It is well known that the optical properties of multi-level atomic and molecular system can be controlled and manipulated efficiently using quantum coherence and interference, which has led to many new effects in quantum optics for e.g. lasing action without population inversion, ultraslow light, high resolution nonlinear spectroscopy etc. Recent experimental and theoretical studies have also provided support for the hypothesis that biological systems uses quantum coherence. Nearly perfect excitation energy transfer in photosynthesis is an excellent example of this. In this dissertation we studied quantum coherence and interference effects in the transient and the continuous-wave regimes. This study led to (i) the first experimental demonstration of carrier-envelope phase effects on bound-bound atomic excitation in multi-cycle regime (~15 cycles), (ii) a unique possibility for standoff detection of trace gases using their rotational and vibrational spectroscopic signals and from herein called Coherent Raman Umklappscattering, (iii) several possibilities for frequency up-conversion and generation of short-wavelength radiation using quantum coherence (iv) the measurement of spontaneous emission noise intensity in Yoked-superfluorescence scheme. Applications of the obtained results are development of XUV (X-Ray) lasers, con- trolled superfluorescent (superradiant) emission, carrier-envelope phase effects, coherent Raman scattering in the backward direction, enhancement of efficiency for generating radiation in XUV and X-Ray regime using quantum coherence with and without population inversion and to extend XUV and X-Ray lasing to ~4.023 nm in Helium-like carbon.

Doctor of Philosophy / Department of Physics / Brett D. Esry / The nuclear rotational period of the simplest molecule H[subscript]2[superscript]+ is about 550 fs, which is more than 35 times longer than its vibrational period of 15 fs. The rotational time scale is also much longer than widely available ultra short laser pulses which have 10 fs or less duration. The large difference in rotational period and ultra short laser pulse duration raises questions about the importance of nuclear rotation in theoretical studies of H[subscript]2[superscript]+ dissociation by these pulses. In most studies, reduced-dimensionality calculations are performed by freezing the molecular axis in one direction, referred to as the aligned model. We have systematically compared the aligned model with our full-dimensionality results for total dissociation probability and field-free dynamics of the dissociating fragments. The agreement between the two is only qualitative even for ultra short 10 fs pulses. Post-pulse dynamics of the bound wave function show rotational revivals. Significant alignment of H[subscript]2[superscript]+ occurs at these revivals. Our theoretical formulation to solve the time-dependent Schrodinger equation is an important step forward to make quantitative comparison between theory and experiment. We accurately calculate observables such as kinetic energy, angular, and momentum distributions. Reduced-dimensionality calculations cannot predict momentum distributions. Our theoretical approach presents the first momentum distribution of H[subscript]2[superscript]+ dissociation by few cycle laser pulses. These observables can be directly compared to the experiment. After taking into account averaging steps over the experimental conditions, we find remarkable agreement between the theory and experiment. Thus, our theoretical formulation can make predictions. In H[subscript]2[superscript]+ dissociation by pulses less than 10 fs, an asymmetry in the momentum distribution occurs by the interference of different pathways contributing to the same energy. The asymmetry, however, becomes negligible after averaging over experimental conditions. In a proposed pump-probe scheme, we predict an order of magnitude enhancement in the asymmetry and are optimistic that it can be observed.