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作者机构:Materials and Engineering Physics Program Ames Laboratory of the United States Department of Energy Iowa State University Ames Iowa 50011-3020 USA Department of Materials Science and Engineering Iowa State University Ames Iowa 50011-2300 USA
出 版 物:《Physical Review B》 (Phys. Rev. B Condens. Matter Mater. Phys.)
年 卷 期:2004年第70卷第14期
页 面:144419-144419页
核心收录:
基 金:Office of Basic Energy Sciences U.S. Department of Energy, USDOE
摘 要:The room temperature crystal structures of Er5SixGe4−x alloys change systematically with the concentration of Ge from the orthorhombic Gd5Si4-type when x=4, to the monoclinic Gd5Si2Ge2 type when 3.5⩽x⩽3.9 and to the orthorhombic Sm5Ge4 type for x⩽3. The Curie-Weiss behavior of Er5SixGe4−x materials is consistent with the Er3+ state. The compounds order magnetically below 30K, apparently adopting complex noncollinear magnetic structures with magnetization not reaching saturation in 50kOe magnetic fields. In Er5Si4, the structural-only transformation from the monoclinic Gd5Si2Ge2-type to the orthorhombic Gd5Si4-type phase occurs around 218K on heating. Intriguingly, the temperature of this polymorphic transformation is weakly dependent on magnetic fields as low as 40kOe (dT∕dH=−0.058K∕kOe) when the material is in the paramagnetic state nearly 200K above its spontaneous magnetic ordering temperature. It appears that a magnetostructural transition may be induced in the 5:4 erbium silicide at ∼18K and above by 75kOe and higher magnetic fields. Only Er5Si4 but none of the other studied Er5SixGe4−x alloys exhibit magnetic field induced transformations, which are quite common in the closely related Gd5SixGe4−x system. The magnetocaloric effects of the Er5SixGe4−x alloys are moderate.