The radiative cooling of naphthalene dimer cations, (CH) was studied experimentally through action spectroscopy using two different electrostatic ion-beam storage rings, DESIREE in Stockholm and Mini-Ring in Lyon. The spectral characteristics of the charge resonance (CR) band were observed to vary significantly with a storage time of up to 30 seconds in DESIREE. In particular, the position of the CR band shifts to the blue, with specific times (inverse of rates) of 0.
View Article and Find Full Text PDFThe unimolecular dissociation and infrared radiative cooling rates of cationic 1-hydroxypyrene (OHPyr, CHO) and 1-bromopyrene (BrPyr, CHBr) are measured using a cryogenic electrostatic ion beam storage ring. A novel numerical approach is developed to analyze the time dependence of the dissociation rate and to determine the absolute scaling of the radiative cooling rate coefficient. The model results show that radiative cooling competes with dissociation below the critical total vibrational energies E = 5.
View Article and Find Full Text PDFThe mutual neutralisation of O with O has been studied in a double ion-beam storage ring with combined merged-beams, imaging and timing techniques. Branching ratios were measured at the collision energies of 55, 75 and 170 (± 15) meV, and found to be in good agreement with previous single-pass merged-beams experimental results at 7 meV collision energy. Several previously unidentified spectral features were found to correspond to mutual neutralisation channels of the first metastable state of the cation (O(D), ≈ 3.
View Article and Find Full Text PDFThis work presents a study of the thermal evaporation and stability of pyrene (CH) clusters. Thermal evaporation rates of positively charged mass-selected clusters are measured for sizes in the range n = 3-40 pyrene units. The experimental setup consists of a gas aggregation source, a thermalization chamber, and a time of flight mass spectrometer.
View Article and Find Full Text PDFIn cosmic environments, polycyclic aromatic hydrocarbons (PAHs) strongly interact with vacuum ultraviolet (VUV) photons emitted by young stars. Trapped PAH cations ranging in size from 30 to 48 carbon atoms were irradiated by tunable synchrotron light (DESIRS beamline at SOLEIL). Their ionization and dissociation cross sections were determined and compared with TD-DFT computed photoabsorption cross sections.
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