Issue 5, 2025

Multi-scale enhanced energy storage performance in Sm(Mg0.5Sn0.5)O3-modified Bi0.47Na0.47Ba0.06TiO3 ceramics with a composite structure

Abstract

Lead-free dielectric capacitors have attracted widespread attention for their high power density, ultra-fast charge–discharge rate and excellent chemical stability. Nevertheless, low energy storage density (Wrec < 9 J cm−3) and energy storage efficiency (η < 85%) limit their further development. The 0.80(Bi0.47Na0.47Ba0.06TiO3)-0.20Sm(Mg0.5Sn0.5)O3 ceramics achieved excellent comprehensive energy storage performance (Wrec ∼ 9.91 J cm−3, η ∼ 87.01%) and stability over a wide temperature range (25–200 °C) at 700 kV cm−1. The introduction of Sm(Mg0.5Sn0.5)O3 (SMS) constructs a local random field, and the large-size ferroelectric macrodomains are decomposed into high dynamic polar nanodomains (PNRs), which effectively suppresses the generation of early polarization saturation and achieves high ΔP (∼31.92 μC cm−2). Interestingly, SMS-modified Bi0.47Na0.47Ba0.06TiO3 ceramics have a 0–3 type composite structure consisting of a pyrochlore phase Sm2Sn2O7 and a main phase. The low dielectric constant of the secondary phase and the refined grains increase the breakdown field strength (Eb). Due to the stable local structure and improved relaxation properties, the ceramics exhibit excellent temperature stability (Wrec and η are maintained at 2.62 ± 0.06 J cm−3 and 87.03 ± 2.96% at 25–200 °C, respectively). This work provides a theoretical basis for the future development and design of high energy storage materials.

Graphical abstract: Multi-scale enhanced energy storage performance in Sm(Mg0.5Sn0.5)O3-modified Bi0.47Na0.47Ba0.06TiO3 ceramics with a composite structure

Supplementary files

Article information

Article type
Paper
Submitted
28 Oct 2024
Accepted
17 Dec 2024
First published
02 Jan 2025

J. Mater. Chem. A, 2025,13, 3749-3764

Multi-scale enhanced energy storage performance in Sm(Mg0.5Sn0.5)O3-modified Bi0.47Na0.47Ba0.06TiO3 ceramics with a composite structure

Y. Pan, Q. Dong, J. Huang, Y. Zhang, X. Chen, X. Li, L. Deng and H. Zhou, J. Mater. Chem. A, 2025, 13, 3749 DOI: 10.1039/D4TA07670B

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