New iron-based multiferroics with improper ferroelectricity

被引:12
|
作者
Peng, Jin [1 ]
Zhang, Yang [1 ]
Lin, Ling-Fang [1 ]
Lin, Lin [2 ,3 ]
Liu, Meifeng [2 ,3 ,4 ]
Liu, Jun-Ming [2 ,3 ,5 ]
Dong, Shuai [1 ]
机构
[1] Southeast Univ, Sch Phys, Nanjing 211189, Jiangsu, Peoples R China
[2] Nanjing Univ, Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
[3] Nanjing Univ, Innovat Ctr Adv Microstruct, Nanjing 210093, Jiangsu, Peoples R China
[4] Hubei Normal Univ, Inst Adv Mat, Huangshi 435002, Peoples R China
[5] South China Normal Univ, Inst Adv Mat, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
multiferroics; improper ferroelectricity; iron oxide; iron selenide; iron fluoride; MAGNETIC-STRUCTURE; RARE-EARTH; ORDER; PHYSICS;
D O I
10.1088/1361-6463/aac345
中图分类号
O59 [应用物理学];
学科分类号
摘要
In this contribution to the special issue on magnetoelectrics and their applications, we focus on some single phase multiferroics, which have been theoretically predicted and/ or experimentally discovered by the authors in recent years. In these materials, iron is the common core element. However, these materials are conceptually different from the mostly-studied BiFeO3, since their ferroelectricity is improper. Our reviewed materials are not simply repeating one magnetoelectric mechanism, but cover multiple branches of improper ferroelectricity, including the magnetism-driven ferroelectrics, geometric ferroelectric, as well as electronic ferroelectric driven by charge ordering. In this sense, these iron-based improper ferroelectrics can be an encyclopaedic playground to explore the comprehensive physics of multiferroics and magnetoelectricity. Furthermore, the unique characteristics of iron's 3d orbitals make some of their magnetoelectric properties quite prominent, comparing with the extensively-studied Mn-based improper multiferroics. In addition, these materials establish the crossover between multiferroics and other fields of functional materials, which enlarges the application scope of multiferroics.
引用
收藏
页数:15
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