Horbatsch, Marko2015-01-262015-01-262014-05-052015-01-26http://hdl.handle.net/10315/28160The 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.enAuthor owns copyright, except where explicitly noted. Please contact the author directly with licensing requests.Atomic physicsMolecular physicsQuantum physicsIonization of the Hydrogen Molecular Ion by Strong Infrared Laser FieldsElectronic Thesis or Dissertation2015-01-26Spectral methodsHydrogen molecular ionIonization rateStrong laser fieldsHigh-harmonic generation