Magnetotransport in core-shell Fe–Fe oxide nanostructures

Magnetic and magnetotransport measurements were performed on gas-phase synthesized Fe nanoparticles subjected to surface oxidation and cold consolidation. Two samples were investigated with α-Fe volume fraction of 0.15 and 0.60. The sample with smaller metallic fraction is below the percolation threshold for metallic conduction and the conduction mechanism is dominated by thermally activated processes across the oxide. In this case, by lowering the temperature, an increase of the negative magnetoresistance is observed up to 5% at 50 K in a magnetic field of 70 kOe. The magnetoresistance dependence on the sample magnetization, temperature and sample composition is discussed considering the magnetic correlations present in these nanostrucuterd systems.     

The Fe–Fe2P phase diagram at 6 GPa

Here, we report experimental results on melting and subsolidus phase relations in the Fe–Fe₂P system at 6?GPa and 900–1600°C. The system has two P-bearing compounds: Fe₃P and Fe₂P. X-ray diffraction patterns of these compounds correspond to schreibersite and barringerite, respectively. The Fe–Fe₃P eutectic appears at 1075°C and 16?mol% P. Schreibersite (Fe₃P) melts incongruently at 1250°C to produce barringerite (Fe₂P) and liquid containing 23?mol% P. Barringerite (Fe₂P) melts congruently at 1575°C. Maximum solid solution of P in metallic iron at 6?GPa is 5?mol%. As temperature increases to 1600°C, the P solubility in the metallic iron decreases to 0.5?mol%, whereas the P content in coexisting liquid decreases to 3?mol%. The composition of quenched phases from Fe–P melt coincides with the compositions of equilibrium phases at corresponding temperature. Consequently, the composition of quenched products of Fe-P melts in meteorites can be used for reconstruction of P–T conditions of their crystallization under ambient or low pressures or during shock melting by impact collisions.     

合成反铁磁Ni81Fe19/Co90Fe10/Ru/Co90Fe10/Ni81Fe19的研究

采用直流磁控溅射方法制备了一系列的合成反铁磁及以其为自由层的自旋阀.研究发现,在Ni81,Fe19与Ru层之间插入适当厚度的Co90Fe10层后,可有效地提高合成反铁磁两磁性层间的反铁磁耦合强度,得到具有饱和场日.更高、饱和磁化强度M.更低、热稳定性更好的合成反铁磁.另外,以这种合成反铁磁作自旋阀的自由层时,可有效提高自旋阀的稳定性.     

Hyperfine fields and Fe magnetic moments in Fe−Ni invar alloys

Mössbauer spectra of Fe_1?x Ni _x withx=0.40, 0.35 and 0.32 were taken at various temperatures and fitted withB _hf distributions. TheP(B _hf) curves generally show a peak and a low-field tail. The peakB ^* and the average \(\bar B\) were obtained in theT→0 limit. Fe moments were deduced from these data with help of a semiempirical equation. While the average \(\bar \mu _{Fe} \) decreases withx (invar anomaly), a large fraction of Fe atoms retain the strong moment (≈ 2.7 μ_B) typical of Ni-rich alloys. This result is consistent with a two-states model for invar.     

Magnetic Thermocouples Made of Co–Fe and Ni–Fe Permalloys

Technical Physics - Magnetized and unmagnetized Co–Fe and Ni–Fe alloys fabricated on a two-high casting installation in the form of thin flexible amorphous films are promising materials...     

Pd/Fe和PdFe/Fe多层膜中的振荡行为

采用磁控溅射法制备了Pd/Fe和Pd_1-xFe_x/Fe多层膜.利用变换梯度磁强计测量了样品的M_s.发现层间耦合是铁磁性的,M_s具有长程振荡,周期为4ML.振荡的相位和周期在Pd_0.966Fe_0.034/Fe和Fd_0.944Fe_0.056/Fe系统中保持不变.就Pd/Fe多层膜中是否存在内层的Pd负极化和长程的铁磁耦合振荡进行了讨论,并分析了不同计算结果以及理论计算与实验结果之间存在差异的原因. 关键词：     

Fe/Dy artificial multilayered films studied by57Fe Mössbauer spectroscopy

Magnetic properties of multilayered Fe/Dy films with artificial superstructures have been investigated by⁵⁷Fe Mössbauer spectroscopy. Doublet peaks are observed at room temperature when the Fe layer is thinner than 20Å. Mössbauer spectra for thicker Fe layers correspond to α-Fe spectra. In certain samples, i.e. [Fe(44Å)/Dy(6Å)], a gradual spin reorientation takes place, which is evidenced from the change of relative intensities of Δm=0 lines with decreasing temperature.     

Fe含量和粒径对Fe/Cu颗粒膜结构和磁性的影响

采用共蒸发法制备不同组分的Fe/Cu颗粒膜,将样品分两组进行退火和不退火处理. 根据测量及分析,确定了不同成分的Fe/Cu颗粒膜的相组成和晶体结构;找出了 Fe/Cu颗粒膜矫顽力与粒径的关系,利用此关系由自发形核理论可知,提高功率,快速蒸镀薄膜,可得到细密颗粒的Fe/Cu颗粒膜,从而降低矫顽力,减少磁滞损耗.     

Studying the properties of Fe and Fe–Co nanotubes in polymer ion-track membranes

Iron and iron–cobalt nanostructures are probed by means of Mössbauer spectroscopy combined with scanning electron microscopy, energy-dispersion analysis, and X-ray diffraction. The obtained nanostructures are single-phase Fe_{1 ? x}Co _x (0 ≤ x ≤ 1) nanotubes that have high degrees of polycrystallinity and a bcc lattice 12 μm long and 110 ± 3 nm in diameter, with walls 21 ± 2 nm thick. A random distribution of the orientations of the magnetic momenta of Fe atoms are observed for Fe nanotubes, while Fe–Co nanotubes are characterized by a magnetic texture along their axes.     

Out-of-equilibrium Sm–Fe based phases

Structure and magnetic properties of nanocrystalline P6/mmm out-of-equilibrium precursors of hard magnetic R-3m Sm₂(Fe,M)₁₇C (M=Ga,Si,) and I4/mmm Sm(Fe,Co,Ti)₁₁ equilibrium phases, are presented. Their structure is explained with a model ground on the R_1???s T_5?+?2s formula (R=rare-earth, s=vacancy rate, T=transition metal) where s Sm atoms are statistically substituted by s transition metal pairs. The Rietveld analysis (RA) provides the stoichiometry of the precursors, 1:9 and 1:10, respectively precursor of 2:17 and 1:12 phases. The interpretation of the Mössbauer spectra of the 1:9 and 1:10 phases, is based on the correlation between δ and the Wigner–Seitz Cell volumes, calculated from the structural parameters. The δ behaviour of each crystallographic site versus Co content, defines the Co location while it confirms that of Si and Ga obtained by RA. Substitution occurs in 3 g site, whatever Co or M. The Sm(Fe,Co,Ti)₁₀ and Sm(Fe,M)₉C Curie temperature (T_c) are compared to those of the equilibrium phases, the effects of Fe substitution and C addition are discussed. The maximum μ ₀H_c is obtained for low M or Co content, for auto-coherent diffraction domain size ～30 nm. SmFe_8.75Ga_0.25C and SmFe_8.75Si_0.25C with T_c of 680 and 690 K, show respectively M_r and μ ₀H_c of 58 emu/g, 27 kOe and 95 emu/g, 15 kOe, values higher than those obtained for Sm₂(Fe,M)₁₇ carbides.     

H2O分子在Fe(100), Fe(110), Fe(111)表面吸附的第一性原理研究

采用第一性原理研究了H2O分子在Fe(100),Fe(110),Fe(111)三个高对称晶面上的表面吸附.结果表明,H2O分子在三个晶面上的最稳定结构皆为平行于基底表面的顶位吸附结构.H2O分子与三个晶面相互作用的吸附能及几何结构计算结果表明H2O分子与三个晶面的相互作用程度不同,H2O分子与Fe(111)晶面的相互作用最强,其次是Fe(100),相互作用最弱的是Fe(110)表面,而这与晶面原子的排列密度相关.吸附体系的电子结构计算结果也得出了相似的结论.同时电荷布居分析表明,H2O分子与Fe表面相互作用时,O原子与基底原子之间的电荷交换使基底Fe原子表面带负电,导致表面电位降低,也促使Fe表面更易于发生电化学腐蚀反应.     

Fe基合金与金刚石单晶生长

 本文通过Fe基催化剂在生长金刚石单晶中获得的不同现象与Fe基合金晶格常数、组分、磁距、Mossbauer谱相比较，揭示了Fe基催化剂常温常压下磁性质与金刚石单晶生长的关系。     

57Fe Mössbauer study of Lu2Fe3Si5 iron silicide superconductor

With the advent of Fe–As based superconductivity it has become important to study how superconductivity manifests itself in details of ⁵⁷Fe Mössbauer spectroscopy of conventional, Fe-bearing superconductors. To this end, the iron-based superconductor Lu₂Fe₃Si₅ has been studied by ⁵⁷Fe Mössbauer spectroscopy over the temperature range from 4.4 K to room temperature with particular attention to the region close to the superconducting transition temperature (T_c=6.1 K). Consistent with the two crystallographic sites for Fe in this structure, the observed spectra appear to have a pattern consisting of two doublets over the whole temperature range. The value of Debye temperature was estimated from temperature dependence of the isomer shift and the total spectral area and compared with the specific heat capacity data. Neither abnormal behavior of the hyperfine parameters at or near T_c, nor phonon softening were observed.     

Fe,Ce原子在A1—Fe—Ce非晶合金中的分布

采用Ｘ射线衍射技术研究了Ａ１－Ｆｅ－Ｃｅ合金的非晶结构,发现非晶态合金Ｘ射线强度曲线上都丰在明显的预峰,合金随铁含量增加,预峰和主峰向大角度偏移;合金随铈含量增加,预峰和主峰向小解度偏移。２５０℃时,非晶合金出现铝相晶化,而预峰的形状和位置并未发生改革;４００℃时央预峰消失的位置形成多种化合物相。Ｆｅ原子大部分存在于预峰所对应的Ａ１－Ｆｅ－Ｃｅ原子团簇中,崦Ｃｅ原子大部分无规分布于Ａ１非晶基体中。     

Reduction of hematite with ethanol to produce magnetic nanoparticles of Fe3O4, Fe1 − x O or Fe0 coated with carbon

The production of magnetic nanoparticles of Fe₃O₄ or Fe⁰ coated with carbon and carbon nanotubes was investigated by the reduction of hematite with ethanol in a Temperature Programmed Reaction up to 950°C. XRD and Mössbauer measurements showed after reaction at 350°C the partial reduction of hematite to magnetite. At 600°C the hematite is completely reduced to magnetite (59%), wüstite (39%) and metallic iron (7%). At higher temperatures, carbide and metallic iron are the only phases present. TG weight losses suggested the formation of 3–56 wt.% carbon deposits after reaction with ethanol. It was observed by SEM images a high concentration of nanometric carbon filaments on the material surface. BET analyses showed a slight increase in the surface area after reaction. These materials have potential application as catalyst support and removal of spilled oil contaminants.     

Mössbauer investigation of the Fe/Cu interfaces in BCC Fe/Cu/Fe(0 0 1) structures

A RHEED study shows quasi layer-by-layer growth in BCC Fe/Cu/Fe(0 0 1) structures. The BCC stacking of Cu layers is maintained up to a critical thickness of 11 layers. The different iron sites at the Fe/Cu interfaces can be identified by Mössbauer spectroscopy from the distinct values measured for the magnetic hyperfine fields H_hf and isomer shifts at the ⁵⁷Fe nuclei. This makes it possible to determine the concentration of ⁵⁷Fe atoms in the different iron sites. The roughness of the Cu on Fe interface estimated from the Mössbauer study is more pronounced than that estimated from a RHEED study of the structure. The growth of Fe on Cu produces CuFe alloy layers at the Cu/Fe interface.     

Fe掺杂ZnO纳米薄膜的光致发光

采用溶胶-凝胶法制备了Zn_1-xFe_xO(x=0.01,0.05,0.10)纳米薄膜。X射线衍射谱显示所有样品均具有六角纤锌矿结构。而且在X射线衍射谱中没有发现其他相存在。研究了在不同的溶液浓度、退火温度和Fe浓度下制备的掺杂ZnO薄膜的光致发光谱。结果表明,热退火提高了样品的光学质量。溶液浓度为0.1mol/L,且Fe含量较低的条件下,样品的光学质量有所提高。     

Fe/Al2O3/Fe隧道结特性分析

用离子束溅射方法制备磁性隧道结(MTJ). 研究MTJ样品的隧道结磁电阻(TMR)效应.用X射线 光电子能谱分析了MTJ的软、硬磁层和非磁层及其界面的化学组成与微结构.研究了MTJ的微 结构对氧化铝势垒高度与有效宽度和TMR效应的影响. 关键词： 磁性隧道结 X射线光电子能谱 隧道结磁电阻