Abstract
Here we report the single phase nanostructured Gd₃Fe₅O₁₂ garnets with different grain sizes (bulk, 75, 47, 35, and 22 nm) were prepared by ball milling for various milling times. Both the average grain size and the lattice parameter were estimated from the x-ray diffraction line broadening. The 57Fe Mӧssbauer spectra were recorded at 300 and 77 K for the samples with different grain sizes clearly evidenced the formation of Fe²⁺ ions induced by milling and the content of Fe²⁺ increases with milling time. At 4.2 K, a significant increase in saturation magnetization (+11%) has been observed for the 47 nm particles. The magnetization is strongly applied field dependent and no saturation effect is observed even at fields as high as of 320 kOe. The results presented here have been explained in terms of the key role played by the Fe²⁺ ions.
Keywords
nanostructures, milling, single phase nanostructured gadolinium iron garnet, 32 tesla, Gd₃Fe₅O₁₂, saturation magnetization
Subject Categories
Magnetic properties, Pulsed laser deposition, Magnetic fields, Garnet, Grain--Milling
Disciplines
Electromagnetics and photonics
Publisher
American Institute of Physics
Publication Date
5-1-2010
Rights Information
Copyright 2010 American Institute of Physics.
Rights Holder
American Institute of Physics
Permanent URL
Recommended Citation
Chinnasamy, C. N.; Greneche, J. M.; Guillot, M.; Latha, B.; Sakai, T.; Vittoria, C.; and Harris, V. G., "Structural and size dependent magnetic properties of single phase nanostructured gadolinium-iron-garnet under high magnetic field of 32 tesla" (2010). Electrical and Computer Engineering Faculty Publications. Paper 126. http://hdl.handle.net/2047/d20002297
Figure 1
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Additional Files
structural_and_size_dependent_fig1.zip (151 kB)Figure 1
structural_and_size_dependent_fig2.zip (756 kB)
Figure 2
structural_and_size_dependent_fig3.zip (54 kB)
Figure 3
structural_and_size_dependent_fig4.zip (228 kB)
Figure 4




Notes
Originally published in Journal of Applied Physics 107, 09A512 (2010). DOI:10.1063/1.3357326 (http://dx.doi.org/10.1063/1.3357326).