Local anodization of permalloy film by atomic force microscope

Local anodization on a permalloy (_Ni80Fe20)${\mathrm{Ni}}_{80}{\mathrm{Fe}}_{20})$ thin film by an atomic force microscope (AFM) in air was studied. Fabrication of uniform structure on the permalloy film was difficult in comparison with that on a Si(1 0 0) substrate. On the permalloy film, threshold voltage for the AFM anodization increased until 3 h after exposure to air. With passage of time, I–V$I–V$ curves on the permalloy film also changed from metallic behavior to insulating one. In addition, I–V$I–V$ curves varied at positions on the permalloy film. The oxide layer with time- and position-dependencies can induce non-uniform structure in AFM anodization. However, uniformity of structure was able to be improved by using method of fabrication of dots.     

On the propensity of magnetism in 3d transition-metal-MgCNi3 alloys

The effects of disorder and incipient magnetism in MgC(_Ni1-xTx)3$\mathrm{MgC}({\mathrm{Ni}}_{1-x}{\mathrm{T}}_x{)}_3$ (T≡Fe$\mathrm{T}\equiv \mathrm{Fe}$, Co or Cu) alloys are studied using coherent-potential approximation and Ginzburg–Landau coefficients. The first-principles, local-density-functional-based calculations for substitutionally disordered Fe and Co impurities in the Ni sub-lattice of MgCNi₃, in low concentrations, show that incipient magnetism resides in these materials. The overestimation of the calculated magnetic properties points to the limitations of the local-density approximation. However, using a phenomenological approach based on Ginzburg–Landau coefficients and the fixed-spin moment method, we show that MgC(_Ni1-xTx)3$\mathrm{MgC}({\mathrm{Ni}}_{1-x}{\mathrm{T}}_x{)}_3$ alloys remain paramagnetic. At expanded volumes, we also find the possibility of a ferromagnetic state for MgC(_{Ni0.95Fe0.05)3}$\mathrm{MgC}({\mathrm{Ni}}_{0.95}{\mathrm{Fe}}_{0.05}{)}_3$ and MgC(_{Ni0.90Co0.10)3}$\mathrm{MgC}({\mathrm{Ni}}_{0.90}{\mathrm{Co}}_{0.10}{)}_3$ alloys.     

Effect of Mg substitution on electromagnetic properties of (Ni0.25Cu0.20Zn0.55)Fe2O4 ferrite prepared by auto combustion method

The ferrite compositions of (Ni_0.25−xMg_xCu_0.2Zn_0.55)Fe₂O₄ with x=0.0$x=0.0$, 0.07, 0.13, 0.18, and 0.25 were synthesized through nitrate-citrate auto-combustion method. The as-burnt powders showed the presence of crystalline cubic spinel ferrite with about 19–22 nm crystallite sizes. The resultant powders were calcined at 700 °C/2 h and pressed ferrites were sintered at 950 °C/4 h. The initial permeability, magnetic loss and AC resistivity were measured in the frequency range 10 Hz–10 MHz. The permeability and AC resistivity were found to increase and the magnetic loss decreased with Mg substitution for Ni, up to x=0.18$x=0.18$. The very high permeability in the composition x=0.18$x=0.18$, was due to better densification, lower magnetostriction constant and inner stresses, etc. The AC resistivity of the composition was also highest. The composition would be better than NiCuZn-based material for more miniaturization of multi layer chip inductor.     

Pressure dependence of the irradiation-induced ferromagnetism in Fe–Ni invar alloys

Pressure dependence of the irradiation-induced ferromagnetism recently found in Fe–Ni invar alloys was investigated under hydrostatic pressures up to 7.5 GPa. A rectangular sheet of Fe–30.2 at% Ni invar alloy was irradiated with 80 MeV Xe ions. The range was much smaller than the thickness of the sample. The Curie temperature of the irradiated part increased by 63 K, and the absolute value of the pressure coefficient, dT_C/dp   was smaller than that of non-irradiated part. The relation p≈(_TC0-_TC)ⁿ$p\approx (T_{{\mathrm{C}}_0}-T_{\mathrm{C}}{)}^n$ holds with n=2$n=2$ for both non-irradiated and irradiated part. The itinerant character was not so much modified by irradiation.     

Effect of carbon content on structure and magnetic properties for (Fe,Ni)1−xCx by mechanical alloying

FCC (Fe₅₅Ni₄₅)_1−xC_x   supersaturated solid solution was prepared in a wide concentration range (0?x?0.9)$(0?x?0.9)$ by mechanical alloying of nanocrystalline Fe₅₅Ni₄₅ with graphite. The lattice constant of Fe₅₅Ni₄₅ increases linearly with increasing carbon content up to x=0.25$x=0.25$. At the same time, it is found that the magnetic moment per metal atom (Fe, Ni) decreases linearly with increasing carbon content for 0?x?0.25$0?x?0.25$ with a slope of 1.2 μ_B/at. For high carbon content, x?0.5$x?0.5$, it is observed that the decrease of lattice constant and increase of moment per metal atom (Fe, Ni) with increasing C content, indicates that the dissolution of carbon is hindered by the high-volume fraction of graphite in the initial powder mixture. The complete amorphization of x=0.5$x=0.5$ does not occur after the extended ball milling. The alloying effect of carbon on the magnetization is compared with other metalloid B, P, and Si in Fe- and Ni-based binary system.     

Ferromagnetic properties of Fe-substituted ZnO-based magnetic semiconductor

The diluted magnetic semiconductor Zn_1−x⁵⁷Fe_xO (x=0.01, 0.02, 0.03) compounds were prepared by the solid-state reaction method. The crystal structure of _Zn0.97⁵⁷_Fe0.03O${\mathrm{Zn}}_{0.97}{}^{57}{\mathrm{Fe}}_{0.03}\mathrm{O}$ at room temperature is determined to be a hexagonal structure of P6₃mc with lattice constants a₀=3.252 Å and c₀=5.205 Å by Rietveld refinement. The Bragg factors R_B and R_F were determined as 3.23% and 2.81%. From the inverse susceptibility versus T curve, the paramagnetic Curie temperature is found to be 2.7 K and effective moment is found to be 4.01 μ_B, thereby suggesting that the exchange interactions between Fe ions are ferromagnetic. Mössbauer spectra of _Zn0.97⁵⁷_Fe0.03O${\mathrm{Zn}}_{0.97}{}^{57}{\mathrm{Fe}}_{0.03}\mathrm{O}$ have been taken at various temperatures ranging from 4.2 to 295 K. Mössbauer spectrum for _Zn0.97⁵⁷_Fe0.03O${\mathrm{Zn}}_{0.97}{}^{57}{\mathrm{Fe}}_{0.03}\mathrm{O}$ at 4.2 K has shown ferromagnetic phase (sextet), and the spectra were fitted based on a random distribution model of Fe ions.     

Effects of Gd substitution on the structural and magnetic properties of strontium hexaferrites

The effect of Gd substitution in M-type strontium hexaferrites has been examined in two series of samples, (_Sr1-xGdx)O·5.25$({\mathrm{Sr}}_{1-x}{\mathrm{Gd}}_x)\mathrm{O}·5.25$_Fe2O3${\mathrm{Fe}}_2{\mathrm{O}}_3$ and _{Sr1-xGdxFe12-xCoxO19}${\mathrm{Sr}}_{1-x}{\mathrm{Gd}}_x{\mathrm{Fe}}_{12-x}{\mathrm{Co}}_x{\mathrm{O}}_{19}$, both prepared by the ceramic method, where x=0–0.40$x=0–0.40$. The samples have been characterized by XRD, VSM and SEM-EDAX techniques. All substituted samples present primarily the hexaferrite structure. Sample (_{Sr0.95Gdx0.05})O·5.25$({\mathrm{Sr}}_{0.95}{\mathrm{Gd}}_{x0.05})\mathrm{O}·5.25$_Fe2O3${\mathrm{Fe}}_2{\mathrm{O}}_3$ is single phase. Formation of impurity phases is affected by stoichiometry and presence of Co. In Sr–Gd samples, coercivity showed a maximum value of 305 kA/m (3.8 kOe) for x=0.20$x=0.20$, while remanence and saturation magnetization did not decrease. Coercivity and magnetization in the Sr–Gd–Co series decreased steadily with substitution degree.     

Time dependence of hysteresis loop displacement in hard–soft magnetic systems

Time dependence of the hysteresis loop asymmetry observed in partially crystallized _{Co66Si16B12Fe4Mo2}${\mathrm{Co}}_{66}{\mathrm{Si}}_{16}{\mathrm{B}}_{12}{\mathrm{Fe}}_4{\mathrm{Mo}}_2$ is here analyzed at room temperature. The results are related to a magnetic aftereffect occurring in the hard crystallites embedded in the residual soft matrix. The coercive field is found to be constant with time, which is explained in terms of the dipolar interaction theory.     

Mössbauer studies on the superparamagnetic behavior of CoFe2O4 with a few nanometers

CoFe₂O₄ nanoparticles with a cubic spinel structure are prepared by a high-temperature thermal decomposition method. The average particle sizes are 4.6  and 5.7 nm for CoFe₂O₄ made with two kinds of solvents by TEM. Mössbauer spectra of 4.6 nm particles displayed a superparamagnetic behavior as demonstrated by a single line with zero hyperfine fields, but that of 5.7 nm particles did not at room temperature. It is considered that anisotropy energy was still more superior to thermal energy because of particle size of 5.7 nm CoFe₂O₄. Furthermore, Mössbauer spectra exhibited the typical spectrum shapes of the CoFe₂O₄ at 4.2 K. The spectrum at 4.2 K was fitted using two magnetic components of hyperfine fields _Hhf=540.4,512.6$H_{\mathrm{hf}}=540.4,512.6$ kOe and isomer shifts δ=0.40,0.30$\delta =0.40,0.30$ mm/s for 4.6 nm and _Hhf=542.7,512.8$H_{\mathrm{hf}}=542.7,512.8$ kOe and δ=0.41,0.29$\delta =0.41,0.29$ mm/s for 5.7 nm corresponding to Fe³⁺ ions at site A and site B, respectively.     

Magnetic linear dichroism studies of in situ grown NiO thin films

We report thickness dependence of magnetic linear dichroism (MLD) of in situ grown NiO(0 0 1) films on Ag(0 0 1) substrate at the Ni L₂ absorption edge. Antiferromagnetic domains at the surface of NiO(0 0 1) films are found to be preferentially aligned in-plane. For films thinner than a critical thickness _tc$t_{\mathrm{c}}$ (20–40ML), we observe a softening of the in-plane magnetic domain alignments with increasing film thickness, arising from the strain-relaxation effects. Films thicker than _tc$t_{\mathrm{c}}$ exhibits a residual in-plane anisotropy, possibly related to the finite-thickness effects.     

The influence of 3d-impurities on magnetic and transport properties of CoSiB metallic glasses

Temperature dependencies of magnetic susceptibility and electric resistivity of Co-based metallic glasses (MGs) of the general composition _Co(72-x)Mex(Si,B₎₂₈${\mathrm{Co}}_{(72-x)}{\mathrm{Me}}_x(\mathrm{Si},\mathrm{B}{)}_{28}$(Me=Fe,Cr,Si:B=18:10)$(\mathrm{Me}=\mathrm{Fe},\mathrm{Cr},\mathrm{Si}:\mathrm{B}=18:10)$ have been studied up to 950 K. The studied MGs were found to be ferromagnets at the room temperature and their Curie point _TC$T_{\mathrm{C}}$ ranges within 260–560 K depending on the dopant contents. At the temperatures higher than _TC$T_{\mathrm{C}}$, a wide paramagnetic region exists. The regularities of magnetic moment variation upon Cr doping evidence a formation of antiferromagnetic clusters, which determine the anomalous behavior of resistivity.     

X-ray magnetic circular dichroism at rare-earth L23 absorption edges in various compounds and alloys

Theoretical interpretations of X-ray magnetic circular dichroism (XMCD) at rare-earth (called R hereafter) L₂₃ absorption edges are reviewed using differing models, depending on the material under investigation. In the first chapter, we present an overview of recent developments for XMCD in XAS with a few general remarks, especially at R atom absorption edges. In Section 2, we first describe basic mechanism of XMCD at L₂₃ edges of R systems, and then we essentially discuss two examples of XMCD spectra in: (i) R₂Fe₁₄B metallic compounds, with the help of a cluster model, and (ii) RFe₂ Laves-phase compounds, using a tight-binding approximation for R 5d and Fe 3d conducting states. A good agreement between theory and experiment for R₂Fe₁₄B suggests that a cluster model provides a valuable method to quantitatively calculate XMCD spectra of R systems, even with quite complicated atomic arrangements. For RFe₂ systems the XMCD spectral shape, especially for the L₂ edge of heavy R elements, is more complicated than those of R₂Fe₁₄B systems, and this is explained by the competition of some different XMCD mechanisms. In Section 3, we focus on special series of Ce systems, related to XAS and XMCD studies at the Ce L₂₃ edges. Two clearly differing cases are interpreted: (i) A well localized 4f¹ system, i.e. CeRu₂Ge₂; (ii) A less localized 4f¹ system, i.e. CeFe₂, with a 3d partner. Then, from a more experimental point of view, we investigate the influence of substitution on the low temperature properties of CePd₃ compounds, i.e. Ce(_Pd1-xMnx)3$\mathrm{Ce}({\mathrm{Pd}}_{1-x}{\mathrm{Mn}}_x{)}_3$ alloys where x   is about 0.03, giving rise to (_CePd3)8Mn$({\mathrm{CePd}}_3{)}_8\mathrm{Mn}$ ordered structure. We give another example: Ce(_Pd1-xNix)3$\mathrm{Ce}({\mathrm{Pd}}_{1-x}{\mathrm{Ni}}_x{)}_3$ alloys with x taken up to about 0.25. Also the Ce L₂₃ XMCD signal measured in pure CePd₃ demonstrates that in the Ce based dense Kondo materials, only the 4f¹ channel yields a magnetic response.     

Exchange bias of mu-metal thin films

The exchange bias of the soft ferromagnet mu-metal, _{Ni77Fe14Cu5Mo4}${\mathrm{Ni}}_{77}{\mathrm{Fe}}_{14}{\mathrm{Cu}}_5{\mathrm{Mo}}_4$, with the metallic antiferromagnet _Fe50Mn50${\mathrm{Fe}}_{50}{\mathrm{Mn}}_{50}$ has been studied as a function of ferromagnet thickness and buffer layer material. Mu-metal exhibits classic exchange bias behavior: the exchange bias (_HEB)$(H_{\mathit{EB}})$ and coercive fields scale inversely with the ferromagnet's thickness, with H_EB varying as the cosine of the in-plane applied field angle. Ta buffers, rather than Cu, allow the mu-metal to retain more of its soft magnetic character while exhibiting exchange bias. The ability to preserve soft ferromagnetic behavior in an exchange biased heterostructure may be useful for low field sensing and other device applications.