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arXiv:1203.0010 · Physical Review Letters

Nonadiabatic Preparation of Spin Crystals with Ultracold Polar Molecules

Mikhail Lemeshko, Roman V. Krems, Hendrik Weimer

Published Jul 16, 2012• 32 citations
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Abstract

We study the growth dynamics of ordered structures of strongly interacting polar molecules in optical lattices. Using a dipole blockade of microwave excitations, we map the system onto an interacting spin-1/2 model possessing ground states with crystalline order, and describe a way to prepare these states by nonadiabatically driving the transitions between molecular rotational levels. The proposed technique bypasses the need to cross a phase transition and allows for the creation of ordered domains of considerably larger size compared to approaches relying on adiabatic preparation.

DOI
10.1103/physrevlett.109.035301

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We study the growth dynamics of ordered structures of strongly interacting polar molecules in optical lattices. Using a dipole blockade of microwave excitations, we map the system onto an interacting spin-1/2 model possessing ground states with crystalline order, and describe a way to prepare these states by nonadiabatically driving the transitions between molecular rotational levels. The proposed technique bypasses the need to cross a phase transition and allows for the creation of ordered domains of considerably larger size compared to approaches relying on adiabatic preparation.
We investigate the dynamical formation of crystalline states with systems of polar molecules or Rydberg atoms loaded into a deep optical lattice. External fields in these systems can be used to couple the atoms or molecules between two internal states: one that is weakly interacting and one that exhibits a strong dipole–dipole interaction. By appropriate time variation of the external fields, we show that it is possible to produce crystalline states of the strongly interacting states with high filling fractions chosen via the parameters of the coupling. We study the coherent dynamics of this process in one dimension (1D) using a modified form of the time-evolving block decimation (TEBD) algorithm, and obtain crystalline states for system sizes and parameters corresponding to realistic experimental configurations. For polar molecules these crystalline states will be long-lived, assisting in a characterization of the state via the measurement of correlation functions. We also show that as the coupling strength increases in the model, the crystalline order is broken. This is characterized in 1D by a change in density–density correlation functions, which decay to a constant in the crystalline regime, but show different regions of exponential and algebraic decay for larger coupling strengths.
We present a technique for engineering quantum magnets via ultracold polar molecules in optical lattices and explore exotic interplay between its spin superfluidity and solidity. The molecular ground and first excited rotational states are resonantly coupled by a linearly polarized microwave field. The spin-up (spin-down) states are presented by molecular rotational states of electric dipole moment along (against) the coupling field. By controlling the angle between the lattice direction and the coupling field, the inter-site interaction can be tuned from antiferromagnetic to ferromagnetic. Furthermore, the dipole-dipole interaction induces an exotic interplay between spin superfluidity and solidity, and spin supersolid phases may appear in mediate regions.
We propose a scheme to realize a pseudospin-1/21/21/2 model of the ${}^{1}\mathrm{\ensuremath{\Sigma}}(v=0)$ bialkali polar molecules with the spin states corresponding to two sublevels of the first excited rotational level. We show that the effective dipole-dipole interaction between two spin-1/21/21/2 molecules couples the rotational and orbital angular momenta and is highly tunable via a microwave field. We also investigate the ground-state properties of a spin-1/21/21/2 molecular condensate. A variety of nontrivial quantum phases, including the doubly quantized vortex states, are discovered. Our scheme can also be used to create spin-1 model of polar molecules. Thus we show that the ultracold gases of bialkali polar molecules provide a unique platform for studying the spinor condensates of rotating molecules.
We describe how to design a large class of always on spin-1 interactions between polar molecules trapped in an optical lattice. The spin degrees of freedom correspond to the hyperfine levels of a ro-vibrational ground state molecule. Interactions are induced using a microwave field to mix ground states in one hyperfine manifold with the spin entangled dipole–dipole coupled excited states. Using multiple fields, anistropic models in one, two, or three dimensions can be built with tunable spatial range. An illustrative example in one-dimension is the generalized Haldane model, which at a specific parameter has a gapped valence bond solid ground state. The interaction strengths are large compared to decoherence rates and should allow for probing the rich phase structure of strongly correlated systems, including dimerized and gapped phases.
The creation of a gas of ultracold polar molecules with a high phase space density brings new possibilities beyond experiments with ultracold atomic gases. In particular, long-range, anisotropic, and tunable dipole-dipole interactions open the way for novel quantum gases, with applications including strongly correlated many-body systems, and ultracold chemistry. This thesis will present the final steps to complete control over both internal and external degrees of freedom of the molecule which allows us to control, and even completely suppress, the chemical reactions between molecules. First, the control over internal states has been achieved through coherent state transfer to the ro-vibronic ground state and coherent manipulations of the hyperfine and rotational states with microwave radiation. Second, external degrees of freedom are controlled by loading the gas into an optical lattice. With the molecules loaded into a one-dimensional lattice, the orientation of the molecular collisions is controlled by manipulating both internal (hyperfine states) and external (motional states in the direction of tight confinement) degrees of freedom. Most striking is that by preparing the molecules all in the lowest band of the lattice in the same internal state, the molecular collisions can only occur in a side-by-side" orientation, where the chemical reaction rate is suppressed by the repulsive dipole-dipole interactions. The chemical reaction can be suppressed completely by further constraining the motion in the trap in a strong 3D lattice. Here we see lifetimes longer than 20 s, limited by o-resonant light scattering. Finally, the ac polarizability of the molecules is explored and controlled. The different rotational states of the molecule have different polarizabilities and will experience a different trapping force in both the optical dipole trap or lattice. We show that there is a magic angle" between the quantization axis and the polarization of the trapping laser at which the polarizabilities of two different rotational states can be matched, eliminating dephasing and allowing for coherent manipulations between rotational states.
Abstract. We describe how to design a large class of always on spin−1 interactions between polar molecules trapped in an optical lattice. The spin degrees of freedom correspond to the hyperfine levels of a ro-vibrational ground state molecule. Interactions are induced using a microwave field to mix ground states in one hyperfine manifold with the spin entangled dipoledipole coupled excited states. Using multiple fields anistropic models in one, two, or three dimensions, can be built with tunable spatial range. An illustrative example in one dimension is the generalized Haldane model, which at a specific parameter has a gapped valence bond solid ground state. The interaction strengths are large compared to decoherence rates and should allow for probing the rich phase structure of strongly correlated systems, including dimerized and gapped phases. PACS numbers: 75.10.Jm, 74.20.Mn, 34.20GjDesigning spin−1 lattice models using polar molecules 2 1.