Claude Krantz

Long term operation of high quantum efficiency GaAs(Cs,O) photocathodes using multiple recleaning by atomic hydrogen

Atomic hydrogen, produced by thermal dissociation of H2 molecules inside a hot tungsten capillary, is shown to be an efficient tool for multiple recleaning of degraded surfaces of high quantum efficiency transmission-mode GaAs photocathodes within an ultrahigh vacuum (UHV) multichamber photoelectron gun. Ultraviolet quantum yield photoemission spectroscopy has been used to study the removal of surface pollutants and the degraded (Cs,O)-activation layer during the cleaning procedure. For photocathodes grown by the liquid-phase epitaxy technique, the quantum efficiency is found to be stable at about 20% over a large number of atomic hydrogen cleaning cycles. A slow degradation of the quantum efficiency is observed for photocathodes grown by metal-organic chemical vapor deposition, although they reached a higher initial quantum efficiency of about 30%–35%. Study of the spatial distributions of photoluminescence intensity on these photocathodes proved that this overall degradation is likely due to insertion o...

M1, M2 and hyperfine-induced decay rates in Mg-like ions of Co, Ni and Cu measured at a heavy-ion storage ring

The optical decay rates of the 3s3p 3 P o level in Mg-like ions of 59 Co, 58 Ni and 63,65 Cu have been measured at a heavy-ion storage ring. The measurement is sensitive to M1, M2 and hyperfine-induced decay rates. The measurement precision is just about high enough to detect the difference in the isotope effect on the level lifetime in the ions 63,65 Cu 17+ . We also discuss our findings when trying to measure the hyperfine-induced decay of the lowest triplet level, 3s3p 3 P o , in the two Cu isotopes.

Imaging the Absolute Configuration of a Chiral Epoxide in the Gas Phase

Foil-Forged Images X-ray diffraction is widely used to determine molecular geometries and can often distinguish mirror image isomers (enantiomers), which generally requires well-ordered crystals. Herwig et al. (p. 1084) report an imaging technique to characterize enantiomers in the gas phase. A succession of ionization events were induced by passage through a carbon foil that culminated in a Coulomb explosion of mutually repelling nuclei. The trajectories of these nuclei precisely reflected the original molecular structure. Ultrafast electron stripping by a carbon foil enables precise elucidation of molecular geometries as the nuclei fly apart. 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. Determining absolute configurations of chiral molecules in the gas phase is still a formidable challenge. Here we demonstrate the determination of the absolute configuration of isotopically labeled (R,R)-2,3-dideuterooxirane by foil-induced Coulomb explosion imaging of individual molecules. Our technique provides unambiguous and direct access to the absolute configuration of small gas-phase species, including ions and molecular fragments.

COLD ELECTRON REACTIONS PRODUCING THE ENERGETIC ISOMER OF HYDROGEN CYANIDE IN INTERSTELLAR CLOUDS

Using event-by-event fragment momentum spectroscopy in a storage-ring merged-beams experiment, we find laboratory evidence that in the dissociative recombination (DR) of HCNH{sup +} with cold electrons the energetic isomer HNC is produced with a high yield, similar to that of HCN. With a newly implemented mass-sensitive fragment imaging detector, we analyze the kinetic energy release of the triatomic fragments DCN/DNC from the DR reaction of the isotopologue DCND{sup +} with cold (near 10 K) electrons. The results show that the internal energy of these fragments is extremely high, far exceeding the isomerization barrier between DNC and DCN. From this laboratory characterization of the DR reaction we conclude that also the triatomic fragment HCN/HNC from the DR of HCNH{sup +} will carry a large amount of ro-vibrational excitation and show that this implies an isomeric production ratio in a narrow range near unity.

Storage Ring Cross Section Measurements for Electron Impact Ionization of Fe11+ Forming Fe12+ and Fe13+

We report ionization cross section measurements for electron impact single ionization (EISI) of Fe11+ forming Fe12+ and electron impact double ionization (EIDI) of Fe11+ forming Fe13+. The measurements cover the center-of-mass energy range from approximately 230 eV to 2300 eV. The experiment was performed using the heavy-ion storage ring TSR located at the Max-Planck-Institut f?r Kernphysik in Heidelberg, Germany. The storage ring approach allows nearly all metastable levels to relax to the ground state before data collection begins. We find that the cross section for single ionization is 30% smaller than was previously measured in a single-pass experiment using an ion beam with an unknown metastable fraction. We also find some significant differences between our experimental cross section for single ionization and recent distorted wave (DW) calculations. The DW Maxwellian EISI rate coefficient for Fe11+ forming Fe12+ may be underestimated by as much as 25% at temperatures for which Fe11+ is abundant in collisional ionization equilibrium. This is likely due to the absence of 3s excitation-autoionization (EA) in the calculations. However, a precise measurement of the cross section due to this EA channel was not possible because this process is not distinguishable experimentally from electron impact excitation of an n = 3 electron to levels of n ? 44 followed by field ionization in the charge state analyzer after the interaction region. Our experimental results also indicate that the EIDI cross section is dominated by the indirect process in which direct single ionization of an inner shell 2l electron is followed by autoionization, resulting in a net double ionization.

Recombination of W18+ ions with electrons: absolute rate coefficients from a storage-ring experiment and from theoretical calculations

We present experimentally measured and theoretically calculated rate coefficients for the electron-ion recombination of W18+([Kr]4d104f10) forming W17+. At low electron-ion collision energies, the merged-beam rate coefficient is dominated by strong, mutually overlapping recombination resonances. In the temperature range where the fractional abundance of W18+ is expected to peak in a fusion plasma, the experimentally derived Maxwellian recombination rate coefficient is 5 to 10 times larger than that which is currently recommended for plasma modeling. The complexity of the atomic structure of the open-4f system under study makes the theoretical calculations extremely demanding. Nevertheless, the results of the present Breit-Wigner partitioned dielectronic recombination calculations agree reasonably well with the experimental findings. This also gives confidence in the ability of the theory to generate sufficiently accurate atomic data for the plasma modeling of other complex ions.

Dissociative Recombination Measurements of HCl+ Using an Ion Storage Ring

We have measured dissociative recombination (DR) of HCl+ with electrons using a merged beams configuration at the TSR heavy-ion storage ring located at the Max Planck Institute for Nuclear Physics in Heidelberg, Germany. We present the measured absolute merged beams recombination rate coefficient for collision energies from 0 to 4.5 eV. We have also developed a new method for deriving the cross section from the measurements. Our approach does not suffer from approximations made by previously used methods. The cross section was transformed to a plasma rate coefficient for the electron temperature range from T = 10 to 5000 K. We show that the previously used HCl+ DR data underestimate the plasma rate coefficient by a factor of 1.5 at T = 10 K and overestimate it by a factor of three at T = 300 K. We also find that the new data may partly explain existing discrepancies between observed abundances of chlorine-bearing molecules and their astrochemical models.

Storage Ring Cross-Section Measurements for Electron Impact Ionization of Fe12+ Forming Fe13+ and Fe14+

We report electron impact ionization cross section measurements for electron impact single ionization of Fe12 + forming Fe13 + and electron impact double ionization of Fe12 + forming Fe14 +. These are the first electron impact ionization data for any Si-like ion uncontaminated by an unknown metastable fraction. Recent distorted wave calculations agree with our single ionization results to within ~15%. Double ionization is dominated by inner shell ionization of a 2l electron resulting in autoionization of a second electron as the inner shell hole is filled.

The cryogenic storage ring CSR

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 (5.5 ± 1) K inside the ring, storage time constants of several minutes up to almost an hour were observed for atomic and molecular, anion and cation beams at an energy of 60 keV. The ion-beam intensity, energy-dependent closed-orbit shifts (dispersion), and the focusing properties of the machine were studied by a system of capacitive pickups. The Schottky-noise spectrum of the stored ions revealed a broadening of the momentum distribution on a time scale of 1000 s. Photodetachment of stored anions was used in the beam lifetime measurements. The detachment rate by anion collisions with residual-gas molecules was found to be extremely low. A residual-gas density below 140 cm(-3) is derived, equivalent to a room-temperature pressure below 10(-14) mbar. Fast atomic, molecular, and cluster ion beams stored for long periods of time in a cryogenic environment will allow experiments on collision- and radiation-induced fragmentation processes of ions in known internal quantum states with merged and crossed photon and particle beams.

Coulomb Explosion Imaged Cryptochiral (R,R)-2,3-Dideuterooxirane: Unambiguous Access to the Absolute Configuration of (+)-Glyceraldehyde

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.