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Dynamical preparation of laser-excited anisotropic Rydberg crystals in 2D optical lattices

Benoît Vermersch, M. Punk, A. W. Glaetzle, C. Gross, P. Zoller

Published Jan 9, 2015• 10 citations
OpenAlex

Abstract

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

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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
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.
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 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.
Ultracold atomic gases have been used extensively in recent years to realize textbook examples of condensed matter phenomena. Recently, phase transitions to ordered structures have been predicted for gases of highly excited, 'frozen' Rydberg atoms. Such Rydberg crystals are a model for dilute metallic solids with tunable lattice parameters, and provide access to a wide variety of fundamental phenomena. We investigate theoretically how such structures can be created in four distinct cold atomic systems, by using tailored laser-excitation in the presence of strong Rydberg-Rydberg interactions. We study in detail the experimental requirements and limitations for these systems, and characterize the basic properties of small crystalline Rydberg structures in one, two and three dimensions.