TY - JOUR A1 - Heitz, J. A1 - Plamadeala, C. A1 - Muck, M. A1 - Habidzadeh, H. A1 - Baumgartner, W. A1 - Weth, A. A1 - Steinwender, C. A1 - Blessberger, H. A1 - Kellermair, J. A1 - Kirner, Sabrina V. A1 - Krüger, Jörg A1 - Bonse, Jörn A1 - Guntner, A. S. A1 - Hassel, A. W. T1 - Laser-induced microstructures on Ti substrates for reduced cell adhesion N2 - The abstract summarizes the poster presented at the "Kardiologie im Zentrum - Fortbildung der Klinik für Kardiologie und Intensivmedizin Kepler Universitätsklinikum Linz", held between October 20th and 31st in Linz, Austria. The poster has been awarded the 2nd place of the "Best Poster Award". T2 - Kardiologie im Zentrum - Fortbildung der Klinik für Kardiologie und Intensivmedizin Kepler Universitätsklinikum Linz CY - Linz, Austria DA - 20.10.2017 KW - Femtosecond laser processing KW - Titanium alloy KW - Cell adhesion KW - Pacemaker PY - 2017 UR - http://www.kup.at/kup/pdf/14098.pdf SN - 1024-0098 VL - 24 IS - 11-12 SP - 292 EP - 292 PB - Krause & Pachernegg GmbH CY - Gablitz, Austria AN - OPUS4-43160 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krüger, Jörg A1 - Kautek, Wolfgang A1 - Niino, H. T1 - Biomaterial immobilization on polyurethane films by XeCl excimer laser processing N2 - Zusammenfassung The surface chemical modification of polyurethane (PU) films was performed by an UV laser-induced chemical reaction in a polysaccharide solution. This process may be applicable as hydrophilic packaging of implantable medical devices and in vivo sensors. When a PU film in contact with an aqueous alginic acid (AAC) solution was irradiated with a XeCl laser, the PU film turned hydrophilic. Contact angles of water on the film were reduced from 110° to 60°. Since light absorption of the AAC solution at 308 nm was negligibly small, reactive sites were generated solely on the PU surface. There, AAC could be immobilized by chemical bonds thus allowing for a nanometer-scaled grafting of this biomolecule. The mechanism was investigated by surface analyses with Fourier-transform infrared spectroscopy (FT-IR), dye staining, ultraviolet-visible (UV-VIS) spectroscopy, and scanning electron microscopy (SEM) techniques. A one-photon photochemical process could beidentified. PY - 2001 DO - https://doi.org/10.1007/s003390000617 SN - 0947-8396 VL - 72 IS - 1 SP - 53 EP - 57 PB - Springer CY - Berlin AN - OPUS4-926 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Shaik, A.-A. A1 - Richter, M. A1 - Kricheldorf, H. A1 - Krüger, Ralph-Peter T1 - New polymer syntheses - CIX. Biodegradable, alternating copolyesters of terephthalic acid, aliphatic dicarboxylic acids, and alkane diols N2 - Copolyesters with an alternating sequence of terephthalic acid and aliphatic dicarboxylic acids were prepared with three different methods. First, dicarboxylic acid dichlorides were reacted with bis(2-hydroxyethyl)terephthalate (BHET) in refluxing 1,2-dichlorobenzene. Second, the same monomers were polycondensed at 0-20 °C in the presence of pyridine. Third, dicarboxylic acid dichlorides and silylated BHET were polycondensed in bulk. Only this third method gave satisfactory molecular weights. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry revealed that the copolyesters prepared by the pyridine and silyl methods might have contained considerable fractions of cyclic oligoesters and polyesters despite the absence of transesterification and backbiting processes. The alternating sequences and thermal properties were characterized with 1H NMR spectroscopy and differential scanning calorimetry measurements, respectively. In agreement with the alternating sequence, all copolyesters proved to be crystalline, but the crystallization was extremely slow [slower than that of poly(ethylene terephthalate)]. A second series of alternating copolyesters was prepared by the polycondensation of silylated bis(4-hydroxybut- yl)terephthalate with various aliphatic dicarboxylic acid dichlorides. The resulting copolyesters showed significantly higher rates of crystallization, and the melting temperatures were higher than those of the BHET-based copolyesters. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 3371-3382, 2001 KW - Poly(ethylene terephthalate) KW - Poly(butylene terephthalate) KW - Alternating sequence KW - Macrocycles KW - Crystallization KW - Biodegradable polyesters PY - 2001 DO - https://doi.org/10.1002/pola.1320 SN - 0360-6376 SN - 0887-624X VL - 39 IS - 19 SP - 3371 EP - 3382 PB - Wiley CY - Hoboken, NJ AN - OPUS4-2173 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bünger, H. A1 - Krüger, Ralph-Peter A1 - Pietschmann, S. A1 - Wüstneck, N. A1 - Kaufner, L. A1 - Tschiersch, R. A1 - Pison, U. T1 - Two hydrophobic protein fractions of ovine pulmonary surfactant: Isolation, characterisation and biophysical activity N2 - Pulmonary surfactant contains two extremely hydrophobic proteins, SP-B and SP-C. We present a novel HPLC method for the preparation of these hydrophobic proteins. It is based on size-exclusion chromatography using the apolar stationary-phase butyl silica gel and isocratic elution with acidified chloroform/methanol. Samples for HPLC were prepared from sheep lung lavage fluid by centrifugation and extraction with chloroform/methanol. Amino acid analyses of the two protein fractions revealed sequences that are consistent with SP-B and SP-C, respectively. MALDI-TOF-MS analyses of the SP-B fraction showed one major peak of dimeric SP-B with m/z 17,361, and additional peaks of monomeric and oligomeric forms, which are predominantly even numbered. The SP-C fraction showed a peak at m/z 4200, consistent with the theoretical mass of the dipalmitoylated form of this protein. The biophysical activity of pure sheep SP-B and SP-C was evaluated by measuring the surface tension using axisymmetric drop shape analysis for captive bubbles. We found distinct surface pressure versus surface area isotherms of SP-B and SP-C indicating different biophysical activities for these surfactant proteins. The new preparative HPLC method is able to replace the established, time-consuming low-pressure liquid chromatography method for the isolation of SP-B and SP-C from lipids. KW - Surfactant proteins KW - SP-B KW - SP-C KW - Preparative HPLC KW - MALDI-TOF-MS KW - Surface pressure KW - Captive bubble PY - 2001 DO - https://doi.org/10.1006/prep.2001.1510 SN - 1046-5928 SN - 1096-0279 VL - 23 IS - 2 SP - 319 EP - 327 PB - Elsevier CY - Amsterdam AN - OPUS4-2174 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H. A1 - Hauser, K. A1 - Krüger, Ralph-Peter A1 - Schulz, Günter T1 - Macrocycles 12. Ring-Opening Polycondensations of Tin-Containing Macrocycles with Bis(Thioarylester)s N2 - 2,2-Dibutyl-2-stanna-1,3-dioxepane (DSDOP) was polycondensed with bis(4-chlorothiophenyl) suberat under various reaction conditions, but only moderate molecular weights (Mn 10000) were obtained. The MALDI-TOF mass spectrosmetry revealed the formation of cyclic oligo- and polyesters in addition to linear species having OH, CO2H, and unreacted 4-chlorothiophenyl ester endgroups. Furthermore, -Caprolactone (-CL) was polymerized with DSDOP as the initiator at monomer/initiator (M/I) ratios of 20 and 50. The resulting tin-containing macrocyclic polylactones were reacted with sebacic acid bis(4-thiocresyl)ester at three different temperatures and with different reaction times. Analogous polycondensations were conducted with suberic acid bis(4-chlorothiophenyl) ester. The presence of thioarylester endgroups in the isolated polyesters was checked by 1H NMR spectroscopy. The highest conversions were found at long reaction times (24 or 72 hours), or after the addition of pyridine and N,N-dimethylaminopyridine as catalysts. Despite high conversions, the number average molecular weights (Mn's) did not exceed values around 20000. Even in the samples having the highest molecular weights, unreacted 4-chlorothiophenylester endgroups were detected by GPC measurements evaluated with a UV-detector. It is concluded that both factors, cyclization and incomplete conversion, contribute to the limitation of the chain growth. KW - Ring-Opening Polycondensations KW - Macrocycles KW - Polyesters PY - 2000 DO - https://doi.org/10.1081/MA-100101099 SN - 1060-1325 SN - 1520-5738 VL - 37 IS - 4 SP - 379 EP - 394 PB - Taylor & Francis CY - Philadelphia, PA AN - OPUS4-2167 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H. A1 - Probst, N. A1 - Schwarz, G. A1 - Schulz, Günter A1 - Krüger, Ralph-Peter T1 - New Polymer Syntheses - 107. Aliphatic Poly(thio ester)s by Ring-Opening Polycondensation of 2-Stanna-1,3-Dithiacycloalkanes N2 - We prepared 2,2-dibutyl-2-stanna-1,3-dithiacycloalkanes from dibutyltin oxide and ,-dimercaptoalkanes. Heterocycles with five-, six-, seven-, or nine-ring members were used as bifunctional monomers for polycondensations with aliphatic dicarboxylic acid chlorides. These polycondensations conducted in bulk were highly exothermic and yielded poly(thio ester)s with number average molecular weights (Mn's) in the range of 5000-30,000 Da. These poly(thio ester)s proved to be rapidly crystallizing materials with melting temperatures in the range of 90-150 °C. In addition to the success of the new synthetic approach, two interesting and unpredictable results were obtained. All volatile species detectable by matrix assisted laser desorption induced-time of flight (MALDI-TOF) mass spectrometry were cyclic oligo- and poly(thio ester)s. Second, several polyesters showed a reversible first-order change of the crystal modification as identified by differential scanning calorimetry measurements and X-ray scattering with variation of the temperature. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 3656-3664, 2000 KW - Poly(thio-ester)s KW - Ring-opening polycondensation KW - Macrocycles KW - Change of crystal structure PY - 2000 DO - https://doi.org/10.1002/1099-0518(20001001)38:19<3656::AID-POLA190>3.0.CO;2-M SN - 0360-6376 SN - 0887-624X VL - 38 IS - 19 SP - 3656 EP - 3664 PB - Wiley CY - Hoboken, NJ AN - OPUS4-2170 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter A1 - Frey, H. T1 - Characterization of unusual Silsesquioxane-Based Polymer Architectures Based on the Coupling of Liquid Chromatography and MALDI-TOF-MS T2 - 11th International Symposium on Organosilicon Chemistry CY - Montpellier, France DA - 1996-09-01 PY - 1996 CY - Montpellier AN - OPUS4-2222 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Kautek, Wolfgang A1 - Hertwig, Andreas A1 - Martin, Sven A1 - Krüger, Jörg A1 - Lenzner, Matthias A1 - Spielmann, C. A1 - Lenner, M. A1 - Bunte, J. A1 - Puester, T. A1 - Burmester, T. A1 - Fiedler, A. A1 - Heberer, E. A1 - Brose, M. A1 - Stingl, A. A1 - Kiehl, P. A1 - Hönigsmann, H. A1 - Trautinger, F. A1 - Grabner, G. T1 - Safety in Femtosecond Laser Technology - Recent Results of a European Research Project (406) T2 - International Laser Safety Conference 2003 ; ILSC 2003 CY - Jacksonville, FL, USA DA - 2003-03-10 PY - 2003 SN - 0-912035-38-2 SP - 1(?) EP - 10(?) PB - Laser Institute of America CY - Orlando, Fla. AN - OPUS4-2259 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bünger, H. A1 - Pison, U. A1 - Krüger, Ralph-Peter ED - Yeung, E. T1 - Separation of hydrophobic pulmonary surfactant proteins using preparative HPLC with UV detection T2 - 24th International Symposium on High Performance Liquid Phase Separations and Related Techniques ; 24th HPLC 2000 CY - Seattle, WA, USA DA - 2000-06-24 PY - 2000 SN - 0021-9673 PB - Elsevier CY - Amsterdam AN - OPUS4-2249 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hoebbel, D. A1 - Weber, Ch. A1 - Schmidt, H. A1 - Krüger, Ralph-Peter T1 - Synthesis and Properties of Perfluoroalkyl Groups Containing Double Four-Ring Spherosilicate (Siloxysilsesquioxane) Precursors N2 - Organically modified cage-like double four-ring spherosilicates have received considerable interest in the construction of nanosized hybrid materials, as well as building units for structural well-defined polymers. This group is extended by perfluoroalkyl ligands containing spherosilicates, synthesized by addition reaction of the octahydridodimethylsiloxyoctasilsesquioxane [H(CH3)2Si]8Si8O20 and heptadecafluorodecyl methacrylate. The resultant liquid spherosilicate substituted with eight terminal perfluoroalkyl groups was characterized by 29Si and 13C NMR spectroscopies and MALDI Time-of-Flight mass spectrometry. Partial substitution of perfluoroalkyl ligands by trimethoxysilyl containing groups provides condensable precursors for the synthesis of hydrophobic and oleophobic materials via the sol-gel process. This new spherosilicate, carrying on average four perfluoroalkyl groups and four trimethoxysilyl groups shows better hydrophobic and oleophobic properties compared with commonly used perfluoroalkyltrialkoxysilanes under identical concentration of perfluoroalkyl chains. In addition a comprehensive literature survey is given on structural well characterized, organically modified cage-like double four-ring spherosilicates. KW - Spherosilicate KW - Siloxysilsesquioxane KW - Perfluoralkylalkoxysilane KW - 29Si NMR KW - Coatings KW - Hydrophobicity PY - 2002 DO - https://doi.org/10.1023/A:1015239707783 SN - 0928-0707 SN - 1573-4846 VL - 24 SP - 121 EP - 129 PB - Kluwer Academic Publ. CY - Dordrecht AN - OPUS4-1658 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krüger, Jörg A1 - Kautek, Wolfgang A1 - Newesely, H. T1 - Femtosecond-pulse laser ablation of dental hydroxyapatite and single-crystalline fluoroapatite N2 - Laser microdrilling of healthy human enamel and dentine using 300 fs pulses at a wavelength of 615 nm and 3 Hz repetition rate leads to an enhanced structuring quality in comparison with nanosecond-laser results. Microcracking and damage to neighboring tissue can be reduced. Ablation threshold fluences for 100 laser pulses of 0.3 J cm-2 (human dentine), 0.6 J cm-2 (human enamel) and 0.8 J cm-2 (single crystalline fluoroapatite) could be determined. Ablation depths per pulse below 1 7m were observed. T2 - 5th International Conference on Laser Ablation ; COLA '99 CY - Göttingen, Germany DA - 1999-07-19 PY - 1999 DO - https://doi.org/10.1007/s003390051426 SN - 0947-8396 VL - 69 IS - 7 SP - S403 EP - S407 PB - Springer CY - Berlin AN - OPUS4-779 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Frübing, P. A1 - Krüger, H. A1 - Goering, Harald A1 - Gerhard-Multhaupt, R. T1 - Relaxation behaviour of thermoplastic polyurethanes with covalently attached nitroaniline dipoles N2 - Thermoplastic polyurethanes with covalently attached nitroaniline chromophores exhibit a strong high-temperature relaxation associated with a glass transition rather than the typical frequency-independent loss due to the aggregation of polymer chains via hydrogen bonds. This relaxation behaviour suggests the formation of an amorphous structure without separation into soft-segment and hard-segment phases. In such a structure, a field-induced orientation of molecular dipoles is stabilised by the high viscosity of the material below its glass transition. The dipole orientation yields a pyroelectric effect caused by dipole-density changes upon thermal expansion and contraction. The changes in phase separation are investigated by varying the chain length of the soft-phase component and studying its influence on the calorimetric, dynamic-mechanical, and dielectrical properties. Good correlation was found between differential scanning calorimetry, dynamic-mechanical analysis and dielectric spectroscopy as well as measured and calculated pyroelectric coefficients. This leads to a uniform picture of the structural changes caused by the incorporation of nitroaniline chromophores into the polyurethane structure. KW - Thermoplastic polyurethane KW - Nitroaniline chromophore KW - Dielectric relaxation PY - 2002 DO - https://doi.org/10.1016/S0032-3861(02)00075-7 SN - 0032-3861 SN - 1873-2291 VL - 43 IS - 9 SP - 2787 EP - 2794 PB - Springer CY - Berlin AN - OPUS4-2062 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Sonnenschein, H. A1 - Kreher, T. A1 - Gründemann, E. A1 - Krüger, Ralph-Peter A1 - Kunath, A. A1 - Zabel, V. T1 - Novel Redox-Active Cyclophanes Based on 3,3'-Bisindolizines - Synthesis and Chirality PY - 1996 SN - 0022-3263 SN - 1520-6904 VL - 61 SP - 710 EP - 714 PB - American Chemical Society CY - Washington, DC AN - OPUS4-2147 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Simone A1 - Goering, Harald A1 - Stark, Wolfgang A1 - Bayerl, H. A1 - Brinkmann, P. T1 - Thermoanalytische Untersuchungen zur Phenolharzhärtung unter hohem Druck - Ein Weg zur Optimierung der Nachtemperung T2 - 3rd International Thermoset Conference CY - Iserlohn, Deutschland DA - 2005-04-21 KW - Post curing KW - High pressure DSC KW - DMA KW - Reaction kinetic KW - Phenolic resin PY - 2005 SP - 107 EP - 114 PB - Fachhochschule Südwestfalen - Hochschule für Technik und Wirtschaft CY - Iserlohn AN - OPUS4-7452 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Simone A1 - Goering, Harald A1 - Stark, Wolfgang A1 - Bayerl, H. A1 - Brinkmann, P. T1 - Thermo Analytical Investigations of Phenol Moulding Compound Curing - Potential for Post-Cure Optimisation T2 - 3rd International Thermoset Conference CY - Iserlohn, Germany DA - 2005-04-21 KW - Post curing KW - High pressure DSC KW - DMA KW - Reaction kinetic KW - Phenolic resin PY - 2005 SP - 219 EP - 225 PB - Fachhochschule Südwestfalen - Hochschule für Technik und Wirtschaft CY - Iserlohn AN - OPUS4-7453 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H. A1 - Chatti, S. A1 - Schwarz, G. A1 - Krüger, Ralph-Peter T1 - Macrocycles 27 - Cyclic Aliphatic Polyesters of Isosorbide N2 - Numerous polycondensations of isosorbide and suberoyl chloride or other aliphatic dicarboxylic acid dichlorides were performed with pyridine as a catalyst and HCl acceptor. The reaction conditions were varied to optimize both the molecular weight and the fraction of cyclic oligo- and polyesters. Furthermore, we attempted to obtain the cyclic monomer by catalyzed back-biting degradation of the molten cyclic polyesters above 220 °C in vacuo. The polyesters were characterized by viscosity and size exclusion chromatographic measurements as well as matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. In selected cases, mixtures of linear and cyclic polyesters were treated with a hot solution of partially methylated ß-cyclodextrin in methanol. This treatment allowed for a selective extraction of the linear chains up to approximately 5000 Da. KW - Polycondensation KW - Cyclization KW - Isosorbide KW - Polyesters KW - MALDI PY - 2003 DO - https://doi.org/10.1002/pola.10933 SN - 0360-6376 SN - 0887-624X VL - 41 IS - 21 SP - 3414 EP - 3424 PB - Wiley CY - Hoboken, NJ AN - OPUS4-12017 LA - eng 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 - JOUR A1 - Markötter, H. A1 - Manke, I. A1 - Krüger, P. A1 - Arlt, Tobias A1 - Huassmann, J. A1 - Klages, M. A1 - Riesemeier, Heinrich A1 - Hartnig, C. A1 - Scholta, J. A1 - Banhart, J. T1 - Investigation of 3D water transport paths in gas diffusion layers by combined in-situ synchrotron X-ray radiography and tomography N2 - The three-dimensional water distribution and water transport paths in the gas diffusion layer (GDL) and the adjacent micro-porous layer (MPL) of a polymer electrolyte membrane fuel cell (PEMFC) were analyzed during cell operation. The technique of quasi in-situ X-ray tomography was used for a 3D visualization of the water distribution and the structure of the GDL at different operating conditions. Based on findings from in-situ radiographic measurements water transport paths were detected and subsequently examined by tomography. The combination of these 2D and 3D techniques allows for a fully three-dimensionally resolved visualization of transport paths through the GDL. KW - Polymer electrolyte membrane fuel cell (PEMFC) KW - Radiography KW - Tomography KW - Synchrotron X-ray imaging KW - Gas diffusion layer (GDL) KW - Water transport paths PY - 2011 DO - https://doi.org/10.1016/j.elecom.2011.06.023 SN - 1388-2481 VL - 13 IS - 9 SP - 1001 EP - 1004 PB - Elsevier B.V. CY - Amsterdam AN - OPUS4-25244 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Geier, M. A1 - Eberstein, M. A1 - Grießmann, H. A1 - Partsch, U. A1 - Völkel, L. A1 - Böhme, R. A1 - Mann, Guido A1 - Bonse, Jörn A1 - Krüger, Jörg T1 - Impact of laser treatment on phosphoric acid coated multicrystalline silicon PV-wafers N2 - The selective emitter is a well-known technology for producing highly doped areas under the metallization grid to improve the solar cell performance. In this work, the influence of laser irradiation on phosphoric acid coated multicrystalline silicon PV-wafers on the wafer surface structure, the phosphorous depth distribution and the electrical contact resistance within the laser treated area as well as the electrical series resistance of laserprocessed solar cells was evaluated. Different laser processing settings were tested including pulsed and continuous wave (cw) laser sources (515 nm, 532 nm, 1064 nm wavelength). Complementary numerical simulations using the finite element method (FEM) were conducted to explain the impact of the laser parameters on the melting behavior (melt duration and geometry). It was found that the melt duration is a key parameter for a successful laser Doping process. Our simulations at a laser wavelengths of 515 nm reveal that low-repetition rate (<500 kHz) laser pulses of 300 ns duration generate a melt duration of ~0.35 µs, whereas upon scanning cw-laser radiation at 532 nm prolongates the melt duration by at least one order of magnitude. Experimentally, the widely used ns-laser pulses did not lead to satisfying laser irradiation results. In contrast, cw-laser radiation and scan velocities of less than 2 m/s led to suitable laser doping featuring low electrical resistances in the laser treated areas. T2 - 26th European photovoltaic solar energy conference and exhibition CY - Hamburg, Germany DA - 05.09.2011 KW - Silicon solar cell KW - Selective emitter KW - Laser processing KW - Doping KW - Simulation PY - 2011 SN - 3-936338-27-2 DO - https://doi.org/10.4229/26thEUPVSEC2011-2BV.1.7 SP - 1243 EP - 1247 AN - OPUS4-24995 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Eberstein, M. A1 - Geier, M. A1 - Grießmann, H. A1 - Partsch, U. A1 - Voelkel, L. A1 - Böhme, R. A1 - Pentzien, Simone A1 - Koter, Robert A1 - Mann, Guido A1 - Bonse, Jörn A1 - Krüger, Jörg T1 - Towards an industrial laser doping process for the selective emitter using phosphoric acid as dopant N2 - Different laser supported approaches have already been realized, proving the great potential of laserdoped selective emitters (LDSE). However, it is challenging to establish a low-cost process by using pulsed laser tools. So far a single-step process only leads to satisfying results utilizing cw-lasers. In this paper we have examined a two-step process to produce laser-doped selective emitters on multicrystalline textured standard silicon photovoltaic wafers (90-Ω/sq-Emitter, SiN-antireflection coating (ARC)). The precise ARC removal by near-infrared fs-laser pulses (30 fs, 800 nm), and the doping of uncoated silicon wafers by ns-laser pulses (8 ns, 532 nm) were systematically investigated. In the fs-experiment, optimum conditions for ARC removal were identified. In the nsexperiments under suitable conditions (melting regime), the phosphorous concentration underneath the wafer surface was significantly increased and the sheet resistance was reduced by nearly a factor of two. Moreover, electrical measurements on fired metallization fingers deposited on the laser processed wafers showed low contact resistances. Hence, wafer conditioning with combined fs-laser- and ns-laser-processes are expected to be a promising technology for producing selective emitters. T2 - 26th European photovoltaic solar energy conference and exhibition CY - Hamburg, Germany DA - 05.09.2011 KW - Laser processing KW - Doping KW - Selective emitter KW - Multicrystalline silicon PY - 2011 SN - 3-936338-27-2 DO - https://doi.org/10.4229/26thEUPVSEC2011-2BV.1.2 SP - 1220 EP - 1223 AN - OPUS4-24996 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -