Following the realization of Bose-Einstein condensates in atomic gases, an experimental challenge is the production of molecular gases in the quantum regime. A promising approach is to create the molecular gas directly from an ultracold atomic gas; for example, bosonic atoms in a Bose-Einstein condensate have been coupled to electronic ground-state molecules through photoassociation or a magnetic field Feshbach resonance. The availability of atomic Fermi gases offers the prospect of coupling fermionic atoms to bosonic molecules, thus altering the quantum statistics of the system. Such a coupling would be closely related to the pairing mechanism in a fermionic superfluid, predicted to occur near a Feshbach resonance. Here we report the creation and quantitative characterization of ultracold 40K2 molecules. Starting with a quantum degenerate Fermi gas of atoms at a temperature of less than 150 nK, we scan the system over a Feshbach resonance to create adiabatically more than 250,000 trapped molecules; these can be converted back to atoms by reversing the scan. The small binding energy of the molecules is controlled by detuning the magnetic field away from the Feshbach resonance, and can be varied over a wide range. We directly detect these weakly bound molecules through their radio-frequency photodissociation spectra; these probe the molecular wavefunction, and yield binding energies that are consistent with theory.
We have measured a p-wave Feshbach resonance in a single-component, ultracold Fermi gas of 40K atoms. We have used this resonance to enhance the normally suppressed p-wave collision cross section to values larger than the background s-wave cross section between 40K atoms in different spin states. In addition to the modification of two-body elastic processes, the resonance dramatically enhances three-body inelastic collisional loss.
We report a unique feature of magnetic field Feshbach resonances in which atoms collide with nonzero orbital angular momentum. P-wave (l = 1) Feshbach resonances are split into two components depending on the magnitude of the resonant state's projection of orbital angular momentum onto the field axis. This splitting is due to the magnetic dipole-dipole interaction between the atoms and it offers a means to tune anisotropic interactions of an ultra-cold gas of atoms. A parameterization of the resonance in terms of an effective range expansion is given.
Three magnetic-field induced heteronuclear Feshbach resonances were identified in collisions between bosonic 87Rb and fermionic 40K atoms in their absolute ground states. Strong inelastic loss from an optically trapped mixture was observed at the resonance positions of 492, 512, and 543+/-2 G. The magnetic-field locations of these resonances place a tight constraint on the triplet and singlet cross-species scattering lengths, yielding (-281+/-15)a(0) and (-54+/-12)a(0), respectively. The width of the loss feature at 543 G is 3.7+/-1.5 G wide; this broad Feshbach resonance should enable experimental control of the interspecies interactions.
We have loaded an ultracold gas of fermionic atoms into a far-off resonance optical dipole trap and precisely controlled the spin composition of the trapped gas. We have measured a magnetic-field Feshbach resonance between atoms in the two lowest energy spin states, /9/2,-9/2> and /9/2,-7/2>. The resonance peaks at a magnetic field of 201.5+/-1.4 G and has a width of 8.0+/-1.1 G. Using this resonance, we have changed the elastic collision cross section in the gas by nearly 3 orders of magnitude.
We investigate the scattering cross section of aligned dipolar molecules in low-temperature gases. Over a wide range of collision energies relevant to contemporary experiments, the cross section declines in inverse proportion to the collision speed, and is given nearly exactly by a simple semiclassical formula. At yet lower energies, the cross section becomes independent of energy, and is reproduced within the Born approximation to within corrections due to the s-wave scattering length. While these behaviors are universal for all polar molecules, nevertheless interesting deviations from universality are expected to occur in the intermediate energy range.
We study the superfluid character of a dipolar Bose-Einstein condensate (DBEC) in a quasi-two dimensional (q2D) geometry. In particular, we allow for the dipole polarization to have some nonzero projection into the plane of the condensate so that the effective interaction is anisotropic in this plane, yielding an anisotropic dispersion for propagation of quasiparticles. By performing direct numerical simulations of a probe moving through the DBEC, we observe the sudden onset of drag or creation of vortex-antivortex pairs at critical velocities that depend strongly on the direction of the probe's motion. This anisotropy emerges because of the anisotropic manifestation of a roton-like mode in the system.A quintessential feature of a superfluid is its ability to support dissipationless flow, for example, when an object moves through a superfluid and experiences no drag force. This, however, only occurs when the object is moving below a certain critical velocity; when it exceeds this critical velocity it dissipates energy into excitations of the superfluid, resulting in a net drag force on the object and the breakdown of superfluid flow.In many superfluids, such as dilute Bose-Einstein condensates (BECs) of atoms, this critical velocity is simply the speed of sound in the system, which is set by the density and the s-wave scattering length of the atoms. However, for a dense superfluid such as liquid 4 He, this is not the case. In 4 He, the critical velocity is set by a roton mode, corresponding to a peak in the static structure factor of the system at some finite, non-zero momentum, with a characteristic velocity that is considerably less than the speed of sound in the liquid. This feature has been verified experimentally via measurements of ion-drift velocity in the fluid [1], thereby providing insight into the detailed structure of the system. Interestingly, a BEC of dipolar constituents (DBEC) is also expected to possess a roton-like dispersion, in spite of existing in a dilute gaseous state [2]. Unlike the dispersion of 4 He, the dispersion of a DBEC is highly tunable as a function of the condensate density and dipole-dipole interaction (ddi) strength. Additionally, the DBEC is set apart from liquid 4 He in that its interactions depend on how the dipoles are oriented in space. Thus, the DBEC provides an ideal system to study the effects that anisotropies have on the bulk properties of a superfluid, such as its critical velocity. Anisotropic dispersions have been predicted for a 1D lattice system of q2D DBECs [3], periodically dressed BECs [4] and for dipolar gases in a 2D lattice [5]. Additionally, anisotropic solitons have been predicted for dipolar gases [6].In this Letter we consider a DBEC in a quasi-twodimensional (q2D) geometry and allow for the dipoles to be polarized at a nonzero angle into this plane so that the in-plane interaction is anisotropic. We perform numerical simulations of a probe moving through the DBEC. This probe experiences a sudden onset of drag at a certain velocity, the critical veloci...
We present measurements of the binding energies of 6 Li p-wave Feshbach molecules formed in combinations of the |F = 1/2, mF = +1/2 (|1 ) and |F = 1/2, mF = −1/2 (|2 ) states. The binding energies scale linearly with magnetic field detuning for all three resonances. The relative molecular magnetic moments are found to be 113 ± 7 µK/G, 111 ± 6 µK/G and 118 ± 8 µK/G for the |1 −|1 , |1 −|2 and |2 −|2 resonances, respectively, in good agreement with theoretical predictions. Closed channel amplitudes and the size of the p-wave molecules are obtained theoretically from full closed-coupled calculations.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.