Environmental effects on vibrational proton dynamics in H5O2+: DFT study on crystalline H5O2+ClO4−

Abstract

The structure as well as IR and inelastic neutron scattering (INS) spectra of H₅O₂⁺ in crystalline H₅O₂⁺ClO₄⁻ were simulated using Car–Parrinello molecular dynamics with the BLYP functional. The potential of the O⋯H⁺⋯O fragment is very shallow. The Pnma structure, assumed in the X-ray study to be the most suitable choice, is a saddle point on the potential energy surface, while the P2₁2₁2₁ minimum structure is only 20 cm⁻¹ lower in energy. The computed INS and IR spectra enable us to achieve a complete assignment of the observed spectra. The broad band between 1000 and 1400 cm⁻¹ is due to the asymmetric stretch and one of the bending vibrations of the O⋯H⁺⋯O fragment, while the band between 1600 and 1800 cm⁻¹ is due to the bending vibration of the water molecules and the second bending of the O⋯H⁺⋯O fragment. Comparison with the vibrational spectra of isolated H₅O₂⁺, obtained using Born–Oppenheimer molecular dynamics simulation, reveals environmental effects on vibrational proton dynamics in strong H-bonded species. The most pronounced changes are found for the O⋯H⁺⋯O bending modes because the two bending coordinates become distinctly different for the structure that the H₅O₂⁺ ion assumes in the crystal.