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Now showing 1 - 10 of 17
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    Delayed relaxation of highly excited naphthalene cations
    (Bristol : IOP Publ., 2020) Reitsma, G.; Hummert, J.; Dura, J.; Loriot, V.; Vrakking, M.J.J.; Lépine, F.; Kornilov, O.
    The efficiency of energy transfer in ultrafast electronic relaxation of molecules depends strongly on the complex interplay between electronic and nuclear motion. In this study we use wavelength-selected XUV pulses to induce relaxation dynamics of highly excited cationic states of naphthalene. Surprisingly, the observed relaxation lifetimes increase with the cationic excitation energy. We propose that this is a manifestation of a quantum mechanical population trapping that leads to delayed relaxation of molecules in the regions with a high density of excited states. © 2019 Published under licence by IOP Publishing Ltd.
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    Intracycle interference in ionization of Ar by a laser assisted XUV pulse
    (Bristol : IOP Publ., 2017) Arbó, D.G.; López, S. D.; Kubin, M.; Hummert, J.; Vrakking, M.J.J.; Kornilov, O.
    Synopsis We present a theoretical and experimental study of the subcycle interference in laser assisted XUV ionization of Ar atoms. Averaging over the focal volume happens to blur the intracycle interference, which thus cannot be measured directly. We show that even at these conditions, the intracycle interference can be obtained through the subtraction of two different angle and energy-resolved distributions at slightly different laser intensities.
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    Photoelectron holography in strong optical and dc electric fields
    (Bristol : Institute of Physics Publishing, 2014) Stodolna, A.; Huismans, Y.; Rouzée, A.; Lépine, F.; Vrakking, M.J.J.
    The application of velocity map imaging for the detection of photoelectrons resulting from atomic or molecular ionization allows the observation of interferometric, and in some cases holographic structures that contain detailed information on the target from which the photoelecrons are extracted. In this contribution we present three recent examples of the use of photoelectron velocity map imaging in experiments where atoms are exposed to strong optical and dc electric fields. We discuss (i) observations of the nodal structure of Stark states of hydrogen measured in a dc electric field, (ii) mid-infrared strong-field ionization of metastable Xe atoms and (iii) the reconstruction of helium electronic wavepackets in an attosecond pump-probe experiment. In each case, the interference between direct and indirect electron pathways, reminiscent of the reference and signal waves in holography, is seen to play an important role.
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    Generation and characterization of isolated attosecond pulses for coincidence spectroscopy at 100 kHz repetition rate
    (Bristol : IOP Publ., 2020) Witting, T.; Furch, F.; Osolodkov, M.; Schell, F.; Menoni, C.; Schulz, C.P.; Vrakking, M.J.J.
    An attosecond pump-probe beamline with 100 kHz repetition rate for coincidence experiments has been developed. It is based on non-collinear optical parametric chirped pulse ampli-cation and delivers 100 µJ sub-4 fs to an high-harmonic generation source. Details on the generation and characterization of isolated attosecond pulses will be presented. © 2019 Published under licence by IOP Publishing Ltd.
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    Signatures of Light-Induced Potential Energy Surfaces in H2+
    (Bristol : IOP Publ., 2020) Kübel, M.; Spanner, M.; Dube, Z.; Naumov, A. Yu; Vrakking, M.J.J.; Corkum, P.B.; Villeneuve, D.M.; Staudte, A.
    Using theory and Cold Target Recoil Ion Momentum Spectroscopy we find signatures of light-induced molecular potential energy surfaces in the 3-dimensional proton momentum distributions of dissociating H+2. © 2020 Journal of Physics: Conference Series. All rights reserved.
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    Highly non-linear ionization of atoms induced by intense high-harmonic pulses
    (Bristol : IOP Publishing, 2020) Senfftleben, B.; Kretschmar, M.; Hoffmann, A.; Sauppe, M.; Tümmler, J.; Will, I.; Nagy, T.; Vrakking, M.J.J.; Rupp, D.; Schütte, B.
    Intense extreme-ultraviolet (XUV) pulses enable the investigation of XUV-induced non-linear processes and are a prerequisite for the development of attosecond pump - attosecond probe experiments. While highly non-linear processes in the XUV range have been studied at free-electron lasers (FELs), high-harmonic generation (HHG) has allowed the investigation of low-order non-linear processes. Here we suggest a concept to optimize the HHG intensity, which surprisingly requires a scaling of the experimental parameters that differs substantially from optimizing the HHG pulse energy. As a result, we are able to study highly non-linear processes in the XUV range using a driving laser with a modest (˜ 10 mJ) pulse energy. We demonstrate our approach by ionizing Ar atoms up to Ar5 + , requiring the absorption of at least 10 XUV photons. © 2020 The Author(s). Published by IOP Publishing Ltd
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    Propagation-assisted generation of intense few-femtosecond high-harmonic pulses
    (Bristol : IOP Publishing, 2020) Major, B.; Kretschmar, M.; Ghafur, O.; Hoffmann, A.; Kovács, K.; Varjú, K.; Senfftleben, B.; Tümmler, J.; Will, I.; Nagy, T.; Rupp, D.; Vrakking, M.J.J.; Tosa, V.; Schütte, B.
    The ongoing development of intense high-harmonic generation (HHG) sources has recently enabled highly non-linear ionization of atoms by the absorption of at least 10 extreme-ultraviolet (XUV) photons within a single atom (Senfftleben et al, arXiv:1911.01375). Here we investigate how the generation of these very intense HHG pulses in our 18-m-long beamline is aided by the reshaping of the fundamental, few-cycle, near-infrared (NIR) driving laser within a 30-cm-long HHG Xe medium. Using an incident NIR intensity that is higher than what is required for phase-matched HHG, signatures of reshaping are found by measuring the NIR blueshift and the fluorescence from the HHG medium along the propagation axis. These results are well reproduced by numerical calculations that show temporal compression of the NIR pulses in the HHG medium. The simulations predict that after refocusing an XUV beam waist radius of 320 nm and a clean attosecond pulse train can be obtained in the focal plane, with an estimated XUV peak intensity of 9 × 1015 W cm-2. Our results show that XUV intensities that were previously only available at large-scale facilities can now be obtained using moderately powerful table-top light sources. © 2020 The Author(s). Published by IOP Publishing Ltd
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    Coulomb explosion of diatomic molecules in intense XUV fields mapped by partial covariance
    (Bristol : Institute of Physics Publishing, 2013) Kornilov, O.; Eckstein, M.; Rosenblatt, M.; Schulz, C.P.; Motomura, K.; Rouzée, A.; Klei, J.; Foucar, L.; Siano, M.; Lübcke, A.; Schapper, F.; Johnsson, P.; Holland, D.M.P.; Schlathölter, T.; Marchenko, T.; Düsterer, S.; Ueda, K.; Vrakking, M.J.J.; Frasinski, L.J.
    Single-shot time-of-flight spectra for Coulomb explosion of N2 and I2 molecules have been recorded at the Free Electron LASer in Hamburg (FLASH) and have been analysed using a partial covariance mapping technique. The partial covariance analysis unravels a detailed picture of all significant Coulomb explosion pathways, extending up to the N 4+-N5+ channel for nitrogen and up to the I 8+-I9+ channel for iodine. The observation of the latter channel is unexpected if only sequential ionization processes from the ground state ions are considered. The maximum kinetic energy release extracted from the covariance maps for each dissociation channel shows that Coulomb explosion of nitrogen molecules proceeds much faster than that of the iodine. The N 2 ionization dynamics is modelled using classical trajectory simulations in good agreement with the outcome of the experiments. The results suggest that covariance mapping of the Coulomb explosion can be used to measure the intensity and pulse duration of free-electron lasers.
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    Carrier-envelope phase-tagged imaging of the controlled electron acceleration from SiO 2 nanospheres in intense few-cycle laser fields
    (Bristol : IOP, 2012) Zherebtsov, S.; Süßmann, F.; Peltz, C.; Plenge, J.; Betsch, K.J.; Znakovskaya, I.; Alnaser, A.S.; Johnson, N.G.; Kübel, M.; Horn, A.; Mondes, V.; Graf, C.; Trushin, S.A.; Azzeer, A.; Vrakking, M.J.J.; Paulus, G.G.; Krausz, F.; Rühl, E.; Fennel, T.; Kling, M.F.
    Waveform-controlled light fields offer the possibility of manipulating ultrafast electronic processes on sub-cycle timescales. The optical lightwave control of the collective electron motion in nanostructured materials is key to the design of electronic devices operating at up to petahertz frequencies. We have studied the directional control of the electron emission from 95 nm diameter SiO 2 nanoparticles in few-cycle laser fields with a well-defined waveform. Projections of the three-dimensional (3D) electron momentum distributions were obtained via single-shot velocity-map imaging (VMI), where phase tagging allowed retrieving the laser waveform for each laser shot. The application of this technique allowed us to efficiently suppress background contributions in the data and to obtain very accurate information on the amplitude and phase of the waveform-dependent electron emission. The experimental data that are obtained for 4 fs pulses centered at 720 nm at different intensities in the range (1-4)×10 13Wcm -2 are compared to quasi-classical mean-field Monte-Carlo simulations. The model calculations identify electron backscattering from the nanoparticle surface in highly dynamical localized fields as the main process responsible for the energetic electron emission from the nanoparticles. The local field sensitivity of the electron emission observed in our studies can serve as a foundation for future research on propagation effects for larger particles and field-induced material changes at higher intensities.
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    Attosecond control of electron-ion recollision in high harmonic generation
    (Bristol : IOP, 2011) Gademann, G.; Kelkensberg, F.; Siu, W.K.; Johnsson, P.; Gaarde, M.B.; Schafer, K.J.; Vrakking, M.J.J.
    We show that high harmonic generation driven by an intense nearinfrared (IR) laser can be temporally controlled when an attosecond pulse train (APT) is used to ionize the generation medium, thereby replacing tunnel ionization as the first step in the well-known three-step model. New harmonics are formed when the ionization occurs at a well-defined time within the optical cycle of the IR field. The use of APT-created electron wave packets affords new avenues for the study and application of harmonic generation. In the present experiment, this makes it possible to study harmonic generation at IR intensities where tunnel ionization does not give a measurable signal.