替代式合金系统的电阻率

本文将文献[1]的无序晶态合金电阻率理论推广到包含长程有序的系统,从而建立了适用于晶态金属,无序及有序替代式合金的Ziman型电阻率理论。根据这个理论我们详细讨论了这类系统电阻率的温度依赖性。文中着重指出:合金系统结构因子的超结构峰对电阻率有重要贡献。这个贡献在低温下是一个T²项,它比电子-电子散射引起的T²项大得多,因而合金系统电阻率在T<<Θ(Θ是德拜温度)时有ρ≈ρ₀+ρ_a(T/Θ)²+ρ_i(T/Θ)⁵的形式。据此,许多A-15化合物正常态电阻率在低温下的反常行为很容易解释。作为例子,我们将低温电阻率的理论表达式与V₃Si的测量值作了比较,符合得很好。     

FeCo基纳米晶合金高温交换耦合作用机理

研究了500和600℃真空退火后的纳米晶Fe_38.4Co₄₀Si₉B₉Nb_2.6Cu合金初始磁导率随温度的变化规律,发现较高温度(600℃)退火的FeCo基纳米晶合金,在非晶相居里温度以上较宽温度范围内磁导率没有明显的衰减,这是在双相纳米晶合金中观察到的一种新现象,其磁特性不同于Fe基纳米晶合金.为了探明这种现象的起源,估算了与剩余非晶相同成分的非晶合金的居里温度及纳米晶粒间发生交换耦合作用的参数 关键词： 交换耦合作用 非晶相居里温度 交换耦合穿透深度     

Hyperfine magnetic fields in Fe−Co alloys and their tempera ture dependences

We obtained⁵⁷Fe hyperfine field parameters from Fe₁−x-Co _x alloys (0≤x≤0.6) from 77 K to 900 K. We first discuss the origin of the low temperature hyperfine fields in terms of the 3d and 4s electrons at⁵⁷Fe atoms. The⁵⁷Fe hyperfine magnetic field (hmf) of Fe-Co alloys depends more weakly on temperature than the hmf of pure Fe. This temperature dependence occurs because the alignment of the magnetic moments at both the Fe atoms and at the Co atoms depend on temperature in the same way as the bulk magnetization of Fe-Co alloys.     

Electron-phonon interaction and coulomb pseudopotential in AuGa alloys from resistivity and superconductivity measurements

Measurements of the electrical resistivity as a function of temperature from 250 to 270 K for Au and f.c.c. phase AuGa alloys are presented. The linear dependence of the resistivity with temperature and previous results of the superconducting transition temperature of the alloys are used to obtain a value for T_c of pure Au. From these results a new method is introduced to estimate the Coulomb pseudopotential μ¹ for gold.     

Structural and magnetic studies of the alloy system GdInxAg1-x

The structural and magnetic studies below room temperature of the alloy system GdIn_xAg_1-x(0?x?1) are reported. It has been found that alloys with x?0.5 crystallize in CsCl type cubic structure, but the distortion of the unit cell starts for alloys with x#62;0.5 and for these alloys the unit cell becomes tetragonal. No phase change is evident from the low temperature (295-8 K) structural studies. However, a break appears in the X^-1_m vs. T linear plot of each alloy of this system at a specific temperature (designated as break temperature T_B). The variation of T_B with x is similar to the variation of phase transition temperature with x reported for LaIn_xAg_1-x. Close agreement has been found in the values of effective magneton number (p), magnetic ordering [Néel (T_N) or Curie (T_C)] and paramagnetic Curie (θ_p) temperature for materials studied by us and earlier workers. The variation of magnetization with applied field strength (2.5-65)×10⁵ Am^-1) at 4.2 K has also been reported for ferromagnetic of this system. It has been concluded that alloys with 0.4?x?0.6 are simple ferromagnets with parallel alignment of magnetic moment in the ground state. The angular arrangement of the magnetic moment starts appearing in the ground state for alloys with x?0.4 for x#62;0.6 and continues till x becomes closure to 0.17 or 0.84. The alloys with x=0.17 or x=0.84 have θ_p and T_C equal to zero and appear paramagnetic. Angular arrangement in spins again appear for alloys with x?0.17 or x#62;0.84, however all materials with 0?x?0.17 or 0.84?x?1 remain antiferromagnetic.     

Influence of lattice instability on the superconducting properties of “La3S4”

The normal state properties (the electronic specific heat constant, Debye temperature and electrical resistivity) and superconducting state properties [the superconducting transition temperature, T_c, and the upper critical field at 0 K, H_c²(0)] have been studied in the La₃S₄-La₂S₃ system. The superconducting properties and the electronic specific heat constant exhibit the maximum values in the alloy with the lowest sulfur content that does not undergo a low temperature crystallographic transformation. At lower sulfur contents the alloys exhibit a cubic to tetragonal transformation at ～80 K with a serious degradation in their superconducting properties, especially H_c² (0). These alloys clearly illustrate that materials which are almost but not quite unstable are good superconductors, relative to the more stable compositions.     

Ti-Pd系合金的比热测量

本文给出了Ti-Pd系合金样品的低温比热的测量结果,得出样品Ti_0.92Pd_0.08及Ti_0.8Pd_0.2的电子比热系数r分别为5.89mJ/mol·K²和4.78mJ/mol·K²,显然比纯Ti的r值3.32mJ/mol·K²高得多。因此,它们的费密面的电子态密度也比纯Ti的高,这正是Ti-Pd系合金的超导转变温度T_c比纯Ti的有较大幅度提高的原因。 关键词：     

预注入对Si1-xCx合金形成的影响

室温下在单晶Si中注入(0.6—1.5)at%的C原子,部分样品在C离子注入之前在其中注入²⁹Si⁺离子产生损伤,然后在相同条件下利用高温退火固相外延了Si_1-xC_x合金,研究了预注入对Si_1-xC_x合金形成的影响.如果注入C离子的剂量小于引起Si非晶化的剂量,在950℃退火过程中注入产生的损伤缺陷容易与C原子结合形成缺陷团簇,难于形成Si_1-xC关键词： 离子注入 固相外延 1-xC_x合金')" href="#">Si_1-xC_x合金     

Muon hyperfine fields in iron and its dilute alloys

The temperature dependence (240 to 633 K) of the interstitial magnetic field, B_μ, as determined by the rotation of the spin of the μ⁺, has been measured for dilute polycrystalline iron alloys with Mo, Ti and Nb additions. In all cases the behaviours differ from one another and from the Fe(A1) alloys previously studied. B_μ, which is negative with respect to the magnetization, is increased in magnitude by A1 and Mo, and decreased greatly by Ti. The addition of Nb creates a two- phase alloy from which we can assess the role of heterogeneity and/or strain on B_μ in iron. If the temperature dependence of the hyperfine field B_hf extracted from B_μ for Fe(Mo) alloys is interpreted on the model previously used to discuss the Fe(A1) data, we would conclude that the muon is attracted to the Mo atom while repelled by the A1 atoms as the temperature decreases. Measurements giving room temperature values of B_μ for iron alloys with Mn, Cr, V and W taken after annealing above the recrystallization temperature are also reported.     

Phase transitions and thermal expansion in Ni<Subscript>51–<Emphasis Type="Italic">x</Emphasis></Subscript>Mn<Subscript>36 + <Emphasis Type="Italic">x</Emphasis></Subscript>Sn<Subscript>13</Subscript> alloys

Thermal expansion and structural and magnetic phase transitions in alloys of the Ni–Mn–Sn system have been investigated. The spontaneous martensitic transformation in Ni_51–xMn_{36 + x}Sn₁₃ (0 ≤ x ≤ 3) alloys is found to be accompanied by high jumps in the temperature dependences of the linear thermal expansion. The relative change in the linear sizes of these alloys at the martensitic transformation is ~1.5 × 10^–3. There are no anomalies in the magnetic-ordering temperature range in the temperature dependences of the coefficient of linear thermal expansion. The differences in the behavior of linear thermal expansion at the martensitic transformation in Ni_51–xMn_{36 + x}Sn₁₃ (0 ≤ x ≤ 3) and Ni₄₇Mn₄₀Sn₁₃(x = 4) alloys have been established.     

Diffusion of Au in amorphous Zr x Ni100−x alloys studied by Rutherford Backscattering Spectrometry

The diffusion coefficients (D) of Au in three binary amorphous Zr _x Ni_100–x (x=61, 65, and 67) alloys were measured in the temperature range 549–623 K using the technique of the Rutherford Backscattering Spectrometry (RBS). The D values were found to lie in the range 1.0×10^–21–9.0×10^–20 m²s^–1 for different alloys. The activation energy (Q) was calculated in each case on the basis of an observed Arrhenius temperature dependence of D. The activation energy was found to scale with the crystallization temperature (T _x) of the alloy. Other published measurements for Au diffusion in amorphous Zr-Ni alloys also appear to follow the scaling relation between Q and T _x.     

Magnetic and electrical transport properties of amorphous Zr-Fe alloys

Amorphous Zr_1?xFe_x samples were prepared in the composition range 0.2 ? x ? 0.9 either by means of vapour deposition or melt spinning. The electrical resistivity was determined in the range 4.2–300 K. Negative temperature coefficients were observed in the whole concentration range. The extended Ziman theory (diffraction model) was found to be able to explain these results only if the effective valence of the Fe atoms involves not only s electrons but also d electrons. The magnetic properties and the ⁵⁷Fe Mössbauer effect of the Zr_1?xFe_x alloys were studied in the range 4.2–300 K. The Fe-rich alloys are ferromagnetic. The Fe moment vanishes in alloys of an Fe concentration lower than about 50 at%. In most alloys (x ? 0.8) the Curie temperature is below room temperature and continuously decreases with Zr concentration. By means of Mössbauer spectroscopy and magnetic measurements it is shown that compositional short-range order (CSRO) is present to a higher degree in melt-spun alloys than in vapour-deposited alloys. The effect of sign and magnitude of the heat of solution on CSRO and the magnetic properties is discussed.     

Densities,molar volumes,and surface tensions of Na-K-Cs ternary alloys along the two sections containing the eutectic alloy

The densities, molar volumes, and surface tensions of 21 ternary alloys of the Na-K-Cs system have been determined in the temperature range 293–453 K for the two sections directed to the Cs and K vertices and containing the eutectic alloy. The polytherms of these parameters for the Na_0.129K_0.435Cs_0.436 eutectic alloy in the temperature range 200–460 K are described by linear equations and their values at 373 K are determined to be 1406 kg m^?3, 54.62 × 10^?6 m³ mol^?1, and 77.0 mN m^?1, respectively. The isotherms of molar volumes of the ternary alloys in both sections obey the additivity rule; in the low-concentration range, cesium exhibits high surface activity.     

Giant forced volume magnetostriction of Fe-rich iron-cobalt-zirconium amorphous alloys

The forced volume magnetostriction has been measured as a function of composition and temperature in amorphous (Fe_1?xCo_x)₉₀Zr₁₀ alloys. The maximum value of $\text{δω}\text{δH}$ (T = 0 K), equal to 285 × 10^-10 Oe^-1, has been observed for Fe₉₀Zr₁₀ alloys. The effect of pressure on the magnetization σ₀ at T = 0 K was calculated from $\text{δω}\text{δH}$ data. The pressure dependence of the Curie temperature T_c and σ₀ behaves in a similar way as those observed for crystalline NiPd and NiRh alloys.     

Hydrogen depth profile in sputtered CuxZr1-x amorphous alloys studied by nuclear reaction analysis. Evolution as a function of annealing temperature.

Hydrogen depth profiles in thin films of sputtered Cu_xZr_1-x amorphous alloys have been measured using the resonant nuclear reaction ¹H (¹⁵N, αγ)¹²C. In Cu_0.3Zr_0.7, Cu_0.4Zr_0.6 and Cu_0.5Zr_0.5 alloys the hydrogen bulk concentrations expressed bythe atomic ratio H/Zr are respectively 0.26, 0.45 and 0.80. Hydrogen mobility under beam impact is observed at both interfaces (air-film, film-substrate) and in the molybdenum substrate. Evolution of the hydrogen profiles has been followed as a function of annealing temperature. No departure of hydrogen is observed below 520K; at temperatures close to the crystallisation, the hydrogen content remains high, in the 20–30 at % range. These results are discussed in correlation with physical properties of the alloys.     

Fe基非晶态合金的低温电阻研究

本文报道Fe_100-xB_x,Fe_87-xSi_xB₁₃,(Fe_1-xCo_x)₇₈Si_9.5B_12.5,(Fe_1-xM_x)_80-84B_16-20(M=Zr,V,Nb,Ta,Cr,Mo,W,Mn)非晶态合金的 关键词：     

Hyperfine interaction parameters of the ScFe2 laves alloy with MgZn2 hexagonal structure

This paper reports on NMR measurement of hyperfine fields, enhancement factors, and quadrupole splitting for ⁴⁵Sc nuclei in the ScFe₂, Sc_0.95Fe_2.05, and ScFe_1.97Al_0.03 alloys at room temperature and 77 K. The NMR spectra are studied, and the hyperfine-field shifts at ⁴⁵Sc nucleus sites in the above alloys, caused by Fe substituting for Sc and Al, for Fe in the nearest Sc coordination shells, are determined.     

Magnetic clusters in Fe3−x V x Al alloys with DO3 type structure forx≤1.1

Polycrystalline Fe_3?x V _x Al alloys with the DO₃ type structure were investigated by magnetostatic and Mössbauer methods. In alloys with 0.2<x<0.5 the ferro- and superpara-magnetic phases coexist. For alloys withx≥0.5 these investigations showed that in spite of the lack of magnetic order, they are characterized by strong nonlinear variations of the magnetization in a magnetic field over a wide temperature range. This indicates the presence of magnetic clusters of Fe atoms with very large magnetic moments. Analysis of the magnetization isotherms indicates that in these alloys a distribution of magnetic moments of clusters (μ_c) from 10 μ_B to 10⁴ μ_B exists.     

Carbon-doping effects on the metamagnetic transition and magnetocaloric effect in MnAsCx

Carbon doping effects in MnAs alloys have been investigated. More carbon doping in MnAs alloys leads to lower Curie temperature, larger thermal hysteresis and sharper slope of the dependence of critical field on reduced temperature due to severe lattice distortion. The obtained maximum of magnetic entropy change for a field change of 5 T is about 12.8 J kg⁻¹ K⁻¹ near room temperature, and increases with more doping carbon content to about 22.4 J kg⁻¹ K⁻¹ in MnAsC_0.03 and 13.2 J kg⁻¹K⁻¹ in MnAsC_0.05.     

Electron paramagnetic resonance in Nd-Ag amorphous alloys

We have studied the EPR of Nd³⁺ ions in Nd_16.7Ag_83.3 amorphous alloys between 4.2 K and room temperature. The resonance observed above 100K at a field corresponding to a g ? 2.3 indicates the existence of sites having a non-axial crystal field of the form J²_x-J²_z.