磁铁矿
兴奋剂
稀土
饱和(图论)
凝聚态物理
轨道(动力学)
离子
磁化
自旋(空气动力学)
自旋轨道相互作用
材料科学
化学
物理
磁场
热力学
冶金
工程类
航空航天工程
数学
量子力学
有机化学
组合数学
作者
M. Hussein N. Assadi,José Julio Gutiérrez Moreno,Dorian Hanaor,Hiroshi Katayama‐Yoshida
摘要
The significance of the spin-orbit interaction is very well known in compounds containing heavier elements such as the rare-earth Eu ion. Here, through density functional calculations, we investigated the effect of the spin-orbit interaction on the magnetic ground state of Eu doped magnetite ($\mathrm{Fe_3O_4:Eu_{Fe}}$). By examining all possible spin alignments between Eu and magnetite's Fe, we demonstrate that Eu, which is most stable when doped at the tetrahedral site, adapts a spin almost opposite the substituted Fe. Consequently, because of smaller spin cancellation between the cations on the tetrahedral site ($\mathrm{Fe_{Tet}}$ and $\mathrm{Eu_{Tet}}$) and the cations on the octahedral sites ($\mathrm{Fe_{Oct}}$), $\mathrm{Fe_3O_4:Eu_{Fe}}$ exhibits a maximum saturation magnetisation of 9.451 $\mu_B/$f.u. which is significantly larger than that of undoped magnetite (calculated to be 3.929 $\mu_B/$f.u.). We further show that this large magnetisation persists through additional electron doping. However, additional hole doping, which may unintentionally occur in Fe deficient magnetite, can reduce the magnetisation to values smaller than that of the undoped magnetite. The results presented here can aid in designing highly efficient magnetically recoverable catalysts for which both magnetite and rare earth dopants are common materials.
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