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Acta Sinica Quantum Optica

Electric Dipole Radiation of Sr Atoms Induced by Polarized Light Field

Shougang Zhang

Published Jan 1, 2009• 0 citations
OpenAlex

Abstract

The atomic fluorescence can be explained perfectly by the classical theories of electric dipole radiation.The changes of fluorescence intensity of Sr atomic beam are detected and analysed by changing the polarization of the laser beam which interacts with Sr atomic beam,and the characterization of the electric dipole radiation of Sr atom is detected in the far zone.It is experimentally demonstrated that the electric dipole radiates energy in the far zone is based upon the relationship of sin2θ,by which the fluorescence can be detected more effectively.

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The atomic fluorescence can be explained perfectly by the classical theories of electric dipole radiation.The changes of fluorescence intensity of Sr atomic beam are detected and analysed by changing the polarization of the laser beam which interacts with Sr atomic beam,and the characterization of the electric dipole radiation of Sr atom is detected in the far zone.It is experimentally demonstrated that the electric dipole radiates energy in the far zone is based upon the relationship of sin2θ,by which the fluorescence can be detected more effectively.
The sodium D2{\mathit{D}}_{2}D2​ transition is resonantly excited by \ensuremath{\pi}-polarized, narrow-band laser radiation. The line polarization of the resulting fluorescence detected normally to the plane containing the electric-field vector of the radiation and its propagation direction, as well as the atomic beam, is measured as a function of radiation intensity and tuning. The data are compared to calculations from a quantum-electrodynamic theory which includes all participating energy states in the hyperfine representation. The quantitative agreement is very good.
The theory of a method to measure electric-dipole polarizabilities is presented. The method uses two-stage laser ablation to produce a pulsed beam of atoms from a solid target. A pair of slits makes the velocity distribution of the atomic beam nonuniform in a way that is well characterized. The light-force technique uses the polarization forces experienced by an atom in the intense, inhomogeneous electromagnetic field of a standing-wave laser to change the velocity distribution of the atomic beam. The large forces cause measurable Doppler shifts in the resonant frequency of the atoms. These frequency shifts change the amount of absorption of resonant light, yielding information about the change in the velocity distribution of the atoms. The detailed shape of the final absorption distribution is polarizability dependent. In the classical picture of the light force, the standing-wave electric field induces a time-varying dipole moment in each atom. Each atom then experiences a Lorentz force due to coherent interaction of the oscillating dipole moment with the time-varying magnetic field. The quantum-mechanical picture corresponds to the Kapitza-Dirac effect for atoms: an atom absorbs a photon from one of the two beams which form the standing wave, and is then stimulated to emit this photon by the other, counterpropagating beam. This paper provides a classical treatment of the light force experienced by an atom in a standing-wave light field; the polarizability is treated quantum mechanically. The theory presented here can be applied to atoms with a scalar polarizability, such as rubidium, and to atoms with significant tensor components, such as uranium. Experimental results from application of the light-force technique to a measurement of the polarizability of rubidium are also presented.
We systematically investigate the far-zone fluorescence from a number of laser-driven two-level atoms with the cooperative effects stemming from the virtual exchange of photons between identical atoms. Due to the large interaction-induced energy level shifts, i.e. the collective Lamb shifts, both atomic excitation and photon emission do not maximize at the resonant light-atom coupling. In addition, the long-range dissipative interactions among atoms lead to the disproportion between the atomic excitation and the photon emission. Moreover, we discuss the temporal properties of the far-field fluorescence light from the atomic ensemble. The first-order correlation function indicates a damped light-atom dynamics combined with a strong background of the elastic photon scattering. The second-order correlation function illustrates that in the weak-excitation limit the scattered light exhibits the nonclassical photon antibunching behavior, while the bunched photons arrive at the photodetector in the saturated-excitation limit.
The phenomenon of resonance fluorescence provides an interesting manifestation of the quantum theory of light and is a “real world” application of the material of the Chapters 8 and 9. In this process, a two-level atom is typically driven by a resonant continuous-wave laser field and the spectral and quantum statistical properties of the fluorescent light emitted by the atom are measured. Experimentally this can be achieved by scattering a laser off a collimated atomic beam such that the directions of the laser beam, atomic beam, and detector axis are mutually perpendicular as shown in Fig. 10.1. If the driving field is monochromatic, then at low excitation intensity the atom absorbs a photon at the excitation frequency and reemits it at the same frequency as a consequence of conservation of energy. The spectral width of the fluorescent light is therefore very narrow. The situation, however, is considerably more complicated when the excitation intensity increases and the Rabi frequency associated with the driving field becomes comparable to, or larger than, the atomic linewidth. At such intensity levels, the Rabi oscillations show up as a modulation of the quantum dipole moment and sidebands start emerging in the spectrum of the emitted radiation. This so-called dynamic Stark splitting is an interesting feature of the atom–field interaction. In addition to that, the fluorescent light exhibits certain nonclassical properties including photon antibunching and squeezing. In this chapter, we develop a theory of resonance fluorescence to explain these phenomena.
Laser-induced fluorescence experiments carried out using linearly polarized photons from a pulsed laser on a excitation - detection scheme in electrical discharges at 0.04 - 0.6 Torr, show that light emitted during the interaction and in the subsequent decay manifests anisotropy in its angular distribution and polarization. A rate equation approach is used to discuss the general features of the interaction between polarized light and atoms observed experimentally. The incident electromagnetic field is decomposed into multipolar components that may interact with the atom through an appropriate coupling. Defining the Einstein coefficients for each coupling, it is possible to introduce the equations for the dynamics of the atomic populations. For each direction and polarization, the temporal profile of the intensity during the transition is calculated. The theoretical prediction explains the outcome of the He experiment satisfactorily, providing that the role of the quenching and of the collision mixing within the manifold of the state is duly taken into account. Fitting of the model calculations to the experimental data then allows one to deduce the value of the `thermally averaged' cross section for collision-induced transitions between fine-structure and degenerate components of the sublevel, , for each J,M in the manifold.
This review deals with the problem of selective detection of single atoms by laser radiaton. It begins with a classification of the detection methods (fluorescence, photoionization, deflection), discusses detection conditions (atomic vapor, atomic beam, buffer gas), and gives estimates of the parameters of laser radiation ensuring effective detection. Next, a detailed comparision is made of each of the detection methods. It is shown that in the fluorescence method the maximum efficiency of the detection process is achieved for cyclic interaction of atoms with laser radiation. In the photoionization method the most suitable technique is multistage photoionization of atoms by laser radiation. The highest ionization selectivity and a high efficiency are obtained by multistage excitation of an atom either to a Rydberg state followed by ionization with an electric field pulse or to a narrow autoionizing state with a large excitation cross section. Both these techniques are considered from the point of view of the sources of background and ways of discriminating against it, detection selectivity, and absolute sensitivity; the experimental results are analyzed. In discussing the deflection method consideration is given to deflection of an atom in a magnetic field after excitation with laser radiation and to deflection of atoms by resonant optical pressure. The review concludes with a brief discussion of the prospective applications of these detection methods in nuclear physics, atomic physics, and chemistry.