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Unveiling the ferrielectric nature of PbZrO3-based antiferroelectric materials.

Authors :
Fu, Zhengqian
Chen, Xuefeng
Li, Zhenqin
Hu, Tengfei
Zhang, Linlin
Lu, Ping
Zhang, Shujun
Wang, Genshui
Dong, Xianlin
Xu, Fangfang
Source :
Nature Communications; 7/30/2020, Vol. 11 Issue 1, p1-8, 8p
Publication Year :
2020

Abstract

Benefitting from the reversible phase transition between antiferroelectric and ferroelectric states, antiferroelectric materials have recently received widespread attentions for energy storage applications. Antiferroelectric configuration with specific antiparallel dipoles has been used to establish antiferroelectric theories and understand its characteristic behaviors. Here, we report that the so-called antiferroelectric (Pb,La)(Zr,Sn,Ti)O<subscript>3</subscript> system is actually ferrielectric in nature. We demonstrate different ferrielectric configurations, which consists of ferroelectric ordering segments with either magnitude or angle modulation of dipoles. The ferrielectric configurations are mainly contributed from the coupling between A-cations and O-anions, and their displacement behavior is dependent largely on the chemical doping. Of particular significance is that the width and net polarization of ferroelectric ordering segments can be tailored by composition, which is linearly related to the key electrical characteristics, including switching field, remanent polarization and dielectric constant. These findings provide opportunities for comprehending structure-property correlation, developing antiferroelectric/ferrielectric theories and designing novel ferroic materials. The large family PbZrO<subscript>3</subscript>-based solid solutions are usually considered as antiferroelectric materials with specific antiparallel polarization configuration. Here, the authors demonstrate the PbZrO<subscript>3</subscript>-based material has ferrielectric dipoles ordering and configure a clear structure-property relationship. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
11
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
144855834
Full Text :
https://doi.org/10.1038/s41467-020-17664-w