12 research outputs found
-Determination of the C-H Bond Dissociation Energies of Ethylene and Acetylene by Observation of the Threshold Energies of H+ Formation by Synchrotron Radiation.
Determination of the carbon-hydrogen bond dissociation energies of ethylene and acetylene by observation of the threshold energies of proton formation by synchrotron radiation
Time-of-flight mass and photoelectron spectroscopy study of LaCn-
Mass spectra of LaCn- were taken by using a laser-vaporization source (LVS) and pulsed arc cluster ion source (PACIS) applied to La-carbon composite rods (1:130 atomic ratio). The mass spectrum using the LVS with annealing procedure has shown several magic numbers for LaCn- (n = 44, 50, 60, and 70), whereas only small LaCn- (up to n = 14) have been observed in the mass spectrum using the PACIS. Photoelectron spectra of some of these have been measured using a magnetic-bottle type time-of-flight electron spectrometer. These results indicate the exsistence of a few conformational isomers for small La-containing carbon cluster negative ions LaCn- (n = 5 8)
Radiative cooling of C7-
The spontaneous and photo-induced neutralization of C_7- produced in a laser ablation source was measured in an electrostatic storage ring. The measurements provide three independent determinations of the radiative cooling of the ions, based on the short time spontaneous decay and on the integrated amplitude and the shape of the photo-induced neutralization signal. The amplitudeof the photo-induced signal was measured between 0.5 ms and 35 ms and found to depend on photon wavelength and ion storage time. All three signals can be reproduced with identical thermal IR radiative cooling rates with oscillator strengths equal to theoretical predictions. In addition,the measurements provide the excitation energy distribution
Photoelectron spectroscopy study of MCn- (M=Sc, Y, and La, 5<=n<=20)
Photoelectron spectra of metal-attached carbon cluster anions MCnâ (M=Sc, Y, and La, 5â€nâ€20) generated in a laser-vaporization ion source were measured using a magnetic bottle time-of-flight photoelectron spectrometer with 6.4 eV photon energy. The vertical detachment energy (vDE) of each species was estimated from the spectra and compared with the vDE of the linear and monocyclic ring forms of Cn. It was found that PES features of MCnâ (5â€nâ€20, n=odd) could be understood under the assumption that the Ï electronic structure of MCnâ is similar to those of the linear carbon chains. However, the PES features of MCnâ (12â€nâ€20, n=even) indicate the presence of a Ï electronic structure similar to the isomers having ring form. Further possible electronic and molecular structures are presented and discussed for MCnâ of odd n and even n, respectively
Inverse internal conversion in C 4 - below the electron detachment threshold
Inverse internal conversion followed by recurrent fluorescence was observed as a fast decay (10 ÎŒs range) in the time profile of neutral yields from photo-excited C4- molecular ions. We also elucidated the contribution of such electronic radiative cooling to the C4- ions with internal energy far below the detachment threshold by an alternative novel approach, observing the laser wavelength and storage time dependence (ms range) of the total yield of the photo-induced neutrals
Femtosecond time-resolved laser desorption/ionization mass spectrometry of perylene crystals using Raman-induced vibrational excitation
Phosphorescence of Hydrogen-Capped Linear Polyyne Molecules C8H2, C10H2 and C12H2 in Solid Hexane Matrices at 20 K
International audienceLaser-ablated polyyne molecules, H(CâĄC)nH, were separated by size in solutions and co-condensed with excess hexane molecules at a cryogenic temperature of 20 K in a vacuum system. The solid matrix samples containing C8H2, C10H2, and C12H2 molecules were irradiated with UV laser pulses and the phosphorescence 0â0 band was observed at 532, 605, and 659 nm, respectively. Vibrational progression was observed for the symmetric stretching mode of the carbon chain in the ground state with increments of ~2190 cmâ1 for C8H2, ~2120 cmâ1 for C10H2, and ~2090 cmâ1 for C12H2. Temporal decay analysis of the phosphorescence intensity revealed the lifetimes of the triplet state as ~30 ms for C8H2, ~8 ms for C10H2, and ~4 ms for C12H2. The phosphorescence excitation spectrum reproduces UV absorption spectra in the hexane solution and in the gas phase at ambient temperature, although the excitation energy was redshifted. The symmetry-forbidden vibronic transitions were observed for C10H2 by lower excitation energies of 25,500â31,000 cmâ1 (320â390 nm). Detailed phosphorescence excitation patterns are discussed along the interaction of the polyyne molecule and solvent molecules of hexane