We present state-selected measurements of rotational cooling and excitation rates of CH^{+} molecular ions by inelastic electron collisions. The experiments are carried out at a cryogenic storage ring, making use of a monoenergetic electron beam at matched velocity in combination with state-sensitive laser dissociation of the CH^{+} ions for simultaneous monitoring of the rotational level populations. Employing storage times of up to 600 s, we create conditions where electron-induced cooling to the J=0 ground state dominates over radiative relaxation, allowing for the experimental determination of inelastic electron collision rates to benchmark state-of-the-art theoretical calculations.
View Article and Find Full Text PDFWe have measured the spectrum of laser photodissociation of OH molecular ions to O + H and O + H fragments for photon energies of 38 100-40 900 cm. The OH ions were stored as a fast beam (5.50 MeV) in the storage ring TSR for several seconds to achieve rovibrational cooling into the lowest rotations N'' = 0-11 of the vibrational ground state XΣ(v'' = 0), close to room temperature (≈300 K).
View Article and Find Full Text PDFWe have studied the photodissociation of CH^{+} in the Cryogenic Storage Ring at ambient temperatures below 10 K. Owing to the extremely high vacuum of the cryogenic environment, we were able to store CH^{+} beams with a kinetic energy of ∼60 keV for several minutes. Using a pulsed laser, we observed Feshbach-type near-threshold photodissociation resonances for the rotational levels J=0-2 of CH^{+}, exclusively.
View Article and Find Full Text PDFWe have measured the photodissociation spectrum of CH(+) and CD(+) molecular ions, stored as fast (MeV) ion beams in the heavy-ion storage ring TSR. Several b (3)Sigma(-)-a (3)Pi bands were observed as strong resonances because a large fraction of the ions in the metastable a (3)Pi(v=0) state were pumped to b (3)Sigma(-) levels and predissociated via the c (3)Sigma(+) state into C(+) and H(D) fragments. From a rotational analysis of the 2-0, 3-0, and 4-0 bands in CH(+) and the 3-0 and 4-0 bands in CD(+), we derive spectroscopic constants for these levels and also revise a previous analysis of the 0-0 and 1-0 bands in CH(+).
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