Sättele Marie S, Windischbacher Andreas, Egger Larissa, Haags Anja, Hurdax Philipp, Kirschner Hans, Gottwald Alexander, Richter Mathias, Bocquet François C, Soubatch Serguei, Tautz F Stefan, Bettinger Holger F, Peisert Heiko, Chassé Thomas, Ramsey Michael G, Puschnig Peter, Koller Georg
Institute of Physical and Theoretical Chemistry, University of Tübingen, Auf der Morgenstelle 18, 72076 Tübingen, Germany.
Institute of Organic Chemistry, University of Tübingen, Auf der Morgenstelle 18, 72076 Tübingen, Germany.
J Phys Chem C Nanomater Interfaces. 2021 Feb 11;125(5):2918-2925. doi: 10.1021/acs.jpcc.0c09062. Epub 2021 Feb 3.
Longer acenes such as heptacene are promising candidates for optoelectronic applications but are unstable in their bulk structure as they tend to dimerize. This makes the growth of well-defined monolayers and films problematic. In this article, we report the successful preparation of a highly oriented monolayer of heptacene on Ag(110) by thermal cycloreversion of diheptacenes. In a combined effort of angle-resolved photoemission spectroscopy and density functional theory (DFT) calculations, we characterize the electronic and structural properties of the molecule on the surface in detail. Our investigations allow us to unambiguously confirm the successful fabrication of a highly oriented complete monolayer of heptacene and to describe its electronic structure. By comparing experimental momentum maps of photoemission from frontier orbitals of heptacene and pentacene, we shed light on differences between these two acenes regarding their molecular orientation and energy-level alignment on the metal surfaces.
诸如七并苯之类的更长并苯是光电子应用的有前途的候选材料,但由于它们倾向于二聚化,其本体结构不稳定。这使得制备结构明确的单层和薄膜存在问题。在本文中,我们报告了通过二聚七并苯的热环化逆反应在Ag(110)上成功制备了高度取向的七并苯单层。通过角分辨光电子能谱和密度泛函理论(DFT)计算相结合的方法,我们详细表征了表面上该分子的电子和结构性质。我们的研究使我们能够明确证实成功制备了高度取向的完整七并苯单层,并描述其电子结构。通过比较七并苯和并五苯前沿轨道光发射的实验动量图,我们揭示了这两种并苯在金属表面上的分子取向和能级排列方面的差异。