Magnetic alignment of MnBi crystals and magnetic properties of MnBi–Bi composites

Below Curie temperature T_C, MnBi crystals are aligned along c-axis in a Bi matrix under a fabrication field H_f of 0.5 T. Above T_C, this alignment is also accomplished by quenching under a high H_f of 10 T. Such a method has a prominent feature that MnBi crystals grow preferentially and congregate along the H_f direction. Magnetic testing shows a pronounced anisotropy in magnetization in directions normal and parallel to H_f, resulting from the alignment. In the case of the alignment below T_C, H_f increases the transition temperature of spin-reorientation and the change in magnetization.     

Effect of a high magnetic field on the morphology and magnetic properties of the MnBi compound during the Mn1.08Bi-MnBi phase transformation process

Effect of a 10 T high magnetic field on the morphology and magnetic properties of the MnBi compounds during the Mn_1.08Bi-MnBi phase transformation has been investigated. Results indicate that the field has split the MnBi crystal along the (0 0 1)-crystal plane during the Mn_1.08Bi-MnBi phase transformation process and the split MnBi crystals align and aggregate along the magnetic field direction. Along with the change of the MnBi phase morphology, the magnetic property changes greatly. Indeed, with the alignment and aggregation of the spit MnBi phases, the saturation magnetization M_s and the magnetic susceptibility χ increase, and the coercive field H_c and the remnant magnetization M_r decrease. This implies that a high magnetic field may have caused the magnetic property of the MnBi phase to transform towards soft magnetism. Above results may be attributed to the enhancement of the magnetization and the Mn_1.08Bi-MnBi phase transformation in a high magnetic field.     

Effect of magnetic field on the TC and magnetic properties for the aligned MnBi compound

In the compound MnBi, a first-order transition from the paramagnetic to the ferromagnetic state can be triggered by an applied magnetic field and the Curie temperature increases nearly linearly with an increase in magnetic field by ∼2 K/T. Under a field of 10 T, T_C increases by 20 and 22 K during heating and cooling, respectively. Under certain conditions a reversible magnetic field or temperature induced transition between the paramagnetic and ferromagnetic states can occur. A magnetic and crystallographic H-T phase diagram for MnBi is given. Magnetic properties of MnBi compound aligned in a Bi matrix have been investigated. In the low temperature phase MnBi, a spin-reorientation takes place during which the magnetic moments rotate from being parallel to the c-axis towards the basal plane at ∼90 K. A measuring Dc magnetic field applied parallel to the c-axis of MnBi suppresses partly the spin-reorientation transition. Interestingly, the fabricated magnetic field increases the temperature of spin-reorientation transition T_s and the change in magnetization for MnBi. For the sample solidified under 0.5 T, the change in magnetization is ∼70% and T_s is ∼91 K.     

磁场诱导制备Bi-Mn合金的结构和低温磁性研究

系统研究了在外加诱导磁场下制备的Bi-Mn 6%合金的结构和低温磁特性.结果表明,在外加诱导磁场下制备的Bi-Mn 6%合金呈现典型的双相结构和各向异性特征,MnBi相c轴沿外加诱导磁场方向定向排列.发现MnBi相的矫顽力随温度的升高而增大,而饱和磁化强度则随温度的升高而减小.MnBi相的自旋重定向温度TSR随测量磁场的增大逐渐向低温区移动,在高的外加测量磁场下这种自旋重定向特征消失,发现了TSR随外加诱导制备磁场的增大而逐渐向高温区移动.对磁场诱导制备织构化MnBi相和该类材料磁各向异性能的物理机制进行了分析和讨论.     

Variations from Zn1-xCoxO Magnetic Semiconductor to Co-ZnCoO Granular Composite

We investigate the variations from as-deposited Zn1-x： Cox O magnetic semiconductors to the post-annealed Co- ZnCoO granular composite. The as-deposited Zn1-x Cox 0 magnetic semiconductor deposited under thermal nonequilibrium conditions is composed of Zn1-x. Cox O nanograins of high Co concentration. The room-temperature ferromagnetism with high magnetization and large negative magnetoresistance are found in the as-deposited samples. By annealing, the samples become of granular composite consisting of the Co metal grains and the remanent Zn1-x CoxO matrix. Although the magnetization is enhanced after annealing, the spin-dependent negative magnetoresistance disappears at room temperature. The magnetoresistance observed in the annealed samples in the high field region has no relation with the ferromagnetism, which in turn indicates that the roomtemperature ferromagnetism and large negative magnetoresistance observed in the as-deposited are the intrinsic properties of the Zn1-x Cox O magnetic semiconductor.     

Spin reorientation transition in (111) textured L10 CoPt layers

In this work, a spin reorientation transition from [001] axis to an in-plane direction occurs near Curie temperature under a small external field for (111) textured L1₀ CoPt layers in an AlN/CoPt multilayer film, indicating the dominant role of the shape anisotropy at elevated temperatures over the magnetocrystalline anisotropy. A large in-plane residual magnetization is also observed after cooling the sample from a temperature above the Curie point. The formation of magnetization during cooling is considered due to the alignment of magnetic moments along the easy axis by the small field in the spin reorientation transition temperature region. Our work reveals the importance of shape anisotropy for the formation of magnetization in the heat assisted magnetic recording process.     

Dielectric Properties of Fine-Grained BaTiO3 Ceramics under High Pressure

We investigate the temperature dependence of the dielectric constant of BaTiO3 ceramic with coarse to nanograin size under different hydrostatic high pressures up to 5000 bar in the range between room temperature and 200℃. The ferroelectric-to-paraelectric phase transition temperatures Tc are determined from the peak of dielectric constant versus temperature. The values of average grain-size are estimated from the SEM images. It is found that the magnitude of dTc/dp varies considerably from sample to sample depending on grain size. The Curie point Tc of the sample with small grain size decreases more sharply than that of samples with larger one.     

Magnetization and magnetocrystalline anisotropy in YCo4B compound

Easy and hard magnetization curves of YCo₄B compound have been measured in the temperature range from 1.5 to 300 K. It was found that the uniaxial magnetic anisotropy field decreases with decreasing temperature, and the magnetic anisotropy changes from the easy c-axis to the easy cone at approximately 150 K. The easy and hard magnetization curves did not cross up to 6 T. High field susceptibility of the compound for magnetic field parallel to the alignment direction seems different from that for a field perpendicular to the alignment direction. A jump was observed along the easy magnetization curve at 1.5 and 77 K. The critical field of the jump is about 1.5 T at 1.5 K and 1.2 T at 77 K. The jump was shown to be reversible at 1.5 K by down hill measurement.     

First observation of ferromagnetism and ferromagnetic domains in a liquid metal

80 Pd₂₀ alloy below the Curie temperature T_C(l)=1257 K of the liquid state. The magnetization of the undercooled liquid sample has been measured as a function of temperature using a modified Faraday balance. Below T_C(l), the magnetization of the liquid metal shows a plateau in the weak external field of μ₀H_z=5.6 mT. The effect is comparable to the behaviour of the corresponding solid phase, indicating the onset of spontaneous magnetization with ferromagnetic domains. T_C(l) is about 20 K lower than the Curie temperature of the solid phase T_C(s). Received: 24 February 1997/Accepted: 16 May 1997     

Magnetic Properties of Exchange-Coupled Dual-Layer SmTbCo Thin Films

Exchange-coupled SmTbCo dual-layer media are prepared by an r.f magnetron sputtering system and their magnetic properties are investigated. The prepared SmTbCo dual layer is composed of a 340 emu/cm^3 TM-rich readout layer and a 5.80 kOe RE-rich memory layer, meeting the requirements of high saturation magnetization and large coercivity for hybrid recording. Through exchange coupling, the coercivity of the high-saturation- magnetization SmTbCo layer is greatly enhanced from 1.85 to 5.96 kOe. The calculated interface wall energy for Sm6.65Tb12.35Co81 （20nm）/Sm1.22Tb42.16Co56.62 （20hm） is about 3.85erg/cm62. The reversal magnetization of the SmTbCo exchange-coupling dual-layer films is analysed based on a micro-magnetic model.     

ErFe11-xCoxTi化合物的结构与磁性研究

粉末样品的X射线衍射和热磁曲线测量表明，所有的ErFe_11-xCo_xTi(x=0—11)化合物都结晶ThMn₁₂型结构，且具有良好的单相性.Co替代Fe导致居里温度的显著提高和晶格常数的单调减小，4.2K下的饱和磁化强度M_s随Co含量的增加在x=3处呈现极大值.ErFe_11-xCo_xTi化合物当x≤4时，在室温下具有单轴磁晶各向异性，当6≤x≤9时，样品的易磁化方向垂直于c轴 关键词：     

Magnetic anisotropy-induced spin-reorientation in spinel FeCr2S4

In this paper, the low-field magnetic behavior of polycrystalline FeCr₂S₄ was investigated by thermal circling the sample from 5 to 200 K at a constant magnetic field. We show that, upon cooling the sample at 50 Oe to a temperature below the Curie temperature then warming back, the magnetization displays irreversibility between cooling and warming sequence. The irreversible behavior was suppressed gradually with increasing magnetic field. By considering spin-reorientation due to the increase of magnetic anisotropy upon cooling, the irreversible behavior has been explained qualitatively.     

Magnetocaloric effect in R2Fe17 (R=Sm,Gd, Tb,Dy, Er)

A series of R₂Fe₁₇ (R=Sm, Gd, Tb, Dy, Er) have been synthesized. The magnetocaloric effect (MCE) of these compounds has been investigated by means of magnetic measurements in the vicinity of their Curie temperature. The Curie temperature of Er₂Fe₁₇ is 294 K. The maximum magnetic entropy change of Er₂Fe₁₇ under 5 T magnetic field is ∼3.68 J/kg K. In the R₂Fe₁₇ (R=Sm, Gd, Tb, Dy, Er) system, the maximum magnetic entropy change under 1.5 T magnetic field is 1.72, 0.89, 1.32, 1.59, 1.68 J/kg K corresponding to their Curie temperature (400, 472, 415, 364, 294 K), respectively.     

Magnetic and magnetocaloric properties of the high-temperature modification of TbTiGe

The high-temperature form (HT) of the ternary germanide TbTiGe was prepared by melting. The investigation of HT-TbTiGe by x-ray and neutron powder diffractions shows that the compound crystallizes in the tetragonal CeScSi-type structure (space group I4/mmm; a?=?404.84(5) and c?=?1530.10(9)?pm as unit cell parameters). Magnetization and specific heat measurements as well as neutron powder diffraction performed on HT-TbTiGe reveal a ferromagnet having T(C)?=?300(1)?K as the Curie temperature; the Tb-moments are aligned along the c-axis. This magnetic ordering is associated with a modest magnetocaloric effect around room temperature. The isothermal magnetic entropy change ΔS(m) was determined from the magnetization data; ΔS(m) reaches, respectively, a maximum value of -?4.3 and -?2.0?J?K(-1)?kg(-1) for a magnetic field change of 5 and 2?T.     

Magnetic phase diagram of the four-sublattice antiferromagnet Tb2O2SO4 for a particular field direction

Tb₂O₂SO₄ orders antiferromagnetically at 3.9 K in a four-sublattice structure with two of the nearest-neighbour moments antiparallel and two almost perpendicular to that of a central ion. Specific-heat and magnetization measurements were carried out and allowed to establish the phase diagram for the external magnetic field along one of the moments' direction. Starting at the Néel temperature, the boundary of the paramagnetic phase is first shifted to lower temperatures for increasing field and then it stays at constant temperature for further increase of field. The shift is caused by the reduction of the staggered field that is existing in the antiferromagnetic phase. The experimental results are corroberated to a large extent by mean-field calculations.     

Preparation of Mg55Ni35Si10 Amorphous Powders by Mechanical Alloying and Consolidation by Vacuum Hot Pressing

Amorphous Mg55Ni35Si10 powders are fabricated by using a mechanical alloying technique. The amorphous powders are found to exhibit a relatively high crystallization temperature of 380℃. The as-milled amorphous Mg55Ni35Si10 powders are consolidated successfully into bulk body by vacuum hot pressing technique. Limited nanocrystallization is noticed. The Vickers microhardness range of the Mg55Ni35Si10 bulk sample is 7834 to 8048 MPa. Its bending strength and compressive strength are 529 MPa and 1466 MPa, respectively.     

Electronic Structure and Magnetic Properties of SmCo7-xZrx

The electronic structure and magnetism of SmCo_7-xZr_x alloy are investigated using the spin-polarized MS-X. method. The results show that a few of electrons are transferred to the Sm(5d⁰) orbital due to orbital hybridization between Sm and Co atoms. The exchange interactions between 3d and 5d electrons are more important than the polarization effects of the conductive electrons, thus it is the main reason resulting in the long-range ferromagnetic order in SmCo_7-xZr_x. The Curie temperature of SmCo_7-xZr_x is generally lower than that of corresponding pure Co, which may be explained by the weaker average coupling strength between Co lattices due to some negative couplings mainly occurring of 2e site. The calculated results for the Sm₅Co₃₂Zr₂ cluster may lead to a better understanding of why SmCo_7-xZr_x is stable phase. Since the spin-up DOS peak of d electrons at E_F arises and the bonding of electrons at E_F strengthens with increasing Zr concentration, which results in the internal energy of the system decrease, the stable ferromagnetic order forms in SmCo_7-xZr_x.     

Electronic States and Spatial Charge Distribution of Single Mn Impurity in Diluted Magnetic Semiconductors

The electronic and magnetic properties as well as the spatial charge distribution of single Mn impurity in III--V diluted magnetic semiconductors are obtained when the degeneracy of the p orbits contributed from the four nearest-neighbouring As(N) atoms is taken into account. We show that in the ground state, the Mn spin is strongly antiferromagnetically coupled to the surrounding As(N) atoms when the p-d hybridization V_pd is large and both the hole level E_v and the impurity level E_d are close to the Fermi energy. The spatial charge distribution of the Mn acceptor in the (110) plane is non-spherically symmetric, in good agreement with the recent STM images.     

Magnetic and magnetocaloric properties of the intermetallic compound TbNiAl

Magnetization measurements have been carried out on the intermetallic compound TbNiAl in applied fields up to 120 kOe. Temperature dependence of magnetization under zero-field-cooled and field-cooled conditions shows thermomagnetic irreversibility, which is attributed to magnetic frustration. With the increase of field, the irreversibility decreases and vanishes completely at high fields. Magnetocaloric effect has been calculated in terms of isothermal magnetic entropy change using magnetization isotherms obtained at various temperatures. The maximum entropy change is 13.8 J kg⁻¹ K⁻¹ near the ordering temperature for a field change of 50 kOe. The refrigerant capacity is found to be 494 J kg⁻¹ for the same field change and for a temperature difference of 52 K between the cold and the hot sinks.     

Magnetic properties of chalcogenide spinel CuCr2Se4 nanocrystals

The magnetic properties of chalcogenide spinel CuCr₂Se₄ nanocrystals have been studied as a function of crystallite size (15-30 nm). A solution-based method is used for the facile synthesis of the nanocrystals with good size control. They have close to cubic morphology with a narrow size distribution and exhibit superparamagnetic behavior at room temperature. The Curie temperature and saturation magnetization of the nanocrystals are lower as compared with the bulk and decrease with decreasing nanocrystal size. A similar trend is observed in the paramagnetic state for the Curie-Weiss temperature and effective magnetic moment. The low temperature magnetization behavior can be qualitatively explained by spin glass dynamics.