Ion detection in the photoionization of a Rb Bose-Einstein condensate

Two-photon ionization of Rubidium atoms in a magneto-optical trap and a Bose-Einstein condensate (BEC) is experimentally investigated. Using 100 ns laser pulses, we detect single ions photoionized from the condenstate with a 35(10)% efficiency. The measurements are performed using a quartz cell with external electrodes, allowing large optical access for BECs and optical lattices.Comment: 14 pages, 7 figure

Effective dynamics of strongly dissipative Rydberg gases

We investigate the evolution of interacting Rydberg gases in the limit of strong noise and dissipation. Starting from a description in terms of a Markovian quantum master equation we derive effective equations of motion that govern the dynamics on a "coarse-grained" timescale where fast dissipative degrees of freedom have been adiabatically eliminated. Specifically, we consider two scenarios which are of relevance for current theoretical and experimental studies --- Rydberg atoms in a two-level (spin) approximation subject to strong dephasing noise as well as Rydberg atoms under so-called electromagnetically induced transparency (EIT) conditions and fast radiative decay. In the former case we find that the effective dynamics is described by classical rate equations up to second order in an appropriate perturbative expansion. This drastically reduces the computational complexity of numerical simulations in comparison to the full quantum master equation. When accounting for the fourth order correction in this expansion, however, we find that the resulting equation breaks the preservation of positivity and thus cannot be interpreted as a proper classical master rate equation. In the EIT system we find that the expansion up to second order retains information not only on the "classical" observables, but also on some quantum coherences. Nevertheless, this perturbative treatment still achieves a non-trivial reduction of complexity with respect to the original problem

Observation of mesoscopic crystalline structures in a two-dimensional Rydberg gas

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.Comment: 10 pages, 7 figure

The physics of dipolar bosonic quantum gases

This article reviews the recent theoretical and experimental advances in the study of ultracold gases made of bosonic particles interacting via the long-range, anisotropic dipole-dipole interaction, in addition to the short-range and isotropic contact interaction usually at work in ultracold gases. The specific properties emerging from the dipolar interaction are emphasized, from the mean-field regime valid for dilute Bose-Einstein condensates, to the strongly correlated regimes reached for dipolar bosons in optical lattices.Comment: Review article, 71 pages, 35 figures, 350 references. Submitted to Reports on Progress in Physic

Cold and Ultracold Molecules: Science, Technology, and Applications

This article presents a review of the current state of the art in the research field of cold and ultracold molecules. It serves as an introduction to the Special Issue of the New Journal of Physics on Cold and Ultracold Molecules and describes new prospects for fundamental research and technological development. Cold and ultracold molecules may revolutionize physical chemistry and few body physics, provide techniques for probing new states of quantum matter, allow for precision measurements of both fundamental and applied interest, and enable quantum simulations of condensed-matter phenomena. Ultracold molecules offer promising applications such as new platforms for quantum computing, precise control of molecular dynamics, nanolithography, and Bose-enhanced chemistry. The discussion is based on recent experimental and theoretical work and concludes with a summary of anticipated future directions and open questions in this rapidly expanding research field.Comment: 82 pages, 9 figures, review article to appear in New Journal of Physics Special Issue on Cold and Ultracold Molecule

Laser frequency stabilization to excited state transitions using electromagnetically induced transparency in a cascade system

We demonstrate laser frequency stabilization to excited state transitions using cascade electromagnetically induced transparency. Using a room temperature Rb vapor cell as a reference, we stabilize a first diode laser to the D2 transition and a second laser to a transition from the intermediate 5P3/2 state to a highly excited state with principal quantum number n = 19–70. A combined laser linewidth of 280±50 kHz over a 100 μs time period is achieved. This method may be applied generally to any cascade system and allows laser stabilization to an atomic reference in the absence of a direct absorption signal