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| 3. |
- Fushitani, Mizuho, et al.
(författare)
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Wave packet dynamics and control in excited states of molecular nitrogen
- 2024
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Ingår i: The Journal of chemical physics. - 0021-9606. ; 160:10
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Tidskriftsartikel (refereegranskat)abstract
- Wave packet interferometry with vacuum ultraviolet light has been used to probe a complex region of the electronic spectrum of molecular nitrogen, N2. Wave packets of Rydberg and valence states were excited by using double pulses of vacuum ultraviolet (VUV), free-electron-laser (FEL) light. These wave packets were composed of contributions from multiple electronic states with a moderate principal quantum number (n ∼ 4-9) and a range of vibrational and rotational quantum numbers. The phase relationship of the two FEL pulses varied in time, but as demonstrated previously, a shot-by-shot analysis allows the spectra to be sorted according to the phase between the two pulses. The wave packets were probed by angle-resolved photoionization using an infrared pulse with a variable delay after the pair of excitation pulses. The photoelectron branching fractions and angular distributions display oscillations that depend on both the time delays and the relative phases of the VUV pulses. The combination of frequency, time delay, and phase selection provides significant control over the ionization process and ultimately improves the ability to analyze and assign complex molecular spectra.
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| 4. |
- Ganguly, Smita, et al.
(författare)
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Coincidence study of core-ionized adamantane: Site-sensitivity within a carbon cage?
- 2022
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Ingår i: Physical chemistry chemical physics : PCCP. - 1463-9084. ; 24:47, s. 28994-29003
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Tidskriftsartikel (refereegranskat)abstract
- We investigate the fragmentation dynamics of adamantane dications produced after core-ionization at the carbon edge followed by Auger decay. The combination of high-resolution electron spectroscopy, energy-resolved electron-ion multi-coincidence spectroscopy and different theoretical models allows us to give a complete characterization of the processes involved after ionization. We show that energy- and site-sensitivity is observed even for a highly-symmetric molecule that lacks any unique atomic site.
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| 5. |
- Ganguly, Smita, et al.
(författare)
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Resonant Inner-Shell Photofragmentation of Adamantane (C10H16)
- 2023
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Ingår i: Molecules. - 1420-3049. ; 28:14
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Tidskriftsartikel (refereegranskat)abstract
- Adamantane, the smallest diamondoid molecule with a symmetrical cage, contains two distinct carbon sites, CH and CH2. The ionization/excitation of the molecule leads to the cage opening and strong structural reorganization. While theoretical predictions suggest that the carbon site CH primarily causes the cage opening, the role of the other CH2 site remains unclear. In this study, we used advanced experimental Auger electron-ion coincidence techniques and theoretical calculations to investigate the fragmentation dynamics of adamantane after resonant inner-shell photoexcitation. Our results demonstrate that some fragmentation channels exhibit site-sensitivity of the initial core-hole location, indicating that different carbon site excitations could lead to unique cage opening mechanisms.
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- Hoflund, Maria, et al.
(författare)
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Focusing Properties of High-Order Harmonics
- 2021
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Ingår i: Ultrafast Science. - : American Association for the Advancement of Science (AAAS). - 2765-8791. ; 2021
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Tidskriftsartikel (refereegranskat)abstract
- Many applications of the extreme ultraviolet (XUV) radiation obtained by high-order harmonic generation (HHG) in gases require a small focus area in order to enable attosecond pulses to reach a high intensity. Here, high-order harmonics generated in Ar with a multiterawatt laser system in a loose focusing geometry are focused to a few micrometers using two toroidal mirrors in a Wolter configuration with a high demagnification factor. Using a knife-edge measurement technique, we determine the position and size of the XUV foci as a function of harmonic order. We show that the focus properties vary with harmonic order and the generation conditions. Simulations, based on a classical description of the harmonic dipole phase and assuming that the individual harmonics can be described as Gaussian beams, reproduce the experimental behavior. We discuss how the generation geometry affects the intensity and duration of the focused attosecond pulses
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| 7. |
- Kockert, Hansjochen, et al.
(författare)
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UV-induced dissociation of CH2BrI probed by intense femtosecond XUV pulses
- 2022
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Ingår i: JOURNAL OF PHYSICS B-ATOMIC MOLECULAR AND OPTICAL PHYSICS. - : IOP Publishing. - 0953-4075 .- 1361-6455. ; 55:1
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Tidskriftsartikel (refereegranskat)abstract
- The ultraviolet (UV)-induced dissociation and photofragmentation of gas-phase CH2BrI molecules induced by intense femtosecond extreme ultraviolet (XUV) pulses at three different photon energies are studied by multi-mass ion imaging. Using a UV-pump-XUV-probe scheme, charge transfer between highly charged iodine ions and neutral CH2Br radicals produced by C-I bond cleavage is investigated. In earlier charge-transfer studies, the center of mass of the molecules was located along the axis of the bond cleaved by the pump pulse. In the present case of CH2BrI, this is not the case, thus inducing a rotation of the fragment. We discuss the influence of the rotation on the charge transfer process using a classical over-the-barrier model. Our modeling suggests that, despite the fact that the dissociation is slower due to the rotational excitation, the critical interatomic distance for charge transfer is reached faster. Furthermore, we suggest that charge transfer during molecular fragmentation may be modulated in a complex way.
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| 8. |
- Lee, Jason W.l., et al.
(författare)
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The Kinetic Energy of PAH Dication and Trication Dissociation Determined by Recoil-Frame Covariance Map Imaging
- 2022
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Ingår i: Physical Chemistry Chemical Physics. - 1463-9084. ; 24:38, s. 23096-23105
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Tidskriftsartikel (refereegranskat)abstract
- We investigated the dissociation of dications and trications of three polycyclic aromatic hydrocarbons (PAHs), fluorene, phenanthrene, and pyrene. PAHs are a family of molecules ubiquitous in space and involved in much of the chemistry of the interstellar medium. In our experiments, ions are formed by interaction with 30.3 nm extreme ultraviolet (XUV) photons, and their velocity map images are recorded using a PImMS2 multi-mass imaging sensor. Application of recoil-frame covariance analysis allows the total kinetic energy release (TKER) associated with multiple fragmentation channels to be determined to high precision, ranging 1.94-2.60 eV and 2.95-5.29 eV for the dications and trications, respectively. Experimental measurements are supported by Born-Oppenheimer molecular dynamics (BOMD) simulations.
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| 9. |
- Muschet, Alexander, 1990-
(författare)
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Non-linear attosecond physics at 100 eV
- 2021
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Non-linear interactions between light and matter have nowadays a broad range of applications. They are used for frequency doubling in simple laser pointers as well as for a variety of purposes in complex laser systems like the one presented in this thesis. For the study of ultrafast phenomena, those non-linear interactions are crucial to trigger and observe events at the fastest timescale, which is currently the attosecond regime (10-15 – 10-18 s). As the duration of a single optical cycle of a visible light wave is longer than this timescale, these investigations necessitate the application of XUV and X-ray pulses. However, the generation of isolated attosecond light pulses sufficiently intense to initiate non-linear interactions with matter is restricted to photon energies below 50 eV. The aim of this thesis is to establish a new light source, which pushes this boundary further and thereby enables the observation of up to now unrevealed electron dynamics.The presented new light source provides attosecond pulses with approximately hundred times more pulse energy than typical systems (up to 55 nJ in the spectral range from approximately 65 eV to 140 eV). This facilitates non-linear measurements at these photon energies. The achieved high energy stability (5 %) of this light source allows precise and time efficient measurements. These parameters are obtained via energy-upscaling of high-harmonic generation in gas medium. For the generation of well isolated attosecond pulses a unique laser, like the Light Wave Synthesizer 20, is necessary. This laser uses optical parametric synthesis to produce the most intense sub-5 fs, sub two-cycle laser pulses in the world (80 mJ, 4.5 fs).Furthermore, an optimal focus of the XUV pulses is crucial to provide the necessary intensity for non-linear interactions. Therefore, different methods for focusing the XUV pulses are investigated. Moreover, the construction and characterization of a robust split and delay stage is presented, which is essential for time resolved measurements.The detection of the non-linear interaction is realized via a spatially resolved ion time-of-flight detector, the ion microscope. This allows for a quantitative measurement of different ionization states. With the combination of this detector and the new light source the non-linear generation of Xe4+ and Xe5+ at photon energies around 100 eV is demonstrated. This enables the determination of the two-photon ionization cross-sections, which could up to now only be measured with much longer pulses at large scientific infrastructures. This paves the way towards time-resolved XUV pump – XUV probe measurements at 100 eV.
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| 10. |
- Nandi, Saikat, et al.
(författare)
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Generation of entanglement using a short-wavelength seeded free-electron laser
- 2024
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Ingår i: Science Advances. - 2375-2548. ; 10:16, s. 0668-0668
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Tidskriftsartikel (refereegranskat)abstract
- Quantum entanglement between the degrees of freedom encountered in the classical world is challenging to observe due to the surrounding environment. To elucidate this issue, we investigate the entanglement generated over ultrafast timescales in a bipartite quantum system comprising two massive particles: a free-moving photoelectron, which expands to a mesoscopic length scale, and a light-dressed atomic ion, which represents a hybrid state of light and matter. Although the photoelectron spectra are measured classically, the entanglement allows us to reveal information about the dressed-state dynamics of the ion and the femtosecond extreme ultraviolet pulses delivered by a seeded free-electron laser. The observed generation of entanglement is interpreted using the time-dependent von Neumann entropy. Our results unveil the potential for using short-wavelength coherent light pulses from free-electron lasers to generate entangled photoelectron and ion systems for studying spooky action at a distance.
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