Role of alkali cations for the excited state dynamics of liquid water near the surface.

Citation data:

The Journal of chemical physics, ISSN: 1089-7690, Vol: 137, Issue: 2, Page: 024503

Publication Year:
2012
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Repository URL:
http://scholarworks.unist.ac.kr/handle/201301/6233
PMID:
22803543
DOI:
10.1063/1.4732582
Author(s):
Buchner, Franziska; Ritze, Hans-Hermann; Beutler, Marcus; Schultz, Thomas; Hertel, Ingolf V.; Luebcke, Andrea
Publisher(s):
AIP Publishing; AMER INST PHYSICS
Tags:
Physics and Astronomy; Chemistry; Ab initio calculations; Alkali cations; Dielectric continuum model; Excited-state dynamics; Hydrated complexes; Liquid jets; Liquid water; Liquid water surface; Solvated electron; Time-resolved; Vacuum ultraviolets; Vertical ionization energy; Water molecule
article description
Time-resolved liquid jet photoelectron spectroscopy was used to explore the excited state dynamics at the liquid water surface in the presence of alkali cations. The data were evaluated with the help of ab initio calculations on alkali-water clusters and an extension of these results on the basis of the dielectric continuum model: 160 nm, sub-20 fs vacuum ultraviolet pulses excite water molecules in the solvent shell of Na(+) or K(+) cations and evolve into a transient hydrated complex of alkali-ion and electron. The vertical ionization energy of this transient is about 2.5 eV, significantly smaller than that of the solvated electron.