The effect of metal cations on the nature of the first electronic transition of liquid water as studied by attenuated total reflection far-ultraviolet spectroscopy
Abstract
The first electronic transition (Ã ← ) of liquid
transition energies of 1 M electrolyte solutions are higher (Li+: 8.024 eV and Cs+: 8.013 eV) than that of pure
transition energies are mostly attributable to the hydrogen bond formation energies of
transition energies of the water–cation complexes depend on the hydration structures of the
transition energies of the
transition bands measured by ATR-FUV