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arXiv:1104.5411 · Physical Chemistry Chemical Physics

Anisotropy in the interaction of ultracold dysprosium

Svetlana Kotochigova, Alexander N. Petrov

Published Jan 1, 2011• 41 citations
arXivHTMLPDF

Abstract

The nature of the interaction between ultracold atoms with a large orbital and spin angular momentum has attracted considerable attention. It was suggested that such interactions can lead to the realization of exotic states of highly correlated matter. Here, we report on a theoretical study of the competing anisotropic dispersion, magnetic dipole-dipole, and electric quadrupole-quadrupole forces between two dysprosium atoms. Each dysprosium atom has an orbital angular momentum of L = 6 and a magnetic moment of μ = 10 μ(B). We show that the dispersion coefficients of the ground state adiabatic potentials lie between 1865 a.u. and 1890 a.u., creating a non-negligible anisotropy with a spread of 25 a.u. and that the electric quadrupole-quadrupole interaction is weak compared to the other interactions. We also find that for interatomic separations R < 50a(0) both the anisotropic dispersion and magnetic dipole-dipole potential are larger than the atomic Zeeman splittings for external magnetic fields of order 10 G to 100 G. At these separations the atomic angular momentum can be reoriented. We finish by describing two scattering models for these inelastic m-changing collisions. A universal scattering theory is used to model loss due to the anisotropy in the dispersion and a Born approximation is used to model losses from the magnetic dipole-dipole interaction for the (164)Dy isotope. These models find loss rates that are of the same order of magnitude as the experimental value.

DOI
10.1039/c1cp21175g

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The nature of the interaction between ultracold atoms with a large orbital and spin angular momentum has attracted considerable attention. It was suggested that such interactions can lead to the realization of exotic states of highly correlated matter. Here, we report on a theoretical study of the competing anisotropic dispersion, magnetic dipole-dipole, and electric quadrupole-quadrupole forces between two dysprosium atoms. Each dysprosium atom has an orbital angular momentum of L = 6 and a magnetic moment of μ = 10 μ(B). We show that the dispersion coefficients of the ground state adiabatic potentials lie between 1865 a.u. and 1890 a.u., creating a non-negligible anisotropy with a spread of 25 a.u. and that the electric quadrupole-quadrupole interaction is weak compared to the other interactions. We also find that for interatomic separations R < 50a(0) both the anisotropic dispersion and magnetic dipole-dipole potential are larger than the atomic Zeeman splittings for external magnetic fields of order 10 G to 100 G. At these separations the atomic angular momentum can be reoriented. We finish by describing two scattering models for these inelastic m-changing collisions. A universal scattering theory is used to model loss due to the anisotropy in the dispersion and a Born approximation is used to model losses from the magnetic dipole-dipole interaction for the (164)Dy isotope. These models find loss rates that are of the same order of magnitude as the experimental value.
We explore the anisotropic nature of Feshbach resonances in the collision between ultracold highly magnetic submerged-shell dysprosium atoms in their energetically lowest magnetic sublevel, which can only occur due to couplings to rotating bound states. This is in contrast to well-studied alkali-metal atom collisions, where broadest (strongest) Feshbach resonances are hyperfine induced and due to rotationless bound states. Our first-principle coupled-channel calculation of the collisions between these spin-polarized bosonic dysprosium atoms reveals a strong interplay between the anisotropies in the dispersion and magnetic dipole-dipole interaction. The former anisotropy is absent in alkali-metal and chromium collisions. We show that both types of anisotropy significantly affect the Feshbach spectrum as a function of an external magnetic field. Effects of the electrostatic quadrupole-quadrupole interaction are small. Over a 20 mT magnetic field range, we predict about 10 Feshbach resonances and show that the resonance locations depend on the dysprosium isotope.
The collisional magnetic reorientation rate constant gR{g}_{R}gR​ is measured for magnetically trapped atomic dysprosium (Dy), an atom with large magnetic dipole moments. Using buffer gas cooling with cold helium, large numbers (>1011>{10}^{11}>1011) of Dy are loaded into a magnetic trap and the buffer gas is subsequently removed. The decay of the trapped sample is governed by collisional reorientation of the atomic magnetic moments. We find ${g}_{R}=1.9\ifmmode\pm\else\textpm\fi{}0.5\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}11}$ cm3{}^{3}3 s${}^{\ensuremath{-}1}$ at 390 mK. We also measure the magnetic reorientation rate constant of holmium (Ho), another highly magnetic atom, and find ${g}_{R}=5\ifmmode\pm\else\textpm\fi{}2\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}12}$ cm3{}^{3}3 ${\mathrm{s}}^{\ensuremath{-}1}$ at 690 mK. The Zeeman relaxation rates of these atoms are greater than expected for the magnetic dipole-dipole interaction, suggesting that another mechanism, such as an anisotropic electrostatic interaction, is responsible. Comparison with estimated elastic collision rates suggests that Dy is a poor candidate for evaporative cooling in a magnetic trap.
We show that for ultracold magnetic lanthanide atoms chaotic scattering emerges due to a combination of anisotropic interaction potentials and Zeeman coupling under an external magnetic field. This scattering is studied in a collaborative experimental and theoretical effort for both dysprosium and erbium. We present extensive atom-loss measurements of their dense magnetic Feshbach-resonance spectra, analyze their statistical properties, and compare to predictions from a random-matrix-theory-inspired model. Furthermore, theoretical coupled-channels simulations of the anisotropic molecular Hamiltonian at zero magnetic field show that weakly bound, near threshold diatomic levels form overlapping, uncoupled chaotic series that when combined are randomly distributed. The Zeeman interaction shifts and couples these levels, leading to a Feshbach spectrum of zero-energy bound states with nearest-neighbor spacings that changes from randomly to chaotically distributed for increasing magnetic field. Finally, we show that the extreme temperature sensitivity of a small, but sizable fraction of the resonances in the Dy and Er atom-loss spectra is due to resonant nonzero partial-wave collisions. Our threshold analysis for these resonances indicates a large collision-energy dependence of the three-body recombination rate.
Zero field splittings in molecules originate from the intrinsic spin and orbital angular momentum of unpaired electrons. Here, we close a knowledge gap on a diatomic molecule built from spin-8 ground-state dysprosium atoms, where zero-field splittings correspond to the energies of states with different alignments of the two spins. We predict a paramagnetic molecular ground state with parallel Dy spins aligned along the internuclear axis. A diamagnetic state with anti-parallel spins is the first excited state with a small energy cost of hc × 2 cm−1 predominantly due to the magnetic dipole-dipole interaction. We also determine the rotations and vibrations of the diatom and show that centrifugal forces double the splittings between these para- and dia-magnetic states. The vibrational spacings and zero-field splittings have similar magnitude. Finally, the Dy2 ground state has a magnetic moment that is twice that of the atom and, thus, arrays of ultracold Dy2 can be used to simulate strongly interacting magnets. Zero-field splittings in molecules arise from the spin and orbital angular momentum of unpaired electrons, yet their behaviour in diatomic molecules with spin-8 dysprosium atoms remains underexplored. Here, the authors predict a paramagnetic ground state with parallel Dy spins and reveal implications for simulating strongly interacting magnets using ultracold Dy2 arrays.
We report the observation of resonancelike loss in the trap population of ultracold dysprosium as a function of magnetic field, which we attribute to anisotropy-induced Fano-Feshbach resonances arising from Dy's large magnetic dipole moment and nonzero electronic orbital angular momentum. We recorded these resonances for four different isotopes, three bosonic and one fermionic, over a field range of 0--6 G and show that the number of resonances changes significantly as a function of temperature, even in the nK regime. Most of the observed resonances are of very narrow width. The fermionic isotope, unlike its bosonic counterparts, possesses nonzero nuclear spin and exhibits a much higher density of resonances.
Since the achievement of quantum degeneracy in gases of chromium atoms in 2004, the experimental investigation of ultracold gases made of highly magnetic atoms has blossomed. The field has yielded the observation of many unprecedented phenomena, in particular those in which long-range and anisotropic dipole-dipole interactions (DDIs) play a crucial role. In this review, we aim to present the aspects of the magnetic quantum-gas platform that make it unique for exploring ultracold and quantum physics as well as to give a thorough overview of experimental achievements. Highly magnetic atoms distinguish themselves by the fact that their electronic ground-state configuration possesses a large electronic total angular momentum. This results in a large magnetic moment and a rich electronic transition spectrum. Such transitions are useful for cooling, trapping, and manipulating these atoms. The complex atomic structure and large dipolar moments of these atoms also lead to a dense spectrum of resonances in their two-body scattering behaviour. These resonances can be used to control the interatomic interactions and, in particular, the relative importance of contact over dipolar interactions. These features provide exquisite control knobs for exploring the few- and many-body physics of dipolar quantum gases. The study of dipolar effects in magnetic quantum gases has covered various few-body phenomena that are based on elastic and inelastic anisotropic scattering. Various many-body effects have also been demonstrated. These affect both the shape, stability, dynamics, and excitations of fully polarised repulsive Bose or Fermi gases. Beyond the mean-field instability, strong dipolar interactions competing with slightly weaker contact interactions between magnetic bosons yield new quantum-stabilised states, among which are self-bound droplets, droplet assemblies, and supersolids. Dipolar interactions also deeply affect the physics of atomic gases with an internal degree of freedom as these interactions intrinsically couple spin and atomic motion. Finally, long-range dipolar interactions can stabilise strongly correlated excited states of 1D gases and also impact the physics of lattice-confined systems, both at the spin-polarised level (Hubbard models with off-site interactions) and at the spinful level (XYZ models). In the present manuscript, we aim to provide an extensive overview of the various related experimental achievements up to the present.