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Physical Review A

Magnetic-field-induced interference of scattering states in ultracold collisions

Felipe Herrera

Published Nov 20, 2008• 9 citations
Publisher

Abstract

We propose a general method to induce interference between scattering wave functions in atomic and molecular collisions at ultracold temperatures by using a static magnetic field. The scheme is based on the preparation of collision partners in coherent superpositions of Zeeman states. The magnetic field is used to induce interference between two incoming channels. As an illustrative example, we consider ultracold collisions between $^{7}\mathrm{Li}$ and $^{133}\mathrm{Cs}$ atoms, and show that ratios of state resolved collision cross sections can be enhanced by engineering the preparation of the initial coherent superpositions.

DOI
10.1103/physreva.78.054702

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We propose a general method to induce interference between scattering wave functions in atomic and molecular collisions at ultracold temperatures by using a static magnetic field. The scheme is based on the preparation of collision partners in coherent superpositions of Zeeman states. The magnetic field is used to induce interference between two incoming channels. As an illustrative example, we consider ultracold collisions between 7Li^{7}\mathrm{Li}7Li and 133Cs^{133}\mathrm{Cs}133Cs atoms, and show that ratios of state resolved collision cross sections can be enhanced by engineering the preparation of the initial coherent superpositions.
We show that quantum interference-based coherent control is a highly efficient tool for tuning ultracold molecular collision dynamics that is free from the limitations of commonly used methods that rely on external electromagnetic fields. By varying the relative populations and phases of initial coherent superpositions of degenerate molecular states, we demonstrate complete coherent control over integral scattering cross sections in the ultracold s-wave regime of both the initial and final collision channels. The proposed control methodology is applied to ultracold O_{2}+O_{2} collisions, showing extensive control over s-wave spin-exchange cross sections and product branching ratios over many orders of magnitude.
Exploiting quantum interference presents a significant challenge in ultracold inelastic scattering. In this study we propose a method to verify quantum interference within the two-body loss rate that arises from multiple inelastic-scattering channels, where the colliding particles are initially prepared in their individual hyperfine states. Our approach employs a ring-coupling configuration, accomplished by combining external radio-frequency and static electric fields during ultracold atomic collisions. To validate our proposal, we perform close-coupling calculations for $^{7}\mathrm{Li}\text{\ensuremath{-}}^{41}\mathrm{K}$ collisions at the ultracold limit. The results reveal that the interference profile, as manifested in the two-body loss rate, can be verified with optimized external field parameters. Notably, our findings indicate that the two-body loss rate coefficient exhibits a distinct pattern of constructive or destructive interference when crossing a magnetically induced ppp-wave resonance in the incoming channel. These interference patterns become increasingly pronounced as the intensities of the external fields increase. This work presents a potential approach to controlling inelastic-scattering processes in ultracold collisions.
We propose a method of controlling two-atom interaction using both magnetic and laser fields. We analyse the role of quantum interference between magnetic and optical Feshbach resonances in controlling cold collision. In particular, we demonstrate that this method allows us to suppress inelastic and enhance elastic scattering cross sections. Quantum interference is shown to modify significantly the threshold behaviour and resonant interaction of ultracold atoms. Furthermore, we show that it is possible to manipulate not only the spherically symmetric s-wave interaction but also the anisotropic higher partial-wave interactions which are particularly important for high-temperature superfluid or superconducting phases of matter.
Ultracold molecules are expected to find applications in cold chemistry, quantum phases, precision measurements and quantum information. In this thesis three novel applications of cold molecules are studied. First the thesis presents a general method for coherent control of collisions between non-identical particles. It is shown that by preparing two alkali-metal atoms in a superposition of hyperfine states, the elastic-to-inelastic cross section ratio can be manipulated at ultracold temperatures by tuning laser parameters in the presence of a magnetic field. The static field is needed to induce quantum interference between scattering states. Extensions of this scheme for ultracold molecular reactive scattering are discussed. Second, the thesis describes rotational excitons and polarons in molecular ensembles trapped in optical lattices. Rotational excitons can be manipulated using static electric and magnetic fields. For a one-dimensional molecular array with substitutional impurities any localized exciton state can be delocalized by applying a suitable electric field. The electric field induces correlations between diagonal and off-diagonal disorder. It is also shown that the translational motion of polar molecules in an optical lattice can lead to phonons. The lattice dynamics and the phonon spectrum depend on the strength and orientation of a static electric field. An array of polar molecules in an optical lattice can be described by generalized polaron model with tunable parameters including diagonal and off-diagonal exciton-phonon interactions. It is shown that in a strong electric field the system is described by a generalized Holstein model, and at weak electric fields by the Su-Schrieffer-Heeger (SSH) model. The possibility of observing a sharp polaron transition in the SSH model using polar alkali-metal dimers is discussed. Finally, the thesis presents a method to generate entanglement of polar molecules using strong off-resonant laser pulses. Bipartite entanglement between alkali-metal dimers separated by hundreds of nanometers can be generated. Maximally entangled states can be prepared by tuning the pulse intensity and duration. A scheme is proposed to observe the violation of Bell’s inequality based on molecular orientation correlation measurements. It is shown that using a combination of microwave and off-resonant optical pulses, arbitrary tripartite and many-particle states can be prepared.
We present an accurate quantum mechanical study of molecule–molecule collisions in the presence of a magnetic field. The work focuses on the analysis of elastic scattering and spin relaxation in collisions of O 2 ( 3 Σ g – ) molecules at cold (∼0.1 K) and ultracold (∼10 –6 K) temperatures. Our calculations show that magnetic spin relaxation in molecule–molecule collisions is extremely efficient except at magnetic fields below 1 mT. The rate constant for spin relaxation at T =0.1 K and a magnetic field of 0.1 T is found to be as large as 6.1 × 10 –11 cm –3 s –1 . The magnetic field dependence of elastic and inelastic scattering cross sections at ultracold temperatures is dominated by a manifold of Feshbach resonances with the density of ∼100 resonances per Tesla for collisions of molecules in the absolute ground state. This suggests that the scattering length of ultracold molecules in the absolute ground state can be effectively tuned in a very wide range of magnetic fields. Our calculations demonstrate that the number and properties of the magnetic Feshbach resonances are dramatically different for molecules in the absolute ground and excited spin states. The density of Feshbach resonances for molecule–molecule scattering in the low-field-seeking Zeeman state is reduced by a factor of 10.
In this work we investigate the potential of controlling cold (O(K)−mK) and ultracold (mK-μK) atom-molecule collisions by tuning scattering states across Feshbach resonances using magnetic fields. We are interested in particular in the prospect of suppressing the often undesirable inelastic collisions. The He-O_2 system provides the vehicle for our study. We calculate bound and quasi-bound states of several isotopic combinations, including their Zeeman structure, to reveal the underlaying pattern for easier characterization of quasi-bound states in terms of rigorous and approximately good quantum numbers. These calculations also help us locate the fields at which zero-energy resonances will occur. Scattering calculations are then performed for collisions of 3^He and 4^He with {16}^O_2 at fixed (1 μK) energy but varying magnetic field. The field is varied to sweep the scattering state across resonance. At low and ultralow energies we enter the Wigner threshold regime where the S-partial wave dominates the wavefunction. The cross sections, and the real and imaginary parts of the scattering length, vary dramatically across resonance. Their profiles are used to analyze the resonances. In a highlight of our results we show that dramatic suppression of inelastic cross sections occur for 4^He-{16}^O_2 . The resonances are relatively wide (of order 100 Gauss), with suppression of inelastic scattering over a similarly wide range of fields and for temperatures ranging from 10 mK down to 1 μK. We conclude that under certain conditions it is possible to almost completely eliminate inelastic collisions. This is potentially very important for cooling techniques, such as evaporative and sympathetic cooling, that require efficient elastic cross sections. Suppression of inelastic collisions can not only increase thermalization efficiency but it can also result in longer trap-lifetimes by reducing transitions to untrapable states.