Publikationsserver der Universitätsbibliothek Marburg

Titel:Investigations of Metal/Organic Interfaces and Metalation Reactions of Organic Semiconductors
Autor:Kachel, Stefan Renato
Weitere Beteiligte: Gottfried, J. Michael (Prof. Dr.)
URN: urn:nbn:de:hebis:04-z2020-06603
DDC:540 Chemie
Titel (trans.):Untersuchungen an Metall/Organischen Grenzflächen und Metallierungsreaktionen Organischer Halbleiter


HAXPES, LEED, Metal/Organic, Metall/Organik, Perfluoropentacene, Naphtha, Anorganik/Organik, Halbleiter, TPD, AES, Pentacene, Tetraphenylporphyrin, Semiconductor, Grenzfläche, Inorganic/Organic, LEED, Tetraphenylporphyrin, Interphase, HAXPES, TPD, Azulen, Pentacen, Interface, Perfluoropentacen, AES

Modern electronic devices are increasingly based on organic semiconductors. The performance of such devices crucially depends on the properties of the interface between the organic semiconductors and the metal contacts. Understanding the influence of the topology of the organic semiconductor’s conjugated pi-electron system on the interface interaction could greatly improve the device’s performance. Furthermore, the knowledge about reactions of heteroatomic organic semiconductors with metal atoms during electrode fabrication may lead to enhanced lifetimes of such devices. This cumulative dissertation comprises several publications and a number of so far unpublished results, addressing metal/organic interface interactions and metalation reactions of heteroatomic organic semiconductors. The properties of the interfaces are tailored by investigating the alternant aromatic molecules naphthalene and pyrene as well as the nonalternant aromatic molecules azulene and azupyrene on different metallic singlecrystal surfaces. Investigations by means of temperature-programmed desorption reveal stronger desorption energies for the non-alternant molecules on both Ag(111) and Cu(111). The biggest difference is observed on Cu(111), on which azulene and azupyrene are chemisorbed, whereas naphthalene and pyrene are physisorbed. The enhanced interface interaction of the non-alternant molecules is associated with the formation of surface dipoles that lead to stronger intermolecular repulsion between the adsorbed molecules. These results are supported by additional surface science methods, such as X-ray photoelectron spectroscopy or near-edge X-ray absorption fine structure spectroscopy, as well as density functional theory calculations conducted by group members and external collaboration partners. Detailed quantitative analysis of temperature-programmed desorption data of benzene on Cu(111) and Ag(111) yields experimental desorption energies that can be used as a benchmark for theoretical adsorption energies derived by density functional theory calculations. The interactions of metal/organic interfaces are compared with organic/inorganic interfaces in the case of pentacene and its fluorinated derivative perfluoropentacene on Au(111) as well as on bulk and two-dimensional MoS2 in a collaboration project. Organic semiconductors often interact weakly with inorganic surfaces, e.g., the thermal desorption of the first molecular layer is indistinguishable from multilayer desorption. No monolayer desorption peaks are observed as is mostly the case on metal surfaces. However, monolayer desorption of pentacene and perfluoropentacene on MoS2 occurs at significantly higher temperatures than the multilayer desorption. Detailed analysis reveals that the monolayers of both molecules are entropically stabilized. Codeposition of both molecules results in strong attractive intermolecular interactions on MoS2, while these interactions are weaker on Au(111). Metalation reactions of organic semiconductors with metal atoms, e.g., Co on tetraphenylporphyrin and Ca on alpha-sexithiophene, during interface preparation were investigated by means of hard X-ray photoelectron spectroscopy and temperature-programmed desorption mass spectrometry. The thickness of the reaction zone is changed by variation of experimental properties during interface formation. It is found that only the sample temperature during metal atom deposition and the metal atom flux in the case of Ca have an impact on the reaction depth, which is usually limited to few nanometers. In contrast to Co and Ca, Li atoms readily diffuse into the organic bulk and react with tetraphenylporphyrin over several tens of nanometers, forming dilithium tetraphenylporphyrin or monolithium monohydrogen tetraphenylporphyrin depending on the deposited Li amount. Furthermore, the transmetalation reaction of lead(II) tetraphenylporphyrin with Cu atoms on the Cu(111) surface was proven by temperature-programmed desorption. In addition, the Ullmann coupling reaction of bromo- and iodobenzene on Cu(111) was examined. While bromobenzene molecules desorb intact from the Cu(111) surface, iodobenzene molecules dissociate into iodine atoms and phenyl radicals. The latter form biphenyl that desorbs in three distinct desorption peaks at different temperatures. In a collaborative project, the oxidation state and electronic structure of Pb atoms in the newly synthesized Pb3F8 were studied by hard X-ray photoelectron spectroscopy and near-edge X-ray absorption fine structure spectroscopy giving evidence for the presence of Pb(II) and Pb(IV) species. The experimental results are complemented by constructional work to improve the temperatureprogrammed desorption setup. Moreover, two Igor Pro 8 scripts were written to quickly import data from different experimental setups and speed up the data treatment.

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