Published March 2009 | Version v1
Journal article

Magnetization reversal process and intrinsic coercivity of sputtered Sm2Co17-based films

  • 1. State Key Laboratory of Electronic Thin Films and Integrated Devices, University of Electronic Science and Technology of China, Chengdu 610054 (China)
  • 2. Department of Physics and Astronomy, University of Delaware, Newark, DE 19716 (United States)

Description

The Sm2Co17-based intermetallic films with additives of Fe, Cu, and Zr have been deposited on Si(1 0 0) substrates by dc magnetron sputtering process. Subsequent thermal treatment and the film thickness are found to have significant contribution to the crystal structure and grain structure, which determines the magnetization reversal process and intrinsic coercivity (HC) of these films. The conventional thermal annealing (CTA) treatment almost failed to crystallize the as-deposited films, leading to a very low HC. Continuous and homogeneous domain walls cannot form in this deteriorated microstructure, so that the pinning mechanism can be excluded. Contrarily, the films with thickness exceeding 0.8 μm treated by rapid recurrent thermal annealing (RRTA) show an improved HC, which is attributed to the observed completed crystallization and compact microstructure. It is suggested that this film structure is responsible for providing continuous and homogeneous domain walls, leading to a magnetization reversal process controlled by domain wall pinning model. In special, the HC of the RRTA-treated film with thickness of 1.8 μm shows a good temperature dependence from 25 to 300 deg. C, with intrinsic coercivity temperature coefficient β of -0.23%/deg. C

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jmmm.2008.10.016

Additional details

Identifiers

DOI
10.1016/j.jmmm.2008.10.016;
PII
S0304-8853(08)01046-9;

Publishing Information

Journal Title
Journal of Magnetism and Magnetic Materials
Journal Volume
321
Journal Issue
6
Journal Page Range
p. 624-629
ISSN
0304-8853
CODEN
JMMMDC

Optional Information

Copyright
Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.