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arXiv:cond-mat/0608250 · Physical Review Letters

Quantum Fluids of Self-Assembled Chains of Polar Molecules

Daw-Wei Wang, Mikhail D. Lukin, Eugene Demler

Published Nov 3, 2006• 139 citations
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Abstract

We study polar molecules in a stack of strongly confined pancake traps. When dipole moments point perpendicular to the planes of the traps and are sufficiently strong, the system is stable against collapse but attractive interaction between molecules in different layers leads to the formation of dipolar chains, analogously to the chaining phenomenon in classical rheological electro- and magnetofluids. We analyze properties of the resulting quantum liquid of dipolar chains and show that only the longest chains undergo Bose-Einstein condensation with a strongly reduced condensation temperature. We discuss several experimental methods for studying chains of polar molecules.

DOI
10.1103/physrevlett.97.180413

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We study polar molecules in a stack of strongly confined pancake traps. When dipole moments point perpendicular to the planes of the traps and are sufficiently strong, the system is stable against collapse but attractive interaction between molecules in different layers leads to the formation of dipolar chains, analogously to the chaining phenomenon in classical rheological electro- and magnetofluids. We analyze properties of the resulting quantum liquid of dipolar chains and show that only the longest chains undergo Bose-Einstein condensation with a strongly reduced condensation temperature. We discuss several experimental methods for studying chains of polar molecules.
Ultracold polar molecules, in highly anisotropic traps and interacting via a repulsive dipolar potential, may form one-dimensional chains at high densities. According to classical theory, at low temperatures there exists a critical value of the density at which a second order phase transition from a linear to a zigzag chain occurs. We study the effect of thermal and quantum fluctuations on these self-organized structures using classical and quantum Monte Carlo methods, by means of which we evaluate the pair correlation function and the static structure factor. Depending on the parameters, these functions exhibit properties typical of a crystalline or of a liquid system. We compare the thermal and the quantum results, identifying analogies and differences. Finally, we discuss experimental parameter regimes where the effects of quantum fluctuations on the linear - zigzag transition can be observed.
We predict that ultracold bosonic dipolar gases, confined within a multilayer geometry, may undergo self-assembling processes, leading to the formation of chain gases and solids. These dipolar chains, with dipoles aligned across different layers, emerge at low densities and resemble phases observed in liquid crystals, such as nematic and smectic phases. We calculate the phase diagram using quantum Monte Carlo methods, introducing a newly devised trial wave function designed for describing the chain gas, where dipoles from different layers form chains without in-plane long-range order. We find gas, solid, and chain phases, along with quantum phase transitions between these states. Specifically, we predict the existence of quantum phase transitions from gaseous to self-ordered phases, as the interlayer distance is decreased. Remarkably, in the self-organized phases, the mean interparticle distance can significantly exceed the characteristic length of the interaction potential, yielding solids and chain gases with densities several orders of magnitude lower than those of conventional quantum solids.
Dipolar interactions support the formation of intersite soliton molecules in a stack of quasi-one-dimensional (quasi-1D) traps. We show that the stability and properties of individual solitons and soliton molecules in such a geometry crucially depend on the interplay between contact and dipolar interactions. In particular, two different quasi-1D soliton regimes are possible: a one-dimensional (1D) soliton characterized by purely repulsive dipole-dipole interactions (DDI) and a three-dimensional (3D) soliton for which a sufficiently large dipole moment renders the DDI attractive. Furthermore, we find that in contrast to the dimers of polar molecules the soliton dimers exhibit a nontrivial behavior of the elementary excitations that stems from the competition between onsite and intersite DDI. Finally, we prove the existence of soliton trimers in a regime where molecular trimers do not occur. We demonstrate that the soliton molecules that we report are well feasible under realistic experimental conditions.
It is well-known that the liquid properties in a strongly confined system can be very different from their ordinary behaviors in an extended system, due to the competition between the thermal energy and the interaction energy. Here we show that, in a low-dimensional self-assembled dipolar crystal, the parabolic optical confinement potential can also strongly affect the quantum many-body properties in the low temperature regime. For example, by changing the confinement aspect ratio, the bulk of the system can undergo a quantum phase transition between a liquid state and a solid state via a nonmonotonic pattern formation of the domain wall. Furthermore, the entropy of a trapped dipolar crystal can be much larger than the liquid state in the weak dipole limit, indicating an intrinsic polarization cooling mechanism via increasing the external field. These highly correlated confinement effects are very important to the experimental preparation of a self-assembled dipolar crystal using ultracold polar molecules.
Bose-Einstein condensation of dipolar molecules can be achieved by shielding loss channels with microwave fields. The microwave coupling can be approximated by effective dipole-dipole interactions with a short-range repulsion. We study properties and stability of these molecular Bose gases with a many-body variational method, the hypernetted-chain Euler-Lagrange method for a wide range of densities and repulsion strengths of the microwave shield. We find a homogeneous gas-like phase which, however, is unstable at low density against density waves: at a critical density, which depends on the repulsion strength, the dipolar fluid undergoes a phase transition to a layer phase. Thus, if the molecular condensate is expanded adiabatically by decreasing the confinement strength, it will spontaneously form layers at the critical density. These quasi-two-dimensional layers can be self-bound, hence form two-dimensional liquids. By varying the microwave shield, the predicted equilibrium densities span more than an order of magnitude.