001     616891
005     20241113213959.0
024 7 _ |a 10.11588/HEIDOK.00034342
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024 7 _ |a urn:nbn:de:bsz:16-heidok-343425
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037 _ _ |a PUBDB-2024-06572
041 _ _ |a English
100 1 _ |a Borisova, Gergana
|0 P:(DE-H253)PIP1030264
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245 _ _ |a Controlling two-electron systems in their excited state by an intense laser field: Strong-field ionization of atomic helium & Wave-packet manipulation in molecular hydrogen
|f 2021-01-16 - 2024-01-16
260 _ _ |c 2024
|b Heidelberg University Library
300 _ _ |a 196
336 7 _ |a Output Types/Dissertation
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336 7 _ |a DISSERTATION
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336 7 _ |a PHDTHESIS
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336 7 _ |a Thesis
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336 7 _ |a Dissertation / PhD Thesis
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336 7 _ |a doctoralThesis
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502 _ _ |a Dissertation, Universität Heidelberg, 2024
|c Universität Heidelberg
|b Dissertation
|d 2024
|o 2024-01-16
520 _ _ |a In this work fundamental light–matter interaction is studied in excited-state two-electron systems under the influence of an intense laser field in two respects: First, motivated by the results of a numerical simulation on the role of initial-state electron correlation for the ionization process, strong-field ionization out of selectively prepared doubly excited states (DESs) in helium is studied in a two-colour extreme ultraviolet (XUV)–infrared (IR) experiment using a reaction microscope (REMI). Detected recoil-ion and photoelectron momentum distributions help to identify a variety of different IR-induced ionization pathways for both single and double ionization out of different DESs as the initial state for strong-field interaction. Turning the focus from the atomic to the molecular two-electron system, in the second study, a novel all-optical approach enables visualisation of the dynamics of a vibrational wave packet in an electronically excited state of neutral H_2 through molecular self-probing by the ground state encoded in the reconstructed time-dependent dipole response of the excited system from XUV spectroscopy data. In a pump–control scheme, an additional interaction with a 5-fs near-infrared (NIR) pulse of adjustable intensity modifies the vibrational wave-packet revival. The adoption of an impulsive control mechanism together with state-resolved extraction of the accumulated strong-field induced phases leading to the observed revival shift brings access to state-dependent polarizability of different vibronic states in the excited wave packet. In future, both experimental approaches can be applied to multi-electron systems to study and control correlation in specifically prepared excited quantum systems.
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650 _ 7 |a 530 Physics
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693 _ _ |a FLASH2
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700 1 _ |a Pfeifer, Thomas
|0 P:(DE-H253)PIP1010834
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700 1 _ |a Jochim, Selim
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773 _ _ |a 10.11588/HEIDOK.00034342
856 4 _ |u https://bib-pubdb1.desy.de/record/616891/files/Dissertation_GerganaDBorisova.pdf
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913 1 _ |a DE-HGF
|b Forschungsbereich Materie
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