Publications by authors named "Heber O"

We demonstrate both experimentally and using a numerical simulation that, under special conditions, the repulsive Coulomb interaction helps to suppress the emittance growth of an rf-driven bunch of ions in an electrostatic ion beam trap. The underlying mechanisms can be explained by the synchronization of ion motion when nonlinear interactions are present. The surprising effect can help in improving the phase space manipulation of ions and the beam control in storage rings and accelerators and may be applied to other systems with many-body interactions in a periodic potential.

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Simultaneous trapping of merged cation and anion beams in the hybrid electrostatic ion beam trap (HEIBT) opens new opportunities for the study of the interactions of isolated atomic molecular or cluster ions with oppositely charged ionic species. Application of the trapped merged beams requires a detailed understanding of the trapping dynamics and the effect of the Coulombic attractive and repulsive forces between the ions on their motion in the trap. The simultaneous trapping regime is explored experimentally for SF anion and SF cation beams and compared to realistic ion trajectory simulations.

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The dynamics of ions in an electrostatic ion beam trap in the presence of an external time-dependent field is studied with a recently developed particle-in-cell simulation technique. The simulation technique, capable of accounting for space-charge effects, has reproduced all the experimental results on the bunch dynamics in the radio frequency mode. With simulation, the motion of ions is visualized in phase space and it is shown that the ion-ion interaction strongly affects the distribution of ions in phase space in the presence of an rf driving voltage.

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The radiative cooling of a stored, initially rotationally hot OH[Formula: see text] ion beam is probed by photodetachment using an electrostatic ion beam trap combined with an in-trap velocity map imaging spectrometer, providing direct measurement of the time-dependent rotational population. The rotational temperatures are estimated from photodetached electron spectra as a function of time using a Boltzmann distribution model and further verified by a rate law model using known Einstein coefficients. We demonstrate that during the entire cooling time, the rotational population can be well described by a Boltzmann distribution.

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We developed a simulation technique to study the effect of space charge interaction between trapped ions in the electrostatic ion beam trap (EIBT). The importance of space charge is demonstrated in both the dispersive and the self-bunching regime of the ion trap. The simulation results provide an estimate for the space charge effect on the trapping efficiency.

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Decay of bound states due to coupling with free particle states is a general phenomenon occurring at energy scales from MeV in nuclear physics to peV in ultracold atomic gases. Such a coupling gives rise to Fano-Feshbach resonances (FFR) that have become key to understanding and controlling interactions-in ultracold atomic gases, but also between quasiparticles, such as microcavity polaritons. Their energy positions were shown to follow quantum chaotic statistics.

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Using dichroic electrostatic mirrors, which can reflect a fast ion beam while transmitting a counterion beam, allows extending the field of electrostatic ion trapping. We present the design and simulations of a hybrid electrostatic ion beam trap that allows simultaneous trapping of velocity matched cation and anion beams. The possible merged beam ion-ion, ion-neutral, and ion-laser experiments are discussed.

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We present an experimental scheme that combines the well-established method of velocity-map imaging with a cold trapped metastable neon target. The device is used for obtaining the branching ratios and recoil-ion energy distributions for the penning ionization process in optical collisions of ultracold metastable neon. The potential depth of the highly excited dimer potential is extracted and compared with theoretical calculations.

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Isomerization and carbon chemistry in the gas phase are key processes in many scientific studies. Here we report on the isomerization process from linear [Formula: see text] to its monocyclic isomer. [Formula: see text] ions were trapped in an electrostatic ion beam trap and then excited with a laser pulse of precise energy.

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Autoresonance (AR) cooling of a bunch of ions oscillating inside an electrostatic ion beam trap is demonstrated for the first time. The relatively wide initial longitudinal velocity distribution is reduced by at least an order of magnitude using AR acceleration and ramping forces. The hot ions escaping the bunch are not lost from the system but continue to oscillate in the trap outside of the bunch and may be further cooled by successive AR processes.

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A Velocity Map Imaging (VMI) spectrometer has been designed and integrated with an electrostatic ion beam trap to study delayed electron emission from trapped polyatomic anions upon photodetachment. The VMI spectrometer is small in size and can record a wide range of photoelectron energies, with variable magnification. Delayed electron emission can be recorded in our experimental setup for any time duration after the photoexcitation of the polyatomic anions.

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Ions in an ion bunch trapped inside an Electrostatic Ion Beam Trap (EIBT) exhibit collective oscillations within the bunch under the influence of an external driving force. These internal oscillations have been measured explicitly using a new method with a particle detector outside the EIBT. In this approach, the evolving ion bunch is monitored along the entire trap length, in contrast to the localized single point measurements that are often carried out in other techniques.

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An electrostatic cryogenic storage ring, CSR, for beams of anions and cations with up to 300 keV kinetic energy per unit charge has been designed, constructed, and put into operation. With a circumference of 35 m, the ion-beam vacuum chambers and all beam optics are in a cryostat and cooled by a closed-cycle liquid helium system. At temperatures as low as (5.

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We observe energy-dependent angle-resolved diffraction patterns in protons from strong-field dissociation of the molecular hydrogen ion H_{2}^{+}. The interference is a characteristic of dissociation around a laser-induced conical intersection (LICI), which is a point of contact between two surfaces in the dressed two-dimensional Born-Oppenheimer potential energy landscape of a diatomic molecule in a strong laser field. The interference magnitude and angular period depend strongly on the energy difference between the initial state and the LICI, consistent with coherent diffraction around a cone-shaped potential barrier whose width and thickness depend on the relative energy of the initial state and the cone apex.

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Photodetachment cross sections as a function of photon energy are measured for cold (SF6)n(-) cluster anions stored in an electrostatic ion beam trap. Absolute photodetachment cross sections near the adiabatic limit are reported. The strong dependence of the SF6(-) absolute photodetachment cross section on the anion equilibrium bond length leads to the conclusion that the excess charge is localized on a SF6(-) ion core that is only subtly perturbed by the neighboring cluster units.

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High sensitivity photodetachment cross-section measurements of SF6(-) are performed near the adiabatic threshold limit. The extraction of adiabatic detachment energy (ADE) from the high sensitivity measurement of the cross-section change as a function of photon energy is discussed. Below the vertical detachment energy a steep 4 orders of magnitude cross-section drop is observed, with cross sections as low as 2 × 10(-6) Å(2) measured for photon energies below 2 eV.

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The absolute configuration of (R,R)-2,3-dideuterooxirane, which has been independently determined using Coulomb explosion imaging, has been unambiguously chemically correlated with the stereochemical key reference (+)-glyceraldehyde. This puts the absolute configuration of D(+)-glyceraldehyde on firm experimental grounds.

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In chemistry and biology, chirality, or handedness, refers to molecules that exist in two spatial configurations that are incongruent mirror images of one another. Almost all biologically active molecules are chiral, and the correct determination of their absolute configuration is essential for the understanding and the development of processes involving chiral molecules. Anomalous x-ray diffraction and vibrational optical activity measurements are broadly used to determine absolute configurations of solid or liquid samples.

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We describe a technique to measure absolute photo-induced cross sections for cluster anions stored in an electrostatic ion beam trap (EIBT) with a central deflector. The setup allows determination of total photo-destruction cross sections as well as partial cross sections for fragmentation and electron detachment. The unique properties of this special EIBT setup are investigated and illustrated using small Al(n)(-) clusters.

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A technique for mass-selective lifetime measurements of keV ions in a linear electrostatic ion beam trap is presented. The technique is based on bunching the ions using a weak RF potential and non-destructive ion detection by a pick-up electrode. This method has no mass-limitation, possesses the advantage of inherent mass-selectivity, and offers a possibility of measuring simultaneously the lifetimes of different ion species with no need for prior mass-selection.

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We present the results of a Coulomb explosion experiment that allows for the imaging of the rovibrational wave function of the metastable H2- ion. Our measurements confirm the predicted large internuclear separation of 6 a.u.

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Photofragmentation of the protonated water dimer H+(H2O)_{2}, a fundamental system both in aqueous solutions and gas-phase water clusters, has been studied at 13.8 nm using the Free Electron Laser FLASH in Hamburg. In a crossed-beam experiment using time-resolved, single-molecule fragment imaging, the two-body breakup into H2O++H3O+ was found as a prominent fragmentation channel with a kinetic energy release of up to 10 eV.

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Individual product channels in the dissociative recombination of deuterated hydronium ions and cold electrons are studied in an ion storage ring by velocity imaging using spatial and mass-sensitive detection of the neutral reaction fragments. Initial and final molecular excitation are analyzed, finding the outgoing water molecules to carry internal excitation of more than 3 eV in 90% of the recombination events. Initial rotation is found to be substantial and in three-body breakup strongly asymmetric energy repartition among the deuterium products is enhanced for hot parent ions.

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We report on the realization and operation of a fast ion beam trap of the linear electrostatic type employing liquid helium cooling to reach extremely low blackbody radiation temperature and residual gas density and, hence, long storage times of more than 5 min which are unprecedented for keV ion beams. Inside a beam pipe that can be cooled to temperatures <15 K, with 1.8 K reached in some locations, an ion beam pulse can be stored at kinetic energies of 2-20 keV between two electrostatic mirrors.

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