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arXiv:0902.4523 · Physical Review A

Universal scaling in a strongly interacting Rydberg gas

Robert Löw, Hendrik Weimer, Ulrich Krohn, Rolf Heidemann, Vera Bendkowsky, Björn Butscher, Hans Peter Büchler, Tilman Pfau

Published Sep 29, 2009• 87 citations
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Abstract

We study a gas of ultracold atoms resonantly driven into a strongly interacting Rydberg state. The long-distance behavior of the spatially frozen effective pseudospin system is determined by a set of dimensionless parameters, and we find that the experimental data exhibit algebraic scaling laws for the excitation dynamics and the saturation of Rydberg excitation. Mean-field calculations as well as numerical simulations provide an excellent agreement with the experimental finding and are evidence for universality in a strongly interacting frozen Rydberg gas.

DOI
10.1103/physreva.80.033422

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We study a gas of ultracold atoms resonantly driven into a strongly interacting Rydberg state. The long-distance behavior of the spatially frozen effective pseudospin system is determined by a set of dimensionless parameters, and we find that the experimental data exhibit algebraic scaling laws for the excitation dynamics and the saturation of Rydberg excitation. Mean-field calculations as well as numerical simulations provide an excellent agreement with the experimental finding and are evidence for universality in a strongly interacting frozen Rydberg gas.
We study the appearance of correlated many-body phenomena in an ensemble of atoms driven resonantly into a strongly interacting Rydberg state. The ground state of the Hamiltonian describing the driven system exhibits a second order quantum phase transition. We derive the critical theory for the quantum phase transition and show that it describes the properties of the driven Rydberg system in the saturated regime. We find that the suppression of Rydberg excitations known as blockade phenomena exhibits an algebraic scaling law with a universal exponent.
In this thesis I present several theoretical methods to explore the excitation dynamics of Ultracold Rydberg systems in various regimes. For some applications the details of interactions between Rydberg atoms have to be carefully examined, while for others, the many-body aspect of Rydberg excitation may be crucial. In both cases, the basic prerequisite is to know the interactions sufficiently well. I will review the basic concepts how to evaluate molecular potentials in various Hund's cases and approximations. Long-range Rydberg-Rydberg interactions between Rydberg atoms induce ℓ-mixing which in certain situations gives rise to molecular resonances. For these resonances, we calculate long-range potentials in Hund's case (c) by diagonalization of an interaction matrix. The excitation dynamics of the resonances is always modeled as pair excitation. At high principal quantum number n, the interactions between Rydberg atoms can blockade the excitation of many surrounding atoms in the range of few μm. The atoms within this range are strongly correlated so that many-body treatments are, in general, needed. To describe this blockading effect and other manifestations of the collective behavior of Rydberg excitation, such as the many-body Rabi oscillations, spatial correlations between atoms and the fluctuations of the number of excited atoms, I have used three different approaches. In the mean-field approach the interactions between different atoms is modeled by a distribution of mean-field shifts for which a distribution of probabilities is calculated, A good agreement between the theoretical model and experimental measurements is found. To study the correlations between atoms the many-body wavefunction is numerically computed. The possibility of observing the many-body Rabi oscillations of Rydberg excitation and other aspects of many-body dynamics is analyzed. Although strong interactions cannot be treated perturbatively other expansions may be feasible. I will show that the expansion in powers of the single atom Rabi frequency can be evaluated in the interaction and Heisenberg picture. The expansion is expected to behave well for arbitrary strong interactions. ^
The properties of a Rydberg atom immersed in an ultracold environment were investigated. Two scenarios were considered, one of which involves the neighbouring ground-state atoms arranged in a spatially structured configuration, while the other involves them distributed randomly in space. To calculate the influence of the multiple ground-state atoms on the Rydberg atom, Fermi-pseudopotential was used, which simplified greatly the numerical effort. In many cases, the few-body interaction can be written down analytically which reveals the symmetry properties of the system. In the structured case, we report the first prediction of the formation of ``Rydberg Borromean trimers''. The few-body interactions and the dynamics of the linear A-B-A trimer, where A is the ground-state atom and B is the Rydberg atom, were investigated in the framework of normal mode analysis. This exotic ultralong-range triatomic bound state exists despite that the Rydberg-ground-state interaction is repulsive. Their lifetimes were estimated using both quantum scattering calculations and semi-classical approximations which are found to be typically sub-microseconds. In the disordered case, the Rydberg-excitation spectra of a frozen-gas were simulated, where the nuclear degrees of freedom can be ignored. The systematic change of the spectral shape with respect to the density of the gas and the excitation of the Rydberg atom were found and studied. Some parts of the spectral shape can be described by simple scaling laws with exponents given by the basic properties of the atomic species such as the polarizability and the zero-energy electron-atom scattering length.
The nonequilibrium dynamics of a gas of cold atoms in which Rydberg states are off-resonantly excited is studied in the presence of noise. The interplay between interaction and off-resonant excitation leads to an initial dynamics where aggregates of excited Rydberg atoms slowly nucleate and grow, eventually reaching long-lived metastable arrangements which then relax further on much longer time scales. This growth dynamics is governed by an effective Master equation which permits a transparent and largely analytical understanding of the underlying physics. By means of extensive numerical simulations we study the many-body dynamics and the correlations of the resulting nonequilibrium states in various dimensions. Our results provide insight into the dynamical richness of strongly interacting Rydberg gases in noisy environments, and highlight the usefulness of these kinds of systems for the exploration of soft-matter-type collective behavior.
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.
The dipole-dipole interaction strongly couples ultracold highly excited atoms, known as Rydberg atoms, and is the dominant mechanism for energy exchange among such atoms on microsecond time scales. I present the results of experiments that investigate this interaction using rubidium atoms excited to Rydberg states with an all-diode laser system. In the first of these, high resolution dipole-dipole interaction spectra for different magnetic sublevels of the 32d5/2 state are collected and analyzed. In the second experiment, ultracold rubidium atoms are implusively excited to coherent superpositions of three closely spaced |mj|sublevels of the 32d5/2 state in a weak electric field. The magnitude of the field sets the energy level spacing between these states, and hence the frequency of the phase dependent oscillations resulting from interference in resonant energy exchange processes. In the third experiment, the dipole-dipole interaction induced resonant energy exchange between columns of ultracold rubidium Rydberg atoms is imaged using a new technique involving selective field ionization with a spatially sensitive ion detector.