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Structural and high-field magnetic properties of Laves phase RFe2-H hydrides

机译:Laves 相 RFe2-H 氢化物的结构和高场磁性

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摘要

The crystal structure and magnetic properties of the multicomponent compounds (Tb1-xYx)(0.8)Sm0.2Fe2Hz (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 LE; x < 0.8. Hydrogen absorption does not change the space group of the (Tb,Y,Sm)Fe-2 compounds but boosts significantly the lattice parameter a. A large volume change of UDelta;V/V SIM; 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 lambda. The magnetic compensation occurs at x AP; 0.6 and 0.2 in (Tb1-xYx)(0.8)Sm0.2Fe2Hz at z = 0 and 3.7, respectively. While maintaining the collinear magnetic structure, the phenomenon of compensation in hydrides should be observed at x AP; 0.4.
机译:研究了多组分化合物(Tb1-xYx)(0.8)Sm0.2Fe2Hz (x = 0, 0.2, 0.4, 0.6, 0.8, 1; z = 0 and 3.7)的晶体结构和磁性.这些化合物以 MgCu2 型结构结晶。虽然母体化合物 Tb0.8Sm0.2Fe2 和 Y0.8Sm0.2Fe2 是单相,但我们在具有 0.2 & LE 的合金中检测到 5%-8% 的第二相具有 PuNi3 型晶体结构(空间组 R3m);x < 0.8。氢吸收不会改变(Tb,Y,Sm)Fe-2化合物的空间基团,但会显著提高晶格参数a。&UDelta的体积变化很大;V/V & SIM卡;观察到氢吸收时为 28%。通过施加高达 58 T 的高磁场,我们观察到磁亚晶格的旋转,因此我们能够确定从亚铁磁态到铁磁态的临界跃迁场 H 以及亚晶格间交换参数 lambda。磁补偿发生在 x 和 AP;在 z = 0 和 3.7 时,分别为 0.6 和 0.2 in (Tb1-xYx)(0.8)Sm0.2Fe2Hz。在保持共线磁结构的同时,应在x&AP处观察氢化物的补偿现象;0.4.

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