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arXiv:1812.10559 · Physical Review A

Roton-induced trapping in strongly correlated Rydberg gases

João D. Rodrigues, Luís F. Gonçalves, Hugo Terças, Luís Gustavo Marcassa, José Tito Mendonça

Published Dec 26, 2018• 1 citation
arXivHTMLPDF

Abstract

Atoms excited into high-lying Rydberg states and under strong dipole-dipole interactions exhibit phenomena associated with highly correlated and complex systems. We perform first-principles numerical simulations on the dynamics of such systems. The emergence of a roton minimum in the excitation spectrum, as expected in strongly correlated gases and accurately described by Feynman's theory of liquid helium, is shown to significantly inhibit particle transport, with a strong suppression of the diffusion coefficient, due to the emerging spatial order. We also demonstrate how the ability to temporally tune the interaction strength among Rydberg atoms can be used in order to overcome the effects of disorder-induced heating, allowing the study of unprecedented highly coupled regimes.

DOI
10.1103/physreva.98.062713

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Atoms excited into high-lying Rydberg states and under strong dipole-dipole interactions exhibit phenomena associated with highly correlated and complex systems. We perform first-principles numerical simulations on the dynamics of such systems. The emergence of a roton minimum in the excitation spectrum, as expected in strongly correlated gases and accurately described by Feynman's theory of liquid helium, is shown to significantly inhibit particle transport, with a strong suppression of the diffusion coefficient, due to the emerging spatial order. We also demonstrate how the ability to temporally tune the interaction strength among Rydberg atoms can be used in order to overcome the effects of disorder-induced heating, allowing the study of unprecedented highly coupled regimes.
We describe the emergence of strong spatial correlations, akin to liquidlike behavior and crystallization effects, in low- (one- and two-)dimensional gases of cold Rydberg atoms. The presence of an external electric field permanently polarizes the atoms, which became highly correlated due to the long-range dipole-dipole interaction. We describe a theoretical approach particularly suited for strongly coupled systems and numerically obtain both the two-particle distribution function and the static structure factor. The experimental implementation of such highly interacting systems is discussed, including detailed calculations of the interaction strength for different Rydberg states. The results provide insights into many-body effects associated with strongly interacting Rydberg atoms, including the possibility of observing highly ordered phases.
The strong interactions between Rydberg excitations can result in spatial correlations between the excitations. The ability to control the interaction strength and the correlations between Rydberg atoms is applicable in future technological implementations of quantum computation. In this thesis, I investigates how both the character of the Rydberg-Rydberg interactions and the details of the excitation process affect the nature of the spatial correlations and the evolution of those correlations in time. I first describes the experimental apparatus and methods used to perform high-magnification Rydberg-atom imaging, as well as three experiments in which these methods play an important role. The obtained Rydberg-atom positions reveal the correlations in the many-body Rydberg-atom system and their time dependence with sub-micron spatial resolution. In the first experiment, atoms are excited to a Rydberg state that experiences a repulsive van der Waals interaction. The Rydberg excitations are prepared with a well-defined initial separation, and the effect of van der Waals forces is observed by tracking the interatomic distance between the Rydberg atoms. The atom trajectories and thereby the interaction coefficient C6 are extracted from the pair correlation functions of the Rydberg atom positions. In the second experiment, the Rydberg atoms are prepared in a highly dipolar state by using adiabatic state transformation. The atom-pair kinetics that follow from the strong dipole-dipole interactions are observed. The pair correlation results provide the first direct visualization of the electric-dipole interaction and clearly exhibit its anisotropic nature. In both the first and the second experiment, results of semi-classical simulations of the atom-pair trajectories agree well with the experimental data. In the analysis, I use energy conservation and measurements of the initial positions and the terminal velocities of the atom pairs to extract the C6 and C3 interaction coefficients. The final experiment demonstrates the ability to enhance or suppress the degree of spatial correlation in a system of Rydberg excitations, using a rotary-echo excitation process in concert with particular excitation laser detunings. The work in this thesis demonstrates an ability to control long-range interactions between Rydberg atoms, which paves the way towards preparing and studying increasingly complex many-body systems.
This thesis experimentally explores the application of strongly interacting states of Rydberg atoms as means to introduce and control correlations in many-body systems. A new apparatus has been built, which combines high atomic densities possible using optical dipole traps with the ability to detect and probe Rydberg atoms via both field ionization detection and electromagnetically induced transparency. In the first study, the interaction induced excitation of Rydberg atom pairs ('antiblockade') is demonstrated using detuned laser excitation. This provides \nthe possibility to engineer spatial correlations and to control interactions between Rydberg atoms. We then investigate the effects of Rydberg-Rydberg interactions \nand correlations on the spontaneous evolution of the system to an ultracold plasma. The initial correlations between Rydberg atoms should be preserved, suggesting a new route to overcome disorder-induced heating and to enter new strongly coupled regimes. Finally the back-action of Rydberg-Rydberg interactions on propagating light fields is explored. Dissipative interactions between dark-state polaritons give rise to a strongly nonlinear optical response and sub-Poissonian statistics of polaritons \nwhich reflect the emergence of correlations in both the atomic and light fields. Combined, these experiments help elucidate the effects of Rydberg induced correlations on diverse physical systems involving atoms, ions and photons.
This thesis investigates different aspects of strongly interacting ultracold Rydberg gases coupled by light, including the excitation of correlated structures called Rydberg aggregates and dipolar energy transport. For this purpose an experimental apparatus has been constructed. We study coherent population trapping (CPT) and electromagnetically induced transparency (EIT) involving Rydberg states. To study the formation of Rydberg aggregates we use full counting statistics (FCS) which makes it possible to infer the size of Rydberg aggregates. Dephasing during the excitation is found to have a dramatic effect on the formation process, leading to sequential growth around an initial grain. Rydberg state EIT is used to realize a new direct optical imaging scheme for Rydberg atoms which combines highly sensitive detection with high spatial and temporal resolution. Applying this technique we observe dipole-mediated energy transport processes between Rydberg atoms. We study classical transport in the presence of strong measurement induced decoherence. The strong interactions are seen to mediate long-range hopping significantly beyond nearest neighbors. We present first indications for coherent transport in this system. These experiments shed light on the role of correlations in the excitation and evolution of strongly interacting quantum systems and e.g. could possibly be used to model energy transport in biological systems. \n
Laser-driven Rydberg gases are many-body quantum systems that exhibit a pronounced collective excitation behavior due to the strong interaction between atoms in high-lying electronic states. Atoms located within a so-called blockade volume share a single Rydberg excitation, which is dynamically created and annihilated. For sufficiently long times, this driven system approaches a steady state, which lends its properties from a maximum entropy state of a Tonks gas. Using this connection, we show that spatial correlations between Rydberg atoms are controlled by the number of atoms contained within a blockade volume. For a small number, the system favors a disordered arrangement of Rydberg atoms, whereas in the opposite limit, Rydberg atoms tend to arrange in an increasingly ordered configuration. We argue that this is an entropic effect which is observable in current experiments. Our work demonstrates how ordered structures can spontaneously emerge in a strongly interacting, closed many-body system out of equilibrium.
Ultracold atomic gases excited to strongly interacting Rydberg states are a promising system for quantum simulations of many-body systems. The dipole blockade of Rydberg excitations is a hallmark of the strong interactions between atoms in these high-lying quantum states. We have measured the Rydberg excitation for rubidium ultracold atoms in magneto-optical traps and for Bose-Einstein condensates loaded into quasi one-dimensional traps. One of the consequences of the dipole blockade is the suppression of fluctuations in the counting statistics of Rydberg excitations. We have obtained experimental results on the dynamics and the counting statistics of Rydberg excitations of ultra-cold Rubidium atoms both on and off resonance, which exhibit sub- and super-Poissonian counting statistics, respectively. We have found strongly bimodal counting distributions in the offresonant regime.