Tunable perpendicular magnetic anisotropy in GdFeCo amorphous films
We report the compositional and temperature dependence of magnetic compensation in amorphous ferrimagnetic GdxFe93−xCo7 alloy films. Magnetic compensation is attributed to the competition between antiferromagnetic coupling of rare-earth (RE) with transition-metal (TM) ions and ferromagnetic interact...
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Veröffentlicht in: | Journal of magnetism and magnetic materials 2013-08, Vol.339, p.51-55 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | We report the compositional and temperature dependence of magnetic compensation in amorphous ferrimagnetic GdxFe93−xCo7 alloy films. Magnetic compensation is attributed to the competition between antiferromagnetic coupling of rare-earth (RE) with transition-metal (TM) ions and ferromagnetic interaction between the TM ions. The low-Gd region of x between 20 and 34 was found to exhibit compensation phenomena characterized by a low saturation magnetization and perpendicular magnetic anisotropy (PMA) near the compensation temperature. Compensation temperature was not observed in previously unreported high-Gd region of x=52–59, in qualitative agreement with results from recent model calculations. However, low magnetization was achieved at room temperature, accompanied by a large PMA with coercivity reaching ~6.6kOe. The observed perpendicular magnetic anisotropy of amorphous GdFeCo films probably has a structural origin consistent with certain aspects of the atomic-scale anisotropy. Our findings have broadened the composition range of transition metal-rare earth alloys for designing PMA films, making it attractive for tunable magnetic anisotropy in nanoscale devices.
► We measure the magnetic anisotropy of amorphous GdxFe93−xCo7 films. ► The magnetization was controlled by varying the composition and temperature. ► At room temperature a large PMA with coercivity of 6.6kOe was achieved. ► The PMA has a structural origin consistent with the atomic-scale anisotropy. |
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ISSN: | 0304-8853 |
DOI: | 10.1016/j.jmmm.2013.03.007 |