Decay studies of neutron-rich isotopes of manganese,iron, cobalt,nickel, copper and zinc

A 46 mg/cm² thick ^natW target was irradiated with an 11.5 MeV/u ⁸²Se beam. On-line massseparated samples of projectile-like neutron-rich products from multi-nucleon transfer reactions were investigated by βγ spectroscopy in the mass region A = 52–79. Decay properties of the nuclei ⁶¹Mn (0.71 s), ⁶⁴Fe (2.0 s), ⁶⁵Co (1.25 s), ⁶⁹Ni (10 s) and ^73mZn (5.8 s) were measured for the first time. For ⁶⁷Ni a decay scheme could be constructed using information from new γ-transitions. The known decay schemes of ⁶⁰Mn, ⁶³Fe, ⁶³Co and ⁶⁹Cu were extended. New half-life values of neutron-rich isotopes are compared with theoretical predictions.     

醇热反应低温合成锰钴镍热敏薄膜

锰钴镍复合氧化物是一种具有半导体性质的热敏材料. 本文采用金属有机沉积技术于室温条件下、在Si衬底上沉积一定 厚度的Mn_1.74Co_0.72Ni_0.54O₄金属 有机化合物薄膜, 并通过醇热反应进行低温结晶化合成, 可得到Mn_1.74Co_0.72Ni_0.54O₄结晶薄膜. 通过X 射线衍射、场发射扫描电子显微镜 (FESEM) 以及阻温特性等测试方法表征, 讨论了醇热反应对锰钴镍热敏薄膜的物相结构、微观形貌以及电学性能的影响. X射线衍射图显示薄膜已出现尖晶石结构的特征峰. 电镜照片说明结晶薄膜的表面较为平整、孔隙率低. 阻温特性关系表明薄膜具有明显的负温度系数效应, 室温(≈27°) 电阻率约为303.13 Ω·cm. 关键词： 醇热反应 锰钴镍薄膜 热敏电阻 低温合成     

A study of the synthesis products of fullerenes with nickel and cobalt

Qualitative analysis of the products of plasmochemical synthesis of fullerenes with metallic nickel and cobalt has been carried out using electron paramagnetic resonance (EPR) and electron microscopy. These studies show that the synthesis products are mainly fullerenes, metallic nanoparticles coated with an insulating layer, and isolated atomic clusters.     

Magnetic behaviour of cobalt,iron and manganese dissolved in palladium

This paper is meant to be a report on the experimental work on dilute Pd-based alloys with Co, Fe and Mn. These alloys exhibit the phenomenon of giant moments. The importance of measurements on paramagnetic alloys is emphasized. From these measurements the conclusion can be drawn that Co and Fe dissolved in Pd does not behave like a normal paramagnet, i.e. according to a Brillouin function. This result makes it possible to explain the existing discrepancy in the interpretations of magnetic measurements on one hand and of specific-heat experiments on the other.

The main conclusions of this paper are:

The giant moment should be accounted for by ‘normal’ values of the magnetic quantum number (3/2 for Co, 2 for Fe and 5/2 for Mn) and a large value of geff.

Paramagnetic alloys of Mn in Pd behave according to Brillouin functions, but alloys of Co or Fe in Pd do not. Hence, a number of interpretations of magnetic measurements should be considered as incorrect.

The localized model for ferromagnetism can well account for the magnetic ordering of dilute Pd-based alloys (certainly if c < 1 at.%). A straightforward generalization of the Weiss molecular-field model may be applied.

The transition temperature of Pd-Mn alloys is not proportional to the concentration, but after scaling the behaviour is similar to what has been found for Pd-Co and Pd-Fe alloys. The concentration dependence can be explained from a calculation of the strength of the interaction between two impurity atoms as a function of the distance.

Comparison between alloys with equal concentrations shows that the magnetic ordering in Pd-Mn is not at all exceptional, but analogous to that in Pd-Co and in Pd-Fe. It should be mentioned, however, that Pd-Mn at c > 3 at.% is a so-called spin glass.

Addition of Ag or Rh to Pd alloys with Co, Fe and Mn has important influences on their properties. Unfortunately these effects are not completely understood.     

Solid solutions of nickel and cobalt disilicides

Lattice parameters, density, thermal expansion coefficients and electrical conductivity of alloys of higher silicide of nickel with cobalt disilicide were measured. The influence of the completeness of the crystal lattice of the continuous series of solid solutions formed by these compounds was analyzed. The anomalous variation in the lattice parameter observed when nickel is replaced by cobalt was attributed to a reduction in the electron concentration in antibonding states.     

镍锰铁氧体纳米线阵列的制备与表征

采用真空负压灌注技术, 结合溶胶-凝胶法在多孔氧化铝模板的纳米孔洞中成功制备了平均直径为80 nm左右的Ni_{1- x}Mn_xFe₂O₄(x=0, 0.25, 0.5, 0.75) 纳米线阵列. XRD结果显示所制备的纳米线阵列为立方尖晶石结构, SEM和TEM的结果表明纳米线是由大量不同晶体取向的亚微晶粒联接组成. 磁测量结果显示, 随着Mn掺杂浓度的增加, 饱和磁化强度先增加而后减小, 这种变化与离子在尖晶石结构中的替代、占位变化有关. 相比于块体材料的NiFe₂O₄, 由于非线性磁结构比例的增加, 导致了线体NiFe₂O₄的饱和磁化强度降低.     

Oxidation of iron,cobalt and nickel at the Curie temperature

The large differences in the logarithmic oxidation kinetics reported as a change in activation energy with the oxidation rate decreasing from ferromagnetic to paramagnetic states are discussed for iron, cobalt and nickel. The observed anomalies at the Curie point are explained by a mechanism which takes into account both surface-state charge at the metal/oxide interface and space charge in the growing oxide.     

Synthesis and characterization of cobalt–manganese oxides

Cobalt doped/un-doped manganese oxides materials were synthesized at various doping rates by soft chemical reactions, oxidation-reduction method, which allows generating a metal-mixed oxide. The synthesized materials were characterized using several techniques including chemical analysis, X-rays diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and vibrating sample magnetometer (VSM). The chemical analysis confirmed the presence of cobalt in the samples. XRD patterns reveal mainly a spinel-like structure and SEM micrographs exhibited morphology with fine aggregate of particles. TGA profiles showed weight loss due to loss of water in a first step, followed by a loss of oxygen from the lattice associated with partial reduction of Mn⁴⁺ to Mn³⁺. VSM was used to measure the magnetization as a function of the applied magnetic field at temperatures T=50 and 300 K. Different magnetic behaviors were observed when cobalt percentage changed in the samples. These behaviors are considered to be related to the size of the particles and composition of the materials. Higher coercive field and lesser magnetization were observed for the sample with higher cobalt content.     

Magnetoresistivity of single-crystal films of iron,cobalt, and nickel binary alloys

Magnetoresistivity measurements of binary systems of alloy films Fe-Co, Fe-Ni, and Co-Ni in the [100] direction for the alloy systems Fe-Co and Fe-Ni up to 25 wt. % Co and Ni, respectively, and in the [100] direction for the remaining alloys are presented. A test of Berger's theory on the influence of spin-orbit interaction on transition processes in ferromagnetic alloys of nickel is carried out. The results obtained are compared with the results derived from bulk polycrystalline samples [1, 2].     

Infrared spectra of the matrix-isolated chlorides of iron,cobalt, and nickel

Iron, cobalt, and nickel metal cathodes were sputtered with various mixtures of ³⁷Cl₂/³⁵Cl₂/Ar to produce Ar matrices at 14 K that contained the mono-, di-, and trichlorides of the corresponding metal. The measured infrared absorption spectra of these matrices allowed the identification and characterization of FeCl₂, FeCl₃, CoCl, CoCl₂, CoCl₃, and NiCl₂. The derived vibrational constants of the electronic ground state of ⁵⁹Co³⁵Cl are ω_e = 457.8 ± 3.0 cm^?1 and ω_eχ_e = 2.0 ± 1.5 cm^?1. The antisymmetric stretching mode frequencies of six isotopomers of FeCl₂ and three isotopomers of CoCl₂ were identified and measured. The dichlorides of iron, cobalt, and nickel were all determined, in contrast with previous work, to be nonlinear with bond angles of 161, 157, and 161°, respectively. The estimated uncertainty is 5°. For both iron and cobalt trichlorides, the measured stretching mode frequencies were used to derive a ClMCl angle in excess of 120°, as would be expected for planar molecules with somewhat anharmonic vibrations. Observed adsorption peaks could be assigned to the ν₃(E) modes of planar (D_3h) Fe and Co trichlorides and the corresponding modes of the isotopomers. These observations strongly suggest that recent data supporting a pyramidal geometry for FeCl₃ should be reexamined. The geometry of CoCl₃ has not previously been determined.     

A study of nitric oxide adsorbed on nickel oxide,cobalt oxide,and graphite by X-ray photoelectron spectroscopy

The nitrogen 1s binding energy of nitric oxide adsorbed on nickel oxide, cobalt oxide and graphite was measured at several temperatures by X-ray photoelectron spectroscopy. For the oxides, a temperature dependent range of binding energies was observed, but for graphite the nitrogen 1s binding energy was independent of temperature. The values obtained suggest that significant back donation of electrons occurs from the oxides to the adsorbed nitric oxides, but no back donation occurs from graphite to adsorbed nitric oxide. However, adsorption did not cause changes in the binding energy of substrate core electrons. It is believed that unless the mean free path of electrons is short, the total photoelectron signal will not reveal changes in binding energy of electrons from substrate atoms at the surface.