PubMed Health⌕ Search

Biomedical subjects

Joong-Won Shin

Publications and source records attributed to Joong-Won Shin.

2 recordsLinked to original sources

How do small water clusters bind an excess electron?

The arrangement of water molecules around a hydrated electron has eluded explanation for more than 40 years. Here we report sharp vibrational bands for small gas-phase water cluster anions, (H2O)(4-6)- and (D2O)(4-6)-. Analysis of these bands reveals a detailed picture of the diffuse electron-binding site. The electron is closely associated with a single water molecule attached to the supporting network through a double H-bond acceptor motif. The local OH stretching bands of this molecule are dramatically distorted in the pentamer and smaller clusters because the excited vibrational levels are strongly coupled to the electron continuum. The vibration-to-electronic energy transfer rates, as revealed by line shape analysis, are mode-specific and remarkably fast, with the symmetric stretching mode surviving for less than 10 vibrational periods [50 fs in (H2O)4-].

Journal Article↗

Spectroscopic determination of the OH- solvation shell in the OH-.(H2O)n clusters.

There has been long-standing uncertainty about the number of water molecules in the primary coordination environment of the OH- and F- ions in aqueous chemistry. We report the vibrational spectra of the OH-.(H2O)n and F-.(H2O)n clusters and interpret the pattern of OH stretching fundamentals with ab initio calculations. The spectra of the cold complexes are obtained by first attaching weakly bound argon atoms to the clusters and then monitoring the photoinduced evaporation of these atoms when an infrared laser is tuned to a vibrational resonance. The small clusters (n </= 3) display an isolated, sharp feature near the free OH stretching vibration, the signature of open solvation morphologies where each water molecule binds independently to the ion. Pronounced changes in the spectra are observed at n = 4 in the hydroxide ion and at n = 5 in the fluoride ion. In both cases, new features appear in the region typically associated with interwater hydrogen bonding. This behavior establishes that the primary hydration shells occur at n = 3 and 4 in hydroxide and fluoride, respectively.

Journal Article↗