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arXiv:1911.09741 · Journal of Optics

Polarization transfer from the twisted light to an atom

Andrei V. Afanasev, Carl E. Carlson, Hao Wang

Published Mar 23, 2020• 11 citations
arXivHTMLPDF

Abstract

Abstract When polarized light is absorbed by an atom, the excited atomic system carries information about the initial polarization of light. For the light that carries an orbital angular momentum, or the twisted light, the polarization states are described by eight independent parameters, as opposed to three Stokes parameters for plane waves. We use a parameterization of the spin-density matrix of the twisted light in terms of vector and tensor polarization, in analogy with massive spin-1 particles, and derive formulae that define atom’s response to specific polarization components of the twisted light. It is shown that for dipole ( S → P ) atomic transitions, the atom’s polarization is in one-to-one correspondence with polarization of the incident light; this relation is violated, however, for the transitions of higher multipolarity ( S → D , S → F , etc) We pay special attention to contributions of the longitudinal electric field into the matrix elements of atomic transitions.

DOI
10.1088/2040-8986/ab8288

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Abstract When polarized light is absorbed by an atom, the excited atomic system carries information about the initial polarization of light. For the light that carries an orbital angular momentum, or the twisted light, the polarization states are described by eight independent parameters, as opposed to three Stokes parameters for plane waves. We use a parameterization of the spin-density matrix of the twisted light in terms of vector and tensor polarization, in analogy with massive spin-1 particles, and derive formulae that define atom’s response to specific polarization components of the twisted light. It is shown that for dipole ( S → P ) atomic transitions, the atom’s polarization is in one-to-one correspondence with polarization of the incident light; this relation is violated, however, for the transitions of higher multipolarity ( S → D , S → F , etc) We pay special attention to contributions of the longitudinal electric field into the matrix elements of atomic transitions.
Twisted light has received a lot of attention in recent years. And there are justified reasons for this. The properties of twisted light are unusual and differ fundamentally from the plane-wave properties. The phase fronts of these light beams have a helical structure, giving them the name twisted. This helical phase structure originates from the well-defined orbital angular momentum (OAM) that they carry along their propagation direction and in addition to the spin angular momentum (SAM). Moreover, they have a characteristic intensity profile, which consists of concentric rings with a central minimum, and a phase singularity in the beam center. This thesis is based on two main parts, each dealing with a different aspect of twisted light. These investigations are carried out using Bessel beams, one type of twisted light. Twisted light beams are cylindrically symmetrical. Therefore, they are defined on the basis of circularly polarized light. This fact leads to the first question: Is it possible to generate twisted light in other polarization states? In this work, we derive how this can be achieved by using the superposition principle and how this can be used to construct linearly, radially, or azimuthally polarized Bessel beams. The focus in the second part is on excitations of atoms by twisted Bessel beams. In particular, we analyze how the use of twisted light can modify individual atomic multipole transitions. The obtained results show that for an efficient modification a precise localization of the target atom is required. In the last chapter, both aspects are combined. We analyze transitions between magnetic hyperfine states in a single trapped atom (or ion), which is exposed to an additional external magnetic field. The presented calculations for these multipole excitations are based on a formalism that accounts for the alignment of the applied external magnetic field with respect to the light propagation direction, and additionally different polarization states of the radiation field are considered. The obtained results indicate that twisted light could be of particular interest for precision experiments. One possible application is the use in single-ion clocks. The work shows that high multipole orders of the vortex beams allow excitations in the intensity minimum in the center of these beams without causing large disturbances, and thus may enable a significant reduction of the light shift in atomic transitions.
A theoretical study is performed for the excitation of a single atom localized in the center of twisted light modes. Here we present the explicit dependence of excitation rates on critical parameters, such as the polarization of light, its orbital angular momentum projection, and the orientation of its propagation axis with respect to the atomic quantization axis. The effect of a spatial spread of the atom is also considered in detail. The expressions for transition rates obtained in this work can be used for any atom of arbitrary electronic configuration. For definiteness we apply them to the specific case of the $^{2}S_{1/2}(F=0)\ensuremath{\rightarrow}^{2}F_{7/2}(F=3,M=0)$ electric octupole (E3) transition in 171Yb+{^{171}\mathrm{Yb}}^{+}171Yb+ ion. Our analytical and numerical results are suitable for the analysis and planning of future experiments on the excitation of electric-dipole-forbidden transitions by twisted light modes in optical atomic clocks.
Equations are derived for the polarisation of light emitted by impulsively excited atoms. A spontaneous electric dipole transition between Russell-Saunders terms is considered. The density matrix of the excited term is described by a double tensor expansion which allows for anisotropy in the directional distribution of the spin as well as the orbital angular momentum. Conditions are discussed under which one may test for the presence of spin anisotropy by polarisation measurements or zero-field quantum beats.
The theory of optical birefringence is discussed from the point of view of the scattering of polarized photons by molecules using the framework of formal scattering theory and quantum electrodynamics. In Part One, those features from noncovariant quantum electrodynamics relevant to the molecular scattering of photons are reviewed. Chapter One contains an outline of classical electrodynamics in the Coulomb gauge, including the Stokes parameter and density matrix formulations of polarization. Chapter Two deals with the quantization of the radiation field, and the occupation number representation is defined. The quantum mechanical description of polarized light is outlined in Chapter Three: operator equivalents of the density matrix and Stokes parameters are invoked, the parameters themselves being obtained from the expectation values of the Stokes operators with the state vector of the photon. The Stokes parameter and density matrix are then applied to the polarization of a general beam containing an arbitrary number of photons, and some new methods are developed. The interaction of the electromagnetic field with bound electrons is formulated in Chapter Four in terms of a canonically transformed interaction Hamiltonian in which the multipole terms are explicit. Since each term is then gauge-invariant, this Hamiltonian is particularly suited to the application of diagrammatic perturbation theory which follows from the iteration of the scattering matrix in the interaction representation (Chapter Five). Also the extension of the theory to multiphoton processes is facilitated "because the field strength is explicit in the transformed Hamiltonian. The S-matrix connects the initial and final asymptotic states of the scattering system, and in Chapter Six the state vector and density operator of the scattered photon beam are obtained from those of the incident beam. Part Two contains the application of the above methods to a variety of linear and nonlinear optical birefringence effects in the absence or presence of external fields. In Chapter Seven, general equations are obtained for the polarization changes imposed on a forward scattered photon in terms of matrix elements of the reaction operator between plane polarized photon base states; whereas Chapter Eight extends this treatment to an n-photon beam, thereby encompassing the hyperpolarizability contributions to the polarization changes of the forward scattered beam. It is then demonstrated that the fundamental process in optical birefringence can be interpreted as an infinitesimal unitary transformation of the polarization spinor. Also the S-matrix approach to birefringence is compared with the methods used in crystal optics, and with the classical treatments of the scattering of polarized light by molecules. The general equations obtained for the polarization changes of the forward scattered beam are subsequently interpreted in the light of the physical circumstances appropriate to the bire- fringence effect of interest. In Chapters Nine, Ten, and Eleven, diagrammatic perturbation theory is used to obtain explicit expressions, in terms of molecular polarizability and rotation tensors, for the linear and nonlinear contributions to the polarization changes involved in natural optical activity, and in birefringence phenomena induced by static and optical electric and magnetic fields. The nonforward scattering of polarized photons by molecules is discussed in Part Three. General equations are calculated in Chapter Twelve for the azimuth, ellipticity, and depolarization ratio of the Rayleigh beam at any scattering angle and for any polarization of the incident beam. Explicit expressions in terms of molecular quantities are then obtained for the polarization at scattering angles of 90° and almost zero from both optically inactive and optically active molecules. It is demonstrated that a determination of the precise polarization state of the scattered beam can provide useful molecular information additional to that obtained from depolarization ratios alone. This is because the depolarization ratio depends on only the diagonal elements of the polarization density matrix and so does not convey all the information about the system. Raman scattering processes are contained in the formulation and the polarization of the Raman light at any scattering angle can be obtained. This is shown to be particularly useful for predicting the polarization of stimulated Raman light for any Raman-active liquid placed within a laser cavity. By extending the nonforward scattering formulation to incorporate multiphoton processes, equations are obtained in Chapter Thirteen for the ellipticity, azimuth, and depolarization ratio of the second harmonic wave at any scattering angle as a function of the incident polarization. Several specific situations are subsequently investigated. Finally, it is shown in Chapter Fourteen that the near-forw- ard Rayleigh and Raman scattering formulations provide an explanation for the observed polarization, as a function of the initial polarization, of the self-trapped filaments that arise from the self-focusing of an intense laser beam.
The nine (9) elements of the density matrix of a general three-level atom interacting with a classically described linearly polarized light are parameterized by eight (8) variables related to the populations of the atomic levels, and the coherences (interference effects) between the levels. The dynamical equations of these eight parameters (that is, the optical Bloch equations for a general three-level atom) are derived under the electric dipole as well as the rotating wave approximations, and under the assumption that the matrix elements of the atomic electric dipole are all real. The general optical Bloch equations so derived are shown to contain the well-known optical Bloch equations for three-level atoms in the , and cascade configurations as well as those for two-level atoms as special cases. Expressing the interaction of light with a three-level atom in all possible configurations as well as with a two-level atom by a single set of generalized optical Bloch equations is the main result of this work.