Ferrimagnetic properties of Co/(Gd–Co) multilayers

Co/(Gd–Co) multilayers have been prepared by rf-sputtering and investigated by means of Transverse Magnetooptic Kerr Effect (TMOKE), SQUID and VSM magnetometry. The composition of amorphous _Gd0.36Co0.64${\mathrm{Gd}}_{0.36}{\mathrm{Co}}_{0.64}$ layers was chosen so that their saturation magnetization was dominated by Gd moments in all the temperature range. Co and Gd–Co layers formed a macroscopic ferrimagnetically coupled system displaying a compensation temperature. Complete magnetic moment compensation was found at such point. An inversion of TMOKE hysteresis loops and a divergent behaviour of coercivity were also observed. By changing the layers thickness it has been possible to control the magnetic characteristics of the Co/(Gd–Co) structures, in particular the compensation takes place at different temperatures.     

Hyperfine anomalies and nuclear γ-factors of56Co,57Co and60Co isotopes studied by NMR/ON

The results of NMR/ON measurements on^56,57,60Co isotopes in iron are presented in the paper. To avoid the uncertainties caused by local demagnetizing field inhomogeneities the measurements on two cobalt isotopes in one sample have been carried out. The values of nuclear-factors ratios ⁵⁷/ ⁶⁰=1·805(20), ⁶⁰/ ⁵⁶ = 0·761(20), ⁵⁶/ ⁵⁷ = 0·726(20) and hyperfme anomalies^{56 60} = –0·036(10),^{60 57} = 0·017(10) and^{57 56} = 0·018(10) have been calculated from the experimental results.Dedicated to the 30th anniversary of the Joint Institute for Nuclear Research.     

Electron Holography of Barrier Structures in Co／ZrAlOx／Co Magnetic Tunnel Junctions

We investigate the potential profiles and elemental distribution of barriers in Co/ZrAlOx/Co magnetic tunnel junctions (MTJs) using electron holography (EH) and scanning transmission electron microscopy. The MTJ barriers are introduced by oxidizing a bilayer consisting with a uniform 0.45-nm Al layer and a wedge-shaped Zr layer (0-2 nm). From the scanning transmission electron microscopy, AlOx and ZrOx layers are mixed together, indicating that compact AlOx layer cannot be formed in such a bilayer structure of barriers. The Eli results reveal that there are no sharp interfaces between the barrier and magnetic electrodes, which may be responsible for a smaller tunnelling magnetoresistance compared with the MTJs of Co/AlOx/Co.     

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.     

Kinetics of Heterogeneous Isotopic Exchange of 60Co/Co3Co(CN)6 2 · 12 H2O in Aqueous Solution

The heterogeneous exchange reaction between cobalt ions in solution and Co₃Co(CN)_{6 2} · 12 H₂O has been studied. It is found that the exchange rate increases as the concentration of Co²⁺ ions in solution decreases. The results show that the exchange rate is controlled by the surface reaction at the solid-liquid interface. The activation parameters E_a, ΔH^#, ΔS^#, and ΔG^# are calculated.     

Co/GaAs(100)界面形成以及Co超薄膜磁性质的研究

利用同步辐射光电发射和铁磁共振(FMR)研究了Co/GaAs(100)界面形成以及Co超薄膜的磁性质.结果表明,在低覆盖度(约为0.2nm)下,Co吸附原子与衬底发生强烈的界面反应,在覆盖度为0.9nm时,形成稳定的界面.从衬底扩散出的Ga原子与Co覆盖层合金化,而部分As原子与Co原子发生反应,形成稳定的键合,这些反应产物都停留在界面处很窄的区域(0.3—0.4nm)内.另一部分As原子偏析在Co覆盖层表面.结合理论模型,详细地讨论了界面结构及Ga，As原子的深度分布.FMR结果表明,生长的Co超薄膜具 关键词：     

第一性原理研究Co2MnSi和Co2MnGe半金属与磁性的稳定性

基于广义梯度近似密度泛函和全势能线性缀加平面波方法,对Co2MnSi和Co2MnGe在晶格常数发生变化的情况下进行电子结构和磁矩的自旋极化计算,得到了它们的自旋态密度分布以及总磁矩和各原子磁矩。计算结果的分析表明：（1）Co2MnSi 和Co2MnGe具有半金属性质;（2）晶格常数的改变分别为-5%~ 4%和-6%~1%时,Co2MnSi 和 Co2MnGe仍保持稳定的半金属质性;（3）Co2MnSi 和Co2MnGe的总磁矩为5.00µB/formula。总磁矩主要来源于Mn和Co的原子磁矩,Si和Ge的原子磁矩对总磁矩的贡献极小而且为负值。（4）Co2MnSi 和 Co2MnGe的晶格常数变化分别为-6% ~ 6%和-7%~ 4%时,虽然各原子磁矩都发生了变化,但是它们总磁矩稳定于5.00µB/formula.     

第一性原理研究Co2MnSi和Co2MnGe半金属与磁性的稳定性

基于广义梯度近似密度泛函和全势能线性缀加平面波方法,对Co2MnSi和Co2MnGe在晶格常数发生变化的情况下进行电子结构和磁矩的自旋极化计算,得到了它们的自旋态密度分布以及总磁矩和各原子磁矩。计算结果的分析表明：（1）Co2MnSi 和Co2MnGe具有半金属性质;（2）晶格常数的改变分别为-5%~ 4%和-6%~1%时,Co2MnSi 和 Co2MnGe仍保持稳定的半金属质性;（3）Co2MnSi 和Co2MnGe的总磁矩为5.00µB/formula。总磁矩主要来源于Mn和Co的原子磁矩,Si和Ge的原子磁矩对总磁矩的贡献极小而且为负值。（4）Co2MnSi 和 Co2MnGe的晶格常数变化分别为-6% ~ 6%和-7%~ 4%时,虽然各原子磁矩都发生了变化,但是它们总磁矩稳定于5.00µB/formula.     

Spin polarization effect for Co2 molecule

The density functional theory (DFT)(b3p86) of Gaussian 03 has been used to optimize the structure of the Co$_{2}$ molecule, a transition metal element molecule. The result shows that the ground state for the Co$_{2}$ molecule is a 7-multiple state, indicating a spin polarization effect in the Co$_{2}$ molecule. Meanwhile, we have not found any spin pollution because the wavefunction of the ground state is not mingled with wavefunctions of higher-energy states. So for the ground state of Co$_{2}$ molecule to be a 7-multiple state is the indicative of spin polarization effect of the Co$_{2}$ molecule, that is, there exist 6 parallel spin electrons in a Co$_{2}$ molecule. The number of non-conjugated electrons is the greatest. These electrons occupy different spacial orbitals so that the energy of the Co$_{2}$ molecule is minimized. It can be concluded that the effect of parallel spin in the Co$_{2}$ molecule is larger than the effect of the conjugated molecule, which is obviously related to the effect of electron d delocalization. In addition, the Murrell--Sorbie potential functions with the parameters for the ground state and the other states of the Co$_{2}$ molecule are derived. The dissociation energy $De$ for the ground state of Co$_{2}$ molecule is 4.0489eV, equilibrium bond length $R_{\rm e}$ is 0.2061~nm, and vibration frequency $\omega _\e $ is 378.13~cm$^{ - 1}$. Its diatomic molecule force constants $f_2$, $f_3$, and $f_4$ are 2.4824~aJ$\cdot$nm$^{ - 2}$, -7.3451~aJ$\cdot$nm$^{ - 3}$, and 11.2222~aJ$\cdot$nm$^{ - 4 }$respectively(1~aJ=$10^{-18}$~J). The other spectroscopic data for the ground state of Co$_{2}$ molecule $\omega_{\e}\chi _{\e}$, $B_{\e}$, and $\alpha_{\e}$ are 0.7202~cm$^{-1}$, 0.1347~cm$^{-1 }$, and 2.9120$\times $ 10$^{-1}$~cm$^{-1}$ respectively. And $\omega_{\e}\chi _{\e}$ is the non-syntonic part of frequency, $B_{\e}$ is the rotational constant, $\alpha_{\e}$ is revised constant of rotational constant for non-rigid part of Co$_2$ molecule.     

Sm–Co high-temperature permanent magnet materials

Permanent magnets capable of reliably operating at high temperatures up to ~450?C are required in advanced power systems for future aircrafts, vehicles, and ships. Those operating temperatures are far beyond the capability of Nd–Fe–B magnets. Possessing high Curie temperature, Sm–Co based magnets are still very important because of their hightemperature capability, excellent thermal stability, and better corrosion resistance. The extensive research performed around the year 2000 resulted in a new class of Sm_2(Co, Fe, Cu, Zr)_(17)-type magnets capable of operating at high temperatures up to 550?C. This paper gives a systematic review of the development of Sm–Co permanent magnets, from the crystal structures and phase diagrams to the intrinsic magnetic properties. An emphasis is placed on Sm_2(Co, Fe, Cu, Zr)_(17)-type magnets for operation at temperatures from 300?C to 550?C. The thermal stability issues, including instantaneous temperature coefficients of magnetic properties, are discussed in detail. The significance of nanograin structure, nanocrystalline, and nanocomposite Sm–Co magnet materials, and prospects of future rare-earth permanent magnets are also given.     

Superconducting property of Zr–Co and Zr–Co–Al alloys fabricated by rapid solidification

The superconducting property of Zr_(1−x)Co_x (x = 10–50 at.%) alloys and a Zr₅₅Co₃₀Al₁₅ bulk metallic glass fabricated using techniques of rapid solidification was investigated. The Zr₅₅Co₃₀Al₁₅ alloy crystallized by heat treatment in a vacuum atmosphere exhibited superconductivity of T_c,on = 2.4 K. This was attributable to the superconducting property of a crystalline Zr–Co alloy precipitated in the Zr₅₅Co₃₀Al₁₅ alloy. The T_c,on of the crystalline Zr_(1−x)Co_x alloy was sensitive to the Co content. The increase of Co content for the Zr_(1−x)Co_x alloy led to the decrease of T_c,on. The Zr_(1−x)Co_x alloy exhibited superconductivity of a maximum T_c,on = 3.9 K for the Zr₈₀Co₂₀ alloy with superconducting nanocrystal particles embedded in the amorphous matrix.     

Relativistic configuration interaction calculations for the K α X-ray transitions of Co XV to Co XXVI ions

Relativistic configuration interaction calculations with the inclusion of the Breit interaction, quantum electrodynamics (QED) and finite nuclear mass corrections have been carried out in the extended optimal level scheme using multiconfiguration Dirac-Fock wave functions on the wavelengths, electric dipole rates, oscillator strengths and line strengths of cobalt ions with a single vacancy in the K shell. The calculated values are compared with the other available data on He-like to Be-like cobalt and are found to be in very good agreement with them. This confirms the present calculations. We predict new data for several levels where no other theoretical and/or experimental results are available. These data provide reference values for level lifetimes, charge state distribution and the average charge of cobalt plasmas.     

非晶Zr—Co的超导转变

测量了非晶态过渡族 Zr_(100-x)Co_x(x=20—41)合金的超导转变温度 T_c、上临界场 B_(c2)(T)和临界电流密度 J_c(H,T).T_c 随着 Co 含量 x 增加而线性地降低.上临界场 B_(c2)(T)的测量数值符合标准的 WHH 理论.电子状态密度和电子比热系数都随着 Co 含量 x 增加而降低.临界电流密度 J_c(H,T)和磁通钉扎力 F_p,相当弱,可以归因于在相干长度尺度上的结构均匀性.     

Influence of Co:Cu ratio on properties of Co–Cu films deposited at different conditions

A series of Co–Cu films with different Co:Cu ratio was electrodeposited at different electrolyte pH, deposition potential and film thickness, and their morphology, crystal structure and magnetic properties were investigated. Compositional analysis by energy dispersive x-ray spectroscopy disclosed that the Co and Cu content were 75 and 25 wt%, respectively, at high pH (3.2) level, while for films at low pH (2.5) level the compositions are 61 Co and 39 wt% Cu, and further decrease of Co:Cu ratio occurred as the film thicknesses increased. The surface morphology of the films changed from an initial dendritic stage to expanded dendrites with increasing Cu content by the electrolyte pH. The dendrites became more obvious at 3 μm and the dendritic structures increased with further increase of film thickness as the Co:Cu ratio decreased. Hence, the increase of the Cu content is thought to be the cause of the increase of dentritic structure. Structural characterizations by x-ray diffraction (XRD) showed that all films have face-centered cubic structure. In the XRD patterns, the peak intensity of Co (111) is lower for the films grown at low pH compared to that of high pH, and the (111) peaks of Co and Cu slightly separated at 3 μm and then the intensity of the Cu (111) increased with increasing film thickness from 4 to 5 μm, so that the Co:Cu ratio changed at all deposition parameters. Magnetic measurements displayed that the saturation magnetization decreased and the coercivity increased as the Co:Cu ratio decreased with all deposition parameters. Also, the magnetic easy axis was found to be in the film plane for all films. It was seen that the variations in the properties of the films might be attributed to the change of Co:Cu ratio caused by the deposition parameters.     

ZnS:Co2+和CdTe:Co2+中配体对g因子的贡献

采用双自旋-轨道耦合模型和分子轨道研究了Co²⁺离子在Ⅱ-Ⅵ半磁半导体ZnS和CdTe中的EPR g因子.计算表明,配体Te有大的SO耦合作用和强的共价性,其对g因子有较大的贡献.     

不同过渡层上Co/Cu/Co三明治结构的巨磁电阻效应研究

通过对不同过渡层上Co(5.5nm)/Cu(3.5nm)/Co(5.5nm)三明治结构的研究,发现过渡层的磁性及过渡层诱导的三明治晶格结构对材料的巨磁电阻效应有重要影响.反铁磁Cr过渡层由于和相邻铁磁Co层之间存在着反铁磁耦合,可以获得6％以上的巨磁电阻值,但它同时使材料的矫顽力较大,因此磁灵敏度不高.Ni和Ti过渡层上Co/Cu/Co三明治结构,由于形成了强的（111）织构,其巨磁电阻值也达到5％以上.磁性材料Ni过度层还使三明治结构材料的矫顽力大为下降,从而显著提高了材料的磁灵敏度. 关键词：     

(Co, Zn)O compound obtained from ZnTe vapor deposition on Co/Si substrates

(Co, Zn)O compound has been obtained by a non-expensive synthesis route. ZnTe thin films were obtained by isothermal close space sublimation on the Co thin layer previously sputtered on silicon substrates. After the annealing process in humid ambient cobalt atoms diffusion and Zn oxidation were obtained besides partial Te evaporation. The detailed characterization of the samples by using XRD, RBS, AFM, XPS, VSM and MFM techniques point to the formation of room temperature ferromagnetic Co _x Zn_(1−x)O phase (x<0.15). This ferromagnetic behavior is mainly attributed to Co atoms substituting Zn atoms in the ZnO network.     

Mössbauer spectroscopy investigation of body centered cubic Co in Co/Fe superlattices prepared with MBE

A new spectrum component is observed in Mössbauer spectra of thin body centered cubic Co layers prepared in Fe/Co superlattices doped with⁵⁷Co. It is characterized by a large magnetic hyperfine field (31.2 T) and an isomer shift nearly equal to that of -Fe. The decrease of the isomer shift in bcc Co with respect to hcp Co is consistent with smaller s to d charge transfer in bcc Co as compared to hcp Co. The cubic structure of the CoFe superlattices is evidenced with X-ray diffraction and ion-channeling measurements. The Fe/Co interface is investigated with conversion electron Mössbauer spectroscopy. It is shown that the interface alloy thickness is about six monolayers for growth temperatures up to 450 K and that increasing alloying occurs for higher growth temperatures.     

Interdiffusion and solid solution strengthening in Ni–Co–Pt and Ni–Co–Fe ternary systems

Diffusion couple experiments are conducted in Co–Ni–Pt system at 1200?°C and in Co–Ni–Fe system at 1150?°C, by coupling binary alloys with the third element. Uphill diffusion is observed for both Co and Ni in Pt rich corner of the Co–Ni–Pt system, whereas in the Co–Ni–Fe system, it is observed for Co. Main and cross interdiffusion coefficients are calculated at the composition of intersection of two independent diffusion profiles. In both the systems, the main interdiffusion coefficients are positive over the whole composition range and the cross interdiffusion coefficients show both positive and negative values at different regions. Hardness measured by performing the nanoindentations on diffusion couples of both the systems shows the higher values at intermediate compositions.     

一维Co单晶纳米线的x射线研究

对电化学沉积法在多孔氧化铝中制备的一维单晶Co纳米线阵列的结构和形态利用各种x射线衍射测量方法进行了细致的表征.确定了阵列中的纳米线在线长方向均为一致的晶体学取向，并以很高的平行度排列.并且发现生长条件可能在一维纳米线中引起不同程度的螺旋晶格曲扭.根据实验观察结果提出了一个具有手性的螺旋曲扭模型.利用超导量子干涉磁强计测量了样品在300K下的磁特性，分析发现螺旋扭曲可以在相当大的程度上改变纳米线阵列的各向异性.说明利用磁弹性效应有可能有效地调节纳米线的磁各向异性. 关键词： 纳米线 单晶 x射线摇摆曲线 x射线极图