The experimental work in this thesis is divided into two distinct parts. In both parts, broadband femtosecond laser pulses are "shaped" by adjusting the relative phase and amplitude of spectral components. In the first set of experiments, time-dependent perturbation theory is used to show that the probability of a quantum transition in atomic rubidium can be substantially enhanced or suppressed using pulse shaping, compared to the probability of transition observed when a transform-limited or "flat phase" optical pulse is used. These enhancement or suppression effects are also demonstrated experimentally. As quantum interference (the material phase having been transferred from the optical phase) is used to enhance or diminish a particular final quantum state, this can be classified as a quantum coherent control experiment. In the second set of experiments, an optical pulse is scattered into a train of pulses by a layered structure. The layered structure is used to simulate the effect of optical pulses travelling through certain types of complex media. One consequence of the disruption of a single pulse into a train of pulses is lower per-pulse peak intensity, and thus a greatly diminished nonlinear signal. It is shown that spectral pulse shaping (in phase only) is sufficient to pre-compensate for the scattering structure, allowing a single transform-limited pulse to be obtained at the output.
The experimental work in this thesis is divided into two distinct parts. In both parts, broadband femtosecond laser pulses are "shaped" by adjusting the relative phase and amplitude of spectral components. In the first set of experiments, time-dependent perturbation theory is used to show that the probability of a quantum transition in atomic rubidium can be substantially enhanced or suppressed using pulse shaping, compared to the probability of transition observed when a transform-limited or "flat phase" optical pulse is used. These enhancement or suppression effects are also demonstrated experimentally. As quantum interference (the material phase having been transferred from the optical phase) is used to enhance or diminish a particular final quantum state, this can be classified as a quantum coherent control experiment. In the second set of experiments, an optical pulse is scattered into a train of pulses by a layered structure. The layered structure is used to simulate the effect of optical pulses travelling through certain types of complex media. One consequence of the disruption of a single pulse into a train of pulses is lower per-pulse peak intensity, and thus a greatly diminished nonlinear signal. It is shown that spectral pulse shaping (in phase only) is sufficient to pre-compensate for the scattering structure, allowing a single transform-limited pulse to be obtained at the output.
Creating and controlling well-defined single-photon states is important for many quantum enhanced technologies. Information can be encoded in any degree of freedom associated with a single-photon field excitation, for example in the polarization or transverse spatial mode structure. The ability to encode multiple qubits in these states is desirable for high data transmission rates and increased information processing capacity. The spectral-temporal domain offers a large Hilbert space for encoding information, well suited to integrated optical architectures owing to the low cross-talk between channels. Indeed, time-frequency encoding is an integral component of existing information technologies infrastructure. Thus, complete, coherent control of the spectral-temporal mode structure of light is essential to advancing optical quantum technologies. Arbitrary control of single-photon states has been demonstrated in the polarization and spatial-momentum degrees of freedom however, is yet to be established in the spectral-temporal domain. Recently it was shown that spectral-temporal pulse shaping is experimentally feasible using nonlinear optical methods. However, such techniques can introduce noise photons, are challenging to implement deterministically and require specially prepared auxiliary pump pulses. Furthermore, they are typically only possible at relatively low repetition rates to avoid damage of nonlinear optical materials. Here, we demonstrate deterministic pulse shaping of single-photon wave packets by introducing a time-varying phase. Applying linear or quadratic phase to the wave packet introduces a spectral shift or spectral broadening, respectively. Achieving significant spectral manipulation requires temporal-phase modulation on the order of π. The phase must also vary on the same time scale as the optical pulses, approximately 1 ps in duration here. This relatively rapid phase variation is achieved using a fast electro-optic phase modulator. The modulator is driven by a time-varying voltage that is synchronized with a pulse train of single-photon wave packets for accurate temporal phase control. In this thesis, we experimentally demonstrate control of the spectral-temporal state of single-photon wave packets using this method. Heralded single-photon wave packets are generated by spontaneous parametric down conversion pumped by a frequency-doubled Titanium-Sapphire laser oscillator with 80 MHz repetition rate. To achieve significant modulation of single-photon pulses a 10 V peak-to-peak radio-frequency signal of 40 GHz drives the phase modulator, which requires approximately 3.6 V to achieve a π phase shift. The signal is synchronized with the oscillator pulse train using custom designed electronics. Details of these electronics are presented, resulting in a robust phase and amplitude controllable 40 GHz voltage source, phase locked to the single-photon pulse train. To demonstrate the utility of this pulse-shaping method we experimentally show spectral shearing of almost 1 nm for single-photon wave packets with 830 nm central wavelength and 1 nm bandwidth. Measurement of the second-order intensity correlation before and after the wave-packet manipulation remains constant within uncertainty of the measurement, showing that the quantum nature of the single-photon source is not deteriorated by the modulator. Preservation of the wave-packet coherence is verified by two-photon interference between spectrally sheared and non-modulated single-photons.
The main goal of this PhD work is an experimental study of coherent excitation of atomic and molecular wavepackets, i.e. superpositions of many quantum eigenstates, by shaped femtosecond pulses. Approaches allowing nearly complete population transfer between quantum eigenstates were well studied in the past within the two level approximation. In this work we focus on adiabatic and non-adiabatic methods of population transfer beyond the two-level approximation. Excitation of multi-level target states is possible due to broad spectrum of an ultrashort pulse which contains frequencies needed for multiple transitions to different states in the final superposition. At the same time, the spectrum of an ultrashort pulse can be modified, or ``shaped'', in order to affect the excitation process and control the amplitudes in the final superposition. Both non-adiabatic and quasi-adiabatic methods were first implemented and studied in electronic wavepackets in alkali atoms. The non-adiabatic approach revealed features linked to the strong-field perturbations of the energy level structure of the quantum system. An adiabatic method was implemented for the first time on a femtosecond time scale, and was thoroughly characterized. The control over complex amplitudes in the target superposition was demonstrated as well as completeness of the population transfer. In the second part of this work, we focused on coherent control of rotational wavepackets in diatomic molecules. Rotational excitation by a periodic train of femtosecond pulses was investigated in the context of ``delta-kicked'' rotor - a paradigm system for studying quantum chaos, and the effect of quantum resonance was demonstrated for the first time in a system of true quantum rotors. Control of uni-directional molecular rotation was proposed and demonstrated with a novel ``chiral pulse train'' - a sequence of femtosecond pulses with polarization rotating from pulse to pulse by a predefined angle. All the developed techniques offer new tools in coherent control of atomic and molecular wavepackets on an ultrashort time scale.
In this thesis, atomic coherence is used to enhance nonlinear optical processes in multi-level atoms. The multi-photon transitions are driven resonantly, and at the same time without absorptive losses, by using electromagnetically induced transparency (EIT), thereby allowing the study of χ(3) and χ(5) nonlinearities using weak driving fields. The coherently modified probe beam(s) and the atom-radiated signal fields arising from four- and six- wave- mixing (FWM and SWM) processes are measured in the spectral, temporal and spatial domains. In a three-level ladder-type atomic system, multiple peaks having spectral asymmetries are observed in the EIT window as well as in the FWM signal waveforms due to the diverse multiplicities of the participating atomic states. Using phase control tailored in the frequency domain, we demonstrate all-optical methods to control these spectral waveforms and discuss applications involving waveform-shaping and metrology. For the EIT study we demonstrate a switching of multiple dark peaks into bright peaks via phase-control of interferences in the underlying dark-states. In the FWM study we demonstrate all-optical spectral line shape symmetrization, linewidth narrowing and bandwidth switching. In a four-level inverted-Y-type atomic system, we drive and measure coexisting and phase-matched FWM and SWM signals. By using precision control of the relative phase and amplitude between these two processes of different nonlinear orders, we demonstrate phase coherence between them. First, a single-phase measurement is performed in the temporal and spatial domains, and the interferogram is used to measure the resonant frequency of the 5D5/2-5P3/2 atomic transition in 85Rb. Second, the method is extended to realize a capacity for two-phase measurement. In this case, the spectral bandwidth of the signal is modified in order to measure the phase-shift occurring in one Mach-Zehnder interferometer, while the intensity of the total signal waveform measures the phase-shift occurring in a second interferometer. Finally, we demonstrate phase-dependent spatial fusion between two ultra-weak optical fields by using a strong coupling field to first convert the weak fields into bosonic dark-state polaritons, which are then steered into a common all-optical waveguide mode arising due to the coupling field's intensity distribution and the resulting cross-Kerr refractive index gradient.
Coherent control schemes are interference-based procedures for the control of quantum mechanical systems informed by a careful analysis of the physical conditions on interference. In this thesis, the coherent control approach is applied to experimental phase control in the condensed phase. Specifically, coherent control schemes are proposed as mechanisms for experimental manifestations of phase interference. First, a simulation of a ``black box'' feedback control experiment using realistic pulse shaping is shown to automatically find a specific, previously devised coherent control scheme. Qualitative features of experiments performed in this way are reproduced. Second, an analysis of interference in one-photon phase control yields an upper bound on the duration of phase effects. One-photon phase control was previously shown to be possible only over the transient (as opposed to steady-state) value of observables. The bound described here quantifies this statement and provide a rigorous definition of ``transient'' control. We propose that phase control beyond this bound, as reported in a number of weak-field experimental and computational studies, is the result of previously unaccounted for multiphoton effects. Third, we analyze a recent experiment showing phase control of the macroscopic current emanating from living brain cells photostimulated by two-photon absorption. We propose mechanisms for the phase dependence of the current that operate over fifteen orders of magnitude in time, from the femtosecond dynamics of light-matter interactions to the macroscopic dynamics of neuron current. Significantly, coherent control is extended to the case of systems repeatedly interacting with pulses of light; we show that macroscopic control is obtained, in this case, from the multi-pulse accumulation of small phase effects. Research into multiphoton control led to the development of a novel algorithm to compute higher order perturbation theory integrals, presented in the final chapter of this thesis. The Fourier-Laplace Inversion of the Perturbation Theory (FLIPT) method is a highly efficient, numerically exact, ``black box'' integration algorithm. The FLIPT method exploits the specific structure of the multidimensional perturbation theory integrals to obtain an exponential improvement in performance over standard quadrature.
Multiphoton transitions can be reached by many routes through a continuum of virtual levels. We show that the transition probability of two-photon and multiphoton processes can be controlled by tailoring the shape of an ultrashort excitation pulse, so that the many paths leading to the final state interfere to give a desired probability amplitude. We analyze the effect of pulse shapes on N-photon absorption as well as on Raman transitions. We show theoretically that certain tailored dark pulses do not excite the system at all, while other shaped pulses induce transitions as effectively as transform limited pulses, even when their peak amplitudes are greatly reduced. These results are confirmed experimentally for two-photon transitions in atomic cesium.
The four-wave mixing produced with two ultrashort phase-locked !-3! laser pulses propagating coherently in a two-level system in the infrared spectral region is shown to depend on the pulses relative phase. The Maxwell-Bloch equations are solved beyond the rotating-wave approximation to account for field frequencies which are largely detuned from the atomic resonance. The relative phase dominating the efficiency of the coupling to the 5! anti-Stokes Raman component is determined by sign of the total ac Stark shift induced in the system, in such a way that the phase influence disappears precisely where the ac Stark effect due to both pulses is compensated. This fundamental quantum interference effect can be the basis for nonlinear ultrafast optical spectroscopy techniques. Phenomena arising from the coherent control of nonlinear interactions are of importance in fields as diverse as optoelectronics and materials research, in high harmonic generation, in photoionization or molecular dissociation, and in biological applications such as spectroscopy and imaging, among others [1, 2, 3, 4, 5, 6, 7]. Optical quantum coherent control is based on the fact that the phases of interfering transition amplitudes in light-matter interactions can be controlled through the optical phase of coherent light sources that drive the interaction, in such a way that the transition rates to final states and the dynamics at various stages of the process can be modified [1]. In a recent paper [8], a theoretical investigation on the quantum coherent control of the optical transient four-wave mixing of two intense phase-locked femtosecond laser pulses of central angular frequencies ω and 3ω propagating in a two-level atom (TLA) was reported. It was shown how the nonlinear (χ (3) ) coupling to the antiStokes Raman field at frequency 5ω depends critically on the initial relative phase φ of the propagating pulses. In Ref. [8], the study was centered to intense pulses in the visible and ultraviolet spectral regions, with frequencies at resonance or lower than the atomic transition. The phenomena observed in [8], however, can be scaled to various laser and material parameters. In the infrared spectral range, for instance, experiments on ultrafast molecular dynamics are frequently performed by help of twocolor pump probe nonlinear spectroscopy techniques. In this type of studies, due to the high intensities inherent to ultrashort (subpicosecond) pulses, nonlinear effects such as stimulated Raman processes may become important and are often utilized as a complementary tool to gain information [9]. In this Letter, we address the conditions for quantum coherent control of transient four-wave mixing interactions with two phase-locked ω-3ω femtosecond laser pulses in the mid-IR spectral region. Our purpose is to reveal the basic physics for a strict two-level medium and to this end the Maxwell-Bloch TLA will be considered. We will study pulses with a duration of 300 fs (with a w 5w