Laves相
铁磁性
铁磁性
晶体结构
结晶学
化学
晶格常数
空间组
凝聚态物理
材料科学
磁场
X射线晶体学
金属间化合物
磁化
物理
衍射
合金
有机化学
光学
量子力学
作者
И. С. Терешина,A. Yu. Karpenkov,D. I. Gorbunov,M. Doerr,E. A. Tereshina-Chitrova,H. Drulis
摘要
The crystal structure and magnetic properties of the multicomponent compounds (Tb1−xYx)0.8Sm0.2Fe2Hz (x = 0, 0.2, 0.4, 0.6, 0.8, 1; z = 0 and 3.7) are investigated. The compounds crystallize in the MgCu2 type of structure. While the parent compounds Tb0.8Sm0.2Fe2 and Y0.8Sm0.2Fe2 are single phase, we detect 5%–8% of a second phase with a crystal structure of the PuNi3 type (space group R3m) in the alloys with 0.2 ≤ x < 0.8. Hydrogen absorption does not change the space group of the (Tb,Y,Sm)Fe2 compounds but boosts significantly the lattice parameter a. A large volume change of ΔV/V ∼ 28% upon hydrogen absorption is observed. By applying high magnetic fields up to 58 T, we observed rotations of the magnetic sublattices and hence we were able to determine the critical transition fields, H, from the ferrimagnetic to the ferromagnetic state and the inter-sublattice exchange parameter λ. The magnetic compensation occurs at x ≈ 0.6 and 0.2 in (Tb1−xYx)0.8Sm0.2Fe2Hz at z = 0 and 3.7, respectively. While maintaining the collinear magnetic structure, the phenomenon of compensation in hydrides should be observed at x ≈ 0.4.
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