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arXiv:1611.05412

Resonant Floquet Scattering of Ultracold Atoms

Dane Hudson Smith

Published Nov 16, 2016• 0 citations
arXivHTMLPDF

Abstract

In systems of ultracold atoms, pairwise interactions are resonantly enhanced by the application of an oscillating magnetic field that is parallel to the spin-quantization axis of the atoms. The resonance occurs when the frequency of the applied field is precisely tuned near the transition frequency between the scattering atoms and a diatomic molecule. The resulting cross section can be made more than two orders of magnitude larger than the cross section in the absence of the oscillating field. The low momentum resonance properties have a universal description that is independent of the atomic species. To arrive at these conclusions, we first develop a formal extension of Floquet theory to describe scattering of atoms with time-periodic, short-range interaction potentials. We then calculate the atomic scattering properties by modeling the atomic interactions with a square well potential with oscillating depth and then explicitly solving the time-dependent Schrodinger equation. We then apply the Floquet formalism to the case of atoms scattering with a contact interaction described by a time-periodic scattering length, obtaining analytic results that agree with those obtained by solving the time-dependent Schrodinger equation.

DOI
10.48550/arxiv.1611.05412

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In systems of ultracold atoms, pairwise interactions are resonantly enhanced by the application of an oscillating magnetic field that is parallel to the spin-quantization axis of the atoms. The resonance occurs when the frequency of the applied field is precisely tuned near the transition frequency between the scattering atoms and a diatomic molecule. The resulting cross section can be made more than two orders of magnitude larger than the cross section in the absence of the oscillating field. The low momentum resonance properties have a universal description that is independent of the atomic species. To arrive at these conclusions, we first develop a formal extension of Floquet theory to describe scattering of atoms with time-periodic, short-range interaction potentials. We then calculate the atomic scattering properties by modeling the atomic interactions with a square well potential with oscillating depth and then explicitly solving the time-dependent Schrodinger equation. We then apply the Floquet formalism to the case of atoms scattering with a contact interaction described by a time-periodic scattering length, obtaining analytic results that agree with those obtained by solving the time-dependent Schrodinger equation.
In systems of ultracold atoms, pairwise interactions can be resonantly enhanced by a new mechanism that does not rely upon a magnetic Feshbach resonance. In this mechanism, interactions are controlled by tuning the frequency of an oscillating parallel component of the magnetic field close to the transition frequency between the scattering atoms and a two-atom bound state. The real part of the resulting s-wave scattering length a is resonantly enhanced when the oscillation frequency is close to the transition frequency. The resonance parameters can be controlled by varying the amplitude of the oscillating field. The amplitude also controls the imaginary part of a, which arises because the oscillating field converts atom pairs into molecules. The real part of a can be made much larger than the background scattering length without introducing catastrophic atom losses from the imaginary part. For the case of a shallow bound state in the scattering channel, the dimensionless resonance parameters are universal functions of the dimensionless oscillation amplitude.
In systems of ultracold atoms, pairwise interactions can be resonantly enhanced by a new mechanism which does not rely upon a magnetic Feshbach resonance. In this mechanism, interactions are controlled by tuning the frequency of an oscillating parallel component of the magnetic field close to the Bohr frequency for the transition to a two-atom bound state. The real part of the s-wave scattering length a has a resonance as a function of the oscillation frequency near the Bohr frequency. The resonance parameters can be controlled by varying the amplitude of the oscillating field. The amplitude also controls the imaginary part of a which arises predominantly because the oscillating field converts atom pairs into molecules. For the case of a shallow bound state in the scattering channel, the dimensionless resonance parameters are universal functions of the dimensionless oscillation amplitude.
In systems of ultracold atoms, pairwise interactions can be resonantly enhanced by a new mechanism which does not rely upon a magnetic Feshbach resonance. In this mechanism, interactions are controlled by tuning the frequency of an oscillating parallel component of the magnetic field close to the Bohr frequency for the transition to a two-atom bound state. The real part of the s-wave scattering length aaa has a resonance as a function of the oscillation frequency near the Bohr frequency. The resonance parameters can be controlled by varying the amplitude of the oscillating field. The amplitude also controls the imaginary part of aaa which arises predominantly because the oscillating field converts atom pairs into molecules. For the case of a shallow bound state in the scattering channel, the dimensionless resonance parameters are universal functions of the dimensionless oscillation amplitude.
It is demonstrated that the effective scattering length can be highly manipulated via time-periodic driving of a short-range interparticle potential. By developing a Floquet-scattering theory we show that sharp Floquet resonances occur at which the effective interaction can be tuned to very large attractive or repulsive values. The resulting s-wave scattering length can be obtained in analytic form and the shape of these resonances is given by a simple formula describing how resonance position and width can be altered by the driving strength. Our approach allows the identification of the underlying physical mechanism of the scattering resonances as Floquet bound states with positive energies, which are dynamically created by the drive. This insight is valuable for a detailed analysis and uncovers a general resource for enhanced or reduced scattering in Floquet systems, as was recently confirmed experimentally.
Scattering resonances are fundamental to many areas of physics, occurring across a wide range of energy scales. In ultracold quantum gases, magnetic Feshbach resonances have transformed quantum many-body research by enabling precise interaction control between atoms. Here, we demonstrate unprecedented control to engineer Feshbach resonances at tunable positions via Floquet driving in a lithium-6 (^{6}Li) atom gas, achieved through strong magnetic field modulation at megacycles per second frequencies. This periodic modulation creates scattering resonances whenever dressed molecular levels cross the atomic threshold. By adding a second modulation at twice the base frequency, we tune the asymmetry of resonance loss profiles and suppress two-body losses from Floquet heating. This technique enhances control over atomic interactions, expanding possibilities for quantum simulations of complex systems and studies of exotic quantum phases.
The pairwise interactions of ultracold atoms can be resonantly enhanced by tuning the scattering length to infinity using a Feshbach resonance.In a gas of ultracold atoms whose scattering length is controlled by a magnetic Feshbach resonance, the atoms can be associated into universal dimers and the dimers can be dissociated into unbound atoms by using an oscillating longitudinal magnetic field with frequency near the binding energy of a dimer.If the gas of ultracold atoms are fermions, the oscillating magnetic field with frequency near the pairing gap can dissociate Cooper pairs into pairs of unbound atoms.In this thesis, we show that the transition rates for association and dissociation can be calculated by treating the oscillating magnetic field as a sinusoidal time-dependent perturbation proportional to the contact operator.We calculate both the harmonic and subharmonic transition rates analytically for association in a thermal gas of atoms and for dissociation in a thermal gas of dimers.We also calculate the harmonic transition rate analytically for the dissociation of Cooper pairs into pairs of unbound atoms in the BCS limit.Our results for the dissociation rate of Cooper pairs can be used to make a direct measurement of the pairing gap for fermionic atoms.