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首页> 外文期刊>Journal of Electron Spectroscopy and Related Phenomena >Electronic states of titanyl phthalocyanine films on alkanethiolate self-assembled monolayers probed by two-photon photoemission
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Electronic states of titanyl phthalocyanine films on alkanethiolate self-assembled monolayers probed by two-photon photoemission

机译:双光子光发射探测链烷硫醇盐自组装单分子膜上钛氧基酞菁薄膜的电子态

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摘要

We studied both occupied and unoccupied states of titanyl phthalocyanine (TiOPc) films formed on an octanethiolate self-assembled monolayer (SAM) on an Au(1 1 1) surface fabricated in a wet chemical process using two-photon photoemission (2PPE) spectroscopy. A 1.90-nm-thick layer of TiOPc formed an unoccupied state at 2.9 eV above the Fermi level. This state was resonantly enhanced at 4.3-4.4 eV photon energy, suggesting that electrons were excited from the highest occupied molecular orbital of TiOPc. The 2PPE measurements of photon energy dependence and light polarization selectivity revealed that the unoccupied state originates from a charge transfer exciton not observed in organic thin films deposited on bare metallic substrates. The formation of a charge transfer exciton implies that the SAM strongly insulates the molecular monolayer.
机译:我们研究了在湿化学过程中使用双光子光电子发射(2PPE)光谱制造的Au(1 1 1)表面上的辛硫醇盐自组装单分子膜(SAM)上形成的钛氧基酞菁(TiOPc)膜的占据和未占据状态。厚度为1.90 nm的TiOPc层在费米能级以上2.9 eV处形成未占据状态。该状态在4.3-4.4 eV光子能量下共振增强,表明电子是从TiOPc的最高占据分子轨道中激发出来的。对光子能量依赖性和光偏振选择性的2PPE测量结果表明,未占据状态源自在裸露的金属基板上沉积的有机薄膜中未观察到的电荷转移激子。电荷转移激子的形成意味着SAM强烈隔离了分子单层。

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