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Exchange-coupled nanocomposite magnets by nanoparticle self-assembly

Author

Listed:
  • Hao Zeng

    (IBM T. J. Watson Research Center
    Louisiana Tech University)

  • Jing Li

    (Georgia Institute of Technology)

  • J. P. Liu

    (Louisiana Tech University)

  • Zhong L. Wang

    (Georgia Institute of Technology)

  • Shouheng Sun

    (IBM T. J. Watson Research Center)

Abstract

Exchange-spring magnets are nanocomposites that are composed of magnetically hard and soft phases that interact by magnetic exchange coupling1. Such systems are promising for advanced permanent magnetic applications, as they have a large energy product—the combination of permanent magnet field and magnetization—compared to traditional, single-phase materials1,2,3. Conventional techniques, including melt-spinning4,5,6, mechanical milling7,8,9 and sputtering10,11,12, have been explored to prepare exchange-spring magnets. However, the requirement that both the hard and soft phases are controlled at the nanometre scale, to ensure efficient exchange coupling, has posed significant preparation challenges. Here we report the fabrication of exchange-coupled nanocomposites using nanoparticle self-assembly. In this approach, both FePt and Fe3O4 particles are incorporated as nanometre-scale building blocks into binary assemblies. Subsequent annealing converts the assembly into FePt–Fe3Pt nanocomposites, where FePt is a magnetically hard phase and Fe3Pt a soft phase. An optimum exchange coupling, and therefore an optimum energy product, can be obtained by independently tuning the size and composition of the individual building blocks. We have produced exchange-coupled isotropic FePt–Fe3Pt nanocomposites with an energy product of 20.1 MG Oe, which exceeds the theoretical limit of 13 MG Oe for non-exchange-coupled isotropic FePt by over 50 per cent.

Suggested Citation

  • Hao Zeng & Jing Li & J. P. Liu & Zhong L. Wang & Shouheng Sun, 2002. "Exchange-coupled nanocomposite magnets by nanoparticle self-assembly," Nature, Nature, vol. 420(6914), pages 395-398, November.
  • Handle: RePEc:nat:nature:v:420:y:2002:i:6914:d:10.1038_nature01208
    DOI: 10.1038/nature01208
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    Cited by:

    1. Chenli Huang & Rong Sun & Lipiao Bao & Xinyue Tian & Changwang Pan & Mengyang Li & Wangqiang Shen & Kun Guo & Bingwu Wang & Xing Lu & Song Gao, 2023. "A hard molecular nanomagnet from confined paramagnetic 3d-4f spins inside a fullerene cage," Nature Communications, Nature, vol. 14(1), pages 1-8, December.
    2. Gharaibeh, Maen & Alqaiem, Samah & Obeidat, Abdalla & Al-Qawasmeh, Ahmad & Abedrabbo, Sufian & Badarneh, Mohammad H.A., 2021. "Magnetic properties of the ferrimagnetic triangular nanotube with core–shell structure: A Monte Carlo study," Physica A: Statistical Mechanics and its Applications, Elsevier, vol. 584(C).
    3. Bum Chul Park & Min Jun Ko & Young Kwang Kim & Gyu Won Kim & Myeong Soo Kim & Thomas Myeongseok Koo & Hong En Fu & Young Keun Kim, 2022. "Surface-ligand-induced crystallographic disorder–order transition in oriented attachment for the tuneable assembly of mesocrystals," Nature Communications, Nature, vol. 13(1), pages 1-11, December.

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