@misc{StaedterMuellerRachowetal., author = {St{\"a}dter, Matthias and M{\"u}ller, Klaus and Rachow, Fabian and Richter, Matthias and Schmeißer, Dieter}, title = {Ambient pressure thermal desorption spectroscopy (AP-TDS) of NiO/SiO2 catalysts}, series = {Environmental Earth Sciences}, volume = {70}, journal = {Environmental Earth Sciences}, number = {8}, issn = {1866-6280}, doi = {10.1007/s12665-013-2835-8}, pages = {3779 -- 3784}, abstract = {The Sabatier reaction is a key process in the "power-to-gas" application which is considered to con-tribute to future chemical energy storage systems. In this contribution we focus on the catalytic active sites of a NiO catalyst supported on SiO2(NiO/SiO2) which is commonly used in the Sabatier reaction. A novel technique for the characterization of the active sites is presented and dis-cussed using thermal desorption spectroscopy at ambient pressure. This analytical tool is operated under reaction conditions and allows element specific measurements during the catalytic process of CO2 reforming towards methane. Beside the desorption experiments, XPS and XAS measurements of pristine and catalytically used samples are performed to determine the influence of the Sabatier reaction conditions on the surface structure of the catalyst.}, language = {en} } @misc{FriedrichHenkelRichteretal., author = {Friedrich, Daniel and Henkel, Karsten and Richter, Matthias and Schmeißer, Dieter}, title = {Fullerenol as probed by Synchrotron X-Ray Photoemission and Absorption Spectroscopy}, language = {en} } @misc{MuellerRichterPhilipetal., author = {M{\"u}ller, Klaus and Richter, Matthias and Philip, Shine and Kunst, Manuel and Schmeißer, Dieter}, title = {Excited states in P3HT and P3HT/PCBM blends}, series = {BioNanoScience}, volume = {2}, journal = {BioNanoScience}, number = {1}, issn = {2191-1630}, pages = {42 -- 51}, language = {en} } @misc{RichterFriedrichSchmeisser, author = {Richter, Matthias and Friedrich, Daniel and Schmeißer, Dieter}, title = {Valence and Conduction band states of PCBM as probed by photoelectron spectroscopy at resonant excitation}, series = {BioNanoScience}, volume = {2}, journal = {BioNanoScience}, number = {1}, issn = {2191-1630}, pages = {59 -- 65}, language = {en} } @misc{MuellerRichterFriedrichetal., author = {M{\"u}ller, Klaus and Richter, Matthias and Friedrich, Daniel and Paloumpa, Ioanna and Kramm, Ulrike Ingrid and Schmeißer, Dieter}, title = {Spectroscopic characterization of Cobalt-Phthalocyanine electrocatalysts for fuel cell applications}, series = {Solid State Ionics}, journal = {Solid State Ionics}, number = {216}, issn = {1872-7689}, doi = {10.1016/j.ssi.2011.12.013}, pages = {78 -- 82}, abstract = {For polymer-electrolyte-membrane fuel cells (PEM-FC), platinumcatalysts on carbon based substrates are state of the art, due to high electrochemical activity and chemical stability in acid electrolytes. High costs of platinum force investigations of alternative catalysts. With respect to the oxygen reduction reaction, possible candidates are transition metal (TM) complexes like TM-porphyrines or TM-phthalocyanines. Pyrolysis on carbon based substrates improves the catalytic activity. Highest activities were found for Fe or Co as transition metal centers. We present results of the pyrolysis of Co-phthalocyanine (CoPc) on carbon black. Besides an investigation of morphology by scanning electron microscopy (SEM) and chemical composition by energy dispersive X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy (XPS) during pyrolysis, we present a near edge X-ray absorption fine structure (NEXAFS) study of the chemical composition for the related annealing steps. This investigation is accompanied by an electrochemical characterization of the catalytic activity and selectivity. The XPS and NEXAFS data indicate a decomposition of the CoN4(chelate-) complex during pyrolysis. The N1s data for 800 °C show graphite-like, formally pyrrolic and pyridinic like features, without any significant contri-bution of Co. The Co2p data for both, XPS and NEXAFS are dominated by CoO/Co2O3. It can be concluded that during the pyrolysis cobalt particles are formed by the disintegration of CoN4-centers, after pyrolysis these par-ticles become oxidized upon contact with air.}, language = {en} } @misc{FischerRohrbeckWehneretal., author = {Fischer, Christian B. and Rohrbeck, Magdalena and Wehner, Stefan and Richter, Matthias and Schmeißer, Dieter}, title = {Interlayer formation of diamond-like carbon coatings on industrial polyethylene: Thickness dependent surface characterization by SEM, AFM and NEXAFS}, series = {Applied Surface Science}, journal = {Applied Surface Science}, number = {271}, issn = {0169-4332}, doi = {10.1016/j.apsusc.2013.01.210}, pages = {381 -- 389}, abstract = {The coating of materials with diamond-like carbon (DLC) is a very common way to change and improve their basic characteristics. Although DLC is used on several substrates, the chemical and physical properties throughout the coating process on plastics are yet sparsely investigated. Two types of protective coatings one sp3-enriched (robust, r-type) and one with more sp2-centers (flexible, f-type) have been realized on polyethylene by PECVD deposition. SEM and AFM analysis of coated samples of DLC types revealed diverse surface topographies on different scales and images appeared even differently smoothed by the carbonaceous deposits. Grains of both DLC types are platelet-shaped and nearly double in size for the robust type indicating fundamental differences in the epitaxial DLC growth. NEXAFS spectroscopy showed significant details of carbon centers in chemically different neighborhood displaying a characteristic fingerprint behavior. Comparison of deposition models revealed a mechanism of interlayer formation which is discussed in detail. Interlayer formation is clearly the appropriate explanation of the process for the current carbon deposition between these two unequal materials. An improved understanding of hard DLC and soft polyethylene assembly is given in the presented work.}, language = {en} } @misc{RichterPaloumpaFriedrichetal., author = {Richter, Matthias and Paloumpa, Ioanna and Friedrich, Daniel and Schmeißer, Dieter}, title = {Multiple Auger Decay At Resonant Photo-Excitation In Carbon Thin Films}, series = {ECS Transactions}, volume = {50}, journal = {ECS Transactions}, number = {20}, doi = {10.1149/05020.0009ecst}, pages = {9 -- 21}, abstract = {We use resonant photoemission at the C1s edge to study the electronic structure of HOPG, graphene flakes and monolayer graphene. We find remarkable differences in the profile of the Auger decay channels, which we attribute to an additional multiple-Auger with a three-hole final state. A prerequisite for the appearance of this decay mechanism is the existence of localized excitonic states, which cause the appearance of the multiple Auger decay. We use those effects to identify the existence and the quantity of such defect states within the π*-band regime in carbon thin films, because the intensity of the three-hole Auger decay is varying with the defect density of the carbon films. We find that the appearance of the multiple Auger decay is different for multilayer and monolayer graphene. In particular the interaction of impurities leads to broadening of the C1s core levels. The three-hole Auger decay spectroscopy is a new method to detect such contaminations with a high sensitivity.}, language = {en} } @misc{RichterSchmeisser, author = {Richter, Matthias and Schmeißer, Dieter}, title = {Spin states in Co-PI catalysts}, series = {Applied Physics Letters}, journal = {Applied Physics Letters}, number = {102}, issn = {1077-3118}, doi = {10.1063/1.4811748}, pages = {253904-1 -- 253904-4}, abstract = {Cobalt based oxygen evolution catalysts (Co-PI, PI=electrodeposited from pH 7 phosphate) are studied by resonant photoemission spectroscopy at the Co L3 and O1s edge. For the individual Co3d states, we determine their configuration, their spin, and their energy level relative to the Fermi energy. We identify the Co divalent high spin state and the trivalent low spin state. In addition, we also find the corresponding oxygen-to-metal charge transfer states. We attribute the trivalent charge transfer state to be the active state for the oxygen evolution reaction.}, language = {en} } @misc{RichterSchmeisser, author = {Richter, Matthias and Schmeißer, Dieter}, title = {The Co2p Oxidation State In Co-PI Catalysts}, series = {ECS Transactions}, volume = {50}, journal = {ECS Transactions}, number = {49}, doi = {10.1149/05049.0113ecst}, pages = {113 -- 126}, abstract = {The electronic structure of Cobalt based catalysts used for photocatalytic water splitting in solar cells is analyzed using synchrotron radiation photoelectron spectroscopy. The catalyst films are prepared by electrochemical deposition. We employ a X-ray photoelectron spectroscopy study to analyze the Co2p and O1s core levels,absorption edges and valence bands. We discuss our resonant data in terms of the partial density of states of the valence and conduction band. We find a difference in the Co oxidation state as a function of film thickness (deposited charge). From the relative amount of Co, O, K and P we favor the molecular cobaltate cluster-like structure as the structural motif of the Co-PI catalyst.}, language = {en} } @misc{RichterStarkeSchmeisser, author = {Richter, Matthias and Starke, Ulrich and Schmeißer, Dieter}, title = {Multiple Auger processes in Graphene}, series = {Journal of Electron Spectroscopy and Related Phenomena}, journal = {Journal of Electron Spectroscopy and Related Phenomena}, number = {Vol. 192}, issn = {0368-2048}, doi = {10.1016/j.elspec.2013.12.009}, pages = {1 -- 6}, abstract = {Resonant Auger decay processes have been studied by resonant photoemission spectroscopy (resPES) and X-ray absorption spectroscopy (XAS) in Graphene systems. The pi*-resonance is used to identify the degree of localization of the lowest pi*-orbitals in the conduction band. Localization and lifetime of the photo-excited intermediate state cause the formation of multiple Auger processes. For the Graphene systems we identify two novel Auger decay combinations with a four hole final state: the (S+S) and the(S+S)* decay. We demonstrate that these processes are sensitive for interlayer coupling and interactions with the metallic free electrons of the substrate.}, language = {en} } @misc{RichterFriedrichSchmeisser, author = {Richter, Matthias and Friedrich, Daniel and Schmeißer, Dieter}, title = {Interlayer-exciton mediated three-hole-Auger-decay in the pi-band of highly oriented pyrolytic graphite}, series = {Physica E}, volume = {Vol. 56}, journal = {Physica E}, issn = {1386-9477}, doi = {10.1016/j.physe.2013.01.015}, pages = {441 -- 446}, abstract = {Resonant photoemission spectroscopy(resPES) is used to probe the occupied pi- and unoccupied pi*-bands of carbon thin films with particular focus on the Auger decay. Highly Oriented Pyrolytic Graphite (HOPG) is studied at the C1s edge. We find strong resonant features at 285.5 eV and 292 eV in the resPES diagram. The normal two-hole Auger decay proceeds under constant kinetic energy (451)only in the sigma*-region. In the pi*-region, however, it proceeds under 67.5° in terms of a Ebind(w) diagram. We attribute this to a multiple Auger decay with a net three hole final state. For this novel decay process we propose a model.We discuss the long lifetime of the first resonant excitation and conclude that it arises from the strong excitonic character of the first resonant state. We use HOPG as a reference system and suggest that this novel process is a tool to identify interlayer-substrate interaction of the carbon layers involved.}, language = {en} } @misc{HaeberleRichterGalazkaetal., author = {Haeberle, J{\"o}rg and Richter, Matthias and Galazka, Zbigniew and Janowitz, Christoph and Schmeißer, Dieter}, title = {Resonant Photoemission at the O1s threshold to characterize In2O3 single crystals}, series = {Thin Solid Films}, volume = {2014}, journal = {Thin Solid Films}, number = {555}, issn = {0040-6090}, doi = {10.1016/j.tsf.2013.03.036}, pages = {53 -- 56}, abstract = {We report on spectroscopic investigations on In2O3 single crystals. We focus on the detailed analysis of the O1s resonance profile by resonant photoelectron spectroscopy. We analyze the electronic structure and assign the O2p to build the valence band and both, O2p and In5s5p states to contribute to the conduction band (CB). We determine the partial density of states for the valence and CBs and find a strong hybridization of O2p and In5s states. This is deduced from constant final state spectra on the O-KLL-Auger over the O K-edge and In M4,5-edge and a comparison to the corresponding X-ray absorption spectroscopy data.We also identify several types of defects. A broad band of oxygen derived defects is identified that extends throughout the gap. These are attributed to small polarons which cause an anti-resonance in the valence states around the O1s threshold. In addition, a separate Auger decay at resonance indicates the existence of localized charge transfer states which involves localized In5s5p states.}, language = {en} } @misc{SchmeisserHaeberleRichteretal., author = {Schmeißer, Dieter and Haeberle, J{\"o}rg and Richter, Matthias and Brazda, Petr}, title = {Spin State and Satellite Structures of ε-Fe₂O₃ as determined by Resonant Photoelectron Spectroscopy}, series = {Nuclear Instruments and Methods in Physics Research B}, volume = {2015}, journal = {Nuclear Instruments and Methods in Physics Research B}, number = {364}, issn = {0168-583X}, doi = {10.1016/j.nimb.2015.08.062}, pages = {127 -- 131}, abstract = {We use resonant photoelectron spectroscopy at the Fe2p and the O1s absorption edges to report on spectroscopic investigation of Fe-oxides nanoparticles. We discuss the spectroscopic details like multiple Auger decays, satellite emission in the X-ray absorption process and the core level data. We explain these data by a novel mechanism in which the resonant excitation between Fe3d and Fe4s states are involved. This mechanism is observed when the photo-excited electron becomes polarized by the electron-hole pairs existing in the conduction and valence bands.}, language = {en} }