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Journal of the Physical Society of Japan

Spin Torque and Zeta Force of Dimer of Alkali Atoms

Masato Senami, Jun Nishikawa, Takaaki Hara, Akitomo Tachibana

Published Aug 10, 2010• 17 citations
Publisher

Abstract

In this work, the novel theoretical approach to predict the torque for spin is studied. This approach is based on the novel quantities, the spin torque and the zeta force, which are proposed by one of the authors. These quantities govern the dynamics of the spin of electrons, and hence, can clarify the essential description of the dynamics of the electron spin. This approach would be applicable to many spin phenomena. In this work, as a first step of the demonstration of this approach, we investigate the spin torque and the zeta force of the dimers of alkali atoms, lithium, sodium, potassium, and rubidium.

DOI
10.1143/jpsj.79.084302

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In this work, the novel theoretical approach to predict the torque for spin is studied. This approach is based on the novel quantities, the spin torque and the zeta force, which are proposed by one of the authors. These quantities govern the dynamics of the spin of electrons, and hence, can clarify the essential description of the dynamics of the electron spin. This approach would be applicable to many spin phenomena. In this work, as a first step of the demonstration of this approach, we investigate the spin torque and the zeta force of the dimers of alkali atoms, lithium, sodium, potassium, and rubidium.
The rapid development of experimental techniques to produce ultracold alkali molecules opens the ways to manipulate them and to control their dynamics using external electric fields. A prerequisite quantity for such studies is the knowledge of their static dipole polarizability. In this paper, we computed the variations with internuclear distance and with vibrational index of the static dipole polarizability components of all homonuclear alkali dimers including Fr(2), and of all heteronuclear alkali dimers involving Li to Cs, in their electronic ground state and in their lowest triplet state. We use the same quantum chemistry approach as in our work on dipole moments [Aymar and Dulieu, J. Chem. Phys. 122, 204302 (2005)], based on pseudopotentials for atomic core representation, Gaussian basis sets, and effective potentials for core polarization. Polarizabilities are extracted from electronic energies using the finite-field method. For the heaviest species Rb(2), Cs(2), and Fr(2) and for all heteronuclear alkali dimers, such results are presented for the first time. The accuracy of our results on atomic and molecular static dipole polarizabilities is discussed by comparing our values with the few available experimental data and elaborate calculations. We found that for all alkali pairs, the parallel and perpendicular components of the ground state polarizabilities at the equilibrium distance R(e) scale as (R(e))(3), which can be related to a simple electrostatic model of an ellipsoidal charge distribution. Prospects for possible alignment and orientation effects with these molecules in forthcoming experiments are discussed.
Following out the ideas of Hund and others on complex spectra, and of Goudsmit and Uhlenbeck on the spinning electron, a model for a complex atom is set up, consisting of electrons whose intrinsic and orbital angular momentum vectors act on each other with torques whose energies are proportional to the cosines of the angles between. The dynamical equations of this model are solved and the quantum conditions are applied. These agree with the quantum conditions previously set up empirically, as far as those go, but also yield new quantum numbers relating to the orientation of electrons. The formula for the energy in terms of the quantum numbers is set up. This is not only in qualitative agreement with what has been previously found, but it furnishes an explanation of inverted multiplets, of the fact that relativity doublets follow the same formula as alkali doublets but are inverted, and of the fact that doublets and triplets both fit on the same "relativity" doublet curve.
Abstract Collisions of alkali atoms in the ground state are accompanied by the exchange of electron polarization between the colliding atoms, which lead to the polarization transfer between particles. As a result of this process, the electronic orientation is transferred from the spin oriented atoms to unpolarized atoms, along with the polarization transfer, the magnetic resonance frequency shifts of polarized atoms occur too. In this work the magnetic resonance frequency shifts of arising from spin exchange collisions in a mixture of alkali potassium and rubidium atoms at the optical orientation of atoms are calculated. The situation when optical pumping by resonant polarized radiation is carried out only for atoms of the one kind is considered. The spin exchange process between alkali atoms was described in the formalism of the complex cross section for spin exchange process. The real and imaginary parts of the complex cross section were calculated using the interaction potentials of alkali atom dimers. The calculation of the frequency shifts is carried out on the basis of data on the interaction potentials for the following pairs of alkali atoms K-K, K-Rb and Rb-Rb. Maxwell averaging of the cross sections over the velocities was done and the temperature dependences of the magnetic resonance frequency shifts for K and Rb atoms were plotted.
Collisions of alkali-metal atoms in the ground state with the electron spin S = 1/2 are accompanied by exchange of electron coordinates between colliding particles, which leads to polarization transfer between them (i.e., to the well-known phenomenon of spin exchange). In addition, along with the polarization transfer from one partner to another, the magnetic resonance lines of colliding atoms are broadened and shifted in spin-exchange collisions. In particular the last two processes depend on the complex spin-exchange cross section. The real part of the cross section determines the so-called "spin-exchange cross section," which is responsible for the broadening of magnetic resonance lines, while the imaginary part determines the shift cross section, which governs the frequency shift of magnetic resonance. In order to describe the spin-exchange process one have to know complex spin-exchange cross sections. Complex spin-exchange cross sections are calculated on the basis of the data on the singlet (X 1 Σ + ) and triplet (a 3 Σ + ) potentials describing the interaction alkali-metal atoms in the ground state. Collisions of alkali-metal atoms Cs, Rb, K, Na in the ground state are considered in the energy interval of 10 −4 −10 −2 au.
A theory for calculating the spin–rotation coupling coefficient in alkali-metal–noble-gas van der Waals molecules was recently presented.1 It assumes the spin–rotation interaction in alkali-metal–noble-gas molecules to be mainly due to the spin–orbit interaction of the alkali-metal valence electron within the core of the noble gas, and predicts that the spin–rotation constant γ should depend on the spin–orbit interaction in the noble gas and be almost independent of the spin–orbit interaction of the alkali-metal atom. Experimentally, only a few of the possible pairs of the different alkali-metal atoms with different noble-gas atoms have been investigated. By measuring the sodium spin relaxation rate as a function of the helium buffer-gas pressure and the width of the sodium magnetic slowing-down curve, we report in this paper our experimentally determined value of the spin–rotation interaction constant in Na–Xe molecules γ = (1.1 ± 0.3)MHz. The measured value is nearly the same as was measured in K–Xe, Rb–Xe, and Cs–Xe.1 This result shows a reasonable agreement with the theoretical prediction.
Spin is an intrinsic form of angular momentum carried by elementary particles, composite particles, and atomic nuclei. It is wildly believed that spin is a purely quantum mechanical concept and has no classical analogue. In fact, elementary particles are conceived as point objects which have no axis to “spin” around. Therefore, there is no explaining how spin arises at the fundamental level, why particles have the values they do, and what underpins the Pauli Exclusion principle and Bose-Einstein behavior. However, spin is like a vector quantity; it has a definite magnitude, and it has a “direction”, in order to spin should be composite. In this paper we propose a physical explanation for spin of the electron at the sub-particle level, relying on the vortex model of the electron. The electron is described as a superfluid frictionless vortex which has a mass, angular momentum and spin to provide a complete explanation of all properties of the electron: it composite, spinning around its own axis, produces a tiny magnetic fields independent of those from its orbital motions. The classical hydrodynamic laws are used to describe the quantum properties of the electron, such as spin, angular momentum, magnetic momentum and a magnetic dipole. The circulation in the vortex is constant, and the angular momentum of the vortex is conserved and has the same value of Planck constant. The direction of the angular momentum of a spinning electron vortex is along the axis of rotation and determined by the direction of spin. The spin quantum number 1/2 has a fixed value which represents the gap between the circulation rate of the core of the vortex and the boundaries of the vortex. The changeable values +1/2 “spin-up” or -1/2 “spin-down” indicate the direction of the magnetic dipole of the vortex. The relation between spin and Planck constant is discussed and the origin h/4pi angular momentum units are revealed.