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.

Oxide ion conductors find important technical applications in electrochemical devices such as solid-oxide fuel cells (SOFCs), oxygen separation membranes and sensors. Na0.5Bi0.5TiO3 (NBT) is a well-known lead-free piezoelectric material; however, it is often reported to possess high leakage conductivity that is problematic for its piezo- and ferroelectric applications. Here we report this high leakage to be oxide ion conduction due to Bi-deficiency and oxygen vacancies induced during materials processing. Mg-doping on the Ti-site increases the ionic conductivity to ~0.01 S cm(-1) at 600 °C, improves the electrolyte stability in reducing atmospheres and lowers the sintering temperature. This study not only demonstrates how to adjust the nominal NBT composition for dielectric-based applications, but also, more importantly, gives NBT-based materials an unexpected role as a completely new family of oxide ion conductors with potential applications in intermediate-temperature SOFCs and opens up a new direction to design oxide ion conductors in perovskite oxides.

Ultrahigh discharge energy density (W_dis = 10.5 J cm⁻³) and efficiency (η = 87%) have been obtained in doped BiFeO₃–BaTiO₃ ceramic multilayers by achieving an electrically rather than chemically homogeneous microstructure. Back scattered scanning and transmission electron microscopy combined with energy dispersive X-ray spectroscopy mapping of (0.7 − x)BiFeO₃–0.3BaTiO₃–xNd(Zn_0.5Zr_0.5)O₃ (0.05 ≤ x ≤ 0.10) ceramics revealed a core–shell grain structure which switched from a bright to dark contrast as x increased. Compositions with x = 0.08 were at the point of cross over between these two manifestations of core–shell contrast. Dielectric measurements together with the absence of macrodomains in diffraction contrast TEM images suggested that compositions with x = 0.08 exhibited relaxor behaviour within both the core and shell regions. Impedance spectroscopy demonstrated that, despite being chemical dissimilar, the grains were electrically homogeneous and insulating with little evidence of conductive cores. Multilayers of x = 0.08 had enhanced breakdown strength, E_BDS > 700 kV cm⁻¹ and a slim hysteresis loop which resulted in large W_dis and high η which were temperature stable to <15% from 25 to 150 °C.

Bismuth ferrite-based lead-free multilayers with a high recoverable energy density of 6.74 J cm⁻³ and an efficiency of 77%, stable up to 125 °C.

Open access articleSolar cells are considered as one of the prominent sources of renewable energy suitable for large-scale adoption in a carbon-constrained world and can contribute to reduced reliance on energy imports, whilst improving the security of energy supply. A new arrival in the family of solar cells technologies is the organic-inorganic halide perovskite. The major thrust for endorsing these new solar cells pertains to their potential as an economically\ud and environmentally viable option to traditional silicon-based technology. To verify this assertion, this paper presents a critical review of some existing photovoltaic (PV) technologies in comparison with perovskite structured solar cells (PSCs), including material and performance parameters, production processes and manufacturing complexity, economics, key technological challenges for further developments and current research efforts. At present, there is limited environmental assessment of PSCs and consequently, a\ud methodologically robust and environmentally expansive lifecycle supply chain assessment of two types of PSC modules A and B is also undertaken within the context of other PV technologies, to assess their potential for environmentally friendly innovation in the energy sector. Module A is based on MAPbX3 perovskite structure while module B is based on CsFAPbX3 with improved stability, reproducibility and high performance efficiency.\ud The main outcomes, presented along with sensitivity analysis, show that PSCs offer more environmentally friendly and sustainable option, with the least energy payback period, as compared to other PV technologies.\ud The review and analysis presented provide valuable insight and guidance in identifying pathways and windows of opportunity for future PV designs towards cleaner and sustainable energy production