Outstanding energy density and hardness in Ba0.85Ca0.15Zr0.1Ti0.9O3-based ceramics via weakly coupled relaxor design
Abstract
Lead-free ceramic-based dielectric capacitors demonstrate significant potential for pulse power energy storage applications due to their high power density and rapid charge/discharge characteristics. In this study, highly dynamic polar nanoregions (PNRs) were constructed in (1 − x)[0.92Ba0.85Ca0.15Zr0.1Ti0.9O3–0.08Bi(Zn2/3Ta1/3)O3]-xBi0.5Na0.5TiO3 (abbreviated as BNTx) dielectric ceramics by introducing the strongly polar relaxor end-member Bi0.5Na0.5TiO3 (BNT). Meanwhile, the hybridization of Bi 6s and O 2p orbitals improves the polarization capability of the ceramics, resulting in a larger polarization difference (ΔP ∼47.8 μC cm−2). Furthermore, due to the high doping concentration of BNT and Ta donor doping, BNTx relaxor ferroelectrics exhibit high bulk resistivity, submicron grain size (∼0.57 μm), and wide bandgap characteristics, leading to a remarkable improvement in breakdown strength (Eb ∼710 kV cm−1). Both the electroactive regions corresponding to the bulk and grain boundaries showed similar characteristics, indicating a homogeneous electrical microstructure and intrinsic resistance which significantly contributed to maintaining the high resistivity of the samples. Through compositional optimization, the 20% BNT-doped BCZT-based relaxor ferroelectric ceramic (BNT20) achieves a Vickers hardness of ∼8.608 GPa while demonstrating exceptional energy storage performance, including an outstanding recoverable energy density (Wrec) of ∼10.6 J cm−3 and ultrahigh energy efficiency (η) of ∼87%. Notably, the stable PNRs significantly improved the temperature and frequency stability of the dielectric constant and energy storage performance. Furthermore, the BNT20 ceramic exhibits a high current density (CD ∼1108.3 A cm−2), power density (PD ∼132.99 MW cm−3), and an ultrafast discharge speed (t0.9 ∼79.9 ns), demonstrating its promising application prospects in pulse power systems.

Please wait while we load your content...