Search

The spread of excitations by Rydberg facilitation bears many similarities to epidemics. Such systems can be modeled with Monte-Carlo simulations of classical rate equations to great accuracy as a result of high dephasing. In this paper, we analyze the dynamics of a Rydberg many-body system in the facilitation regime in the limits of high and low temperatures. While in the high-temperature limit a homogeneous mean-field behaviour is recovered, characteristic effects of heterogeneity can be seen in a frozen gas. At large temperatures the system displays an absorbing-state phase transition and, in the presence of an additional loss channel, self-organized criticality. In a frozen or low-temperature gas, excitations are constrained to a network resembling an Erd\"os-Renyi graph. We show that the absorbing-state phase transition is replaced with an extended Griffiths phase, which we accurately describe by a susceptible-infected-susceptible model on the Erd\"os-Renyi network taking into account Rydberg blockade. Furthermore, we expand upon an existing macroscopic Langevin equation to more accurately describe the density of Rydberg atoms in the frozen and finite temperature regimes., Comment: 14 pages, 11 figures

We report the engineering of molecular potentials at large interatomic distances. The molecular states are generated by off-resonant optical coupling to a highly excited, long-range Rydberg molecular potential. The coupling produces a potential well in the low-lying molecular potential, which supports a bound state. The depth of the potential well, and thus the binding energy of the molecule, can be tuned by the coupling parameters. We characterize these molecules and find good agreement with a theoretical model based on the coupling of the two involved adiabatic potential energy curves. Our results open numerous possibilities to create long-range molecules between ultracold ground state atoms and to use them for ultracold chemistry and applications such as Feshbach resonances, Efimov physics or the study of halo molecules.

Randomness and disorder have strong impact on transport processes in quantum systems and give rise to phenomena such as Anderson localization [1-3], many-body localization [4] or glassy dynamics [5]. Their characteristics thereby depend on the strength and type of disorder. An important class are hopping models, where particles or excitations move through a system which has randomized couplings. This includes, e.g., spin glasses [5], coupled optical waveguides [6], or NV center arrays [7]. They are also key to understand excitation transport in molecular and biological systems, such as light harvesting complexes [8]. In many of those systems, the microscopic coupling mechanism is provided by the dipole-dipole interaction. Rydberg systems [9] are therefore a natural candidate to study random hopping models. Here, we experimentally study a three-dimensional many-body Rydberg system with random dipole-dipole couplings. We measure the spectrum of the many-body system and find good agreement with an effective spin model. We also find spectroscopic signatures of a localization-delocalization transition. Our results pave the way to study transport processes and localization phenomena in random hopping models in detail. The inclusion of strong correlations is experimentally straightforward and will allow to study the interplay between random hopping and localization in strongly interacting systems., Comment: 7 pages, 4 figures

When atomic gases are laser driven to Rydberg states in an off resonant way, a single Rydberg atom may enhance the excitation rate of surrounding atoms. This leads to a facilitated excitation referred to as Rydberg anti-blockade. In the usual facilitation scenario, the detuning of the laser from resonance compensates the interaction shift. Here, we discuss a different excitation mechanism, which we call anomalous facilitation. This occurs on the "wrong side" of the resonance and originates from inhomogeneous broadening. The anomalous facilitation may be seen in experiments of attractively interacting atoms on the blue detuned side, where facilitation is not expected to appear., 5 pages, 3 figures

We investigate the possibility of a bistable phase in an open many-body system. To this end we discuss the microscopic dynamics of a continuously off-resonantly driven Rydberg lattice gas in the regime of strong decoherence. Our experimental results reveal a prolongation of the temporal correlations with respect to the lifetime of a single Rydberg excitation and show strong evidence for the formation of finite-sized Rydberg excitation clusters in the steady state. We simulate our data using a simplified and a full many-body rate-equation model. The results are compatible with the formation of metastable states associated with a bimodal counting distribution as well as dynamic hysteresis. A scaling analysis reveals however, that the correlation times remain finite for all relevant system parameters. This suggest that the Rydberg aggregate is composed of many small clusters and all correlation lengths remain finite. This is a strong indication for the absence of a global bistable phase, previously suggested to exist in this system., 13 pages, 13 figures

We have performed high resolution photoassociation spectroscopy of rubidium ultra long-range Rydberg molecules in the vicinity of the 25$P$ state. Due to the hyperfine interaction in the ground state perturber atom, the emerging mixed singlet-triplet potentials contain contributions from both hyperfine states. We show that this can be used to induce remote spin-flips in the perturber atom upon excitation of a Rydberg molecule. When furthermore the spin-orbit splitting of the Rydberg state is comparable to the hyperfine splitting in the ground state, the orbital angular momentum of the Rydberg electron is entangled with the nuclear spin of the perturber atom. Our results open new possibilities for the implementation of spin-dependent interactions for ultracold atoms in bulk systems and in optical lattices., 6 pages, 3 figures

Obtaining full control over the internal and external quantum states of molecules is the central goal of ultracold chemistry and allows for the study of coherent molecular dynamics, collisions and tests of fundamental laws of physics. When the molecules additionally have a permanent electric dipole moment, the study of dipolar quantum gases and spin-systems with long-range interactions as well as applications in quantum information processing are possible. Rydberg molecules constitute a class of exotic molecules, which are bound by the interaction between the Rydberg electron and the ground state atom. They exhibit extreme bond lengths of hundreds of Bohr radii and giant permanent dipole moments in the kilo-Debye range. A special type with exceptional properties are the so-called butterfly molecules, whose electron density resembles the shape of a butterfly. Here, we report on the photoassociation of butterfly Rydberg molecules and their orientation in a weak electric field. Starting from a Bose-Einstein condensate of rubidium atoms, we fully control the external degrees of freedom and spectroscopically resolve the rotational structure and the emerging pendular states in an external electric field. This not only allows us to extract the bond length, the dipole moment and the angular momentum of the molecule but also to deterministically create molecules with a tunable bond length and orientation. We anticipate direct applications in quantum chemistry, many-body quantum physics and quantum information processing., Comment: 6 pages, 4 figures; Supplementary Material included

We have studied the associative ionization of a Rydberg atom and a ground state atom in an ultracold Rydberg gas. The measured scattering cross section is three orders of magnitude larger than the geometrical size of the produced molecule. This giant enhancement of the reaction kinetics is due to an efficient directed mass transport which is mediated by the Rydberg electron. We also find that the total inelastic scattering cross section is given by the geometrical size of the Rydberg electron's wavefunction., 5 pages, 4 figures

Controlling strongly interacting many-body systems enables the creation of tailored quantum matter, with properties transcending those based solely on single particle physics. Atomic ensembles which are optically driven to a Rydberg state provide many examples of this, such as atom-atom entanglement, many-body Rabi oscillations, strong photon-photon interaction and spatial pair correlations. In its most basic form, Rydberg quantum matter consists of an isolated ensemble of strongly interacting atoms spatially confined to the blockade volume - a so-called superatom. Here we demonstrate the controlled creation and characterization of an isolated mesoscopic superatom by means of accurate density engineering and excitation to Rydberg $p$-states. Its variable size allows to investigate the transition from effective two-level physics for strong confinement to many-body phenomena in extended systems. By monitoring continuous laser-induced ionization we observe a strongly anti-bunched ion emission under blockade conditions and extremely bunched ion emission under off-resonant excitation. Our experimental setup enables in vivo measurements of the superatom, yielding insight into both excitation statistics and dynamics. We anticipate straightforward applications in quantum optics and quantum information as well as future experiments on many-body physics., 7 pages, 5 figures

We report on the realization of high resolution electron microscopy of Rydberg-excited ultracold atomic samples. The implementation of an ultraviolet laser system allows us to excite the atom, with a single-photon transition, to Rydberg states. By using the electron microscopy technique during the Rydberg excitation of the atoms, we observe a giant enhancement in the production of ions. This is due to $l$-changing collisions, which broaden the Rydberg level and therefore increase the excitation rate of Rydberg atoms. Our results pave the way for the high resolution spatial detection of Rydberg atoms in an atomic sample.

We characterize the two-photon excitation of an ultracold gas of rubidium atoms to Rydberg states analyzing the induced atomic losses from an optical dipole trap. Extending the duration of the Rydberg excitation to several milliseconds, the ground-state atoms are continuously coupled to the formed positively charged plasma. In this regime we measure the $n$ dependence of the plasma-induced blockade effect and we characterize the interaction of the excited states and the ground state with the plasma. We also investigate the influence of the quasielectrostatic trapping potential on the system, confirming the validity of the ponderomotive model for states with $20\ensuremath{\le}n\ensuremath{\le}120$.

We show that the excitation of long-range Rydberg molecules in a three-dimensional optical lattice can be used as a position- and time-sensitive probe of the site occupancy in the system. To this end, we detect the ions which are continuously generated by the decay of the formed Rydberg molecules. While a superfluid gas shows molecule formation for all parameters, a Mott insulator with $n=1$ filling reveals a strong suppression of the number of formed molecules. In the limit of weak probing, the technique can be used to probe the superfluid to Mott-insulator transition in real-time. Our method can be extended to higher fillings and has various applications for the real-time diagnosis and manipulation of ultracold lattice gases., 6 pages, 5 figures