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Physical Review A

Adiabatic theorem for a condensate system in an atom-molecule dark state

Hong Yuan Ling, P. Maenner, Weiping Zhang, Han Pu

Published Mar 26, 2007• 41 citations
Publisher

Abstract

We consider the adiabatic evolution of an atom-molecule dark state in a collisional two-color Raman photoassociation condensate system. By linking nonadiabaticity with the population growth in the collective excitations of the dark state, we develop an adiabatic theorem where we have consistently addressed the issues related to the Goldstone mode and the biorthonormality of the collective modes. We apply this theorem to specific examples to demonstrate its use in designing pulses that can optimize the yield of ground molecule production in the stimulated Raman adiabatic passage process.

DOI
10.1103/physreva.75.033615

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We consider the adiabatic evolution of an atom-molecule dark state in a collisional two-color Raman photoassociation condensate system. By linking nonadiabaticity with the population growth in the collective excitations of the dark state, we develop an adiabatic theorem where we have consistently addressed the issues related to the Goldstone mode and the biorthonormality of the collective modes. We apply this theorem to specific examples to demonstrate its use in designing pulses that can optimize the yield of ground molecule production in the stimulated Raman adiabatic passage process.
We consider a Raman photoassociation model in a field configuration in which a Gaussian and a first-order Laguerre Gaussian laser field are applied between the bound-bound and free-bound transitions, respectively. We show that such a configuration can lead to a coherent population trapping superposition of an atomic condensate and a ground molecular vortex of unit winding number. We develop stimulated Raman adiabatic passages that minimize the effect of mean-field shifts due to collisions, for optimal conversion of an atomic condensate into a ground molecular vortex.
Collective two-color photoassociation of a freely interacting 87Rb^{87}\mathrm{Rb}87Rb Bose-Einstein condensate is theoretically examined, focusing on stimulated Raman adiabatic passage (STIRAP) from an atomic to a stable molecular condensate. In particular, Drummond et al. [Phys. Rev. A. 65, 063619 (2002)] have predicted that particle-particle interactions can limit the efficiency of collective atom-molecule STIRAP, and that optimizing the laser parameters can partially overcome this limitation. We suggest that the molecular conversion efficiency can be further improved by treating the initial condensate density as an optimization parameter.
The adiabaticity of the stimulated Raman adiabatic passage (STIRAP) for the 87Rb atom–molecule conversion in a condensate system is investigated in terms of a newly defined adiabatic fidelity. The evolution of the dark state in the STIRAP is simulated numerically by considering the interparticle interactions and spontaneous emissions of the excited molecular state. We find that these terms will reduce the adiabatic fidelity; however, one can still achieve higher adiabatic fidelity through optimizing the external parameters of the STIRAP. Our discussions are helpful in obtaining higher conversion efficiency from an atomic Bose–Einstein condensate to its molecular counterpart in experiment.
We theoretically examine Raman photoassociation of a Bose-Einstein condensate, revisiting stimulated Raman adiabatic passage (STIRAP). Due to collisional mean-field shifts, efficient molecular conversion requires strong coupling and low density, either of which can bring about rogue photodissociation to noncondensate modes. We demonstrate explicitly that rogue transitions are negligible for low excited-state fractions and photodissociation that is slower than the STIRAP time scale. Moreover, we derive a reduced-parameter model of collisions, and thereby find that a gain in the molecular conversion efficiency can be obtained by adjusting the atom-atom scattering length with off-resonant magnetoassociation. This gain saturates when the atom-atom scattering length is tuned to a specific fraction of either the molecule-molecule or atom-molecule scattering length. We conclude that a fully optimized STIRAP scheme may offer the best chance for achieving coherent conversion from an atomic to a molecular condensate with photoassociation.
We study the dynamics of a two-color photoassociation of atoms into diatomic molecules via nonlinear stimulated Raman adiabatic passage process. The system has a famous counterpart in (linear) quantum mechanics, and has been discussed recently in the context of generalizing the quantum adiabatic theorem to nonlinear systems. Here we use another approach to study adiabaticity and stability in the system: we apply methods of classical Hamiltonian dynamics. We find nonlinear dynamical instabilities, cases of complete integrability, and improved conditions of adiabaticity.
We analyze coherent two-color photoassociation of a Bose-Einstein condensate, focusing on stimulated Raman adiabatic passage (STIRAP) in free-bound-bound transitions from atoms to molecules. This problem raises an interest because STIRAP has been predicted to be absent in the nondegenerate case [Javanainen and Mackie, Phys. Rev. A 58, R789 (1998)]. Nevertheless, we find that Bose stimulation enhances the free-bound dipole matrix element for an atomic condensate, and photoassociative STIRAP turns out to be a viable mechanism for converting an atomic condensate to a molecular condensate with near-unit efficiency.