学术文献库

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 $μ_B/$f.u. which is significantly larger than that of undoped magnetite (calculated to be 3.929 $μ_B/$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.