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Cambridge University Press eBooks

Ground state angular momenta polarization

Marcis P. Auzinsh, R. Ferber

Published Mar 30, 1995• 0 citations
Publisher

Abstract

We know now how alignment and orientation of angular momenta arise in the excited state as a result of optical excitation from the primarily isotropic distribution of the ensemble of angular momenta. This phenomenon reflects, in essence, the anisotropy of absorption probability G (θ,ϕ). Since spatial structures of the type shown in Fig. 2.2 appear in the excited state the same structure must be ‘eaten out’ from the angular momentum distribution in the ground (initial) state. If the gap created is not closed quickly enough, the ensemble of the remaining angular momenta of the absorbing molecules in the ground state must necessarily also be polarized. If, from another point of view, fluorescent decay leads to a considerable population of the ground state level c, (see, e.g., Fig. 1.2), then molecules on this level may exhibit angular momenta polarization, being particularly noticeable for thermally unpopulated, high lying levels. In the present chapter we intend to discuss the conditions necessary for the creation of ground state angular momenta polarization, the possibilities of its experimental observation, and to develop the theoretical description of broad line radiation interaction with molecules further. Angular momenta polarization via depopulation For many years there existed the widespread opinion that in molecules we obtain an anisotropic distribution of angular momenta only in the excited state in the absorption process, whilst in the ground state isotropy is conserved [124]. This conjecture is based essentially on the assumption of the existence of a so-called ‘weak’ excitation. At first sight it may appear, for instance, from Eq. (2.20) that, as is usual in non-linear spectroscopy, such an admission is correct if condition Γ p /Γ ≫ 1 is valid.

DOI
10.1017/cbo9780511564093.004

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We know now how alignment and orientation of angular momenta arise in the excited state as a result of optical excitation from the primarily isotropic distribution of the ensemble of angular momenta. This phenomenon reflects, in essence, the anisotropy of absorption probability G (θ,ϕ). Since spatial structures of the type shown in Fig. 2.2 appear in the excited state the same structure must be ‘eaten out’ from the angular momentum distribution in the ground (initial) state. If the gap created is not closed quickly enough, the ensemble of the remaining angular momenta of the absorbing molecules in the ground state must necessarily also be polarized. If, from another point of view, fluorescent decay leads to a considerable population of the ground state level c, (see, e.g., Fig. 1.2), then molecules on this level may exhibit angular momenta polarization, being particularly noticeable for thermally unpopulated, high lying levels. In the present chapter we intend to discuss the conditions necessary for the creation of ground state angular momenta polarization, the possibilities of its experimental observation, and to develop the theoretical description of broad line radiation interaction with molecules further. Angular momenta polarization via depopulation For many years there existed the widespread opinion that in molecules we obtain an anisotropic distribution of angular momenta only in the excited state in the absorption process, whilst in the ground state isotropy is conserved [124]. This conjecture is based essentially on the assumption of the existence of a so-called ‘weak’ excitation. At first sight it may appear, for instance, from Eq. (2.20) that, as is usual in non-linear spectroscopy, such an admission is correct if condition Γ p /Γ ≫ 1 is valid.
Anisotropy of angular momenta: ideas and methods The fundamental idea forming the basis of early quantum theory was the quantization of the angular momentum of the atom, which, at a later stage, assumed the form of the Bohr–Sommerfeld quantization rule [360], namely ∲ pdq = n ℏ where p and q are the generalized momentum and coordinate. This concept has retained its physical meaning in modern-day quantum mechanics [371, 372]. In the course of the further development of quantum mechanical concepts it became increasingly clear that in the theory of atoms and molecules the angular momentum is a ‘dominant’ notion, the fundamental significance of which is in no small degree connected with its dimension of action, which coincides with that of Planck's constant ℏ. In the interaction between particles and a directed beam of photons the angular momentum of the system is conserved, thus forming the basis for the optical method of producing spatial anisotropy of the distribution of the angular momenta of the ensemble of particles, i.e. its optical polarization . In terms of quantum concepts, spatial anisotropy means that in an ensemble of particles a non-equilibrium population of magnetic sublevels m j of angular momenta is created. We make a distinction between the alignment of momenta, for instance in the absorption of linear polarized light, when there is no difference between the population of ± m j -sublevels, and orientation , when such a difference exists. Anisotropic distribution of angular momenta in an excited state, as produced in absorption, manifests itself directly in the polarization of fluorescence. It is rather likely that understanding of the anisotropic distribution of the angular momenta of atoms was enhanced by Hanle's [184] discovery in 1924.
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.
If an ensemble of atoms or molecules is excited by linearly polarized light, then usually one expects linearly polarized fluorescence form the ensemble. This reflects a symmetry of the excitation process, namely the fact that the electric field in a light wave and consequently the angular momentum distribution of atoms or molecules in an excited state can be characterized by a double headed arrow . An ensemble of particles in an excited state possesses a net alignment. In this paper some processes that for molecules'in an external field can break this symmetry are reviewed. As a result of symmetry breaking the ensemble of molecules acquires a net orientation of angular momentum, that can be characterized by a single headed arrow , and one can expect a circularly polarized fluorescence from this ensemble.
The Wigner representation of angular-momentum orientation in the classical limit on $J\ensuremath{\gg}1$ has been used to derive an equation of angular-momentum motion in the case of a closed two-level system interacting with an arbitrary polarized radiation. This equation enables us to carry out a theoretical analysis of angular-momentum motion and consider final states of the quantum system for all types of dipole transitions. We have found that in the case of a zero magnetic field in the final state of the system with $\stackrel{\ensuremath{\rightarrow}}{J}J$ or $\stackrel{\ensuremath{\rightarrow}}{J}J+1$ optical transition, the angular momentum is directed along or opposite to the wave vector of the radiation depending on the sign of the polarization ellipsity, while for a linear polarization the angular momentum is isotropically distributed on the plane orthogonal to the polarization vector. For the $\stackrel{\ensuremath{\rightarrow}}{J}J\ensuremath{-}1$ transition two directions of angular momentum are possible in the final state. These directions are determined by the ellipsity of polarization. The spatial size of the final distribution of the angular momentum has been defined by the quantum uncertainty, 1/J,1/\sqrt{J},1/J​, of the angular-momentum orientation. In the case of the $\stackrel{\ensuremath{\rightarrow}}{J}J\ensuremath{-}1$ or $\stackrel{\ensuremath{\rightarrow}}{J}J,$ transition particles come into ``dark'' states while for the $\stackrel{\ensuremath{\rightarrow}}{J}J+1$ transition they occupy the ``brightest'' state. In the presence of a nonzero magnetic field, particles with $\stackrel{\ensuremath{\rightarrow}}{J}J$ transition have in the final state only one angular-momentum orientation, i.e., along or opposite to the direction of the magnetic field depending on the polarization ellipsity sign. For the $\stackrel{\ensuremath{\rightarrow}}{J}J+1$ transition both directions are possible, i.e., along and opposite to the magnetic field. In the case of the $\stackrel{\ensuremath{\rightarrow}}{J}J\ensuremath{-}1$ transition the directions of the angular momentum form a cone around the magnetic field.
Optical pumping of the electronic ground state of molecules has been investigated under conditions of plane, elliptically, and circularly polarized light broadband excitation. The analysis has been performed assuming arbitrary angular momentum values, and applying the apparatus of polarization moments, the latter forming the coefficients in the expansion of the density matrix over irreducible tensor operators, including simplifications due to asymptotic limits for large momentum values. In addition to accounting for the external magnetic field, attention has been also given to the dynamical Stark effect arising from the absence of coincidence between the centers of the exciting line and the absorption line. An alternative classical description is also proposed using multiple moments as coefficients of the expansion of a classical quasidensity of states over spherical harmonics. The equivalence of both approaches of description in the limit of infinitely large angular moments is demonstrated, and the meaning of the origin of coherence is clarified, as well as its destruction by the magnetic field in the classical description of the system.