TY - GEN A1 - Kühn, Danilo A1 - Sorgenfrei, Nomi A1 - Giangrisostomi, Erika A1 - Jay, Raphael Martin A1 - Musazayb, Abdurrahman A1 - Ovsyannikov, Ruslan A1 - Stråhlman, Christian A1 - Svensson, Svante A1 - Mårtensson, Nils A1 - Föhlisch, Alexander T1 - Capabilities of angle resolved time of flight electron spectroscopy with the 60 degrees wide angle acceptance lens T2 - Postprints der Universität Potsdam Mathematisch-Naturwissenschaftliche Reihe N2 - The simultaneous detection of energy, momentum and temporal information in electron spectroscopy is the key aspect to enhance the detection efficiency in order to broaden the range of scientific applications. Employing a novel 60 degrees wide angle acceptance lens system, based on an additional accelerating electron optical element, leads to a significant enhancement in transmission over the previously employed 30 degrees electron lenses. Due to the performance gain, optimized capabilities for time resolved electron spectroscopy and other high transmission applications with pulsed ionizing radiation have been obtained. The energy resolution and transmission have been determined experimentally utilizing BESSY II as a photon source. Four different and complementary lens modes have been characterized. (C) 2017 The Authors. Published by Elsevier B.V. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 782 KW - Artof KW - electron spectroscopy KW - wide angle KW - time of flight KW - energy resolution KW - synchrotron Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-436629 SN - 1866-8372 IS - 782 SP - 45 EP - 50 ER - TY - JOUR A1 - Kühn, Danilo A1 - Müller, Moritz A1 - Sorgenfrei, Nomi A1 - Giangrisostomi, Erika A1 - Jay, Raphael Martin A1 - Ovsyannikov, Ruslan A1 - Martensson, Nils A1 - Sanchez-Portal, Daniel A1 - Föhlisch, Alexander T1 - Directional sub-femtosecond charge transfer dynamics and the dimensionality of 1T-TaS2 JF - Scientific reports N2 - For the layered transition metal dichalcogenide 1T-TaS2, we establish through a unique experimental approach and density functional theory, how ultrafast charge transfer in 1T-TaS2 takes on isotropic three-dimensional character or anisotropic two-dimensional character, depending on the commensurability of the charge density wave phases of 1T-TaS2. The X-ray spectroscopic core-hole-clock method prepares selectively in-and out-of-plane polarized sulfur 3p orbital occupation with respect to the 1T-TaS2 planes and monitors sub-femtosecond wave packet delocalization. Despite being a prototypical two-dimensional material, isotropic three-dimensional charge transfer is found in the commensurate charge density wave phase (CCDW), indicating strong coupling between layers. In contrast, anisotropic two-dimensional charge transfer occurs for the nearly commensurate phase (NCDW). In direct comparison, theory shows that interlayer interaction in the CCDW phase - not layer stacking variations - causes isotropic three-dimensional charge transfer. This is presumably a general mechanism for phase transitions and tailored properties of dichalcogenides with charge density waves. Y1 - 2019 U6 - https://doi.org/10.1038/s41598-018-36637-0 SN - 2045-2322 VL - 9 IS - 488 PB - Nature Publ. Group CY - London ER - TY - JOUR A1 - Giangrisostomi, Erika A1 - Ovsyannikov, Ruslan A1 - Sorgenfrei, Nomi A1 - Zhang, Teng A1 - Lindblad, Andreas A1 - Sassa, Yasmine A1 - Cappel, Ute B. A1 - Leitner, Torsten A1 - Mitzner, Rolf A1 - Svensson, Svante A1 - Martensson, Nils A1 - Föhlisch, Alexander T1 - Low Dose Photoelectron Spectroscopy at BESSY II BT - electronic structure of matter in its native state JF - Journal of electron spectroscopy and related phenomena : the international journal on theoretical and experimental aspects of electron spectroscopy N2 - The implementation of a high-transmission, angular-resolved time-of-Right electron spectrometer with a 1.25 MHz pulse selector at the PM4 soft X-ray dipole beamline of the synchrotron BESSY II creates unique capabilities to inquire electronic structure via photoelectron spectroscopy with a minimum of radiation dose. Solid-state samples can be prepared and characterized with standard UHV techniques and rapidly transferred from various preparation chambers to a 4-axis temperature-controlled measurement stage. A synchronized MHz laser system enables excited-state characterization and dynamical studies starting from the picosecond timescale. This article introduces the principal characteristics of the PM4 beamline and LowDosePES end-station. Recent results from graphene, an organic hole transport material for solar cells and the transition metal dichalcogenide MoS2 are presented to demonstrate the instrument performances. Y1 - 2018 U6 - https://doi.org/10.1016/j.elspec.2017.05.011 SN - 0368-2048 SN - 1873-2526 VL - 224 SP - 68 EP - 78 PB - Elsevier CY - Amsterdam ER - TY - JOUR A1 - Fondell, Mattis A1 - Eckert, Sebastian A1 - Jay, Raphael Martin A1 - Weniger, Christian A1 - Quevedo, Wilson A1 - Niskanen, Johannes A1 - Kennedy, Brian A1 - Sorgenfrei, Nomi A1 - Schick, Daniel A1 - Giangrisostomi, Erika A1 - Ovsyannikov, Ruslan A1 - Adamczyk, Katrin A1 - Huse, Nils A1 - Wernet, Philippe A1 - Mitzner, Rolf A1 - Föhlisch, Alexander T1 - Time-resolved soft X-ray absorption spectroscopy in transmission mode on liquids at MHz repetition rates JF - Structural dynamics N2 - We present a setup combining a liquid flatjet sample delivery and a MHz laser system for time-resolved soft X-ray absorption measurements of liquid samples at the high brilliance undulator beamline UE52-SGM at Bessy II yielding unprecedented statistics in this spectral range. We demonstrate that the efficient detection of transient absorption changes in transmission mode enables the identification of photoexcited species in dilute samples. With iron(II)-trisbipyridine in aqueous solution as a benchmark system, we present absorption measurements at various edges in the soft X-ray regime. In combination with the wavelength tunability of the laser system, the set-up opens up opportunities to study the photochemistry of many systems at low concentrations, relevant to materials sciences, chemistry, and biology. (C) 2017 Author(s). Y1 - 2017 U6 - https://doi.org/10.1063/1.4993755 SN - 2329-7778 VL - 4 PB - American Institute of Physics CY - Melville ER - TY - JOUR A1 - Sorgenfrei, Nomi A1 - Giangrisostomi, Erika A1 - Kühn, Danilo A1 - Ovsyannikov, Ruslan A1 - Föhlisch, Alexander T1 - Time and angle-resolved time-of-flight electron spectroscopy for functional materials science JF - Molecules : a journal of synthetic chemistry and natural product chemistry N2 - Electron spectroscopy with the unprecedented transmission of angle-resolved time-of-flight detection, in combination with pulsed X-ray sources, brings new impetus to functional materials science. We showcase recent developments towards chemical sensitivity from electron spectroscopy for chemical analysis and structural information from photoelectron diffraction using the phase transition properties of 1T-TaS2. Our development platform is the SurfaceDynamics instrument located at the Femtoslicing facility at BESSY II, where femtosecond and picosecond X-ray pulses can be generated and extracted. The scientific potential is put into perspective to the current rapidly developing pulsed X-ray source capabilities from Lasers and Free-Electron Lasers. KW - photoelectron spectroscopy KW - surface science KW - time-resolved KW - ultrafast KW - instrumentation KW - dichalcogenides KW - phase transition Y1 - 2022 U6 - https://doi.org/10.3390/molecules27248833 SN - 1420-3049 VL - 27 IS - 24 PB - MDPI CY - Basel ER -