We report on the current status and performance of the toroidal grating monochromator beamline at the Brazilian Synchrotron Light Laboratory (Laboratorio Nacional de Luz Sincrotron). This beamline provides photons in the vacuum ultraviolet and soft x-ray regions from 12 to 330 eV with three interchangeable gratings. We report on the improvement, which allows the possibility of choosing the light polarization degree from linear to almost circular. Here, we also describe the development of a new apparatus, namely, the mirror-inserted harmonic attenuator and calibrating-device with a long length (MIRHACLLE). All beamlines based on diffraction gratings suffer from the problem of high harmonics contaminations to some extent. The MIRHACLLE provides a way to efficiently suppress high harmonics from 25% to 1 ppm in a grazing incidence bending magnet beamline. Its principle of operation relays on the absorption of the high energy photons in a gas phase region. It allows negligible high harmonics contamination for photon energies ranging from 12 eV to the gas first ionization threshold, 21.6 eV, in the case of neon. We also demonstrate the possibility to use this device for energy calibration and resolution evaluation together with any experiment needing its filtering capabilities. The device is also very cost effective compared to other filters presented previously in the literature.

Total ion yield spectra and photoinduced fragmentations following S 2p, C 1s, O 1s, and F 1s inner shell excitations of methyl thiofluoroformate, FC(O)SCH(3), have been studied in the gaseous phase by using synchrotron radiation and multicoincidence techniques, which include photoelectron-photoion coincidence (PEPICO) and photoelectron-photoion-photoion coincidence (PEPIPICO) time-of-flight mass spectrometry. Fragmentation patterns deduced from PEPICO spectra at the various excitation energies show a moderate site-specific fragmentation. The dissociation dynamic for the main ion-pair production has been discussed. Two-, three-, and four-body dissociation channels have been observed in the PEPIPICO spectra, and the dissociation mechanisms were proposed. The high stability of the interstellar HCS(+) ion can be observed over the whole range of photon energies analyzed.

No abstract

A study of valence electronic properties of S-ethyl chlorothioformate (S-ethyl chloromethanethioate), ClC(O)SCH(2)CH(3), using HeI photoelectron spectra (PES) and synchrotron radiation is presented. Moreover, the photon impact excitation and dissociation dynamics of ClC(O)SCH(2)CH(3) excited at the S 2p and Cl 2p levels are elucidated by analyzing the total ion yield (TIY) spectra and time-of-flight mass spectra acquired in multicoincidence mode [photoelectron-photoion coincidence (PEPICO) and photoelectron-photoion-photoion coincidence (PEPIPICO)]. The HeI photoelectron spectrum is dominated by features associated with lone-pair electrons from the ClC(O)S- group, the HOMO at 9.84 eV being assigned to the n(π)(S) sulfur lone-pair orbital. Whereas the formation of C(2)H(5)(+) ion dominates the fragmentation in the valence energy region, the most abundant ion formed in both the S and Cl 2p energy ranges is C(2)H(3)(+). Comparison with related XC(O)SR (X = H, F, Cl and R = -CH(3), -C(2)H(5)) species reveals the impact of the alkyl chain on the photodissociation behavior of S-alkyl (halo)thioformates.

A new possibility of laser cooling of alkaline-earth-metal and Ytterbium atoms using a twophoton transition is analyzed. We consider a 1 S0 -1 S0 transition, with excitation in near resonance with the 1 P1 level. This greatly increases the two-photon transition rate, allowing an effective transfer of momentum. The experimental implementation of this technique is discussed and we show that for Calcium, for example, two-photon cooling can be used to achieve a Doppler limit of 123 microKelvin. The efficiency of this cooling scheme and the main loss mechanisms are analyzed.