Deutsch
 
Hilfe Datenschutzhinweis Impressum
  DetailsucheBrowse

Datensatz

DATENSATZ AKTIONENEXPORT
  Dissociative Photoionization of Molecular Hydrogen : A Joint Experimental and Theoretical Study of the Electron-Electron Correlations induced by XUV Photoionization and Nuclear Dynamics on IR-Laser Dressed Transition States

Fischer, A. (2015). Dissociative Photoionization of Molecular Hydrogen: A Joint Experimental and Theoretical Study of the Electron-Electron Correlations induced by XUV Photoionization and Nuclear Dynamics on IR-Laser Dressed Transition States. PhD Thesis, Ruprecht-Karls-Universität, Heidelberg.

Item is

Dateien

einblenden: Dateien
ausblenden: Dateien
:
fischer.pdf (Verlagsversion), 24MB
Name:
fischer.pdf
Beschreibung:
-
OA-Status:
Sichtbarkeit:
Öffentlich
MIME-Typ / Prüfsumme:
application/pdf / [MD5]
Technische Metadaten:
Copyright Datum:
-
Copyright Info:
-
Lizenz:
-
:
fischer.pdf (beliebiger Volltext), 24MB
Name:
fischer.pdf
Beschreibung:
In this thesis, the dissociative single-ionization of molecular hydrogen is investigated in a kinematically complete experiment by employing extreme ultraviolet attosecond pulse trains and infrared femtosecond laser pulses. Induced by the absorption of a single XUV photon, a pronounced energy-dependent asymmetry of the relative emission direction of the photoelectron and the ion is observed. The asymmetry pattern is explained in terms of an interference of two ionization pathways involving a doubly-excited state. This interpretation is validated by a semi-classical model which only takes the nuclear motion into account. Using this model and the observed asymmetry, it is furthermore possible to disentangle the two dissociation pathways which allows for the determination of the autoionization lifetime of the contributing doubly-excited state as a function of the internuclear distance. Moreover, using a pump{probe experiment the dissociation dynamics of molecular hydrogen is investigated. A time-delay dependent momentum distribution of the fragments is observed. With a combined quantum mechanical and semi-classical approach the mechanism giving rise to the observed time-dependence is identified in terms of an intuitive elevator mechanism.
OA-Status:
Sichtbarkeit:
Öffentlich
MIME-Typ / Prüfsumme:
application/pdf / [MD5]
Technische Metadaten:
Copyright Datum:
-
Copyright Info:
-
Lizenz:
-

Externe Referenzen

einblenden:

Urheber

einblenden:
ausblenden:
 Urheber:
Fischer, Andreas1, Autor           
Moshammer, Robert, Gutachter
Jochim, Selim, Gutachter
Affiliations:
1Division Prof. Dr. Thomas Pfeifer, MPI for Nuclear Physics, Max Planck Society, ou_2025284              

Inhalt

einblenden:
ausblenden:
Schlagwörter: -
 Zusammenfassung: In this thesis, the dissociative single-ionization of molecular hydrogen is investigated in a kinematically complete experiment by employing extreme ultraviolet attosecond pulse trains and infrared femtosecond laser pulses. Induced by the absorption of a single XUV photon, a pronounced energy-dependent asymmetry of the relative emission direction of the photoelectron and the ion is observed. The asymmetry pattern is explained in terms of an interference of two ionization pathways involving a doubly-excited state. This interpretation is validated by a semi-classical model which only takes the nuclear motion into account. Using this model and the observed asymmetry, it is furthermore possible to disentangle the two dissociation pathways which allows for the determination of the autoionization lifetime of the contributing doubly-excited state as a function of the internuclear distance. Moreover, using a pump{probe experiment the dissociation dynamics of molecular hydrogen is investigated. A time-delay dependent momentum distribution of the fragments is observed. With a combined quantum mechanical and semi-classical approach the mechanism giving rise to the observed time-dependence is identified in terms of an intuitive elevator mechanism.

Details

einblenden:
ausblenden:
Sprache(n): eng - English
 Datum: 2015-01-13
 Publikationsstatus: Angenommen
 Seiten: II, 153 S.
 Ort, Verlag, Ausgabe: Heidelberg : Ruprecht-Karls-Universität
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: DOI: 10.17617/2.2084601
 Art des Abschluß: Doktorarbeit

Veranstaltung

einblenden:

Entscheidung

einblenden:

Projektinformation

einblenden:

Quelle

einblenden: