Enhanced dipole-interaction in Nd-Dy-Fe-Co-B/Fe composite thick stacked trilayer

被引:1
作者
Li, C. H. [1 ,2 ]
Zhao, X. T. [1 ]
Liu, L. [1 ]
Liu, W. [1 ]
Ye, Z. X. [1 ,2 ]
Wu, J. X. [1 ,2 ]
Ma, J. [1 ,2 ]
Zhang, Z. D. [1 ]
机构
[1] Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China
[2] Univ Sci & Technol China, Sch Mat Sci & Engn, Shenyang 110016, Peoples R China
基金
国家重点研发计划;
关键词
ENERGY PRODUCT; REMANENCE ENHANCEMENT; NANOCOMPOSITE MAGNETS; FILMS; OPTIMIZATION; COERCIVITY; ANISOTROPY; BEHAVIOR; NDFEB; HARD;
D O I
10.1063/5.0227572
中图分类号
O59 [应用物理学];
学科分类号
摘要
It is crucial to better understand the magnetization reversal process between soft and hard magnets and to achieve a high maximum energy product in thick composite multilayers. In this study, we find that the exchange interactions dominate in soft-hard-magnetic composite bilayers, while dipole interactions are predominant in soft-hard-magnetic composite trilayers. Based on the first-order reversal curve, magnetization reversal models are developed for both the thick composite bilayer and trilayer. Dipole interactions play an important role in the long range, resulting in higher coercivity and remanence in the thick trilayer. A multilayer in a stacked trilayer structure is achieved, which is composed of thick films with a perpendicular magnetic anisotropy at a thickness of up to 16 mu m. The enhanced dipole interactions lead to a remanent polarization of 1 T and a maximum energy product of 22.5 MGOe. This work contributes to the preparation of thick films with a high maximum energy product for applications in magnetic microelectromechanical systems.
引用
收藏
页数:9
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共 45 条
  • [1] Optimization study of the nanostructure of hard/soft magnetic multilayers
    Amato, M
    Pini, MG
    Rettori, A
    [J]. PHYSICAL REVIEW B, 1999, 60 (05): : 3414 - 3420
  • [2] Permanent Magnets for MEMS
    Arnold, David P.
    Wang, Naigang
    [J]. JOURNAL OF MICROELECTROMECHANICAL SYSTEMS, 2009, 18 (06) : 1255 - 1266
  • [3] Magnetic properties of exchange-coupled PtFe/Fe films with spacer layers
    Cui, W. B.
    Liu, W.
    Yang, F.
    Li, D.
    Delikanli, S.
    Guo, S.
    Gong, W. J.
    Zhang, Z. D.
    [J]. JOURNAL OF APPLIED PHYSICS, 2011, 109 (07)
  • [4] Anisotropic behavior of exchange coupling in textured Nd2Fe14B/α-Fe multilayer films
    Cui, W. B.
    Zheng, S. J.
    Liu, W.
    Ma, X. L.
    Yang, F.
    Yao, Q.
    Zhao, X. G.
    Zhang, Z. D.
    [J]. JOURNAL OF APPLIED PHYSICS, 2008, 104 (05)
  • [5] Nd2Fe14B/FeCo Anisotropic Nanocomposite Films with a Large Maximum Energy Product
    Cui, Wei-Bin
    Takahashi, Yukiko K.
    Hono, Kazuhiro
    [J]. ADVANCED MATERIALS, 2012, 24 (48) : 6530 - 6535
  • [6] Magnetic interactions in anisotropic Nd-Dy-Fe-Co-B/α-Fe multilayer magnets
    Dai, Z. M.
    Liu, W.
    Zhao, X. T.
    Han, Z.
    Kim, D.
    Choi, C. J.
    Zhang, Z. D.
    [J]. JOURNAL OF APPLIED PHYSICS, 2016, 120 (16)
  • [7] High performance hard magnetic NdFeB thick films for integration into micro-electro-mechanical systems
    Dempsey, N. M.
    Walther, A.
    May, F.
    Givord, D.
    Khlopkov, K.
    Gutfleisch, O.
    [J]. APPLIED PHYSICS LETTERS, 2007, 90 (09)
  • [8] Optimization of energy product and reversal process for Nd2Fe14B/α"-(FeCo)16N2/Nd2Fe14B exchange-spring trilayer films
    Fan, J. P.
    Zhang, X. Y.
    Jiang, Y. N.
    Liang, R. Y.
    Sun, J.
    Bai, Y. H.
    Xu, X. H.
    [J]. JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS, 2017, 441 : 43 - 48
  • [9] Micromagnetization patterning of sputtered NdFeB/Ta multilayered films utilizing laser assisted heating
    Fujiwara, Ryogen
    Shinshi, Tadahiko
    Kazawa, Elito
    [J]. SENSORS AND ACTUATORS A-PHYSICAL, 2014, 220 : 298 - 304
  • [10] Exchange-coupling interaction, effective anisotropy and coercivity in nanocomposite permanent materials
    Gao, RW
    Feng, WC
    Liu, HQ
    Wang, B
    Chen, W
    Han, GB
    Zhang, P
    Li, H
    Li, W
    Guo, YQ
    Pan, W
    Li, XM
    Zhu, MG
    Li, X
    [J]. JOURNAL OF APPLIED PHYSICS, 2003, 94 (01) : 664 - 668