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Role of Spin-Orbital Splitting of 5f-Orbitals of Uranium Atom in the Formation of Its Chemical State

机译:旋转轨道分裂5F轨道的作用在其化学状态中形成的铀原子中的作用

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Chemical shifts (ChSh) of nine emission lines of the uranium L-series in uranium oxides UCW (x=0-1) with respect to UO2 were studied by using a precise crystal-diffraction X-ray spectrometer and the changes in energy of spin-orbital splitting (SOS) - Δδnl_± of inner nl-orbitals of the uranium atom were calculated from the data of ChSh of spin-doublet lines. For UO_(2+x) oxides, a linear decrease in Δδnl_± values with increasing degree of uranium oxidation was found. On the basis of the comparison of experimental Δδnl_± values with Dirac-Hartree-Fock atomic calculations, it was concluded that the observed variations in Δδnl_± values are due to the redistribution of electron and spin density between the 5f_(7/2)- and 5_f_(5/2)-levels of the fine structure of the uranium atom without changes in atomic charge state.
机译:通过使用精确的晶体 - 衍射X射线光谱仪和旋转能量的变化,研究了氧化铀L-系列铀L-系列铀L-系列的铀L-系列的铀L-系列的化学位移(CHSH)。从旋转双重线的CHSH的数据计算铀原子的内部NL-轨道的内部NL-轨道的硼分裂(SOS) - ΔΔNL_±。对于UO_(2 + x)氧化物,发现随着氧化铀氧化程度增加的ΔΔNL_±值的线性降低。基于具有Dirac-hartree-Fock原子计算的实验ΔΔnl_±值的比较,得出结论是,ΔΔnl_±值的观察变化是由于5f_(7/2)之间的电子和旋转密度的重新分配 - 和5_F_(5/2) - 铀原子的细结构没有变化原子充电状态。

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