基质(水族馆)
X射线光电子能谱
图层(电子)
扫描隧道显微镜
轨道能级差
吸附
分子
材料科学
光电发射光谱学
化学物理
光谱学
吸收(声学)
氧化物
化学
光电子学
纳米技术
物理化学
化学工程
有机化学
海洋学
量子力学
地质学
复合材料
工程类
冶金
物理
作者
P. Palmgren,Katharina Nilson,Shun Yu,Franz Hennies,T. Angot,Cajetan Ikenna Nlebedim,J.M. Layet,G. Le Lay,M. Göthelid
摘要
Phthalocyanines (Pcs) are capable of converting sunlight into electric energy when adsorbed on TiO2 in a dye-sensitized solar cell. Of special interest in this type of cell is the energy level alignment as well as how molecules adsorb on the surface as it determines the output of the cell. We investigated the FePc-TiO2(110) interface using scanning tunneling microscopy, synchrotron-based photoelectron spectroscopy, and X-ray absorption spectroscopy. We found a strong coupling of the first-layer FePc to the substrate resulting in an alteration of the electronic structure and charge transfer from the molecules. The FePc in the second layer is not severely affected by the bonding to the surface and has bulk-like electronic properties. The growth of FePc thin films proceeds in a layer plus island mode, and the molecular plane is parallel to the surface. The energy level alignment at the interface is determined, and the lowest unoccupied molecular orbital is found above the conduction band minimum of the oxide substrate.
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