| 1. |
- Jahnke, T., et al.
(författare)
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Inner-Shell-Ionization-Induced Femtosecond Structural Dynamics of Water Molecules Imaged at an X-Ray Free-Electron Laser
- 2021
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Ingår i: Physical Review X. - : American Physical Society. - 2160-3308. ; 11:4
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Tidskriftsartikel (refereegranskat)abstract
- The ultrafast structural dynamics of water following inner-shell ionization is a crucial issue in high-energy radiation chemistry. We have exposed isolated water molecules to a short x-ray pulse from a free-electron laser and detected momenta of all produced ions in coincidence. By combining experimental results and theoretical modeling, we can image dissociation dynamics of individual molecules in unprecedented detail. We reveal significant molecular structural dynamics in H2O2+, such as asymmetric deformation and bond-angle opening, leading to two-body or three-body fragmentation on a timescale of a few femtoseconds. We thus reconstruct several snapshots of structural dynamics at different time intervals, which highlight dynamical patterns that are relevant as initiating steps of subsequent radiation-damage processes.
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| 2. |
- Li, S., et al.
(författare)
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Manifestation of postcollision interaction in Krypton LMN Auger spectra following K-shell photoionization
- 2022
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Ingår i: Physical Review A: covering atomic, molecular, and optical physics and quantum information. - : American Physical Society. - 2469-9926 .- 2469-9934. ; 106:2
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Tidskriftsartikel (refereegranskat)abstract
- We report on an experimental and theoretical study of postcollision interaction (PCI) effects on L-2 - M4,5N2,3 Auger electrons measured above the Kr K-edge in which L-2 vacancies are primarily generated by KL2 x-ray emission. Such cascade processes, in which a deep inner-shell vacancy decays first by x-ray emission followed by Auger electron emission, is a strong decay mode in heavy atoms. The L-2 - M4,5N2,3 Auger electron peak is observed to become increasingly asymmetric with a shifting peak maximum as the absorbed x-ray energy approaches the K-shell ionization threshold. This is attributed to PCI energy exchanges of the Auger electron with the 1s photoelectron. To model the PCI effects, we have applied a semiclassical approach modified to account for the combined lifetimes of the K and L-2 hole states. In addition, our analysis treats several closely spaced Auger transitions with final ionic states having different terms and angular momenta.
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| 3. |
- Travnikova, O., et al.
(författare)
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Photochemical Ring-Opening Reaction of 1,3-Cyclohexadiene: the True Reactive State
- 2022
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Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 144:48, s. 21878-21886
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Tidskriftsartikel (refereegranskat)abstract
- The photochemically induced ring-opening isomeriza-tion reaction of 1,3-cyclohexadiene to 1,3,5-hexatriene is a textbook example of a pericyclic reaction and has been amply investigated with advanced spectroscopic techniques. The main open question has been the identification of the single reactive state which drives the process. The generally accepted description of the isomerization pathway starts with a valence excitation to the lowest lying bright state, followed by a passage through a conical intersection to the lowest lying doubly excited state, and finally a branching between either the return to the ground state of the cyclic molecule or the actual ring-opening reaction leading to the open-chain isomer. Here, in a joint experimental and computational effort, we demonstrate that the evolution of the excitation-deexcitation process is much more complex than that usually described. In particular, we show that an initially high-lying electronic state smoothly decreasing in energy along the reaction path plays a key role in the ring-opening reaction.
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| 4. |
- Martins, J. B., et al.
(författare)
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Electron delocalisation in conjugated sulfur heterocycles probed by resonant Auger spectroscopy
- 2022
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Ingår i: Physical Chemistry Chemical Physics. - : Royal Society of Chemistry (RSC). - 1463-9076 .- 1463-9084. ; 24:14, s. 8477-8487
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Tidskriftsartikel (refereegranskat)abstract
- We propose a novel approach for an indirect probing of conjugation and hyperconjugation in core-excited molecules using resonant Auger spectroscopy. Our work demonstrates that the changes in the electronic structure of thiophene (C4H4S) and thiazole (C3H3NS), occurring in the process of resonant sulfur K-shell excitation and Auger decay, affect the stabilisation energy resulting from pi-conjugation and hyperconjugation. The variations in the stabilisation energy manifest themselves in the resonant S KL2,3L2,3 Auger spectra of thiophene and thiazole. The comparison of the results obtained for the conjugated molecules and for thiolane (C4H8S), the saturated analogue of thiophene, has been performed. The experimental observations are interpreted using high-level quantum-mechanical calculations and the natural bond orbital analysis.
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| 5. |
- Püttner, R., et al.
(författare)
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Argon KLL Auger spectrum: Initial states, core-hole lifetimes, shake, and knock-down processes
- 2020
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Ingår i: Physical Review A. - : AMER PHYSICAL SOC. - 2469-9926 .- 2469-9934. ; 102:5
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Tidskriftsartikel (refereegranskat)abstract
- State-of-the-art argon KLL Auger spectra measured using photon energies of hν=3216 and 3400 eV are presented along with an Ar [1s] photoelectron spectrum (square brackets indicate holes in the respective orbital). The two different photon energies used for measuring the Auger spectra allow distinguishing between the shake transitions during the Auger decay and the Auger transitions of the photoelectron satellites. A complete assignment of satellite transitions is provided, partially based on configuration-interaction calculations. In addition, Ar [1s3(s,p)]n′l′→[2p2(1D2)] transitions are observed, which can be explained by knock-down transitions leading to a direct exchange of angular momentum between the excited electron and the Auger electron. The lifetime broadenings of the Ar [2s] single-core-hole state and the [2s2] and [2s2p] double-core-hole states are also determined, confirming previously observed trends for double-core-hole states. © 2020 American Physical Society.
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| 6. |
- Püttner, R., et al.
(författare)
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Nonstatistical behavior of the photoionization of spin-orbit doublets
- 2021
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Ingår i: Journal of Physics B: Atomic, Molecular and Optical Physics. - : IOP Publishing. - 0953-4075 .- 1361-6455. ; 54:8
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Tidskriftsartikel (refereegranskat)abstract
- The photoionization branching ratios of spin-orbit doublets are studied both experimentally and theoretically at energies several keV above threshold. The results show significant relativistic effects for Ar 2p in the autoionizing region below the 1s threshold, and large many-body effects for Xe 3d and 4d in the vicinity of the L-shell thresholds. The branching ratios in Xe are also found to vary significantly over very broad multi-keV energy regions both above and below the inner-shell thresholds. In addition, the Ar 2p study confirms experimentally the decades-old theoretical prediction that the nonresonant branching ratio does not approach the statistical (nonrelativistic) value, and, in fact, progressively diverges from statistical with increasing photon energy. © 2021 The Author(s). Published by IOP Publishing Ltd.
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| 7. |
- Santos, A. C. F., et al.
(författare)
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Resonant Auger decay induced by the symmetry-forbidden 1a(1g)? 6a(1g) transition of the SF6 molecule
- 2022
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Ingår i: Journal of Vacuum Science & Technology A. - : American Vacuum Society. - 0734-2101 .- 1520-8559. ; 40:4
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Tidskriftsartikel (refereegranskat)abstract
- Resonant Auger electron spectroscopic study at the symmetry-forbidden 1 a 1 g -> 6 a 1 g excitation below the S K-shell threshold of SF 6 is reported. Partial electron yield and resonant K L L Auger spectra have been measured by using monochromatized undulator synchrotron radiation. By changing the photon energy in small steps, a so-called 2D map is produced. In this map, the dipole-forbidden transition exhibits spectral features (e.g., an S-shaped dispersion relation), which are well known and understood for dipole-allowed transitions. We validate by a theory that for the case of dipole-forbidden transitions, these spectral features can be analyzed in the same way as previously established for the dipole-allowed ones. This approach grants information on the nuclear dynamics in the K-shell core-excited states of SF 6 on the femtosecond (fs) timescale. In particular, for the potential-energy curves of the states S 1 s(-1) 6(a1g) and S 2p(-2)6a(1g), the slopes at the equilibrium distance of the ground state are derived. Symmetry breaking as a result of ultrafast vibronic coupling is revealed by the population of the electronically forbidden excited state. Published under an exclusive license by the AVS.
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