Structure and magnetostriction of Tb0.2Pr0.8(Fe0.4Co0.6)1.93−xCx intermetallic compounds

The structure and magnetostriction of Tb_0.2Pr_0.8(Fe_0.4Co_0.6)_1.93−xC_x intermetallic compounds were studied by X-ray diffraction and magnetic measurements. Almost a single cubic Laves phase forms in the alloys for x ≤0.20, and a small amount of C can inhibit the formation of the 1:3 phase. The lattice parameter increases when 0≤x≤0.15, while the T_c and the spontaneous magnetization decreases with increasing x. The lattice parameter decreases slowly when 0.15≤x≤0.30, while the T_c decreases evidently with increasing x. The magnetostriction λ_a (=λ_∥-λ_⊥) is improved at low magnetic fields at room temperature for the compounds with 0.05≤x≤0.10, indicating that these C-containing compounds are promising magnetostrictive materials.     

Synthesis and magnetic properties of Pr(Fe 1-xCo x) 2 and Pr 1-yTb y(Fe 0.4Co 0.6) 2 alloys

Measurement of X-ray diffraction, magnetization and magnetostriction was made on the Pr(Fe_1-xCo_x)₂ (x=0.4, 0.5 and 0.6) and Pr_1-yTb_y(Fe_0.4Co_0.6)₂ (y=0, 0.1, 0.2 and 0.3) alloy series. It was found that a cubic phase with the MgCu₂ structure can be obtained in the Pr(Fe_1-xCo_x)₂ series only at x=0.6. The Pr_1-yTb_y(Fe_0.4Co_0.6)₂ system has the cubic MgCu₂ structure over the studied range for y. The lattice constant and magnetization decrease and the Curie temperature increases with increasing y. At 7 K, Pr_1-yTb_y(Fe_0.4Co_0.6)₂ samples are found to have huge intrinsic coercivities, which are associated with narrow domain walls. It is also found from X-ray measurement that in Pr_1-yTb_y(Fe_0.4Co_0.6)₂ the spontaneous magnetostriction ₁₁₁ increases due to Tb substitution, while the saturation magnetostriction _s is much lower than ₁₁₁. This can be attributed to the large value of ₁₀₀ with an opposite sign to ₁₁₁, which may be caused by the filling of the d band due to Co substitution. PACS 75.80.-g; 61.10.-i; 75.60.-d     

Preparation and magnetic properties of the conductive Co(1−x)NixFe2O4/polyaniline microsphere composites

Core-shell Co_(1−x)Ni_xFe₂O₄/polyaniline nanoparticles, where the core was Co_(1−x)Ni_xFe₂O₄ and the shell was polyaniline, were prepared by the combination of sol-gel process and in-situ polymerization methods. Nanoparticles were investigated by Fourier transform spectrometer, X-ray diffraction diffractometer, Scanning electron microscope, Differential thermal analysis and Superconductor quantum interference device. The results showed that the saturation magnetization of pure Co_(1−x)Ni_xFe₂O₄ nanoparticles were 57.57 emu/g, but Co_(1−x)Ni_xFe₂O₄/polyaniline composites were 37.36 emu/g. It was attributed to the lower content (15 wt%), smaller size and their uneven distribution of Co_(1−x)Ni_xFe₂O₄ nanoparticles in the final microsphere composites. Both Co_(1−x)Ni_xFe₂O₄ and PANI/Co_(1−x)Ni_xFe₂O₄ showed superparamagnetism.     

Magnetic transitions and magnetostrictive properties of Laves compounds Sm0.88Nd0.12(Fe1−xCox)1.93

The structure, magnetic and magnetostrictive properties of Sm_0.88Nd_0.12(Fe_1−xCo_x)_1.93 (0≤x≤1.0) alloys have been investigated. The alloys have the cubic MgCu₂ structure over the whole composition range and the lattice parameter a decreases with increasing x. For 0≤x≤0.2, substitution of Co for Fe slightly increases the saturation magnetization M_s and Curie temperature T_c, while further substitution causes a decrease in both M_s and T_c. The spin reorientation is observed, and a phase diagram for the spin configurations of the Sm_0.88Nd_0.12(Fe_1−xCo_x)_1.93 system is determined. The spontaneous magnetostriction λ₁₁₁ increases as x is increased, while a monotonic decrease of the saturation magnetostriction λ_s with x originates from the increase of λ₁₀₀ with opposite sign to that of λ₁₁₁, which may be caused by the filling of the d band due to Co substitution.     

Structure,magnetic properties and magnetostriction of laves compounds Nd1−xPrx(Fe0.35Co0.55B0.1)2

The C15 Laves phases with composition Nd_1−xPr_x(Fe_0.35Co_0.55B_0.1)₂ (0?x?1) have been synthesized by arc melting and subsequent annealing. The Curie temperature T_c and the saturation magnetizations M_s at 5 and 295 K decrease with increasing Pr content. The linear anisotropic magnetostriction λ_a=λ_∥−λ_⊥ at room temperature for Nd_1−xPr_x(Fe_0.35Co_0.55B_0.1)₂ alloys with 0?x?0.4 initially reaches a negative minimum, then increases and changes its sign with increasing magnetic field H, and the λ_a for the alloys with x?0.6 is positive and increases as magnetic field H increases.     

A study on magnetoelastic properties of Tb3 (Fe28−xCox) V1.0 (x=0, 3, 6) compounds

In this work, The magnetoelastic properties of polycrystalline samples of Tb₃ (Fe_28−xCo_x) V_1.0 (x=0, 3, 6) intermetallic compounds are investigated by means of linear thermal expansion and magnetostriction measurements in the temperature range of 77–515 K under applied magnetic fields up to 1.5 T. The linear thermal expansion increases with the Co content. The well-defined anomalies observed in the linear thermal expansion coefficients for Tb₃ (Fe_28−xCo_x) V_1.0 (x=0, 3, 6) compounds are associated with the magnetic ordering temperature for x=0 and spin reorientation temperatures for x=3, 6. Below transition temperatures, the value of the longitudinal magnetostriction (λ_Pa) at 1.6 T increases with Co content.     

Field and temperature induced colossal strain in Gd5(SixGe1−x)4

Gd₅(Si_xGe_1−x)₄, known for its giant magnetocaloric effect, also exhibits a colossal strain of the order of 10,000 ppm for a single crystal near its coupled first-order magnetic-structural phase transition, which occurs near room temperature for the compositions 0.41≤x≤0.575. Such colossal strain can be utilised for both magnetic sensor and actuator applications. In this study, various measurements have been carried out on strain as a function of magnetic field strength and as a function of temperature on single crystal Gd₅Si₂Ge₂ (x=0.5), and polycrystalline Gd₅Si_1.95Ge_2.05 (x=0.487) and Gd₅Si_2.09Ge_1.91 (x=0.52). Additionally a giant magnetostriction/thermally induced strain of the order of 1800 ppm in polycrystalline Gd₅Si_2.09Ge_1.91 was observed at its first order phase transition on varying temperature using a Peltier cell without the use of bulky equipment such as cryostat or superconducting magnet.     

A magnetic, magnetostrictive and Mössbauer study of Tb0.3Dy0.7−xPrx(Fe0.9Al0.1)1.95 alloys

The effect of Pr substitution for Dy on the magnetization, magnetostriction, anisotropy and spin reorientation of a series of Tb_0.3Dy_0.7−xPr_x(Fe_0.9Al_0.1)_1.95 alloys (x=0, 0.1, 0.20, 0.25, 0.30, 0.35) at room temperature has been investigated. It was found that the magnetization and magnetostriction of the homogenized Tb_0.3Dy_0.7−xPr_x(Fe_0.9Al_0.1)_1.95 alloys decreases drastically with increasing x and the magnetostrictive effect disappears for x>0.2, but the spontaneous magnetostriction λ₁₁₁ increases approximately linearly with increasing x. Moreover, the magnetostriction exhibits slightly bigger value at x=0.1 than the free alloys and is saturated more easily with the magnetic field H, showing that a small amount of Pr substitution is beneficial to a decrease in the magnetocrystalline anisotropy. The analysis of the Mössbauer spectra indicated that the easy magnetization direction in the {1 1 0} plane deviates slightly from the main axis of symmetry with Pr concentration x, namely spin reorientation. Comparing with the Al substitution, the effect of Pr substitution for Dy on the spin reorientation is smaller.     

Effect of Sr concentration on microstructure and magnetic properties of (Ba1−xSrx)(Ti0.3Fe0.7)O3 ceramics

Fe-doped (Ba_1−xSr_x)TiO₃ ceramics were prepared by solid-state reaction, and ferromagnetism was realized at room temperature. The microstructure and magnetism were modified by the Sr concentration control (0≤x≤75 at%) at a fixed Fe concentration, and the relevant magnetic exchange mechanism was discussed. All the samples are shown to have a single perovskite structure. When increasing the Sr concentration, the phase structure is transformed from a hexagonal perovskite into a cubic perovskite, with a monotonic decrease in lattice parameters induced by ionic size effect. The room-temperature ferromagnetism is expected to originate from the super-exchange interactions between Fe³⁺ on pentahedral and octahedral Ti sites mediated by the O²⁻ ions. The increase in Sr addition modifies two main influencing factors in magnetic properties: the ratio of pentahedral to octahedral Fe³⁺ and the concentration of oxygen vacancies, leading to a gradually enhanced saturation magnetization. The highest value, obtained for Fe-doped (Ba_0.25Sr_0.75)TiO₃, is an order of magnitude higher than that of the Fe-doped BaTiO₃ system with similar Fe concentration and preparation conditions, which may indicate (Ba_1−xSr_x)TiO₃ as a more suitable matrix material for multiferroic research.     

熔体快淬Pr(Fe1-xCox)2合金的结构和磁性

通过熔体快淬方法获得Pr(Fe_1-xCo_x)₂合金条带,经过X射线衍射、差示扫描量热计和磁性测量对其结构、磁性和热稳定性进行了研究.发现当Co的含量x大于0.2时才可能获得Pr(Fe,Co)₂立方Laves相化合物.对Pr(Fe_0.6Co_0.4)₂合金,在快淬速度为30m/s时,条带由Pr₂(Fe,Co)₁₇,Pr(Fe,Co)₂和富稀土相组成;在速度为40m/s时,获得了几乎单相的Pr(Fe_0.6Co_0.4)₂化合物,其居里温度为305℃;在速度为45m/s时,除了Pr(Fe_0.6Co_0.4)₂化合物外,还存在少量的非晶相.Pr(Fe_0.6Co_0.4)₂化合物在770℃以上发生分解.用40m/s快淬纳米晶粉胶粘磁体有大的磁致伸缩系数（λ_∥-λ_⊥=140×10^-6)和高的硬磁性能（_iH_c=398kA/m). 关键词：     

Spontaneous volume magnetostriction in Y(Fe1−xCox)2 and Zr(Fe1−xCox)2

The spontaneous volume magnetostriction is calculated for Y(Fe_1?xCo_x)₂ and Zr(Fe_1?xCo_x)₂ in the simple itinerant-electron model. The density of states for various compositions is calculated by the recursion method. The calculated results on the composition dependence of the spontaneous volume magnetostriction are shown to be consistent with the experimental ones.     

R3(Fe1-xCox)29-yCry(R=Gd,Sm)化合物相稳定性研究

在制备出Gd₃(Fe_1-xCo_x)_29-yCr_{y化合物基础上，成功制备出Sm3(Fe1-xCox)29 -yCry化合物，通过x射线衍射和热磁分析对R3(Fe1-x< /sub>Co x)29-yCry 关键词： 3(Fe1-xCox)29-yCry化合物')" href="#">R3(Fe1-xCox)29-yCry化合物 相结构 单轴磁晶各向异性}     

RECa4O(BO3)3 thin films as new Luminescent materials screened by the combinatorial method

A new phosphor material, Y_1−xTb_xCa₄O(BO₃)₃ (0≤x≤1) film was grown on SiO₂ substrates by the combinatorial pulsed laser deposition (PLD) method, which enabled us to fabricate continuous composition spread film libraries. Photoluminescence (PL) and PL decay were measured for these film libraries to identify the optimum composition as well as to determine the luminescence mechanism. The film libraries showed strong dependence of luminescence intensities on the chemical composition of Tb ion. The optimum concentration of Tb ions in Y_1−xTb_xCa₄O(BO₃)₃ was experimentally and theoretically determined to be x=0.2-0.3.     

Luminescent properties of HTP AgGd1−xW2O8:Eux and AgGd1−x(W1−yMoy)2O8:Eux phosphor for white LED

Intense red phosphors, AgGd_1−xEu_x(W_1−yMo_y)₂O₈ (x=0.0-1.0, y=0.0-1.0), have been synthesized through traditional solid-state reaction and characterized by X-ray diffraction (XRD) and photoluminescence (PL). XRD results reveal that AgGd_1−xEu_xW₂O₈ synthesized at 1000 °C has a tetragonal crystal structure, which is named as high temperature phase (HTP) AgGdW₂O₈. All phosphors compositions with Eu³⁺ show red and green emission on excitation either in the charge-transfer or Eu³⁺ levels. Analysis of the emission spectra with different Eu³⁺ concentrations reveal that the optimum dopant concentration for Eu³⁺ is x=0.6 in the HTP AgGd_1−xEu_xW₂O₈ (x=0.0-1.0). Studies on the AgGd_0.4Eu_0.6(W_1−yMo_y)₂O₈ (y=0.0-1.0) and AgGd_1−xEu_x(W_0.7Mo_0.3)₂O₈ (x=0.0-1.0) show that the emission intensity is maximum for compositions with y=0.3 and x=0.5, respectively, and a decrease in emission intensity is observed for higher y or x values. The Mo⁶⁺ and Eu³⁺ co-doped AgGd(WO₄)₂ phosphors show higher emission intensity in comparison with the singly Eu³⁺-doped AgGd(WO₄)₂ in UV region. The intense emission of the tungstate/molybdate phosphors under 394 and 465 nm excitations, respectively, suggests that these materials are promising candidates as red-emitting phosphors for near-UV/blue GaN-based white LED for white light generation.     

Y2(Fe1-x-y,Coy,Crx)17化合 物的结构及居里温度

通过x射线衍射及磁测量手段研究了Y₂(Fe_1-y-x,Co_y,C r_x)₁₇化合物的结 构及居里温度.研究结果表明Y₂(Fe_1-y-x,Co_y,Crx)₁₇化合物具有六 角相的Th₂Ni₁₇型结构.随着x的增加，Y₂(Fe 关键词： 2(Fe_1-y-x')" href="#">Y₂(Fe_1-y-x y')" href="#">Co_y x)_{1 7}化合物')" href="#">Cr_x)_{1 7}化合物 x射线衍射 居里温度     

Magnetocaloric effects in (Gd1−xTbx)Co2

The structures and magnetocaloric effects of (Gd_1−xTb_x)Co₂ (x=0, 0.25, 0.4, 0.5, 0.6, 0.7, 0.8, and 1) pseudobinary compounds were investigated by X-ray powder diffraction and magnetic properties measurement. The results show that the T_c of the alloy is near room temperature when X=0.6. The magnetic entropy changes of the compounds increase from 1.7 to 3.6 J/kg K with increasing the content of Tb under an applied field up to 2 T. All the compounds exhibit second order magnetic change. As a result, the values of their ΔS_M are lower than that of some large magnetocaloric effect materials.     

Structure and magnetic properties of melt-spun Tb0.27Dy0.73Fex ribbons

The structure and magnetic properties of the melt-spun ribbons of Tb_0.27Dy_0.73Fe_x alloy are investigated as a function of various wheel speeds during melt-quenching using a single-roll technique. It is found that Tb_0.27Dy_0.73Fe_x alloy is difficult to be fabricated as amorphous state by using the melt-quenching method. X-ray diffractions show that all these ribbons for x=1.7−2.0 are the MgCu₂-type phase at the wheel speed of 45 m s⁻¹. For Tb_0.27Dy_0.73Fe_x alloy, the high wheel speed is beneficial to eliminate the RFe₃ phase and form the perfect MgCu₂-type phase. Compared with the bulk of Tb_0.27Dy_0.73Fe_1.95, these ribbons exhibit higher intrinsic coercivity value and their saturation magnetizations increase as well. The magnetostriction of Tb_0.27Dy_0.73Fe_1.95 composite with 4% epoxy resin is 640×10⁻⁶ at 900 kA m⁻¹.     

Magnetostriction, Curie temperature and microstructure of Tb0.29(Dy1−xPrx)0.71Fe1.97 oriented alloys

The Tb_0.29(Dy_1−xPr_x)_0.71Fe_1.97 (x=0, 0.1, 0.2 and 0.3) alloys were prepared by directional solidification method. The orientation, magnetostriction λ, Curie temperature T_c and microstructure of alloys were characterized by XRD, standard resistant strain gauge technique, VSM and SEM-EDS. The results reveal that the alloys have a preferred orientation of 〈1 1 0〉 and 〈1 1 3〉 direction when x>0. With the increase in Pr content, the T_c of alloys decreases gradually and the non-cubic phase appears, resulting in the decline of λ dramatically, from 1935.2×10⁻⁶ for x=0 to 695.9×10⁻⁶ for x=0.3 at a compressive stress of 6 MPa and a magnetic field of H=240 kA m⁻¹.     

Crystal structure and magnetic properties of Nd（Mn1-xFex）2Si2 compounds

X-ray powder diffraction,resistivity and magnetization studies have been performed on polycrystalline Nd(FexMn1-x)2Si2 (0 ≤ x ≤ 1) compounds which crystallize in a ThCr2Si2-type structure with the space group I4/mmm.The field-cooled temperature dependence of the magnetization curves shows that,at low temperatures,NdFe2Si2 is antiferromagnetic,while the other compounds show ferromagnetic behaviour.The substitution of Fe for Mn leads to a decrease in lattice parameters a,c and unit-cell volume V .The Curie temperature of the compounds first increases,reaches a maximum around x = 0.7,then decreases with Fe content.However,the saturation magnetization decreases monotonically with increasing Fe content.This Fe concentration dependent magnetization of Nd(FexMn1-x)2Si2 compounds can be well explained by taking into account the complex effect on magnetic properties due to the substitution of Mn by Fe.The temperature’s square dependence on electrical resistivity indicates that the curve of Nd(Fe0.6Mn0.4)2Si2 has a quasi-linear character above its Curie temperature,which is typical of simple metals.     

Structure and magnetostrictive properties of melt-spun Pr(Fe0.4Co0.6)1.93 alloys

Pr(Fe_0.4Co_0.6)_1.93 ribbons were prepared by a melt-spinning method. Their structure and magnetic properties are investigated as functions of wheel speed and annealing temperature. The as-spun ribbon consists of a Pr(Fe, Co)₂ cubic Laves phase and an amorphous phase at a wheel speed of v≥35 m/s, while the non-cubic phases of PuNi₃-type and rare earth appear when the speed lower than 30 m/s. A single Pr(Fe, Co)₂ phase with MgCu₂-type structure has been synthesized by the process for the wheel speed of v≥35 m/s and subsequent annealing at 500 °C for 30 min. The epoxy/Pr(Fe_0.4Co_0.6)_1.93 composite has been produced by a cold isostatic pressing technique, and the magnetic properties have been investigated. The composite rod sample possesses good magnetostrictive properties, i.e., a large magnetostriction (λ_a=λ_∥−λ_⊥) of 710 ppm at 800 kA/m and a dynamic coefficient d₃₃ of 0.67 nm/A at 100 kA/m, and is of practical value.