D. A. Orlov

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...

Energy distributions of electrons emitted from GaAs(Cs, O)

A method to map out the energy distribution N(E∥,E⊥) of an electron beam as a function of the longitudinal (E∥) and transverse (E⊥) energy has been developed and applied to study the photoemission process from GaAs(Cs, O) at 90 K. The method proceeds by “marking” electrons with fixed longitudinal energy E∥b and a subsequent measurement of the associated differential transverse energy distribution N⊥(E∥b,E⊥), applying an adiabatic magnetic compression technique. The complete energy distribution N(E∥,E⊥) of electrons from a GaAs(Cs, O) photocathode obtained by a stepwise variation of E∥b provides details about the transfer of electrons through the GaAs(Cs, O)–vacuum interface and demonstrates that not only electron energy loss, but also elastic electron scattering is of crucial importance in the escape process.

Physics with colder molecular ions: The Heidelberg Cryogenic Storage Ring CSR

A novel cryogenic electrostatic storage ring is planned to be built at the Max-Planck Institute for Nuclear Physics in Heidelberg. The machine is expected to operate at low temperatures (∼ 2K) and to store beams with kinetic energies between 20 to 300 keV. An electron target based on cooled photocathode technology will serve as a major tool for the study of reactions between molecular ions and electrons. Moreover, atomic beams can be merged and crossed with the stored ion beams allowing for atom molecularion collision studies at very low up to high relative energies. The proposed experimental program, centered around the physics of cold molecular ions, is shortly outlined.

A cryogenic electrostatic trap for long-time storage of keV ion beams

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. Along with an overview of the cryogenic trap design, we present a measurement of the residual gas density inside the trap resulting in only 2 x 10(3) cm(-3), which for a room temperature environment corresponds to a pressure in the 10(-14) mbar range. The device, called the cryogenic trap for fast ion beams, is now being used to investigate molecules and clusters at low temperatures, but has also served as a design prototype for the cryogenic heavy-ion storage ring currently under construction at the Max-Planck Institute for Nuclear Physics.

Storage-ring measurement of the hyperfine induced 47Ti18+(2s2p 3P0 --> 2s2 1S0) transition rate.

The hyperfine induced 2s2p (3)P(0) --> 2s(2) (1)S(0) transition rate A(HFI) in berylliumlike (47)Ti(18+) is measured. Resonant electron-ion recombination in a heavy-ion storage ring is employed to monitor the time dependent population of the (3)P(0) state. The experimental value A(HFI)=0.56(3) s(-1) is almost 60% larger than theoretically predicted.

Preparation and performance of transmission-mode GaAs photocathodes as sources for cold dc electron beams

Photoemission from GaAs cathodes with negative electron affinity (NEA) is applied for producing electron beams with very low longitudinal and transverse velocity spread. GaAs transmission-mode cathodes were activated with Cs and either O2 or NF3 in an extremely high vacuum setup (base pressure below 10−12 mbar). Quantum efficiencies of 20%–25% (at 670 nm) and long dark lifetimes (about 1000 h) could be achieved for both types of activation in a reproducible way. Using a method based on the adiabatic transverse expansion of an electron beam in a spatially decreasing magnetic field, the mean transverse energy (MTE) of the photoemitted electrons was measured systematically, recording longitudinal energy distribution curves. Both the MTE and the longitudinal energy spread strongly depend on the value of NEA and the position of the extracted distribution relative to the bulk conduction band minimum. Electrons with energies above the conduction band minimum are thermalized with the lattice temperature of the ca...

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.

Energy-sensitive imaging detector applied to the dissociative recombination of D2H+

We report on an energy-sensitive imaging detector for studying the fragmentation of polyatomic molecules in the dissociative recombination of fast molecular ions with electrons. The system is based on a large area (10x10 cm{sup 2}) position-sensitive, double-sided Si-strip detector with 128 horizontal and 128 vertical strips, whose pulse height information is read out individually. The setup allows us to uniquely identify fragment masses and is thus capable of measuring branching ratios between different fragmentation channels, kinetic energy releases, and breakup geometries as a function of the relative ion-electron energy. The properties of the detection system, which has been installed at the Test Storage Ring (TSR) facility of the Max-Planck Institute for Nuclear Physics in Heidelberg, is illustrated by an investigation of the dissociative recombination of the deuterated triatomic hydrogen cation D{sub 2}H{sup +}. A huge isotope effect is observed when comparing the relative branching ratio between the D{sub 2} + H and the HD + D channel; the ratio 2B(D{sub 2} + H)/B(HD + D), which is measured to be 1.27{+-}0.05 at relative electron-ion energies around 0 eV, is found to increase to 3.7{+-}0.5 at {approx}5 eV.

Electron-ion recombination for Fe viii forming Fe vii and Fe ix forming Fe viii: Measurements and theory

The photorecombination rate coefficients of potassium-like Fe viii ions forming calcium-like Fe vii and of argon-like Fe ix forming potassium-like Fe viii were measured by employing the merged electron-ion beams method at the Heidelberg heavy-ion storagering TSR. New theoretical calculations with the AUTOSTRUCTURE code were carried out for dielectronic recombination (DR) and trielectronic recombination (TR) for both ions. We compare these experimental and theoretical results and also compare with previously recommended rate coefficients. The DR and TR resonances were experimentally investigated in the electron-ion collision energy ranges 0–120 eV and 0–151 eV for Fe viii and Fe ix. Experimentally derived Fe viii and Fe ix DR + TR plasma rate coefficients are provided in the temperature range kBT = 0.2 to 1000 eV. Their uncertainties amount to <±26% and <±35% at a 90% confidence level for Fe viii and Fe ix, respectively.

Electron collisions and rovibrational action spectroscopy of cold H3+ molecules

Electron recombination of H3+ has found a lot of attention due to its outstanding relevance for the chemistry of the interstellar medium (ISM) and its role as a benchmark for the treatment of dissociative recombination (DR) of polyatomic ions. We report DR measurements performed at the TSR storage ring utilizing a cryogenic ion trap injector. Furthermore, a chemical probing spectroscopy technique is described that allows for a very sensitive monitoring of the populated states inside the ion injector. Since H3+ exists in two different nuclear spin modifications, a controlled manipulation of the ortho/para fraction is needed in order to perform state-selective measurements.