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弱相互作用基底上的异分子双层:铜-十六氟酞菁的物理吸附键合与分子畸变

Heteromolecular Bilayers on a Weakly Interacting Substrate: Physisorptive Bonding and Molecular Distortions of Copper-Hexadecafluorophthalocyanine.

作者信息

Wang Qi, Franco-Cañellas Antoni, Yang Jiacheng, Hausch Julian, Struzek Samuel, Chen Mengting, Thakur Pardeep Kumar, Gerlach Alexander, Duhm Steffen, Schreiber Frank

机构信息

Institut für Angewandte Physik, Universität Tübingen, 72076 Tübingen, Germany.

Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices and Joint International Research Laboratory of Carbon-Based Functional Materials and Devices, Soochow University, Suzhou 215123, People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2020 Mar 25;12(12):14542-14551. doi: 10.1021/acsami.9b22812. Epub 2020 Mar 11.

Abstract

Heteromolecular bilayers of π-conjugated organic molecules on metals, considered as model systems for more complex thin film heterostructures, are investigated with respect to their structural and electronic properties. By exploring the influence of the organic-metal interaction strength in bilayer systems, we determine the molecular arrangement in the physisorptive regime for copper-hexadecafluorophthalocyanine (FCuPc) on Au(111) with intermediate layers of 5,7,12,14-pentacenetetrone and perylene-3,4,9,10-tetracarboxylic diimide. Using the X-ray standing wave technique to distinguish the different molecular layers, we show that these two bilayers are ordered following their deposition sequence. Surprisingly, FCuPc as the second layer within the heterostructures exhibits an inverted intramolecular distortion compared to its monolayer structure.

摘要

金属上π共轭有机分子的异质分子双层被视为更复杂薄膜异质结构的模型系统,对其结构和电子性质进行了研究。通过探索双层系统中有机-金属相互作用强度的影响,我们确定了在Au(111)上铜十六氟酞菁(FCuPc)与5,7,12,14-并五苯四酮和苝-3,4,9,10-四羧酸二亚胺中间层形成的物理吸附体系中的分子排列。利用X射线驻波技术区分不同的分子层,我们发现这两种双层按照其沉积顺序排列。令人惊讶的是,与单层结构相比,作为异质结构中第二层的FCuPc表现出分子内扭曲反转。

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