Synthesis and characterization of FePt nanoparticles and FePt nanoparticle/SiO2-matrix composite films
Superparamagnetic face-centered cubic (fcc) FePt nanoparticles were synthesized using a polyol process. The effect of reaction temperature and molar ratio of Fe(CO) 5 to Pt(acac) 2 on the structure, composition and morphology of nanoparticles has been investigated. The optimum processing condition h...
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Published in | Journal of sol-gel science and technology Vol. 64; no. 2; pp. 269 - 275 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Boston
Springer US
01.11.2012
Springer Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Superparamagnetic face-centered cubic (fcc) FePt nanoparticles were synthesized using a polyol process. The effect of reaction temperature and molar ratio of Fe(CO)
5
to Pt(acac)
2
on the structure, composition and morphology of nanoparticles has been investigated. The optimum processing condition has been obtained for producing well-monodisperse fcc-phase FePt nanoparticles with the 2:1 molar ratio of Fe-Pt at 220 °C. In order to circumvent the problem of FePt particle coalescence during high temperature annealing for the
L
1
0
ordering, FePt nanoparticle/SiO
2
-matrix composite films have been fabricated by sol–gel method. The experimental results confirm that the amorphous SiO
2
matrix effectively inhibits the grain growth and particle aggregation during 700 °C annealing for 1 h. Well-monodisperse face-centered tetragonal (fct) FePt particles embedded in the SiO
2
matrix can be obtained with the long-range chemical order parameter
S
of ~0.74, indicating partially ordered
L
1
0
phase transition in FePt/SiO
2
composite films. The FePt/SiO
2
system exhibits a hysteretic behavior with smaller coercive field of 1,450 Oe. The incomplete phase transition from cubic deredat height maxsium (
A
1
-disordered phase to tetragonal
L
1
0
-ordered phase) might be responsible for it. |
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ISSN: | 0928-0707 1573-4846 |
DOI: | 10.1007/s10971-010-2373-8 |