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Ionization of the Hydrogen Molecular Ion by Strong Infrared Laser Fields

dc.contributor.advisorHorbatsch, Marko
dc.creatorTsednee, Tsogbayar
dc.date.accessioned2015-01-26T14:05:15Z
dc.date.available2015-01-26T14:05:15Z
dc.date.copyright2014-05-05
dc.date.issued2015-01-26
dc.date.updated2015-01-26T14:05:15Z
dc.degree.disciplinePhysics And Astronomy
dc.degree.levelDoctoral
dc.degree.namePhD - Doctor of Philosophy
dc.description.abstractThe ionization of simple molecular targets, such as molecular hydrogen, or even the molecular hydrogen ion ($\mbox{H}^{+}_{2}$) by strong laser fields has become the focus of experimental research in the past few decades. On the theoretical side the problem presents two challenges: on the one hand one has to solve the problem numerically even in the one-electron case ($\mbox{H}^{+}_{2}$), since no analytic closed-form solution is possible; on the other hand there is the many-electron problem ($\mbox{H}_{2}$ and other diatomic molecules, such as $\mbox{N}_{2}$, $\mbox{O}_{2}$, etc.), which currently is at the limit of computational feasibility ($\mbox{H}_{2}$), or exceeds it for molecules with more than two electrons. In this thesis the single-electron problem of the hydrogen molecular ion in intense continuous-wave laser fields is addressed. The focus is on ionization rates of the molecule as a function of internuclear separation within the framework that the motion of the nuclei can be neglected (Born-Oppenheimer approximation). First, the problem of the DC limit is considered, i.e., a strong static electric field is applied along the internuclear axis. The field ionization rate is calculated by solving a stationary non-hermitean Schr\"odinger equation in a suitable coordinate system (prolate spheroidal coordinates). Some previously obtained values from the literature are reproduced; for larger internuclear separations improved values are obtained. For the more interesting case of an infrared (continuous-wave) laser field Floquet theory is applied to transform the time-dependent Schr\"odinger equation for the electronic motion into a non-hermitean coupled-channel stationary problem. Ionization rates are found as a function of laser frequency ($\omega$), and the low-frequency limit is pursued to understand how one can establish a connection to the DC limit. Results are obtained for the two lowest electronic states, which are named the {\it gerade} and {\it ungerade} (or even and odd) ground states in the field-free limit. From the calculated results it is observed that the ionization rates peak at certain internuclear separations, such that a dissociating $\mbox{H}^{+}_{2}$ molecule will be preferentially field ionized. In addition, the thesis reports on calculations of so-called high harmonic generation - a process where photo-electrons acquire energy from the laser field, are deflected back by the linearly polarized laser and recombine under the emission of photons with energies that correspond to odd-integer multiples of the laser photon energy.
dc.identifier.urihttp://hdl.handle.net/10315/28160
dc.language.isoen
dc.rightsAuthor owns copyright, except where explicitly noted. Please contact the author directly with licensing requests.
dc.subjectAtomic physics
dc.subjectMolecular physics
dc.subjectQuantum physics
dc.subject.keywordsSpectral methodsen_US
dc.subject.keywordsHydrogen molecular ionen_US
dc.subject.keywordsIonization rateen_US
dc.subject.keywordsStrong laser fieldsen_US
dc.subject.keywordsHigh-harmonic generationen_US
dc.titleIonization of the Hydrogen Molecular Ion by Strong Infrared Laser Fields
dc.typeElectronic Thesis or Dissertation

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