Multi-element addition to construct multiphase high-entropy glass-ceramics with ultra-high energy storage efficiency

SPS prepared NN-24SBT lead-free relaxor-antiferroelectric ceramics with ultrahigh energy-storage density and efficiency

Advanced energy storage properties and multi-scale regulation mechanism in (1-x)(Bi0.5Na0.5)0.7Sr0.3TiO3-xCa(Nb0.5Al0.5)O3 relaxor ferroelectric ceramics

Although extensive studies have been done on lead-free dielectric ceramics to achieve excellent dielectric behaviors and good energy storage performance, the major problem of low energy density has not been solved so far. Here, we report on designing the crossover relaxor ferroelectrics (CRFE), a crossover region between the normal ferroelectrics and relaxor ferroelectrics, as a solution to overcome the low energy density. CRFE exhibits smaller free energy and lower defect density in the modified Landau theory, which helps to obtain ultrahigh energy density and efficiency. The (1-x)Ba0.65Sr0.35TiO3-xBi(Mg2/3Nb1/3)O3 ((1-x)BST-xBMN) (x = 0, 0.08, 0.1, 0.18, 0.2) ceramic was synthesized by a solid-state reaction method. The solid solutions exhibit dielectric frequency dispersion, which suggests typical relaxor characteristics with the increasing BMN content. The crossover ferroelectrics of 0.9BST-0.1BMN ceramic possesses a high energy storage efficiency (η) of 85.71%, a high energy storage density (W) of 3.90 J/cm3, and an ultrahigh recoverable energy storage density (Wrec) of 3.34 J/cm3 under a dielectric breakdown strength of 400 kV/cm and is superior to other lead-free BaTiO3 (BT)-based energy storage ceramics. It also exhibits strong thermal stability in the temperature range from 25 to 150 °C under an electric field of 300 kV/cm, with the fluctuations below 3% and with the energy storage density and energy efficiency at about 2.8 J/cm3 and 82.93%, respectively. The enhanced recoverable energy density and breakdown strength of BT-based materials with significantly high energy efficiency make it a promising candidate to meet the wide requirements for high power applications.

Ultra-high energy storage density BaTiO3 amorphous thin film via multi-ion synergistic optimization

The advancement of lead-free glass ceramics (GCs) possessing appropriate energy storage characteristics is crucial for the renewable energy and electronics industry. In this study, we synthesized lead-free GCs predominantly composed of the tungsten bronze phase, Ba3.3Nb10O28.3. Ab initio molecular dynamics initially reveal nonuniform distribution within the Ba/Nb-O regions in niobite glassy melts, offering valuable insights for the subsequent crystallization process. The proposal of a B-site engineering strategy is suggested, which entails the concurrent reduction of grain size and augmentation of the band gap in tungsten bronze GCs doped with Ta. This approach results in a substantial enhancement of the dielectric breakdown strength (BDS). Phase-field simulations have indicated that the refinement of grain sizes plays a pivotal role in augmenting the local electric field distribution and breakdown path, thereby contributing to the enhancement of BDS. As a consequence of these modifications, a notably high recoverable energy density (Wrec) of 5.23 J/cm3 can be achieved, accompanied by an ultrahigh efficiency (η) of 94%, and superior thermal stability in energy storage. These outcomes are particularly evident in the case of 2 mol % Ta2O5-doped P2O5-K2O-BaO-Bi2O3-TeO2-Nb2O5 (PKBBTN-T) GCs, where the Wrec and η can be determined to be 2.87 ± 3% J/cm3 and 95.46 ± 4%, respectively, over a temperature range spanning from 20 to 150 °C. Additionally, this specimen exhibits an exceptionally high discharge energy density (Wdis) of 4.01 J/cm3. This comprehensive investigation, comprising experimental and theoretical analyses, establishes an effective pathway and paradigm for the development of dielectric materials with ultrahigh energy storage properties.

Ultrahigh energy density and efficiency of BaTiO3-based ceramics via multiple design strategies

Ultrahigh energy storage density and efficiency in PLZST antiferroelectric ceramics via multiple optimization strategy

Antiferroelectric domain modulation enhancing energy storage performance by phase-field simulations

Polymer dielectrics need to operate at high temperatures to meet the demand of electrostatic energy storage in modern electronic and electrical systems. The polymer nanocomposite approach, an extensively proved strategy for the performance improvement, encounters the bottleneck of reduced energy density and poor discharge efficiency beyond 150°C. Here, we report a polymer/metal oxide cluster composite prepared based on the "site isolation" strategy. Capitalizing on the quantum size effect, the bandgap and surface defect states of the ultra-small inorganic clusters (2.2nm diameter) are modulated to markedly differ from the regular-sized nanoparticles. Experimental results in conjunction with computational simulation demonstrate that, the presence of ultra-small inorganic clusters can introduce more abundant, deeper traps in the composite dielectric with respect to the conventional polymer/nanoparticle blends. Unprecedented high-temperature capacitive performance including colossal energy density (6.8 Jcm-3 ), ultra-high discharge efficiency (95%) and superior stability at different electric field frequencies, are achieved in these polymer/cluster composites up to 200°C. Along with the advantages in material preparation (inexpensive precursors and one-pot synthesis), such polymer/inorganic cluster composite approach is promising for high-temperature dielectric energy storage in practical power apparatus and electronic devices. This article is protected by copyright. All rights reserved.

Scalable high-temperature polypropylene dielectrics with ultrahigh energy storage and efficiency via slightly crosslinked organic fillers

Antiferroelectric-liner dielectric solid solutions leading to large energy density and ultrahigh efficiency in PBLZST-CZT ceramics

The inherent risk of explosion in widely used lithium-ion-batteries has ignited greater interest in the development of more efficient and safer energy storage. Notably, there is growing attention on all-solid-state batteries for their ability of providing both safe and efficient energy storage. Among the promising candidates, we focused on argyrodite-type electrolytes exhibiting high ionic conductivity on the order of some mS/cm at room temperature.In this study, we compared dual-substituted argyrodite-type electrolytes to observe the effect of the anion substitution on the physical properties of the solid electrolytes using solid state NMR. We investigated the correlation between anion substitution and the local dynamics of lithium ions through NMR relaxometry. We measured 7Li spin-lattice relaxation times (T1) in various temperature, fitted the T1 values into the Arrhenius equation and calculated the activation energy. Furthermore, by comparing the peak intensity of NMR 1D spectra before and after cycling, we confirmed the movement of Li ions between cathode and electrolyte.In short, our findings, obtained via solid-state NMR, deepen our insights on electrolytes down to the atomic level. This work gained ground for future research to develop the efficient and safe energy storage systems and drive innovation in all-solid-state batteries.

BCZT-xLa (x = 0.0, 0.04) ceramics were synthesized by solid state reaction method. Structure, microstructure, dielectric, and energy storage characteristics were investigated. SEM analysis shows the decrease in grain size with La doping. Addition of La disrupted the long-range ordering and promoted the polar nano regions, resulting in significant increase in relaxor behaviour. This leads to slimmer PE loop and outstanding energy storage properties. We observed high storage density (W)~187 mJ/cm <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">3</sup> and efficiency (n)~91.5% in La-doped BCZT ceramics.

A trans-critical carbon dioxide energy storage system with heat pump to recover stored heat of compression

Elastic materials that store and release elastic energy play pivotal roles in both macro and micro mechanical systems. Uniting high elastic energy density and efficiency is crucial for emerging technologies such as artificial muscles, hopping robots, and unmanned aerial vehicle catapults, yet it remains a significant challenge. Here, a nanocrystalline structure embedded with elliptical martensite nanodomains in ferroelastic alloys wasutilized to enable high yield strength, large recoverable strain, and low energy dissipation simultaneously. As a result, the designed Ti-Ni-V alloys demonstrate ultrahigh energy density (>40 MJ m-3) with ultrahigh efficiency (>93%) and exceptional durability. This concept, which combines nano-sized embryos to minimize energy dissipation of psuedo-elasticity and employs a fine-grained structure to enhance yield strength, can be applied to other ferroelastic materials. Furthermore, it holds promise for the development of phase transformation-involved functionalities such as high-performance dielectric energy storage, ultralow-hysteresis magnetostrain, and high-efficiency solid-state caloriccooling.