DocumentCode
38256
Title
Magnetic and Magnetization Properties of Co-Doped Fe2O3 Thin Films
Author
Akbar, Arslan ; Riaz, S. ; Ashraf, Robina ; Naseem, Shahzad
Author_Institution
Centre of Excellence in Solid State Phys., Univ. of the Punjab, Lahore, Pakistan
Volume
50
Issue
8
fYear
2014
fDate
Aug. 2014
Firstpage
1
Lastpage
4
Abstract
Amongst the various phases of iron oxide, hematite (Fe2O3) is the most stable form, which shows antiferromagnetic behavior with ferromagnetic canting at room temperature. Doping of different metal ions in α-Fe2O3 will not only lead to its new technological and industrial applications but also enhance its performance in existing applications. In this paper, we report synthesis and characterization of cobalt (Co)-doped Fe2O3 thin films with dopant concentration in the range of 0%-10%. XRD peaks shift to slightly higher angles as compared with undoped thin films due to smaller ionic radii of cobalt (72 pm) as compared with iron (74 pm). Room temperature magnetic properties, studied using vibrating sample magnetometer, show increase in saturation magnetization with increase in dopant concentration up to 8%. Further increase in dopant concentration to 10% degrades magnetic properties, which might be because of the presence of more atoms at the grain boundaries.
Keywords
X-ray diffraction; antiferromagnetic materials; cobalt; dilute magnetic materials; ferromagnetic materials; grain boundaries; iron compounds; magnetic thin films; magnetisation; magnetometry; sol-gel processing; Fe2O3:Co; XRD peaks; antiferromagnetic behavior; cobalt ionic radii; cobalt-doped hematite thin films; dopant concentration; ferromagnetic canting; grain boundaries; iron oxide phases; metal ion doping; saturation magnetization; temperature 293 K to 298 K; vibrating sample magnetometer; Cobalt; Iron; Lattices; Magnetic properties; Magnetic tunneling; Magnetometers; Saturation magnetization; Ferromagnetic; hematite; sol-gel; thin films;
fLanguage
English
Journal_Title
Magnetics, IEEE Transactions on
Publisher
ieee
ISSN
0018-9464
Type
jour
DOI
10.1109/TMAG.2014.2311826
Filename
6880908
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