FeCrB非晶合金带铁磁共振研究

本文报道用电子自旋共振谱仪所测得的FeCrB非晶合金带的铁磁共振谱,给出了谱形随温度变化的实验结果。用“独立晶粒近似”理论解释了样品中的磁相变化,并讨论了线宽△H随温度T的变化。为研究非晶合金带材料的性能提供了新的实验结果。 关键词：     

铁磁共振实验中值得注意的几个问题

与顺磁样品相比铁磁样品的磁共振信号不仅是强得多,铁磁样品的许多特点都会在铁磁共振(FMR)谱中反映出来.诸如,起始磁化过程的FMR谱线与有剩余磁化强度Mr的FMR谱是不同的,起始磁化过程中的巴克豪森跳跃也会在FMR谱中反映出来.样品的磁晶各向异性、形状各向异性,铁磁高温顺磁的磁性相变等等都能用FMR方法加以研究.     

Fe/[NiFe/Cu]30多层膜线列阵的铁磁共振研究

用铁磁共振(FMR)技术研究Fe/［NiFe/Cu］₃₀多层膜线列阵的特性,线列阵采用激光全息光刻和离子束刻蚀技术加工,线密度为250线/mm和500线/mm.线列阵样品的FMR谱在稍高于主峰（声学峰）的共振场下有光学峰出现,相当层间交换耦合为反铁磁型.光学峰与声学峰的峰位间距沿易轴小于沿难轴.又,来自非磁Cu夹层的顺磁共振峰的幅度远大于原始的连续膜,说明线列阵加工致使层结构退化. 关键词：     

磁共振法研究(Fe1-xCox)84Zr3.5Nb3.5B8Cu1纳米晶薄带的磁各向异性

铁磁共振(FMR)实验研究(Fe1-xCox)84Zr3.5 Nb3.5B8Cu1(x=0.0,0.2,0.4,0.6, 0.8)合金薄带的各向异性,易轴在薄带的横向方向,同等宽度样品的各向异性常数K′随Co掺杂量的增加而减小, K′值在4.67×10-5 J/m(x=0.0)到2.54×10-5 J/m4(x=0.8)之间.由于磁化率的虚部χ″(H)随磁场强度H非线性变化,在低场(0-12 mT)有一个与FMR信号强度相当的低场非共振信号.特别是对Fe84Zr3.5 Nb3.5B8Cu1合金薄带的磁化,在可逆磁化(0-2.0 mT)和趋近饱和磁化(9.0-12 mT)区域, dχ″/dH=0;不可逆畴壁移动过程中,交流磁化率虚部χ″(H)与磁场强度的n次方即Hn(n≥3)有关;在磁畴转动过程中χ″(H)正比于H2(瑞利区),(dχ″)/(dH)为常数;而且发现,有不可逆畴壁移动-磁畴转动三段交替变化的过程,此过程对应三种磁畴的消失过程.     

磁共振法研究(Fe1-xCox)84Zr3.5Nb 3.5B8Cu1纳米晶薄带的磁各向异性

铁磁共振（FMR）实验研究(Fe_1-xCo_x)₈₄Zr_{3.5 Nb3.5B8Cu1（x=0.0,0.2,0.4,0.6, 0.8）合金薄 带的各向异性，易轴在薄带的横向方向,同等宽度样品 的各向异性常数K′随Co掺杂量的增加而减小, K′值在4.67×10^-5　J/m（x=0. 0）到 2.54×10^-5　J 关键词： 铁磁共振 各向异性常数 低场非共振信号 磁化过程}     

垂直磁各向异性自旋阀结构中的铁磁共振

本文在理论上研究了垂直磁各向异性自旋阀结构中磁场激发和调节的铁磁共振. 通过线性展开包含自旋转移矩项的Landau-Lifshitz-Gilbert方程,获得了磁场激发和调节的铁磁共振谱. 给出了共振线宽、共振频率和共振磁场随直流电流密度大小和方向以及直流磁场的变化关系. 通过调节直流电流密度的大小和方向,系统的有效阻尼可以达到最小. 关键词： 自旋阀 自旋转移矩 垂直磁各向异性 铁磁共振     

石榴石薄膜中的条畴铁磁共振

本文详细报道了条畴铁磁共振(FMR)特性与微波磁场和条畴间夹角的依赖关系。实验结果表明,由Smit和Beljers等人所提出来的关于磁畴共振的理论需要进一步改进和完善。 关键词：     

基于锁相放大器的微扰型共面波导铁磁共振测试参量研究

铁磁共振测试是自旋电子学研究的重要手段，为实现简单高效的FMR测试，基于瑞士苏黎世仪器500k MFLI锁相放大器，搭建了微扰型宽频带共面波导式铁磁共振测试系统，并对坡莫合金等材料进行了测试.为了得到材料的真实性质，对影响实验结果的参量进行优化，在深入讨论了这些参量对实验结果的影响及其物理和数学机制后，得到准确铁磁共振测试结果的实验条件为：电磁铁定点增加模式下，锁相放大器的时间常量为100 ms,滤波阶数在2阶以上，微扰线圈驱动信号振幅为1～2 V,频率为33～200 Hz.     

垂直场下磁性薄膜中的铁磁共振现象

将铁磁共振频率看成外磁场的函数, 讨论了垂直场下磁性膜中的铁磁共振现象. 结果显示: 当外磁场平行于膜面, 并考虑磁膜具有垂直磁晶各向异性情形时, 其磁共振频率随外磁场的变化分为高频支和低频支两种情况, 具体的依赖关系取决于磁膜内磁晶的各向异性; 当外磁场垂直于膜面, 其磁共振频率随外磁场的关系仅存在一支, 一般地, 磁共振频率随外磁场的增加单调地非线性减小, 但当立方磁晶各向异性场H_k1 与单轴磁晶各向异性场H_a之比值介于2/3 < H_k1/H_a <1时, 其磁共振频率随外磁场的增加单调增加, 这与相关的实验结果一致. 研究结果表明: 磁薄膜中有无垂直于膜面的磁各向异性可以通过其磁共振谱的测量进行辨析.     

Co-SiO2颗粒膜中颗粒相互作用的温度和尺寸依赖关系

我们在真空离子束溅射设备中制备了Co-SiO2颗粒膜，其结构和磁性分别利用透射电子显微术（TEM）和铁磁共振（FMR）来研究。TEM分析表明Co纳米颗粒相互独立地分布在SiO2介质中，且尺寸分布非常窄。室温转角FMR实验显示薄膜具有单轴各向异性，变温FMR实验被用来研究在100－300K温度范围内的颗粒间相互作用强度随温度变化的关系（我们利用一理论模型计算了颗粒集合体中的铁磁部分所占比例和超顺磁部分所占比例）。我们发现颗粒间相互作用强度除了与温度有关之外，还与Co颗粒的尺寸直接相关。     

Local structure of amorphous and microcrystalline Fe-B alloys

Amorphous and microcrystalline Fe-B alloys in the composition range (4–25) at % B, fabricated by melt spinning, were investigated by pulse nuclear magnetic resonance (NMR) on ¹¹B nuclei at 4.2 K. Alloy samples were prepared both from a natural mixture of isotopes and an isotope mixture ⁵⁶Fe-¹¹B. The NMR spectra were measured at different boron contents. The local atomic structure of amorphous Fe-B alloys has been determined. The amorphous alloys consist of microregions (clusters) with short-range order of the tetragonal and orthorhombic Fe₃B-phase types, as well as of the α-Fe type.     

穆斯堡尔谱学研究非晶TM80M20合金的微观结构

在室温下和4.2K下测定了非晶Fe₈₀B_20-xM_x合金(M=P,C)的穆斯堡尔吸收谱。利用分布参数拟合程序得到了超精细内场H_i和同质异能移IS同类金属成份的变化关系。利用这些结果考察了非晶合金的微观结构,比较了两类结构模型:Bernal-Polk模型和微晶模型。对比非晶合金和它们的相应晶相的行为得知,这类非晶合金中不存在微晶近程序,Bernal-Polk模型对描述TM-M类非晶合金的微观结构优于微晶模型。 关键词：     

NMR study of rapidly quenched crystalline and amorphous Fe-B alloys

Amorphous and microcrystalline Fe-B alloys (4–25 at % B) obtained by rapid quenching of the melt were studied using the pulsed nuclear magnetic resonance (NMR) of ¹¹B nuclei at 4.2 K. Alloy samples were prepared from both a natural isotope mixture and a mixture of the ⁵⁶Fe and ¹¹B isotopes. The NMR spectra were measured as a function of the boron content. The maximum hyperfine fields at the ¹¹B nuclei sites are 25–29 kOe and overlap the values of the hyperfine fields at the ¹¹B nuclei sites in the tetragonal and orthorhombic Fe₃B phases and also in the α-Fe phase containing boron as a substitutional impurity. The short-range order and local atomic structure of the amorphous Fe-B alloys were determined. The amorphous alloys are found to consist of microregions (clusters) with a short-range order similar to that in the tetragonal or orthorhombic Fe₃B phase or the α-Fe phase.     

On the FMR absorption in Pd-Si based amorphous alloys

Ferromagnetic resonance(FMR) spectra of ternary amorphous Pd-Si based system with 3d-metal (Co,Fe) are reported. The measurements have been performed at 9.37 GHz and room temperature on the as-quenched and annealed samples. For the Co-Pd-Si alloys an additional signal was observed at lower fields which can be ascribed to the antiresonance effect. This work was supported by the Slovak Ministry of Education and Science (Research Project No. 1/3201/96). The authors express their thanks to dr. Z. Frait for help and valuable discussions.     

Structural and Mössbauer studies of Fe1−xAlx alloys over the entire composition range

Metastable Fe_1?xAl_x alloys over the entire composition range have been investigated by X-ray diffraction and Mössbauer effect measurements. Alloys with x less than 0.55 are bec, whereas those with x>0.9 are fce, in between, the samples are amorphous. The Mössbauer spectra at 300 K for the bce alloys with x<0.5 consist of a broadened sextet and the spectra for the alloys with x≥0.5 are quadrupole-split doublets with a slight asymmetry. The magnetic hyperfine field at 4.2 K decreases monotonically with Al concentration from 340 kOe in pure Fe to zero at x=0.7. The isomer shift increases essentially linearly with Al concentration, and reaches a maximum at x=0.75. It is noted that at the boundary of x=0.55 separating the bce and the amorphous states, there is no discernible change in elther hyperfine field or lsomer shift.     

Magnetism in amorphous Fe-Si alloys

Fe-Si alloys have been obtained by the vapor quenching technique. Resistance measurements, electron microscopy and diffraction results are typical of an amorphous system. The Mössbauer spectra of these amorphous alloys, fitted in terms of a distribution of hyperfine fields, show the existence of a local magnetic order with, however, a proportion of weakly or even no coupled Fe atoms which is temperature and Fe-concentration dependent.     

Study of nano-scale diffusion in thin films and multilayers

It is shown that x-ray reflectivity and x-ray fluorescence under standing wave conditions can be used to study atomic diffusion with an accuracy of a fraction of a nanometer. Both the techniques can be made isotope selective by making use of nuclear resonance scattering from a Mössbauer active isotope. The techniques have been used to study self-diffusion of Fe in amorphous and nano-crystalline alloys of FeZr and FeN. The observed correlation of the activation energy E with pre-exponent factor D₀ confirms that in amorphous FeZr alloy diffusion takes place via collective motion of a group of atoms. Even in nanocrystalline alloys it is found that atomic diffusion occurs mainly through grain boundaries which are amorphous or highly disordered in nature.     

Unified analysis of diffusion and relaxation processes in amorphous metallic alloys

Abstract

Self-diffusion data on amorphous metallic alloys determined in long-time radio-tracer experiments and activation-enthalpy spectra deduced from short-time structural relaxation studies on such materials are reviewed and analyzed in terms of current random transition rate models. It is shown that the seeming discrepancy between the self-diffusion enthalpies and the comparatively small enthalpies obtained from measurements of the magnetic after-effect arises from the existence of activation-enthalpy spectra. Whereas the short-time experiments reveal the small-activation-enthalpy parts of these spectra, the long-time self-diffusion experiments are controlled by the larger activation enthalpies. Assuming that the activation-enthalpy distributions are Gaussian, their characteristic parameters have been determined by comparing the two types of measurements. It is shown that the Arrhenius-type diffusion coefficients found by experiment are compatible with half-widths of the activation-enthalpy spectra of about 0.3 eV. Based on an analysis of the pre-exponential factors and other typical properties of the diffusion coefficients, potential mechanisms of the diffusion in amorphous alloys are proposed.     

Multiple scattering approach to Co K-edge XMCD and XANES spectra in Gd–Co alloys

We have measured and analyzed Co K-edge X-ray absorption near edge structure (XANES) and X-ray magnetic circular dichroism (XMCD) near edge spectra in crystalline and amorphous GdCo₂ alloys. We have used a semi-relativistic full multiple scattering approach to the analyses of the XMCD spectra. A general formula is obtained which is applicable to randomly oriented systems in space. Useful information is obtained on both the electronic and geometric structure around a Co atom. The difference in XANES and XMCD spectra between crystalline and amorphous GdCo₂ is well explained by models referring to the anomalous X-ray scattering result, where three Gd atoms in the second shell are removed away. The calculated XANES are not so sensitive to the electronic structure, whereas the calculated XMCD spectra are rather sensitive to the spin polarization on Co atoms. The result shows that the spin polarization on Co atoms in GdCo₂ alloys is smaller than that in Co metals.     

Specific features of the magnetoreflection of co-based amorphous ribbons in the IR region

The light reflection spectra and the magnetorefractive effect in the cobalt-based amorphous ribbons in the IR spectral region (λ = 2.5–25 μm) are studied. These amorphous alloys are characterized by the magnetoimpedance effect, which is enhanced after thermal and laser annealing. It is found that the magnetoimpedance and magnetorefractive effects correlate with each other. The magnetorefractive effect reveals a feature at λ = 15–20 μm and the change of sign in the wavelength region 20–25 μm. It is shown that, in the first approximation, the optical properties of the amorphous alloys in the IR spectral region can be explained on the basis of a modified Hagen-Rubens relation. It is found that the change in the reflection coefficient of amorphous metal films in the IR spectral region under action of a magnetic field is caused by the change in both their magnetic permeability and conductivity, which is caused by the degree of polarization of localized electronic states at the Fermi level.