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Physical Review A

Light-induced conical intersection effect enhancing the localization of molecules in optical lattices

Mariusz Pawlak, Nimrod Moiseyev

Published Aug 6, 2015• 15 citations
Publisher

Abstract

The cold weakly bound ${\mathrm{Rb}}_{2}$ molecule dressed by a standing linear polarized laser wave is investigated. In such a case the light-induced conical intersections (LICIs) occur. We demonstrate that when the LICI conditions are fulfilled the transition from the weakly trapped rubidium dimer in the red-detuned optical lattice to the strongly trapped rubidium dimer in the blue-detuned optical lattice takes place. A significant localization enhancement of the molecule is observed.

DOI
10.1103/physreva.92.023403

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The cold weakly bound Rb2{\mathrm{Rb}}_{2}Rb2​ molecule dressed by a standing linear polarized laser wave is investigated. In such a case the light-induced conical intersections (LICIs) occur. We demonstrate that when the LICI conditions are fulfilled the transition from the weakly trapped rubidium dimer in the red-detuned optical lattice to the strongly trapped rubidium dimer in the blue-detuned optical lattice takes place. A significant localization enhancement of the molecule is observed.
Conical intersections of potential energy surfaces widely appear in molecules which consist of more than two atoms. No conical intersections exist in the case of free diatomic molecules. We show here that diatomic molecules interacting with standing laser waves produce periodic arrays of conical intersections. At these laser-induced intersections the non-adiabatic effects are infinitely strong. The translational and rovibrational molecular motions become strongly coupled to each other and energy exchange between the various degrees of freedom influences the dynamics of the system. As an illustrative example, an effect of the laser-induced conical intersections on trapping of ultracold diatomic molecules by light is discussed.
High Resolution Image Download MS PowerPoint Slide Conical intersections are crossing points or lines between two or more adiabatic electronic potential energy surfaces in the multidimensional coordinate space of colliding atoms and molecules. Conical intersections and corresponding nonadiabatic coupling can greatly affect molecular dynamics and chemical properties. In this paper, we predict significant or measurable nonadiabatic effects in an ultracold atom–ion charge-exchange reaction in the presence of laser-induced conical intersections (LICIs). We investigate the fundamental physics of these LICIs on molecular reactivity under unique conditions: those of relatively low laser intensity of 10 8 W/cm 2 and ultracold temperatures below 1 mK. We predict irregular interference effects in the charge-exchange rate coefficients between K and Ca + as functions of the laser frequency. These irregularities occur in our system due to the presence of two LICIs. To further elucidate the role of the LICIs on the reaction dynamics, we compare these rate coefficients with those computed for a system where the CIs have been “removed”. In the laser frequency window, where conical interactions are present, the difference in rate coefficients can be as large as 1 × 10 –9 cm 3 /s.
We show that conical intersections can be created in laboratory coordinates by dressing a parabolic trap for ultracold atoms or molecules with a combination of optical and static magnetic fields. The resulting ring trap can support single-particle states with half-integer rotational quantization and many-particle states with persistent flow. Two well-separated atomic or molecular states are brought into near resonance by an optical field and tuned across each other with an inhomogeneous magnetic field. Conical intersections occur at the nodes in the optical field.
We find that energy surfaces of more than two atoms or molecules interacting via transition dipole-dipole potentials generically possess conical intersections (CIs). Typically only few atoms participate strongly in such an intersection. For the fundamental case, a circular trimer, we show how the CI affects adiabatic excitation transport via electronic decoherence or geometric phase interference. These phenomena may be experimentally accessible if the trimer is realized by light alkali atoms in a ring trap, whose interactions are induced by off-resonant dressing with Rydberg states. Such a setup promises a direct probe of the full many-body density dynamics near a CI.
We observe a series of conical intersections in the potential energy curves governing both the collision between a Rydberg atom and a ground-state atom and the structure of Rydberg molecules. By employing the electronic energy of the Rydberg atom as a synthetic dimension we circumvent the von Neumann-Wigner theorem. These conical intersections can occur when the Rydberg atom's quantum defect is similar in size to the electron-ground-state atom scattering phase shift divided by π, a condition satisfied in several commonly studied atomic species. The conical intersections have an observable consequence in the rate of ultracold l-changing collisions of the type Rb(nf)+Rb(5s)→Rb(nl>3)+Rb(5s). In the vicinity of a conical intersection, this rate is strongly suppressed, and the Rydberg atom becomes nearly transparent to the ground-state atom.
Abstract We experimentally demonstrate optical trapping of atoms using a two-color evanescent field around an optical nanofiber. In our trapping geometry, a blue-detuned traveling wave whose polarization is nearly parallel to the polarization of a red-detuned standing wave produces significant vector light shifts that lead to broadening of the absorption profile of a near-resonant beam at the trapping site. A model that includes scalar, vector, and tensor light shifts of the probe transition - from the trapping beams, weighted by the temperature-dependent position of the atoms in the trap, qualitatively describes the observed asymmetric profile and explains differences with previous experiments that used Cs atoms. The model provides a consistent way to extract the number of atoms in the trap.