Electron gun for diffraction experiments off controlled molecules

A dc electron gun, generating picosecond pulses with up to $8\times10^{6}$ electrons per pulse, was developed. Its applicability for future time-resolved-diffraction experiments on state- and conformer-selected laser-aligned or oriented gaseous samples was characterized. The focusing electrodes were arranged in a velocity-map imaging spectrometer configuration. This allowed to directly measure the spatial and velocity distributions of the electron pulses emitted from the cathode. The coherence length and pulse duration of the electron beam were characterized by these measurements combined with electron trajectory simulations. Electron diffraction data off a thin aluminum foil illustrated the coherence and resolution of the electron-gun setup

Strongly aligned and oriented molecular samples at a kHz repetition rate

We demonstrate strong adiabatic laser alignment and mixed-field orientation at kHz repetition rates. We observe degrees of alignment as large as cos\Theta=0.94 at 1 kHz operation for iodobenzene. The experimental setup consist of a kHz laser system simultaneously producing pulses of 30 fs (1.3 mJ) and 450 ps (9 mJ). A cold 1 K state-selected molecular beam is produced at the same rate by appropriate operation of an Even-Lavie valve. Quantum state selection has been obtained using an electrostatic deflector. A camera and data acquisition system records and analyzes the images on a single-shot basis. The system is capable of producing, controlling (translation and rotation) and analyzing cold molecular beams at kHz repetition rates and is, therefore, ideally suited for the recording of ultrafast dynamics in so-called "molecular movies".Comment: 6 pages, 4 figures, in press in Mol. Phys., accepted in February 2013, in final production (galley proofs done) since March 8, 2013, v3 only adds publication dat

Strongly driven quantum pendulum of the OCS molecule

We demonstrate and analyze a strongly driven quantum pendulum in the angular motion of stateselected and laser aligned OCS molecules. Raman-couplings during the rising edge of a 50-picosecond laser pulse create a wave packet of pendular states, which propagates in the confining potential formed by the polarizability interaction between the molecule and the laser field. This wave-packet dynamics manifests itself as pronounced oscillations in the degree of alignment with a laser-intensity dependent period.Comment: 6 pages, 4 figure

Power scaling of an extreme ultraviolet light source for future lithography

For future lithography applications, high-power extreme ultraviolet (EUV) light sources are needed at a central wavelength of 13.5 nm within 2% bandwidth. We have demonstrated that from a physics point of view the Philips alpha-prototype source concept is scalable up to the power levels required for high-volume manufacturing (HVM) purposes. Scalability is shown both in frequency, up to 100 kHz, and pulse energy, up to 55 mJ collectable EUV per pulse, which allows us to find an optimal working point for future HVM sources within a wide parameter space. (C) 2008 American Institute of Physics

Emission of volatile halogenated compounds, speciation and localization of bromine and iodine in the brown algal genome model Ectocarpus siliculosus

This study explores key features of bromine and iodine metabolism in the filamentous brown alga and genomics model Ectocarpus siliculosus. Both elements are accumulated in Ectocarpus, albeit at much lower concentration factors (2-3 orders of magnitude for iodine, and < 1 order of magnitude for bromine) than e.g. in the kelp Laminaria digitata. Iodide competitively reduces the accumulation of bromide. Both iodide and bromide are accumulated in the cell wall (apoplast) of Ectocarpus, with minor amounts of bromine also detectable in the cytosol. Ectocarpus emits a range of volatile halogenated compounds, the most prominent of which by far is methyl iodide. Interestingly, biosynthesis of this compound cannot be accounted for by vanadium haloperoxidase since the latter have not been found to catalyze direct halogenation of an unactivated methyl group or hydrocarbon so a methyl halide transferase-type production mechanism is proposed

Single-photon-emitting optical centers in diamond fabricated upon Sn implantation

The fabrication of luminescent defects in single-crystal diamond upon Sn implantation and annealing is reported. The relevant spectral features of the optical centers (emission peaks at 593.5 nm, 620.3 nm, 630.7 nm and 646.7 nm) are attributed to Sn-related defects through the correlation of their photoluminescence (PL) intensity with the implantation fluence. Single Sn-related defects were identified and characterized through the acquisition of their second-order auto-correlation emission functions, by means of Hanbury-Brown-Twiss interferometry. The investigation of their single-photon emission regime as a function of excitation laser power revealed that Sn-related defects are based on three-level systems with a 6 ns radiative decay lifetime. In a fraction of the studied centers, the observation of a blinking PL emission is indicative of the existence of a dark state. Furthermore, absorption dependence from the polarization of the excitation radiation with about 45 percent contrast was measured. This work shed light on the existence of a new optical center associated with a group-IV impurity in diamond, with similar photo-physical properties to the already well-known Si-V and Ge-V emitters, thus providing results of interest from both the fundamental and applicative points of view.Comment: 10 pages, 4 figure

Photoelectron Soft X-Ray Fluorescence Coincidence Spectroscopy on Free Molecules

A technique for measuring core-level photoemission from free molecules in coincidence with the soft x-ray fluorescence decay is presented. Zero-kinetic-energy photoelectrons are detected in a time-of-flight electron spectrometer, and photons are collected in a large solid angle by a detector situated close to the interaction region. The coincidence spectrum of N2 shows an adiabatic 1s line, free from electron-electron postcollision interaction effects. The results open up new aspects on core-hole excitation-emission dynamics