High-entropy relaxor ferroelectric ceramics for ultrahigh energy storage.

Nat Commun

State Key Laboratory of Infrared Physics, Shanghai Institute of Technical Physics, Chinese Academy of Sciences, Shanghai, 200083, China.

Published: June 2024

AI Article Synopsis

  • Dielectric ceramic capacitors are essential for modern electronics but face challenges in energy density and breakdown strength.
  • A new high-entropy tungsten bronze-type relaxor ferroelectric was developed, achieving a significant recoverable energy density of 11.0 J·cm and an efficiency of 81.9%.
  • The improved performance is due to the unique atomic-scale structure created by high configuration entropy, which enhances energy storage capabilities while reducing polarization hysteresis and increasing breakdown endurance.

Article Abstract

Dielectric ceramic capacitors with ultrahigh power densities are fundamental to modern electrical devices. Nonetheless, the poor energy density confined to the low breakdown strength is a long-standing bottleneck in developing desirable dielectric materials for practical applications. In this instance, we present a high-entropy tungsten bronze-type relaxor ferroelectric achieved through an equimolar-ratio element design, which realizes a giant recoverable energy density of 11.0 J·cm and a high efficiency of 81.9%. Moreover, the atomic-scale microstructural study confirms that the excellent comprehensive energy storage performance is attributed to the increased atomic-scale compositional heterogeneity from high configuration entropy, which modulates the relaxor features as well as induces lattice distortion, resulting in reduced polarization hysteresis and enhanced breakdown endurance. This study provides evidence that developing high-entropy relaxor ferroelectric material via equimolar-ratio element design is an effective strategy for achieving ultrahigh energy storage characteristics. Our results also uncover the immense potential of tetragonal tungsten bronze-type materials for advanced energy storage applications.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11187193PMC
http://dx.doi.org/10.1038/s41467-024-49107-1DOI Listing

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