Ding, Xiaoyan2018-11-292018-11-292018-11-29http://hdl.handle.net/10393/38504http://dx.doi.org/10.20381/ruor-22757With more atoms in a system, coupling between quantum states complicates the system dynamics. We shine intense laser pulses on three systems with increasing complexity: a molecule, a dimer, and a solid. For single molecules, a 400 nm photon excites NO_2 and initiates a dissociation process. We probe the dynamics using a strong laser pulse to ionize the molecule, and detect the resulting electrons and ions. The evolution of the NO-O molecular bond was directly measured in our experiment. For dimers, a laser pulse removes three electrons from (CO)_2. The dimer breaks up into C^+, O^+ and CO^+. Compared to a monomer, CO^{2+} in the dimer has a new prompt dissociation pathway that produces fragments with higher kinetic energy. Calculation shows that the Coulomb field of the neighboring CO^+ modifies the electronic state of the dimer, giving rise to a prompt channel. Coupling between different charge state configurations results in a new dimer electronic state, which leads to dissociation with higher kinetic energy. For solids, coupling among many atoms creates bands and a bandgap that plays the role of the ionization potential and reduces the threshold for electron-hole pair generation. Thus, solids are a good medium for high-order harmonic generation at the high repetition rates needed for frequency combs. We generate up to the 7th harmonic in silicon and zinc oxide with femtosecond pulses from a thulium fiber laser.enIntense laser fieldsMolecular dynamicsSolidsPhotodissociationHarmonic generationThesis