46 research outputs found

    Manipulating Rydberg atoms close to surfaces at cryogenic temperatures

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    Helium atoms in Rydberg states have been manipulated coherently with microwave radiation pulses near a gold surface and near a superconducting NbTiN surface at a temperature of 3K3 \text{K}. The experiments were carried out with a skimmed supersonic beam of metastable (1s)1(2s)1 1S0(1\text{s})^1(2\text{s})^1\, {}^1\text{S}_0 helium atoms excited with laser radiation to npn\text{p} Rydberg levels with principal quantum number nn between 3030 and 4040. The separation between the cold surface and the center of the collimated beam is adjustable down to 250μm250 \mu\text{m}. Short-lived npn\text{p} Rydberg levels were coherently transferred to the long-lived nsn\text{s} state to avoid radiative decay of the Rydberg atoms between the photoexcitation region and the region above the cold surfaces. Further coherent manipulation of the nsn\text{s} Rydberg levels with pulsed microwave radiation above the surfaces enabled measurements of stray electric fields and allowed us to study the decoherence of the atomic ensemble. Adsorption of residual gas onto the surfaces and the resulting slow build-up of stray fields was minimized by controlling the temperature of the surface and monitoring the partial pressures of H2_2O, N2_2, O2_2 and CO2_2 in the experimental chamber during the cool-down. Compensation of the stray electric fields to levels below 100mV/cm100 \text{mV}/\text{cm} was achieved over a region of 6mm6 \text{mm} along the beam-propagation direction which, for the 1770m/s1770 \text{m}/\text{s} beam velocity, implies the possibility to preserve the coherence of the atomic sample for several microseconds above the cold surfaces.Comment: 12 pages, 10 figure

    The Role of Nebulizer Gas Flow in Electrosonic Spray Ionization (ESSI)

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    In this work, we investigated the role of the nebulizer gas flow in electrosonic spray ionization (ESSI), by systematically studying the relation between the flow and the ion signals of proteins, such as cytochrome c and holomyoglobin using ESSI-mass spectrometry (MS). When a neutral solution was delivered with a small sample flow rate (≤5μL/min), no obvious transition from electrospray ionization (ESI) to ESSI was found as the gas velocity varies from subsonic to supersonic speed. Droplets mostly experienced acceleration instead of breakup by the high-speed nebulizer gas. On the contrary, using particular experimental conditions, such as an acidic solution or high sample flow rate (≥200μL/min), more folded protein ions appear to be kept in droplets of diminishing size due to breakup by the high-speed nebulizer gas in ESSI compared with ESI. Theoretical analyses and numerical simulations were also performed to explain the observed phenomena. These systematic studies clarify the ionization mechanism of ESSI and provide valuable insight for optimizing ESSI and other popular pneumatically assisted electrospray ionization methods for future application

    Observation of enhanced rate coefficients in the H2+_2^+ + H2_2 →\rightarrow H3+_3^+ + H reaction at low collision energies

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    The energy dependence of the rate coefficient of the H2+ +H2→H3++H_2^+\ + {\rm H}_2 \rightarrow {\rm H}_3^+ + {\rm H} reaction has been measured in the range of collision energies between kB⋅10k_\mathrm{B}\cdot 10 K and kB⋅300k_\mathrm{B}\cdot 300 mK. A clear deviation of the rate coefficient from the value expected on the basis of the classical Langevin-capture behavior has been observed at collision energies below kB⋅1k_\mathrm{B}\cdot 1 K, which is attributed to the joint effects of the ion-quadrupole and Coriolis interactions in collisions involving ortho-H2_2 molecules in the j=1j = 1 rotational level, which make up 75% of the population of the neutral H2_2 molecules in the experiments. The experimental results are compared to very recent predictions by Dashevskaya, Litvin, Nikitin and Troe (J. Chem. Phys., in press), with which they are in agreement.Comment: 14 pages, 3 figure

    New method to study ion-molecule reactions at low temperatures and application to the H2+_2^+ + H2_2 →\rightarrow H3+_3^+ + H reaction

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    Studies of ion-molecule reactions at low temperatures are difficult because stray electric fields in the reaction volume affect the kinetic energy of charged reaction partners. We describe a new experimental approach to study ion-molecule reactions at low temperatures and present, as example, a measurement of the H2++H2→H3++H{\rm H}_2^+ + {\rm H}_2\rightarrow {\rm H}_3^+ + {\rm H} reaction with the H2+{\rm H}_2^+ ion prepared in a single rovibrational state at collision energies in the range Ecol/kB=5E_{\rm col}/k_{\rm B} = 5-60 K. To reach such low collision energies, we use a merged-beam approach and observe the reaction within the orbit of a Rydberg electron, which shields the ions from stray fields. The first beam is a supersonic beam of pure ground-state H2_2 molecules and the second is a supersonic beam of H2_2 molecules excited to Rydberg-Stark states of principal quantum number nn selected in the range 20-40. Initially, the two beams propagate along axes separated by an angle of 10∘^\circ. To merge the two beams, the Rydberg molecules in the latter beam are deflected using a surface-electrode Rydberg-Stark deflector. The collision energies of the merged beams are determined by measuring the velocity distributions of the two beams and they are adjusted by changing the temperature of the pulsed valve used to generate the ground-state H2{\rm H}_2 beam and by adapting the electric-potential functions to the electrodes of the deflector. The collision energy is varied down to below Ecol/kB=10E_{\rm col}/k_{\rm B}= 10 K, i.e., below Ecol≈1E_{\rm col}\approx 1 meV, with an energy resolution of 100 μ\mueV. We demonstrate that the Rydberg electron acts as a spectator and does not affect the cross sections, which are found to closely follow a classical-Langevin-capture model in the collision-energy range investigated. Because all neutral atoms and molecules can be excited to Rydberg states, this method of studyingComment: 39 pages, 10 figure

    Experimental study of the ion-molecule reaction H2+ + H2 → H3+ + H at low collision energies

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    We present a new method to study ion-molecule reactions at low temperatures or low collision energies and illustrate its application to the study of the H2+ + H2 → H3+ + H reaction.ISSN:1742-6588ISSN:1742-659

    Surface-electrode decelerator and deflector for Rydberg atoms and molecules

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    ISSN:1094-1622ISSN:0556-2791ISSN:1050-294
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