磁场对液态铝和固态铁界面微观组织的影响

研究了直流磁场、交流磁场对液态铝和固态铁界面微观组织的影响，采用金相显微镜、电子探针和x射线衍射等方法对其扩散层内生成物进行了分析.结果表明，在直流磁场和交流磁场作用下，固态铁界面内形成的扩散层厚度均比无磁场时小；在交流磁场作用下，液态铝和固态铁的界面变得凹凸不平；在垂直于磁场方向上，直流磁场抑制了铝原子和铁原子之间的扩散，交流磁场则促进了扩散；无磁场时固态铁内扩散层中生成的金属间化合物由FeAl₃和Fe₂Al₅组成，直流磁场条件下只有Fe₂Al_{5生成，交流磁场作用下由Fe2Al5和Fe4Al13组成. 关键词： 磁场 铝 铁 金属间化合物 扩散}     

强磁场对Al-Si合金凝固组织中硅分布的影响

为了揭示强磁场对金属凝固组织的影响规律，本文研究了Al-14.98%Si(质量分数)和Al-9.2%Si(质量分数)合金在强磁场作用下凝固组织的变化趋势，分析了强磁场对合金凝固组织中Si分布的影响.研究发现，均恒磁场和梯度磁场分别通过洛伦兹力和磁化力的作用对合金的凝固组织产生影响，强磁场可以显著改变初晶硅在合金中的分布状况.在均恒磁场作用条件下初晶硅在合金中均匀分布；在梯度磁场条件下，由于磁化力和浮力的共同作用，初晶硅在试样的上部或下部聚集.同时，磁化力也改变了共晶体在合金中的组织形态，使试样上部和下部共晶体的层片间距明显不同.理论和实验分析表明，Al-Si合金在强磁场中凝固时，磁场能作用于凝固过程，使共晶体中的Al含量增大，共晶点向左偏移. 关键词： 强磁场 凝固过程 共晶组织 Al-Si合金     

稳恒磁场下金属电沉积枝晶生长的模拟

采用Monte-Carlo模拟方法,给出用于描述稳恒磁场作用下电沉积枝晶生长的模型.该模型综合考虑了外加磁场B,电解溶液浓度和离子在阴极发生还原反应的几率P_s等因素对电沉积过程的影响,模拟得到与实验结果一致的枝晶生长图形.模拟结果表明:团簇的形状和它们的分形维数都与外加磁场B的强弱,即体现在模型中离子的旋转角速度ω的大小有关;随着磁场强度的增加,沉积团簇会从分形向非分形转变;在相对强的外加磁场作用下,较高离子浓度时的沉积物是非分形的;离子在阴极的反应概率P_s越小,随着磁场强度的增加枝晶生长越易趋向非分形.     

急冷Al-Si合金超导电性的研究

本文研究了热处理对急冷Al-11.3at％Si合金的微观结构及超导电性的影响,结构分析表明,液态淬火的样品由两相组成:过饱和α-Al(Si)固溶体晶体相和Al,Si原子按统计分布的非晶相,经100℃/50小时热处理后,α-Al(Si)固溶体贫化,非晶相中析出Si的小颗粒,经200℃/100小时热处理的样品已趋向平衡态结构,测量了样品的临界温度,在研究磁场中的超导-正常转变时发现了反常的磁阻效应,它可以用样品中存在两个超导相的模型予以解释。 关键词：     

深过冷液态Al-Ni合金中枝晶与共晶生长机理

在自由落体条件下实现了液态Al-4 wt.%Ni亚共晶、Al-5.69 wt.%Ni共晶和Al-8 wt.%Ni过共晶合金的深过冷与快速凝固. 计算表明, (Al+Al₃Ni)规则纤维状共晶的共生区是4.8–15 wt.%Ni成分范围内不闭合区域, 且强烈偏向Al₃Ni相一侧. 实验发现, 随液滴直径的减小, 合金熔体冷却速率和过冷度增大, (Al)和Al₃Ni相枝晶与其共晶的竞争生长引发了Al-Ni 共晶型合金微观组织演化. 在快速凝固过程中, Al-4 wt.%Ni亚共晶合金发生完全溶质截留效应, 从而形成亚稳单相固溶体. 当过冷度超过58K时, Al-5.69 wt.%Ni 共晶合金呈现从纤维状共晶向初生(Al) 枝晶为主的亚共晶组织演变. 若过冷度连续增大, Al-8 wt.%Ni过共晶合金可以形成全部纤维状共晶组织, 并且最终演变为粒状共晶.     

强磁场条件下Mn-Sb梯度复合材料的制备

研究了Mn-898wt%Sb合金在无磁场以及磁场为B=88 T、不同强度的磁场梯度作用下的凝固组织变化,并分析了上述不同强磁场条件对合金凝固组织影响的作用机理.研究表明,在较大梯度磁场作用时,试样中出现了初生MnSb相与Sb相以及共晶组织共存的现象,而且初生MnSb相与Sb相产生了明显的分层现象.此外,磁场梯度作用下初生MnSb相和Sb相的含量随着磁场梯度的增大而增加.论文对初生MnSb相和Sb相的分离机理进行了探讨,发现在梯度磁场作用下,熔融金属中不同磁化率的合金组元团簇受力不同,造成 关键词： 强磁场 Mn-Sb合金 磁化力 梯度功能材料     

室温下磁场对基于Alq3的有机电致发光器件的影响

制备了ITO/NPB/LiF/Alq₃/LiF/Al的器件,测量了该组器件效率和亮度的磁效应.结果表明,在50 mT磁场中,当LiF缓冲层厚度为0.8 nm时,器件的效率最大增加了12.4%,磁致亮度最大变化率17%.同时,制备的磷光器件ITO/NPB/LiF/CBP:6 wt% Ir(ppy)₃/BCP/Alq₃/ LiF/Al,在50mT磁场作用下,当LiF缓冲层的厚度为0.8 nm时,器件的效率最大增加12.1%.在Alq_{3 关键词： 有机发光 磁场 效率 磁致亮度}     

3 T强磁场对真空蒸发Zn薄膜晶体结构的影响

在3 T强磁场下采用真空蒸发沉积在玻璃基片上制备了三种厚度分别为1,2,3 μm的Zn薄膜,并和无磁场下制备的薄膜进行了对比研究.对施加磁场和无磁场环境下制备的试样分别进行了X射线衍射研究.研究表明,3 T磁场下制备的Zn薄膜都是沿（002）面取向,而0 T磁场下制备的薄膜随着厚度的增加c轴取向逐渐减弱. 3 T磁场的取向作用可以维持Zn晶粒沿着c轴取向.利用扫描电子显微镜对薄膜表面形貌的研究发现,施加磁场制备的Zn薄膜表面晶粒要比无磁场条件下制备的薄膜有明显的细化.对磁场下Zn原子团形成进行了热力学分析,推导了磁场作用下的临界形核半径r^*_M和临界形核自由能ΔG^*_M.初步分析表明,r^*_M和ΔG^*_M减小从而增加临界形核浓度是Zn晶粒细化的原因. 关键词： 强磁场 晶体结构 真空蒸发沉积 薄膜     

准2-2型磁电多层复合材料的磁电性能

用带底座的Pb（Zr,Ti）O₃薄片阵列作为压电相,Terfenol-D粉末与树脂的混合物作为磁致伸缩相,灌注复合得到准2-2型磁电多层三相复合材料.研究了这种准2-2型多层结构在不同偏置磁场和不同角度下的磁电效应.其面内相互垂直的两个方向磁电电压系数分别在0.15和0.225 T磁场下达到峰值,低频下分别为1.62×10⁵ V·m^-1T^-1和1.75×10⁵ V·m^-1T^-1;而在垂直于面内方向,低频下磁电系数仅有1.3×10⁴ V·m^-1T^-1,体现出显著的磁电各向异性.这种准2-2型磁电多层复合材料具有较好的交流磁场灵敏度,在谐振频率下可以探测到10^-9 T的交流磁场的变化.进行合适的设计和排列,可以探测空间磁场的大小和方向,有望应用于磁场传感器等领域. 关键词： 磁电效应 多铁性 多层复合材料     

LiF插层对有机发光二极管磁场效应的调控

制备了有LiF插层的有机发光二极管,以八羟基喹啉铝（Alq₃）作为电子传输层,N, N′-二苯基-N, N′-二(1-萘基)-1,1′-联苯-4,4′-二胺（NPB）作为空穴传输层.通过改变Alq₃与NPB间LiF插层的厚度,研究了不同温度下器件的光电特性及电致发光的磁场效应.测量结果表明:LiF插层可以影响器件内部载流子的输运和激发态的形成.较厚的插层阻碍了空穴的传输,使器件的电流效率变低.但实验中发现, 关键词： LiF插层结构 磁场效应 三重态激子     

Diffusion interaction between Al and Mg controlled by a high magnetic field

The effects of an 11.5 T high magnetic field on the growth behavior of compounds layers during reactive diffusion in solid Al/solid Mg diffusion couples have been investigated. After annealing with and without a magnetic field, the interfacial zone was still composed of two layers of stable compounds β (Mg₂Al₃) and γ (Mg₁₇Al₁₂), but the thicknesses of the layers were increased by the magnetic field. Data analysis of the thicknesses of compound layers showed that the growth of the γ layer was controlled by grain boundary diffusion as well as volume diffusion at B=0 T, but only controlled by volume diffusion when an 11.5 T high magnetic field was applied. The interdiffusion coefficients for the samples annealed at 643–693 K were calculated from the parabolic relationship between the migration of the interface and the annealing time. The results show that the diffusion constant increased due to the high magnetic field, increasing the chemical potential gradient, and in turn it caused the interdiffusion coefficient to increase.     

Studies on the coupling of interlayers in multilayered FeSi/Si amorphous films by cems

Multilayered FeSi/Si amorphous films with fixed FeSi layer thickness and different Si layer thicknesses have been studied by conversion electron Mössbauer spectroscopy at room temperature. The results showed that with decreasing the Si layer thickness, the hyperfine field of samples increased and the thickness of interface dead layers arisen from the atomic interdiffusion effect decreased. These are due to the coupling effect between the magnetic layers.     

Size effects and magnetoelastic couplings: a link between Hall–Petch behaviour and coercive field in soft ferromagnetic metals

Size effects regarding Hall–Petch (HP) relation are studied in this work for cobalt, nickel and Fe–3wt.%Si (FeSi), from polycrystalline to multicrystalline states. The materials show a breakdown in HP plot for thickness (t) to grain size (d) ratio less than a critical value. This appears in the beginning of plasticity for cobalt and FeSi whereas a plastic strain threshold must be overcome for nickel. Measurements of the coercive field on strained samples are able to depict such modification for low t/d ratio. Values of the coercive field in the polycrystalline domain allow an estimation of the magnetocrystalline anisotropy energy, related to the grain volume fraction concerned by reversal mechanisms for magnetic domains. Multicrystalline samples of cobalt and FeSi becomes magnetically softer at the yield stress. This is linked to a delay of the maximum intergranular stress towards higher strains for FeSi. For cobalt, non-linear elasticity and strong basal texture modify the magnetoelastic effects in coarse grain samples. For nickel, size effect on the coercive field appears after a few per cent of plastic strain as for HP relationship. A mean internal stress can be captured by magnetic measurements on polycrystals, related to the intragranular part of the kinematic stress. The softening of the magnetic properties for strained nickel multicrystals is due to a competition between the apparition of dislocation cells, which increases the coercive field by mechanisms of magnetic domain wall pinning, and surface softening of multicrystals, which tends to decrease the value of H_c.     

Reaction diffusion and interdiffusion in some binary metallic systems

This paper reviews studies from the Münster laboratory on multiphase and interdiffusion performed on several binary metallic systems. Optical microscopy and electron microprobe analysis were used to study interdiffusion and growth of the intermetallic layer(s) in infinite diffusion couples. Both methods have resolutions at the micron level. Thus, the results summarised in this paper concern the diffusion-controlled regime of the reaction diffusion process. We first remind the reader of some of the basics of multiphase diffusion and interdiffusion. Then we discuss results reported for the following systems: cobalt–niobium, nickel–niobium, nickel–aluminium and magnesium–aluminium. In the case of Co₂Nb we also compare interdiffusion and tracer diffusion of the components. Multiphase diffusion experiments also contain information about solid–solid equilibria of the phase diagram(s).     

EBSD study of crystallographic identification of Fe-Al-Si intermetallic phases in Al-Si coating on Cr-Mo steel

5Cr-0.5Mo steel was coated by hot-dipping in a molten Al-10 wt.% Si bath at 700 °C for 10, 60, 120 or 180 s. The identification of the phases in the Fe-Al-Si intermetallic phases formed in the aluminide layers during hot-dipping was carried out by using a combination of scanning electron microscope (SEM) with energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD) and electron backscatter diffraction (EBSD). The EDS results show a τ_5(H)-Al₇Fe₂Si phase, which exhibited 2 distinct morphologies, small particles widely dispersed and a continuous layer. Also revealed by EDS were τ₆-Al₄FeSi and τ₄-Al₃FeSi₂ phases, which showed plate-shaped morphology, in an Al-Si topcoat. However, the XRD results show the intermetallic phases in the aluminide layer were composed of outer cubic τ_5(C)-Al₇(Fe,Cr)₂Si and inner hexagonal τ_5(H)-Al₇Fe₂Si. EBSPs and mapping functions in EBSD helped to clarify the confused phase identifications yielded by EDS and XRD. In this way, the small intermetallic particles and the continuous intermetallic layer were identified as cubic τ_5(C)-Al₇(Fe,Cr)₂Si and hexagonal τ_5(H)-Al₇Fe₂Si, respectively, and the plate-shaped intermetallic phase was identified as monoclinic τ₆-Al₄FeSi and tetragonal τ₄-Al₃FeSi₂ with the same metallographic morphology. EBSD proved to be a very effective technique for local phase identification of aluminide layers with complicated multiphase morphologies.     

A transfer matrix analysis of quaternary diffusion

A transfer matrix method (TMM), developed recently by Ram-Mohan and Dayananda, has been employed for the first time to generate error function solutions for quaternary diffusion in solid–solid metallic diffusion couples. The method was validated with the aid of a hypothetical couple with known quaternary interdiffusion coefficients and applied to two experimental Cu–Ni–Zn–Mn quaternary couples annealed at 775°C. Quaternary interdiffusion coefficients were determined by the Dayananda analysis from the concentration profiles of the couples over selected composition ranges in the diffusion zone and employed for the subsequent TMM calculation of error function solutions. For the hypothetical test couple, identical sets of constant interdiffusion coefficients were determined on either side of the Matano plane and utilized for the calculation of concentration profiles by TMM. For the experimental Cu–Ni–Zn–Mn couples, interdiffusion coefficients determined over selected regions in the diffusion zone were employed for the TMM generation of the concentration profiles.     

Solid–state diffusion–controlled growth of the phases in the Au–Sn system

The solid state diffusion-controlled growth of the phases is studied for the Au–Sn system in the range of room temperature to 200 °C using bulk and electroplated diffusion couples. The number of product phases in the interdiffusion zone decreases with the decrease in annealing temperature. These phases grow with significantly high rates even at the room temperature. The growth rate of the AuSn₄ phase is observed to be higher in the case of electroplated diffusion couple because of the relatively small grains and hence high contribution of the grain boundary diffusion when compared to the bulk diffusion couple. The diffraction pattern analysis indicates the same equilibrium crystal structure of the phases in these two types of diffusion couples. The analysis in the AuSn₄ phase relating the estimated tracer diffusion coefficients with grain size, crystal structure, the homologous temperature of experiments and the concept of the sublattice diffusion mechanism in the intermetallic compounds indicate that Au diffuses mainly via the grain boundaries, whereas Sn diffuses via both the grain boundaries and the lattice.     

A pseudobinary approach to study interdiffusion and the Kirkendall effect in multicomponent systems

Interdiffusion studies become increasingly difficult to perform with the increasing number of elements in a system. It is rather easy to calculate the interdiffusion coefficients for all the compositions in the interdiffusion zone in a binary system. The intrinsic diffusion coefficients can be calculated for the composition of Kirkendall marker plane in a binary system. In a ternary system, however, the interdiffusion coefficients can only be calculated for the composition where composition profiles from two different diffusion couples intersect. Intrinsic diffusion coefficients are possible to calculate when the Kirkendall markers are also present at that composition, which is a condition that is generally difficult to satisfy. In a quaternary system, the composition profiles for three different diffusion couples must intersect at one particular composition to calculate the diffusion parameters, which is a condition that is almost impossible to satisfy. To avoid these complications in a multicomponent system, the average interdiffusion coefficients are calculated. I propose a method of calculating the intrinsic diffusion coefficients and the variation in the interdiffusion coefficients for multicomponent systems. This method can be used for a single diffusion couple in a multicomponent pseudobinary system. The compositions of the end members of a diffusion couple should be selected such that only two elements diffuse into the interdiffusion zone. A few hypothetical diffusion couples are considered in order to validate and explain our method. Various sources of error in the calculations are also discussed.     

Effect of Pt on interdiffusion and mechanical properties of the γ and γ′ phases in the Ni–Pt–Al system

The effect of Pt on the growth kinetics of the γ′-[Ni(Pt)]₃Al ordered intermetallic phase and the γ-Ni(Pt, Al) solid solution diffusion rates of the species, hardness and elastic modulus was examined by employing the diffusion couple experimental technique. Experiments were conducted by using the β-Ni(Pt)Al phase and Ni(Pt) alloy couples, each of which had a fixed amount of Pt (5, 10 and 15 at. %) in both the end members so that the Pt content is more or less constant throughout the interdiffusion zone. The results suggest that the growth kinetics of both phases and the average effective interdiffusion coefficients of Ni and Al increase with the increase in Pt content. Nanoindentation studies across the compositional gradients show that the mechanical properties of the intermetallic phase in the superalloy are relatively insensitive to the presence of Pt but are more sensitive to the Ni/Al ratio. In contrast, the marked variation in the hardness of the γ phase were noted, increasing markedly with Al concentration in a given couple and also increasing with increasing Pt content. Possible causes for the observed variations are discussed.     

The Kinetics of the Cd21Ni5 Intermetallic Growth under High Hydrostatic Pressure

The kinetics of growth of the Cd₂₁Ni₅ intermetallic phase in two-layer Cd-Ni samples has been studied at hydrostatic pressures 0.05–0.9 GPa and at temperatures 200–280°C. Arrhenius equations for both interdiffusion through the growing phase layer and the interfacial reaction have been obtained for different pressures. The activation volumes have been found to be 0.9V₀ for interdiffusion and 1.6V₀ for interfacial reaction, where V_{_0} 1.8 × 10_-29m₃ is the average volume per atom in the Cd₂₁Ni₅ lattice. Atomistic mechanisms of intermetallic growth are discussed.