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Pulse power energy conversion materials with ultrafast discharge processes and ultrahigh power densities have been widely used in the defense, energy, medical, and mining fields. The pressure‐driven depolarization in ferroelectric materials is significant and accounts for the discharge processes. In this study, we focus on pressure‐induced depolarization in (Pb1‐1.5xLax)(Zr0.80Ti0.20)O3 (PLZT) (x = 0‐0.07) ceramics, and their corresponding phase structure, dielectric properties, ferroelectric properties, and thermal depolarization performances. Although a satisfactory pulse power energy conversion performance has been achieved in Pb(Zr0.95Ti0.05)O3 materials, poor temperature stability negatively influences their application. The static charge densities of PLZT (x = 0.04, 0.06) decreased from 29.11 μC/cm2 and 31.53 μC/cm2 to 19.76 μC/cm2 and 6.56 μC/cm2 under 400 MPa hydrostatic pressure, respectively, which is attributed to a pressure‐driven ferroelectric‐antiferroelectric phase structural transition. In particular, the temperature stability of PLZT (x = 0.06) materials is up to 87°C. This study may guide the further development pulse power energy conversion devices. [ABSTRACT FROM AUTHOR]

Antiferroelectrics (AFE) are considered a promising energy storage material for components that require nanosecond-level discharge. Pb(Yb 1/2 Nb 1/2)O 3 (PYN) is an AFE material with potential energy storage applications. However, the unmatched critical phase transition field (E F) and breakdown electric field (E B) conceal most of energy storage capacitance. This work is aimed to settle imbalanced E F / E B via a compositional design strategy. E F and E B were tuned in order to obtain 5.18 J cm−3 in recoverable energy density, 65% energy efficiency, and thermal and frequency stability varying within 15%, producing excellent comprehensive energy storage properties. A modified kinetic model of energetic path was used to understand the mechanism governing the variation of E F. We expect our work to contribute to further development of novel AFE materials for energy storage. [ABSTRACT FROM AUTHOR]