DECAY OF CS2 AND OCS AFTER SULFUR IS PHOTOEXCITATION .2. DISSOCIATIONCHANNELS AND KINEMATICS

Citation
U. Ankerhold et al., DECAY OF CS2 AND OCS AFTER SULFUR IS PHOTOEXCITATION .2. DISSOCIATIONCHANNELS AND KINEMATICS, Journal of physics. B, Atomic molecular and optical physics, 30(5), 1997, pp. 1207-1222
Citations number
26
Categorie Soggetti
Physics, Atomic, Molecular & Chemical",Optics
ISSN journal
09534075
Volume
30
Issue
5
Year of publication
1997
Pages
1207 - 1222
Database
ISI
SICI code
0953-4075(1997)30:5<1207:DOCAOA>2.0.ZU;2-C
Abstract
CS2 and OCS molecules were excited and fragmented by x-rays of variabl e energy around the sulphur Is threshold (2478 eV). Coincident detecti on of three ionic fragments by a time-of-flight mass spectrometer enab led the determination of branching ratios for 18 dissociation channels with total ionic charges between 2 and 7. While the electronic de-exc itation is similar in both molecules (see the preceding paper), the di ssociation shows differences, notably a more asymmetric distribution o f charge onto the fragments of OCS. Branching among channels of the sa me total charge is independent of photon energy although the dominant de-excitation cascades are not. This is interpreted as an indication o f strong interchannel mixing. A simple, parameter-free Coulomb explosi on model to simulate the dissociative kinematics is described. Detaile d results based on this model give, contrary to opinions to be found i n the literature, very good agreement with observed momentum correlati ons whereas maximum kinetic energies are somewhat overestimated for ch annels of higher total charge.