Cluster size distribution and collision-induced dissociation (CID) studies of protonated methanol and protonated methanol-water clusters yield information on the structure and energetics of such ions. Ions were formed at atmospheric pressure in a corona discharge source, and were subjected to CID in
Ionization of water clusters by surface collision
β Scribed by A.A. Vostrikov; D.Yu. Dubov; M.R. Predtechenskiy
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- English
- Weight
- 439 KB
- Volume
- 139
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
We present experiments in which a beam of neutti #i,O), clusters are scsttered at various solid surfaces. ft is shown that at cluster sizes ~r~spond~ng to NS 300 cluster cations, anions and electrons appear in the scattered Bow. As Nincreases the current of cluster cations f, and anions I_ becomes greater. The currents I, and I_ are not identical and depend on the target material and the angle of incidence of the water cluster beam on the target. The phenomenon of charge formation and separation can be explained by the autoprotolysis of water molecules in clusters: H,O(aq)+N*(aq) i-OH-faq}. This reaction is enhanced by increasing the cluster collision energy. The difference between I+ and f_ seems to be connected with the different rates of neutralization of positive and negative ions in clusters by the surface. The presence of electrons in the scattered particle flow is explained by Auger neutralization of some af the cations.
π SIMILAR VOLUMES
Structures of the negatively charged water clusters H O with n up to 2 n 6 were optimized at the UHFr4-31 q q G\*\* level without any geometrical restriction. There was found a chainlike structure for the trimer anion and both chainlike and cyclic geometries for the larger clusters. According to t
We present ab initio molecular orbital calculations on vertical ionization potentials of surface and interior anion structures of I -( HzO), (n = 7, 8) clusters. The 'magic number' in the differential ionization potential of I-(HsO), is accounted for by the dominance of surface structures for n = 2-