The recently observed linear dependence of the lifetime of excited hydrated electrons upon the inverse of the cluster size is explained in terms of a nonadiabatic long range coupling mechanism. It is due to dipolar interactions between the p→s transition and the excitation of the infrared active modes of the solvent water molecules.
Print ISSN: 0942-9352
Volume: 221, 05/2007
Pages: 585 - 595