Lead-free antiferroelectric AgNbO3: Phase transitions and structure engineering for dielectric energy storage applications

Jing Gao, Qian Li, Shujun Zhang, Jing-Feng Li*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

The development of electronic materials for storing electrical energy is a thriving research field, where the materials used in batteries, supercapacitors, dielectric capacitors have attracted extensive interest in last decades. The dielectric capacitors showing unique characteristics such as high power density and large charge/discharge rate have been actively studied, where the antiferroelectrics demonstrate great potentials for dielectric energy storage applications by storing and releasing energy upon a reversible electric-field induced antiferroelectric-ferroelectric phase transition. Recently, lead-free antiferroelectric AgNbO3 has emerged as a promising candidate to substitute conventional lead-based antiferroelectrics (such as PbZrO3) in energy storage applications. The phase transition dynamics of AgNbO3 is driven by a complex sequence of oxygen octahedron tilting orders in addition to cation displacement, which can be effectively engineered by a doping strategy. In this article, we present a succinct overview of the phase transition mechanisms in AgNbO3-based ceramics and describe how the phase transition characteristics are affected by the dopants. By exploring the composition related average structure and local structural evolutions, we provide a view toward the goal of establishing a link between the phase transition and physical properties tailored for dielectric energy storage applications. © 2020 Author(s).
Original languageEnglish
Article number070903
JournalJournal of Applied Physics
Volume128
Issue number7
Online published19 Aug 2020
DOIs
Publication statusPublished - 21 Aug 2020
Externally publishedYes

Funding

This work was supported by the Basic Science Center Project of NSFC under Grant No. 51788104 and the International Collaboration Project of NSFC under Grant No. 51761135118.

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