Loading…
Magnetic, Structural, and Dielectric Properties of Bi1-xKxFeO3 Thin Films Using Sol-Gel
Bismuth iron oxide (Bi 1-x K x FeO 3 ) thin films are prepared using sol-gel and the spin coating method. Films are deposited onto copper substrates and are annealed in the presence of vacuum with 500 Oe magnetic field at 300 °C. Potassium has an ionic radius of 1.64 Å and replaces Bi, which has an...
Saved in:
Published in: | IEEE transactions on magnetics 2014-08, Vol.50 (8), p.1-4 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Bismuth iron oxide (Bi 1-x K x FeO 3 ) thin films are prepared using sol-gel and the spin coating method. Films are deposited onto copper substrates and are annealed in the presence of vacuum with 500 Oe magnetic field at 300 °C. Potassium has an ionic radius of 1.64 Å and replaces Bi, which has an ionic radius of 1.17 Å. Based on the ionic radii difference of Bi 3+ and K + , the dopant concentration is varied in the range x = 0.0-0.3. X-ray diffractometer analysis shows that at x = 0.3 an impurity phase (K 2 O) appears, which was not present at low dopant concentrations. It is shown here that ferromagnetic behavior arises in doped BiFeO 3 films due to suppression of helical spin structure. In addition, as K+ replaces Bi 3+ the charge compensation mechanism gives rise to oxygen vacancies and to the formation of Fe 4+ cations, thus inducing ferromagnetic behavior. Variation in dopant concentration strongly affects the dielectric properties. Increase in dielectric constant up to 84 was observed with increase in dopant concentration up to 0.15. Decrease in dielectric constant ( 25), beyond 0.15 doping concentration, might have been observed because of the appearance of impurity phase as is observed in structural and magnetic properties. |
---|---|
ISSN: | 0018-9464 1941-0069 |
DOI: | 10.1109/TMAG.2014.2310691 |