DocumentCode :
1070437
Title :
Magnetization and coercivity studies in amorphous Nd50Fe 50/BN multilayers
Author :
Wan, H. ; Tsoukatos, A. ; Hadjipanayis, G.C.
Author_Institution :
Dept. of Phys. & Astron., Delaware Univ., Newark, DE, USA
Volume :
29
Issue :
6
fYear :
1993
fDate :
11/1/1993 12:00:00 AM
Firstpage :
3084
Lastpage :
3086
Abstract :
Amorphous Nd50Fe50/BN multilayers are fabricated by sputtering over a wide range of bilayer thickness. A superparamagnetic behavior is found above 20 K in samples with a dNdFe thickness below 15 Å which may be due to the particulate like nature of the thinner films. In samples with dNdFe above 15 Å, the spontaneous magnetization is found to be independent of thickness. The coercivity increases with the NdFe layer thickness according to 1/dNdFe. This may be related to the out of plane effective surface anisotropy. The spontaneous magnetization does not follow Bloch´s law above 50 K. A linear temperature dependence is observed in the temperature range of 50-300 K, with the temperature range extending to lower temperature in samples with thinner NdFe layers
Keywords :
amorphous state; boron compounds; coercive force; ferromagnetic properties of substances; iron alloys; magnetic multilayers; magnetic properties of amorphous substances; magnetic properties of fine particles; magnetic thin films; neodymium alloys; spontaneous magnetisation; sputtered coatings; superparamagnetism; 50 to 300 K; amorphous Nd50Fe50-BN multilayers; bilayer thickness; coercivity studies; linear temperature dependence; particulate like nature; plane effective surface anisotropy; spontaneous magnetization; sputtering; superparamagnetic behavior; temperature range; Amorphous materials; Anisotropic magnetoresistance; Coercive force; Iron; Magnetic multilayers; Magnetization; Neodymium; Sputtering; Temperature dependence; Temperature distribution;
fLanguage :
English
Journal_Title :
Magnetics, IEEE Transactions on
Publisher :
ieee
ISSN :
0018-9464
Type :
jour
DOI :
10.1109/20.280892
Filename :
280892
Link To Document :
بازگشت