Understanding ferroelectricity in layered perovskites: new ideas and insights from theory and experiments

被引:245
作者
Benedek, Nicole A. [1 ]
Rondinelli, James M. [2 ]
Djani, Hania [3 ]
Ghosez, Philippe [4 ]
Lightfoot, Philip [5 ,6 ]
机构
[1] Univ Texas Austin, Mat Sci & Engn Program, Austin, TX 78712 USA
[2] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[3] Ctr Dev Technol Avancees, Baba Hassen, Alger, Algeria
[4] Univ Liege, Theoret Mat Phys, B-4000 Liege, Belgium
[5] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[6] Univ St Andrews, EaStCHEM, St Andrews KY16 9ST, Fife, Scotland
基金
美国国家科学基金会;
关键词
INVERSION SYMMETRY-BREAKING; METAL-ANION ARRAYS; POLARIZATION ENHANCEMENT; CRYSTAL-STRUCTURE; STRUCTURAL DISTORTIONS; IMPROPER FERROELECTRICITY; ELECTRONIC-STRUCTURE; PHASE-TRANSITIONS; THIN-FILMS; A-SITE;
D O I
10.1039/c5dt00010f
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
ABO(3) perovskites have fascinated solid-state chemists and physicists for decades because they display a seemingly inexhaustible variety of chemical and physical properties. However, despite the diversity of properties found among perovskites, very few of these materials are ferroelectric, or even polar, in bulk. In this Perspective, we highlight recent theoretical and experimental studies that have shown how a combination of non-polar structural distortions, commonly tilts or rotations of the BO6 octahedra, can give rise to polar structures or ferroelectricity in several families of layered perovskites. We discuss the crystal chemical origin of the polarization in each of these families - which emerges through a so-called 'trilinear coupling' or 'hybrid improper' mechanism - and emphasize areas in which further theoretical and experimental investigation is needed. We also consider how this mechanism may provide a generic route for designing not only new ferroelectrics, but also materials with various other multifunctionalities, such as magnetoelectrics and electric field-controllable metal-insulator transitions.
引用
收藏
页码:10543 / 10558
页数:16
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