Abstract
The influence of synthesis procedure on the yttrium iron garnet (YIG; Y3Fe5O12) formation has been investigated by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Mössbauer and magnetization measurements. The samples were prepared by coprecipitation or ceramic processing using the starting molar ratio Y2O3/Fe2O3=3:5. The fractions of Y2O3, α-Fe2O3, YFeO3 and YIG present in the samples depended on the method of materials processing and the calcination temperature. XRD of the thermally treated hydroxide coprecipitate at 1173 K showed the formation of YIG as a dominant phase, and YFeO3 and Y2O3 as associated phases, whereas upon heating at 1473 K, YIG and a small amount of YFeO3 were found. The samples produced by combining ball-milling of the starting powder and ceramic processing at 1573 K contained YIG and a smaller amount of YFeO3, as found by XRD. It was shown that high-energy ball-milling with stainless steel can be substituted by milling with agate bowl and balls, thus decreasing the contamination of the oxide system due to wear. FT-IR and 57Fe Mössbauer spectroscopic measurements were in agreement with XRD; however, the smaller amount of YFeO3 produced at 1573 K could not be detected with certainty by means of FT-IR and 57Fe Mössbauer spectroscopies. The magnetization values of end-products measured at 5 K were in agreement with their phase composition.
Original language | English |
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Pages (from-to) | 2584-2590 |
Number of pages | 7 |
Journal | Materials Letters |
Volume | 57 |
Issue number | 16-17 |
DOIs | |
State | Published - May 2003 |
Keywords
- Fe Mössbauer
- FT-IR
- Magnetic oxides
- Magnetization measurements
- XRD
- Yttrium iron garnet