V-type three-level systems, where two excited states share a common ground state, serve as fundamental models for exploring coherent light-matter interactions in a range of quantum systems, from atomic gases to semiconductor nanostructures. In this work, we investigate the coherent evolution of such a system under strong femtosecond-pulse excitation by numerically solving the optical Bloch equations. Our analysis shows that the coherent evolution of a three-level system critically depends on the product of the excitation-pulse duration and energy separation between the excited states. Building on this understanding, we extend our analysis to simulate two-dimensional coherent spectra in a high-intensity regime. We demonstrate a control over the coherent pathway contributions to the nonlinear optical response of a V-type system by varying the intensity of the excitation pulses. This control is manifested through the ability to selectively turn individual spectral features on or off in the 2D spectra, each corresponding to distinct quantum pathways. Furthermore, the pulse intensities are varied to precisely adjust the phase of these peaks. Our approach provides a simple and robust framework for achieving control of coherent response of multilevel systems.
V-type three-level systems, where two excited states share a common ground state, serve as fundamental models for exploring coherent light-matter interactions in a range of quantum systems, from atomic gases to semiconductor nanostructures. In this work, we investigate the coherent evolution of such a system under strong femtosecond-pulse excitation by numerically solving the optical Bloch equations. Our analysis shows that the coherent evolution of a three-level system critically depends on the product of the excitation-pulse duration and energy separation between the excited states. Building on this understanding, we extend our analysis to simulate two-dimensional coherent spectra in a high-intensity regime. We demonstrate a control over the coherent pathway contributions to the nonlinear optical response of a V-type system by varying the intensity of the excitation pulses. This control is manifested through the ability to selectively turn individual spectral features on or off in the 2D spectra, each corresponding to distinct quantum pathways. Furthermore, the pulse intensities are varied to precisely adjust the phase of these peaks. Our approach provides a simple and robust framework for achieving control of coherent response of multilevel systems.
Simple analytical approaches for implementing strong field coherent control schemes are often elusive due to the complexity of the interaction between the intense excitation field and the system of interest. Here, we demonstrate control over multiphoton excitation in a three-level resonant system using simple, analytically derived ultrafast pulse shapes. We utilize a two-dimensional spatiotemporal control technique, in which temporal focusing produces a spatially dependent quadratic spectral phase, while a second, arbitrary phase parameter is scanned using a pulse shaper. In the current work, we demonstrate weak-to-strong field excitation of 85Rb, with a $\ensuremath{\pi}$ phase step and the quadratic phase as the chosen control parameters. The intricate dependence of the multilevel dynamics on these parameters is exhibited by mapping the data onto a two-dimensional control landscape. Further insight is gained by simulating the complete landscape using a dressed-state, time-domain model, in which the influence of individual shaping parameters can be extracted using both exact and asymptotic time-domain representations of the dressed-state energies.
The evolution of a V-type three-level system is studied, whose two resonances are coherently excited and coupled by two ultrashort laser pump and probe pulses, separated by a varying time delay. We relate the quantum dynamics of the excited multilevel system to the absorption spectrum of the transmitted probe pulse. In particular, by analyzing the quantum evolution of the system, we interpret how atomic phases are differently encoded in the time-delay-dependent spectral absorption profiles when the pump pulse either precedes or follows the probe pulse. This scheme is experimentally applied to atomic Rb, whose fine-structure-split 5s (2)S{1/2}→5p(2)P{1/2} and 5s(2)S_{1/2}→5p(2)P{3/2} transitions are driven by the combined action of a pump pulse of variable intensity and a delayed probe pulse. The provided understanding of the relationship between quantum phases and absorption spectra represents an important step towards full time-dependent phase reconstruction (quantum holography) of bound-state wave packets in strong-field light-matter interactions with atoms, molecules, and solids.
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
The calculation of the coherent nonlinear response of a system is essential to correctly interpret results from advanced techniques such as two-dimensional coherent spectroscopy. Usually, even for the simplest systems, such calculations are either performed for low-intensity excitations where perturbative methods are valid and/or by assuming a simplified pulse envelope, such as a δ-function in time. Here, we use the phase-cycling method for the exact calculation of the nonlinear response without making the aforementioned approximations even for high-intensity excitation. We compare the simulation results to several experimental observations to prove the validity of these calculations. The saturation of the photon-echo signal from excitons in a semiconductor quantum well sample is measured. The excitation-intensity dependent measurement shows nonlinear contributions up to twelfth order. Intensity-dependent simulations reproduce this effect without explicitly considering higher-order interactions. In addition, we present simulation results that replicate previously reported experiments with high-intensity excitation of semiconductor quantum dots. By accurately reproducing a variety of phenomena such as higher-order contributions, switching of coherent signals, and changes in photon-echo transients, we prove the efficacy of the phase-cycling method to calculate the coherent nonlinear signal for high-intensity excitation. This method would be particularly useful for systems with multiple, well-separated peaks and/or large inhomogeneities.
We theoretically demonstrate that selective resonant excitation can be achieved in a dense collection of V-type three-level atoms by optimizing the pulse delay and peak intensity ratio of an applied phase-tailored ultrashort pulse pair. Near-dipole-dipole interaction plays an important role in the quantum control of selective excitations since it brings about an intrinsic frequency shift in the atomic resonance, which builds up various excitation pathways. As a consequence, we can control the quantum interference between various pathways by shaping the excitation pulse pair to steer the atomic excitation selectively toward a desired quantum state.
The last two decades have marked a revolution in materials science with the appearance of two novel groups of materials with promising features for future optoelectronics. The first are artificially fabricated metamaterials, composed of carefully engineered nanoparticle arrays, displaying tailored mie and plasmonic resonant responses [1]. The second are atomically thin two-dimensional (2D) semiconductor crystals, characterized by tightly bound excitons, promising for their flexible heterostructure stacking capabilities [2]. In this work we introduce a novel pulse-shaping approach, to study and control the coherent dynamics of resonant quasparticle excitations in such materials. By constructing a state-of-the-art pulse shaper for controlling the spectral phase of our sub-10 fs laser, we tailor the temporal order of instantaneous frequencies driving the noninstantaneous electronic response of the material on resonance [3]. We measure the response to various pulse shapes through monitoring the four-wave mixing (FWM) generation. Our contribution can be described by to three key aspects: We retrace the resonant dispersion by synchronizing the phase-dependent intra-pulse nonlinear wave-mixing with the prediction of the anharmonic oscillator model (AHO). We disentangle the multitude of interfering quantum pathways caused by the resonant dynamics, and reassemble them to achieve a strong nonlinear enhancement as well as near-complete destruction of the nonlinear yield. By controlling two successive resonant states, we present a glimpse into inter-state selectivity. We display nonlinear generation by improving the coherence in one state while suppressing the coherence in another. We believe this work places the control of coherent quasiparticle dynamics in condensed matter systems as a highly appealing field for both fundamental and applied research, such as improved nonlinear sensing, broadband compressed light sources and various ultrafast optoelectronic applications.