Interface Properties of CoPc on Nanographene-Covered Au(111) and the Influence of Annealing.

Organic bilayer systems and heterostructures are of enormous importance for optoelectronic devices. We study interface properties and the structural ordering of cobalt phthalocyanine (CoPc) on a highly ordered monolayer hexa-peri-hexabenzocoronene (HBC), grown on Au(111), using photoemission, X-ray absorption, scanning tunneling microscopy, and low-energy electron diffraction. A charge transfer between CoPc and the gold substrate is almost completely prevented by the HBC intermediate layer. We show that HBC acts as a template for the initial growth of CoPc molecules. After annealing to 630 K, a molecular exchange takes place, resulting in a coexistence of domains of both CoPc and HBC molecules on the surface.

Visualization of the Borazine Core of B3N3-Doped Nanographene by STM.

Electronic interface properties and the initial growth of hexa-peri-hexabenzocoronene with a borazine core (BN-HBC) on Au(111) have been studied by using X-ray photoelectron spectroscopy (XPS), low-energy electron diffraction (LEED), and scanning tunneling microscopy (STM). A weak, but non-negligible, interaction between BN-HBC and Au(111) was found at the interface. Both hexa-peri-hexabenzocoronene (HBC) and BN-HBC molecules form well-defined monolayers. The different contrast in STM images of HBC and BN-HBC at different tunneling voltages with submolecular resolution can be ascribed to differences in the local density of states (LDOS). At positive and negative tunneling voltages, STM images reproduce the distribution of the highest occupied and lowest unoccupied molecular orbitals (HOMO and LUMO) as determined by density functional theory (DFT) calculations very well.

FePc and FePcF16 on Rutile TiO2(110) and (100): Influence of the Substrate Preparation on the Interaction Strength.

Interface properties of iron phthalocyanine (FePc) and perfluorinated iron phthalocyanine (FePcF16) on rutile TiO2(100) and TiO2(110) surfaces were studied using X-ray photoemission spectroscopy (XPS), X-ray absorption spectroscopy (XAS), and low-energy electron diffraction (LEED). It is demonstrated that the interaction strength at the interfaces is considerably affected by the detailed preparation procedure. Weak interactions were observed for all studied interfaces between FePc or FePcF16 and rutile, as long as the substrate was exposed to oxygen during the annealing steps of the preparation procedure. The absence of oxygen in the last annealing step only had almost no influence on interface properties. In contrast, repeated substrate cleaning cycles performed in the absence of oxygen resulted in a more reactive, defect-rich substrate surface. On such reactive surfaces, stronger interactions were observed, including the cleavage of some C-F bonds of FePcF16.