Department of Physical Chemistry, Fritz-Haber Institute of the Max-Planck Society , Faradayweg 4-6, 14195 Berlin, Germany.
J Am Chem Soc. 2015 Feb 11;137(5):1844-9. doi: 10.1021/ja510528x. Epub 2015 Jan 7.
The adsorption of porphyrin derivatives on a Au(111) surface was studied by scanning tunneling microscopy and spectroscopy at low temperatures in combination with density functional theory calculations. Different molecular appearances were found and could be assigned to the presence of single gold adatoms bonded by a coordination bond underneath the molecular monolayer, causing a characteristic change of the electronic structure of the molecules. Moreover, this interpretation could be confirmed by manipulation experiments of individual molecules on and off a single gold atom. This study provides a detailed understanding of the role of metal adatoms in surface-molecule bonding and anchoring and of the appearance of single molecules, and it should prove relevant for the imaging of related molecule-metal systems.
通过低温下的扫描隧道显微镜和光谱学与密度泛函理论计算的结合,研究了卟啉衍生物在 Au(111)表面的吸附。发现了不同的分子外观,并可以归因于单个金原子在分子单层下方通过配位键结合,导致分子电子结构的特征变化。此外,通过在单个金原子上操纵单个分子的实验可以证实这种解释。这项研究提供了对金属原子在表面-分子键合和锚固以及单个分子出现中的作用的详细理解,并且应该对相关分子-金属系统的成像具有重要意义。