Doctor of Philosophy / Department of Physics / Charles L. Cocke / An underlying goal of studying atomic or molecular dynamics with short laser pulses is to reach a time scale short enough to study the evolution of the system in the time domain. In this thesis, the strong field ionization of atoms and molecules has been investigated with the highly resolved technique known as cold target recoil momentum spectroscopy (COLTRIMS). The thesis can be divided into two parts: single and double ionization. In the first part, we studied the momentum vectors of low energy electrons generated by short laser pulses of wavelengths varying from 400 to 800 nm with atomic and molecular targets with intensities in the tunneling region. Most of the structures observed in the momentum spectra of atomic and molecular targets can be explained as due to above-threshold ionization, and Freeman resonances. The most significant structure in our observed spectra is the angular structure in the lowest part of the momentum image, and this is attributed to the diffraction pattern evolved by tunneling electrons. Surprisingly, we observed that the structure produced by the electrons from high Rydberg states is independent of the internal structure of the target atom and molecules. The same work is extended to aligned molecules. The basic idea of this part of the work is to see whether the angular distribution of electrons from aligned molecules resembles the orbital structures of the molecules. The rotational revival structure was used to align the molecules. We observed pronounced energy and angular structures of the momentum images which show a dependence on the alignment of the molecule. The last part of this work mainly focuses on double ionization, i.e. the removal of two electrons from the target atoms sequentially by a short laser pulse. Measuring the complete momentum vector of Ar2+ and Ne2+, we demonstrate that these can be used to extract the angular correlation between two electrons sequentially released in the circularly polarized pulse. We demonstrate how the measurement of full momentum vectors of the doubly ionized argon and neon ions can be used to extract the time gap of the two emissions.

Doctor of Philosophy / Department of Physics / Brett D. DePaola / Many people in the science community are interested in the prospect of cold molecules for such applications as quantum computing and molecular Bose-Einstein condensates. Current methods of production fall short of the requirements for such projects. Photo association is a promising technique for forming cold molecules, but is currently facing significant obstacles. By understanding the photo association process and utilizing higher excited states, it is hoped that cold molecules can be formed from more easily produced cold atoms. Photo associative Ionization (PAI) is presented as a means to study excited state molecular dynamics at large internuclear separation, including photo association. This thesis presents a number of techniques for studying PAI in cold rubidium and a number of results obtained with the techniques. Excitation pathways for the process are explored in both narrow linewidth (MHz) and ultrafast (fs), large bandwidth (20 nm) domains.

Doctor of Philosophy / Department of Physics / Zenghu Chang / The few-cycle femtosecond laser pulse has proved itself to be a powerful tool for controlling the electron dynamics inside atoms and molecules. By applying such few-cycle pulses as a driving field, single isolated attosecond pulses can be produced through the high-order harmonic generation process, which provide a novel tool for capturing the real time electron motion. The first part of the thesis is devoted to the state of the art few-cycle near infrared (NIR) laser pulse development, which includes absolute phase control (carrier-envelope phase stabilization), amplitude control (power stabilization), and relative phase control (pulse compression and shaping). Then the double optical gating (DOG) method for generating single attosecond pulses and the attosecond streaking experiment for characterizing such pulses are presented. Various experimental limitations in the attosecond streaking measurement are illustrated through simulation. Finally by using the single attosecond pulses generated by DOG, an attosecond transient absorption experiment is performed to study the autoionization process of argon. When the delay between a few-cycle NIR pulse and a single attosecond XUV pulse is scanned, the Fano resonance shapes of the argon autoionizing states are modified by the NIR pulse, which shows the direct observation and control of electron-electron correlation in the temporal domain.

Doctor of Philosophy / Department of Physics / Jingyu Lin / Time-resolved deep ultraviolet (DUV) Photoluminescence (PL) spectroscopy system has been employed to systematically monitor crystalline quality, identify the defects and impurities, and investigate the light emission mechanism in III-nitride semiconducting materials and photonic structures. A time correlated single photon counting system and streak camera with corresponding time resolutions of 20 and 2 ps, respectively, were utilized to study the carrier excitation and recombination dynamics. A closed cycle He-flow cryogenic system was employed for temperature dependent measurements. This system is able to handle sample temperatures in a wide range (from 10 to 900 K). Structural, electrical, and morphological properties of the material were monitored by x-ray diffraction (XRD), Hall-effect measurement, and atomic force microscopy (AFM), respectively. Most of the samples studied here were synthesized in our laboratory by metal organic chemical vapor deposition (MOCVD). Some samples were bulk AlN synthesized by our collaborators, which were also employed as substrates for homoepilayer growth. High quality AlN epilayers with (0002) XRD linewidth as narrow as 50 arcsec and screw type dislocation density as low as 5x10[superscript]6 cm[superscript]-2 were grown on sapphire substrates. Free exciton transitions related to all valence bands (A, B, and C) were observed in AlN directly by PL, which allowed the evaluation of crystal field (Δ[subscript]CF) and spin-orbit (Δ[subscript]SO) splitting parameters exerimentally. Large negative Δ[subscript]CF and, consequently, the difficulties of light extraction from AlN and Al-rich AlGaN based emitters due to their unique optical polarization properties have been further confirmed with these new experimental data. Due to the ionic nature of III-nitrides, exciton-LO phonon Frohlich interaction is strong in these materials, which is manifested by the appearance of phonon replicas accompanying the excitonic emission lines in their PL spectra. The strength of the exciton-phonon interactions in AlN has been investigated by measuring the Huang-Rhys factor. It compares the intensity of the zero phonon (exciton emission) line relative to its phonon replica. AlN bulk single crystals, being promising native substrate for growing nitride based high quality device structures with much lower dislocation densities (<10[superscript]4 cm[superscript]-2), are also expected to be transparent in visible to UV region. However, available bulk AlN crystals always appear with an undesirable yellow or dark color. The mechanism of such undesired coloration has been investigated. MOCVD was utilized to deposit ~0.5 μm thick AlN layer on top of bulk crystal. The band gap of strain free AlN homoepilayers was 6.100 eV, which is ~30 meV lower compared to hetero-epitaxial layers on sapphire possessing compressive strain. Impurity incorporation was much lower in non-polar m-plane growth mode and the detected PL signal at 10 K was about an order of magnitude higher from a-plane homo-epilayers compared to that from polar c-plane epilayers. The feasibility of using Be as an alternate p-type dopant in AlN has been studied. Preliminary studies indicate that the Be acceptor level in AlN is ~330 meV, which is about 200 meV shallower than the Mg level in AlN. Understanding the optical and electronic properties of native point defects is the key to achieving good quality material and improving overall device performance. A more complete picture of optical transitions in AlN and GaN has been reported, which supplements the understanding of impurity transitions in AlGaN alloys described in previous reports.

Doctor of Philosophy / Department of Physics / Zenghu Chang / In this research, the carrier-envelope phase (CE phase) evolution of the pulse train from a Kerr-lens mode-locked chirped-mirror dispersion compensated Ti:Sapphire laser oscillator was stabilized. The offset frequency corresponding to the rate of change of the CE phase was obtained by spectrally broadening the oscillator pulses in a photonic crystal fiber and interfering the f and 2f components. An offset frequency linewidth of 100 mHz was obtained and could be locked over several hours. The effect of path length drift in the interferometer used for CE phase stabilization of the laser oscillator was investigated. By stabilizing the path length drift, the interferometer noise was reduced by several orders of magnitude. The CE phase drift through a grating-based chirped-pulse multi-pass amplifier was investigated. Varying the grating separation by 1μm in the stretcher was found to cause a shift of 3.7 +/- 1.2 rad of the CE phase. The CE phase could be stabilized to within 160 mrad rms error by feedback controlling the grating separation. By locking the path length in the f-to-2f interferometer used to stabilize the CE phase of the oscillator pulses, the fast (>3 Hz) CE phase drift of the amplified laser pulses was reduced from 79 to 48 mrad. It was also found that the CE phase could be shifted and set to any value within a 2π range by changing the grating separation. Also, the CE phase could be continuously modulated within a 2π range while maintaining a relative phase error of 171 mrad. The CE phase shift of a grating-based compressor was found to be stabilized to 230 mrad rms. The effect of laser power fluctuation on the CE phase measurement was also investigated. It was found that a 1% fluctuation of the laser energy caused a 160 mrad error in the CE phase measurement. A two-step model is proposed to explain the phase-energy coupling in the CE phase measurement. The model explains the experimentally observed dependence of the group delay between the f and 2f pulses on the laser energy. Few-cycle pulses were CE phase stabilized to 134 mrad rms and were used to perform above-threshold ionization and high harmonic generation.

Doctor of Philosophy / Department of Physics / Kristan L. Corwin / We have made significant accomplishments in the development of portable frequency standard inside hollow optical fibers. Such standards will improve portable optical frequency references available to the telecommunications industry. Our approach relies on the development of a stabilized Cr:forsterite laser to generate the frequency comb in the near-IR region. This laser is self referenced and locked to a CW laser which in turn is stabilized to a sub-Doppler feature of a molecular transition. The molecular transition is realized using a hollow core fiber filled with acetylene gas. We finally measured the absolute frequency of these molecular transitions to characterize the references. In this thesis, the major ideas, techniques and experimental results for the development and absolute frequency measurement of the portable frequency references are presented. A prism-based Cr:forsterite frequency comb is stabilized. We have effectively used the prism modulation along with power modulation inside the cavity in order to actively stabilize the frequency comb. We have also studied the carrier-envelope-offset frequency (f0) dynamics of the laser and its effect on laser stabilization. A reduction of f0 linewidth from [similar to]2 MHz to [similar to]20 kHz has also been observed. Both our in-loop and out-of-loop measurements of the comb stability showed that the comb is stable within a part in 10^11 at 1-s gate time and is currently limited by our reference signal. In order to develop this portable frequency standard, saturated absorption spectroscopy is performed on the acetylene v1+v3 band near 1532 nm inside different kinds of hollow optical fibers. The observed linewidths are a factor 2 narrower in the 20 um fiber as compared to 10 um fiber, and vary from 20-40 MHz depending on pressure and power. The 70 um kagome fiber shows a further reduction in linewidth to less than 10 MHz. In order to seal the gas inside the hollow optical fiber, we have also developed a technique of splicing the hollow fiber to solid fiber in a standard commercial arc splicer, rather than the more expensive filament splicer, and achieved comparable splice loss. We locked a CW laser to the saturated absorption feature using a Frequency Modulation technique and then compared to an optical frequency comb. The stabilized frequency comb, providing a dense grid of reference frequencies in near-infrared region is used to characterize and measure the absolute frequency reference based on these hollow optical fibers.

Doctor of Philosophy / Department of Physics / Kristan L. Corwin / Current portable near-infrared optical frequency references offer modest accuracy and instability compared to laboratory references. Low pressure reference cells are necessary to realize features narrower than the Doppler broadened overtone transitions, and most setups to date have occurred in free-space. Hollow-core photonic crystal fibers offer a potential alternative to free-space setups through their small cores (~10’s of µm) and low-loss guidance. Furthermore, HC-PCF can be made into fiber cells that could be directly integrated into existing telecommunications networks. Efforts were made to fabricate these fiber cells with a low pressure of molecules trapped inside, but this has proven to be quite challenging. Therefore, investigation of these fibers is conducted by placing the ends of the fiber inside vacuum chambers loaded with acetylene (12C2H2). The linewidths of several P branch transitions (near 1.5 µm) are investigated as a function of acetylene pressure and optical pump power in three different HC-PCFs. Frequency modulation spectroscopy is then implemented on the acetylene-filled HC-PCF to generate sub-Doppler dispersion features that are useful for frequency stabilization using standard servo electronics. Instability and accuracy of this near-IR optical reference were then determined by analysis of heterodyne experiments conducted with frequency combs referenced to a GPS-disciplined rubidium oscillator. The instability and accuracy of this HC-PCF reference are within an order of magnitude of free-space experiments, as expected based on the ratio of linewidths observed in the two experiments. Therefore, HC-PCF has been shown to be suitable for potential frequency references. Further work is necessary to fabricate gas fiber cells with high optical transmission and low molecular contamination.

Doctor of Philosophy / Department of Physics / Itzhak Ben-Itzhak / Present laser technology allows for the production of ultra short (&7 fs) intense (.1016 W/cm2)pulses, which are comparable in duration and interaction strength to the vibrational period and the interaction that binds the electron in molecules, respectively. In this intense-field ultra short-pulse regime one can both measure and manipulate dynamics on the femtosecond timescale. To probe the dynamics of laser-matter interactions in this regime, we have chosen to start from the simplest possible molecule - H+ 2 , which can either dissociate into H + p or ionize into p + p + e. We have designed and employ a coincidence three-dimensional momentum imaging technique which allows us to measure ionization and dissociation of a molecular ion beam target simultaneously, while completely separating the two channels from each other. By varying the laser intensity and the pulse duration, we measure the intensity and pulse length dependent momentum distributions for laser induced fragmentation of H+ 2 at 790 nm. These dissociation measurements are in agreement with the phenomena predicted using the adiabatic Floquet picture, e.g. bond softening, in addition to more sophisticated calculations done by solving the time-dependent Schrodinger equation in the Born-Oppenheimer representation. Furthermore, the structure seen in ionization in our measurements and soon after by others is explained via a unified diabatic Floquet picture, which includes both ionization and dissociation in a single intensity and wavelength dependent picture that includes nuclear motion. Additionally, we use the same experimental techniques and apparatus to probe the laser-induced dynamics of multi-electron diatomic molecules, e.g. O+2, N+2, and ND+. The most probable dissociation and ionization pathways producing the features seen in these measurements are discerned using the angular and kinetic-energy-release distributions in conjunction with the diabatic Floquet picture. Finally, we extend these experimental techniques and interpretive models to the simplest polyatomic molecule - H+ 3 , whose fragmentation presents challenges both in our first-of-their-kind experiments and in physical interpretation.

Master of Science / Department of Physics / Brian R. Washburn / This thesis reports our attempt towards achieving a phase stabilized free-space nonlinear polarization rotation (NPR) mode locked erbium doped fiber laser frequency comb system. Optical frequency combs generated by mode-locked femtosecond fiber lasers are vital tools for ultra-precision frequency metrology and molecular spectroscopy. However, the comb bandwidth and average output power become the two main limiting elements in the application of femtosecond optical frequency combs. We have specifically investigated the free-space mode locking dynamics of erbium-doped fiber (EDF) mode-locked ultrafast lasers via nonlinear polarization rotation (NPR) in the normal dispersion regime. To do so, we built a passively mode-locked fiber laser based on NPR with a repetition rate of 89 MHz producing an octave-spanning spectrum due to supercontinuum (SC) generation in highly nonlinear fiber (HNLF). Most significantly, we have achieved highly stable self-starting NPR mode-locked femtosecond fiber laser based frequency comb which has been running mode locked for the past one year without any need to redo the mode locking. By using the free-space NPR comb scheme, we have not only shortened the cavity length, but also have obtained 5 to 10 times higher output power (more than 30 mW at central wavelength of 1570 nm) and much broader spectral comb bandwidth (about 54 nm) compared to conventional all-fiber cavity structure with less than 1 mW average output power and only 10 nm spectral bandwidth. The pulse output from the NPR comb is amplified through a 1 m long EDF, then compressed by a length of anomalous dispersion fiber to a near transform limited pulse duration. The amplified transform limited pulse, with an average power of 180 mW and pulse duration of 70 fs, is used to generate a supercontinuum of 140 mW. SC generation via propagation in HNLF is optimized for specific polling period and heating temperature of PPLN crystal for SHG around 1030 nm. At last, we will also discuss the attempt of second harmonic generation (SHG) by quasi phase matching in the periodically polled lithium niobate (PPLN) crystal due to nonlinear effect corresponding to different polling period and heating temperature.

Master of Science / Department of Physics / Brett D. Esry / The two-state field-aligned (1-D) model has been employed to investigate the dissociation dynamics of a hydrogen molecular ion and its isotopes under the Born-Oppenheimer approximation without rotation. The emphasis of this work was on the role of mass during the dynamical dissociation processes and on the laser-induced branching ratios between different photon pathways. Firstly, we have found that scaling the pulse duration of the laser pulse, applied to H[subscript]2+ and D[subscript]2+ , by the square root of the mass ratio of these isotopes will produce similar structure in the nuclear kinetic energy release (KER) spectra. In fact, the similarity of the spectra is enhanced by including some averaging that is necessary for comparison with experiment. For this to occur, the same broad initial vibrational distribution and a short pulse are preferred. Using this scaling idea, it is possible to produce effectively shorter laser pulses by studying heavier isotopes, like D[subscript]2+. Secondly, we have demonstrated analytically and numerically that there is a carrier-envelope phase effect in the total dissociation probability (TDP) of H[subscript]2+, and this effect grows with nuclear mass. We further show that under the same laser conditions, the CEP effect in the asymmetry between breakup channels decreases with mass. Our analytic expressions enhance the idea that CEP effects can be understood as an interference between different n-photon processes. Thirdly, the trends in the dissociation dynamics of H[subscript]2+ and D[subscript]2+ in a 800nm ultra short intense laser field were demonstrated by studying the dissociation branching ratios of multiphoton processes as a function of the laser peak intensity (from 8[times]10[superscript]9 to 10[superscript]14 W/cm[superscript]2) or pulse length (5fs-7.5fs). Based on the two-state approximation, an energy-analysis method (EAM) was employed to separate multiphoton processes. The results show that the one-photon dissociation process dominates over all other photon processes under all the laser conditions applied in the calculations and that the zero-photon process contributes to a surprisingly large fraction of the total dissociation. Two- and three- photon dissociation are weaker processes, but become more and more important as the laser peak intensity and pulse length increases. A two-state Floquet method was used to check the accuracy of the EAM, and good agreement between the two methods was found, demonstrating the reliability of the EAM. In comparison with H[subscript]2+, D[subscript]2+ displays stronger two and three photon branching ratios (above-threshold dissociation - ATD), which can be attributed to the late arrival of D[subscript]2+ to the critical distance for ATD to occur due to its heavier mass. Therefore, this "mass" effect can be used to steer the molecular dissociation pathways.