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Chiba, Masafumi;Uemura, Chikao;Arima, Hiroshi;Koizumi, Yoshiharu
- Journal of the Korean Magnetics Society
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- v.5 no.5
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- pp.659-662
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- 1995
Co-ferrite ($CoO-Fe_{2}O_{3}$) thin films have been prepared by two ways of low temperature solid reaction including oxidation process, being based on $Co-layer/{\alpha}-Fe_{2}O_{3}$ films and $Co-layer/Fe_{3}O_{4}$ films. Magnetic properties of both Co-ferrite films have been measured and compared. The samples from $Co-layer/Fe_{3}O_{4}$ films have a large coercive force in the direction perpendicular and have a great poler kerr rotation angle at wavelength 700 nm than ones from $Co-layer/{\alpha}-Fe_{2}O_{3}$ films. The typical magnetic properties are as follows; saturation magnetization $4{\pi}Ms$, 2.9 kG; remnant magnetization $4{\pi}Mr$, 2.0 kG; coercive force Hc, 4.0 kOe; kerr rotation angle ${\PHI}k$, 0.39 deg($\lambda\;=\;700\;nm$); and initial magnetization energy E, $3.3\;{\times}\;10^6\;erg/\textrm{m}^3$, respectively.
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Chong-Shik Chin;L. Vaska
- Journal of the Korean Chemical Society
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- v.24 no.5
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- pp.380-392
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- 1980
Six coordinate low spin iron(Ⅱ) complexes of vicinal-dioximes, [Fe$(DH)_2B_2$] and [Fe$(DH)_2$B(CO)]($(DH)_2$=$(CHDH)_2$(bis(1,2-cyclohexadinedioximato) bivalent anion), $(DPGH)_2$-(bis(diphenylglyoximato) bivalent anion), $(F{\alpha}DH)_2(bis(furil-{\alpha}-dioximato)$ bivalent anion); B = monodentate neutral nitrogen base), have been prepared and their physical properties have been investigated with respect to the effects of the equatorial ligands, $(DH)_2$. The order of ${\pi}$-acceptor CO stretching frequency for [Fe$(DH)_2$B(CO)] is $(F{\alpha}DH)_2$ > $(DPGH)_2$> $(CHDH)_2$, while non-${\pi}$-acceptor $NH_3$ stretching frequencies for [Fe$(DH)_2(NH_3)_2$] show the opposite order to that of CO, i.e., $(CHDH)_2$ > $(DPGH)_2$ > $(F{\alpha}DH)_2$. These infrared spectral data together with Fe-N (oxime) and Fe-N (oxime) and Fe-N (B) stretching frequency data suggest that the nitrogen atoms of $(CHDH)_2$ are more basic and poorer ${\pi}$-acceptors than the corresponding nitrogen atoms of $(DPGH)_2$ and $(F{\alpha}DH)_2$, respectively. It has been found from the electronic spectral data of [Fe$(DH)_2$] and [Fe$(DH)_2$B(CO)] that the energy of the charge transfer band from iron(Ⅱ) to $(DH)_2$ increases as the basicity of $(DH)_2$ increases.
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김보경;이진용;함상희;김순섭;이상석;황도근;김선욱;이장로
- Proceedings of the Korean Magnestics Society Conference
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- 2003.06a
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- pp.130-131
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- 2003
The magnetic and thermal properties of NiFe/IrMn/CoFe with Mn additions have been studied. As grown CoFe pinned-layers with IrMn-Mn have dominantly larger exchange biasing field( $H_{ex}$) and blocking temperature( $T_{b}$) than when pure I $r_{22}$M $n_{78}$ is used. The magnetic properties improve, $H_{ex}$ and $T_{b}$ improve with 77-78 vol% Mn, but drop considerably with more Mn additions, losing magnetic properties of theb NiFe/IrMn/CoFe with addition 0.6 vol % Mn. The average x-ray diffraction peak ratios fcc (111)CoFe of (111)IrM $n_3$ textures for the Mn inserted total vol of 75, 77, and 79 vol% were about 1.4, 0.8, and 0.6, respectively. For the sample without Mn inserted layer, the $H_{ex}$ between I $r_{22}$M $n_{78}$ and CoFe layers is almost nothing. For two multilayer as-grown samples with ultra-thin Mn layers of 77 vol % and 79 vol %, the $H_{ex}$s are 250 Oe and 150 Oe, respectively. In case of IrMn with 77.5 vol% Mn, the $H_{ex}$ was 444 Oe up to 30$0^{\circ}C$ endured of 363 Oe at 40$0^{\circ}C$, respectively. Mn additions improve the magnetic properties and thermal stabilities of NiFe/IrMn/CoFe. Those increase the $H_{ex}$ and $T_{b}$. In applications where higher $H_{ex}$ and $T_{b}$ are accept, proper concentrations of Mn can be used.n can be used.be used.
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