Coercivity enhancement of sintered Nd-Fe-B magnets by efficiently diffusing DyF3 based on electrophoretic deposition

被引:73
作者
Cao, X. J. [1 ,2 ]
Chen, L. [2 ]
Guo, S. [2 ]
Li, X. B. [1 ]
Yi, P. P. [3 ]
Yan, A. R. [2 ]
Yan, G. L. [1 ]
机构
[1] Wuhan Univ, Sch Phys & Technol, Wuhan 430072, Peoples R China
[2] Chinese Acad Sci, Ningbo Inst Mat Technol & Engn, Zhejiang Prov Key Lab Magnet Mat & Applicat Techn, Ningbo 315201, Zhejiang, Peoples R China
[3] Ningbo Songke Magnet Mat Co Ltd, Ningbo 315517, Zhejiang, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Sintered Nd-Fe-B magnet; Electrophoretic deposition; DyF3; diffusion; Core-shell microstructure; GRAIN-BOUNDARY; MICROSTRUCTURAL CHARACTERISTICS; PERMANENT-MAGNETS; MECHANISM;
D O I
10.1016/j.jallcom.2015.01.078
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
Using electrophoretic deposition (EPD) method, we coated DyF3 powder onto the sintered Nd-Fe-B magnets, investigated the changes in magnetic and microstructural properties of DyF3 EPD-coated magnets and clarified the optimum diffusion temperature and time. Through controlling the process parameters (such as temperature and time), the coercivity was increased from 16.1 to 22.8 kOe with a slight reduction in remanence after the diffusion. A significant increment in coercivity of more than 6.5 kOe was achieved with less than 1.2 wt.% Dy in the Dy-free original magnets. Microstructure analysis suggested that the increase of the coercivity was closely related to the concentration and the distribution of Dy. At 100 mu m from the surface of the magnet, Dy concentration gradually increased with the diffusion temperature and time, which corresponds well with the change of coercivity. During the diffusion, Dy favors to substitute for Nd to form the (Nd, Dy)(2)Fe14B core-shell phases in the outer region of Nd2Fe14B grains. The higher magnetocrystalline anisotropy of the core-shell phase and the improved decoupling by the continuous grain boundary phase contribute to the coercivity enhancement. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:315 / 320
页数:6
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