J. Plenge
Free University of Berlin
20 Papers
175 Citations
J. Plenge is an academic researcher from Free University of Berlin. The author has contributed to research in topics: Ionization & Laser. The author has an hindex of 12, co-authored 20 publications.
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Papers
Controlled near-field enhanced electron acceleration from dielectric nanospheres with intense few-cycle laser fields
Sergey Zherebtsov,Thomas Fennel,J. Plenge,E. Antonsson,Irina Znakovskaya,Adrian Wirth,O. Herrwerth,Frederik Süßmann,Christian Peltz,Izhar Ahmad,Sergei A. Trushin,Vladimir Pervak,Stefan Karsch,Marc J. J. Vrakking,Burkhard Langer,Christina Graf,Mark I. Stockman,Ferenc Krausz,Eckart Rühl,Matthias F. Kling +19 more
TL;DR: In this article, the authors demonstrate the attosecond control of the collective electron motion and directional emission from isolated dielectric (SiO2) nanoparticles with phase-stabilized few-cycle laser fields.
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Absolute photoionization cross sections of the primary photofragments of chlorine dioxide and dichlorine monoxide
TL;DR: In this paper, the primary photofragments of chlorine dioxide (OClO) and dichlorine monoxide (Cl2O) are reported, and partial photoionization cross sections of the parent cations and their photolysis products are derived from mass spectral intensities.
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Photoelectron-recoil-induced rotational excitation of the B 2Σ+u state in N2+
T. D. Thomas,Edwin Kukk,Hironobu Fukuzawa,K. Ueda,Ralph Püttner,Yusuke Tamenori,T. Asahina,Nobuhiko Kuze,Hisatoyo Kato,M. Hoshino,H. Tanaka,Michael Meyer,J. Plenge,A. Wirsing,Ertugrul Serdaroglu,R. Flesch,Eckart Rühl,Sergey Gavrilyuk,Faris Gel'mukhanov,Andreas Lindblad,Leif J. Sæthre +20 more
TL;DR: In this article, the role of the electronic structure and vibrational motions on interactions between molecules and electromagnetic radiation, ranging from optical to x-ray, was discussed in both linear and nonlinear regimes of the light-matter interaction.
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A pump-probe photoionization mass spectrometer utilizing tunable extreme ultraviolet laser-produced-plasma radiation
TL;DR: In this article, an experimental device that utilizes time-correlated nanosecond light pulses in combination with photoionization mass spectrometry is reported. But the performance of this experimental approach is characterized by investigating the primary photolysis products of chlorine dioxide.
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Coherent control of the ultrafast dissociative ionization dynamics of bromochloroalkanes.
TL;DR: Optimal pulse shapes are obtained from closed-loop control experiments on bromochloroethane, where the fragment ion yield of CH(2)Br(+) is optimized with respect to that of C( 2)H(4)BrCl(+) as well as the fragment ions ratios C(2).
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