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arXiv:1004.0636 · New Journal of Physics

Creation and manipulation of Feshbach resonances with radiofrequency radiation

Thomas M. Hanna, Eite Tiesinga, Paul S. Julienne

Published Aug 12, 2010• 40 citations
arXivHTMLPDF

Abstract

We present a simple technique for studying the collisions of ultracold atoms in the presence of a magnetic field and radiofrequency (rf) radiation. Resonant control of scattering properties can be achieved by using rf to couple a colliding pair of atoms to a bound state. We show, using the example of 6 Li, that in some ranges of rf frequency and magnetic field this can be done without giving rise to losses. We also show that halo molecules of large spatial extent allow resonant control with much less rf power than deeply bound states. Another way to exert resonant control is with a set of rf-coupled bound states, linked to the colliding pair through the molecular interactions that give rise to magnetically tunable Feshbach resonances. This was recently demonstrated for 87 Rb (Kaufman et al 2009 Phys. Rev. A 80 050701) [1]. We examine the underlying atomic and molecular physics that made this possible. Lastly, we consider the control that may be exerted over atomic collisions by placing atoms in superpositions of Zeeman states, and suggest that it could be useful where small changes in scattering length are required. We suggest other species for which rf and magnetic field control could together provide a useful tuning mechanism.

DOI
10.1088/1367-2630/12/8/083031

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We present a simple technique for studying the collisions of ultracold atoms in the presence of a magnetic field and radiofrequency (rf) radiation. Resonant control of scattering properties can be achieved by using rf to couple a colliding pair of atoms to a bound state. We show, using the example of 6 Li, that in some ranges of rf frequency and magnetic field this can be done without giving rise to losses. We also show that halo molecules of large spatial extent allow resonant control with much less rf power than deeply bound states. Another way to exert resonant control is with a set of rf-coupled bound states, linked to the colliding pair through the molecular interactions that give rise to magnetically tunable Feshbach resonances. This was recently demonstrated for 87 Rb (Kaufman et al 2009 Phys. Rev. A 80 050701) [1]. We examine the underlying atomic and molecular physics that made this possible. Lastly, we consider the control that may be exerted over atomic collisions by placing atoms in superpositions of Zeeman states, and suggest that it could be useful where small changes in scattering length are required. We suggest other species for which rf and magnetic field control could together provide a useful tuning mechanism.
This thesis has investigated the dynamics of ultracold atomic collisions in the presence of both static magnetic and oscillating radio-frequency (rf) fields. The bound state structure and scattering length of 39K+133Cs was examined in the presence of only a static magnetic field, where it was found that no Feshbach resonance of suitable width for magnetoassociation existed at a magnetic field where caesium can be cooled to degeneracy. We then showed that zero-energy Feshbach resonances may be engineered using an rf field in places where they did not previously exist. An rf field with frequency 79.9 MHz was chosen to induce a resonance near 21 G. The widths of such rf-induced Feshbach resonances increase quadratically with rf field strength. The resonances presented are lossless with circularly polarized rf, and the molecules created are long-lived even with plane-polarized RF. Collisional losses in rf-dressed magnetic traps were also investigated. An rf-induced loss mechanism that does not exist in the absence of rf radiation was identified. This mechanism is not suppressed by a centrifugal barrier in the outgoing channel, and can be much faster than spin relaxation, which is centrifugally suppressed. We explore the dependence of the rf-induced loss rate on singlet and triplet scattering lengths, hyperfine splittings and the strength of the rf field. The results were interpreted in terms of an adiabatic model of the collision dynamics, and calculate the corresponding nonadiabatic couplings. The loss rate can vary by 10 orders of magnitude as a function of singlet and triplet scattering lengths. 87Rb is a special case, where several factors combine to reduce rf-induced losses; as a result, they are slow compared to spin-relaxation losses. For most other alkali-metal pairs, rf-induced losses are expected to be much faster and may dominate. For heteronuclear mixtures an rf-modified spin-exchange mechanism was identified that results in loss rates orders of magnitude greater than the rf-induced loss rates in homonuclear cases. Fast loss is expected in mixtures where the Lande g-factors differ.
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.
It is crucial to control the collision between ultracold atoms by applying external fields. We developed a theoretical model for investigating the s-wave scattering of ultracold atoms controlled by the magnetic field and laser field. The calculation is performed by using the close-coupling method and mapped Fourier grid method. Due to the interference between the photoassociation and bound-to-bound transitions, the bound state in the continuum, which is a resonance with a vanishing width, occurs at the magnetic field position near the magnetic Feshbach resonance. The widths of resonances in the neighborhood of the bound state in the continuum are narrow. Changing the laser intensity can shift the magnetic field position where the bound state in the continuum occurs through modifying the ground molecular state to induce wide resonances at desired magnetic field positions. By increasing the resonance width, the tunability of the real part of the scattering length at resonances can be significantly improved. Changing the laser intensity can also adjust the coupling between the ground and excited molecular states. When the coupling between the ground and excited molecular states approaches zero, a resonance is induced, and the photoassociation and bound-to-bound transitions are both significantly suppressed at this resonance. Therefore, the atomic loss peak due to spontaneous emission does not appear at this resonance. The magnetic field position of this resonance is stable against the change in laser frequency.
A rigorous quantum theory of atomic collisions in the presence of radio frequency (rf) magnetic fields is developed and applied to elucidate the effects of combined dc and rf magnetic fields on ultracold collisions of Rb atoms. We show that rf fields can be used to induce Feshbach resonances, which can be tuned by varying the amplitude and frequency of the rf field. The rf-induced Feshbach resonances occur also in collisions of atoms in low-field-seeking states at moderate rf field strengths easily available in atom chip experiments, which opens up the world of tunable interactions to magnetically trappable atomic quantum gases.
This thesis reports on a novel scheme for controlling the scattering properties of an ultracold atomic gas with laser light. We show theoretically and experimentally that light near-resonant with a molecular bound-to-bound transition can be used to shift the magnetic field at which a magnetic Feshbach resonance occurs. This makes it possible to tune the interaction strength with laser light and at the same time induce considerably less loss than an optical Feshbach resonance would do. To find an appropriate bound-to-bound transition for this scheme, we perform excited-state spectroscopy. When applying laser light resonant with one such bound-to-bound transition we observe an Autler-Townes splitting of the magnetic Feshbach resonance. We find good agreement between the theoretical model and experimental data. Our scheme can be used for a variety of future applications. For example, light patterns created by holographic masks could serve as a tool for changing the scattering length of ultracold atoms on very short time and length scales.
We have generalized the BOUND and MOLSCAT packages to allow calculations in basis sets where the monomer Hamiltonians are off diagonal and used this capability to carry out bound-state and scattering calculations on $^{3}\mathrm{He}\text{\ensuremath{-}}\mathrm{NH}$ and $^{4}\mathrm{He}\text{\ensuremath{-}}\mathrm{NH}$ as a function of magnetic field. Following the bound-state energies to the point where they cross thresholds gives very precise predictions of the magnetic fields at which zero-energy Feshbach resonances occur. We have used this to locate and characterize two very narrow Feshbach resonances in $^{3}\mathrm{He}\text{\ensuremath{-}}\mathrm{NH}$. Such resonances can be used to tune elastic and inelastic collision cross sections, and sweeping the magnetic field across them will allow a form of quantum control in which separated atoms and molecules are associated to form complexes. For the first resonance, where only elastic scattering is possible, the scattering length shows a pole as a function of magnetic field and there is a very large peak in the elastic cross section. For the second resonance, however, inelastic scattering is also possible. In this case the pole in the scattering length is dramatically suppressed and the cross sections show relatively small peaks. The peak suppression is expected to be even larger in systems with stronger inelasticity. The results suggest that calculations on ultracold molecular inelastic collisions may be much less sensitive to details of the potential energy surface than has been believed.