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Pentacene on Au(111), Ag(111) and Cu(111): From physisorption to chemisorption

机译:在Au(111),Ag(111)和Cu(111)上并五苯:从物理吸附到化学吸附

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We measured the electronic and the molecular surface structure of pentacene deposited on the (1 1 1)-surfaces of coinage metals by means of ultraviolet photoelectron spectroscopy (UPS) and low-energy electron diffraction (LEED). Pentacene is almost flat-lying in monolayers on all three substrates and highly ordered on Au(1 1 1) and on Cu(1 1 1). On Ag(1 1 1), however, weak chemisorption leads to almost disordered monolayers, both, at room temperature and at 78 K. On Cu(1 1 1) pentacene is strongly chemisorbed and the lowest unoccupied molecular orbital becomes observable in UPS by a charge transfer from the substrate. On Ag(1 1 1) and Cu(1 1 1) multilayers adopt a tilted orientation and a high degree of crystallinity. On Au(1 1 1), most likely, also in multilayers the molecular short and long axes are parallel to the substrate, leading to a distinctively different electronic structure than on Ag(1 1 1) and Cu(1 1 1). Overall, it could be demonstrated that the substrate not only determines the geometric and electronic characteristics of molecular monolayer films but also plays a crucial role for multilayer film growth.
机译:我们通过紫外光电子能谱(UPS)和低能电子衍射(LEED)测量了并五苯金属沉积在造币金属(1 1 1)表面上的电子和分子表面结构。并五苯几乎在所有三个基材上均呈单层平铺,并在Au(1 1 1)和Cu(1 1 1)上高度有序。然而,在Ag(1 1 1)上,弱的化学吸附作用会导致在室温和78 K时几乎无序的单层。在Cu(1 1 1)上,并五苯被强烈地化学吸附,UPS可以观察到最低的未占据分子轨道来自基板的电荷转移。在Ag(1 1 1)和Cu(1 1 1)上,多层采用倾斜取向和高结晶度。在Au(1 1 1)上,最有可能的是,在多层结构中,分子的短轴和长轴也平行于基板,从而导致与Ag(1 1 1)和Cu(1 1 1)截然不同的电子结构。总的来说,可以证明基材不仅决定了分子单层膜的几何和电子特性,而且对多层膜的生长起着至关重要的作用。

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