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Register a new userSolids and supersolids of three-body interacting polar molecules in an optical lattice
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We study the physics of cold polar molecules loaded into an optical lattice in the regime of strong three-body interactions, as put forward recently by Buchler [Nature Phys. 3, 726 (2007)]. To this end quantum Monte Carlo simulations, exact diagonalization and a semiclassical approach are used to explore hardcore bosons on the two-dimensional square lattice which interact solely by long ranged three-body terms. The resulting phase diagram shows a sequence of solid and supersolid phases. Our findings are directly relevant for future experimental implementations and open a new route towards the discovery of a lattice supersolid phase in experiment.
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We study the possibility of associating meta-stable Efimov trimers from three free Bose atoms in a tight trap realised, for instance, via an optical lattice site or a microchip. The suggested scheme for the production of these molecules is based on magnetically tunable Feshbach resonances and takes advantage of the Efimov effect in three-body energy spectra. Our predictions on the energy levels and wave functions of three pairwise interacting 85Rb atoms rely upon exact solutions of the Faddeev equations and include the tightly confining potential of an isotropic harmonic atom trap. The magnetic field dependence of these energy levels indicates that it is the lowest energetic Efimov trimer state that can be associated in an adiabatic sweep of the field strength. We show that the binding energies and spatial extents of the trimer molecules produced are comparable, in their magnitudes, to those of the associated diatomic Feshbach molecule. The three-body molecular state follows Efimovs scenario when the pairwise attraction of the atoms is strengthened by tuning the magnetic field strength.
Optical conductivity of an interacting polaron gas is calculated within an extended random phase approximation which takes into account mixing of collective excitations of the electron gas with LO phonons. This mixing is important for the optical response of strongly polar crystals where the static dielectric constant is rather high: strontium titanate is the case. The present calculation sheds light on unexplained features of experimentally observed optical conductivity spectra in $n$-doped SrTiO$_{3}$. These features appear to be due to dynamic screening of the electron-electron interaction by polar optical phonons and hence do not require additional mechanisms for the explanation.
In this work, we discuss the emergence of $p$-wave superfluids of identical fermions in 2D lattices. The optical lattice potential manifests itself in an interplay between an increase in the density of states on the Fermi surface and the modification of the fermion-fermion interaction (scattering) amplitude. The density of states is enhanced due to an increase of the effective mass of atoms. In deep lattices, for short-range interacting atoms, the scattering amplitude is strongly reduced compared to free space due to a small overlap of wavefunctions of fermions sitting in the neighboring lattice sites, which suppresses the $p$-wave superfluidity. However, we show that for a moderate lattice depth there is still a possibility to create atomic $p$-wave superfluids with sizable transition temperatures. The situation is drastically different for fermionic polar molecules. Being dressed with a microwave field, they acquire a dipole-dipole attractive tail in the interaction potential. Then, due to a long-range character of the dipole-dipole interaction, the effect of the suppression of the scattering amplitude in 2D lattices is absent. This leads to the emergence of a stable topological $p_x+ip_y$ superfluid of identical microwave-dressed polar molecules.
The production of molecules from dual species atomic quantum gases has enabled experiments that employ molecules at nanoKelvin temperatures. As a result, every degree of freedom of these molecules is in a well-defined quantum state and exquisitely controlled. These ultracold molecules open a new world of precision quantum chemistry in which quantum statistics, quantum partial waves, and even many-body correlations can play important roles. Moreover, to investigate the strongly correlated physics of many interacting molecular dipoles, we can mitigate lossy chemical reactions by controlling the dimensionality of the system using optical lattices formed by interfering laser fields. In a full three-dimensional optical lattice, chemistry can be turned on or off by tuning the lattice depth, which allows us to configure an array of long-range interacting quantum systems with rich internal structure. Such a system represents an excellent platform for gaining fundamental insights to complex materials based on quantum simulations and also for quantum information processing in the future.
We introduce a simple model of SO($N$) spins with two-site interactions which is amenable to quantum Monte-Carlo studies without a sign problem on non-bipartite lattices. We present numerical results for this model on the two-dimensional triangular lattice where we find evidence for a spin nematic at small $N$, a valence-bond solid (VBS) at large $N$ and a quantum spin liquid at intermediate $N$. By the introduction of a sign-free four-site interaction we uncover a rich phase diagram with evidence for both first-order and exotic continuous phase transitions.
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