@misc{HenkelDasKotetal., author = {Henkel, Karsten and Das, Chittaranjan and Kot, Małgorzata and Schmeißer, Dieter and Naumann, Franziska and K{\"a}rkk{\"a}nen, Irina and Gargouri, Hassan}, title = {In-gap states in titanium dioxide and oxynitride atomic layer deposited films}, series = {Journal of Vacuum Science and Technology: A}, volume = {35}, journal = {Journal of Vacuum Science and Technology: A}, number = {1}, issn = {0734-2101}, doi = {10.1116/1.4972247}, pages = {01B135-1 -- 01B135-8}, abstract = {Valence band (VB) spectra of titanium dioxide (TiO2) and oxynitride (TiOxNy) films prepared by different atomic layer deposition (ALD) processes are compared and related to electrical characterization [current-voltage (JV) and capacitance-voltage (CV)] results. By increasing the nitrogen amount in the TiO2 film, band-gap narrowing is observed. The band-gap decrease is related to the contribution of the nitrogen density of states, which induces defects within the band-gap and thus reduces its optical band-gap. In-gap states are found in the VB spectra at 1 eV below the Fermi energy in all investigated ALD samples, i.e., in TiO2 as well as in TiOxNy films. An exponential correlation between leakage current density and in-gap state intensity is derived by the combination of JV measurements and VB spectra, whereas the in-gap states seem to have no influence on hysteresis and fixed oxide charges found in the CV data. It is argued that the in-gap states in TiO2 and TiOxNy have an excitonic or polaronic origin. Both, band-gap narrowing and in-gap state intensity can be tuned by the ALD process selection and the variation of its parameters.}, language = {en} } @inproceedings{GarainAdhikaryMandaletal., author = {Garain, Samiran and Adhikary, Prakriti and Mandal, Dipankar and Sen, Shrabanee and Henkel, Karsten and Schmeißer, Dieter}, title = {Electro-active β-Phase Formation in Poly(vinylidene fluoride) Films by Hydrated Rare earth Metal Salt}, series = {Proceeding of the International Conference on Nanotechnology 2013 (ICNT 2013)}, booktitle = {Proceeding of the International Conference on Nanotechnology 2013 (ICNT 2013)}, publisher = {Institute of Technology, Haldia, WB, India}, address = {Haldia}, isbn = {978-81-927756-0-9}, pages = {S. 127}, abstract = {Polyvinylidene fluoride (PVDF) is a typical fluoro-polymer with complicated polymorphisms due to the semi-crystalline nature. Generally, four crystalline phases, α, β, γ and δ may exist in PVDF crystals. The nonpolar α- and δ-phase has a monoclinic lattice with trans-gauche conformation (TGTG⁄), which is thermodynamically most stable for PVDF. The polar β phase with all-trans (TTTT) planar zigzag conformation is attractive for its piezo-, pyro-, and ferroelectric properties. The polar β-Phase and also semi-polar γ-phase (TTTGTTTG⁄) have obtained wide device applications such as acoustic transducers, piezoelectric sensors, energy harvesting generators, pyroelectric sensors, non-volatile memories and energy storage capacitors. In this work, we explore the possibility to nucleate β-phase in PVDF hydrated salt composite films by addition of the hydrated Rare earth metal salt, (NH4)4 Ce (SO4)4, 2H2O) for the piezo- ferro and high dielectric based device applications. It has been found that the water molecules in (NH4)4 Ce (SO4)4, 2H2O could form hydrogen bonds with PVDF during the crystallization process and the hydrogen bonds promoted the electro-active crystalline β- phase in PVDF with all -trans conformations. In addition, the DMF (solvent used for films preparation) can also assist the rare-earth based nanoparticle preparation, as a result the electrostatic interaction of the surface charge of the nanoparticles and molecular dipoles in PVDF can resist the electroactive β- phase in PVDF.}, language = {en} } @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} } @misc{MenezesIndraDasetal., author = {Menezes, Prashanth W. and Indra, Arindam and Das, Chittaranjan and Walter, Carsten and G{\"o}bel, Caren and Gutkin, Vitaly and Schmeißer, Dieter and Driess, Matthias}, title = {Uncovering the Nature of Active Species of Nickel Phosphide Catalysts in High-Performance Electrochemical Overall Water Splitting}, series = {ACS Catalysis}, volume = {7}, journal = {ACS Catalysis}, number = {1}, issn = {2155-5435}, doi = {10.1021/acscatal.6b02666}, pages = {103 -- 109}, abstract = {A systematic structural elucidation of the near-surface active species of the two remarkably active nickel phosphides Ni12P5 and Ni2P on the basis of extensive analytical, microscopic, and spectroscopic investigations is reported. The latter can serve as complementary efficient electrocatalysts in the hydrogen (HER) versus oxygen evolution reaction (OER) in alkaline media. In the OER Ni12P5 shows enhanced performance over Ni2P due to the higher concentration of nickel in this phase, which enables the formation of an amorphous NiOOH/Ni(OH)2 shell on a modified multiphase with a disordered phosphide/phosphite core. The situation is completely reversed in the HER, where Ni2P displayed a significant improvement in electrocatalytic activity over Ni12P5 owing to a larger concentration of phosphide/phosphate species in the shell. Moreover, the efficiently combined use of the two nickel phosphide phases deposited on nickel foam in overall electrocatalytic water splitting is demonstrated by a strikingly low cell voltage and high stability with pronounced current density, and these catalysts could be an apt choice for applications in commercial alkaline water electrolysis.}, language = {en} } @misc{IndraMenezesDasetal., author = {Indra, Arindam and Menezes, Prashanth W. and Das, Chittaranjan and G{\"o}bel, Caren and Tallarida, Massimo and Schmeißer, Dieter and Driess, Matthias}, title = {A facile corrosion approach to the synthesis of highly active CoOxwater oxidation catalysts}, series = {Journal of Materials Chemistry A}, journal = {Journal of Materials Chemistry A}, number = {5}, issn = {2050-7488}, doi = {10.1039/c6ta10650a}, pages = {5171 -- 5177}, abstract = {Ultra-small rock salt cobalt monoxide (CoO) nanoparticles were synthesized and subjected to partial oxidation ('corrosion') with ceric ammonium nitrate (CAN) to form mixed-valence CoOx(1 < x< 2) water oxidation catalysts. Spectroscopic, microscopic and analytical methods evidenced a structural reformation of cubic CoO to active CoOx with a spinel structure. The superior water oxidation activity of CoOx has been established in electrochemical water oxidation under alkaline conditions. Electrochemical water oxidation with CoOx was recorded at a considerably low overpotential of merely 325 mV at a current density of 10 mA cm-2 in comparison to 370 mV for CoO. Transformation of both octahedral CoII and CoIII sites into amorphous Co(OH)2-CoOOH is the key to high electrochemical activity while the presence of a higher amount of octahedral CoIII sites in CoOx is imperative for an efficient oxygen evolution process.}, language = {en} } @inproceedings{ŁobazaKotSchmeisser, author = {Łobaza, Justyna and Kot, Małgorzata and Schmeißer, Dieter}, title = {Analysis of surface oxidation of TiON ALD films}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, issn = {0420-0195}, pages = {S. 202}, abstract = {Titanium oxynitride (TiON) films are interesting due to their remarkable optical and electronic properties which strongly depend on the O/N ratio. However, it is known that films containing Ti are prone to oxidation in contact with the air [1]. In this work, we study the thickness of a surface oxidation layer which is inherently formed on the atomic layer deposition (ALD) grown TiON/TiN films on Si substrate. We use an Ar+ ion bombardment source and X-ray photoelectron spectroscopy (XPS) for this analysis. We calibrate the sputter rate by using substrate signal intensity decay (here Si 2p) in the XPS spectra of the 5 nm thick TiON sample accordingly. This rate is assumed to be constant when films with a larger thickness are analyzed. We find that the surface oxidation layer is about 1 nm thick, independent on the detailed ALD parameters of the films. The TiN films found underneath are close to the stoichiometric values and have a residual O content below 5\%. Finally, we compare these data to our previous results collected with synchrotron-based radiation source [2,3]. References: [1] Sowinska et al., Applied Physics Letters 100, 233509 (2012). [2] M. Sowinska et al., Applied Surface Science 381, 42-47 (2016). [3] M. Sowińska et al., Journal of Vacuum Science and Tech- nology A, 01A12734 (2016).}, language = {en} } @inproceedings{KotWojciechowskiSnaithetal., author = {Kot, Małgorzata and Wojciechowski, Konrad and Snaith, Henry J. and Schmeißer, Dieter}, title = {Characterization of the perovskite solar cells containing atomic layer deposited Al2O3 buffer layer}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft e.V.}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft e.V.}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, issn = {0420-0195}, pages = {S. 147}, abstract = {Hybrid perovskites have potential to overcome performance limits of the current solar cell technologies and achieve low cost and high versatility. Nonetheless, they are prone to degradation in presence of moisture within a couple of hours or days. In this work, we use the atomic layer deposition (ALD) of Al2O3 on the CH3NH3PbI3 perovskite at room temperature in order to verify if this thin ALD layer may protect the perovskite film against moisture degradation and to check the impact of the Al2O3 on the solar to power conversion efficiency (PCE). Depth profiling X-ray photoelectron spectroscopy study shows that the ALD precursors are chemically active only at the perovskite surface and the film bulk is not affected. The perovskite film coated with Al2O3 layer has enhanced moisture stability. Solar cells with a fresh-made CH3NH3PbI3 perovskite film have shown PCE of 15.4\%, while the one with 50 days aged perovskite only 6.1\%. However, when the aged perovskite is covered with RT-ALD-Al2O3 the PCE value is clearly enhanced.[1] [1] M. Kot et al., Room temperature ALD impact on efficiency, stability and surface properties in perovskite solar cells, ChemSusChem,acctepted.}, language = {en} } @inproceedings{HenkelKotSchmeisser, author = {Henkel, Karsten and Kot, Małgorzata and Schmeißer, Dieter}, title = {Localized defect states and charge trapping in Al₂O₃ films prepared by atomic layer deposition}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, issn = {0420-0195}, pages = {S. 205}, abstract = {The evaluation of the electronic structure and intrinsic defect mechanisms in Al₂O₃ thin films is essential for their effective use in applications with desired functionality such as surface passivation schemes for solar cells [1]. We present a comparative study of different Al₂O₃ films grown by atomic layer deposition (ALD) [2]. The layers were deposited on different substrates using the same aluminum precursor (TMA, trimethylalumium) and employing different process parameters (thermal-ALD, plasma-enhanced-ALD, substrate temperature). These films were characterized by resonant photoelectron spectroscopy and by electrical measurements (capacitance-voltage). For all films investigated intrinsic defect states within the electronic band gap were observed including excitonic, polaronic, and charge-transfer defect states, where their relative abundance is subject of the choice of ALD parameters and of the used substrate. The spectroscopic assigned in-gap defect states are related with electronic charges as determined in the electrical measurements. [1] G. Dingemans and W.M.M. Kessels, J. Vac. Sci. Technol. A 30, 040802 (2012). [2] K. Henkel, M. Kot, D. Schmeißer, J. Vac. Sci. Technol. A 35, (2017), accepted.}, language = {en} } @inproceedings{IsraelRachowSchwiertzetal., author = {Israel, Johannes and Rachow, Fabian and Schwiertz, Carola and Charlafti, Evgenia and M{\"u}ller, Klaus and Schmeißer, Dieter}, title = {Direct CO2-Methanation of flue gas emitted by conventional power plants}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, pages = {S. 255}, abstract = {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.}, language = {en} } @inproceedings{RachowHagendorfMuelleretal., author = {Rachow, Fabian and Hagendorf, Moritz and M{\"u}ller, Klaus and Schmeißer, Dieter}, title = {Synthesis of Methanol from CO2 for Power-to-Liquid applications}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, pages = {S. 256}, abstract = {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.}, language = {en} } @misc{DasKotRouissietal., author = {Das, Chittaranjan and Kot, Małgorzata and Rouissi, Zied and Kędzierski, Kamil and Henkel, Karsten and Schmeißer, Dieter}, title = {Selective Deposition of an ultrathin Pt Layer on a Au-Nanoisland-Modified Si Photocathode for Hydrogen Generation}, series = {ACS Omega}, volume = {2}, journal = {ACS Omega}, number = {4}, issn = {2470-1343}, doi = {10.1021/acsomega.6b00374}, pages = {1360 -- 1366}, abstract = {Platinum, being the most efficient and stable catalyst, is used in photoelectrochemical (PEC) devices. However, a minimal amount of Pt with maximum catalytic activity is required to be used to minimize the cost of production. In this work, we use an environmentally friendly, ost-effective, and less Pt-consuming method to prepare PEC devices for the hydrogen evolution reaction (HER). The Pt monolayer catalyst is selectively deposited on a Au-nanoisland-supported boron-doped p-type Si (100) photocathode. The PEC device based on the Si photocathode with an ultralow loading of the Pt catalyst exhibits a comparable performance for the HER to that of devices with a thick Pt layer. In addition, we demonstrate that by using a thin TiO2 layer deposited by atomic layer deposition photo-oxidation of the Si photocathode can be blocked resulting in a stable PEC performance.}, language = {en} } @misc{KotHenkelDasetal., author = {Kot, Małgorzata and Henkel, Karsten and Das, Chittaranjan and Brizzi, Simone and K{\"a}rkk{\"a}nen, Irina and Schneidewind, Jessica and Naumann, Franziska and Gargouri, Hassan and Schmeißer, Dieter}, title = {Analysis of titanium species in titanium oxynitride films prepared by plasma enhanced atomic layer deposition}, series = {Surface and Coatings Technology}, volume = {324}, journal = {Surface and Coatings Technology}, issn = {0257-8972}, doi = {10.1016/j.surfcoat.2016.11.094}, pages = {586 -- 593}, abstract = {A comparative study of thin titanium oxynitride (TiOxNy) films prepared by plasma enhanced atomic layer deposition using tetrakis(dimethylamino)titanium (TDMAT) and N2 plasma as well as titanium(IV)isopropoxide and NH3 plasma is reported. The comparison is based on the combination of Ti2p core level and valence band spectroscopy and current-voltage measurements. The TDMAT/N2 process delivers generally higher fractions of TiN and TiON within the Ti2p spectra of the films and stronger photoemissions within the bandgap as resolved in detail by high energy resolution synchrotron-based spectroscopy. In particular, it is shown that higher TiN contributions and in-gap emission intensities correlate strongly with increased leakage currents within the films and might be modified by the process parameters and precursor selection.}, language = {en} } @misc{IndraMenezesDasetal., author = {Indra, Arindam and Menezes, Prashanth W. and Das, Chittaranjan and Schmeißer, Dieter and Driess, Matthias}, title = {Alkaline electrochemical water oxidation with multi-shelled cobalt manganese oxide hollow spheres}, series = {Chemical Communications}, volume = {53}, journal = {Chemical Communications}, number = {62}, issn = {1359-7345}, doi = {10.1039/C7CC03566G}, pages = {8641 -- 8644}, abstract = {Multi-shelled hollow spheres of cobalt manganese oxides (CMOs) deposited on Ni foam exhibited superior alkaline electrochemical water oxidation activity and surpassed those of bulk CMO and commercial noble metal-based catalysts. A higher amount of cobalt in the spinel structure resulted in the transformation of the tetragonal to the cubic phase with a decrease in the overpotential of oxygen evolution.}, language = {en} } @misc{BiswasHenkelSchmeisseretal., author = {Biswas, Anirban and Henkel, Karsten and Schmeißer, Dieter and Mandal, Dipankar}, title = {Comparison of the thermal stability of the α, β and γ phases in poly(vinylidene fluoride) based on in situ thermal Fourier transform infrared spectroscopy}, series = {Phase Transitions}, volume = {90}, journal = {Phase Transitions}, number = {12}, issn = {0141-1594}, doi = {10.1080/01411594.2017.1337902}, pages = {1205 -- 1213}, abstract = {The electroactive β phase of poly(vinylidenefluoride) (PVDF) is induced due to the aging time of PVDF solutions. The feasibility of the combination of the three crystalline polymorphs (α, β and γ) is demonstrated where their relative proportion within the PVDF film can be tailored by the simple monitoring of the preparation conditions. To identify all these phases, Fourier transform infrared (FT-IR) spectroscopy is carried out and it is spotlighted that the vibrational bands at 510 and 841 cm-1 are not sufficient to state the formation of the β phase. The main aim of this work is devoted to develop a better understanding on the thermal stability of these several phases of PVDF, which has a longstanding ambiguity persisting in this area. It has been found that the in situ thermal FT-IR spectroscopy is one of the best alternatives to understand this important issue. It is ascertained that the β phase is the least thermally stable phase among α, β and γ phases, whereas the γ phase is the most thermally stable phase.}, language = {en} } @misc{CibrevTallaridaDasetal., author = {Cibrev, Dejan and Tallarida, Massimo and Das, Chittaranjan and Lana-Villarreal, Teresa and Schmeißer, Dieter and Gómez, Roberto}, title = {New insights into water photooxidation on reductively pretreated hematite photoanodes}, series = {Physical Chemistry Chemical Physics}, volume = {19}, journal = {Physical Chemistry Chemical Physics}, number = {32}, issn = {1463-9076}, doi = {10.1039/C7CP03958A}, pages = {21807 -- 21817}, abstract = {It has been recently demonstrated that the photoactivity toward oxygen evolution of a number of n-type metal oxides can be substantially improved by a reductive electrochemical pretreatment. Such an enhancement has been primarily linked to the formation of low valent metal species that increase electrode conductivity. In this work, we report new insights into the electrochemical doping using highly ordered (110)-oriented hematite nanorods directly grown on FTO. The reductive pretreatment consists in applying negative potentials for a controlled period of time. Such a pretreatment was optimized in both potentiostatic and potentiodynamic regimes. We show that the optimized pretreatment enhances electrode conductivity due to an increase in charge carrier density. However, it additionally triggers changes in the morphologic, catalytic and electronic properties that facilitate the separation and collection of the photogenerated charge carriers causing an up to 8-fold enhancement in the photocurrent for water oxidation. The reductive pretreatment can be considered as a highly controllable electrochemical n-type doping with the amount of generated Fe2+/polaron species and the change in film morphology as the main factors determining the final efficiency for water photooxidation of the resulting electrodes.}, language = {en} } @misc{KotDasHenkeletal., author = {Kot, Małgorzata and Das, Chittaranjan and Henkel, Karsten and Wojciechowski, Konrad and Snaith, Henry J. and Schmeißer, Dieter}, title = {Room temperature atomic layer deposited Al₂O₃ on CH₃NH₃PbI₃ characterized by synchrotron-based X-ray photoelectron spectroscopy}, series = {Nuclear Instruments and Methods in Physics Research B}, volume = {411}, journal = {Nuclear Instruments and Methods in Physics Research B}, issn = {0168-583X}, doi = {10.1016/j.nimb.2017.01.082}, pages = {49 -- 52}, abstract = {An ultrathin Al₂O₃ film deposited on methylammonium lead triiodide (CH₃NH₃PbI₃) perovskite has the capability to suppress the carrier recombination process and improve the perovskite solar cells efficiency and stability. However, annealing at temperatures higher than 85°C degrades the CH₃NH₃PbI₃ perovskite film. The X-ray photoelectron spectroscopy study performed in this work indicates that it is possible to grow Al₂O₃ by atomic layer deposition on the perovskite at room temperature, however, besides pure Al₂O₃ some OH groups are found and the creation of lead and iodine oxides at the Al₂O₃/CH₃NH₃PbI₃ interface takes place.}, language = {en} } @misc{SchmeisserJanowitz, author = {Schmeißer, Dieter and Janowitz, Christoph}, title = {Two polarization dependent Auger decays observed by resonant photoelectron spectroscopy at the Cu2p-edge of superconducting BiSrCu-oxides}, series = {Nuclear Instruments and Methods in Physics Research B}, volume = {411}, journal = {Nuclear Instruments and Methods in Physics Research B}, issn = {0168-583X}, doi = {10.1016/j.nimb.2017.01.084}, pages = {53 -- 56}, abstract = {We report on a resonant photoemission (resPES) study of PbxBi2-xSr2-yLayCan-1CunO2n+4+d (BISCO) single crystals to unravel the resonant decay mechanisms at the Cu2p absorption edge. The resPES studies on superconducting BISCO are performed at Bessy U49/2. We investigated BISCO single crystals with different hole doping concentrations at temperatures between 300 K and 17 K. CuO films have been used as a reference. We focus on the resPES data recorded at the Cu2p absorption edge. We find a strong polarization dependence for in-plane and out-of-plane geometries (with respect to the Cu-O plane) in our data which are caused by two independent Auger processes. We also report on the influence of different doping concentrations. Our resPES data enable us to sort the individual resonant mechanisms at the Cu2p edge in more detail than recently anticipated (Brookes et al., 2015). We discuss our data in the context of the recent discussion about the applicability of the Zhang-Rice model (Chen et al., 2013).}, language = {en} } @misc{MuellerBaerHenkeletal., author = {M{\"u}ller, Klaus and B{\"a}r, Werner and Henkel, Karsten and Jahnke, Agnes and Schwiertz, Carola and Schmeißer, Dieter}, title = {Organische Feldeffekttransistoren als Transducer in der Biosensorik}, series = {Technisches Messen}, volume = {70}, journal = {Technisches Messen}, number = {12}, issn = {0171-8096}, doi = {10.1524/teme.70.12.565.20261}, pages = {565 -- 568}, abstract = {In diesem Beitrag wird der Einsatz neuartiger Sensortypen f{\"u}r die medizinische Diagnostik beschrieben. Diese Sensoren sollen komplett organisch sein und auf dem Prinzip des Feldeffekttransistors basieren. Als Modellsystem f{\"u}r die Anwendung in der Biosensorik soll die Einsatzm{\"o}glichkeit dieser Sensoren in der nicht-invasiven Diagnostik der Helicobacter-pylori-Infektion {\"u}berpr{\"u}ft werden.}, language = {de} } @misc{MuellerRachowIsraeletal., author = {M{\"u}ller, Klaus and Rachow, Fabian and Israel, Johannes and Charlafti, Evgenia and Schwiertz, Carola and Schmeißer, Dieter}, title = {Direct Methanation of Flue Gas at a Lignite Power Plant}, series = {International Journal of Environmental Science}, journal = {International Journal of Environmental Science}, number = {2}, issn = {2367-8941}, pages = {425 -- 437}, abstract = {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.}, language = {en} } @misc{KotŁobazaNaumannetal., author = {Kot, Małgorzata and Łobaza, Justyna and Naumann, Franziska and Gargouri, Hassan and Henkel, Karsten and Schmeißer, Dieter}, title = {Long-term ambient surface oxidation of titanium oxynitride films prepared by plasma-enhanced atomic layer deposition: An XPS study}, series = {Journal of Vacuum Science and Technology A}, volume = {36}, journal = {Journal of Vacuum Science and Technology A}, number = {1}, issn = {0734-2101}, doi = {10.1116/1.5003356}, abstract = {The surface oxidation of a titanium oxynitride (TiOxNy) film after long-time storage of 25 month in ambient conditions is investigated. The TiOxNy film is prepared by plasma-enhanced atomic layer deposition using etrakis(dimethylamino)titanium and nitrogen plasma, and the film is characterized by Ar+ ion sputtering of the film surface in combination with x-ray photoelectron spectroscopy (XPS) as well as by angle-resolved XPS. The total thickness of an oxygen-enriched layer at the surface of the TiOxNy films is found to be about 0.7 nm and it consists of a sequence of a 0.4 nm thick TiON/TiO2 enriched layer followed by a 0.3 nm thick TiO2 enriched layer underneath compared to the bulk composition of the film which shows constant values of 29\% TiN, 29\% TiO2, and 42\% TiON. The results suggest that the TiON enrichment takes place initially at the surface followed by a surface and subsurface oxidation.}, language = {en} }