TY - CHAP A1 - Henkel, Karsten A1 - Paloumpa, Ioanna A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - P(VDF/TrFE) as a ferroelectric dielectric for Organic Field effect Transistors in MFIS structure T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - MFIS structures consisting of metal, ferroelectric poly[vinylidene fluoride trifluoroethylene](P[VDF/TrFE]), insulator, semiconductor (Si) are fabricated and the influence of the polarization of the P(VDF/TrFE) on the CV characteristics of these structures is investigated. We find a characteristic ferroelectric hysteresis in the CV curves upon increasing the voltage scan window (e.g.-U...U,U=6...30V, |UP(VDF/TrFE)|≤15V, dP(VDF/TrFE)=300 nm). A writing process with adequate electric fields causes large shifts in the flatband voltage ( Δ UFB>4V for the quoted example before) which are stable over days. We report on our investigations which focus on the switching behavior by varying the parameters like polymer thickness, writing field strength and time, long time stability, reversing voltage and insulating material (SiO2, PMMA (Polymethylmetacrylate)). This material combination is favorable for transfer into our full organic concept of field effect transistors for application as a nondestructive readout memory (NDRO) cell. KW - P(VDF/TrFE) KW - Organic ferroelectric field effect transistor KW - capacitance voltage measurements Y1 - 2005 UR - http://www.dpg-verhandlungen.de/year/2005/conference/berlin/part/syoo/session/6/contribution/39?lan=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Müller, Klaus A1 - Burkov, Yevgen A1 - Schmeißer, Dieter T1 - Surface potential profiling on organic thin film transistors by photoemission-electron-microscopy (PEEM) T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - Surface potential imaging with Photoemission-electron-microskopy (PEEM) in high lateral resolution is introduced as a new tool for the characterisation of organic transistor structures. We use source-drain- electrode structures of different organic materials like carbon-black or graphite plotted on a printing foil. Semiconducting regioregular Poly(3-Hexylthiophene-2,5-diyl) (P3HT) was deposited by spin coating. For our measurements we used radiation of a standard high pressure Hg-lamp (4,9 eV) and synchrotron radiation at the BESSYII-U49/2 beam line. In contrast to Kelvin-AFM measurements of the surface potential, PEEM enables a simultaneous analysis of chemical composition by photoelectron spectroscopy. UPS, for example, at zero potential gives information on chemical homogeneity of the organic semiconductor in lateral resolution. PEEM images at applied voltages, compared with UPS-spectra, gives informations on doping profiles in the semiconductor, for example. In conclusion, PEEM should be a complementary method for characterisation of the surface potential with Kelvin-AFM. In addition, PEEM gives opportunities for measurements of chemical composition in the working state of the transistor (applied voltages). KW - organic field effect transistor KW - Photoemission-electron-microscopy (PEEM) KW - Kelvin-AFM KW - X-Ray photoelectron spectroscopy Y1 - 2005 UR - http://www.dpg-verhandlungen.de/year/2005/conference/berlin/part/syoo/session/6/contribution/41?lan=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Müller, Klaus A1 - Paloumpa, Ioanna A1 - Henkel, Karsten A1 - Schmeißer, Dieter T1 - Organic Field Effect Transistors with polymer high-k dielectric insulator T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - Organic field effect transistors consisting of the copolymer poly(vinylidene fluoridetrifluoroethylene) (P(VDF-TrFE)) and P3HT (poly(3-hexlythiophene)) as active layer have been fabricated. The influence of P(VDF-TrFE) on the transconductance of organic field effect transistors was investigated and enhanced gate effects are observed compared to similar transistors with PMMA (Polymethylmetacrylate) as gate dielectric. Due to the high dielectric constant of P(VDF-TrFE) (DK=12) an operation voltage smaller than for a conventional organic dielectric like PMMA (DK=3.3) was observed. The thickness of the spincoated dielectric layers is in the range of 2microns and in consequence, no significant hysteresis was found, a prerequisite for transistor operation. KW - organic field effect transistor KW - P(VDF/TrFE) KW - high-k organic Y1 - 2005 UR - http://www.dpg-verhandlungen.de/year/2005/conference/berlin/part/syoo/session/6/contribution/30?lan=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Geuss, Markus A1 - Müller, Klaus A1 - Paloumpa, Ioanna A1 - Schmeißer, Dieter T1 - Surface Potential profiling on operating full organic thin film transistors by Kelvin probe force microscopy T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - Kelvin-AFM is employed to study all polymer organic thin film transistors which are promising candidates for low cost - low performance applications like active matrix displays, sensors or single-serving devices. We use bottom contact source-drain- electrode structures of different organic materials like carbon-black or graphite plotted on a printing foil. Semiconducting regioregular Poly(3-Hexylthiophene-2,5-diyl) (P3HT) was subsequently deposited by spin coating. Surface potential profiles across the transistor channel were measured by Kelvin-AFM for various source-drain potential differences and signs. We found that contact resistances cause characteristic steps in the surface potential near the channel edges which vary with the electrode material. Furthermore, nonlinearities appear in the potential gradient which possibly give evidence for lateral inhomogeneities of the carrier mobilities. In summary, surface potential imaging with high lateral resolution ( approx. 100 nm) is introduced as a powerful tool for the characterisation of the transistor performance and the selection of suitable low cost electrode materials. KW - organic field effect transistor KW - Kelvin probe force microscopy Y1 - 2005 UR - http://www.dpg-verhandlungen.de/year/2005/conference/berlin/part/syoo/session/6/contribution/36?lan=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - GEN A1 - Birkhofer, Klaus A1 - Diehl, Eva A1 - Andersson, Jesper A1 - Ekroos, Johan A1 - Früh-Müller, Andrea A1 - Machnikowski, Franziska A1 - Mader, Viktoria A1 - Nilsson, Lovisa A1 - Sasaki, Keiko A1 - Rundlöf, Maj A1 - Wolters, Volkmar A1 - Smith, Henrik G. T1 - Ecosystem services – current challenges and opportunities for ecological research T2 - Frontiers in Ecology and Evolution Y1 - 2015 U6 - https://doi.org/10.3389/fevo.2014.00087 SN - 2296-701X VL - 2 SP - 35 ER - TY - CHAP A1 - Israel, Johannes A1 - Rachow, Fabian A1 - Schwiertz, Carola A1 - Charlafti, Evgenia A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - Direct CO2-Methanation of flue gas emitted by conventional power plants T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - The catalytic conversion of CO2 with H2 into CH4 is possible by the Sabatier reaction CO2+4H2→CH4+2H2O. Using excess energy from renewable electricity generation, this approach offers an opportunity for recycling of CO2 as synthetic natural gas. In a new concept, we investigate the performance of the Sabatier reaction as direct methanation of flue gas, emitted by conventional power plants. We investigate the Sabatier process in an upscaled system, with a maximum input flow rate of 45 Nm3/h Gas. The performance is investigated in a simulated composition of flue gas and under real conditions at a lignite power plant in Schwarze Pumpe, Brandenburg, Germany. We can achieve a CO2-conversion of up to 90%, with approx. 100% selectivity towards CH4. Under flue gas conditions and at a certain limit of gas flow the system is operated at an autothermal running modus, a steady state equilibrium of exothermic heat production and thermal flow that needs neither external annealing nor cooling. KW - CO2 KW - methanation KW - Sabatier reaction KW - power plant KW - Schwarze Pumpe KW - autothermal mode Y1 - 2017 UR - http://www.dpg-verhandlungen.de/year/2017/conference/muenster/part/ake/session/8/contribution/5 SP - S. 255 PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Rachow, Fabian A1 - Hagendorf, Moritz A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - Synthesis of Methanol from CO2 for Power-to-Liquid applications T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - The direct synthesis of methanol [CO2+3H2->CH3OH+H2O] represent a possibility to reduce the global CO2-emission by recycling the CO2 and also to store excess energy from renewable energy sources into a common fuel or chemical feedstock (Power-to-Liquid). For an acceptable conversion rate of CO2 a catalyst is needed, together with high temperatures (>200°C) and high pressure (50-200bar). Methanol is normally produced form synthesis gas, a mixture of CO and H2. By directly using CO2 for the exothermic reaction, we avoid the conversion of CO2 to CO by the reversed water gas shift reaction. We also present new concepts for the conversion from CO2-rich flue gases, eliminating the need for a separation of the CO2. The concept is backed up by measurements in laboratory scale. Here we use a Cu−ZnO catalyst on a ZrO2 substrate prepared by impregnation and compare the results with commercially available catalysts. We achieved a conversion of around 7% and a selectivity of 60% at a temperature of 240°C and 45bar. The reaction is thermodynamically limited with a maximum conversion rate of 15% at 250°C and 50bar. The conversion and the selectivity towards methanol is highly influenced by the catalyst used, the temperature, the pressure as well as the flow rate of the reactants. KW - direct methanol synthesis KW - power to liquide KW - Cu-ZnO catalyst KW - CO2 utilization Y1 - 2017 UR - http://www.dpg-verhandlungen.de/year/2017/conference/muenster/part/ake/session/8/contribution/5 SP - S. 256 PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - GEN A1 - Müller, Klaus A1 - Bär, Werner A1 - Henkel, Karsten A1 - Jahnke, Agnes A1 - Schwiertz, Carola A1 - Schmeißer, Dieter T1 - Organische Feldeffekttransistoren als Transducer in der Biosensorik T1 - Organic Field Effect Transistors as Biosensors T2 - Technisches Messen N2 - In diesem Beitrag wird der Einsatz neuartiger Sensortypen für die medizinische Diagnostik beschrieben. Diese Sensoren sollen komplett organisch sein und auf dem Prinzip des Feldeffekttransistors basieren. Als Modellsystem für die Anwendung in der Biosensorik soll die Einsatzmöglichkeit dieser Sensoren in der nicht-invasiven Diagnostik der Helicobacter-pylori-Infektion überprüft werden. N2 - In this contribution we describe the investigation of new types of sensors in medical diagnosis. These sensors are completely organic and are based on the principle of organic field effect transistors. As model system for application in medical diagnosis we test the usability of this sensors for the diagnosis of helicobacter pylori. KW - Feldeffekttransistor KW - Biosensorik KW - Helicobacter pylori KW - Field effect transistors KW - biosensors KW - helicobacter pylori Y1 - 2003 U6 - https://doi.org/10.1524/teme.70.12.565.20261 SN - 0171-8096 VL - 70 IS - 12 SP - 565 EP - 568 ER - TY - GEN A1 - Müller, Klaus A1 - Rachow, Fabian A1 - Israel, Johannes A1 - Charlafti, Evgenia A1 - Schwiertz, Carola A1 - Schmeißer, Dieter T1 - Direct Methanation of Flue Gas at a Lignite Power Plant T2 - International Journal of Environmental Science N2 - The combustion of fossil fuels results in CO2 emission, which is one of the primary causes of global warming. An important approach for solving this problem is the fixation, the chemical utilization and the recycling of CO2. Therefore, we investigate the catalytic conversion of CO2 with H2 into methane (CH4) with an upscaled test station at a brown coal power plant. In a completely new strategy, we realize the direct conversion of the CO2 content of the flue gas, without a cleaning process like amine scrubbing or optimized combustion like oxyfuel. Our experiments are performed in matters of catalytic performance, heat production and stability of the catalytic Sabatier process, as a function of the gas flow rate. The catalytic performance is investigated with a simulated composition of flue gas and under real conditions directly at the power plant. The CH4 production by the Sabatier process is realized with a maximum input flow rate of near 50Nm3/h, with 30Nm3/h flue gas and 20Nm3/h hydrogen. For these values, the necessary power scale for hydrogen generation by electrolysis is around 100kW. With synthetic and real flue gas, a conversion up to 99% (for hydrogen surplus) with 100% selectivity is stabilized. The reaction operates in thermal steady state equilibrium without any external energy supply. In consequence, the process of CO2 recycling could be integrated directly as a post combustion process of conventional power plants, without an expensive capturing step, for example. KW - CO2 recycling KW - Power to Gas (PtG) KW - Synthetic Natural Gas (SNG) KW - Sabatier-Reaction KW - Flue Gas Y1 - 2017 UR - http://www.iaras.org/iaras/home/caijes/direct-methanation-of-flue-gas-at-a-lignite-power-plant SN - 2367-8941 IS - 2 SP - 425 EP - 437 ER - TY - CHAP A1 - Henkel, Karsten A1 - Haeberle, Jörg A1 - Müller, Klaus A1 - Janowitz, Christoph A1 - Schmeißer, Dieter ED - Fornari, Robert T1 - Preparation, properties and electronic structure of SnO₂ T2 - Single Crystals of Electronic Materials N2 - This chapter reports about tin oxide (SnO₂), a material which belongs to the transparent conducting oxide family and is best characterized by its high conductivity, high carrier mobility, and the ability to form p-type conductivity. We correlate these properties in terms of localized intrinsic electronic defect states which are resolved by resonant photoelectron spectroscopy measurements. We describe SnO₂ in terms of an inhomogeneous, mixed-ionic-covalent semiconductor in which these intrinsic electronic defects state are stabilized. KW - electronic structure KW - tin oxide (SnO₂) KW - resonant photoelectron spectroscopy KW - intrinsic defect states Y1 - 2018 SN - 978-0-08-102096-8 SN - 978-0-08-102097-5 SP - 547 EP - 572 PB - Elsevier, Woodhead Publishing CY - Duxford ER - TY - GEN A1 - Müller, Klaus A1 - Rachow, Fabian A1 - Günther, Vivien A1 - Schmeißer, Dieter T1 - Methanation of Coke Oven Gas with Nickel-based catalysts T2 - International Journal of Environmental Science N2 - For a complete transition from fossil to CO₂ neutral energy supply new energy storage concepts are needed that allow energy supply in times of absence of regenerative power production as during dark doldrums. A promising renewable energy storage approach is the power to gas (to power) technique based on the production of synthetic natural gas (also called e-methane) by methanation of CO₂ with H₂. The latter is usually produced by electrolysis. In any power to gas concept, electrolysis is a very critical part, due to its high costs, stability issues, or limited power of required electrolysers. As an alternative source of hydrogen, we investigate the methanation of coke oven gas (COG). COG is a byproduct of the carbon rich coke production from coal for the steel industry, with a high amount of hydrogen (~60vol%). Coke oven gas furthermore contains CH₄(~25vol%), CO (5-8vol%), and CO₂(1-3vol%), making it an attractive feedstock for the production of synthetic energy carriers like methane. In the present study, the authors investigate the direct conversion of CO and CO₂ from COG into e-methane. Compared to stoichiometric conversion, the COG hydrogen content is too high for catalytic methanation of CO₂. In order to achieve a higher methane yield, the addition of CO₂ from air, flue gas, or coal gasification can compensate the surplus of hydrogen in the coke oven gas. The process is evaluated by the conversion of CO and CO₂, the catalyst selectivity towards higher hydrocarbons for varying temperatures, and the CH₄ yield. KW - Coke Oven Gas KW - CO₂ recycling KW - Power to Gas (PtG) KW - Synthetic Natural Gas (SNG) KW - e-methane KW - Sabatier-Reaction Y1 - 2019 UR - https://www.iaras.org/iaras/home/caijes/methanation-of-coke-oven-gas-with-nickel-based-catalysts UR - https://iaras.org/iaras/filedownloads/ijes/2019/008-0009(2019).pdf SN - 2367-8941 IS - 4 SP - 73 EP - 79 ER - TY - GEN A1 - Kot, Małgorzata A1 - Henkel, Karsten A1 - Müller, Klaus A1 - Kegelmann, Lukas A1 - Albrecht, Steve A1 - Tsud, Nataliya A1 - Kús, Peter A1 - Matolinová, Iva A1 - Schmeißer, Dieter T1 - Al2O3-Atomic Layer Deposited Films on CH3NH3PbI3 : Intrinsic Defects and Passivation Mechanisms T2 - Energy Technology , The Journal of Physical Chemistry C N2 - The initial interaction of atomic layer deposited films of Al2O3 at room temperature on CH3NH3PbI3 (MAPI) films is studied. Synchrotron radiation–based photoelectron spectroscopy is applied to analyze the initial changes in the Al-derived features by comparing samples with different Al2O3 film thicknesses. It is found that polarons and excitons, both intrinsic defects of Al2O3, play a key role in the interface formation. The polaronic states uptake a charge from the MAPI substrate. This charge is transferred to and stabilized in the excitonic state of Al2O3 which is assigned to predominately tetrahedral coordinated Al sites. This charge transfer is initiated by vacancies present in the MAPI substrate and stabilizes a covalent bonding at the Al2O3–MAPI interface but also causes a roughening of the interface which may lead to the formation of grain boundaries. On top of the rough interface, 2D Al2O3 clusters with an increasing number of octahedrally coordinated Al—O bonds grow, and with increasing Al2O3 coverage, they introduce self-healing of the structural defects. KW - charge donation and transfer cycles KW - covalent interfaces KW - defect monitoring KW - model of Al2O3–CH3NH3PbI3 interactions KW - resonant photoelectron spectroscopy Y1 - 2019 U6 - https://doi.org/10.1002/ente.201900975 SN - 2194-4288 SN - 2194-4296 VL - 7 IS - 11 ER -