The history of the discovery, study, and explanation of the effect discovered fifty years ago by the German physicist Hanle and its development and generalization by the French school of physicists led by Kastler are described. The effect is observed optically in an increase in the degree of depolarization of the resonance fluorescence. It is studied in the range of magnetic fields in which the Zeeman splitting of the atomic magnetic sublevels does not exceed the level widths determined by thermal relaxation mechanisms and electromagnetic interaction. It is a direct optical manifestation of interference of degenerate atomic states and is intimately connected with the conservation law for the angular momentum of the photon-atom system. In the review, different applications of the effect to the measurement of mean lifetimes, linewidths, and Stark splitting constants of atoms in excited states are given. The resonance scattering of light by atoms in the ground state in a weak magnetic field is considered in detail—in particular, in the presence of radio-frequency magnetic fields oriented in different ways. The different possible types of parametric resonances in one or two radio-frequency fields for arbitrary orientation of the constant magnetic field are interpreted as the effect of crossing of the levels of an atom that is dressed by the radio-frequency field. Applications of the effect in the quantum magnetometry of ultraweak fields (down to 10-10 Oe) are examined.
The history of the discovery, study, and explanation of the effect discovered fifty years ago by the German physicist Hanle and its development and generalization by the French school of physicists led by Kastler are described. The effect is observed optically in an increase in the degree of depolarization of the resonance fluorescence. It is studied in the range of magnetic fields in which the Zeeman splitting of the atomic magnetic sublevels does not exceed the level widths determined by thermal relaxation mechanisms and electromagnetic interaction. It is a direct optical manifestation of interference of degenerate atomic states and is intimately connected with the conservation law for the angular momentum of the photon-atom system. In the review, different applications of the effect to the measurement of mean lifetimes, linewidths, and Stark splitting constants of atoms in excited states are given. The resonance scattering of light by atoms in the ground state in a weak magnetic field is considered in detail—in particular, in the presence of radio-frequency magnetic fields oriented in different ways. The different possible types of parametric resonances in one or two radio-frequency fields for arbitrary orientation of the constant magnetic field are interpreted as the effect of crossing of the levels of an atom that is dressed by the radio-frequency field. Applications of the effect in the quantum magnetometry of ultraweak fields (down to 10-10 Oe) are examined.
In the optical excitation of atoms with polarized light, producing excited atoms, only some of the Zeeman sublevels of the excited state are actually reached, so that large differences of population can be built up between Zeeman sublevels or between hyperfine structure (hfs) levels. This property can be used to detect radio-frequency resonance in optically excited atomic states. These resonances produce a characteristic change in intensity or in the degree of polarization of the light re-emitted. Zeeman intervals, Stark effects, and hfs intervals can be measured in this manner. (The Stark constant of the 63P1 level of Hg and the electric quadrupole moments of the alkali atoms have been obtained in this way.)The technique of “optical pumping” gives a way to concentrate atoms in some of the Zeeman sublevels of one of the hfs levels of the ground state.Atomic orientation has been obtained with the Na atom, in an atomic beam and in the vapor in equilibrium with the metal. The orientation effects have been studied by detection of radio-frequency resonance signals in the ground state. Orientation can be increased many times by adding a variable pressure of a foreign gas to the pure Na vapor. Because of the coupling between nuclear spin and electron spin, nuclear orientation is produced at the same time as atomic orientation.
The absorption of a light wave interacting with optical transitions in the D1line of an alkali metal atom subjected to microwave radiation that is in resonance with magnetic dipole transitions between hyperfine ground-state components, has been investigated. It is known that when scanning a longitudinal magnetic field (B||k, wherekis the wavevector), one may observe a magneto-optical resonance due to the ground-state Hanle effect. In addition, the effect of double radio-optical resonance takes place because of the presence of the resonance microwave field. The joint influence of these effects on the formation of a narrow magneto-optical resonance in light wave absorption has been studied theoretically and experimentally. It has been shown analytically that the effects compete with each other and destructively act on the resonance formation. As a result, the amplitude of the resonance is small and its shape is complicated. However, in the presence of a buffer gas the pressure of which is such that the hyperfine splitting of the ground state remains spectrally unresolved, it becomes possible to observe a magneto-optical resonance with a relatively large amplitude. Experiments have been carried out with the use of a miniature glass cell (V~ 0.1 cm3) filled with87Rb vapor and a buffer gas argon (a pressure of about 95 Torr). In particular, the theoretically predicted resonance narrowing with increasing light field intensity has been experimentally observed. A configuration for magneto-optical resonance excitation suggested here may be applied in quantum magnetometry to measure weak permanent magnetic fields and resonance microwave fields using cells filled with alkali metal vapor.
According to the quantum theory of the optical-pumping cycle, one can describe the effect of a nonresonant light beam on the different Zeeman sublevels of an atomic ground state by an effective Hamiltonian He which depends on the polarization and spectral profile of the incident light. In order to check the structure of He, we have performed a detailed experimental study of the ground-state energy sublevels of various kinds of atoms perturbed by different types of nonresonant light beams. Attention is paid to the modification of the Zeeman structure due to He. We have been able to obtain experimentally in the ground state of 199Hg, 201Hg, and 87Rb, Zeeman light shifts that are larger than the width of the levels due to the thermal relaxation. The removal of the Zeeman degeneracy in zero external field, due to a nonresonant light irradiation, is observed by different optical-pumping techniques; the full Zeeman diagram of the perturbed atoms is also determined when a static field ${\stackrel{\ensuremath{\rightarrow}}{\mathrm{H}}}_{0}$ is added. We have checked that the effect of He can be described in terms of fictitious static electric or magnetic fields. These fictitious fields can be used to act selectively on a given atomic level.
Abstract The degree of Zeeman splitting of ground-state sublevels in the presence of a magnetic field can be measured using atomic sensors. The coherence of the spins in the ensemble affects the efficiency of an atomic magnetometer. The sensitivity of these sensors depends on the line width of the magnetic resonance curve, which is related to the coherence lifetime of the atomic spins. Atomic polarization influences the optical properties of the medium, making it anisotropic. The relatively long lifetime of ground-state polarization is a useful tool for measuring the energy-level splitting. The modification associated with the atomic coherence in the presence of an external magnetic field leads to interesting absorption effects in the atomic environment. The splitting of magnetic sublevels and the transition between them under the application of a magnetic field are quantum mechanical images of the interaction between a field and an atomic spin that must be analyzed using a density matrix. In the present work, magneto-optical effects with circularly polarized light such as the dynamic properties and evolution of sublevels of the rubidium-87 D1 line and the absorption properties of the atomic polarized environment are studied theoretically using the reduced density matrix approach.
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.
The polarization of the resonance fluorescence of interacting atoms and the transfer of coherence, due to the exchange of excitation, are studied theoretically. The treatment is for the general case where both the excited and the ground states can have arbitrary angular momenta, except that they can be connected to each other by an allowed transition. Electrostatic dipole–dipole interaction and electromagnetic radiative interaction are considered simultaneously as the perturbations on the system. Heitler and Ma's generalized time-dependent perturbation method is used. The system is quantized with respect to the space-fixed z axis and a static magnetic field along the z axis may be present, so that the magnetic sublevels (m, m′, etc., for the excited state J, and α, β, etc., for the ground state J′) are not necessarily degenerate. The intensity of the scattered light of a given polarization, in a given direction, is expressed as a function of kR (where ℏck is the energy of excitation and R is the internuclear distance), and of the orientation of R with respect to z axis. The matrix elements (ℏ / 2)γmβ,αm′ and Vmβ,αm′, which cause resonant transfer of excitation between two atoms through radiative and electrostatic interaction, respectively, are also expressed as a function of kR, and of the orientation of R. For randomly oriented atoms, the polarization after being averaged over the random orientation of R becomes a function of kR. Numerical calculations have been carried out for S01 → 1P1 transition. The coherence is shown to be conserved upon resonant transfer of excitation when R is parallel to the quantization axis.