546 research outputs found

    Correlations between interacting Rydberg atoms

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    This paper is a short introduction to Rydberg physics and quantum nonlinear optics using Rydberg atoms. It has been prepared as a compliment to a series of lectures delivered during the Latin American School of Physics "Marcos Moshinsky" 2017. We provide a short introduction to the properties of individual Rydberg atoms and discuss in detail how the interaction potential between Rydberg atom pairs is calculated. We then discuss how this interaction gives rise to the Rydberg blockade mechanism. With the aid of hallmark experiments in the field applications of the blockade for creating correlated quantum systems are discussed. Our aim is to give an overview of this exciting and rapidly evolving field. The interested reader is referred to original work and more comprehensive reviews and tutorials for further details on these subjects.</p

    Tunable quantum criticality in multicomponent Rydberg arrays

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    Arrays of Rydberg atoms have appeared as a remarkably rich playground to study quantum phase transitions in one dimension. One of the biggest puzzles that was brought forward in this context are chiral phase transitions out of density waves. Theoretically predicted chiral transition out of period-four phase is still pending experimental verification mainly due to extremely short interval over which this transition is realized in a single-component Rydberg array. In this letter we show that multi-component Rydberg arrays with extra experimentally tunable parameters provide a mechanism to manipulate quantum critical properties without breaking translation symmetry explicitly. We consider an effective blockade model of two component Rydberg atoms. Weak and strong components obey nearest- and next-nearest-neighbor blockades correspondingly. When laser detuning is applied to either of the two components the system is in the period-3 and period-2 phases. But laser detuning applied to both components simultaneously stabilizes the period-4 phase partly bounded by the chiral transition. We show that relative ratio of the Rabi frequencies of the two components tunes the properties of the conformal Ashkin-Teller point and allows to manipulate an extent of the chiral transition. The prospects of multi-component Rydberg arrays in the context of critical fusion is briefly discussed.Comment: 11 pages, 14 figure

    RYDBERG SERIES IN SMALL MOLECULES

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    Author Institution: Physics Department, The Royal Institute of TechnologyA qualitative discussion of the Rydberg series of a diatomic molecule, consisting of atoms such as C, N, O, shows that the quantum defect is approximately independent of the nature of the molecule, and depends only on the type of the Rydberg orbital. It is shown that the orbitals npσnp\sigma and npπnp\pi probably have different quantum defects and that ndσnd\sigma has a much larger quantum defect than ndπnd\pi and ndσnd\sigma. The systematics has been applied to CO,N2CO, N_{2}, and O2O_{2} and a number of new Rydberg series have been found and others have been reinterpreted

    THE RYDBERG STATES OF NO.

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    This work was supported by NASA Grant NsG-414.Author Institution: Department of Astrophysical Sciences, Princeton UniversityThe interpretation of the lowest Rydberg states of NO given recently by Huber and Miescher1Miescher^{1} has been fully confirmed by the identification in the absorption spectrum, of several higher members of the proposed Rydberg series.2series.^{2} The exceedingly complex spectrum can now be interpreted, owing to the work of Miescher and his collaborators,3collaborators,^{3} in terms of a relatively simple electronic energy level diagram. The pattern of Rydberg states resembles strongly that of an atom with closed-shell core. The molecular states corresponding to atomic p- and d- states split into components with different λ\lambda, but in NO the sign of this splitting is opposite to the one expected and found in Rydberg states of H2+,H2,He2,N2H_{2}^{+}, H_{2}, He_{2}, N_{2}, and CO. The pattern observed in NO has been reproduced rather well in the recent theoretical calculation by LeFebvre-Brion and Moser4Moser^{4} who have taken into account the configuration interaction between the unoccupied (Rydberg-) orbitals though they have not included the interaction with excited valence-shell configurations. The relative absorption intensities of the Rydberg bands and the interactions with non-Rydberg states are well explained by the assignment of approximate gg- and uu- symmetries to the states of the nearly symmetric NO molecule. The pp- type Rydberg states of configurations npσunp\sigma_{u} and npπunp\pi_{u} appear with much greater absorption intensities than those resembling atomic ss- and dd- states and they interact strongly with the non-Rydberg states 2Hu^{2}H_{u} and with the repulsive state (σu2p)2Σu+(\sigma_{u} 2p) ^{2}\Sigma_{u}^{+}. These and other observations confirm that it is meaningful to describe the lowest Rydberg states of NO with quantum numbers 3s, 3p, 3d of an atom with a closed n=2n=2 -shell core such as Boron or Sodium

    COOPERATIVE EFFECTS IN A RYDBERG GAS

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    Author Institution: Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02319Rydberg-Rydberg transitions of Ca atoms are directly detected by chirped-pulse millimeter-wave spectroscopy with broadband, high-resolution spectra with accurate relative intensities. At moderate high number density, the radiation of a Rydberg gas behaves as strong cooperative effects. Compared to a rotational transition, Rydberg-Rydberg transitions have enormous electric dipole transition moments and polarizabilities, which are sensitive to external and self-induced electric fields. In a dense Rydberg gas, a large group of molecules can share an electric field, and absorb and radiate cooperatively. A model with semiclassical method describes several significant cooperative effects in the time-domain and frequency-domain in two-level systems and Λ\Lambda-type three-level systems. Several experimental evidences which partly support this model will be discussed and a new experiment with buffer gas cooling technique will be proposed

    MILLIMETER WAVE SPECTROSCOPY OF HIGH RYDBERG STATES OF Kr

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    Author Institution: ETH Z\""{u}rich, Laboratorium f\""{u}r Physikalische Chemie, ETH-H\""{o}nggerberg HClA phase-stabilized backward wave oscillator (BWO) in the 260380260-380 GHz range was combined with an XUV laser system to record high-resolution spectra of high Rydberg states of krypton. The millimeter wave transitions between high n Rydberg states were detected by pulsed field-ionization, at sub-MHz resolution. Results are presented on the hyperfine structure of high n Rydberg states of 83Kr^{83}Kr

    RYDBERG STATES OF POLYATOMIC FREE RADICALS

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    Author Institution: Purdue University, West LafayetteOpen Shell acyl free radical produce closed shell cations that support sharp Rydberg states. Ion-detected absorption shows extensive structure in HCO and CH3OCH_{3}O. Presented here are the first resolved spectra of CH3OCH_{3}O obtained by (1+1) double-resonant photoionization. These states are analyzed and used as intermediate to probe higher level Rydberg states near the ionization threshold

    HIGH-RYDBERG AND AUTOIONIZING STATES OF HCO

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    Author Institution: Purdue University, West Lafayette, IN 47906Double-resonant transitions through the 3pπ3p\pi Rydberg state of HCO state-select autoionizing series converging to specific vibrationally excited thresholds of HCO+HCO^{+}. Extrapolation of series, combined with exisiting knowledge of the vibrational structure of the cation, provides the first accurate determination of the adiabatic ionization potential of HCO, Lineshapes and intensities of resonances reflect mode-specific trends in Rydberg-core coupling dynamics

    RYDBERG STATES: STEALTHY SPIES OF MOLECULAR STRUCTURE

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    Author Institution: Department of Chemistry, Brown University, Providence R.I., 02912Electrons in Rydberg orbits are sensitive spies of molecular structure. Typically, the motions of flexible hydrocarbon chains are famously difficult to observe. Large amplitude vibrations born from high internal temperatures where the molecules vibrate in soft potentials blur the conformeric snapshot. We explore the equilibrium composition and dynamics between conformeric structures of NN,NN-dimethyl-2-butanamine (DM2BA) and NN,NN-dimethyl-3-hexanamine (DM3HA) using the Rydberg Fingerprint method. Initial excitation prepares the molecule in the 3pp state and subsequent relaxation to 3ss deposits 1.8 eV of vibrational energy, elevating the internal temperature to some 900 K. The time-dependent Rydberg spectrum reveals the conformational dynamics of the hot hydrocarbon chains, enabling us to measure time constants for both the forward and backward reactions
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