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arXiv:cond-mat/0612524 · Physical Review Letters

Confinement Effects on the Stimulated Dissociation of Molecular Bose-Einstein Condensates

Igor Tikhonenkov, Amichay Vardi

Published Feb 21, 2007• 18 citations
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Abstract

We show that a molecular Bose-Einstein condensate in a trap is stabilized against stimulated dissociation if the trap size is smaller than the resonance healing length (Planck's 2/2mgsqrt[n]);1/2. The condensate shape determines the critical atom-molecule coupling frequency. We discuss an experiment for triggering dissociation by a sudden change of coupling or trap parameters. This effect demonstrates one of the unique collective features of "superchemistry" in that the yield of a chemical reaction depends critically on the size and shape of the reaction vessel.

DOI
10.1103/physrevlett.98.080403

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We show that a molecular Bose-Einstein condensate in a trap is stabilized against stimulated dissociation if the trap size is smaller than the resonance healing length (Planck's 2/2mgsqrt[n]);1/2. The condensate shape determines the critical atom-molecule coupling frequency. We discuss an experiment for triggering dissociation by a sudden change of coupling or trap parameters. This effect demonstrates one of the unique collective features of "superchemistry" in that the yield of a chemical reaction depends critically on the size and shape of the reaction vessel.
We study the collective two-channel dissociation dynamics of a molecular Bose-Einstein condensate into bosonic fragments under tight harmonic confinement. Bose-stimulated dissociation in either channel can only take place provided that the respective trap size lil_ili​ for the fragments is large with respect to the healing length ζiζ_iζi​ of the atom-molecule resonance. Thus, even when both channels are equally coupled, differences in mass or in dynamical polarizability enable the control of the reaction outcome by variation of the trap frequency. In particular, if l1>ζ1l_1>ζ_1l1​>ζ1​ and $l_2
We solve a model that describes a stimulated conversion between ultracold bosonic atoms and molecules. The reaction is triggered by a linearly time-dependent transition throughout the Feshbach resonance. Our solution predicts a dependence, with a dynamic phase transition, of the reaction efficiency on the transition rate for both atoms-to-molecule pairing and molecular dissociation processes. We find that for the latter process with a linear energy dispersion of atomic modes, the emerging phase can have a thermalized energy distribution of noninteracting bosons with the temperature defined by the rate of the transition. This provides a simple interpretation of the phase transition in terms of the creation of equilibrium Bose-Einstein condensate.
As it was proposed and recently verified experimentally, the mechanism of Feshbach resonance in a condensate can create a second condensate component of molecules that coexists with the atomic condensate. In this work we investigate signatures of the presence of the molecular condensate through the equilibrium properties and collective excitations of the hybrid system of atoms and molecules, subjected to a trap, employing a time-dependent variational ansatz. We show that the shape of the condensate changes significantly by the presence of the molecules and that modes unique to this hybrid system appear at observable frequencies.
State-selected rubidium-87 molecules were created at rest in a dilute Bose-Einstein condensate of rubidium-87 atoms with coherent free-bound stimulated Raman transitions. The transition rate exhibited a resonance line shape with an extremely narrow width as small as 1.5 kilohertz. The precise shape and position of the resonance are sensitive to the mean-field interactions between the molecules and the atomic condensate. As a result, we were able to measure the molecule-condensate interactions. This method allows molecular binding energies to be determined with unprecedented accuracy and is of interest as a mechanism for the generation of a molecular Bose-Einstein condensate.