TY - JOUR A1 - Dietrich, Paul M. A1 - Glamsch, Stephan A1 - Ehlert, Christopher A1 - Lippitz, Andreas A1 - Kulak, Nora A1 - Unger, Wolfgang E. S. T1 - Synchrotron-radiation XPS analysis of ultra-thin silane films: Specifying the organic silicon JF - Applied surface science : a journal devoted to applied physics and chemistry of surfaces and interfaces N2 - The analysis of chemical and elemental in-depth variations in ultra-thin organic layers with thicknesses below 5 nm is very challenging. Energy- and angle-resolved XPS (ER/AR-XPS) opens up the possibility for non-destructive chemical ultra-shallow depth profiling of the outermost surface layer of ultra-thin organic films due to its exceptional surface sensitivity. For common organic materials a reliable chemical in-depth analysis with a lower limit of the XPS information depth z(95) of about 1 nm can be performed. As a proof-of-principle example with relevance for industrial applications the ER/AR-XPS analysis of different organic monolayers made of amino- or benzamidosilane molecules on silicon oxide surfaces is presented. It is demonstrated how to use the Si 2p core-level region to non-destructively depth-profile the organic (silane monolayer) - inorganic (SiO2/Si) interface and how to quantify Si species, ranging from elemental silicon over native silicon oxide to the silane itself. The main advantage of the applied ER/AR-XPS method is the improved specification of organic from inorganic silicon components in Si 2p core-level spectra with exceptional low uncertainties compared to conventional laboratory XPS. (C) 2015 Elsevier B.V. All rights reserved. KW - Synchrotron radiation XPS KW - Depth profiling KW - Silanes KW - Monolayer KW - Amines KW - Amides Y1 - 2016 U6 - https://doi.org/10.1016/j.apsusc.2015.12.052 SN - 0169-4332 SN - 1873-5584 VL - 363 SP - 406 EP - 411 PB - Elsevier CY - Amsterdam ER - TY - JOUR A1 - Dietrich, Paul M. A1 - Streeck, Cornelia A1 - Glamsch, Stephan A1 - Ehlert, Christopher A1 - Lippitz, Andreas A1 - Nutsch, Andreas A1 - Kulak, Nora A1 - Beckhoff, Burkhard A1 - Unger, W. E. S. T1 - Quantification of Silane Molecules on Oxidized Silicon: Are there Options for a Traceable and Absolute Determination? JF - Analytical chemistry N2 - Organosilanes are used routinely to functionalize various support materials for further modifications. Nevertheless, reliable quantitative information about surface functional group densities after layer formation is rarely available. Here, we present the analysis of thin organic nanolayers made from nitrogen containing silane molecules on naturally oxidized silicon wafers with reference-free total reflection X-ray fluorescence (TXR.F) and X-ray photoelectron spectroscopy (XPS). An areic density of 2-4 silane molecules per nm(2) was calculated from the layer's nitrogen mass deposition per area unit obtained by reference-free TXRF. Complementary energy and angle-resolved XPS (ER/AR-XPS) in the Si 2p core-level region was used to analyze the outermost surface region of the organic (silane layer)-inorganic (silicon wafer) interface. Different coexisting silicon species as silicon, native silicon oxide, and silane were identified and quantified. As a result of the presented proof-of-concept, absolute and traceable values for the areic density of silanes containing nitrogen as intrinsic marker are obtained by calibration of the XPS methods with reference-free TXRF. Furthermore, ER/AR-XPS is shown to facilitate the determination of areic densities in (mono)layers made from silanes having no heteroatomic marker other than silicon. After calibration with reference-free TXRF, these areic densities of silane molecules can be determined when using the XPS component intensity of the silane's silicon atom. Y1 - 2015 U6 - https://doi.org/10.1021/acs.analchem.5b02846 SN - 0003-2700 SN - 1520-6882 VL - 87 IS - 19 SP - 10117 EP - 10124 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Sheen, Susanne Fienhold A1 - Sander, Björn A1 - Eibisch, Frank A1 - Koch, Nicole A1 - Telschow, Stephan A1 - Schwuchow, Franka A1 - Dietrich, Ralf A1 - Laflör, Anja T1 - Portal alumni T2 - Das Ehemaligen-Magazin der Universität Potsdam N2 - Liebe Leserin,lieber Leser,das sind doch gute Nachrichten: Ein Studienabschluss schafft nach einer aktuellen Studie des Hochschul-Informations-Systems (HIS) in Hannover nach wie vor die besten Chancen auf einen Arbeitsplatz. Die Arbeitslosenquote von Akademikern pendelt sich ein halbes Jahr nach dem Examen bei fünf Prozent ein. Bei Absolventen einer Lehre liegt sie dagegen doppelt so hoch. Doch auch für Akademiker ist der Einstieg ins Berufsleben kein Selbstläufer mehr. Mit nichts als eingleisigem Fachwissen als Kapital haben es auch Akademiker inzwischen schwer, denn der Arbeitsmarkt hat sich in den letzten Jahren stark verändert. Welche Veränderungen das sind und wie man am besten darauf reagiert, beleuchtet die Rubrik "wissenstransfer". Das man an der Universität Potsdarn mehr als reines Fachwissen erwerben kann, zeigen die Berichte der Alumni über ihren Berufsweg in der Rubrik "umbrüche". Von geradlinigen Entwicklungen ist da zu lesen, von enttäuschten Erwartungen und ergriffenen Chancen. Sie dokumentieren, wie Brüche im beruflichen Werdegang zwar manchen vom geplanten Weg abkommen ließen, doch auf den persönlich richtigen Pfad fuhrten. Wer sich gerade in der Phase der beruflichen Neuorientierung befindet, oder gerade erst ins Arbeitsleben startet, findet Tipps und Adressen im "wegweiser". Die Redaktion wünscht Ihnen viel Vergnügen beim Lesen von Portal alumni. Mit den besten Grüßen, Ihr Alumni-Team. N2 - Dear reader, these are good news indeed: Following a survey ofthe Hochschul-lnformations-System(HIS) in Hannover an university degree is still the best guarantee for getting a Job. The rate of unemployment among those with an university grand is about five percent. For those who finished an apprenticeship it is twice as high. But also for university graduates just knowing scientific facts is not enough for starting a career, because the Job market has changed over the last few years. What kind of changes these are and what is the best way to react is shown at the chapter "wissenstransfer". That one can not only attain exclusive specialised knowledge is shown at the chapter "umbrüche" where alumni describing their career. They talk about straight ways, disappointed expectations and taken chances. They show how they found their way despite changes in their career. Those who are lookingfor a new Job or Just started their professionallife can find addresses and tips under "wegweiser". The editorial staffhope you will enjoy reading Portal alumni. T3 - Portal alumni : das Ehemaligen-Magazin der Universität Potsdam - 2/2004 Y1 - 2004 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-481140 N1 - Aus urheberrechtlichen Gründen wurde die Onlineveröffentlichung des Hefts zurückgezogen. VL - 2004 IS - 2 EP - 58 ER - TY - JOUR A1 - Patel, Dhananjay I. A1 - Noack, Sebastian A1 - Vacogne, Charlotte D. A1 - Schlaad, Helmut A1 - Bahr, Stephan A1 - Dietrich, Paul A1 - Meyer, Michael A1 - Thissen, Andreas A1 - Linford, Matthew R. T1 - Poly(L-lactic acid), by near-ambient pressure XPS JF - Surface Science Spectra N2 - Near ambient pressure - x-ray photoelectron spectroscopy (NAP-XPS) is a less traditional form of XPS that allows samples to be analyzed at relatively high pressures, i.e., at 2500Pa or higher. With NAP-XPS, one can analyze moderately volatile liquids, biological samples, porous materials, and/or polymeric materials that outgas significantly. In this submission we show C 1s, O 1s, and survey NAP-XPS spectra from poly(L-lactic acid). The C 1s and O 1s envelopes were fit with three and two Gaussian-Lorentzian sum functions, respectively. Water vapor (800Pa) was used as the residual gas for charge compensation, which was confirmed by the sharp peak at 535.0 eV in the O 1s narrow scan. The uniqueness plot corresponding to the C 1s fit shows that the fit parameters had statistical significance. C 1s and O 1s spectra of PLLA damaged by exposure to x-rays for ca. 1 hour are also included. Published by the AVS. KW - near-ambient pressure X-ray photoelectron spectroscopy KW - NAP-XPS KW - XPS KW - Water Vapor Y1 - 2019 U6 - https://doi.org/10.1116/1.5110309 SN - 1055-5269 SN - 1520-8575 VL - 26 IS - 2 PB - American Institute of Physics CY - Melville ER - TY - JOUR A1 - Jain, Varun A1 - Wheeler, Joshua J. A1 - Ess, Daniel H. A1 - Noack, Sebastian A1 - Vacogne, Charlotte D. A1 - Schlaad, Helmut A1 - Bahr, Stephan A1 - Dietrich, Paul A1 - Meyer, Michael A1 - Thissen, Andreas A1 - Linford, Matthew R. T1 - Poly(gamma-benzyl l-glutamate), by near-ambient pressure XPS JF - Surface science spectra : SSS : an international journal & database devoted to archiving spectra from surfaces & interfaces N2 - Near-ambient pressure x-ray photoelectron spectroscopy (NAP-XPS) is a less traditional form of XPS that allows samples to be analyzed at relatively high pressures, i. e., at greater than 2500 Pa. In this study, poly(.- benzyl L- glutamate) (PBLG) with a molar mass of 11.3 kg/mol was analyzed by NAP-XPS; here, we show the survey, C 1s, N 1s, and O 1s narrow scans of PBLG. The C 1s peak envelope was fitted in three different ways, to five, six, or seven synthetic peaks. In each fit, there was also a shake-up signal. The O 1s narrow scan was well fit with three peaks: CZO and CvO in a 1:2 ratio from the polymer, and a higher energy signal from water vapor. Hartree-Fock orbital energies of a model monomer served as a guide to an additional fit of the C 1s envelope. KW - near-ambient pressure x-ray photoelectron spectroscopy KW - NAP-XPS KW - XPS KW - polymer KW - poly(gamma-benzyl L-glutamate) KW - PBLG Y1 - 2019 U6 - https://doi.org/10.1116/1.5109121 SN - 1055-5269 SN - 1520-8575 VL - 26 IS - 2 PB - American Institute of Physics CY - Melville ER - TY - JOUR A1 - Sirocko, Frank A1 - Dietrich, Stephan A1 - Veres, Daniel A1 - Grootes, Pieter M. A1 - Schaber-Mohr, Katja A1 - Seelos, Klemens A1 - Nadeau, Marie-Josee A1 - Kromer, Bernd A1 - Rothacker, Leo A1 - Roehner, Marieke A1 - Krbetschek, Matthias A1 - Appleby, Peter G. A1 - Hambach, Ulrich A1 - Rolf, Christian A1 - Sudo, Masafumi A1 - Grim, Stephanie T1 - Multi-proxy dating of Holocene maar lakes and Pleistocene dry maar sediments in the Eifel, Germany JF - Quaternary science reviews : the international multidisciplinary research and review journal N2 - During the last twelve years the ELSA Project (Eifel Laminated Sediment Archive) at Mainz University has drilled a total of about 52 cores from 27 maar lakes and filled-in maar basins in the Eifel/Germany. Dating has been completed for the Holocene cores using 6 different methods (Pb-210 and Cs-137 activities, palynostratigraphy, event markers, varve counting, C-14) In general, the different methods consistently complement one another within error margins. Event correlation was used for relating typical lithological changes with historically known events such as the two major Holocene flood events at 1342 AD and ca 800 BC. Dating of MIS2-MIS3 core sections is based on greyscale tuning, radiocarbon and OSL dating, magnetostratigraphy and tephrochronology. The lithological changes in the sediment cores demonstrate a sequence of events similar to the North Atlantic rapid climate variability of the Last Glacial Cycle. The warmest of the MIS3 interstadials was GI14, when a forest with abundant spruce covered the Eifel area from 55 to 48 ka BP, i.e. during a time when also other climate archives in Europe suggested very warm conditions. The forest of this "Early Stage 3 warm phase" developed subsequently into a steppe with scattered birch and pine, and finally into a glacial desert at around 25 ka BP. Evidence for Mono Lake and Laschamp geomagnetic excursions is found in two long cores. Several large eruptions during Middle and Late Pleistocene (Ulmener Maar - 11,000 varve years BP, Laacher See - 12,900 varve years BP, Mosenberg volcanoes/Meerfelder Maar 41-45 cal ka BP, Dumpel Maar 116 ka BP, Glees Maar - 151 ka BP) produced distinct ash-layers crucial for inter-core and inter-site correlations. The oldest investigated maar of the Eifel is Ar-40/Ar-39 dated to the time older than 520 ka BP. KW - Eifel maar KW - Laminated lake sediments KW - Tuning KW - Historical events KW - C-14-derived chronology KW - Varve counting KW - Luminescence dating KW - Palynostratigraphy KW - (CS)-C-137 and Pb-210 dating KW - Palaeomagnetism KW - Tephrostratigraphy KW - Argon-Argon dating KW - GIS Y1 - 2013 U6 - https://doi.org/10.1016/j.quascirev.2012.09.011 SN - 0277-3791 VL - 62 SP - 56 EP - 76 PB - Elsevier CY - Oxford ER - TY - JOUR A1 - Bormann, Helge A1 - de Brito, Mariana Madruga A1 - Charchousi, Despoina A1 - Chatzistratis, Dimitris A1 - David, Amrei A1 - Grosser, Paula Farina A1 - Kebschull, Jenny A1 - Konis, Alexandros A1 - Koutalakis, Paschalis A1 - Korali, Alkistis A1 - Krauzig, Naomi A1 - Meier, Jessica A1 - Meliadou, Varvara A1 - Meinhardt, Markus A1 - Munnelly, Kieran A1 - Stephan, Christiane A1 - de Vos, Leon Frederik A1 - Dietrich, Jörg A1 - Tzoraki, Ourania T1 - Impact of Hydrological Modellers’ Decisions and Attitude on the Performance of a Calibrated Conceptual Catchment Model BT - Results from a ‘Modelling Contest’ JF - Hydrology N2 - In this study, 17 hydrologists with different experience in hydrological modelling applied the same conceptual catchment model (HBV) to a Greek catchment, using identical data and model code. Calibration was performed manually. Subsequently, the modellers were asked for their experience, their calibration strategy, and whether they enjoyed the exercise. The exercise revealed that there is considerable modellers’ uncertainty even among the experienced modellers. It seemed to be equally important whether the modellers followed a good calibration strategy, and whether they enjoyed modelling. The exercise confirmed previous studies about the benefit of model ensembles: Different combinations of the simulation results (median, mean) outperformed the individual model simulations, while filtering the simulations even improved the quality of the model ensembles. Modellers’ experience, decisions, and attitude, therefore, have an impact on the hydrological model application and should be considered as part of hydrological modelling uncertainty. Y1 - 2018 U6 - https://doi.org/10.3390/hydrology5040064 SN - 2306-5338 VL - 5 IS - 4 PB - MDPI CY - Basel ER - TY - JOUR A1 - Chaurasia, Swami Vivekanandji A1 - Dietrich, Tim A1 - Rosswog, Stephan T1 - Black hole-neutron star simulations with the BAM code BT - first tests and simulations JF - Physical review : D, Particles, fields, gravitation, and cosmology N2 - The first detections of black hole-neutron star mergers (GW200105 and GW200115) by the LIGO-Virgo-Kagra Collaboration mark a significant scientific breakthrough. The physical interpretation of pre- and postmerger signals requires careful cross-examination between observational and theoretical modelling results. Here we present the first set of black hole-neutron star simulations that were obtained with the numerical-relativity code BAM. Our initial data are constructed using the public LORENE spectral library, which employs an excision of the black hole interior. BAM, in contrast, uses the moving-puncture gauge for the evolution. Therefore, we need to "stuff" the black hole interior with smooth initial data to evolve the binary system in time. This procedure introduces constraint violations such that the constraint damping properties of the evolution system are essential to increase the accuracy of the simulation and in particular to reduce spurious center-of-mass drifts. Within BAM we evolve the Z4c equations and we compare our gravitational-wave results with those of the SXS collaboration and results obtained with the SACRA code. While we find generally good agreement with the reference solutions and phase differences less than or similar to 0.5 rad at the moment of merger, the absence of a clean convergence order in our simulations does not allow for a proper error quantification. We finally present a set of different initial conditions to explore how the merger of black hole neutron star systems depends on the involved masses, spins, and equations of state. Y1 - 2021 U6 - https://doi.org/10.1103/PhysRevD.104.084010 SN - 2470-0010 SN - 2470-0029 VL - 104 IS - 8 PB - American Physical Society CY - Ridge, NY ER -