纳米晶永磁Pr2Fe14B微磁学有限元法的模拟计算研究

根据实验数据，构造了接近实际纳米晶永磁Pr2Fe14B的样品，用微磁学有限元法进行了模拟计算.计算结果表明，晶界处各向异性的下降会导致矫顽力减小、剩磁值增大，而晶界处交换作用常数的减小则会使剩磁值减小、矫顽力增大.通过对实验样品的模拟研究发现，晶界处各向异性和交换作用常数的共同减小能够同时拟合出真实的矫顽力和剩磁值.模拟计算与实验在退磁曲线形状上的差距则说明模拟还存在不足. 关键词： 纳米晶永磁 磁滞回线 矫顽力 剩磁     

Non-coercive Linear Elliptic Problems

We study here some linear elliptic partial differential equations (with Dirichlet, Fourier or mixed boundary conditions), to which convection terms (first order perturbations) are added that entail the loss of the classical coercivity property. We prove the existence, uniqueness and regularity results for the solutions to these problems.     

Fe40—45Cr30—35Co20—25Mo0—4Zr0—2合金微观结构对矫顽力的影响

研究了高矫顽力型FeCrCo合金的磁性和微观结构.实验结果表明，适当的合金成分及热处理 条件可以明显提高FeCrCo合金的矫顽力.通过透射电镜、x射线衍射等手段得出结论：主体元 素含量的提高和微量元素的掺杂可以有效地控制相的组成，磁场热处理导致强磁性相和弱磁 性相的分离，回火后形成起磁硬化作用的调幅结构.该调幅结构中较大的两相成分差有利于 提高FeCrCo合金的矫顽力. 关键词： 矫顽力 调幅分解 磁场热处理 两相结构 成分差     

Monotone generalized variational inequalities and generalized complementarity problems

Some existence results for generalized variational inequalities and generalized complementarity problems involving quasimonotone and pseudomonotone set-valued mappings in reflexive Banach spaces are proved. In particular, some known results for nonlinear variational inequalities and complementarity problems in finite-dimensional and infinite-dimensional Hilbert spaces are generalized to quasimonotone and pseudomonotone set-valued mappings and reflexive Banach spaces. Application to a class of generalized nonlinear complementarity problems studied as mathematical models for mechanical problems is given.The research of the first author was supported by the National Natural Science Foundation of P. R. China and by the Ethel Raybould Fellowship, University of Queensland, St. Lucia, Brisbane, Australia.     

The magnetization reversal behaviour for SmCo6.8Zr0.2 and SmCo6.8Zr0.2/α-（Fe,Co） nanocrystalline magnets at low temperature

This paper reports that the SmCo 6.8 Zr 0.2 nanocrystalline permanent magnets and SmCo 6.8 Zr 0.2 /α-(Fe,Co) nanocomposite permanent magnets are successfully produced by mechanical alloying and subsequently annealing at 700 C for 10 minutes.The x-ray diffraction results show that the phase structure of SmCo 6.8 Zr 0.2 nanocrystalline permanent magnets is composed of SmCo 7 phase and SmCo 6.8 Zr 0.2 /α-(Fe,Co) nanocomposite permanent magnets is composed of SmCo 7 and α-(Fe,Co) phases.The mechanism of magnetization reversal is mainly controlled by inhomogeneous domain wall pinning in SmCo 6.8 Zr 0.2 and SmCo 6.8 Zr 0.2 /α-(Fe,Co) magnets.The inter-grain exchange interaction at low temperature is investigated,which shows that the inter-grain exchange interaction of SmCo 6.8 Zr 0.2 /α-(Fe,Co) magnets increases greatly by the decrease of the measured temperature.According to Δm irr-H/H cj,Δm rev-H/H cj and χ irr-H/H cj curves at room temperature and 100 K,the changes of irreversible and reversible magnetization behaviours of SmCo 6.8 Zr 0.2 and SmCo 6.8 Zr 0.2 /α-(Fe,Co) magnets with the decreasing temperature are analysed in detail.The magnetic viscosity and the activation volume of SmCo 6.8 Zr 0.2 and SmCo 6.8 Zr 0.2 /α-(Fe,Co) magnets at different temperatures are also studied.     

Structural and magnetic properties in Bi1−xRxFeO3 (x=0-1, R=La, Nd, Sm, Eu and Tb) polycrystalline ceramics

A series of rare-earth doped BiFeO₃ samples, Bi_1−xR_xFeO₃ (x=0-1, R=La, Nd, Sm, Eu and Tb), were prepared in this work. X-ray diffraction analysis showed that the structure of rare-earth doped BiFeO₃ was transformed from rhombohedral lattice to orthorhombic one by increasing x. The lattice constants and unit-cell volume decreased with the increasing of the doping content, while both the Néel temperature and magnetization were enhanced. A magnetic phase transition was observed at about 35 K for BiFeO₃. The variation of the magnetization with temperature depended on applied field strength and magnetizing history, which was explained according to the antiferromagnetic exchange interaction between Fe and R sites in Bi_1−xR_xFeO₃(x>0). The magnetocrystalline anisotropy contributed by Fe sublattice gave rise to a large coercivity in Bi_xNd_1−xFeO₃ with an orthorhombic structure.     

分子束外延制备的垂直易磁化MnAl薄膜结构和磁性

系统地研究了利用分子束外延方法在GaAs(001) 衬底上外延生长的MnAl_x薄膜的结构和垂直易磁化特性随组分及生长温度的依赖关系. 磁性测试表明, 可在较大组分范围内 (0.4≤x≤1.2) 获得大矫顽力的垂直易磁化MnAl_x薄膜, 然而同步辐射X射线衍射和磁性测试发现当x≤0.6时MnAl薄膜出现较多的软磁相, 当x >0.9时, MnAl薄膜晶体质量和化学有序度逐渐降低, 组分为MnAl_0.9时制备的薄膜有最好的[001]取向. 随着生长温度的增加, MnAl_0.9薄膜的有序度、垂直磁各向异性常数、矫顽力和剩磁比均增加, 350℃时制备的MnAl_0.9薄膜化学有序度高达0.9, 其磁化强度、剩磁比、矫顽力和垂直磁各向异性常数分别为265emu/cm³、93.3%、8.3kOe (1 Oe=79.5775A/m)和7.74Merg/cm³ (1 erg=10^-7J). 不含贵金属及稀土元素、良好的垂直易磁化性质、 与半导体材料结构良好的兼容性以及磁性能随不同生长条件的可调控 性使得MnAl薄膜有潜力应用于多种自旋电子学器件. 关键词： 分子束外延 大矫顽力材料 磁各向异性     

Theoretical Investigation of Exchange Bias in Compensated Cases

The exchange bias （EB） of the ferromagnetic （FM）/antiferromagnetic （AFM） bilayers in a compensated case is studied by use of the many-body Green＇s function method of quantum statistical theory. The so-called compensated case is that there is no net magnetization on the AFM side of the interface. Our conclusion is that the EB in this case is primarily from the asymmetry of the interracial exchange coupling strengths between the FM and the two sublattices of the AFM. The effects of the layer thickness, temperature and the interracial coupling strength oi2 the exchange bias HE are investigated. The dependence of HE on the FM layer thickness and temperature is qualitatively in agreement with experimental results. HE is nearly inversely proportional to FM thickness. When temperature varies, both HE and He decrease with temperature increasing. The anisotropy of the FM layer only slightly influence He, but does not influence HE.     

Annealing dependence of magnetic properties in nanostructured Sm0.5Y0.5Co5

Nanocrystalline Sm_0.5Y_0.5Co₅ powders with high coercivity H_C and enhanced remanence M_r were prepared by mechanical milling and subsequent annealing. Annealing temperatures T ranging from 973 to 1173 K, and times t ranging from 1 to 5 min were used. X-ray diffraction (XRD) and DC-magnetization measurements were carried out to study the microstructure and magnetic properties of these samples. XRD patterns demonstrate that the average grain size D of the nanocrystalline powders depends on the annealing temperature T and time t: D ranges from 11 nm (for T=973 K and t=1 min) to 93 nm (for T=1173 K and t=5 min). Magnetic measurements performed at room temperature indicate high coercivity values (H_C>955 kA/m), and enhanced remanence (M_r/M_max>0.5) for all samples. A strong annealing-induced grain size dependence of these magnetic properties was found.     

Magnetic properties of YCo5 (70%wt)+Y2Co17 (30%wt) nanocomposite powders at low temperatures

Nanostructured YCo₅ (70%wt)+Y₂Co₁₇ (30%wt) composite powders were prepared by mechanical milling and subsequent annealing at 1073 K for 1.5 min. The average grain size D of the YCo₅ and Y₂Co₁₇ phases, obtained from XRD data, was 14 and 12 nm, respectively. The temperature dependence of the magnetic properties was studied by DC magnetization measurements at temperatures T ranging from 3 to 300 K. Hysteresis loops (H_max=70 kOe) show that both the coercivity H_C and the squareness σ_r/σ_max are temperature-dependent. The coercivity increases from 12 kOe at room temperature to 18 kOe at T=3 K. The observed enhanced remanence (σ_r/σ_max>0.5) indicates that a strong exchange coupling is present at all temperatures used in this study. The maximum magnetization σ_max changes little with temperature and has a value of about 70% of the effective saturation magnetization of the title compound.