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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Transition-Metal Phthalocyanines on Transition-Metal Oxides: Iron and Cobalt Phthalocyanine on Epitaxial MnO and TiOx Films
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Transition-Metal Phthalocyanines on Transition-Metal Oxides: Iron and Cobalt Phthalocyanine on Epitaxial MnO and TiOx Films

机译:过渡金属氧化物上的过渡金属酞菁:外延MnO和TiOx薄膜上的铁和钴酞菁

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摘要

The interaction at interfaces between transition-metal phthalocyanines and ultrathin transition-metal oxide films is studied by means of photoemission (PES) and X-ray absorption spectroscopy (XAS). Our results are compared to the recently investigated system CoPc on MnO. A flat-lying adsorption geometry of iron and cobalt phthalocyanines (Fe Pc and CoPc) on the different oxide substrates was observed: ultrathin epitaxially grown MnO films and' ultrathin TiOx films. A charge transfer from the MnO, in particular, to the Fe atom of the FePc molecule is observed by both PES and XAS. X-ray absorption spectra of the N K-edge of FePc do not hint at a nitrogen involvement in the interaction process. As a consequence of the charge transfer, a shift of the Fermi level of the semiconducting MnO films is observed, which is visible as a shift of MnO related core levels to lower binding energy. In contrast, CoPc and FePc deposited on TiOx show no hints for a charge transfer, although the flat-lying adsorption geometry allows in principle a maximum interaction between the pi-system and the substrate. Increased surface roughness (compared to MnO) and an oxygen termination of the surface of the TiOx films is considered to suppress a possible strong interaction between the organic molecules and the substrate.
机译:借助光发射(PES)和X射线吸收光谱(XAS)研究了过渡金属酞菁与超薄过渡金属氧化物膜之间的界面相互作用。我们的结果与最近研究的MnO系统CoPc进行了比较。观察到铁和钴酞菁(Fe Pc和CoPc)在不同氧化物基底上的平坦吸附几何形状:超薄外延生长的MnO膜和超薄TiOx膜。 PES和XAS均可观察到从MnO到FePc分子的Fe原子的电荷转移。 FePc的N K边缘的X射线吸收光谱并不暗示氮参与了相互作用过程。作为电荷转移的结果,观察到了半导体MnO薄膜的费米能级的变化,这是与MnO相关的核能级向较低结合能的变化可见的。相反,沉积在TiOx上的CoPc和FePc没有显示电荷转移的迹象,尽管平坦的吸附几何结构原则上允许pi系统与基材之间的相互作用最大。认为增加的表面粗糙度(与MnO相比)和TiOx膜表面的氧封端可以抑制有机分子与基材之间可能的强相互作用。

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