Transient coherent oscillations in a closed L system under far-off resonant Raman fields were investigated theoretically. It has been found that the coherent superposition of the ground states can be formed due to the absorption even for initial maximal mixed ground states. The absorption oscillates with a period depending on the two-photon detuning when the system is initially in a transparent state and the two-photon Raman detuning is suddenly changed. The amplitude of the absorption decays with the decay rate of the ground states, which is different from the case when the lasers are applied resonantly. These transient coherent oscillations can be used to measure the relaxation rate of the ground states.
Transient coherent oscillations in a closed L system under far-off resonant Raman fields were investigated theoretically. It has been found that the coherent superposition of the ground states can be formed due to the absorption even for initial maximal mixed ground states. The absorption oscillates with a period depending on the two-photon detuning when the system is initially in a transparent state and the two-photon Raman detuning is suddenly changed. The amplitude of the absorption decays with the decay rate of the ground states, which is different from the case when the lasers are applied resonantly. These transient coherent oscillations can be used to measure the relaxation rate of the ground states.
The phenomenon of coherent Raman beats observed recently by Shoemaker and Brewer is analyzed through solutions of the coupled Maxwell-Schr\"odinger equations. The effect arises in coherently prepared molecular samples where the level degeneracy is suddenly removed by Stark-pulse switching. The problem divides into two parts: (a) a steady-state preparative regime whereby the initially degenerate quantum levels are placed in superposition by a resonant laser field, and (b) a transient regime in which coherent forward Raman scattering decays in the presence of the same laser field during a nonresonant condition. The laser and Raman light thus propagate together and produce at a detector a coherent beat with a frequency that corresponds to the level splitting between initial and final states. The beat signal possesses the remarkable property of being entirely independent of longitudinal molecular velocity in the case of a plane-wave laser beam and of being almost so for milliradian divergence. It follows that relaxation involving velocity-changing collisions and that Doppler dephasing effects are absent in coherent Raman beats, in agreement with experimental measurements of the decay rate. The effect of off-resonance excitation on the dephasing time and on the period of the beat signal is also discussed, and the possibility of a small rotation of the plane of polarization of the scattered light is included. The subject presents a new aspect of Raman scattering which can now yield precise radio-frequency splittings directly and offers a selective way of examining relaxation phenomena.
Quantum coherence and interference in atomic systems can lead to interesting optical phenomena such as nonabsorbing resonances, lasing without inversion, generating an ultrahigh index of refraction without absorption, propagation of light pulses without losses. In the last-named is given the title transparency. Up to now it is known some types of transparency in multi-level resonant media. One of them is electromagnetically induced transparency (EIT). The phenomenon of EIT in the propagation of laser radiation through an absorbing medium has been recently investigated and explained in terms of quantum coherence and interference for multi-level atomic system. For instance in the (Lambda) -system, if the atomic medium is prepared in a quantum superposition of states, matched pulses, i.e., a pair of optical pulses whose amplitude and phase have a well defined relation, propagate without absorption. The mechanism of coherent population trapping is responsible for EIT in a (Lambda) -system. There is another, well known mechanism for creating transparency in a two-state atom: self-induced transparency, or SIT. Here, a single pulse whose area (the integral of its Rabi frequency over time) is 2(pi) is applied to the medium. Such a pulse causes the atoms to cycle smoothly from the ground to the excited state and then back again. In principle, such a pulse can propagate over long distances. SIT can be generalized to multi-level systems and multiple quasi-monochromatic fields. Generalization of SIT in a (Lambda) -system was obtained in reference 2. In this report we present a new type of transparency (combined transparency). This type describes propagation of laser pulse through a (Lambda) -type medium where the initial atomic state is prepared in the form of spatially varying coherent superposition of low-energetic states (initial coherency gradient). The common envelope behaves as usual 2(pi) hyperbolic secant pulse, but the ratio between the components of frequencies transitions 1> yields 3> and 2> yields 3> changes due to coherent Raman scattering so (phi) equals atan(E1/E2) equals (pi) /2-Gz, where z is the coordinate, G is the constant determined by both the incident pulse parameters and the initial coherence between the atomic states. Our solution demonstrates a direct connection of EIT in adiabatic regime to the SIT effects. This type of a transparency is given the title screw-type transparency, because for the given form of incident pulse (pitch of screw) medium is transparent, if medium's the initial coherence gradient is correspondingly prepared (thread on a engine nut). Besides a transparency, this phenomenon contains a transformation of the incident pulse frequency during the process of the propagation. This property of the phenomena can be result in a complete conversion of the frequency.
A class of molecular two-photon processes, occurring under transient or steady-state conditions, is analyzed exactly for certain cases using a density-matrix formalism. Our results are relevant to the recently observed phenomena of transient coherent Raman beats and steady-state two-photon absorption of oppositely directed laser beams. Lowest-order perturbation theories have shown that these processes are insensitive to the Doppler effect, and consequently the linewidth is unaffected by Doppler broadening and by elastic collisions that change molecular velocity. The solutions presented here are of the same form for the Raman and two-photon problems and reveal significant power-dependent frequency shifts and line broadening that correct the ideal Doppler-free solutions. For the transient case, we assume a molecular three-level quantum structure that can be switched in or out of optical resonance with cw laser radiation by means of a pulsed dc Stark field, but the solutions also apply when resonant optical pulses are introduced. During the resonant condition when the Stark pulse is on, the three levels are prepared in coherent superposition, and during the nonresonant condition following the Stark pulse, the laser field(s) stimulates the coherently prepared sample in a transient two-photon process. One of these processes, the Ramanbeat effect, has been observed in forward scattering, but the second one, transient two-photon emission, should be observable in backward scattering. Bloch-like equations are derived for this three-level problem that facilitate an exact pulse solution for state preparation. Following the pulse, transient decay is well-approximated by a perturbation calculation. For the steady-state case, an exact solution is also obtained and is of interest for continuous-wave spectroscopy or for transient experiments requiring an initial preparation of quantum states, prior to Stark switching. These solutions exhibit a power-dependent line broadening and a frequency shift of magnitude $\ensuremath{\sim}\frac{\ensuremath{\Delta}({\ensuremath{\alpha}}^{2}\ensuremath{-}{\ensuremath{\beta}}^{2})}{({\ensuremath{\Delta}}^{2}+\frac{1}{{T}_{2}^{2}})}$, in agreement with our earlier estimate, where $\ensuremath{\alpha}$ and $\ensuremath{\beta}$ are the Rabi flopping frequencies for the two intermediate transitions and $\ensuremath{\Delta}$ is the off-resonance tuning behavior for one of them.
The temporal evolution of coherent population trapping (CPT) was observed in rubidium atomic vapor when sudden changes were made to the detuning of a weak Raman field. The subsequent creation and destruction of CPT are caused by the temporal oscillations of optically induced Raman coherence, with their period depending on the Raman detuning. The oscillating signal was observed over a time of order of tens of milliseconds, and the dependence of the relaxation time on the cell temperature and laser power were investigated. The main features of the experimental observations were well explained by the time-dependent density-matrix equations.
Optical response of an active medium can substantially be modified when coherent superpositions of states are excited, that is, when systems display quantum coherence and interference. This has led to fascinating applications in atomic and molecular systems. Examples include coherent population trapping, lasing without inversion, electromagnetically induced transparency, cooperative spontaneous emission, and quantum entanglement. \n \nWe study quantum coherence effects in several quantum optical systems and find interesting applications. We show that quantum coherence can lead to transient Raman lasing and lasing without inversion in short wavelength spectral regions--extreme ultraviolet and x-ray--without the requirement of incoherent pumping. For example, we demonstrate transient Raman lasing at 58.4 nm in Helium atom and transient lasing without inversion at 6.1 nm in Helium-like Boron (triply-ionized Boron). We also investigate dynamical properties of a collective superradiant state prepared by absorption of a single photon when the size of the sample is larger than the radiation wavelength. We show that for large number of atoms such a state, to a good approximation, decays exponentially with a rate proportional to the number of atoms. We also find that the collective frequency shift resulting from repeated emission and reabsorption of short-lived virtual photons is proportional to the number of species in the sample. Furthermore, we examine how a position-dependent excitation phase affects the evolution of entanglement between two dipole-coupled qubits. It turns out that the coherence induced by position-dependent excitation phase slows down the otherwise fast decay of the two-qubit entanglement. We also show that it is possible to entangle two spatially separated and uncoupled qubits via interaction with correlated photons in a cavity quantum electrodynamics setup. Finally, we analyze how quantum coherence can be used to generate continuous-variable entanglement in quantum-beat lasers in steady state and propose possible implementation in quantum lithography.