Materials exhibiting high energy/power density are currently needed to meet the growing demand of portable electronics, electric vehicles and large-scale energy storage devices. The highest energy densities are achieved for fuel cells, batteries, and supercapacitors, but conventional dielectric capacitors are receiving increased attention for pulsed power applications due to their high power density and their fast charge-discharge speed. The key to high energy density in dielectric capacitors is a large maximum but small remanent (zero in the case of linear dielectrics) polarization and a high electric breakdown strength. Polymer dielectric capacitors offer high power/energy density for applications at room temperature, but above 100 °C they are unreliable and suffer from dielectric breakdown. For high-temperature applications, therefore, dielectric ceramics are the only feasible alternative. Lead-based ceramics such as La-doped lead zirconate titanate exhibit good energy storage properties, but their toxicity raises concern over their use in consumer applications, where capacitors are exclusively lead free. Lead-free compositions with superior power density are thus required. In this paper, we introduce the fundamental principles of energy storage in dielectrics. We discuss key factors to improve energy storage properties such as the control of local structure, phase assemblage, dielectric layer thickness, microstructure, conductivity, and electrical homogeneity through the choice of base systems, dopants, and alloying additions, followed by a comprehensive review of the state-of-the-art. Finally, we comment on the future requirements for new materials in high power/energy density capacitor applications.

Electroceramics for High-Energy Density Capacitors: Current Status and Future Perspectives

Dielectric capacitors, which store electrical energy in the form of an electrostatic field via dielectric polarization, are used in pulsed power electronics due to their high power density and ultrashort discharge time. In pursuit of developing high‐performance dielectric capacitors, special attention has been given to the improvement of their energy density and storage efficiency, which would make them useful for an even wider variety of applications. Among the different dielectric materials studied so far, including polymers, glasses, and both bulk and film‐based ceramics, dielectric ceramic films, which are of particular interest for miniature power electronics and mobile platforms, have demonstrated the greatest energy storage performances. In this regard, several interesting approaches involving physical, chemical, and microstructural modifications of the dielectric ceramic films are adopted. In addition to a brief discussion of the polymers, glasses, and ceramics used in dielectric capacitors and key parameters related to their energy storage performance, this review article presents a comprehensive overview of the numerous efforts made toward enhancing the energy storage properties of linear dielectric, paraelectric, ferroelectric, relaxor ferroelectric, and anti‐ferroelectric ceramic films for their applications in pulsed power capacitors.

High-Performance Dielectric Ceramic Films for Energy Storage Capacitors: Progress and Outlook

Low‐dimensional materials have been long sought after for their particular electromagnetic (EM) functions, with promising applications in EM wave absorbing and shielding, communicating and imaging, sensing and detecting, driving and actuating, etc. Herein, across the whole EM spectrum, low‐dimensional EM functional materials and devices are highly focused on. The crystal engineering and function‐guiding features addressed relate to crystal and electronic structures, EM responses and properties, energy conversion, as well as EM wave absorbing and shielding. Moreover, insight is given into this rapidly broadening field, the main challenges are proposed and future directions are predicted.

Electromagnetic Response and Energy Conversion for Functions and Devices in Low‐Dimensional Materials

Compared with fuel cells and electrochemical capacitors, dielectric capacitors are regarded as promising devices to store electrical energy for pulsed power systems due to their fast charge/discharge rates and ultrahigh power density. Dielectric materials are core components of dielectric capacitors and directly determine their performance. Over the past decade, extensive efforts have been devoted to develop high-performance dielectric materials for electrical energy storage applications and great progress has been achieved. Here, we present an overview on the current state-of-the-art lead-free bulk ceramics for electrical energy storage applications, including SrTiO3, CaTiO3, BaTiO3, (Bi0.5Na0.5)TiO3, (K0.5Na0.5)NbO3, BiFeO3, AgNbO3 and NaNbO3-based ceramics. This review starts with a brief introduction of the research background, the development history and the basic fundamentals of dielectric materials for energy storage applications as well as the universal strategies to optimize their energy storage performance. Emphases are placed on the design strategies for each type of dielectric ceramic based on their special physical properties with a summary of their respective advantages and disadvantages. Challenges along with future prospects are presented at the end of this review. This review will not only accelerate the exploration of higher performance lead-free dielectric materials, but also provides a deeper understanding of the relationship among chemical composition, physical properties and energy storage performance.

High-performance lead-free bulk ceramics for electrical energy storage applications: design strategies and challenges

Transition-metal oxides exhibiting a bistable resistance state are attractive for non-volatile memory applications. The relevance of oxygen vacancies (VO) for the resistance-change memory was investigated with x-ray fluorescence, infrared microscopy, and x-ray absorption spectroscopy using Cr-doped SrTiO3 as example. We propose that the microscopic origin of resistance switching in this class of materials is due to an oxygen-vacancy drift occurring in close proximity to one of the electrodes.

Role of oxygen vacancies in Cr-doped SrTiO3 for resistance-change memory

Optical properties of amorphous Al2O3 thin films prepared by a sol–gel process

Dielectric constant and energy density of poly(vinylidene fluoride) nanocomposites filled with core-shell structured BaTiO3@Al2O3 nanoparticles

A novel core-shell structured Pb0.91La0.06(Zr0.552Sn0.368Ti0.08)O3@PbO–B2O3-SiO2-Al2O3-ZnO-MnO2 (PLZST@PBSAZM) antiferroelectric particles were successfully fabricated via sol-gel method. As expected, the sintering temperature was notably reduced from 1250 oC to 1100 oC with the increasing glass contents. More importantly, the breakdown strengths of PLZST@PBSAZM ceramics were significantly increased from 252 kV/cm to 402 kV/cm. As a result, the energy density was up to 7.4 J/cm3 with 1 wt.% of coating glass content, a 55.3% enhancement over the pure PLZST (4.7 J/cm3). Furthermore, the simulations of electric field distribution provided a powerful evidence that the enhancement of the breakdown strength was induced by the core-shell structure, since the glass coating layer could not only undertake the most of electric field, but also impede the grain growth to achieve the smaller grains, which led to the reduction of electric field intensity on the grain cores.

Ultrahigh breakdown strength and energy density in PLZST@ PBSAZM antiferroelectric ceramics based on core-shell structure

A periodic layer structure consisting of sol–gel-derived SrTiO3 and anodized Al2O3 has been designed and fabricated by interface engineering. Utilizing the anodized Al2O3 to be the blocking layer, ...

Achieving Ultrahigh Breakdown Strength and Energy Storage Performance through Periodic Interface Modification in SrTiO3 Thin Film.

Effect of crystallization on the band structure and photoelectric property of SrTiO3 sol–gel derived thin film

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