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arXiv:1306.0320 · Physical Review A

Two-dimensional crystals of Rydberg excitations in a resonantly driven lattice gas

David Petrosyan

Published Oct 28, 2013• 26 citations
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Abstract

The competition between resonant optical excitation of Rydberg states of atoms and their strong, long-range van der Waals interaction results in spatial ordering of Rydberg excitations in a two-dimensional lattice gas, as observed in a recent experiment of Schau\ss{} et al. [Nature (London) 491, 87 (2012)]. Here we use semiclassical Monte Carlo simulations to obtain stationary states for hundreds of atoms in finite-size lattices. We show the formation of regular spatial structures of Rydberg excitations in a system of increasing size, and find highly sub-Poissonian distribution of the number of Rydberg excitations characterized by a large negative value of the Mandel $Q$ parameter which is nearly independent of the system size.

DOI
10.1103/physreva.88.043431

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The competition between resonant optical excitation of Rydberg states of atoms and their strong, long-range van der Waals interaction results in spatial ordering of Rydberg excitations in a two-dimensional lattice gas, as observed in a recent experiment of Schau\ss{} et al. [Nature (London) 491, 87 (2012)]. Here we use semiclassical Monte Carlo simulations to obtain stationary states for hundreds of atoms in finite-size lattices. We show the formation of regular spatial structures of Rydberg excitations in a system of increasing size, and find highly sub-Poissonian distribution of the number of Rydberg excitations characterized by a large negative value of the Mandel QQQ parameter which is nearly independent of the system size.
We study the conditions for attaining crystalline order in the stationary state of a continuously driven, open many-body system. Specifically, we consider resonant optical excitations of atoms in a one-dimensional lattice to the Rydberg states interacting via the van der Waals potential. Strong blockade of excitations at neighboring lattice sites steers the system toward a crystalline state while competing with the fluctuations associated with relaxation. We analyze the stationary state of the many-body system and the dynamics of its buildup employing numerically exact time-dependent density-matrix renormalization-group simulations for two- and three-level excitation schemes. We also present an approximate rate equation model which provides qualitative conditions for attaining crystalline order.
Rydberg atoms have experimentally interestingproperties such as strong long-range Van der Waals interactions and the dipole blockade effect. In optical lattices the blockade effect ensures that only one Rydberg excitation per site is allowed, effectively creating a Rydberg crystal. We theoretically show that it is also possible for a one-dimensional Rydberg crystal to spontaneously form in a random ensemble of atoms, e.g. a magneto-optical trap. This is done using an existing Monte Carlo model [1] to simulate the excitation dynamics inside the intersection of two lasers for a two-step excitation scheme. With a blue-detuned laser for the upper transition, the first Rydberg excitation will occur after a relatively long time. That first Rydberg atom will then seed further Rydberg excitations, as the blockade effect shifts atoms at a certain distance into resonance. If two dimensions of the laser intersection are smaller than the blockade radius, a one-dimensional Rydberg crystal will form.
Abstract We examine the adiabatic preparation of crystalline phases of Rydberg excitations in a one-dimensional lattice gas by frequency sweep of the excitation laser, as proposed by Pohl et al (2010 Phys. Rev. Lett. 104 043002 ) and recently realized experimentally by Schauß et al (2015 Science 347 1455 ). We find that the preparation of crystals of a few Rydberg excitations in a unitary system of several tens of atoms requires exceedingly long times for the adiabatic following of the ground state of the system Hamiltonian. Using quantum stochastic (Monte Carlo) wavefunction simulations, we show that realistic decay and dephasing processes affecting the atoms during the preparation lead to a final state of the system that has only a small overlap with the target crystalline state. Yet, the final number and highly sub-Poissonian statistics of Rydberg excitations and their spatial order are little affected by the relaxations.
We study many-body correlations in the stationary state of a continuously driven, strongly interacting dissipative system. Specifically, we examine resonant optical excitations of Rydberg states of atoms interacting via long-range dipole-dipole and van der Waals potentials employing numerical and analytical techniques. Collection of atoms within a blockade distance form a ``superatom'' that can accommodate at most one Rydberg excitation. The superatom excitation probability saturates to 12\frac{1}{2}21​ for coherently driven atoms but is significantly higher in the presence of dephasing, approaching unity as the number of atoms increases. Using the exact numerical solution of the density-matrix equations for a small system, we demonstrate that strong dephasing of the optically driven dipoles renders the many-body problem amenable to semiclassical Monte Carlo simulations. We employ the Monte Carlo algorithm for a large number of atoms and find that in the steady state of a uniformly driven, extended one-dimensional system, the saturation of superatoms leads to quasicrystallization of Rydberg excitations whose correlations exhibit damped spatial oscillations. We show that the behavior of the system under the van der Waals interaction potential can be approximated by a rate-equations model based on a ``hard-rod'' interatomic potential, and by solving it we obtain the period and correlation length for the density wave of Rydberg excitations.
Abstract. We describe the dynamical preparation of anisotropic crystalline phases obtained by laser-exciting ultracold Alkali atoms to Rydberg p-states where they interact via anisotropic van der Waals interactions. We develop a time-dependent variational mean field ansatz to model large, but finite two-dimensional systems in experimentally accessible parameter regimes, and we present numerical simulations to illustrate the dynamical formation of anisotropic Rydberg crystals. PACS numbers: 32.80.Ee,34.20.Cf,64.70.Tg
Strong, long-range interactions between atoms in high-lying Rydberg states can suppress multiple Rydberg excitations within a micron-sized trapping volume and yield sizable Rydberg level shifts at larger distances. Ensembles of atoms in optical microtraps then form Rydberg superatoms with collectively enhanced transition rates to the singly excited state. These superatoms can represent mesoscopic, strongly interacting spins. We study a regular array of such effective spins driven by a laser field tuned to compensate the interaction-induced level shifts between neighboring superatoms. During the initial transient, a few excited superatoms seed a cascade of resonantly facilitated excitation of large clusters of superatoms. Due to spontaneous decay, the system then relaxes to the steady state having nearly universal Rydberg excitation density . This state is characterized by highly non-trivial equilibrium dynamics of quasi-particles—excitation holes in the lattice of Rydberg excited superatoms. We derive an effective many-body model that accounts for hole mobility as well as continuous creation and annihilation of holes upon collisions with each other. We find that holes exhibit a nearly incompressible liquid phase with highly sub-Poissonian number statistics and finite-range density–density correlations.