We study exotic orbits in the photoassociation process by considering both the vibrational and rotational motions in a classical model. In the presence of rotational motion, the exotic orbits possess regular bound segments even when the total energy exceeds the threshold energy of the interaction potential. Such features of the exotic orbits are interpreted by introducing an effective potential. We employ Lagrangian descriptors and escape time to characterize the phase-space structure and show that exotic orbits are distributed around the stable region in the short-range phase space. We further calculate the photoassociation probability. Our work provides new insights into the dynamical mechanisms of photoassociation processes.
We study exotic orbits in the photoassociation process by considering both the vibrational and rotational motions in a classical model. In the presence of rotational motion, the exotic orbits possess regular bound segments even when the total energy exceeds the threshold energy of the interaction potential. Such features of the exotic orbits are interpreted by introducing an effective potential. We employ Lagrangian descriptors and escape time to characterize the phase-space structure and show that exotic orbits are distributed around the stable region in the short-range phase space. We further calculate the photoassociation probability. Our work provides new insights into the dynamical mechanisms of photoassociation processes.
We investigate the effects of a particular kind of orbits, which we call exotic orbits, on the process of classical molecular photoassociation. As a starting model system, we consider the process described by the Morse potential with a time-dependent perturbation consisting of the interaction of an external laser field with the molecular dipole. When the external perturbation is turned off, the bound molecular states are classically represented by librational motion, whereas the unbound, the collisional states, are represented by unbound motion, and in both cases, the energy is a constant of motion. When the perturbation is turned on, the total energy is no longer a constant of motion and initial conditions in the unbound region can reach the bound region, and vice versa, through chaotic orbits. Alternatively, we have found that the connection between the bound and unbound sectors can be achieved through exotic orbits, which are comprised by librationlike parts, a localized chaotic region, and an unbounded constant-energy part. Thus, if a colliding atomic pair is in an exotic orbit, it penetrates a chaotic region coming from the unbound sector, subsequently performing librationlike motion, during which the molecule with constant bound energy is formed. Afterwards, the molecule returns to the chaotic region and from this region, it can either access a distinct bound energy or dissociate. We call this phenomenon, in which a metastable molecule is formed, intermittent photoassociation. We show that the key for the emergence of exotic orbits is the relatively short range of the dipole as compared to the interacting potential range. In order to further verify our results, we have considered realistic forms for the potentials and dipole functions of several molecules and found the emergence of exotic orbits, and consequently of intermittent photoassociation, for the MgLi and SrLi molecular parameters.
A quantum dynamical description of an atomic collision pair interacting with the electric field of a short infrared laser pulse is developed. Inelastic processes in the electronic ground state are due to stimulated emission resulting in photoassociation, or absorption leading to photoacceleration. A perturbative approach based on a state space representation is compared with a numerical treatment using a grid representation in coordinate space. Special emphasis is on the role of rotations and, in particular, of shape resonances. It is shown that these quasibound states which are supported by the centrifugal barrier (for J ≠ 0) can be used as initial states to effectively populate a selected bound state with specific vibrational and rotational quantum number (photoassociation), or a partial wave of a scattering state with defined energy and rotational quantum number (photoacceleration). Simulations are carried out for the prototype H + Cl collision pair. Also the effect of averaging over initial conditions (velocity, angular momenta) is investigated for a supersonic beam experiment. For a narrow velocity distribution, we predict the presence of a resonance structure of the association and acceleration probability as a function of the mean collision energy.
A new theoretical study for the photoassociation of metastable helium is presented, based on fully ab initio short-range potentials. Optimization of the exponents of the Gaussian orbitals of a smaller basis set than employed previously allowed the calculation of potentials dissociating to He(2 3 S)+He(2 3 P) at the multi-reference configuration interaction level down to internuclear separations of 3.5 a 0 . The good agreement with observed near-dissociation levels obtained previously using extrapolated short-range potentials is confirmed and almost all levels observed to the red of the He D 2 line, associated with the He 2 3 S + 2 3 P 2 dissociation limit, are assigned. The agreement is less satisfactory with the levels observed to the red of the He D 1 line, although vibrational levels have been found in the outer ultra-long-range well of a double-well potential with the He 2 3 P 1 dissociation limit. A semiclassical analysis is presented to explain the limited sensitivity of the near-dissociation binding energies to the short-range potential.
Introduction If, while approaching on an unbound ground-state potential, two atoms absorb a photon and couple to an excited bound molecular state, they are said to undergo photoassociation. Figure 5.1 illustrates the process. At long range electrostatic dispersion forces give rise to the ground-state molecular potential varying as C 6 / R 6 . If the two atoms are homonuclear, then a resonant dipole–dipole interaction sets up ± C 3 / R 3 excited-state repulsive and attractive potentials. Figure 5.2 shows the actual long-range excited potential curves for the sodium dimer, originating from the 2 S ½ + 2 P 3/2 and 2 S ½ + 2 P ½ separated atom states. For cold and ultracold photoassociation processes the long-range attractive potentials play the key role; the repulsive potentials figure importantly in optical shielding and suppression, the subject of Chapter 6. In the presence of a photon with frequency ω p the colliding pair with kinetic energy k B T couples from the ground-state to the attractive molecular state in a free–bound transition near the Condon point R C , the point at which the difference potential just matches ћω p . Scanning the probe laser ω p excites population of vibration–rotation states in the excited bound potential and generates a free–bound spectrum. This general class of measurements is called photoassociative spectroscopy (PAS) and can be observed in several different ways. The observation may consist of bound-state decay by spontaneous emission, most probably as the nuclei move slowly around the outer turning point, to some distribution of continuum states on the ground potential controlled by bound–free nuclear Franck–Condon overlap factors.
We explore the classical dynamics of atoms in an optical dipole trap formed by two identical Gaussian beams propagating in perpendicular directions. The phase space is a mixture of regular and chaotic orbits, the latter becoming dominant as the energy of the atoms increases. The trapping capabilities of these perpendicular Gaussian beams are investigated by considering an atomic ensemble in free motion. After a sudden turn on of the dipole trap, a certain fraction of atoms in the ensemble remains trapped. The majority of these trapped atoms has energies larger than the escape channels, which can be explained by the existence of regular and chaotic orbits with very long escape times.
A theoretical study is performed for the photoassociation of metastable helium. Combining short-range, high-level, ab initio calculations for 5 Σ g / u + and 5 Π g / u symmetries and long-range behaviour, better described in Hund's case (c), potential-energy curves for attractive, 5 Σ u + and 5 Π g , as well as repulsive, 5 Π u and 5 Σ g + , states of quintet metastable helium molecules dissociating to 2 3 S + 2 3 P are obtained. Taking into account the atomic spin-orbit couplings, vibrational levels are derived for near-dissociation levels at the 3 P 2 asymptote. Comparison with results from three recent photoassociation experiments obtained under different conditions (μK temperatures with spin alignment and mK temperatures without) allowed for an assignation of about three quarters of the observed levels. The robustness of the vibrational numbering is confirmed by testing a modification of the short-range potentials.