TY - GEN A1 - Koval, Yuri A1 - Lazareva, I. A1 - Müller, P. A1 - Müller, Klaus A1 - Henkel, Karsten A1 - Friedrich, Daniel T1 - Field effect transistors on graphitized polymer surfaces KW - transistors KW - polymer Y1 - 2011 ER - TY - GEN A1 - Lazareva, I. A1 - Koval, Yuri A1 - Müller, P. A1 - Müller, Klaus A1 - Henkel, Karsten A1 - Schmeißer, Dieter T1 - Interface screening and imprint in pol(vinylidene fluoride/trifluoroethylene) ferroelectric field effect transistors KW - interface KW - screening KW - transistors Y1 - 2009 ER - TY - GEN A1 - Henkel, Karsten A1 - Lazareva, I. A1 - Mandal, Dipankar A1 - Paloumpa, Ioanna A1 - Müller, Klaus A1 - Koval, Yuri A1 - Müller, P. A1 - Schmeißer, Dieter T1 - Electrical investigations on metal/ferroelectric/insulator/semiconductor structures using Poly[vinylidene fluoride trifluoroethylene] as ferroelectric layer for organic nonvolatile memory applications KW - metal KW - frerroelectric KW - insulator KW - semiconductor Y1 - 2009 ER - TY - CHAP A1 - Lazareva, I. A1 - Koval, Yuri A1 - Müller, P. A1 - Paloumpa, Ioanna A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - Field effect transistor of graphitized polyimide with P(VDF-TrFE) as gate insulator T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft, Reihe 6, Bd. 43 N2 - Surfaces of polyimide films were graphitized by low-energy ion irradiation. The conductivity was between 10−5 to 200 S/cm [1]. We prepared field effect transistors using this material. Ferroelectric P(VDF-TrFE) was used as gate insulator. The thickness of P(VDF-TrFE) varied from 120 nm to 1200 nm. Properties of P(VDF-TrFE) were investigated by current-voltage measurements of metal/ P(VDF-TrFE)/metal capacitors. We have found that at room temperature, the coercive field of P(VDF-TrFE) does not depend on the film thickness. At lower temperatures the coercive field increases proportionally to the reciprocal temperature. Remnant polarization is 9.5 µC/cm2. It slightly rises with decreasing temperature. Our recent results of field effect mobility, carrier concentration and threshold voltage are presented. [1] I. Lazareva, Y. Koval, M. Alam, S. Strömsdörfer, P. Müller, Appl. Phys. Lett. 90, 262108 (2007) Y1 - 2008 UR - http://www.dpg-verhandlungen.de/year/2008/conference/berlin/part/df/session/11/contribution/6 SN - 0420-0195 SP - S. 195 PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Schmeißer, Dieter A1 - Müller, Sebastian A1 - Henkel, Karsten A1 - Müller, Klaus A1 - Wehner, Stefan T1 - In-situ analysis of moving reaction fronts for the bistable CO oxidation reaction on noble metal catalyst T2 - Extended Abstracts Book of First International Conference on Materials for Energy N2 - 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. KW - CO oxidation KW - Ir KW - Pd KW - photo electron emission microscopy (PEEM) Y1 - 2010 SN - 978-3-89746-117-8 SP - S. 932 PB - Dechema e.V. CY - Frankfurt ER - TY - GEN A1 - Müller, Felix A1 - Torger, Bernhard A1 - Allertz, Peter J. A1 - Jähnichen, Klaus A1 - Keßler, Stefan A1 - Müller, Martin A1 - Simon, Frank A1 - Salchert, Katrin A1 - Mäurer, Haike A1 - Pospiech, Doris T1 - Multifunctional crosslinkable itaconic acid copolymers for enzyme immobilization T2 - European Polymer Journal N2 - UV-Crosslinkable itaconic copolymers are developed to provide new multifunctional materials for coatings which combine crosslinkable functionalities and the possibility to immobilize enzymes. The polymer-immobilized enzymes were used for water treatment to decompose persistent organic molecules. Introduction of suitable comonomers allows tailoring the mechanical and chemical properties for special applications. Copolymers containing MMA and itaconic anhydride were chosen because of the formation of long-term stable anhydride functionalities. These anhydride functionalities are employed to attach enzymes covalently. 4-Benzoylphenyl methacrylate is used as comonomer for UV-initiated crosslinking. Terpolymers are successfully obtained by radical copolymerization in solution. The copolymers are compared to poly(ethylene-alt-maleic anhydride) [P(EMA)] often used with respect to enzyme immobilization, activity and hydrolytic stability. The hydrolysis stability of the copolymers against water is studied by ATR-FTIR spectroscopy. Thin films are prepared on glass substrates in a layer-by-layer procedure by spin-coating. The layer formation is monitored by ATR-FTIR spectroscopy. UV-crosslinking of the copolymer films is performed taking the optimal irradiation dose that avoids polymer degradation. ATR-FTIR spectroscopy verifies the coupling reaction between amino groups of the enzyme and the anhydride groups on the surface of the crosslinked polymer film. The syringaldazine (4-hydroxy-3,5-dimethoxybenzaldehyde azine) test and 2,2´-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) assay demonstrate that the immobilized enzymes maintain their activities. The functional copolymers showed a significant effect in reduction of persistent organic pollutants in contaminated waste water. KW - ATR-FTIR spectroscopy KW - Crosslinking KW - Enzyme-immobilization KW - Itaconc acid KW - Methacrylate copolymer Y1 - 2018 U6 - https://doi.org/10.1016/j.eurpolymj.2018.03.014 VL - 102 SP - 47 EP - 55 ER - TY - GEN A1 - Boch, Steffen A1 - Allan, Eric A1 - Birkhofer, Klaus A1 - Bossdorf, Oliver A1 - Blüthgen, Nico A1 - Christ-Breulmann, Sabina A1 - Diekötter, Tim A1 - Dormann, Carsten F. A1 - Gossner, Martin M. A1 - Hallmann, Christine A1 - Hemp, Andreas A1 - Hölzel, Norbert A1 - Jung, Kirsten A1 - Klaus, Valentin H. A1 - Klein, Alexandra M. A1 - Kleinebecker, Till A1 - Lange, Markus A1 - Müller, Jörg A1 - Nacke, Heiko A1 - Prati, Daniel A1 - Renner, Swen C. A1 - Rothenwöhrer, Christoph A1 - Schall, Peter A1 - Schulze, Ernst-Detlef A1 - Socher, Stephanie A. A1 - Tscharntke, Teja A1 - Türke, Manfred A1 - Weiner, Christiane N. A1 - Weisser, Wolfgang W. A1 - Westphal, Catrin A1 - Wolters, Volkmar A1 - Wubet, Tesfaye A1 - Fischer, Markus T1 - Extensive und jährlich wechselnde Nutzungsintensität fördert den Artenreichtum im Grünland T2 - ANLIEGEN NATUR Y1 - 2016 UR - https://www.biom.uni-freiburg.de/mitarbeiter/dormann/boch2016anliegennatur.pdf SN - 1864-0729 VL - 38 IS - 1 SP - 86 EP - 95 ER - TY - GEN A1 - Neyret, Margot A1 - Le Provost, Gaëtane A1 - Boesing, Andrea Larissa A1 - Schneider, Florian D. A1 - Baulechner, Dennis A1 - Bergmann, Joana A1 - Vries, Franciska T. de A1 - Fiore-Donno, Anna Maria A1 - Geisen, Stefan A1 - Goldmann, Kezia A1 - Merges, Anna A1 - Saifutdinov, Ruslan A. A1 - Simons, Nadja K. A1 - Tobias, Joseph A. A1 - Zaitsev, Andrey S. A1 - Gossner, Martin M. A1 - Jung, Kirsten A1 - Kandeler, Ellen A1 - Krauss, Jochen A1 - Penone, Caterina A1 - Schloter, Michael A1 - Schulz, Stefanie A1 - Staab, Michael A1 - Wolters, Volkmar A1 - Apostolakis, Antonios A1 - Birkhofer, Klaus A1 - Boch, Steffen A1 - Boeddinghaus, Runa S. A1 - Bolliger, Ralph A1 - Bonkowski, Michael A1 - Buscot, François A1 - Dumack, Kenneth A1 - Fischer, Markus A1 - Gan, Huei Ying A1 - Heinze, Johannes A1 - Hölzel, Norbert A1 - John, Katharina A1 - Klaus, Valentin H. A1 - Kleinebecker, Till A1 - Marhan, Sven A1 - Müller, Jörg A1 - Renner, Swen C. A1 - Rillig, Matthias C. A1 - Schenk, Noëlle V. A1 - Schöning, Ingo A1 - Schrumpf, Marion A1 - Seibold, Sebastian A1 - Socher, Stephanie A. A1 - Solly, Emily F. A1 - Teuscher, Miriam A1 - Kleunen, Mark van A1 - Wubet, Tesfaye A1 - Manning, Peter T1 - A slow-fast trait continuum at the whole community level in relation to land-use intensification T2 - Nature Communications N2 - AbstractOrganismal functional strategies form a continuum from slow- to fast-growing organisms, in response to common drivers such as resource availability and disturbance. However, whether there is synchronisation of these strategies at the entire community level is unclear. Here, we combine trait data for 2800 above- and belowground taxa from 14 trophic guilds spanning a disturbance and resource availability gradient in German grasslands. The results indicate that most guilds consistently respond to these drivers through both direct and trophically mediated effects, resulting in a ‘slow-fast’ axis at the level of the entire community. Using 15 indicators of carbon and nutrient fluxes, biomass production and decomposition, we also show that fast trait communities are associated with faster rates of ecosystem functioning. These findings demonstrate that ‘slow’ and ‘fast’ strategies can be manifested at the level of whole communities, opening new avenues of ecosystem-level functional classification. KW - General Physics and Astronomy KW - General Biochemistry KW - General Chemistry KW - Multidisciplinary KW - Genetics and Molecular Biology Y1 - 2024 U6 - https://doi.org/10.1038/s41467-024-45113-5 SN - 2041-1723 VL - 15 IS - 1 ER - TY - GEN A1 - Müller, Klaus A1 - Henkel, Karsten A1 - Mikalo, Ricardo Pablo A1 - Paloumpa, Ioanna A1 - Schmeißer, Dieter T1 - Elektronik mit organischen Materialien N2 - Plastikelektronik, flexible Solarzellen, intelligente Kleidung, neuartige und maßgeschneiderte Transducer für die Gas-, Flüssigkeits- und Biosensorik, all dies sind Anwendungen, die ohne halbleitende Polymere nicht denkbar wären und die Bereiche erschließen, in denen zur Zeit eine regelrechte Goldgräberstimmung herrscht. Mit wichtigen Beiträgen im Grundlagen- und Anwendungsbereich nimmt die BTU Cottbus an dieser Entwicklung teil, u. a. auch durch eine Kooperation mit dem Institut für Mikrobiologie des Carl-Thiem-Klinikums Cottbus.In diesem Artikel werden die Voraussetzungen für die Konstruktion organischer Feldeffekt-Transistoren mit gassensitiver Gate-Elektrode vorgestellt. Untersuchungen zur elektronischen Struktur des organischen Halbleiters Poly(3-Hexylthiophen), die Anwendung dieses Materials als aktive Schicht in organischen Feldeffekt-Transitoren, die Gassensitivität von Polypyrrolelektroden auf Quarz-Mikrowaagen und die Mikrorstukturierung organischer Elektroden werden beschrieben. Y1 - 2002 PB - BTU Cottbus, Eigenverlag ER - TY - CHAP A1 - Müller, Klaus A1 - Henkel, Karsten A1 - Paloumpa, Ioanna A1 - Schmeißer, Dieter T1 - Low-cost-Plot-Technologie fur die Mikrostrukturierung von Gassensoren T2 - Sensoren im Fokus neuer Anwendungen, 5. Dresdner Sensor-Symposium, 10. - 12. Dezember 2001, Dresden N2 - Bei der Herstellung von Mikrosensoren ist die Strukturierung von Elektroden oder elektrischen Zu-leitungen mit einem hohen Miniaturisierungsgrad ein entscheidender Punkt. Dazu müs-sen häufig teure Verfahren (Lithographie, Maskentechniken) herangezogen werden.Dieser Beitrag beschreibt eine low-cost-Technologie zur Herstellung organischer Mikrostrukturen für elektronische und messtechnische Anwendungen im Bereich der Sensorik. Geplottete Strukturen mit Polypyrrol und Poly(3,4-Ethylen-Dioxy-Thiophen), dotiert mit Polystyrolsulfonat (PEDOT/PSS) wurden als Widerstandssensoren für die Detektion von Luftfeuchte ein-gesetzt. Die prinzipielle Ein-satzmöglichkeit unserer Technik im Bereich der organischen Elektronik konnten wir mit dem Bau organischer Feldeffekttransistoren nachweisen. Mit einem computergesteu-erten Plotter des Typs Rol-land DXY-1150A, Plot-Kapillaren für das Tuschezeichnen, handelsüblichen Folien für wasserlösliche Tinten als Substrat und kolloidalen Graphit als leitendes Material konnten wir Auflösungen, das heißt insbesondere Kanalbreiten bzw. Elektrodenabstände im Bereich von 20+10%B5m (auf 2cm Länge) her-stellen. Y1 - 2002 SN - 3-935712-71-5 SP - 166 EP - 169 PB - w.e.b. Universitätsverlag CY - Dresden ER - TY - JOUR A1 - Müller, Klaus A1 - Hoffmann, Patrick A1 - Milko, S. A1 - Burkov, Yevgen A1 - Schmeißer, Dieter T1 - PEEM and µ-NEXAFS of Cu-In-S-Surfaces N2 - The composition of CuInS2-films tends to differ from the ideal ratio of 1:1:2. A molecularlyvariation of dm=[Cu]/[In]-1 not equal 0 occurs due to the formation of binary phases as segregation's at the surface, as crystallites in the bulk of the film or at the surface of grains [1]. Furthermore, the range of homogeneity of the phase CuInS2 is relatively large caused by a low enthalpy of formation of defects like Cu-vacancies [2]. Segregation's at surfaces can be removed by KCN etching or by an electrochemical process [3, 4] We investigated the effect of an in-situ-heat-treatment of samples, prepared in the Cu-rich regime with additional amounts of copper, deposited on the surface of the Cu-In-S-films.We used Cu-In-S-films on molybdenum, prepared from precursors of Cu/In and a following reactive annealing-process in a sulphur-atmosphere. The experiments were performed as follows: The surface of the films was cleaned in situ to remove CuS-Phases by Argon-bombardment. The thin layers of additional Copper were prepared by evaporation of copper metal in Knudsen-cells. The thickness of this copper-films is in the range of monolayers, revealed by a calibration with copper on iron-substrates. After this deposition the samples were heated up to several temperatures (up to 550 ºC) for ten minutes, respectively. Here the molybdenum back-contact was used as electrical heater. Y1 - 2002 ER - TY - JOUR A1 - Müller, Klaus A1 - Milko, S. A1 - Schmeißer, Dieter T1 - Preparation of stoichiometric CuInS2-surfaces - an XPS, UPS-study JF - Thin Solid Films N2 - CuInS2 films are investigated with photoelectron spectroscopy. We find significant deviation from the stoichiometric composition depending on the preparation on the films. For Cu-rich films (start composition) we show that by Ar sputtering and annealing the surface composition varies along a binary cut of the Cu-In-S ternary phase diagram. We also present a novel technique which brings the surface composition close to the stoichiometric stability range of the CuInS2 phase. The technique used the evaporation of Cu on the sputter cleaned surface. KW - Stoichiometric CuInS2-films KW - Annealing KW - XPS KW - UPS Y1 - 2003 SN - 0040-6090 VL - 431-432 SP - 312 EP - 316 ER - TY - GEN A1 - Müller, Klaus A1 - Burkov, Yevgen A1 - Schmeißer, Dieter T1 - PEEM and my-NEXAFS of Cu-In-S2-surfaces T2 - Thin Solid Films N2 - Polycrystalline CuInS2 samples are an ideal system for photoemission electron microscope studies. The polycrystalline grains have a diameter of approximately 5 small mu, Greekm and the system is expected to be highly inhomogeneous because of the existence of many sub-phases. We used a recently established procedure to reproducibly obtain stoichiometric CuInS2-surfaces and follow the changes in the morphology, the elemental inhomogeneous distribution, and the development of the electronic structure upon its preparation. We find that the individual grains trend to coagulate, the surface composition becomes more homogeneous, and identify characteristic features of the unoccupied DOS. KW - CuInS2 films KW - Annealing-process KW - PEEM KW - small mu KW - NEXAFS Y1 - 2003 SN - 0040-6090 VL - 431-432 SP - 307 EP - 311 ER - TY - GEN A1 - Müller, Klaus A1 - Paloumpa, Ioanna A1 - Schmeißer, Dieter T1 - Carbon-plot-microstructuring for all-polymer-transistors T2 - Synthetic Metals N2 - This contribution describes the use of a low-cost technology to produce organic microstructures for electronically applications. With a computer driven plotter, substrates like printing foil and colloidal graphite (diluted in water) for the electrodes, we realised channel lengths of 20±10 microm. Compared with transistor devices, fabricated using conventional photolithographic methods and the same semiconducting material, this technique is a hopeful approach to produce microelectronic structures that are low-cost and all-organic. KW - Ten micrometer carbon-plot KW - Organic field-effect-transistors KW - Low-cost-technique Y1 - 2003 SN - 0379-6779 VL - 138 IS - 1-2 SP - 271 EP - 273 ER - TY - CHAP 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 Y1 - 2003 SN - 3-935712-92-8 SP - 119 EP - 223 PB - w.e.b.-Univ.-Verl. CY - Dresden ER - TY - GEN A1 - Müller, Klaus A1 - Goryachko, Andriy A1 - Burkov, Yevgen A1 - Schwiertz, Carola A1 - Ratzke, Markus A1 - Köble, J. A1 - Reif, Jürgen A1 - Schmeißer, Dieter T1 - Scanning Kelvin Probe Microscopy and Photoemission electron microscopy of organic source-drain structures T2 - Synthetic Metals N2 - n order to optimize organic field effect transistors (OFETs), the characterisation of active-layer surfaces in terms of their roughness, chemical composition and distribution of surface potentials is important. We report on high-resolution microscopic mapping of organic source-drain structures with P3HT as the semiconductor by scanning Kelvin probe microscopy (SKPM) and photoemission electron microscopy (PEEM). It was shown that PEEM is able to characterise the surface morphology (roughness), the chemical homogeneity and the composition of organic structures. The two-dimensional mapping of surface potentials by SKPM with applied source-drain voltages is shown to be an important ingredient of OFETs failure mode analysis. KW - Photoemission electron microscopy (PEEM) KW - Scanning Kelvin probe microscopy (SKPM) KW - OFET Y1 - 2004 SN - 0379-6779 VL - 146 IS - 3 SP - 377 EP - 382 ER - TY - JOUR A1 - Müller, Klaus T1 - PEEM studies of KCN-etched CuInS2 surfaces Y1 - 2004 ER - TY - JOUR A1 - Müller, Klaus T1 - PEEM imaging contrast in an operating organic electronic device Y1 - 2005 ER - TY - JOUR A1 - Müller, Klaus T1 - Spectro-Microscopic Characterisation of CuInS2 Surfaces N2 - hotoemission electron microscopy (PEEM) is used to study CuInS2 surfaces. CuInS2 (CIS) is used as polycrystalline absorber layer for thin film solar cells. A characterisation in terms of morphological information, elemental distribution, and of doping inhomogeneities at the surface is very important. We demonstrate that the method is capable for such surface studies in high lateral resolution. The use of synchrotron radiation allows the visualization of chemical inhomogeneities in single grains. By taking PEEM images around the absorption edges of Cu, In, or S, we are able to map elemental distributions, separated from morphology-dependent information in the PEEM image. KW - High-resolution PEEM KW - CuInS2 KW - Solar cells KW - Surface characterisation Y1 - 2005 ER - TY - GEN A1 - Müller, Klaus A1 - Paloumpa, Ioanna A1 - Henkel, Karsten A1 - Schmeißer, Dieter T1 - A polymer high-k dielectric insulator for organic field effect Transistors T2 - Journal of Applied Physics Y1 - 2005 SN - 0021-8979 VL - 98 IS - 5 SP - S. 056104 ER - TY - GEN A1 - Henkel, Karsten A1 - Sohal, Rakesh A1 - Torche, Mohamed A1 - Paloumpa, Ioanna A1 - Müller, Klaus A1 - Hoffmann, Patrick A1 - Schmeißer, Dieter T1 - Grenzflächenoptimierung für funktionale Dünnschichtsysteme: Oxide und Polymere T2 - Forum der Forschung Y1 - 2005 SN - 0947-6989 VL - 9 IS - 18 SP - 49 EP - 56 ER - TY - JOUR A1 - Müller, Klaus A1 - Scheer, R. A1 - Schmeißer, Dieter A1 - Burkov, Yevgen T1 - Preparation of stoichiometric CuInS2-Surfaces JF - Thin Solid Films KW - preparation Y1 - 2004 SN - 0040-6090 VL - 451–452 SP - 120 EP - 123 ER - TY - JOUR A1 - Müller, Klaus A1 - Burkov, Yevgen A1 - Schmeißer, Dieter T1 - Photo-Emission-Electron-Microscopy for Characterization of an Operating Organic Electronic Device KW - photo-emission-electron-microscopy Y1 - 2006 ER - TY - JOUR A1 - Müller, Klaus A1 - Paloumpa, Ioanna A1 - Schmeißer, Dieter A1 - Henkel, Karsten T1 - Organic thin film transistors with polymer high-k dielectric insulator KW - high-k Y1 - 2006 ER - TY - JOUR A1 - Müller, Klaus A1 - Henkel, Karsten A1 - Schmeißer, Dieter T1 - Organic field effect transistors with ferroelectric hysteresis Y1 - 2007 ER - TY - JOUR A1 - Müller, Klaus A1 - Mandal, Dipankar A1 - Schmeißer, Dieter T1 - No interfacial layer for PEDOT electrodes on PVDF: Characterization of reactions at the interface P(VDF/TrFE)/Al and P(VDF/TrFE)/PEDOT:PSS Y1 - 2007 ER - TY - GEN A1 - Müller, Klaus A1 - Henkel, Karsten A1 - Mandal, Dipankar A1 - Seime, Bernd A1 - Paloumpa, Ioanna A1 - Schmeißer, Dieter T1 - Spin coated organic ferroelectric films for non volatile memories KW - organic KW - ferroelectric Y1 - 2011 ER - TY - GEN A1 - Mandal, Dipankar A1 - Henkel, Karsten A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - Band gab determination of P(VDF-TrFE) copolymer film by electron energy loss spectroscopy Y1 - 2010 ER - TY - GEN A1 - Henkel, Karsten A1 - Seime, Bernd A1 - Paloumpa, Ioanna A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - Buffer layer incestigaions on MFIS capacitors consisting of ferroelectric poly[vinylidene fluoride trifluoroethylene] T2 - IOP conference series : Materials Science and Engineering KW - MFIS capacitors KW - ferroelectric Y1 - 2010 SN - 1757-899X VL - 8 IS - 1 SP - 012036 ER - TY - GEN A1 - Schmeißer, Dieter A1 - Henkel, Karsten A1 - Müller, Klaus A1 - Tallarida, Massimo T1 - Interface Reactions in Ultrathin Functional Dielectric Films KW - ultrathin KW - dielectric Y1 - 2009 ER - TY - GEN A1 - Schmeißer, Dieter A1 - Tallarida, Massimo A1 - Henkel, Karsten A1 - Müller, Klaus A1 - Mandal, Dipankar A1 - Chumakov, Dmytro A1 - Zschech, Ehrenfried T1 - Characterization of oxidic and organic materials with synchrotron radiation based XPS and XAS KW - oxidic KW - organic KW - materials KW - synchrotron radiation KW - XPS KW - XAS Y1 - 2009 ER - TY - CHAP A1 - Müller, Klaus A1 - Burkov, Yevgen A1 - Mandal, Dipankar A1 - Henkel, Karsten A1 - Paloumpa, Ioanna A1 - Goryachko, Andriy A1 - Schmeißer, Dieter ED - Wöll, Christof T1 - Microscopic and spectroscopic characterization of interfaces and dielectric layers for OFET devices T2 - Organic Electronics : structural and Electronic Properties of OFETs KW - microscopic KW - spectrocsopic KW - dielectric Y1 - 2009 SN - 978-3-527-40810-8 SP - 445 EP - 468 PB - Wiley-VCH CY - Weinheim ER - TY - JOUR A1 - Müller, Klaus A1 - Mandal, Dipankar A1 - Henkel, Karsten A1 - Paloumpa, Ioanna A1 - Schmeißer, Dieter T1 - Ferroelectric properties of spin-coated ultrathin (down to 10nm) copolymer films KW - ferroelectric KW - spin-coated KW - copolymer Y1 - 2008 ER - TY - CHAP A1 - Henkel, Karsten A1 - Mandal, Dipankar A1 - Seime, Bernd A1 - Paloumpa, Ioanna A1 - Lazareva, I. A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - Electrical investigations on MFIS structures consisting P[VDF/TrFE] as ferro-electric layer for non-volatile memory applications T2 - Proceedings of 15th Workshop on Dielectrics in Microelectronics, Bad Saarow, 23 - 25 June 2008, Bad Saarow (Berlin) KW - MFIS, P[VDF/TrFE] KW - ferroelectric KW - non-volatile Y1 - 2008 SP - 159 EP - 160 ER - TY - GEN A1 - Henkel, Karsten A1 - Seime, Bernd A1 - Paloumpa, Ioanna A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - Optimization of MFIS structures containing poly(vinylidene-fluoride trifluoroethylene) for non-volatile memory applications Y1 - 2010 ER - TY - GEN A1 - Henkel, Karsten A1 - Seime, Bernd A1 - Paloumpa, Ioanna A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - Buffer layer investigations on MFIS capacitors consisting of ferroelectric poly[vinylidene fluoride trifluoroethylene] Y1 - 2010 ER - TY - CHAP A1 - Müller, Klaus A1 - Paloumpa, Ioanna A1 - Schmeißer, Dieter T1 - Carbon-Plot-Micostructuring for All-Polymer-Transistors Y1 - 2001 ER - TY - GEN A1 - Müller, Klaus A1 - Richter, Matthias A1 - Philip, Shine A1 - Kunst, Manuel A1 - Schmeißer, Dieter T1 - Excited states in P3HT and P3HT/PCBM blends T2 - BioNanoScience Y1 - 2012 SN - 2191-1630 VL - 2 IS - 1 SP - 42 EP - 51 ER - TY - GEN A1 - Müller, Klaus A1 - Richter, Matthias A1 - Friedrich, Daniel A1 - Paloumpa, Ioanna A1 - Kramm, Ulrike Ingrid A1 - Schmeißer, Dieter T1 - Spectroscopic characterization of Cobalt–Phthalocyanine electrocatalysts for fuel cell applications T2 - Solid State Ionics N2 - 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. KW - Co-phthalocyanine KW - Catalysis KW - Oxygen reduction reaction (ORR) KW - XPS KW - NEXAFS Y1 - 2012 U6 - https://doi.org/10.1016/j.ssi.2011.12.013 SN - 1872-7689 IS - 216 SP - 78 EP - 82 ER - TY - GEN A1 - Mandal, Dipankar A1 - Müller, Klaus A1 - Henkel, Karsten A1 - Schmeißer, Dieter T1 - The effect of X-ray photoelectron spectroscopy measurement on P(VDF-TrFE) copolymer thin films T2 - Applied Surface Science N2 - The impact of prolonged X-ray irradiation during X-ray photoelectron spectroscopy (XPS) measurement was investigated on poly(vinylidene-trifluoroethylene) (P(VDF-TrFE)) thin films. It was observed that prolonged X-ray irradiation can accelerate the crosslinking of P(VDF-TrFE) and diminish the ferroelectric phase. Fourier transform infrared spectroscopy (FT-IR) data indicate that the ferroelectric phase diminishes completely after 360 kJ of X-ray irradiation dose and it induces the paraelectric phase. In this work, the main emphasis was given to the optimization of the X-ray irradiation dose during XPS measurements to maintain the ferroelectric phase within the copolymer films. KW - P(VDF-TrFE) copolymer thin film KW - XPS measurement KW - X-ray irradiation KW - Ferroelectric to paraelectric phase transformation Y1 - 2012 U6 - https://doi.org/10.1016/j.apsusc.2012.07.144 SN - 0169-4332 SN - 1873-5584 IS - 261 SP - 209 EP - 213 ER - TY - GEN A1 - Müller, Klaus A1 - Fleige, Michael A1 - Rachow, Fabian A1 - Schmeißer, Dieter T1 - Sabatier based CO2-methanation of flue gas emitted by conventional power plants T2 - Energy Procedia N2 - The hydrogenation CO2+ 4H2 ->CH4 + 2H2O discovered by Paul Sabatier nowadays is discussed as "Power-to-approach" to utilize excess energy from renewable electricity generation. In a laboratory scale, we investigate the Sabatier process in a simulated flue gas atmosphere of conventional base load power plants. The reaction is investigated with regard to conversion rates, yield, selectivity and long-term stability. Using a catalyst based on nickel,we extract selectivities near 100% with a conversion around 85%. Beside the influence of oxygen, we investigate further typical contaminations like NO2 and SO2. KW - Power to gas KW - CO2 -Methanation KW - Sabatier-reaction KW - flue gas Y1 - 2013 U6 - https://doi.org/10.1016/j.egypro.2013.08.028 SN - 1876-6102 VL - 40 SP - 240 EP - 248 ER - TY - GEN A1 - Müller, Klaus A1 - Städter, Matthias A1 - Rachow, Fabian A1 - Hoffmannbeck, David A1 - Schmeißer, Dieter T1 - Sabatier-based CO2-methanation by catalytic conversion T2 - Environmental Earth Sciences N2 - The catalytic conversion of CO2is an important component for the reintegration of secondary products like CO2 or H2 into the energy supply. An example is the "power to gas’" concept with a conversion of CO2 into CH4. The CO2 is transferred into a carrier of chemical energy, with the possibility to feed the produced CH4 into the existing network of natural gas. At temperatures of around 350 °C, hydrogenation of CO2 to CH4 is possible by the Sabatier reaction CO2+4H2->CH4+H2O. One prerequisite for efficient kinetics of the Sabatier reaction is the application and optimization of catalysts. The focus of catalyst development is given to their performance under the conditions to be expected in the special application. As a part of the project Geoenergy-Research (GeoEn), we address questions related to the catalytic utilization of CO2 produced in the course of the oxyfuel combustion of lignite. In this contribution, we report on the experimental setup in laboratory scale, which enables an advanced characterization of the catalytic performance, including thermodesorption measurements at atmospheric pressure in order to determine the amount of adsorbed CO2 under real conditions. We also show data for activation energies, the catalytic performance as function of temperature and the long time stability of a commercial Ru-based catalyst. KW - CO2 KW - Sabatier reaction KW - Catalysis KW - RuO2 Y1 - 2013 U6 - https://doi.org/10.1007/s12665-013-2609-3 SN - 1866-6280 VL - 70 IS - 8 SP - 3771 EP - 3778 ER - TY - GEN A1 - Städter, Matthias A1 - Müller, Klaus A1 - Rachow, Fabian A1 - Richter, Matthias A1 - Schmeißer, Dieter T1 - Ambient pressure thermal desorption spectroscopy (AP-TDS) of NiO/SiO2 catalysts T2 - Environmental Earth Sciences N2 - 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. KW - CO2 KW - NiO KW - TDS KW - XAS KW - XPS Y1 - 2013 U6 - https://doi.org/10.1007/s12665-013-2835-8 SN - 1866-6280 VL - 70 IS - 8 SP - 3779 EP - 3784 ER - TY - GEN A1 - Walter, Andreas A1 - Keuler, Klaus A1 - Block, Alexander A1 - Knoche, Richard A1 - Block, Alexander A1 - Kotlarski, Sven A1 - Müller-Westermeier, Gerhard A1 - Rechid, Diana A1 - Ahrens, Wilfried T1 - A high resolution reference data set of german wind velocity 1951-2001 and comparison with regional climate model results T2 - Meteorologische Zeitschrift Y1 - 2006 U6 - https://doi.org/10.1127/0941-2948/2006/0162 SN - 1610-1227 VL - 15 IS - 6 SP - 585 EP - 596 ER - TY - CHAP A1 - Seime, Bernd A1 - Henkel, Karsten A1 - Paloumpa, Ioanna A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - Buffer layer investigation of MFIS stacks with an organic ferroelectric layer T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft ; Reihe 6, Bd. 42 N2 - Ferroelectric field effect transistors are considered as future non volatile and non destructive readout memory cells. Conventional Perowskite-type ferroelectric materials are shown to work but they need expensive high temperature and high partial pressure processing steps inducing also unintentional and undefined interfacial layers.A possible low cost solution is the use of poly[vinylidene fluoride trifluoroethylene (P[VDF/TrFE]). This is a ferroelectric polymer which can be spin coated at room temperature onto silicon suited with well defined buffer layers. Using P[VDF/TrFE] we focus on metal ferroelectric insulator semi-conductor (MFIS) structures. In MFIS structure a part of the programming voltage drops over the buffering insulator. We report on attempts to minimize this fraction by optimizing the voltage divider over the buffer and the ferroelectric layers. CV measurements for different thickness of the buffer (10-235nm) and the ferroelectric layer(100nm-1μm) and for different permittivity values of the buffer layer(SiO2, Al2O3, HfO2) will be presented. This work is supported by Deutsche Forschungsgemeinschaft within priority program 1157 (DSCH 745/11-1). Y1 - 2007 UR - http://www.dpg-verhandlungen.de/year/2007/conference/regensburg/part/df/session/11/contribution/1 SN - 0420-0195 SP - S. 216 PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Mandal, Dipankar A1 - Müller, Klaus A1 - Seifarth, Olaf A1 - Hoffman, Patrick A1 - Henkel, Karsten A1 - Schmeißer, Dieter T1 - Study of reactions at the interface P(VDF/TrFE)/Al and P(VDF/TrFE)/PEDOT:PSS T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft ; Reihe 6, Bd. 42 N2 - Due to potential use in non volatile memory application, Poly(vinylidene fluoride/trifluoroethylene) (P(VDF-TrFE)) is a great deal of interest, especially to produce organic field effect transistors (OFET). Right now it was found that Aluminum is one of the cost-effective inorganic electrode candidate. On the other hand, poly(3,4 ethylenedioxythiophene):poly(4-styrenesulfonate)(PEDOT:PSS) shows promising behavior for the application as organic electrode. In part of our investigations we have systematically studied surface interactions of organic ferroelectric thin films (P(VDF-TrFE))with inorganic (Al) and organic layers (PEDOT:PSS). By X-ray photoelectron spectroscopy (XPS) is has been found that there is a interfacial reaction with Al and the copolymer. In contrast, for electrodes, made of PEDOT: PSS, we found not such kind of behavior. In this case, we found no evidence for any surface reaction. Furthermore, we present our results concerning the orientation of permanent dipoles in the co-polymer (formed between hydrogen and fluorine atom). Here, we use Near-edge X-ray absorption fine structure (NEXAFS) analysis at the U 49/2 - PGM2 beam line of the BESSY-II Synchrotron. This work is supported by Deutsche Forschungsgemeinschaft (DFG) within priority program 1157 (DSCH 745/11-1). Y1 - 2007 UR - http://www.dpg-verhandlungen.de/year/2007/conference/regensburg/part/syoe/session/8/contribution/18 SN - 0420-0195 SP - S. 797 PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Kachel, Krzysztof A1 - Richter, Matthias A1 - Philip, Shine A1 - Paloumpa, Ioanna A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - Performance of organic solar cells with a ferroelectric component T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft, Reihe 6, Bd. 45 N2 - Charge dissociation and recombination are important factors for the efficiency of organic solar cells, even in blended systems of different polymers. As a new approach, the influence of additional blended ferroelectric nanoparticles on the solar cell performance is investigated. The ferroelectric dipole of the nanoparticle causes a local field, which could lead to a longer recombination time of the polaron pairs. As solar cell system we use bulk heterojunction cells or bilayer structures based on regioregular poly(3-hexylthiophene) (P3HT) as the donor and phenyl-C61-butyric acid methyl ester (PCBM) as the acceptor molecule. As ferroelectric additive we use the ferroelectric copolymer poly(vinylidene fluoride trifluoroethylene) (P(VDF-TrFE)) or BaTiO3. The copolymer is spincoated as ultrathin film of 20nm, whereas the BaTiO3 is incorporated as nanodispersion into the donor-acceptor blend. We present the solar cell parameters for the different geometries and ferroelectric materials as a function of ferroelectric content and of the alignment of the ferroelectric dipoles after application of an external electric field. Y1 - 2010 UR - http://www.dpg-verhandlungen.de/year/2010/conference/regensburg/part/cpp/session/27/contribution/6 SN - 0420-0195 SP - S. 153 PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Philip, Shine A1 - Richter, Matthias A1 - Friedrich, Daniel A1 - Paloumpa, Ioanna A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - Spectroscopic investigations of P3HT/PCBM films for organic BHJ solar cells T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft, Reihe 6, Bd. 45 N2 - Investigations of the electronic structure and composition of regioregular poly(3-hexylthiophene) (P3HT) and phenyl-C61-butyric acid methyl ester (PCBM) based films using Near Edge X-Ray Absorption Fine Structure (NEXAFS) are presented. The measurements were performed at the U49/2-PGM2 beam line of BESSY II, Berlin recording TEY (total electron yield) and TFY (total fluorescence yield) data. Samples prepared by spin coating a mixture of P3HT dissolved in chloroform and PCBM dissolved in chlorobenzene onto ITO (indium tin oxide) coated glass slides were analyzed. Upon measuring the pure P3HT and PCBM, all reported excitations were observed, whereas the blended system is a weighted superposition of the related peaks. Analyzing the data we calculate the composition of the mixture. We also show angular dependent NEXAFS measurements of the P3HT/PCBM blend in order to measure the orientation and distribution of the P3HT polymer. Additionally, we show a new approach for organic solar cell application. BaTiO3 nanoparticles were incorporated as nanodispersion into the donor-acceptor blend or the ferroelectric copolymer poly(vinylidene fluoride trifluoroethylene) (P(VDF-TrFE)) was spincoated as an ultrathin film below the blend. Y1 - 2010 SN - 0420-0195 SP - S. 153 PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Richter, Matthias A1 - Friedrich, Daniel A1 - Philip, Shine A1 - Paloumpa, Ioanna A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - Study of P3HT/PCBM based films by NEXAFS T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft, Reihe 6, Bd. 45 N2 - In this contribution we report on investigations of the electronic structure and composition of regioregular poly(3-hexylthiophene) (P3HT) and phenyl-C61-butyric acid methyl ester (PCBM) based films by using Near Edge X-Ray Absorption Fine Structure (NEXAFS). The measurements were done at the U49/2-PGM2 beam line of BESSY II, Berlin using TEY (total electron yield) and TFY (total fluorescence yield) detection. The samples were produced by spin casting a mixture of P3HT (dissolved in chloroform) and PCBM (dissolved in chlorobenzene) on ITO (indium tin oxide) coated glass slides. Measurements of pure P3HT and PCBM show all typical excitations, whereas the blended system is a weighted superposition of the related peaks. Analyzing these weighted superposition, we observe in the surface sensitive TEY data an accumulation of P3HT, whereas in the bulk sensitive TFY signal an as expected mixture is found. We also show angular dependent NEXAFS measurements of the P3HT/PCBM blend in order to measure the orientation and distribution of the P3HT polymer. Additionally, we will show a new approach for organic solar cell application by introducing ferroelectric nanoparticles into the mixture. Y1 - 2010 UR - http://www.dpg-verhandlungen.de/year/2010/conference/regensburg/part/df/session/7/contribution/4 SN - 0420-0195 SP - S. 194 PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Henkel, Karsten A1 - Seime, Bernd A1 - Paloumpa, Ioanna A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - C(V) and C(t) measurements on MFIS structures consisting P[VDF/TrFE] as ferroelectric layer T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft ; Reihe 6, Bd. 43 N2 - Ferroelectric Field Effect Transistors (FeFETs) are considered as a candidate for future non volatile and non destructive readout memory cells. A possible low cost solution is the use of poly[vinylidene fluoride trifluoroethylene (P[VDF/TrFE]). Using P[VDF/TrFE] we focus on metal ferroelectric insulator semiconductor (MFIS) capacitor structures. In this contribution we will summarize our investigations related to capacitance measurements in dependence of applied bias (C(V)) and time (C(t)). The thickness of the ferroelectric layer as well as the thickness and the material of the buffer layer have been investigated for optimization of the write voltage. CV measurements at higher temperatures deliver decreased flatband voltage shifts within one CV loop resulting in lower memory windows. At temperatures around 100∘C the hysteresis totally vanished, pointing out the ferroelectric behavior of the system. C(t) measurements at a constant bias have been performed for retention analysis of the MFIS stack. After applying a writing pulse we could distinguish between a higher and a lower capacitance state for more than 5 days. This work is supported by Deutsche Forschungsgemeinschaft within priority program 1157 (SCHM 745/11-2). Y1 - 2008 UR - http://www.dpg-verhandlungen.de/year/2008/conference/berlin/part/sysa/session/4/contribution/7 SN - 0420-0195 SP - S. 828 PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Mandal, Dipankar A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - Dipole orientation of the P[VDF-TrFE] co-polymer films: A NEXAFS study T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft ; Reihe 6, Bd. 43 N2 - Ferroelectric properties of copolymers of vinylidene fluoride with trifluoroethylene (P[VDF-TrFE]) has become great deal of interest due to potential use in non volatile memory technology. Permanent dipoles (formed between the alternating hydrogen and fluorine atom within the copolymer) ordering of orientation are crucial for device efficiency. Here we focus on thickness dependence dipole orientation in these co-polymer films. In our systematic studies, we found there is prominent dipole re-orientation effect also for the intrinsic films (~10 nm thickness) before applying the electric field. It is observed after the application of the field, the dipoles re-oriented in opposite direction. Therefore, we conclude that the lowest thickness of the film should have well grown crystalline lamellae structure. As a result, c-axis of crystallites acts as well define manner in plane of the surface and for that reason the b-axis is more free. Because the b-axis is parallel to the polarization direction, it is easy to get a preferred orientation of the dipoles. For thicker films (here up to 100 nm), the average orientation effect is hindered, so a very low re-orientation effect has been observed. For this investigation, we used Near Edge X-ray Absorption Spectroscopy, at the U 49/2-PGM beam line of BESSY-II, Berlin. This work is supported by DFG within SPP1157 (SCHM 745/11-2). Y1 - 2008 UR - http://www.dpg-verhandlungen.de/year/2008/conference/berlin/part/sysa/session/5/contribution/76 SN - 0420-0195 SP - S. 840 PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER -