Nebraska Center for Materials and Nanoscience, Department of Physics and Astronomy, University of Nebraska-Lincoln, 68588-0299, USA.
J Phys Condens Matter. 2013 Jan 9;25(1):012001. doi: 10.1088/0953-8984/25/1/012001. Epub 2012 Nov 16.
The valence band occupied state electronic structure of Co(1-x)Fe(x)S(2) in the region of the Fe/Co 3d bands has been investigated using photoemission and spin-polarized photoemission. As measured by using spin-polarized ultraviolet photoemission, the surface Fermi level spin polarization of Co(1-x)Fe(x)S(2) thin films at 50 K, specifically at x = 0, 0.05, 0.10 and 0.15, was found to be much reduced compared to that of the bulk. The spin polarization nonetheless increases with Fe concentration. The resonant photoemission spectroscopy provides evidence that S bands have a strong resonance at the photon energy corresponding to the Co 2p core level, indicating strong hybridization between Co and S bands in Co(1-x)Fe(x)S(2) (at small x). Similar evidence exists for Fe hybridization with the S bands.
使用光电子能谱和自旋极化光电子能谱研究了 Co(1-x)Fe(x)S(2)在 Fe/Co 3d 能带区域中占据价带的电子结构。自旋极化紫外光电子能谱测量发现,Co(1-x)Fe(x)S(2)薄膜在 50 K 时的表面费米能级自旋极化,特别是在 x = 0、0.05、0.10 和 0.15 时,与体相相比大大降低。然而,自旋极化随 Fe 浓度的增加而增加。共振光电子能谱提供的证据表明,S 带在对应于 Co 2p 芯能级的光子能量处具有强烈的共振,表明 Co(1-x)Fe(x)S(2)中 Co 和 S 带之间存在强烈的杂化(在小 x 时)。Fe 与 S 带之间的杂化也存在类似的证据。