Abstract As was recently shown in Abumwis et al (2020 Phys. Rev. Lett. 124 193401), many eigenstates of a random Rydberg gas with resonant dipole–dipole interactions are highly delocalized. Although the high degree of delocalization is generic to various types of power-law interactions and to both two and three-dimensional systems, in their detailed aspects the coherence distributions are sensitive to these parameters and vary dramatically between different systems. We calculate the eigenstates of both two and three-dimensional gases and quantify their delocalization throughout the atoms in the gas using a coherence measure. By contrasting the angular dependence of the dipole–dipole interaction with an isotropic interaction we obtain additional information about the generic physical principles underlying random interacting systems. We also investigate the density of states and microwave absorption spectra to obtain information about the types of measurements where these delocalized states play a role, and to check that these delocalized eigenstates are robust against various types of perturbation.
Abstract As was recently shown in Abumwis et al (2020 Phys. Rev. Lett. 124 193401), many eigenstates of a random Rydberg gas with resonant dipole–dipole interactions are highly delocalized. Although the high degree of delocalization is generic to various types of power-law interactions and to both two and three-dimensional systems, in their detailed aspects the coherence distributions are sensitive to these parameters and vary dramatically between different systems. We calculate the eigenstates of both two and three-dimensional gases and quantify their delocalization throughout the atoms in the gas using a coherence measure. By contrasting the angular dependence of the dipole–dipole interaction with an isotropic interaction we obtain additional information about the generic physical principles underlying random interacting systems. We also investigate the density of states and microwave absorption spectra to obtain information about the types of measurements where these delocalized states play a role, and to check that these delocalized eigenstates are robust against various types of perturbation.
The long-range dipole-dipole interaction can create delocalized states due to the exchange of excitation between Rydberg atoms. We show that even in a random gas many of the single-exciton eigenstates are surprisingly delocalized, composed of roughly one quarter of the participating atoms. We identify two different types of eigenstates: one which stems from strongly-interacting clusters, resulting in localized states, and one which extends over large delocalized networks of atoms. These two types of states can be excited and distinguished by appropriately tuned microwave pulses, and their relative contributions can be modified by the Rydberg blockade and the choice of microwave parameters.
Abstract Two-dimensional (2D) spectroscopy uses multiple electromagnetic pulses to infer the properties of a complex system. A paradigmatic class of target systems are molecular aggregates, for which one can obtain information on the eigenstates, various types of static and dynamic disorder and on relaxation processes. However, two-dimensional spectra can be difficult to interpret without precise knowledge of how the signal components relate to microscopic Hamiltonian parameters and system-bath interactions. Here we show that two-dimensional spectroscopy can be mapped in the microwave domain to highly controllable Rydberg quantum simulators. By porting 2D spectroscopy to Rydberg atoms, we firstly open the possibility of its experimental quantum simulation, in a case where parameters and interactions are very well known. Secondly, the technique may provide additional handles for experimental access to coherences between system states and the ability to discriminate different types of decoherence mechanisms in Rydberg gases. We investigate the requirements for a specific implementation utilizing multiple phase coherent microwave pulses and a phase cycling technique to isolate signal components.
Scientific advance is often driven by identifying conceptually simple models underlying complex phenomena. This process commonly ignores imperfections which, however, might give rise to non-trivial collective behavior. For example, already a small amount of disorder can dramatically change the transport properties of a system compared to the underlying simple model. While systems with disordered potentials were already studied in detail, experimental investigations on systems with disordered hopping are still in its infancy. To this end, we experimentally study a dipole-dipole-interacting three-dimensional Rydberg system and map it onto a simple XY model with random couplings by spectroscopic evidence. We discuss the localization-delocalization crossover emerging in the model and present experimental signatures of it. Our results demonstrate that Rydberg systems are a useful platform to study random hopping models with the ability to access the microscopic degrees of freedom. This will allow to study transport processes and localization phenomena in random hopping models with a high level of control.
The spectral structure underlying excitonic energy transfer in ultracold Rydberg gases is studied numerically, in the framework of random matrix theory, and via self-consistent diagrammatic techniques. Rydberg gases are made up of randomly distributed, highly polarizable atoms that interact via strong dipolar forces. Dynamics in such a system is fundamentally different from cases in which the interactions are of short range, and is ultimately determined by the spectral and eigenvector structure. In the energy levels' spacing statistics, we find evidence for a critical energy that separates delocalized eigenstates from states that are localized at pairs or clusters of atoms separated by less than the typical nearest-neighbor distance. We argue that the dipole blockade effect in Rydberg gases can be leveraged to manipulate this transition across a wide range: As the blockade radius increases, the relative weight of localized states is reduced. At the same time, the spectral statistics, in particular, the density of states and the nearest-neighbor level-spacing statistics, exhibits a transition from approximately a 1-stable L\'evy to a Gaussian orthogonal ensemble. Deviations from random matrix statistics are shown to stem from correlations between interatomic interaction strengths that lead to an asymmetry of the spectral density and profoundly affect localization properties. We discuss approximations to the self-consistent Matsubara-Toyozawa locator expansion that incorporate these effects.
Assemblies of highly excited Rydberg atoms in an ultracold gas can be set into motion by a combination of van der Waals and resonant dipole-dipole interactions. Thereby, the collective electronic Rydberg state might change due to nonadiabatic transitions, in particular if the configuration encounters a conical intersection. For the experimentally most accessible scenario, in which the Rydberg atoms are initially randomly excited in a three-dimensional bulk gas under blockade conditions, we numerically show that nonadiabatic transitions can be common when starting from the most energetic repulsive Born-Oppenheimer surface. We outline how this state can be selectively excited using a microwave resonance, and demonstrate a regime where almost all collisional ionization of Rydberg atoms can be traced back to a prior nonadiabatic transition. Since Rydberg ionization is relatively straightforward to detect, the excitation and measurement scheme considered here renders nonadiabatic effects in Rydberg motion easier to demonstrate experimentally than in scenarios considered previously.
Using state-selective field ionization, the state distributions of Rydberg atoms in cold Rydberg gases are measured for various initially excited Rydberg levels, populations, and evolution times. We provide direct experimental evidence for l-changing collisions that we previously observed indirectly [S. K. Dutta, D. Feldbaum, A. Walz-Flannigan, J. R. Guest, and G. Raithel, Phys. Rev. Lett. 86, 3993 (2001)]. We also observe n-mixing and find that its effects are largely in agreement with recent theoretical work on n-changing collisions between electrons and Rydberg atoms, thus enabling an estimation of the electron temperature. Unexpectedly large populations of atoms are found in states with principal quantum numbers much lower than that of the initially excited atoms. We explain this observation by collisions between high-l Rydberg atoms, which are highly polar and can collide due to static electric-dipole forces between them.