The quantum dynamics of an ultracold diatomic molecule tunneling and diffusing in a one-dimensional optical lattice exhibits unusual features. While it is known that the process of quantum tunneling through potential barriers can break up a bound-state molecule into a pair of dissociated atoms, interference and reassociation produce intricate patterns in the time-evolving site-dependent probability distribution for finding atoms and bound-state molecules. We find that the bound-state molecule is unusually resilient against break up at ultralow binding energy ${E}_{b}$ ( ${E}_{b}$ much smaller than the barrier height of the lattice potential). After an initial transient, the bound-state molecule spreads with a width that grows as the square root of time. Surprisingly, the width of the probability of finding dissociated atoms does not increase with time as a power law.The quantum dynamics of an ultracold diatomic molecule tunneling and diffusing in a one-dimensional optical lattice exhibits unusual features. While it is known that the process of quantum tunneling through potential barriers can break up a bound-state molecule into a pair of dissociated atoms, interference and reassociation produce intricate patterns in the time-evolving site-dependent probability distribution for finding atoms and bound-state molecules. We find that the bound-state molecule is unusually resilient against break up at ultralow binding energy ${E}_{b}$ (${E}_{b}$ much smaller than the barrier height of the lattice potential). After an initial transient, the bound-state molecule spreads with a width that grows as the square root of time. Surprisingly, the width of the probability of finding dissociated atoms does not increase with time as a power law.

Physical Review AMar 21, 20123 citations

Collision dynamics of ultracold atoms confined in 1D optical lattices

Z. Li, Roman V. Krems

Bulletin of the American Physical SocietyMay 27, 20100 citations

Tunneling, Diffusion and Dissociation of Feshbach Molecules in Optical Lattices

T. L. Bailey, C. A. Bertulani, Eddy Timmermans

The quantum dynamics of an ultracold diatomic molecule tunneling and diffusing in a one-dimensional optical lattice exhibits unusual features. While it is known that the process of quantum tunneling through potential barriers can break up a bound-state molecule into a pair of dissociated atoms, interference and reassociation produce intricate patterns in the time-evolving site-dependent probability distribution for finding atoms and bound-state molecules. We find that the bound-state molecule is unusually resilient against break up at ultralow binding energy Eb (Eb much smaller than the barrier height of the lattice potential). After an initial transient, the bound-state molecule spreads with a width that grows as the square root of time. Surprisingly, the width of the probability of finding dissociated atoms does not increase with time as a power law.The quantum dynamics of an ultracold diatomic molecule tunneling and diffusing in a one-dimensional optical lattice exhibits unusual features. While it is known that the process of quantum tunneling through potential barriers can break up a bound-state molecule into a pair of dissociated atoms, interference and reassociation produce intricate patterns in the time-evolving site-dependent probability distribution for finding atoms and bound-state molecules. We find that the bound-state molecule is unusually resilient against break up at ultralow binding energy Eb (Eb much smaller than the barrier height of the lattice potential). After an initial transient, the bound-state molecule spreads with a width that grows as the square root of time. Surprisingly, the width of the probability of finding dissociated atoms does not increase with time as a power law.

Bulletin of the American Physical SocietyOct 7, 20110 citations

Quantum dynamics of ultracold atom-molecule and molecule-molecule systems

Goulven Quéméner, N. Balakrishnan, Roman V. Krems

Bulletin of the American Physical SocietyMay 30, 20080 citations

Dissociation dynamics of resonantly coupled Bose-Fermi mixtures in an optical lattice

Takahiko Miyakawa, Pierre Meystre

We consider the photodissociation of ground-state bosonic molecules trapped in an optical lattice potential into a two-component gas of fermionic atoms. The system is assumed to be described by a single-band resonantly coupled Bose-Fermi Hubbard model. We show that in the strong fermion-fermion interaction limit the dissociation dynamics is governed by a spin-boson lattice Hamiltonian. In the framework of a mean-field analysis based on a generalized Gutzwiller ansatz, we then examine the crossover of the dissociation from a regime of independent single-site dynamics to a regime of cooperative dynamics as the molecular tunneling increases. We also show that in the limits of weak and strong intersite tunneling the mean-field solutions agree well with the results from the quantum optical Jaynes-Cummings and Tavis-Cummings models, respectively. Finally, we identify two types of self-trapping transitions, a coherent and an incoherent one, depending on the ratio of the repulsive molecule-molecule interaction strength to molecular tunneling.We consider the photodissociation of ground-state bosonic molecules trapped in an optical lattice potential into a two-component gas of fermionic atoms. The system is assumed to be described by a single-band resonantly coupled Bose-Fermi Hubbard model. We show that in the strong fermion-fermion interaction limit the dissociation dynamics is governed by a spin-boson lattice Hamiltonian. In the framework of a mean-field analysis based on a generalized Gutzwiller ansatz, we then examine the crossover of the dissociation from a regime of independent single-site dynamics to a regime of cooperative dynamics as the molecular tunneling increases. We also show that in the limits of weak and strong intersite tunneling the mean-field solutions agree well with the results from the quantum optical Jaynes-Cummings and Tavis-Cummings models, respectively. Finally, we identify two types of self-trapping transitions, a coherent and an incoherent one, depending on the ratio of the repulsive molecule-molecule interaction strength to molecular tunneling.

arXiv:cond-mat/0603469Physical Review AOct 23, 20068 citations

{E}_{b}

(

{E}_{b}

much smaller than the barrier height of the lattice potential). After an initial transient, the bound-state molecule spreads with a width that grows as the square root of time. Surprisingly, the width of the probability of finding dissociated atoms does not increase with time as a power law.