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Register a new userObservation of mesoscopic crystalline structures in a two-dimensional Rydberg gas
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The ability to control and tune interactions in ultracold atomic gases has paved the way towards the realization of new phases of matter. Whereas experiments have so far achieved a high degree of control over short-ranged interactions, the realization of long-range interactions would open up a whole new realm of many-body physics and has become a central focus of research. Rydberg atoms are very well-suited to achieve this goal, as the van der Waals forces between them are many orders of magnitude larger than for ground state atoms. Consequently, the mere laser excitation of ultracold gases can cause strongly correlated many-body states to emerge directly when atoms are transferred to Rydberg states. A key example are quantum crystals, composed of coherent superpositions of different spatially ordered configurations of collective excitations. Here we report on the direct measurement of strong correlations in a laser excited two-dimensional atomic Mott insulator using high-resolution, in-situ Rydberg atom imaging. The observations reveal the emergence of spatially ordered excitation patterns in the high-density components of the prepared many-body state. They have random orientation, but well defined geometry, forming mesoscopic crystals of collective excitations delocalised throughout the gas. Our experiment demonstrates the potential of Rydberg gases to realise exotic phases of matter, thereby laying the basis for quantum simulations of long-range interacting quantum magnets.
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Dominating finite-range interactions in many-body systems can lead to intriguing self-ordered phases of matter. Well known examples are crystalline solids or Coulomb crystals in ion traps. In those systems, crystallization proceeds via a classical transition, driven by thermal fluctuations. In contrast, ensembles of ultracold atoms laser-excited to Rydberg states provide a well-controlled quantum system, in which a crystalline phase transition governed by quantum fluctuations can be explored. Here we report on the experimental preparation of the crystalline states in such a Rydberg many-body system. Fast coherent control on the many-body level is achieved via numerically optimized laser excitation pulses. We observe an excitation-number staircase as a function of the system size and show directly the emergence of incompressible ordered states on its steps. Our results demonstrate the applicability of quantum optical control techniques in strongly interacting systems, paving the way towards the investigation of novel quantum phases in long-range interacting quantum systems, as well as for detailed studies of their coherence and correlation properties.
We report the experimental observation of strong two-color optical nonlinearity in an ultracold gas of $^{85}mathrm{Rb}$-$^{87}mathrm{Rb}$ atom mixture. By simultaneously coupling two probe transitions of $^{85}$Rb and $^{87}$Rb atoms to Rydberg states in electromagnetically induced transparency (EIT) configurations, we observe significant suppression of the transparency resonance for one probe field when the second probe field is detuned at $sim1~mathrm{GHz}$ and hitting the EIT resonance of the other isotope. Such a cross-absorption modulation to the beam propagation dynamics can be described by two coupled nonlinear wave equations we develope. We further demonstrate that the two-color optical nonlinearity can be tuned by varying the density ratio of different atomic isotopes, which highlights its potential for exploring strongly interacting multi-component fluids of light.
A microscopic understanding of molecules is essential for many fields of natural sciences but their tiny size hinders direct optical access to their constituents. Rydberg macrodimers - bound states of two highly-excited Rydberg atoms - feature bond lengths easily exceeding optical wavelengths. Here we report on the direct microscopic observation and detailed characterization of such macrodimers in a gas of ultracold atoms in an optical lattice. The size of about 0.7 micrometers, comparable to the size of small bacteria, matches the diagonal distance of the lattice. By exciting pairs in the initial two-dimensional atom array, we resolve more than 50 vibrational resonances. Using our spatially resolved detection, we observe the macrodimers by correlated atom loss and demonstrate control of the molecular alignment by the choice of the vibrational state. Our results allow for precision testing of Rydberg interaction potentials and establish quantum gas microscopy as a powerful new tool for quantum chemistry.
We present a quantum many-body description of the excitation spectrum of Rydberg polarons in a Bose gas. The many-body Hamiltonian is solved with functional determinant theory, and we extend this technique to describe Rydberg polarons of finite mass. Mean-field and classical descriptions of the spectrum are derived as approximations of the many-body theory. The various approaches are applied to experimental observations of polarons created by excitation of Rydberg atoms in a strontium Bose-Einstein condensate.
We demonstrate three-dimensional trapping of individual Rydberg atoms in holographic optical bottle beam traps. Starting with cold, ground-state $^{87}$Rb atoms held in standard optical tweezers, we excite them to $nS_{1/2}$, $nP_{1/2}$, or $nD_{3/2}$ Rydberg states and transfer them to a hollow trap at 850 nm. For principal quantum numbers $60 leqslant n leqslant 90$, the measured trapping time coincides with the Rydberg state lifetime in a 300~K environment. We show that these traps are compatible with quantum information and simulation tasks by performing single qubit microwave Rabi flopping, as well as by measuring the interaction-induced, coherent spin-exchange dynamics between two trapped Rydberg atoms separated by 40 $mu$m. These results will find applications in the realization of high-fidelity quantum simulations and quantum logic operations with Rydberg atoms.
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