TY - JOUR A1 - Young, Linda A1 - Ueda, Kiyoshi A1 - Gühr, Markus A1 - Bucksbaum, Philip H. A1 - Simon, Marc A1 - Mukamel, Shaul A1 - Rohringer, Nina A1 - Prince, Kevin C. A1 - Masciovecchio, Claudio A1 - Meyer, Michael A1 - Rudenko, Artem A1 - Rolles, Daniel A1 - Bostedt, Christoph A1 - Fuchs, Matthias A1 - Reis, David A. A1 - Santra, Robin A1 - Kapteyn, Henry A1 - Murnane, Margaret A1 - Ibrahim, Heide A1 - Legare, Francois A1 - Vrakking, Marc A1 - Isinger, Marcus A1 - Kroon, David A1 - Gisselbrecht, Mathieu A1 - Wörner, Hans Jakob A1 - Leone, Stephen R. T1 - Roadmap of ultrafast x-ray atomic and molecular physics JF - Journal of physics : B, Atomic, molecular and optical physics N2 - X-ray free-electron lasers (XFELs) and table-top sources of x-rays based upon high harmonic generation (HHG) have revolutionized the field of ultrafast x-ray atomic and molecular physics, largely due to an explosive growth in capabilities in the past decade. XFELs now provide unprecedented intensity (10(20) W cm(-2)) of x-rays at wavelengths down to similar to 1 Angstrom, and HHG provides unprecedented time resolution (similar to 50 attoseconds) and a correspondingly large coherent bandwidth at longer wavelengths. For context, timescales can be referenced to the Bohr orbital period in hydrogen atom of 150 attoseconds and the hydrogen-molecule vibrational period of 8 femtoseconds; wavelength scales can be referenced to the chemically significant carbon K-edge at a photon energy of similar to 280 eV (44 Angstroms) and the bond length in methane of similar to 1 Angstrom. With these modern x-ray sources one now has the ability to focus on individual atoms, even when embedded in a complex molecule, and view electronic and nuclear motion on their intrinsic scales (attoseconds and Angstroms). These sources have enabled coherent diffractive imaging, where one can image non-crystalline objects in three dimensions on ultrafast timescales, potentially with atomic resolution. The unprecedented intensity available with XFELs has opened new fields of multiphoton and nonlinear x-ray physics where behavior of matter under extreme conditions can be explored. The unprecedented time resolution and pulse synchronization provided by HHG sources has kindled fundamental investigations of time delays in photoionization, charge migration in molecules, and dynamics near conical intersections that are foundational to AMO physics and chemistry. This roadmap coincides with the year when three new XFEL facilities, operating at Angstrom wavelengths, opened for users (European XFEL, Swiss-FEL and PAL-FEL in Korea) almost doubling the present worldwide number of XFELs, and documents the remarkable progress in HHG capabilities since its discovery roughly 30 years ago, showcasing experiments in AMO physics and other applications. Here we capture the perspectives of 17 leading groups and organize the contributions into four categories: ultrafast molecular dynamics, multidimensional x-ray spectroscopies; high-intensity x-ray phenomena; attosecond x-ray science. KW - ultrafast molecular dynamics KW - x-ray spectroscopies and phenomena KW - table-top sources KW - x-ray free-electron lasers KW - attosecond phenomena Y1 - 2018 U6 - https://doi.org/10.1088/1361-6455/aa9735 SN - 0953-4075 SN - 1361-6455 VL - 51 IS - 3 PB - IOP Publ. Ltd. CY - Bristol 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 - GEN A1 - Young, Linda A1 - Ueda, Kiyoshi A1 - Gühr, Markus A1 - Bucksbaum, Philip H. A1 - Simon, Marc A1 - Mukamel, Shaul A1 - Rohringer, Nina A1 - Prince, Kevin C. A1 - Masciovecchio, Claudio A1 - Meyer, Michael A1 - Rudenko, Artem A1 - Rolles, Daniel A1 - Bostedt, Christoph A1 - Fuchs, Matthias A1 - Reis, David A. A1 - Santra, Robin A1 - Kapteyn, Henry A1 - Murnane, Margaret A1 - Ibrahim, Heide A1 - Légaré, François A1 - Vrakking, Marc A1 - Isinger, Marcus A1 - Kroon, David A1 - Gisselbrecht, Mathieu A1 - L'Huillier, Anne A1 - Wörner, Hans Jakob A1 - Leone, Stephen R. T1 - Roadmap of ultrafast x-ray atomic and molecular physics T2 - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - X-ray free-electron lasers (XFELs) and table-top sources of x-rays based upon high harmonic generation (HHG) have revolutionized the field of ultrafast x-ray atomic and molecular physics, largely due to an explosive growth in capabilities in the past decade. XFELs now provide unprecedented intensity (1020 W cm−2) of x-rays at wavelengths down to ~1 Ångstrom, and HHG provides unprecedented time resolution (~50 attoseconds) and a correspondingly large coherent bandwidth at longer wavelengths. For context, timescales can be referenced to the Bohr orbital period in hydrogen atom of 150 attoseconds and the hydrogen-molecule vibrational period of 8 femtoseconds; wavelength scales can be referenced to the chemically significant carbon K-edge at a photon energy of ~280 eV (44 Ångstroms) and the bond length in methane of ~1 Ångstrom. With these modern x-ray sources one now has the ability to focus on individual atoms, even when embedded in a complex molecule, and view electronic and nuclear motion on their intrinsic scales (attoseconds and Ångstroms). These sources have enabled coherent diffractive imaging, where one can image non-crystalline objects in three dimensions on ultrafast timescales, potentially with atomic resolution. The unprecedented intensity available with XFELs has opened new fields of multiphoton and nonlinear x-ray physics where behavior of matter under extreme conditions can be explored. The unprecedented time resolution and pulse synchronization provided by HHG sources has kindled fundamental investigations of time delays in photoionization, charge migration in molecules, and dynamics near conical intersections that are foundational to AMO physics and chemistry. This roadmap coincides with the year when three new XFEL facilities, operating at Ångstrom wavelengths, opened for users (European XFEL, Swiss-FEL and PAL-FEL in Korea) almost doubling the present worldwide number of XFELs, and documents the remarkable progress in HHG capabilities since its discovery roughly 30 years ago, showcasing experiments in AMO physics and other applications. Here we capture the perspectives of 17 leading groups and organize the contributions into four categories: ultrafast molecular dynamics, multidimensional x-ray spectroscopies; high-intensity x-ray phenomena; attosecond x-ray science. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 668 KW - ultrafast molecular dynamics KW - x-ray spectroscopies and phenomena KW - table-top sources KW - x-ray free-electron lasers KW - attosecond phenomena Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-424238 SN - 1866-8372 IS - 668 ER - TY - BOOK A1 - Karg, Detlef A1 - Schopper, Franz A1 - Paschke, Ralph A1 - Meyer, Michael A1 - Ackermann, Irmgard A1 - Baxmann, Matthias A1 - Buchinger, Marie-Luise A1 - Cante, Marcus A1 - Dreger, Hans-Joachim A1 - Gramlich, Sybille A1 - Schwarz, Ulrike A1 - Hübener, Dieter A1 - Metzler, Matthias A1 - Niemann, Alexander A1 - Rohowski, Ilona A1 - Senst, Ingetraud A1 - Groß, Wera ED - Brandenburgisches Landesamt für Denkmalpflege und Archäologisches Landesmuseum, T1 - Denkmalentdeckungen BT - Bilder aus dem Land Brandenburg N2 - »Wenn du reisen willst, mußt du die Geschichte dieses Landes kennen und lieben. Das ist ganz unerläßlich. [...] Wag’ es getrost und du wirst es nicht bereuen. Eigentümliche Freuden und Genüsse werden dich begleiten. Du wirst Entdeckungen machen, denn überall wohin du kommst, wirst du, vom Touristenstandpunkt aus, eintreten wie in ›jungfräuliches Land‹. Du wirst Klosterruinen begegnen, von deren Existenz höchstens die nächste Stadt eine leise Kenntnis hatte; du wirst inmitten alter Dorfkirchen, deren zerbröckelter Schindelturm nur auf Elend deutete, große Wandbilder oder in den treppenlosen Grüften reiche Kupfersärge mit Kruzifix und vergoldeten Wappenschildern finden; du wirst Schlachtfelder überschreiten, Wendenkirchhöfe, Heidengräber, von denen die Menschen nichts mehr wissen.« Die in diesem Bildband gesammelten »Denkmalentdeckungen« verstehen sich als Einladung zu einer Reise durch das Land Brandenburg. Theodor Fontane hatte für ein solches Unternehmen genau den richtigen Blick, als er in seinen »Wanderungen durch die Mark Brandenburg« 1864 diese Sätze schrieb. Auch heute noch sollten wir seiner Anregung zu Begegnungen mit der Geschichte und der Kunstgeschichte des Landes folgen, die uns im Dialog der Kulturen und der Zeiten eine Standortbestimmung in der Gegenwart und eine Orientierung für die Zukunft zugleich bietet. KW - Brandenburg KW - Denkmal KW - Denkmalpflege KW - Bildband KW - Tourismus Y1 - 2007 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-72290 SN - 978-3-88462-244-5 PB - Wernersche Verlagsgesellschaft CY - Worms ET - 1200 ER -