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Physical Review Letters

Imaging Spatial Correlations of Rydberg Excitations in Cold Atom Clouds

Andrew Schwarzkopf, Rachel Sapiro, Georg A. Raithel

Published Aug 31, 2011• 109 citations
Publisher

Abstract

We use direct spatial imaging of cold 85Rb Rydberg atom clouds to measure the Rydberg-Rydberg correlation function. The results are in qualitative agreement with theoretical predictions [F. Robicheaux and J. V. Hernández, Phys. Rev. A 72, 063403 (2005)]. We determine the blockade radius for states 44D(5/2), 60D(5/2), and 70D(5/2) and investigate the dependence of the correlation behavior on excitation conditions and detection delay. Experimental data hint at the existence of long-range order.

DOI
10.1103/physrevlett.107.103001

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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.

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We use direct spatial imaging of cold 85Rb Rydberg atom clouds to measure the Rydberg-Rydberg correlation function. The results are in qualitative agreement with theoretical predictions [F. Robicheaux and J. V. Hernández, Phys. Rev. A 72, 063403 (2005)]. We determine the blockade radius for states 44D(5/2), 60D(5/2), and 70D(5/2) and investigate the dependence of the correlation behavior on excitation conditions and detection delay. Experimental data hint at the existence of long-range order.
We use direct spatial ion imaging of cold 85{}^{85}85Rb Rydberg atom clouds to measure the Rydberg-Rydberg correlation function, with and without light-shift potentials generated by an optical dipole trap. We find that the blockade radius depends on laser detunings and spatially varying light shifts. At certain laser detunings the probability of exciting Rydberg atoms at particular separations is enhanced, which we interpret to be a result of direct two-photon excitation of Rydberg atom pairs. The results are in accordance with predictions [F. Robicheaux and J. V. Hern\'andez, Phys. Rev. A 72, 063403 (2005)] and a model we develop that accounts for a one-dimensional dipole-trap potential.
When cold atoms are laser-excited to Rydberg states, the strong interactions between Rydberg excitations can lead to complex many-body entanglement in the system. The excitation process results in spatial correlations between excitations in the system. In most cases, Rydberg excitation positions are anticorrelated such that no two excitations are within a "blockade radius" of each other. Such systems are well-suited for studying basic many-body physics, as well as for future technological applications such as quantum computation. This thesis describes an experimental apparatus we constructed to perform spatially-sensitive detection of Rydberg atoms. We use the apparatus to perform measurements of the Rydberg-Rydberg pair-correlation function. This results in the first direct spatial images of the Rydberg blockade effect. We measure the blockade radius for a variety of S and D Rydberg states in rubidium. We investigate the dependence of the blockade radius on laser detunings and energy level shifts induced by optical potentials due to trapping lasers. Our results have some implications for atom traps used for neutral atom quantum computation. We also present simulations results used to characterize the performance of the imaging system.
One of the most striking features of the strong interactions between Rydberg atoms is the Rydberg blockade effect, which allows only a single excitation to the Rydberg state within the volume of the blockade sphere. Here we present a method that spatially visualizes this phenomenon in an inhomogeneous gas of ultracold rubidium atoms. In our experiment we scan the position of one of the excitation lasers across the cold cloud and determine the number of Rydberg excitations detected as a function of position. Comparing this distribution to the one obtained for the number of ions created by a two-photon ionization process via the intermediate 5P5P5P level, we demonstrate that the blockade effect modifies the width of the Rydberg excitation profile. Furthermore, we study the dynamics of the Rydberg excitation and find that the time scale for the excitation depends on the atomic density at the beam position.
Abstract We present a depletion imaging technique to map out the spatial and temporal dependency of the density distribution of an ultracold gas of Rydberg atoms. Locally resolved absorption depletion, observed through differential ground state absorption imaging of a 87 Rb cloud in presence and absence of pre-excited Rydberg atoms, reveals their projected two-dimensional distribution. By employing a closed two-level optical transition uncoupled from the Rydberg state, the highly excited atoms are preserved during imaging. We measure the excitation dynamics of the ∣ 48 S 〉 state of 87 Rb, observing a saturation of the two-dimensional Rydberg density. Such outcome can be explained by the Rydberg blockade effect which prevents resonant excitation of close-by Rydberg atoms due to strong dipolar interactions. By combining the superatom description, where atoms within a blockade radius are represented as collective excitations, with a Monte Carlo sampling, we can quantitatively model the observed excitation dynamics and infer the full three-dimensional distribution of Rydberg atoms, that can serve as a starting point for quantum simulation of many-body dynamics involving Rydberg spin systems.
Rydberg atoms, i.e. atoms with one or more highly excited electrons, show exaggerated properties compared to ground state atoms. For example, their energy levels are very sensitive to external electric fields (Stark effect) and they exhibit strong interatomic interactions, which can lead to a suppression of excitation known as the Rydberg blockade. The latter property makes Rydberg atoms promising candidates for quantum simulation and quantum computing. This work describes the direct observation of the excitation blockade for highly Stark-shifted Rydberg atoms induced by controllable dipole-dipole interactions. We investigate the electric field region around and above the classical ionization threshold, which is typically not considered suitable for blockade experiments. We excite Rydberg atoms in the energy region corresponding to the unperturbed 43S1/2 state at electric fields around 127V/cm out of a magneto-optically trapped cloud of 87Rb atoms with a temperature of 150 μK. We tune the dipole-dipole interaction by the applied electric field thus changing the electric dipole moment of the excited state. The position of the Rydberg atoms is detected by ionization and subsequent ion imaging; the controlled ionization of the atoms is achieved by adiabatic transfer of the Rydberg state to an ionizing state. For the spatially resolved detection of the atoms, a high resolution ion microscope for cold atoms has been developed and experimentally characterized. It features a maximum magnification of 1000 and sub-micrometer spatial resolution. A theoretical treatment of highly Stark-shifted Rydberg states is developed introducing a complex absorbing potential. It is capable of predicting the ionization rates of the Rydberg states for a wide range of electric fields and energies with only one free parameter. Together with the numerical calculations, measurements of the ionization spectra for different Rydberg states are presented. The 43S1/2 state is measured in an electric-field range from 125V/cm to 165V/cm (classical ionization limit 127V/cm), the 70S1/2 state in an electric-field range from 15V/cm to 35V/cm (classical ionization limit 16.1V/cm) and the 100S1/2 state in an electric-field range from 7V/cm to 19V/cm (classical ionization limit 3.7V/cm). Our results show an intricate energy level structure with broad, strongly ionizing states as well as sharp, nearly non-ionizing states. The numerical calculations are also used for the prediction of selective field ionization spectra and the results are used to identify Förster resonances in the Stark spectrum of the 45D5/2 state. Complementary to the spatially resolved measurements in high electric fields, the Rydberg blockade effect is also observed via the excitation number statistics at Förster resonances.
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.