TY - JOUR A1 - Al-Falahat, A.M. A1 - Kupsch, Andreas A1 - Hentschel, M.P. A1 - Lange, A. A1 - Kardjilov, N. A1 - Markötter, Henning A1 - Manke, I. T1 - Correction approach of detector backlighting in radiography N2 - In various kinds of radiography, deficient transmission imaging may occur due to backlighting inside the detector itself arising from light or radiation scattering. The related intensity mismatches barely disturb the high resolution contrast, but its long range nature results in reduced attenuation levels which are often disregarded. Based on X-ray observations and an empirical formalism, a procedure is developed for a first order correction of detector backlighting. A backlighting factor is modeled as a function of the relative detector coverage by the sample projection. Different cases of sample transmission are regarded at different backlight factors and detector coverage. The additional intensity of backlighting may strongly affect the values of materials’ attenuation up to a few 10%. The presented scenario provides a comfortable procedure for corrections of X-ray or neutron transmission imaging data. KW - X-ray imaging KW - Neutron imaging KW - Radiology KW - Backlighting KW - Digital detector array PY - 2019 DO - https://doi.org/10.1063/1.5097170 SN - 0034-6748 VL - 90 IS - 12 SP - 125108 PB - American Institute of Physics CY - Melville, NY, USA AN - OPUS4-50217 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Alrwashdeh, S. S. A1 - Markötter, H. A1 - Haußmann, J. A1 - Hilger, A. A1 - Klages, M. A1 - Müller, Bernd R. A1 - Kupsch, Andreas A1 - Riesemeier, Heinrich A1 - Scholta, J. A1 - Manke, I. T1 - Investigation of water transport in newly developed micro porous layers for polymer electrolyte membrane fuel cells N2 - In this investigation, synchrotron X-ray imaging was used to investigate the water distribution inside newly developed gas diffusion media in polymer electrolyte membrane fuel cells. In-situ radiography was used to reveal the relationship between the structure of the microporous layer (MPL) and the water flow in a newly developed MPL equipped with randomly arranged holes. A strong influence of these holes on the overall water transport was found. This contribution provides a brief overview to some of our recent activities on this research field. KW - Polymer electrolyte membrane fuel cell KW - Microporous layer KW - Water distribution KW - Radiography KW - Synchrotron X-ray imaging PY - 2017 DO - https://doi.org/10.9729/AM.2017.47.3.101 SN - 2287-4445 SN - 2287-5123 VL - 47 IS - 3 SP - 101 EP - 104 AN - OPUS4-43356 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Arlt, T. A1 - Kardjilov, N. A1 - Kupsch, Andreas A1 - Manke, I. A1 - Salvemini, F. A1 - Grazzi, F. T1 - Neutronen-Laminografie am Beispiel eines historischen Artefakts T1 - Neutron computed laminography on an ancient metal artifact N2 - Die Computer-gestützte Laminografie (CL) wurde als komplementäre Methode zur Computertomografie für die dreidimensionale Bildgebung von lateral ausgedehnten Objekten entwickelt. Ursprünglich für medizinische Zwecke verwendet, wurde diese Methode kürzlich als zerstörungsfreie nicht-invasive Methode nicht nur in der Materialforschung, sondern auch mit steigendem Interesse für kunsthandwerkliche und historische Objekte eingesetzt. Hier wird die Computer-gestützten Laminografie mit polychromatischer Neutronenstrahlung an einer historischen Tsuba eingesetzt, einem Stichblatt eines japanischen Schwerts. Eine Analyse der Lötstellen gibt Rückschlüsse auf das Herstellungsverfahren. Zudem wurden unterschiedliche Materialsysteme gefunden, vermutlich um dem Tsuba lokal eine höhere Stabilität zu verleihen. Die Messungen wurden an der Imaging-Beamline CONRAD-2 an der Neutronenquelle BER 2 des Helmholtz-Zentrums Berlins (HZB) durchgeführt. KW - Neutronenlaminographie KW - Computertomographie PY - 2018 DO - https://doi.org/10.3139/120.111261 SN - 0025-5300 VL - 60 IS - 12 SP - 1209 EP - 1214 PB - Carl Hanser Verlag CY - München AN - OPUS4-46936 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Arlt, Tobias A1 - Grothausmann, R. A1 - Manke, I. A1 - Markötter, H. A1 - Hilger, A. A1 - Kardjilov, N. A1 - Tötzke, C. A1 - Banhart, J. A1 - Kupsch, Andreas A1 - Lange, Axel A1 - Hentschel, Manfred P. A1 - Krüger, P. A1 - Haußmann, J. A1 - Hartnig, C. A1 - Wippermann, K. T1 - Tomografische Methoden für die Brennstoffzellenforschung N2 - Aufgrund des hohen Wirkungsgrades und der vielfältigen Einsatzmöglichkeiten können Brennstoffzellen einen wichtigen Beitrag zur zukünftigen Energieversorgung leisten. Für die Optimierung der Brennstoffzellentechnik ist es erforderlich, die während des Zellbetriebs ablaufenden Prozesse zu verstehen und exakt zu charakterisieren. Ein ausbalanciertes Wassermanagement ist die Grundlage für die optimale Leistungsfähigkeit einer wasserstoffbetriebenen Zelle. Das während des Betriebs entstehende Wasser muss die Membran ausreichend befeuchten, um deren Protonenleitfähigkeit aufrechtzuerhalten. Andererseits behindern zu große Wasseransammlungen in der Zelle die Gaszufuhr durch die porösen Materialien sowie in den Kanälen der Gasverteilerstrukturen. Alterungsphänomene einzelner Zellkomponenten können die Verteilung der Wasseransammlungen und somit das Wassermanagement empfindlich stören und so die Leistungsfähigkeit der Brennstoffzelle herabsetzen. Zur Analyse der Wasserverteilung werden zerstörungsfreie, bildgebende Methoden, wie die Ex-situ-Neutronentomografie und die In-situ-Synchrotronradiografie, eingesetzt. Diese Methoden können während des Brennstoffzellenbetriebs mit weiteren Messverfahren, beispielsweise der ortsaufgelösten Stromdichtemessung, kombiniert werden. Auf diese Weise werden einzelne Komponenten, wie zum Beispiel die Gasdiffusionsschichten, charakterisiert. KW - Computertomographie KW - Elektronentomographie KW - Neutronentomographie KW - Brennstoffzelle KW - Stromdichtemessung KW - Wassermanagement PY - 2013 DO - https://doi.org/10.3139/120.110429 SN - 0025-5300 VL - 55 IS - 3 SP - 207 EP - 213 PB - Hanser CY - München AN - OPUS4-27950 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Arlt, Tobias A1 - Grothausmann, R. A1 - Manke, I. A1 - Markötter, H. A1 - Krüger, P. A1 - Haussmann, J. A1 - Hilger, A. A1 - Kardjilov, N. A1 - Hartnig, C. A1 - Kupsch, Andreas A1 - Lange, Axel A1 - Hentschel, Manfred P. A1 - Wippermann, K. A1 - Banhart, J. T1 - Tomografische Methoden für die Brennstoffzellenforschung N2 - Auf Grund des hohen Wirkungsgrades und der vielfältigen Einsatzmöglichkeiten stellen Brennstoffzellen sowie Brennstoffzellenverbünde eine vielversprechende Energiequelle dar. Daher ist es wichtig, die Prozesse während des Betriebs einer Brennstoffzelle exakt charakterisieren zu können, um diese im nächsten Schritt zu optimieren. So ist ein ausbalanciertes Wassermanagement in einer mit Wasserstoff betriebenen Zelle ausschlaggebend für ihre Leistungsfähigkeit. Für eine dauerhafte Leistungsfähigkeit muss das entstehende Wasser die Membran feucht halten, um so die Protonenleitfähigkeit aufrecht zu erhalten. Zu viel Wasser kann jedoch die Gaszufuhr durch die porösen Materialien in Richtung Membran verhindern. Alterungsphänomene der einzelnen Komponenten können dieses sensible Wassermanagement stören und so die Leistungsfähigkeit einer Brennstoffzelle herabsetzen. Zum tieferen Verständnis der Wasserverteilung werden zerstörungsfreie Methoden, wie zum Beispiel die ex situ Neutronentomografie oder die in situ Synchrotronradiografie eingesetzt. Letztere Methode kann während des Brennstoffzellenbetriebs in Kombination mit weiteren Messmethoden, wie der ortsaufgelösten Stromdichtemessung, eingesetzt werden. So können einzelne Brennstoffzellenkomponenten, wie die Gasdiffusionsschichten, charakterisiert werden. T2 - DGZfP-Jahrestagung 2011 CY - Bremen, Germany DA - 30.05.2011 KW - Computer-Tomographie KW - Rekonstruktionsalgorithmen KW - Röntgen-Kanten-Tomographie KW - Neutronen-Tomographie KW - Elektronen-Tomographie PY - 2011 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-250023 SN - 978-3-940283-33-7 IS - DGZfP-BB 127 (P7) SP - 1 EP - 8 PB - Deutsche Gesellschaft für Zerstörungsfreie Prüfung (DGZfP) AN - OPUS4-25002 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Arlt, Tobias A1 - Klages, M. A1 - Messerschmidt, M. A1 - Riesemeier, Heinrich A1 - Scholta, J. A1 - Banhart, J. A1 - Manke, I. T1 - Influence of artificial aging of gas diffusion layers on the water management of PEM fuel cells N2 - The influence of artificial aging of gas diffusion layers (GDL) on the water management within the GDL was investigated in-operando by synchrotron X-ray radiography. One GDL was subjected to an accelerated aging procedure in 30% H2O2 solution, while another GDL was pristine. Radiographic measurements were combined with temporally resolved electrical analyzes. Significant differences in cell voltage and water accumulation were observed during cell operation at steady-state conditions. The cell which contained the aged GDL featured a higher water amount especially at the anode side and a lower cell voltage. KW - Degradation KW - Liquid water PY - 2014 DO - https://doi.org/10.1149/2.004402eel SN - 2162-8726 VL - 3 IS - 2 SP - F7 EP - F9 PB - ECS CY - Pennington, NJ, USA AN - OPUS4-32410 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Arlt, Tobias A1 - Manke, I. A1 - Wippermann, K. A1 - Riesemeier, Heinrich A1 - Mergel, J. A1 - Banhart, J. T1 - Investigation of the local catalyst distribution in an aged direct methanol fuel cell MEA by means of differential synchrotron X-ray absorption edge imaging with high energy resolution N2 - Synchrotron X-ray absorption edge imaging with high energy resolution was applied to study aging of fuel cell catalyst materials. The combination of an imaging and a high X-ray energy resolution set-up allows acquiring spatially resolved XAS (XANES and EXAFS) spectra. We analyzed the two-dimensional distribution of Pt and Ru in fresh and aged fuel cell catalysts. Spatially resolved XAS images were taken at the RuK edge and at the PtL3 edge. Taking radiographs above and below the absorption edges provides quantitative information about the thickness of the catalytic materials and additional chemical information. A strong influence of the flow field channels and the structure of the gas diffusion layers on the thicknesses of the catalytic elements were found: a thinner catalyst layer was found below the ribs of the flow field geometries as well as under crossing points of fiber bundles of the woven gas diffusion layers. KW - XAS KW - X-ray energy edge KW - Membrane electrode assembly KW - Direct methanol fuel cell KW - Aging mechanism KW - X-ray synchrotron radiography PY - 2013 DO - https://doi.org/10.1016/j.jpowsour.2012.08.038 SN - 0378-7753 VL - 221 SP - 210 EP - 216 PB - Elsevier CY - Amsterdam [u.a.] AN - OPUS4-27372 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Arlt, Tobias A1 - Manke, I. A1 - Wippermann, K. A1 - Schröder, A. A1 - Mergel, J. A1 - Riesemeier, Heinrich A1 - Banhart, J. T1 - Röntgen-Kanten-Tomografie und -Radiografie zur Untersuchung von Alterungseffekten in Brennstoffzellenmaterialien KW - Resolution neutron-radiography KW - Local current distribution KW - Water transport KW - Carbon-dioxide KW - Methanol KW - Platinum KW - Oxidation PY - 2010 SN - 0025-5300 VL - 52 IS - 10 SP - 692 EP - 697 PB - Hanser CY - München AN - OPUS4-23045 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Arlt, Tobias A1 - Manke, I. A1 - Wippermann, K. A1 - Tötzke, C. A1 - Markötter, H. A1 - Riesemeier, Heinrich A1 - Mergel, J. A1 - Banhart, J. T1 - Investigation of the three-dimensional ruthenium distribution in fresh and aged membrane electrode assemblies with synchrotron X-ray absorption edge tomography N2 - Synchrotron X-ray absorption edge imaging was used to investigate the ruthenium distribution in both fresh and aged Pt/Ru-based membrane electrode assemblies (MEA) of direct methanol fuel cells. MEAs aged in different ways were analyzed: artificially aged by MeOH depletion and aged for 1700 h in an operating fuel cell stack. An element sensitive tomographic technique – differential X-ray absorption edge tomography – was applied allowing for a 3D-visualization of the ruthenium distribution within the MEA. We found a markedly changed Ru distribution after aging which is correlated to the GDL structure, the flow field geometry, and CO2 transport in the methanol solution. KW - Edge tomography KW - Ruthenium distribution KW - Direct methanol fuel cells KW - Synchrotron X-ray KW - PtRu corrosion PY - 2011 DO - https://doi.org/10.1016/j.elecom.2011.05.013 SN - 1388-2481 VL - 13 IS - 8 SP - 826 EP - 829 PB - Elsevier B.V. CY - Amsterdam AN - OPUS4-25243 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bevilacqua, N. A1 - Asset, T. A1 - Schmid, M. A. A1 - Markötter, Henning A1 - Manke, I. A1 - Atanassov, P. A1 - Zeis, R. T1 - Impact of catalyst layer morphology on the operation of high temperature PEM fuel cells N2 - Electrochemical impedance spectroscopy (EIS) is a well-established method to analyze a polymer electrolyte membrane fuel cell (PEMFC). However, without further data processing, the impedance spectrum yields only qualitative insight into the mechanism and individual contribution of transport, kinetics, and ohmic losses to the overall fuel cell limitations. The distribution of relaxation times (DRT) method allows quantifying each of these polarization losses and evaluates their contribution to a given electrocatalyst's depreciated performances. We coupled this method with a detailed morphology study to investigate the impact of the 3D-structure on the processes occurring inside a high-temperature polymer electrolyte membrane fuel cell (HT-PEMFC). We tested a platinum catalyst (Pt/C), a platinum-cobalt alloy catalyst (Pt3Co/C), and a platinum group metal-free iron-nitrogen-carbon (Fe–N–C) catalyst. We found that the hampered mass transport in the latter is mainly responsible for its low performance in the MEA (along with its decreased intrinsic performances for the ORR reaction). The better performance of the alloy catalyst can be explained by both improved mass transport and a lower ORR resistance. Furthermore, single-cell tests show that the catalyst layer morphology influences the distribution of phosphoric acid during conditioning. KW - High-temperature polymer electrolyte membrane fuel cell KW - Platinum-free catalyst KW - Mass transport KW - Oxygen reduction reaction KW - Distribution of relaxation times analysis PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-520917 DO - https://doi.org/10.1016/j.powera.2020.100042 VL - 7 SP - 100042 PB - Elsevier Ltd. AN - OPUS4-52091 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dabah, Eitan A1 - Pfretzschner, Beate A1 - Schaupp, Thomas A1 - Kardjilov, N. A1 - Manke, I. A1 - Boin, M. A1 - Woracek, R. A1 - Griesche, Axel T1 - Time-resolved Bragg-edge neutron radiography for observing martensitic phase transformation from austenitized super martensitic steel N2 - Neutron Bragg-edge imaging was applied for the visualization of a γ-Austenite to α'-martensite phase transformation. In the present study, a super martensitic stainless steel sample was heated until complete austenitization and was subsequently cooled down to room temperature. The martensitic phase Transformation started at Ms = 190 °C. Using a monochromatic neutron beam with λ = 0.390 nm, the transmitted intensity was significantly reduced during cooling below Ms, since the emerging martensitic phase has a higher attenuation coefficient than the austenitic phase at this wavelength. The phase Transformation process was visualized by filming the transmission images from a scintillator screen with a CCD camera with a temporal resolution of 30 s and a spatial resolution of 100 µm. KW - Neutron imaging KW - Bragg-edge imaging KW - Phase transformation PY - 2017 DO - https://doi.org/10.1007/s10853-016-0642-9 SN - 0022-2461 SN - 1573-4803 VL - 52 IS - 6 SP - 3490 EP - 3496 AN - OPUS4-38574 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Duan, K. A1 - Zhu, L. A1 - Li, M. A1 - Xiao, L. A1 - Bevilacqua, N. A1 - Eifert, L. A1 - Manke, I. A1 - Markötter, Henning A1 - Zhang, R. A1 - Zeis, R. A1 - Sui, P. -C. T1 - Multiphase and Pore Scale Modeling on Catalyst Layer of High-Temperature Polymer Electrolyte Membrane Fuel Cell N2 - Phosphoric acid as the electrolyte in high-temperature polymer electrolyte membrane fuel cell plays an essential role in ist performance and lifetime. Maldistribution of phosphoric acid in the catalyst layer (CL) may result in performance degradation. In the present study, pore-scale simulations were carried out to investigate phosphoric acid’s multiphase flow in a cathode CL. A reconstructed CL model was built using focused ion beam-SEM images, where distributions of pore, carbon support, binder, and catalyst particles can be identified. The multi-relaxation time lattice Boltzmann method was employed to simulate phosphoric Acid invading and leaching from the membrane into the CL during the membrane electrode assembly fabrication process. The predicted redistribution of phosphoric acid indicates that phosphoric acid of low viscosity or low wettability is prone to leaching into the CL. The effective transport properties and the active electrochemical active surface area (ECSA) were computed using a pore-scale model. They were subsequently used in a macroscopic model to evaluate the cell performance. A parametric study shows that cell performance first increases with increasing phosphoric acid content due to the increase of ECSA. However, further increasing phosphoric acid content results in performance degradation due to mass transfer limitation caused by acid flooding. KW - Gas diffusion layers KW - Lattice Boltzmann simulation KW - Electrochemical impedance spectra KW - Phosphoric acid KW - HT-PEFC PY - 2021 DO - https://doi.org/10.1149/1945-7111/abff03 VL - 168 IS - 5 SP - 054521 PB - IOP Science AN - OPUS4-53836 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Griesche, Axel A1 - Dabah, Eitan A1 - Hilger, A. A1 - Kardjilov, N. A1 - Manke, I. A1 - Kannengießer, Thomas T1 - Neutron imaging of hydrogen in steels T2 - Materials Science & Technology (MS&T) 2013 CY - Montreal, Quebec, Canada DA - 2013-10-27 KW - Neutron radiography KW - Hydrogen KW - Diffusion KW - Steel PY - 2013 SP - 945 EP - 950 PB - Curran CY - Red Hook, NY AN - OPUS4-29506 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Griesche, Axel A1 - Dabah, Eitan A1 - Kannengießer, Thomas A1 - Hilger, A. A1 - Kardjilov, N. A1 - Manke, I. A1 - Schillinger, B. T1 - Measuring hydrogen distributions in iron and steel using neutrons N2 - Neutron tomography has been applied to investigate the mechanism of hydrogen assisted cracking in technical iron and supermartensitic steel. Rectangular technical iron block samples showed blistering due to intense hydrogen charging and the tomographic method revealed in situ the spatial distribution of hydrogen and cracks. Hydrogen accumulated in a small region around cracks and the cracks are filled with hydrogen gas. Cracks close to the surface contained no hydrogen. Hydrogenous tensile test samples of supermartensitic steel were pulled until rupture and showed hydrogen accumulations at the notch base and in the plastically deformed region around the fracture surface. T2 - 10th World Conference on Neutron Radiography (WCNR) CY - Grindelwald, Switzerland DA - 05.10.2014 PY - 2015 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-348022 DO - https://doi.org/10.1016/j.phpro.2015.07.062 SN - 1875-3892 VL - 69 SP - 445 EP - 450 PB - Elsevier B.V. CY - Amsterdam AN - OPUS4-34802 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Griesche, Axel A1 - Dabah, Eitan A1 - Kannengießer, Thomas A1 - Kardjilov, N. A1 - Hilger, A. A1 - Manke, I. T1 - Three-dimensional imaging of hydrogen blister in iron with neutron tomography N2 - We investigated hydrogen embrittlement and blistering in electrochemically hydrogen-charged technical iron samples at room temperature. Hydrogen-stimulated cracks and blisters and the corresponding hydrogen distributions were observed by neutron tomography. Cold neutrons were provided by the research reactor BER II to picture the sample with a spatial resolution in the reconstructed three-dimensional model of ~25 µm. We made the unique observation that cracks were filled with molecular hydrogen and that cracks were surrounded by a 50 µm wide zone with a high hydrogen concentration. The zone contains up to ten times more hydrogen than the bulk material. The hydrogen enriched zone can be ascribed to a region of increased local defect density. Hydrogen also accumulated at the sample surface having the highest concentration at blistered areas. The surfaces of the brittle fractured cracks showed micropores visualized by scanning electron microscopy. The micropores were located at grain boundaries and were surrounded by stress fields detected by electron backscattered diffraction. The cracks clearly originated from the micropores. KW - Hydrogen embrittlement KW - Hydrogen diffusion KW - In situ KW - Neutron tomography KW - Iron PY - 2014 DO - https://doi.org/10.1016/j.actamat.2014.06.034 SN - 1359-6454 SN - 1873-2453 VL - 78 SP - 14 EP - 22 PB - Elsevier Science CY - Kidlington AN - OPUS4-31068 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Griesche, Axel A1 - Dabah, Eitan A1 - Kardjilov, N. A1 - Hilger, A. A1 - Manke, I. A1 - Kannengießer, Thomas T1 - Imaging of hydrogen in steels using neutrons N2 - We investigated the hydrogen distribution spatially and temporally in technical iron at room temperature. Samples were charged electrochemically and subsequently analysed by means of neutron radiography and tomography. The radiographic images allowed for a time-resolved analysis of hydrogen fluxes. The three-dimensional distribution of hydrogen measured by neutron tomography delivered valuable information for the damage analysis of hydrogen-induced cracks. For the first time hydrogen concentration gradients inside the material could be detect directly together with the cracks. The neutron radiography and tomography results were gained at the Research Reactor BER II of the HZB in Berlin. KW - Hydrogen embrittlement KW - Hydrogen diffusion KW - Neutron tomography KW - Blister PY - 2014 DO - https://doi.org/10.3139/146.111043 SN - 1862-5282 VL - 105 IS - 7 SP - 640 EP - 644 PB - Carl Hanser CY - München AN - OPUS4-31084 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Grothausmann, R. A1 - Manke, I. A1 - Zehl, G. A1 - Dorbandt, I. A1 - Bogdanoff, P. A1 - Fiechter, S. A1 - Hentschel, Manfred P. A1 - Lange, Axel A1 - Kupsch, Andreas A1 - Hilger, A. T1 - Charakterisierung von Katalysatormaterialien für Brennstoffzellen mittels Elektronentomografie N2 - Zur Optimierung moderner Katalysatoren für Brennstoffzellen werden diese elektronen-tomografisch charakterisiert. Die Elektronentomografie ermöglicht einzigartige Einblicke in die Nanometer-Strukturen der metallischen Katalysatorpartikel, die auf einem elektrisch leitenden, inerten Kohlenstoffträger abgeschieden werden. Die dreidimensional bildgebende Methode ermöglicht über qualitative Untersuchungen hinaus detaillierte quantitative Form- und Strukturanalysen der Katalysatormaterialien. So werden beispielsweise die Positionen der Katalysatorpartikel relativ zum Trägermaterial analysiert. Ihre Form und Einbettung in den Träger, welche die für die katalytische Reaktion maßgebliche "freie Oberfläche" definieren, werden bestimmt. Die Elektronentomografie ermöglicht somit quantitative Vergleiche zwischen verschiedenen Katalysatormaterialien und Herstellungsverfahren. Sie erweitert die Möglichkeiten der Korrelation gewünschter elektrochemischer Eigenschaften mit der Nanostruktur dieser Materialien und macht so weitere Optimierungen der Katalysatormaterialien möglich. KW - Computed tomography KW - Reconstruction algorithm KW - Electron tomography KW - Catalyst KW - Fuel cell PY - 2010 SN - 0025-5300 VL - 52 IS - 10 SP - 706 EP - 711 PB - Hanser CY - München AN - OPUS4-22072 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Grothausmann, R. A1 - Zehl, G. A1 - Manke, I. A1 - Fiechter, S. A1 - Bogdanoff, P. A1 - Dorbandt, I. A1 - Kupsch, Andreas A1 - Lange, Axel A1 - Hentschel, Manfred P. A1 - Schumacher, G. A1 - Banhart, J. T1 - Dreidimensionale Charakterisierung von Katalysatornanopartikeln N2 - We present transmission electron microscope (TEM) tomography investigations of ruthenium-based fuel cell catalyst materials as employed in direct methanol fuel cells (DMFC). The digital three-dimensional representation of the samples not only enables detailed studies on number, size, and shape but also on the local orientation of the ruthenium particles to their support and their freely accessible surface area. The shape analysis shows the ruthenium particles deviate significantly from spherical symmetry which increases their surface to volume ratio. The morphological studies help to understand the structure formation mechanisms during the fabrication as well as the high effectiveness of these catalysts in the oxygen reduction reaction at the cathode side of fuel cells. KW - Radiography KW - Tomography KW - Neutrons KW - Polymer electrolyte membrane fuel cell (PEMFC) KW - Fuel cell stack PY - 2012 SN - 1862-5282 VL - 103 IS - 1 SP - 135 EP - 136 PB - Carl Hanser CY - München AN - OPUS4-25976 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Grothausmann, R. A1 - Zehl, G. A1 - Manke, I. A1 - Fiechter, S. A1 - Bogdanoff, P. A1 - Dorbandt, I. A1 - Kupsch, Andreas A1 - Lange, Axel A1 - Hentschel, Manfred P. A1 - Schumacher, G. A1 - Banhart, J. T1 - Nanometer-Tomographie: kleinste Katalysatorteilchen erblicken - Mit Elektronen und Computern die mobile Brennstoffzelle erforschen KW - Electron tomography KW - Polymer electrolyte membrane fuel cell (PEMFC) KW - Reconstruction algorithm KW - DIRECTT PY - 2012 DO - https://doi.org/10.1002/maco.201290007 SN - 0947-5117 SN - 1521-4176 VL - 63 IS - 2 SP - 1 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-26348 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Grothausmann, R. A1 - Zehl, G. A1 - Manke, I. A1 - Fiechter, S. A1 - Bogdanoff, P. A1 - Dorbandt, I. A1 - Kupsch, Andreas A1 - Lange, Axel A1 - Hentschel, Manfred P. A1 - Schumacher, G. A1 - Banhart, J. T1 - Quantitative structural assessment of heterogeneous catalysts by electron tomography N2 - We present transmission electron microscope (TEM) tomography investigations of ruthenium-based fuel cell catalyst materials as employed in direct methanol fuel cells (DMFC). The digital three-dimensional representation of the samples not only enables detailed studies on number, size, and shape but also on the local orientation of the ruthenium particles to their support and their freely accessible surface area. The shape analysis shows the ruthenium particles deviate significantly from spherical symmetry which increases their surface to volume ratio. The morphological studies help to understand the structure formation mechanisms during the fabrication as well as the high effectiveness of these catalysts in the oxygen reduction reaction at the cathode side of fuel cells. KW - Electron tomography KW - Reconstruction algorithm KW - Catalyst KW - Fuel cell PY - 2011 DO - https://doi.org/10.1021/ja2032508 SN - 0002-7863 SN - 1520-5126 VL - 133 IS - 45 SP - 18161 EP - 18171 PB - American Chemical Society CY - Washington, DC AN - OPUS4-24833 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -