation with energy up to 5 pJ under the electron emission during ultrafast optical discharge of a vacuum photodiode. We use a femtosecond optical excitation of metallic copper photocathode for the generation of ultrashort electron bunch and up to 45 kV/cm external electric field for the photo-emitted electron acceleration. Measurements of terahertz pulses energy as a function of emitted charge density, incidence angle of optical radiation and applied electric field have been provided. Spectral and polarization characteristics of generated terahertz pulses have also been studied. The proposed semi-analytical model and simulations in COMSOL Multiphysics prove the experimental data and allow for the optimization of experimental conditions aimed at flexible control of radiation parameters.Graphical

High Energy Storage Performance in BiFeO3-Based Lead-Free High-Entropy Ferroelectrics.

Dielectric capacitors are widely used in advanced electrical and electronic systems due to the rapid charge/discharge rates and high power density. High comprehensive energy storage properties are the ultimate ambition in the field of application achievements. Here, the high-entropy strategy is proposed to design and fabricate single-phase homogeneous (Bi0.5Ba0.1Sr0.1Ca0.2Na0.1)(Fe0.5Ti0.3Zr0.1Nb0.1)O3 ceramic, the hierarchical heterostructure including rhombohedral-tetragonal multiphase nanoclusters and locally disordered oxygen octahedral tilt can lead to the increased dielectric relaxation, diffused phase transition, diverse local polarization configurations, grain refinement, ultrasmall polar nanoregions, large random field, delayed polarization saturation and improved breakdown field. Accordingly, a giant Wrec ≈13.3 J cm-3 and a high η ≈78% at 66.4kV mm-1 can be simultaneously achieved in the lead-free high-entropy BiFeO3-based ceramic, showing an obvious advantage in overall energy-storage properties over BiFeO3-based lead-free ceramics. Moreover, an ultrafast discharge rate (t0.9 = 18ns) can be achieved at room temperature, concomitant with favorable temperature stability in the range of 20-160 °C, due to the enhanced diffuse phase transition and fast polarization response. This work provides a feasible pathway to design and generate dielectric materials exhibiting high comprehensive energy-storage performance.

Novel NaNbO3-based relaxors featuring ultrahigh energy storage performance

Ferroelectric ceramics with ultrahigh power density and fast charging/discharging are attracting increasing attention. The practical application of most antiferroelectric ceramics in current electronics is significantly limited by their poor recoverable energy storage density. Here, a novel system ceramic of (1-x) Na0.84Ca0.16Nb0.84Ti0.16O3-xBiZn2/3Nb1/3O3 (NCNT-xBZN) solid solutions, possessing a giant Wrec∼7.05 J cm−3 and excellent conversion efficiency (η)∼83.7% under 53 kV mm−1, was synthesized to exhibit superior stability with changing temperature, frequency and fatigue behavior, together with the large current density (CD=571.8 A cm−2), ultrahigh power density (PD=85.7 MW cm−3) and ultrafast discharge rate (∼200 ns). These outstanding properties are attributed to the phase transformation from the AFE R to the FE Q phase, accompanied by the smashing of sub-microdomains into polar nanoregions, as the BZN content raises. The experimental results disclose that the synergistic effect of the highly dynamic response of polar nanoregions and the local lattice distortion arising from the disruption of long-range polar ordering by heterovalent ion filling generates a delayed saturation polarization with a strong relaxor behavior, thereby optimizing the energy storage density. The unique combination, together with a simple synthesis strategy, offers a refreshing strategy for the development of dielectric materials.

Low diffusion barrier in black phosphorene/graphdiyne heterostructure for ultrafast Li-ion battery anode

Black phosphorene (BlackP) with low diffusion barriers has been extensively researched as one of the new Li-ion batteries (LIBs) anode materials. Nevertheless, the poor mechanical properties and elastic stiffness of BlackP obviously limit its practical application. Thus, owing to the excellent mechanical properties and good elastic stiffness exhibited by Graphdiyne (GDY), the BlackP/GDY Van der Waals (vdW) heterostructure was investigated in our study to overcome those disadvantages on the basis of the density functional theory (DFT). Our results suggest that the BlackP/GDY vdW heterostructure has favorable mechanical properties and high thermodynamic stability with a small lattice mismatch, which is owing to the synergistic effect existed in BlackP and GDY. Besides, the adsorption energy of Li adsorption on the BlackP/GDY vdW heterostructure evidently enhanced along with the changing of the heterostructure from semiconductor to metallic. Moreover, the maximum theoretical storage capacity (384.703 mA h/g) of the BlackP/GDY vdW heterostructure is larger than that of Graphite (372 mA h/g). Above all, the minimum diffusion barrier (0.083 eV) is extremely low, which is vital for achieving ultrafast charge and discharge rates. These favorable advantages suggest that the BlackP/GDY vdW heterostructure is a viable ultrafast LIBs anode material.

Ultrafast discharge properties and enhanced energy density in lead‐free NaNbO3‐based relaxor ferroelectric ceramics

AbstractNaNbO3‐based (NN) energy storage ceramics are known for exhibiting high maximum polarization (Pmax) and large recoverable energy density (Wrec). However, the huge energy loss density (Wloss) has been a limiting factor in improving energy storage performance. Therefore, a ternary system was designed to achieve both huge Wrec and efficiency (η). The combination of 0.35Bi(Zn0.5Ti0.5)O3–0.65BaTiO3 (BZTBT) was chosen to reduce grain size and disrupt the long‐range ordered domains, thereby inducing the polar‐nano‐regions to mitigate Wloss. The optimal performance was achieved with the 0.75NaNbO3–0.25(0.35Bi(Zn0.5Ti0.5)O3–0.65BaTiO3) (0.75NN–0.25BZTBT) ceramic, which exhibited a high Wrec = 2.68 J/cm3 and superior η = 82.7% under 310 kV/cm. Remarkably, the 0.75NN–0.25BZTBT ceramic displayed an exceptionally fast discharge time to 90%, t0.9 = 88 ns, coupled with a huge energy density Wd = 0.95 J/cm3. This study demonstrates the significant potential of 0.75NN–0.25BZTBT ceramic in the realm of energy storage and rapid charge–discharge applications.

Achieving improved dielectric energy storage properties and temperature stability in 0.91Na0.5Bi0.5TiO3-0.09K0.7La0.1NbO3 based ferroelectric ceramics by composition design and processing optimization

In this study, a ternary solid solution was designed by incorporating varying concentrations of the B-site composite perovskite Ba(Mg1/3Ta2/3)O3 (BMT) into 0.91Na0.5Bi0.5TiO3-0.09K0.7La0.1NbO3 (NBT-KLN-based) ferroelectric ceramics to optimize their energy storage performance. The introduction of BMT disrupted the long-range ordered state of the A/B site in the original perovskite structure, resulting in increased structural disorder and enhanced relaxor characteristics. The viscous polymer processing (VPP) method was employed to attain a significantly denser structure. The 0.10BMT-vpp ceramic has ultimately achieved optimal energy storage performance, along with exceptional temperature and frequency stability. It boasts a high dielectric breakdown strength (BDS) of 440 kV/cm, an ultra-high effective energy storage density (Wrec) of 6.7 J/cm3, and an energy storage efficiency (η) of 82%. Moreover, the 0.10BMT-vpp ceramic exhibits robust pulse performance, characterized by an ultra-fast discharge time (t0.9) of only 77 ns. Furthermore, within the temperature range of −66 °C–354 °C, the temperature coefficient of capacitance (TCC) of the 0.25BMT ceramics undergoes a variation of no more than ±15%, in compliance with X9R specifications (−55 °C–200 °C). The introduction of BMT endows NBT-KLN-based ceramics with remarkable temperature stability and comprehensive energy storage performance, making it a ceramic material with practical potential for industrial applications.

Excellent energy storage properties in BNT-based relaxor ceramics via composition optimization strategy

In this work, lead-free energy storage ceramics, (1−x)(0.95Bi0.5Na0.5TiO3-0.05Ba0.85Ca0.15Zr0.1Ti0.9O3)-xSr0.7La0.2SnO3 (BNT-BZCT-xSLS, x = 0.05, 0.10, 0.15, and 0.20), were prepared. The crystal structure, microstructure, dielectric properties, ferroelectric properties, energy storage properties, and charge-discharge performance of BNT-BZCT-xSLS were systematically studied. Among the products, BNT-BZCT-0.15SLS exhibited the highest energy storage performances (W = 2.95 J/cm3, W rec = 2.09 J/cm3, and η = 71%) due to its dense microstructure, finer grain size, and improved relaxation. Furthermore, the BNT-BZCT-0.15SLS also showed an ultra-fast charge and discharge speed (t0.9 = 0.033 μs) and a large power density (P D = 28.0 MW/cm3).

Ultrafast charge‐discharge and enhanced energy storage properties of lead‐free K0.5Na0.5NbO3‐based ceramics

AbstractFor dielectric capacitors in pulsed power systems, ultrafast charge‐discharge rates and good energy storage performances are essential. The relatively low efficiency η and the low energy density of potassium sodium niobate ceramics will restrict their applications. In this work, a local distortion of the crystal structure of ceramics is made by introducing the Bi and Ce ions, promoting the growth of polar nano‐regions, resulting in more obvious relaxation behavior and lower remnant polarization Pr. The average grain size is reduced, further increasing of breakdown strength. Eventually, fine comprehensive energy storage performances and good mechanical properties are simultaneously obtained. Enhanced recoverable energy storage density Wrec (∼5.30 J/cm3) and a high energy storage efficiency η (∼76.81%) are achieved in 0.970(K0.5Na0.5)NbO3‐0.030CeBiO3 (KNN‐0.030CB) ceramics with an ultrafast discharge rate t0.9 (31 ns) and a high current density (1008.5 A/cm2). All of these results indicate that this work provides a resultful way to design excellent comprehensive properties for advanced energy storage materials.

BaTiO3-based lead-free relaxor ferroelectric ceramics for high energy storage

Barium titanate (BaTiO3, BT) is widely used in capacitors because of its excellent dielectric properties. However, owing to its high remanent polarisation (Pr) and low dielectric breakdown field strength (Eb), achievement of high energy storage performance is challenging. Herein, a systematic strategy was proposed to reduce Pr and elevate Eb of BT via: (i) modification of the relaxor behavior by alloying it with Bi(Mg2/3Ta1/3)O3 (BMT) and (ii) heightening Eb by introducing NaTaO3 (NT) with high band gap. Consequently, the energy storage efficiency (η) of 90 % and high Eb of 780 kV cm−1 were achieved simultaneously for the BT-BMT-xNT system, which facilitated the recoverable energy density (Wrec) of 6.02 J cm−3. At 300 kV cm−1, its temperature (20–120 °C) and frequency (1–500 Hz) stabilities were found to be good. Moreover, the BT-BMT-0.15NT possessed ultrafast discharge rate (t0.9 < 51 ns) and ultrahigh power density (PD > 94 MW cm−3). This study offers an effective strategy for the design of novel high-performance dielectric energy storage materials.

Superior Energy Storage Capability and Fluorescence Negative Thermal Expansion of NaNbO3-Based Transparent Ceramics by Synergistic Optimization.

Transparent dielectric ceramics are splendid candidates for transparent pulse capacitors (TPCs) due to splendid cycle stability and large power density. However, the performance and service life of TPCs at present are threatened by overheating damage caused by dielectric loss. Here, a cooperative optimization strategy of microstructure control and superparaelectric regional regulation is proposed to simultaneously achieve excellent energy storage performance and real-time temperature monitoring function in NaNbO3-based ceramics. By introducing aliovalent ions and oxides with large bandgap energy, the size of polar nanoregions is continuously reduced. Due to the combined effect of increased relaxor behavior and fine grains, excellent comprehensive performances are obtained through doping appropriate amounts of Bi, Yb, Tm, and Zr, Ta, Hf in A- and B-sites of the NaNbO3 matrix, including recoverable energy storage density (5.39Jcm-3), extremely high energy storage efficiency (91.97%), ultra-fast discharge time (29ns), and superior optical transmittance (≈47.5% at 736nm). Additionally, the phenomenon of abnormal fluorescent negative thermal expansion is realized due to activation mechanism of surface phonon at high temperatures that can promote the formation of [Yb···O]-Tm3+ pairs, showing great potential in real-time temperature monitoring of TPCs. This research provides ideas for developing electronic devices with multiple functionalities.

Improved energy storage performance and thermal stability of hafnium-substituted strontium sodium niobate tungsten bronze ceramics.

Dielectric capacitors are widely used in the field of pulsed power systems owing to their ultra-fast charge and discharge capacity; however, considering the complex environment they face in practical applications, how to further improve their thermal stability is an urgent issue that needs to be solved. Tungsten bronzes have the potential to broaden the temperature stability range owing to their unique structure, but only few studies have focused on them. Herein, lead-free Sr4-x La x Na2Hf x Nb10-x O30 ceramics with a tungsten bronze structure were synthesized, and their energy storage properties were comprehensively characterized. With proper Hf substitution in the B site and rare earth substitution in the A site, significantly enhanced relaxor behavior is induced, leading to a broad plateau of the dielectric curve, slim polarization-electric field loop, high energy storage efficiency and stable capacitive performance over a wide temperature range. In addition, an improved microstructure with fewer defects, decreased average grain size, increased band gap and resistance were obtained, which benefit to the increase in breakdown strength and energy storage density. Finally, improved energy storage performance and thermal stability were achieved for the compounds, with W total = 3.6 J cm-3, W rec = 2.9 J cm-3, η = 80% and stable temperature range = 20-160 °C. Thus, the current system is a promising candidate for application in temperature-stable dielectric capacitors.