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银(111)表面的金属/酞菁混合界面态

Metal/Phthalocyanine Hybrid Interface States on Ag(111).

作者信息

Caplins Benjamin W, Suich David E, Shearer Alex J, Harris Charles B

机构信息

Department of Chemistry, University of California at Berkeley, Berkeley, California 94720, United States.

Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.

出版信息

J Phys Chem Lett. 2014 May 15;5(10):1679-84. doi: 10.1021/jz500571z. Epub 2014 Apr 28.

Abstract

A phthalocyanine/Ag(111) interface state is observed for the first time using time- and angle-resolved two-photon photoemission. For monolayer films of metal-free (H2Pc) and iron phthalocyanine (FePc) on Ag(111), the state exists 0.23 ± 0.03 and 0.31 ± 0.03 eV above the Fermi level, respectively. Angle-resolved spectra show the state to be highly dispersive with an effective mass of 0.50 ± 0.15 me for H2Pc and 0.67 ± 0.14 me for FePc. Density functional theory calculations on the H2Pc/Ag(111) surface allow us to characterize this state as being a hybrid state resulting from the interaction between the unoccupied molecular states of the phthalocyanine ligand and the Shockley surface state present on the bare Ag(111) surface. This work, when taken together with the extensive literature on the 3,4,9,10-perylene tetracarboxylic dianhydride/Ag interface state, provides compelling evidence that the hybridization of metal surface states with molecular electronic states is a general phenomenon.

摘要

利用时间分辨和角分辨双光子光电子能谱首次观测到酞菁/Ag(111)界面态。对于Ag(111)上的无金属酞菁(H2Pc)和铁酞菁(FePc)单层膜,该态分别存在于费米能级之上0.23±0.03和0.31±0.03电子伏特处。角分辨光谱表明,对于H2Pc,该态具有高度色散性,有效质量为0.50±0.15me;对于FePc,有效质量为0.67±0.14me。对H2Pc/Ag(111)表面进行的密度泛函理论计算使我们能够将该态表征为酞菁配体的未占据分子态与裸露Ag(111)表面上存在的肖克利表面态之间相互作用产生的杂化态。这项工作与关于3,4,9,10-苝四羧酸二酐/Ag界面态的大量文献一起,提供了令人信服的证据,表明金属表面态与分子电子态的杂化是一种普遍现象。

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