Intermolecular Coulombic Decay: Geometric and Electronic Structures of Ionized Water

Intermolecular Coulombic decay (ICD) in liquid water is a relatively novel type of nonlocal electronic decay mechanism, competing with the traditional mechanism of proton transfer between neighboring water molecules. Key features of ICD are its ultrafast non-radiative decay process and ultralong-range for excess energy transfer from the excited atom/molecule to its neighbors. Since detecting unambiguous ICD signatures in bulk liquid water is technically challenging, small water clusters have often been utilized to gain insights into ICD and other ionization processes in aqueous environment. Here, we present results from quantum mechanical calculations of the electronic structures of neutral to multiply-ionized water monomer, dimer, trimer, and tetramer. Core-level electrons of water are also considered here since recent studies demonstrated that emission site and energy of the electrons released during resonant-Auger-ICD cascade can be controlled by coupling ICD to resonant core excitation. Previous studies of ICD and electronic structures of neutral and ionized small water clusters and liquid water are briefly discussed.