Multiferroic properties of Ba2+-Ti4+co-doped YFeO3 ceramics

被引:5
|
作者
Wang, Zhao [1 ]
Zhao, Wenyue [1 ]
Li, Ze [1 ]
Peng, Yazhou [1 ]
Gao, Chang [1 ]
Shi, Lei [1 ]
Hua, Wenjing [1 ]
Fei, Weidong [1 ,2 ]
Zhao, Yu [1 ,3 ,4 ]
机构
[1] Harbin Inst Technol, Sch Mat Sci & Engn, Harbin 150001, Peoples R China
[2] Harbin Inst Technol, State Key Lab Adv Welding & Joining, Harbin 150001, Peoples R China
[3] Harbin Inst Technol, Lab Space Environm & Phys Sci, Harbin 150001, Peoples R China
[4] Minist Educ, Harbin Inst Technol, Key Lab Microsyst & Microstruct Mfg, Harbin 150001, Peoples R China
基金
中国国家自然科学基金;
关键词
Multiferroic; Acceptor-donor co-doping; Magnetoelectric coupling; YFeO3 based ceramics; HEXAGONAL FERROELECTRICITY; PHASE-RELATIONS; DOPED YFEO3;
D O I
10.1016/j.jallcom.2023.170718
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The search for multiferroic materials with ferroelectric and ferromagnetic properties at room temperature continues to be driven by the prospect of new devices. In this paper, Ba2+-Ti4+ co-doped Y1-x(Ba0.5Ti0.5)xFeO3 were prepared by a traditional solid-state reaction method. The ferroelectricity and ferromagnetism of the co-doped ceramics have been enhanced simultaneously with the maximum polarization of 0.48 & mu;C/cm2 and the maximum magnetization of 3.25 emu/g, the switched charge density (0.26 & mu;C/cm2) measured by PUND tests indicating the intrinsic and switchable remanent polarization. The increase of Fe2+ content (increased to 28 % with the increase of doping content) caused by Ba2+-Ti4+ co-doping destroys the antiferromagnetic ground state, and the doping strategy enlarges the tilt angle of oxygen octahedron from 144.93 & DEG; to 148.63 & DEG;. The magnetic domain switches caused by the external electric field were directly observed by magnetic force microscopy, indicating the modulation of magnetic domain by polarization at room temperature. This work may provide useful information for the structural design and performance improvement of multi-ferroic materials.& COPY; 2023 Elsevier B.V. All rights reserved.
引用
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页数:10
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