首页 | 本学科首页   官方微博 | 高级检索  
     


Enhanced ferroelectric,magnetic and magnetoelectric properties of multiferroic BiFeO3–BaTiO3–LaFeO3 ceramics
Authors:Min Zhang  Xiaoyan Zhang  Xiwei Qi  Hongen Zhu  Ying Li  Yaohang Gu
Affiliation:1. School of Materials Science and Engineering, Northeastern University, Shenyang 110819, China;2. School of Resources and Materials, Northeastern University at Qinhuangdao, Qinhuangdao 066004, China;3. Key Laboratory of Dielectric and Electrolyte Functional Materials Hebei Province, School of Resources and Materials, Northeastern University at Qinhuangdao, Qinhuangdao 066004, China
Abstract:A lead–free multiferroic ceramic 0.7BiFeO3–0.3BaTiO3 showed strong ferroelectric and piezoelectric properties, but weak magnetic and magnetoelectric properties. We herein expected that the electrical and magnetic properties of 0.7BiFeO3–0.3BaTiO3 ceramics could be enhanced by introducing LaFeO3. (0.7–x) BiFeO3–0.3BaTiO3xLaFeO3 (x?=?0–0.2) were synthesized by solid-state reaction. All the ceramics formed a perovskite structure, and a morphotropic phase boundary (MPB) between rhombohedral and orthorhombic phases formed at x?=?0.025. The ceramics with MPB composition had high unipolar strain (Smax = 0.14%), piezoelectricity (d33 = 223 pC/N, d33 * = 350?pm/V), ferroelectricity (Pr = 25.67 mC/cm2) and magnetoelectricity (aME = 466.6?mV/cm·Oe), which can be attributed to addition of La ions. The improved phase angle also demonstrated augmentation of ferroelectricity on the microscopic view. The ferromagnetism was evidently improved after LaFeO3 doping, and the remanent magnetization Mr increased from 0.0207 to 0.0622?emu/g with rising x from 0 to 0.075. In conclusion, with strong magnetoelectric properties, the prepared ceramics may be applicable as promising lead–free multiferroic ceramic materials for novel electronic devices.
Keywords:C  Piezoelectric properties  C  Ferroelectric properties  C  Ferromagnetism properties  C  Magnetoelectric properties
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号