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van der Waals Interaction Activated Strong ElectronicCoupling at the Interface between Chloro Boron-Subphthalocyanine andCu(111)

机译:范德华相互作用法激活强电子氯硼-亚酞菁与氯之间的界面偶联铜(111)

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摘要

In this article, we investigate the interface between shuttlecock-shaped chloro boron-subphthalocyanine molecules and the Cu(111) surface. We highlight how molecular planarization induced by van der Waals forces can fundamentally alter the interface properties and how it can enable a particularly strong hybridization between molecular and metal states. In our simulations, we start from a situation in which we disregard van der Waals forces and then introduce them gradually by rescaling the interaction parameter, thereby “pulling” the molecule toward the surface. This reveals two adsorption regimes with significantly different adsorption distances, molecular conformations, and adsorbate-induced changes of the work function. Notably, the above-mentioned massive hybridization of electronic states, also observed in photoelectron spectroscopy, is obtained solely for one of the regimes. We show that this regime is accessible only as a consequence of the planarization of the molecular backbone resulting from the van der Waals attraction between the molecule and the surface. The results of this study indicatethat for certain metal–molecule combinations unusually stronginterfacial electronic interactions can be triggered by van der Waalsforces creating a situation that differs from the usually describedcases of physisorptive and chemisorptive interactions.
机译:在本文中,我们研究了shuttle球形的氯硼-亚酞菁分子与Cu(111)表面之间的界面。我们重点介绍了范德华力引起的分子平面化如何从根本上改变界面性质,以及如何实现分子态与金属态之间特别强的杂交。在我们的模拟中,我们从不考虑范德华力的情况开始,然后通过重新调整相互作用参数逐步引入它们,从而将分子“拉”向表面。这揭示了两种吸附方式,它们的吸附距离,分子构象和被吸附物诱导的功函变化都显着不同。值得注意的是,上述电子态的大规模杂交,也可以在光电子光谱学中观察到,仅针对其中一种方案即可获得。我们表明,仅由于分子主链的平面化导致分子与表面之间的范德华力吸引,该机制才可访问。这项研究的结果表明对于某些金属-分子组合,异常强范德华斯可以触发界面电子相互作用造成与通常描述不同的情况物理吸附和化学吸附相互作用的案例。

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