@inproceedings{SchmeisserMuellerHenkeletal., author = {Schmeißer, Dieter and M{\"u}ller, Sebastian and Henkel, Karsten and M{\"u}ller, Klaus and Wehner, Stefan}, title = {In-situ analysis of moving reaction fronts for the bistable CO oxidation reaction on noble metal catalyst}, series = {Extended Abstracts Book of First International Conference on Materials for Energy}, booktitle = {Extended Abstracts Book of First International Conference on Materials for Energy}, publisher = {Dechema e.V.}, address = {Frankfurt}, isbn = {978-3-89746-117-8}, pages = {S. 932}, abstract = {Experimental data on the reaction kinetics of catalytic processes are prerequisite for modeling of such reactions and their output. We investigate the CO oxidation on some noble metal catalysts, like Iridium(111) and Palladium(111) which is a bistable surface reaction. In a specific range of CO content in the feed gas islands of one or the other adsorbate nucleate and grow, which is recorded with photo electron emission microscopy (PEEM). During these transients the coverage on the surface changes from predominantly oxygen covered to predominantly CO covered resp. vice versa. But the resolution of PEEM and especially its unknown and nonlinear dependence of coverage of the two adsorbates (oxygen and CO) and image intensity make it impossible to extract the changes in coverage. On the other hand the reaction diffusion model based on the Langmuir-Hinshelwood-mechanism delivers the coverage of oxygen and carbon monoxide. The shapeand wall velocity of those islands has been connected perfectly to each other [CPL 423 (2006) 39], but not the absolute coverage and their variation during the reaction. Since the domain wall velocity is small on Iridium(111), this has opened the possibility for a detailed analysis of the changing coverage inside this domain wallutilizing synchrotron radiation and photo electron spectroscopy at BESSY II. The coverage profile of oxygen and CO inside a moving domain wall was measured for both cases using XPS spectra at O1s, C1s and the valence band during thereaction. Comparison with the reaction-diffusion-model and other catalytic surfaces, like Palladium(111) are done.}, language = {en} } @inproceedings{MuellerSchoelzel, author = {M{\"u}ller, Sebastian and Sch{\"o}lzel, Mario}, title = {Combining Hardware and Software Based Self Repair Methods for Statically Scheduled Data Paths}, series = {2010 IEEE 25th International Symposium on Defect and Fault Tolerance in VLSI Systems (DFT 2010), Kyoto, Japan, 6 - 8 October 2010}, booktitle = {2010 IEEE 25th International Symposium on Defect and Fault Tolerance in VLSI Systems (DFT 2010), Kyoto, Japan, 6 - 8 October 2010}, publisher = {IEEE}, address = {Piscataway, NJ}, isbn = {978-1-424-48447-8}, pages = {90 -- 98}, language = {en} } @phdthesis{Mueller, author = {M{\"u}ller, Sebastian}, title = {Synchrotron radiation spectroscopy studies of the initial interaction of Chromium and Cobalt with the surface of Titanium Dioxide}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:co1-opus-18914}, abstract = {In the framework of this thesis, synchrotron radiation based spectroscopy methods are applied to study the electronic structures of stoichiometric Rutile single crystals and TiO2 thin films, and the initial stage of chromium and cobalt growth on TiO2 thin films. Resonance photoemission spectroscopy of clean TiO2 at the Ti L2,3 edges led to Auger-like features, with kinetic energies corresponding to the Ti L2,3M4,5M4,5 Auger decay channels. The presence of these features is assigned to origin from a d2L2 charge transfer state. The resonance of the Ti L3M2,3V Auger channel at the Ti L2 edge is assigned to the L2L3V Coster-Kronig Auger, followed by the normal L3M2,3V Auger decay. The deposition of chromium on the TiO2 film causes a strong interaction at the interface, in which TiO(2-x) is formed together with chromium in the Cr 3+ state. Besides the oxidized component, contribution of metallic chromium is found as well. In the ultra-low coverage regime, post-deposition oxidation is observed, in which metallic chromium is oxidized to Cr2O3, accompanied by re-oxidation of the substrate to TiO2. The interface reaction is also reflected by the appearance of two defect states in the band gap. Resonant photo-emission at the Cr 2p and Ti 2p edges shows well distinguishable Cr 3d respectively Ti 3d character of the respective states. Indications for self-cleaning properties are found by removal of surface carbon during storage in UHV, but the influence of chromium on these properties is not studied in detail. The interaction between cobalt and TiO2 is weaker than that of chromium and TiO2. Nevertheless, an interface reaction is found, in which some of the deposited cobalt is oxidized, while the oxide support is partly reduced. The particular oxidation state of Cobalt is identified by means of multiplet calculation including charge transfer and crystal field effects. The calculated XAS and XPS spectra indicate Co 2+ in a tetrahedral coordination with four oxygen atoms. The metallic component of cobalt gives rise to a broad resonance in the valence band down to -20 eV, with a pronounced satellite feature that reflects the oxidized component.}, language = {en} } @inproceedings{MuellerSchmeisser, author = {M{\"u}ller, Sebastian and Schmeißer, Dieter}, title = {Synchrotron radiation spectroscopy studies of the initial interaction between cobalt and titanium dioxide}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft, Reihe 6, Bd. 45}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft, Reihe 6, Bd. 45}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, issn = {0420-0195}, pages = {S. 652}, abstract = {Small metallic particles deposited on oxide surfaces can serve as heterogeneous catalysts, as for example TiO2 supported cobalt is a known Fischer-Tropsch-Catalyst. The goal of the presented studies is to investigate the interaction between cobalt and TiO2 in the initial step of growth by synchrotron radiation based spectroscopy. PES studies of TiO2 supported cobalt show a reduction of the oxide support, accompanied by an oxidation of the deposited material. The oxidation is not complete, but metallic cobalt is found already in the very first step of growth. Uniform decrease of both substrate PES lines indicate very weak interaction between overlayer and TiO2. An atomic multiplet calculation including charge transfer and crystal field effects is applied to simulate the experimental Co 2p XAS and XPS spectra of the oxidized component. The results allow the identification of the local coordination as well as the identification of the oxidation state of cobalt.}, language = {en} }