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Register a new userDynamical Crystallization in the Dipole Blockade of Ultracold Atoms
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We describe a method for controlling many-body states in extended ensembles of Rydberg atoms, forming crystalline structures during laser excitation of a frozen atomic gas. Specifically, we predict the existence of an excitation number staircase in laser excitation of atomic ensembles into Rydberg states. Each step corresponds to a crystalline state with a well-defined of regularly spaced Rydberg atoms. We show that such states can be selectively excited by chirped laser pulses. Finally, we demonstarte that, sing quantum state transfer from atoms to light, such crystals can be used to create crystalline photonic states and can be probed via photon correlation measurements.
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In the laser excitation of ultracold atoms to Rydberg states, we observe a dramatic suppression caused by van der Waals interactions. This behavior is interpreted as a local excitation blockade: Rydberg atoms strongly inhibit excitation of their neighbors. We measure suppression, relative to isolated atom excitation, by up to a factor of 6.4. The dependence of this suppression on both laser irradiance and atomic density are in good agreement with a mean-field model. These results are an important step towards using ultracold Rydberg atoms in quantum information processing.
We present a combined experimental and theoretical study of the effects of Rydberg interactions on Autler-Townes spectra of ultracold gases of atomic strontium. Realizing two-photon Rydberg excitation via a long-lived triplet state allows us to probe the thus far unexplored regime where Rydberg state decay presents the dominant decoherence mechanism. The effects of Rydberg interactions are observed in shifts, asymmetries, and broadening of the measured atom-loss spectra. The experiment is analyzed within a one-body density matrix approach, accounting for interaction-induced level shifts and dephasing through nonlinear terms that approximately incorporate correlations due to the Rydberg blockade. This description yields good agreement with our experimental observations for short excitation times. For longer excitation times, the loss spectrum is altered qualitatively, suggesting additional dephasing mechanisms beyond the standard blockade mechanism based on pure van der Waals interactions.
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 show that the dipole-dipole interaction between three identical Rydberg atoms can give rise to bound trimer states. The microscopic origin of these states is fundamentally different from Efimov physics. Two stable trimer configurations exist where the atoms form the vertices of an equilateral triangle in a plane perpendicular to a static electric field. The triangle edge length typically exceeds $Rapprox 2,mutext{m}$, and each configuration is two-fold degenerate due to Kramers degeneracy. The depth of the potential wells and the triangle edge length can be controlled by external parameters. We establish the Borromean nature of the trimer states, analyze the quantum dynamics in the potential wells and describe methods for their production and detection.
We show that nuclear motion of Rydberg atoms can be induced by resonant dipole-dipole interactions that trigger the energy transfer between two energetically close Rydberg states. How and if the atoms move depends on their initial arrangement as well as on the initial electronic excitation. Using a mixed quantum/classical propagation scheme we obtain the trajectories and kinetic energies of atoms, initially arranged in a regular chain and prepared in excitonic eigenstates. The influence of off-diagonal disorder on the motion of the atoms is examined and it is shown that irregularity in the arrangement of the atoms can lead to an acceleration of the nuclear dynamics.
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