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

Relaxor ferroelectrics are promising candidates for pulsed power dielectric capacitor applications because of their excellent energy-storage properties. Different from most relaxor ferroelectrics whose energy-storage density was improved by increasing the breakdown strength and reducing the remanent polarization, in this study, anti-ferroelectric (AFE) AgNbO3 (AN) was used to partially substitute the relaxor ferroelectric 0.76Bi0.5Na0.5TiO3–0.24SrTiO3 (BNT–ST) of morphotropic phase boundary (MPB) composition to reduce the remanent polarization while maintaining large maximum polarization. In this way, a large recoverable energy-storage density (2.03 J cm−3) was obtained in the BNT–ST–5AN ceramics under lower electric field of 120 kV cm−1, which is superior to other lead-free energy-storage materials under similar electric fields. Moreover, excellent temperature (25–175 °C) and frequency (1–100 Hz) stabilities are achieved. This performance demonstrates that the BNT–ST–5AN ceramics form a promising class of dielectric capacitive material for high-temperature pulsed power capacitors with large energy-storage density.

Enhanced energy-storage performance with excellent stability under low electric fields in BNT–ST relaxor ferroelectric ceramics

Sr0.7Bi0.2TiO3 (SBT) was introduced into Bi0.5Na0.5TiO3 (BNT) via a standard solid-state route to modulate its relaxation behaviour and energy storage performance. With increasing SBT content, the perovskite structure of BNT transforms from a rhombohedral phase to a weakly polarized pseudo-cubic phase, and the relaxation behaviour is enhanced. In particular, the EDBS is improved from 120 kV/cm of BNT to 160 kV/cm of 0.6BNT-0.4SBT, which displays a large recoverable energy storage density (Wrec = 2.20 J/cm3), implying a large potential ability of energy storage for the 0.6BNT-0.4SBT ceramic. Moreover, both dielectric properties (28–326 °C) and energy storage properties (20–140 °C) exhibit a good thermal stability for the same 0.6BNT-0.4SBT composition. These characteristics suggest 0.6BNT-0.4SBT ceramic could be a promising candidate to be applied in a pulse power system over a broad temperature range.

Enhanced energy density and thermal stability in relaxor ferroelectric Bi0.5Na0.5TiO3-Sr0.7Bi0.2TiO3 ceramics

Phase structure and properties of sodium bismuth titanate lead-free piezoelectric ceramics

Progress and perspective of high strain NBT-based lead-free piezoceramics and multilayer actuators

Large electric field-induced strain in AgNbO3-modified 0.76Bi0.5Na0.5TiO3-0.24SrTiO3 lead-free piezoceramics

Large electric-field-induced strain in B-site complex-ion (Fe0.5Nb0.5)4+-doped Bi1/2 (Na0.82K0.12)1/2TiO3 lead-free piezoceramics

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Large electric field-induced strain in AgNbO3-modified 0.76Bi0.5Na0.5TiO3-0.24SrTiO3 lead-free piezoceramics

Large electric-field-induced strain in B-site complex-ion (Fe0.5Nb0.5)4+-doped Bi1/2 (Na0.82K0.12)1/2TiO3 lead-free piezoceramics