Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.
Nature Communications volume 15, Article number: 6754 (2024 ) Cite this article all film induction heating capacitor
Superparaelectrics are considered promising candidate materials for achieving superior energy storage capabilities. However, due to the complicated local structural design, simultaneously achieving high recoverable energy density (Wrec) and energy storage efficiency (η) under high electric fields remains a challenge in bulk superparaelectrics. Here, we propose utilizing entropy engineering to disrupt long-range ferroic orders into local polymorphic distortion disorder with multiple BO6 tilt types and diverse heterogeneous polarization configurations. This strategy reduces the switching barriers, thereby facilitating the emergence of superparaelectric behaviors with ideal polarization forms. Furthermore, it enables high polarization response, negligible remnant polarization, delayed polarization saturation, and enhanced breakdown electric fields (Eb) in high-entropy superparaelectrics. Consequently, an extraordinary Wrec of 15.48 J cm–3 and an ultrahigh η of 90.02% are achieved at a high Eb of 710 kV cm–1, surpassing the comprehensive energy storage performance of previously reported bulk superparaelectrics. This work demonstrates that entropy engineering is a viable strategy for designing high-performance superparaelectrics.
With an increasing international focus on environmental protection, efficient energy storage technologies have become a focal point of societal concern1,2,3. Dielectric ceramic capacitors, with their ultrafast charge/discharge rate and ultrahigh power density, are extensively studied as a potential solution for energy storage4,5,6. However, the relatively low recoverable energy density (Wrec) and energy storage efficiency (η) of dielectric ceramic capacitors hinder their development towards miniaturization and integration7,8,9. Therefore, there is an urgent need to develop lead-free bulk ceramics with both ultrahigh Wrec and η.
In recent years, numerous lead-free bulk ceramics have been developed for capacitive energy storage. For instance, high Wrec of 11.4 J cm–3 and 18.5 J cm–3 have been realized in AgNbO3 (AN)-based and NaNbO3 (NN)-based antiferroelectric (AFE) ceramics, respectively10,11. Nevertheless, their η values are capped at or below 80%, which is mainly caused by the AFE-ferroelectric (FE) phase transition. Similar low η phenomena are often observed in FEs or relaxor ferroelectrics (RFEs), such as K0.5Na0.5NbO3 (KNN)-based, Bi0.5K0.5TiO3 (BKT)-based, and BiFeO3 (BF)-based ceramics12,13,14. Although a high η (>90%) can be obtained in some linear dielectrics, such as CaTiO3 (CT)-based and SrTiO3 (ST)-based ceramics15,16,17,18, the relatively low intrinsic polarization leads to their Wrec usually being <7 J cm–3. In addition, although an increase in the electric field contributes to an enhancement of Wrec, it is usually accompanied by an increase in remnant polarization (Pr), hysteresis losses, and leakage currents, all of which have negative impacts on η7,19. Therefore, the trade-off between Wrec and η has become a primary challenge in designing high-performance dielectric ceramics.
Recently, superparaelectrics (SPEs) developed in RFEs have been considered as promising candidate materials for energy storage20,21,22. The state of SPEs appears within the temperature range from Tm (the temperature corresponding to the maximum dielectric constant) to TB (the Burns temperature) and is characterized by weakly coupled polar nanoregions (PNRs). Therefore, SPEs not only maintain a high maximum polarization (Pm) but also allow for flexible polarization redirection with small hysteresis, leading to a higher η compared to conventional RFEs. Based on SPE engineering23,24, Bi0.5Na0.5TiO3 (BNT)-based ceramics achieved a Wrec of 7.2 J cm–3 and a η of 86% at a breakdown electric field (Eb) of 430 kV cm–1, and further, BaTiO3-Bi0.5Na0.5TiO3-NaNbO3 (BT-BNT-NN) ternary ceramics reached a Wrec of 10.59 J cm–3 and a η of 87.6% at a relatively high Eb of 550 kV cm–1. Despite advancements in researching SPEs, the challenge of simultaneously achieving ultrahigh energy density (Wrec ≥ 15 J cm–3) and minimal losses (η ≥ 90%) under high electric fields in bulk SPEs persists due to the lack of precise local structural design. From a thermodynamic perspective, when the long-range FE order in RFE materials shrinks down to nanodomains (or PNRs), the switching energy barriers also decrease. As the energy barrier diminishes to a level comparable to or lower than the thermal disturbance energy (kBT, where kB represents the Boltzmann constant), nanodomains (or PNRs) can undergo flexible switching processes with minimal hysteresis, thus exhibiting ideal polarization form with SPE properties on the macroscopic scale25,26. In this sense, it should be feasible to design ideal SPEs by disrupting long-range FE order to construct flexible local polarization configurations, thereby lowering the switching energy barriers.
Here, we consider that entropy engineering has been demonstrated as an advanced strategy for regulating FE polarization in piezoelectric and energy storage dielectrics27,28,29,30. This is primarily due to the disordered component distribution leading to unmatched atomic size, mass, valence state, and electronegativity, which induce random local strain and electric fields, providing infinite possibilities for tuning the local polarization configurations. Therefore, we design high-entropy SPEs with superior comprehensive energy storage performance through entropy engineering, as shown in Fig. 1. To ensure a large polarization response, Bi0.47Na0.47Ba0.06TiO3 (BNBT), known for its high polarization characteristics, is selected as the base material. The coexistence of tetragonal (T) and rhombohedral (R) phases in BNBT can reduce polarization anisotropy and promote polarization rotation, thereby lowering the switching energy barriers. Meanwhile, Sr0.7La0.2Ta0.2Ti0.75O3 (SLTT) is added to BNBT to regulate configuration entropy (Sconfig) and create the (1 – x)BNBT-xSLTT system (abbreviated as SLTT-x). The high-entropy effect, combined with the small Pr, the low hysteresis loss of SrTiO3, and the large bandgap (Eg) of La2O3 (5.0 eV) and Ta2O5 (4.0 eV), further enhances the energy storage performance. Through entropy engineering, the long-range order is effectively disrupted, resulting in the formation of locally diverse ferroic distortions. These distortions encompass rich heterogeneous polarization configurations of R, T, and monoclinic (M)-like phases embedded in a cubic (C) matrix, as well as in-phase tilted, anti-phase tilted, and non-tilted BO6 types. The induction of these heterogeneous configurations leads to the eventual realization of ideal SPE behavior, while the engineered multiple BO6 tilt types effectively prevent premature polarization saturation. As expected, the high-entropy SPE (SLTT-0.30) exhibits a slender P-E loop at a large Eb of 710 kV cm–1, yielding an impressive Wrec of 15.48 J cm–3 and an ultrahigh η of 90.02%. These results signify a breakthrough in achieving superior energy storage capacities for bulk SPE ceramics.
Schematic diagram of using entropy engineering to achieve excellent comprehensive energy storage performance.
As shown in Supplementary Table 1, the Sconfig values of the SLTT-x system are 0.88 R (x = 0), 1.47 R (x = 0.20), 1.54 R (x = 0.25), 1.61 R (x = 0.30), and 1.66 R (x = 0.35), respectively. Supplementary Fig. 1 illustrates the entropy-dependent dielectric properties. When Sconfig reaches 1.61 (SLTT-0.30) and 1.66 R (SLTT-0.35), the Tm drops below room temperature, indicating that both samples have reached room temperature SPE states. Supplementary Fig. 2 shows the unipolar P-E loops of SLTT-x under low applied electric fields. As Sconfig increases, the P-E loops become thinner, which signifies a transition from RFE to SPE. The overall energy storage performance under the same electric field is evaluated by the figure of merit WF = Wrec/(1 – η)31, as depicted in Supplementary Fig. 2c. SLTT-0.30 high-entropy SPE achieves the optimal WF of 44.17, which is attributed to its high Wrec and η, thus highlighting its excellent potential for energy storage compared to SLTT-0.35.
X-ray diffraction (XRD) reveals that all SLTT-x ceramics possess a typical perovskite structure without impurities (Supplementary Fig. 3). The refinement results and phase compositions obtained by Rietveld refinement via GSAS-II software are shown in Supplementary Fig. 432. SLTT-x ceramics exhibit a phase structure in which the R and T phases coexist. As x increases, the proportion of R phase decreases and the proportion of T phase increases. Supplementary Fig. 5 shows the Raman spectra of SLTT-x ceramics. Characteristic variations of the peaks related to cation disorder and BO6 octahedral distortion are observed33,34. Moreover, double splitting is detected in both B–O bond (200–400 cm–1) and BO6 octahedral (400–700 cm–1) vibrational modes, further indicating the coexistence of R phase and T phase in SLTT-x ceramics35. Figure 2a, b and Supplementary Fig. 6 show the transmission electron microscope (TEM) images and selected area electron diffraction (SAED) patterns of the SLTT-0.30 ceramic along the [100]c and [110]c directions. The absence of the large-scale ferroelectric domain in both the low-magnification and high-resolution TEM images points to the lack of both long-range polarization and BO6 tilt order. The SAED patterns exhibit 1/2(ooe) type superlattice diffraction dots caused by the in-phase tilt of the oxygen octahedron and 1/2(ooo) type superlattice diffraction points caused by the anti-phase tilt of the oxygen octahedron, respectively36,37. These results demonstrate that different localized BO6 tilt types are induced in SLTT-0.30 ceramic, which can impede the appearance of electric field-induced texture domain states, thereby delaying polarization saturation27.
High-resolution TEM images and SAED patterns along (a) [100]c and (b) [110]c. c High-resolution TEM image and (d, e) corresponding inverse fast Fourier transform patterns. f Out-of-plane PFM phase image after ± 30 V poling treatment and corresponding piezoresponse phase profile generated from the line scan. g HAADF-STEM polarization vector image recorded along [100]c. h–j The magnified images of the labeled region in (g). The insets show the (h) anti-phase tilted, (i) in-phase tilted, and (j) non-tilted modes of the oxygen octahedron. k Statistical distribution of the amplitude and angle of the polarization vector. l Quantitative analysis of polarization angle. m Quantitative analysis of polarization amplitude.
High-resolution TEM image in Fig. 2c and the corresponding inverse Fourier transform patterns in Fig. 2d, e of SLTT-0.30 ceramics display pronounced local lattice distortions and PNRs38. The presence of these small-sized PNRs is further confirmed by piezoresponse force microscopy (PFM), as illustrated in Fig. 2f. The PFM image after poling treatment with ±30 V of SLTT-0.30 ceramic shows no domain switching and no abrupt change in the corresponding phase profile. This observation contrasts with the PFM images and phase profile of SLTT-0 ceramic (Supplementary Fig. 7), proving the formation of the highly dynamic PNRs in SLTT-0.30 ceramic12,39,40. In high-entropy systems, the introduction of foreign ions with different properties enhances the local random field, which can disrupt the long-range order into small-sized PNRs, a phenomenon that provides for lowering the switching energy barriers as well as modulating the polarization configuration in polymorphic phase coexistence systems. Moreover, the presence of highly dynamic PNRs suppresses the heat induced by polarization rotation and carrier migration in the electric field, which contributes to an improved Eb and reduced energy loss.
In order to characterize the local structure in more detail and accuracy, high-resolution scanning TEM with high-angle annular dark-field imaging (HAADF-STEM) is performed on SLTT-0.30 ceramic. The displacement of the B (A) site cation from the four nearest neighboring A (B) site cation centers in the HAADF-STEM images can describe the local polarization41. The polarization vector mappings of the A-site and B-site atoms are shown in Supplementary Fig. 8a, b, respectively. Different colors and lengths of arrows are further used to represent the direction and magnitude of the polarization vector, as depicted in Fig. 2g. Inter-nested polar and non-polar clusters are observed. Magnified images of the marked regions in Fig. 2g show the R phase, T phase, and C phase regions, as well as the corresponding anti-phase tilt, in-phase tilt, and non-tilt models of the BO6 octahedron, respectively (Fig. 2h–j). The C phase can also be identified from the dark blue region in the polarization amplitude mapping (Supplementary Fig. 8c), which not only reduces the internal stresses when applying an electric field, but also promotes rapid polarization recovery after unloading the electric field42. In addition, transition regions independent of the R, C, and T phases are detected, which can be further demonstrated in the statistical distribution of polarization vectors (Fig. 2k) and the polarization angle mapping (Supplementary Fig. 8d). Such transition regions are considered to be M-like symmetries with different vector angles and amplitudes28,43,44. The random distribution of local C-R-T-M-like phases indicates the decrease in polarization anisotropy and the existence of a strongly perturbed random field27,45,46,47, which can effectively reduce the switching energy barriers and thereby lead to ideal macroscopic SPE behavior. To quantitatively study the distribution of polarization vectors, the polarization angle is transformed to a range from 0° (T phase) to 45° (R phase) based on the projection direction and unit cell symmetry, as displayed in Fig. 2l. The number of polarization vectors at each angle is almost equal, which not only reaffirms the weak polarization anisotropy but also further confirms the existence of M-like configurations with multiple vector angles. Furthermore, the weak ferroelectricity with a small average ferroelectric displacement (~2.9 pm) suggests that the polarization configurations exhibit weakly coupled characteristics, as illustrated in Fig. 2m.
The high-entropy effect leads to significant differences in atom size, mass, valence state, and electronegativity, amplifying local structure disorder and causing random local fields. This phenomenon disrupts long-range ferroic order into locally diverse ferroic distortion with multiple BO6 tilt types and rich heterogeneous configurations. The BO6 tilt types can hinder the formation of electric field-induced long-range polarization. Locally interconnected C-R-T-M-like phases can drastically reduce the polarization anisotropy, thereby reducing the switching barrier, resulting in a flatter switching pathway and minimizing the hysteresis loss in the SPEs. Moreover, diverse polarization configurations can also increase the polarization direction and intensity, providing a strong polarization response.
Figure 3a illustrates the slim unipolar P-E loops of SLTT-0.30 high-entropy SPE, indicating the insensitivity of the Pr to the electric field. Remarkably, a high Pm of 57.36 μC cm–2 and a low Pr of 2.52 μC cm–2 are achieved at a large Eb of 710 kV cm–1. The realization of these energy storage-friendly parameters is attributed to the design of local ferroic distortion. The high Eb is also associated with entropy-induced lattice distortion, small average grain size (Ga), clear and dense grain boundaries, wide Eg, and ultralow dielectric loss (tanδ) (Supplementary Fig. 9)48. We further simulate the electric field distribution, electric potential distribution, and electric tree evolution of SLTT-0 and SLTT-0.30 samples under applied electric fields, respectively. As depicted in Supplementary Fig. 10, the SLTT-0.30 high-entropy SPE not only exhibits more uniform potential and electric field distributions but also more effectively hinders electric tree propagation compared to the SLTT-0 sample. This is associated with the uniform grain distribution, higher grain boundary density, and lower dielectric constant (εr) in the SLTT-0.30 sample49,50. The reliability of Eb is verified using Weibull distribution analysis, as shown in Supplementary Fig. 11. The Weibull modulus (β) of the SLTT-0.3 sample is 19.8, indicating that the sample possesses high reliability and homogeneity51. The calculated Eb is 725.6 kV cm–1, which is very close to the Eb obtained in the P-E loop. Figure 3b displays the increase of electric field from 100 kV cm–1 to 710 kV cm–1 with an approximately parabolic increase in both the total energy density (Wtot) and Wrec, while η is consistently >90%. Consequently, the SLTT-0.30 high-entropy SPE achieves a “dual high” performance with Wrec of ~15.48 J cm–3 and η of ~90.02%, which is a significant improvement in performance compared to the SLTT-0 ceramic (Sconfig increased by 82%, Eb increased by 610%, Wrec increased by 1885%, and η increased by 175%), as shown in Fig. 3c. Importantly, compared to reported bulk SPEs, RFEs, AFEs, high-entropy ceramics, and linear dielectrics, SLTT-0.30 high-entropy SPE exhibits a greater advantage in comprehensive energy storage performance (Fig. 3d and Supplementary Table 2). Furthermore, compared to these lead-free ceramics with η > 90%, the SLTT-0.30 high-entropy SPE shows a higher Wrec (Fig. 3e and Supplementary Table 2). These results suggest a breakthrough in overcoming the bottleneck of simultaneously achieving high Wrec and low energy loss under high electric fields.
a Electric field-dependent unipolar P-E loops of SLTT-0.30 ceramic. b Calculated Wrec, Wtot and η of SLTT-0.30 ceramic. c Comparison of Sconfig, Wrec, η, and Eb between SLTT-0 and SLTT-0.30 ceramics. d Comparison of Wrec and η between SLTT-0.30 and reported lead-free bulk ceramics. e Comparison of Wrec between SLTT-0.30 and reported lead-free bulk ceramics with a η > 90%.
In situ Raman spectra are measured to evaluate the temperature-dependent structural properties of SLTT-0.30 high-entropy SPE. As depicted in Fig. 4a, the deconvolution results indicate that the number of Raman peaks remains constant with increasing temperature, suggesting the local symmetry is maintained over a wide temperature range. The intensity of the peaks at ~291 cm–1 and ~510 cm–1 decreases, along with an increase in full width at half maximum (FWHM) and a gradual shift towards lower wavenumbers (Fig. 4b, c). This phenomenon demonstrates an increase in structural disorder, which helps suppress the increase of Pr during a rise in temperature52,53. In situ XRD measurements from 25 °C to 250 °C are also used to investigate the stability of SLTT-0.30 ceramic. As shown in Fig. 4d, e, the (111) and (200) peaks both remain in their initial states without significant splitting or merging, proving the structural stability of SLTT-0.30 ceramic54. As illustrated in Supplementary Fig. 12, the SLTT-0.30 ceramic is in the SPE state over a wide temperature range from Tm of ~20.3 °C to TB of ~347.3 °C, which guarantees excellent temperature stability. As observed in Supplementary Fig. 13, the εr and tanδ of SLTT-0.30 ceramic fluctuate weakly with frequency, favoring the realization of frequency-insensitive energy storage performance. Furthermore, the entropy-induced polymorphic PNRs weaken the inter-coupling effect, lower the switching barrier, and promote the polarization rotation. Thus, these PNRs can respond quickly to the applied electric field, leading to enhanced stability43,51. Benefiting from these synergistic effects, the energy storage performance of SLTT-0.30 ceramic demonstrates excellent stability at different temperatures and frequencies. As illustrated in Supplementary Fig. 14a, b, the unipolar P-E loops maintain slim shapes at different temperatures and frequencies. Therefore, the SLTT-0.30 ceramic achieves superior temperature insensitivity over the temperature range of 25–175 °C, with Wrec ≈ 6.59 ± 0.51 J cm–3 and η ≈ 90.55 ± 2.84% (Fig. 4f). It also exhibits significant frequency insensitivity over the frequency range of 1–500 Hz, with Wrec ≈ 7.43 ± 0.22 J cm–3 and η ≈ 87.58 ± 0.91% (Supplementary Fig. 14c). These superior stabilities are superior to most reported high-performance lead-free bulk ceramics32,34,55,56,57,58.
a Temperature-dependent in situ Raman spectra of SLTT-0.30 ceramic. The variations in peak intensity, wavenumber, and FWHM of the peak at (b) 291 cm–1 and (c) 510 cm–1. d Temperature dependence of the (111) and (200) peaks in situ XRD of SLTT-0.30 ceramic. e Contour maps of the (111) and (200) peaks of SLTT-0.30 ceramic. f Temperature-dependent Wrec and η of SLTT-0.30 ceramic at 400 kV cm–1.
Supplementary Fig. 15 shows the excellent charge-discharge properties of the SLTT-0.30 high-entropy SPE. It achieves a high discharge energy density (Wdis = 2.37 J cm–3) in an ultrafast time (t0.9 = 33 ns) under 320 kV cm–1. The maximum current (Imax), current density (CD), and power density (PD) reach 19.5 A, 621.7 A cm–2, and 93.3 MW cm–3 under an electric field of 300 kV cm–1, respectively. Additionally, the charge-discharge parameters demonstrate excellent temperature stability at 240 kV cm–1. Minimal change in performance even at temperatures from 25 °C – 150 °C, with Wdis ≈ 1.42 ± 0.05 J cm–3, t0.9 ≈ 31 ± 2 ns, Imax ≈ 13.37 ± 0.02 A, CD ≈ 425.56 ± 0.78 A cm–2, and PD ≈ 46.83 ± 0.09 MW cm–3. Overall, the SLTT-0.30 ceramic shows great promise as a dielectric for energy storage capacitors due to its stability and impressive charge-discharge performance.
In summary, a lead-free bulk SPE has been developed using entropy engineering, demonstrating exceptional comprehensive energy storage performance with a large Wrec of ~15.48 J cm–3 and an ultrahigh η of ~90.02% at 710 kV cm–1. This performance represents the best reported to date for bulk SPEs. Moreover, the high-entropy SPE exhibits remarkable temperature stability, frequency stability, and superior charge-discharge performance. The impressive performance is attributed to the induction of locally diverse ferroic distortion by entropy engineering, including various BO6 tilt types and heterogeneous symmetries, resulting in a room temperature SPE state with simultaneous lower Pr, improved Eb, and delayed polarization saturation. This work provides valuable insights into the interplay between entropy engineering, SPE behavior, local structure, and energy storage performance.
The (1 – x)BNBT-xSLTT system (abbreviated as SLTT-x, x = 0, 0.20, 0.25, 0.30, 0.35) was fabricated by raw powders of Bi2O3 (purity of ≥99%), Na2CO3 (purity of 99.99%), BaCO3 (purity of 99.8%), TiO2 (purity of 99.5%), SrCO3 (purity of 99.5%), La2O3 (purity of 99.9%), and Ta2O5 (purity of 99.5%) through a conventional solid-state reaction. The corresponding raw material powders were weighed according to the chemical formulas of BNBT and SLTT, with 1 mol% of Bi2O3 and Na2CO3 added to BNBT to prevent the volatilization of Bi and Na. The BNBT and SLTT raw material powders were dispersed for 18 h by ball milling with zirconia balls in ethanol, respectively, and then dried. The dried BNBT slurry was calcined at 850 °C for 5 h, while the dried SLTT slurry was calcined at 1000 °C for 5 h. Subsequently, the calcined powders of both materials were mixed and ball-milled for 20 h, followed by drying. The dried powder was mixed with polyvinyl alcohol (PVA) binder and pressed into pellets with a diameter of ~10 mm and a thickness of ~1 mm. The pellets were held at 600 °C for 3 h to volatilize PVA, then sintered at 1050–1180 °C for 2 h to obtain ceramic samples.
The phase structures of the ceramics at room temperature were examined by X-ray powder diffraction (XRD, Philips X’Pert Pro MPD, Netherlands). The surface microstructure of the ceramics after thinning, polishing, and thermal etching was analyzed using field emission scanning electron microscopy (SEM, FEI, Quanta FEG250, USA). Selected area electron diffraction (SAED), domain morphology, and lattice fringes were examined by transmission electron microscopy (TEM, JEOL, JEM-2100, Japan). The response of domain structure to electric fields was characterized using piezoresponse force microscopy (PFM, Asylum Research, MFP-3D-Infinity, USA). The local structure of well-polished ceramics was analyzed by a Raman scattering spectrometer (Renishaw, inViaTM, UK). To analyze temperature-dependent structural properties, Raman spectra were obtained using a Raman spectrometer (Horiba Jobin Yvon HR800, France) with a heating stage (Linkam, THM 600, UK) under 532 nm excitation, ranging from 25 °C to 250 °C, on the polished SLTT-0.30 ceramic samples. Additionally, temperature-dependent X-ray diffraction (XRD) of SLTT-0.30 ceramic was obtained using CuKα radiation at temperatures ranging from 25 °C to 250 °C with an XRD instrument (X’pert PRO, PANalytical, Netherlands). To analyze polarization vectors, amplitudes, and angles, high-angle annular dark-field (HAADF) atomic-scale images of the SLTT-0.30 ceramic were obtained using atomic-resolution STEM (aberration-corrected Titan Themis 3300), and custom MATLAB scripts were employed for analysis.
For energy storage measurements, the samples were thinned and polished to ~0.05 ± 0.01 mm thickness, and gold electrodes with a diameter of 1.5 mm were prepared on their surfaces using ion sputtering. The ferroelectric analyzer (Aix ACCT, TF analyzer 1000, Germany) was utilized to measure the unipolar P-E loops at room temperature and 10 Hz frequency. Additionally, the same equipment was employed to measure unipolar P-E loops at different temperatures and frequencies to calculate the temperature-dependent and frequency-dependent energy storage performance. The dielectric properties were tested by a dielectric analysis instrument (Tongguo Technology, HCT1821, China). The charge-discharge performance of the ceramics were investigated using a charge-discharge tester (Tongguo Technology, CFD-003, China).
To obtain the bandgap of the samples, the absorption spectra ranging from 200 to 800 nm wavelength were measured using an ultraviolet-visible (UV-Vis) spectrophotometer (Cary 5000; Agilent, USA).
Details of the finite element simulation are elaborated in the Supplementary information.
All data supporting this study and its findings are available within the article and its Supplementary Information. Any data deemed relevant are available from the corresponding author upon request.
Chen, J. et al. Ladderphane copolymers for high-temperature capacitive energy storage. Nature 615, 62–66 (2023).
Article ADS CAS PubMed Google Scholar
Kim, J. et al. Ultrahigh capacitive energy density in ion-bombarded relaxor ferroelectric films. Science 369, 81–84 (2020).
Article ADS CAS PubMed Google Scholar
Peddigari, M. et al. Giant energy density via mechanically tailored relaxor ferroelectric behavior of PZT thick film. Adv. Mater. 9, 2302554 (2023).
Li, J. et al. Grain-orientation-engineered multilayer ceramic capacitors for energy storage applications. Nat. Mater. 19, 999–1005 (2020).
Article ADS CAS PubMed Google Scholar
Yang, L. et al. Perovskite lead-free dielectrics for energy storage applications. Prog. Mater. Sci. 102, 72–108 (2019).
Li, J. et al. Multilayer lead‐free ceramic capacitors with ultrahigh energy density and efficiency. Adv. Mater. 30, 1802155 (2018).
Zhao, P. et al. High-performance relaxor ferroelectric materials for energy storage applications. Adv. Energy Mater. 9, 1803048 (2019).
Wang, G. et al. Electroceramics for high-energy density capacitors: current status and future perspectives. Chem. Rev. 121, 6124–6172 (2021).
Article CAS PubMed PubMed Central Google Scholar
Luo, H. et al. Outstanding energy-storage density together with efficiency of above 90% via local structure design. J. Am. Chem. Soc. 146, 460–467 (2024).
Article CAS PubMed Google Scholar
Chen, L. et al. Compromise optimized superior energy storage performance in lead‐free antiferroelectrics by antiferroelectricity modulation and nanodomain engineering. Small 20, 2306486 (2023).
Jiang, J. et al. Ultrahigh energy storage density in lead-free relaxor antiferroelectric ceramics via domain engineering. Energy Storage Mater. 43, 383–390 (2021).
Wang, H. et al. Significantly enhanced energy storage performance in high hardness BKT-based ceramic via defect engineering and relaxor tuning. ACS Appl. Mater. Interfaces 14, 54021–54033 (2022).
Article CAS PubMed Google Scholar
Chai, Q. et al. Superior energy storage properties and optical transparency in K0.5Na0.5NbO3-based dielectric ceramics via multiple synergistic strategies. Small 19, 2207464 (2023).
Wang, M. et al. Energy storage properties under moderate electric fields in BiFeO3-based lead-free relaxor ferroelectric ceramics. Chem. Eng. J. 440, 135789 (2022).
Liu, J. et al. A synergistic two-step optimization design enables high capacitive energy storage in lead-free Sr0.7Bi0.2TiO3-based relaxor ferroelectric ceramics. J. Mater. Chem. A 11, 609–620 (2023).
Article ADS CAS Google Scholar
Liu, L. et al. Multi-scale collaborative optimization of SrTiO3-based energy storage ceramics with high performance and excellent stability. Nano Energy 109, 108275 (2023).
Li, C. et al. Superior energy storage capability and stability in lead-free relaxors for dielectric capacitors utilizing nanoscale polarization heterogeneous regions. Small 19, 2206662 (2023).
Pu, Y. et al. Enhancing the energy storage properties of Ca0.5Sr0.5TiO3-based lead-free linear dielectric ceramics with excellent stability through regulating grain boundary defects. J. Mater. Chem. C. 7, 14384–14393 (2019).
Sun, Z. et al. Strong local polarization fluctuations enabled high electrostatic energy storage in Pb-free. Relaxors. J. Am. Chem. Soc. 146, 13467–13476 (2024).
Article CAS PubMed Google Scholar
Wang, K. et al. Superparaelectric (Ba0.95,Sr0.05)(Zr0.2,Ti0.8)O3 ultracapacitors. Adv. Energy Mater. 10, 2001778 (2020).
Pan, H. et al. Ultrahigh energy storage in superparaelectric relaxor ferroelectrics. Science 374, 100–104 (2021).
Article ADS CAS PubMed Google Scholar
Chu, Y.-H. et al. The superparaelectric battery. Science 374, 33–344 (2021).
Article ADS CAS PubMed Google Scholar
Zheng, Q. et al. Remarkable energy storage properties in (Bi0.5Na0.5)TiO3-based quasilinear relaxor ferroelectrics via superparaelectric regulation. Chem. Eng. J. 483, 149154 (2024).
Chen, L. et al. Local diverse polarization optimized comprehensive energy-storage performance in lead-free superparaelectrics. Adv. Mater. 34, 2205787 (2022).
Lan, S. et al. Constructing superparaelectric polar structure for dielectric energy storage. Appl. Phys. Lett. 124, 090501 (2024).
Article ADS CAS Google Scholar
Bell, A. Calculations of dielectric properties from the superparaelectric model of relaxors. J. Phys. Condens. Matter 5, 8773 (1993).
Article ADS CAS Google Scholar
Chen, L. et al. Giant energy-storage density with ultrahigh efficiency in lead-free relaxors via high-entropy design. Nat. Commun. 13, 3089 (2022).
Article ADS CAS PubMed PubMed Central Google Scholar
Liu, Y. et al. Flexible polarization configuration in high-entropy piezoelectrics with high performance. Acta Mater. 236, 118115 (2022).
Qiao, W. et al. High-performance energy storage in BNST-based lead-free ferroelectric ceramics achieved through high-entropy engineering. Chem. Eng. J. 477, 147167 (2023).
Yang, B. et al. High-entropy enhanced capacitive energy storage. Nat. Mater. 21, 1074–1080 (2022).
Article ADS CAS PubMed Google Scholar
Yang, B. et al. Engineering relaxors by entropy for high energy storage performance. Nat. Energy 8, 956–964 (2023).
Article ADS CAS Google Scholar
Li, D. et al. Lead-free relaxor ferroelectric ceramics with ultrahigh energy storage densities via polymorphic polar nanoregions design. Small 19, 2206958 (2022).
Yan, F. et al. Superior energy storage properties and excellent stability achieved in environment-friendly ferroelectrics via composition design strategy. Nano Energy 75, 105012 (2020).
Yan, F. et al. Optimization of polarization and electric field of bismuth ferrite-based ceramics for capacitor applications. Chem. Eng. J. 417, 127945 (2021).
Wang, Z. et al. (Bi0.5Na0.5)TiO3-based relaxor ferroelectrics with medium permittivity featuring enhanced energy-storage density and excellent thermal stability. Chem. Eng. J. 427, 131989 (2022).
Jo, W. et al. On the phase identity and its thermal evolution of lead free (Bi1/2Na1/2)TiO3-6 mol% BaTiO3. J. Appl. Phys. 110, 074106 (2011).
Ma, Q. et al. Excellent energy‐storage performance in lead‐free capacitors with highly dynamic polarization heterogeneous nanoregions. Small 19, 2303768 (2023).
Liu, H. et al. Local chemical clustering enabled ultrahigh capacitive energy storage in Pb-free relaxors. J. Am. Chem. Soc. 145, 19396–19404 (2023).
Article CAS PubMed Google Scholar
Kang, R. et al. Enhanced energy storage performance in Sr0.7La0.2Zr0.15Ti0.85O3-modified Bi0.5Na0.5TiO3 ceramics via constructing local phase coexistence. Chem. Eng. J. 446, 137105 (2022).
Article ADS CAS Google Scholar
Qi, H. et al. Superior energy‐storage capacitors with simultaneously giant energy density and efficiency using nanodomain engineered BiFeO3‐BaTiO3‐NaNbO3 lead‐free bulk ferroelectrics. Adv. Energy Mater. 10, 1903338 (2019).
Sun, Z. et al. Superior capacitive energy-storage performance in Pb-free relaxors with a simple chemical composition. J. Am. Chem. Soc. 145, 6194–6202 (2023).
Article CAS PubMed Google Scholar
Chen, L. et al. Near‐zero energy consumption capacitors by controlling inhomogeneous polarization configuration. Adv. Mater. 36, 2313285 (2024).
Zhang, Y. et al. High‐performance ferroelectric based materials via high‐entropy strategy: design, properties, and mechanism. InfoMat 5, 12488 (2023).
Zhang, Y. et al. Ultrahigh piezoelectric performance benefiting from quasi-isotropic local polarization distribution in complex lead-based perovskite. Nano Energy 104, 107910 (2022).
Li, D. et al. A high-temperature performing and near-zero energy loss lead-free ceramic capacitor. Energy Environ. Sci. 16, 4511–4521 (2023).
Guo, J. et al. Multi-symmetry high-entropy relaxor ferroelectric with giant capacitive energy storage. Nano Energy 112, 108458 (2023).
Zhao, W. et al. Broad-high operating temperature range and enhanced energy storage performances in lead-free ferroelectrics. Nat. Commun. 14, 5725 (2023).
Article ADS CAS PubMed PubMed Central Google Scholar
Liu, J. et al. Giant comprehensive capacitive energy storage in lead-free quasi-linear relaxor ferroelectrics via local heterogeneous polarization configuration. J. Mater. Chem. A 11, 15931–15942 (2023).
Article ADS CAS Google Scholar
Chen, L. et al. Large energy capacitive high-entropy lead-free ferroelectrics. Nano Micro Lett. 15, 65 (2023).
Wang, W. et al. Enhancing energy storage performance in Na0.5Bi0.5TiO3-based lead-free relaxor ferroelectric ceramics along a stepwise optimization route. J. Mater. Chem. A 11, 2641–2651 (2023).
Zhang, M. et al. Ultrahigh energy storage in high-entropy ceramic capacitors with polymorphic relaxor phase. Science 384, 185–189 (2024).
Article ADS CAS PubMed Google Scholar
Xie, A. et al. NaNbO3-(Bi0.5Li0.5)TiO3 lead-free relaxor ferroelectric capacitors with superior energy-storage performances via multiple synergistic design. Adv. Energy Mater. 11, 2101378 (2021).
Zhang, Y. et al. Superior energy-storage properties in Bi0.5Na0.5TiO3-based lead-free ceramics via simultaneously manipulating multiscale structure and field-induced structure transition. ACS Appl. Mater. Interfaces 14, 40043–40051 (2022).
Article CAS PubMed Google Scholar
Zhao, J. et al. Delayed polarization saturation induced superior energy storage capability of BiFeO3-based ceramics via introduction of non-isovalent ions. Small 19, 2206840 (2023).
Luo, N. et al. Constructing phase boundary in AgNbO3 antiferroelectrics: pathway simultaneously achieving high energy density and efficiency. Nat. Commun. 11, 4824 (2020).
Article ADS CAS PubMed PubMed Central Google Scholar
Li, S. et al. Giant energy density and high efficiency achieved in silver niobate-based lead-free antiferroelectric ceramic capacitors via domain engineering. Energy Storage Mater. 34, 417–426 (2021).
Chen, L. et al. Outstanding energy storage performance in high‐hardness(Bi0.5K0.5)TiO3‐based lead‐free relaxors via multi‐scale synergistic design. Adv. Funct. Mater. 32, 2110478 (2022).
Chen, Z. et al. Phase engineering in NaNbO3 antiferroelectrics for high energy storage density. J. Materiomics. 8, 753–762 (2022).
This work was supported by the National Natural Science Foundation of China (No.52102129, H.L.), the Hunan Provincial Natural Science Foundation of China (No.2023JJ30138, H.L.), the Science and Technology Innovation Program of Hunan Province (2023RC3094, H.L.), and the Shenzhen Science and Technology Program (Grant No. RCYX20200714114733204 and JCYJ20200109115219157, G.K.Z.).
College of Electrical and Information Engineering, Hunan University, Changsha, 410082, China
Jianhong Duan, Kun Wei, Qianbiao Du, Linzhao Ma & Hao Li
Beijing Advanced Innovation Center for Materials Genome Engineering, Department of Physical Chemistry, University of Science and Technology Beijing, Beijing, 100083, China
Huifen Yu & He Qi
Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China
Yangchun Tan & Gaokuo Zhong
You can also search for this author in PubMed Google Scholar
You can also search for this author in PubMed Google Scholar
You can also search for this author in PubMed Google Scholar
You can also search for this author in PubMed Google Scholar
You can also search for this author in PubMed Google Scholar
You can also search for this author in PubMed Google Scholar
You can also search for this author in PubMed Google Scholar
You can also search for this author in PubMed Google Scholar
You can also search for this author in PubMed Google Scholar
This work was conceived and designed by J.H.D., H.Q., G.K.Z., and H.L. Sample fabrication was performed by J.H.D. and K.W., who also conducted energy storage, dielectric, and charge-discharge performance tests, as well as analyzed relevant data. Finite element simulations of breakdown characteristics were conducted by H.F.Y. SEM and Raman spectroscopy were performed by H.L. and L.Z.M. UV-Vis data was collected and processed by H.L. PFM images were captured and processed by G.K.Z. HAADF-STEM imaging was carried out by H.Q. and processed accordingly. Temperature-dependent Raman and XRD data were collected by H.Q. and analyzed by J.H.D. XRD testing and corresponding data analysis were carried out by Y.C.T. The manuscript was drafted by J.H.D. and revised by H.L., Q.B.D., H.Q., G.K.Z., and Y.C.T. All authors participated in data analysis and discussions.
Correspondence to He Qi, Gaokuo Zhong or Hao Li.
The authors declare no competing interests
Nature Communications thanks Dibakar Das, Jigong Hao and the other anonymous reviewer(s) for their contribution to the peer review of this work. A peer review file is available.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
Duan , J. , Wei , K. , Du , Q. et al. High-entropy superparaelectrics with locally diverse ferroic distortion for high-capacitive energy storage. Commun Nat 15, 6754 (2024). https://doi.org/10.1038/s41467-024-51058-6
DOI: https://doi.org/10.1038/s41467-024-51058-6
Anyone you share the following link with will be able to read this content:
Sorry, a shareable link is not currently available for this article.
Provided by the Springer Nature SharedIt content-sharing initiative
Nature Communications (Nat Commun) ISSN 2041-1723 (online)
ge high voltage capacitor Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.