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钾插层 H2Pc 薄膜:碱诱导的电子和几何结构修饰。

Potassium-intercalated H2Pc films: alkali-induced electronic and geometrical modifications.

机构信息

Department of Physics, Uppsala University, Box 530, S-751 21 Uppsala, Sweden.

出版信息

J Chem Phys. 2012 Jul 28;137(4):044708. doi: 10.1063/1.4738755.

Abstract

X-ray spectroscopy studies of potassium intercalated metal-free phthalocyanine multilayers adsorbed on Al(110) have been undertaken. Photoelectron spectroscopy measurements show the presence of several charge states of the molecules upon K intercalation, due to a charge transfer from the alkali. In addition, the comparison of valence band photoemission spectra with the density functional theory calculations of the density of states of the H(2)Pc(-) anion indicates a filling of the formerly lowest unoccupied molecular orbital by charge transfer from the alkali. This is further confirmed by x-ray absorption spectroscopy (XAS) studies, which show a decreased density of unoccupied states. XAS measurements in different experimental geometries reveal that the molecules in the pristine film are standing upright on the surface or are only slightly tilted away from the surface normal but upon K intercalation, the molecular orientation is changed in that the tilt angle of the molecules increases.

摘要

我们对钾嵌入的无金属酞菁多分子层在 Al(110)上吸附的 X 射线能谱进行了研究。光电子能谱测量结果表明,由于碱金属的电荷转移,在钾嵌入后,分子存在几种电荷态。此外,价带光电子能谱与 H(2)Pc(-)阴离子态密度的密度泛函理论计算的比较表明,通过碱金属的电荷转移填充了以前的最低未占据分子轨道。X 射线吸收光谱(XAS)研究进一步证实了这一点,其表明未占据态密度降低。不同实验几何形状的 XAS 测量表明,原始薄膜中的分子垂直于表面或以稍微偏离表面法线的方式站立,但在钾嵌入后,分子取向发生变化,分子的倾斜角增加。

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