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Bragg diffraction of an atomic wave packet in a retroreflective geometry with two counterpropagating optical lattices exhibits a light shift induced phase. We show that the temporal shape of the light pulse determines the behavior of this phase shift: In contrast to Raman diffraction, Bragg diffraction with Gaussian pulses leads to a significant suppression of the intrinsic phase shift due to a scaling with the third power of the inverse Doppler frequency. However, for box-shaped laser pulses, the corresponding shift is twice as large as for Raman diffraction. Our results are based on approximate, but analytical expressions as well as a numerical integration of the corresponding Schrodinger equation.
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Alkali-metal-vapor magnetometers, using coherent precession of polarized atomic spins for magnetic field measurement, have become one of the most sensitive magnetic field detectors. Their application areas range from practical uses such as detections of NMR signals to fundamental physics research such as searches for permanent electric dipole moments. One of the main noise sources of atomic magnetometers comes from the light shift that depends on the frequency of the pump laser. In this work, we theoretically study the light shift, taking into account the relaxation due to the optical pumping and the collision between alkali atoms and between alkali atoms and the buffer gas. Starting from a full master equation containing both the ground and excited states, we adiabatically eliminate the excited states and obtain an effective master equation in the ground-state subspace that shows an intuitive picture and dramatically accelerates the numerical simulation. Solving this effective master equation, we find that in the light-narrowing regime, where the line width is reduced while the coherent precession signal is enhanced, the frequency-dependence of the light shift is largely reduced, which agrees with experimental observations in cesium magnetometers. Since this effective master equation is general and is easily solved, it can be applied to an extensive parameter regime, and also to study other physical problems in alkali-metal-vapor magnetometers, such as heading errors.
We demonstrate coherent storage and retrieval of pulsed light using the atomic frequency comb quantum memory protocol in a room temperature alkali vapour. We utilise velocity-selective optical pumping to prepare multiple velocity classes in the $F=4$ hyperfine ground state of caesium. The frequency spacing of the classes is chosen to coincide with the $F=4 - F=5$ hyperfine splitting of the $6^2$P$_{3/2}$ excited state resulting in a broadband periodic absorbing structure consisting of two usually Doppler-broadened optical transitions. Weak coherent states of duration $2,mathrm{ns}$ are mapped into this atomic frequency comb with pre-programmed recall times of $8,mathrm{ns}$ and $12,mathrm{ns}$, with multi-temporal mode storage and recall demonstrated. Utilising two transitions in the comb leads to an additional interference effect upon rephasing that enhances the recall efficiency.
We show that coherent multiple light scattering, or diffuse light propagation, in a disordered atomic medium, prepared at ultra-low temperatures, can be be effectively delayed in the presence of a strong control field initiating a stimulated Raman process. On a relatively short time scale, when the atomic system can preserve its configuration and effects of atomic motion can be ignored, the scattered signal pulse, diffusely propagating via multiple coherent scattering through the medium, can be stored in the spin subsystem through its stimulated Raman-type conversion into spin coherence. We demonstrate how this mechanism, potentially interesting for developing quantum memories, would work for the example of a coherent light pulse propagating through an alkali-metal atomic vapor under typical conditions attainable in experiments with ultracold atoms.
We identify significant quantum many-body effects, robust to position fluctuations and strong dipole--dipole interactions, in the forward light scattering from planar arrays and uniform-density disks of cold atoms, by comparing stochastic electrodynamics simulations of a quantum master equation and of a semiclassical model that neglects quantum fluctuations. Quantum effects are pronounced at high atomic densities, light close to saturation intensity, and around subradiant resonances. We show that such conditions also maximize spin--spin correlations and entanglement of formation for the atoms, revealing the microscopic origin of light-induced quantum effects. In several regimes of interest, an enhanced semiclassical model with a single-atom quantum description reproduces light transmission remarkably well, and permits analysis of otherwise numerically inaccessible large ensembles, in which we observe collective many-body analogues of resonance power broadening, vacuum Rabi splitting, and significant suppression in cooperative reflection from atomic arrays.
We investigate dynamics of atomic and molecular systems exposed to intense, shaped chaotic fields and a weak femtosecond laser pulse theoretically. As a prototype example, the photoionization of a hydrogen atom is considered in detail. The net photoionization undergoes an optimal enhancement when a broadband chaotic field is added to the weak laser pulse. The enhanced ionization is analyzed using time-resolved wavepacket evolution and the population dynamics of the atomic levels. We elucidate the enhancement produced by spectrally-shaped chaotic fields of two different classes, one with a tunable bandwidth and another with a narrow bandwidth centered at the first atomic transition. Motivated by the large bandwidth provided in the high harmonic generation, we also demonstrate the enhancement effect exploiting chaotic fields synthesized from discrete, phase randomized, odd-order and all-order high harmonics of the driving pulse. These findings are generic and can have applications to other atomic and simple molecular systems.
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