33 research outputs found

    Mixing of Au in Si induced by secondary and high-order recoil implantation

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    The mixing of Au in Si induced by secondary and high-order recoil implantation was investigated using 350 keV Ar + and 350 keV Kr + ions to fluences from 1?×?10 16 to 3?×?10 16 ions/cm 2 at room temperature. The thickness of the Au layer evaporated on Si substrate was ~2400 .The ranges of the Ar and Kr ions were chosen to be lower than the thickness of the Au layer in order to avoid the ballistic mixing produced by the primary knock-on atoms. Rutherford backscattering spectrometry (RBS) experiments were carried out to study the effects induced by Ar and Kr irradiation at the interface of Au-Si system. We observed that in the case of the irradiation with Ar + ions, a broadening of the Au-Si interface occurred only at the fluence of 3?×?10 16 Ar + /cm 2 and it is attributed to the surface roughening induced by ion bombardment. In contrast, the RBS analysis of a sample irradiated with 2?×?10 16 Kr + /cm 2 clearly showed, in addition to the broadening effect, the formation of a mixed zone of Au and Si atoms at the interface. The mixing of Au in Si atoms can be explained by the secondary and high-order recoil implantation followed by subsequent collision cascade

    Effect of thickness on the physical properties of ITO thin films

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    We have studied the effect of thickness on the structural, optical and electrical properties of In2O3:Sn (ITO) thin films. Two series of ITO thin films have been deposited onto glass substrates by DC sputtering at two partial pressures of oxygen (ppo): 4 × 10−4 and 4.75 × 10−4 mbar. Each series consists of samples with thickness ranging from 306 nm to 1440 nm. We observed a change of texture with thickness; the thinner films grow with a 〈111〉 preferred orientation; however as the thickness increased, the preferred orientation becomes in the 〈100〉 direction. The lattice constant and the grain size have also been obtained from the X-ray spectra. The energy gap, Eg, has been obtained from the transmission curve; Eg is found to decrease with increasing thickness for both series. The electrical resistivity ρ has been studied as a function of thickness, ppo and temperature (T). The temperature was varied from room temperature (RT) to 450 °C and back to RT; a hysteresis effect was observed in the ρ vs. T curve. Also, a minimum in ρ was observed, in all these samples, in the temperature range 260 to 280 °C. For these temperatures, we have studied the effect of annealing time on the electrical resistivity for samples having both textures. We noted that ρ increased with annealing time and reaches a saturation value equal to the RT temperature value. Hall effect experiments were done on all these samples. The concentration n and the mobility μH were obtained. These parameters are found to be sensitive to the thickness and the texture of these films. All these results will be correlated and discussed

    A comparative structural and magnetic study of Fe100-xPdx(x=15, 20 and 36) thin films deposited on Si (100) and glass substrates

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    Various structural and magnetic characterization techniques have been used to investigate Fe100-xPdx (x=15, 20 and 36) thin films deposited onto silicon and glass substrates, by thermal evaporation technique. X-ray diffraction analysis shows the presence of supersaturated solid solution with bcc structure for Pd concentrations of 15% and 20%. However, for 36% of Pd, in addition to the supersaturated α-FePd (bcc) phase, another disordered FePd3 phase with fcc structure is present. At 20 at% Pd, the magnetic characterization shows a saturation of the bcc (α-FePd) phase and the appearance of the fcc phase. The correlation between the structure and magnetic properties allows us to compare the two substrates effects on deposited thin films. As results, the measurements indicate that the grain size D, the thin film thickness and the d(110) spacing significantly affect the magnetic coercivity HC. The Fe-Pd alloys deposited on a monocrystalline Si (100) and glass substrate show that the coercivity HC is given by the random anisotropy model. & 201

    Structural, electrical and magnetic properties of evaporated permalloy thin films: effect of substrate and thickness

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    We have studied the effects of the substrate and the thickness on the structural, electrical and magnetic properties of permalloy thin films Ni81Fe19 (Py). Series of Py thin films were evaporated on four various substrates: glass, kapton, Si(1 0 0) and Si(1 1 1). The thickness ranges from 13 nm to 190 nm. We show that evaporated permalloy on kapton and Si(1 1 1) present a strong ⟨1 1 1⟩ preferred orientation for samples thicker than 85 nm; however, the films grown on glass and Si(1 0 0) present a weak (1 1 1) texture for most of these samples. Generally, the lattice constant for Py/glass, Py/Si(1 0 0) and Py/Si(1 1 1) samples is found to be smaller than the bulk value (abulk), while for the Py/kapton, it is larger than abulk. There is an overall increase of the grain sizes (100 Å–480 Å) with thickness for Py/Si(1 1 1), Py/Si(1 0 0) and Py/glass. For the Py/kapton samples, the grain sizes (about 130 Å) seem to be independent of the thickness. The resistivity, ρ, decreases with increasing thickness for all samples. The highest values of ρ were observed in the Py/kapton thin films, diffusion at the grain boundaries might be in part responsible for these high values. The magnetization easy axis is found to be in the film plane for all samples. For all series, the two thinner films seem to exhibit a perpendicular magnetocrystalline anisotropy. The coercive field, HC//, values range from 1 Oe to 67 Oe. A peak in the HC// vs. t curve is observed for Py/Si while for Py on glass and Py/kapton, HC// seems to be constant. We also observed that for the thicker Py/Si(1 1 1) samples, the coercivity decreases as the grain sizes increase

    Pulsed excimer laser deposition of Permalloy thin films: structural and electrical properties

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    We report on the effect of thickness on the structural and electrical properties of permalloy thin films Ni81Fe19 (Py). Permalloy films were deposited onto Si(100) substrates at room temperature using a KrF (wavelength of 248 nm, pulse duration of 30 ns) excimer laser at a fluence of 3 J/cm2. The thickness ranges from 25 nm to 250 nm. The micrographs reveal the formation of irregular droplets with dimensions between 4.6 μm and 0.24 μm. We show that all samples presented a strong 100 \langle 100 \rangle texture. The lattice constant (a) monotonously increases with increasing thickness. Also, we note that for thickness below 127 nm, the lattice constant (a) is lower than the bulk value, however, for thickness more than 127 nm, (a) is higher than abulka_{\rm bulk} . The grain size increases from 30 nm to 54 nm as the thickness increases from 45 nm to 250 nm. The different contributions to the electrical resistivity are investigated as a function of the Py thickness

    Irradiation-induced gold silicide formation and stoichiometry effects in ion beam-mixed layer

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    The irradiation-induced silicide formation in ion beam-mixed layer of Au/Si(1 0 0) system was investigated by using 200 keV Kr+ and 350 keV Xe+ ions to fluences ranging from 8×1014 to 1×1016 ions/cm2 at room temperature. The thickness of Au layer evaporated on Si substrate was ∼500 Å. Rutherford backscattering spectrometry (RBS) experiments were carried out to study the irradiation effects on the mixed layers. We observed that at the fluence of 1×1016 Kr+/cm2 and starting from the fluence of 8×1014 Xe+/cm2, a total mixing of the deposited Au layer with Si was obtained. RBS data corresponding to the fluences of 1×1016 Kr+/cm2 and 8×1014 Xe+/cm2 clearly showed mixed layers with homogenous concentrations of Au and Si atoms which can be attributed to gold silicides. The samples irradiated to fluences of 1×1016 Kr+/cm2 and 1×1016 Xe+/cm2 were also analyzed by X-ray photoelectron spectroscopy (XPS). The observed chemical shift of Au 4f and Si 2p lines confirmed the formation of gold silicides at the surface of the mixed layers. Au2Si phase is obtained with Kr+ irradiation whereas the formed phase with Xe+ ions is more enriched in Si atoms. © 2006 Elsevier Ltd. All rights reserve

    Structural, microstructural and Mössbauer studies of nanocrystalline Fe100-x Alx powders elaborated by mechanical alloying

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    Nanocrystalline Fe100-xAlx powders (x= 25, 30, 34 and 40 at %) were prepared by the mechanical alloying process using a vario-planetary high-energy ball mill for a milling time of 35 h. The formation and physical properties of the alloys were investigated as a function of Al content by means of X-ray diffraction, scanning electron microscopy (SEM), energy dispersive X-ray and Mössbauer spectroscopy. For all Fe100-xAlx samples, the complete formation of bcc phase was observed after 35 h of milling. As Al content increases, the lattice parameter increases, whereas the grain size decreases from 106 to 12 nm. The powder particle morphology for different compositions was observed by SEM. The Mössbauer spectra were adjusted with a singlet line and a sextet containing two components. The singlet was attributed to the formation of paramagnetic A2 disordered structure rich with Al. About the sextet, the first component indicated the formation of Fe clusters/ Fe-rich phases; however, the second component is characteristic of disordered ferromagnetic phase

    Electrical properties and Kerr effect study of evaporated Fe/Si and Fe/glass thin films

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    Electrical and magnetic properties were studied for evaporated Fe thin films on glass and Si substrates. These properties were investigated by means of the four point probe and the magneto-optical Kerr effect techniques. Rutherford backscattering (RBS) and scanning electron microscopy (SEM) experiments show no interdiffusion at the interface Fe/Si for these samples. The electrical resistivity ρ\rho is found to be larger in Fe/glass than in Fe/Si for the same thickness. Diffusion at the grain boundaries seems to be the dominant factor in the ρ\rho values in this 6 to 110 nm thickness range; the reflection coefficient is smaller in Fe/glass (R ≈ 0.40) than in Fe/Si(100) (R ≈ 0.65). Saturation field and strain values confirm that Fe films have a stress induced magnetic anisotropy. Coercive field HC values range from 2.45 Oe for Fe/Si(100) to 17.65 Oe for Fe/Si(111) for the same Fe thickness (45 nm)
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