Crystal structure and magnetic characteristics of solid solutions Ni1–xCrxMnSb

The results of an experiment on studying the features of the crystal structure and magnetic studies of substitutional solid solutions of the Ni1–xCrxMnSb system (0 m х m 0.2) are presented. It was found that an increase in the concentration of chromium in solid solutions does not lead to significant changes in the size of the unit crystal cell. It was found that solid-phase quenching can be used to expand the limit of chromium solubility in Ni1–xCrxMnSb solid solutions. The temperature and field dependences of the specific magnetization of the synthesized compositions have been studied. It was found that the substitution of chromium for nickel in the NiMnSb compound leads to a decrease in the temperature of the “magnetic order – magnetic disorder” phase transformation with an increase in the concentration x from 0 to 20 mol.%. The values of specific magnetization and Curie temperature of hardened hard rasters are higher than those of slowly cooled ones. The results obtained contribute to the creation of a physical basis for the elemental base of spintronics.

Кристаллическая структура и магнитные характеристики твердых растворов Mn-=SUB=-1-x-=/SUB=-Fe-=SUB=-x-=/SUB=-NiGe

Substitutional solid solutions Mn1-xFexNiGe (0.05≤x≤1.00) were synthesized. The crystal structure in the temperature range of 20 - 300 K has been studied by X-ray and neutron diffraction. At T = 200 K, a phase transformation from a hexagonal structure of the Ni2In type to an orthorhombic structure (S.G. Pnma) has been observed. The magnetic properties of these compounds were also investigated in the temperature range of 5 - 300 K and external magnetic fields up to 10 T. The temperature of the "magnetic order - magnetic disorder" phase transformation was found to decrease from 272 to 132 K with an increase in concentration x from 5 to 30 mol%.

Exploring the Different Degrees of Magnetic Disorder in TbxR1−xCu2 Nanoparticle Alloys

Recently, potential technological interest has been revealed for the production of magnetocaloric alloys using Rare-Earth intermetallics. In this work, three series of TbxR1−xCu2 (R ≡ Gd, La, Y) alloys have been produced in bulk and nanoparticle sizes via arc melting and high energy ball milling. Rietveld refinements of the X-ray and Neutron diffraction patterns indicate that the crystalline structure in all alloys is consistent with TbCu2 orthorhombic Imma bulk crystalline structure. The analyses of the DC-magnetisation (MDC) and AC-susceptibility (χAC) show that three distinct degrees of disorder have been achieved by the combination of both the Tb3+ replacement (dilution) and the nanoscaling. These disordered states are characterised by transitions which are evident to MDC, χAC and specific heat. There exists an evolution from the most ordered Superantiferromagnetic arrangement of the Tb0.5La0.5Cu2 NPs with Néel temperature, TN∼ 27 K, and freezing temperature, Tf∼ 7 K, to the less ordered weakly interacting Superparamagnetism of the Tb0.1Y0.9Cu2 nanoparticles (TN absent, and TB∼ 3 K). The Super Spin Glass Tb0.5Gd0.5Cu2 nanoparticles (TN absent, and Tf∼ 20 K) are considered an intermediate disposition in between those two extremes, according to their enhanced random-bond contribution to frustration.