Reinvestigation of the Infrared Spectrum of the Gas-Phase Protonated Water Tetramer.

Abstract

Gas-phase H9O4+ has been considered an archetypal Eigen cation, H3O+(H2O)3. Yet ab initio molecular dynamics (AIMD) suggested that its infrared spectrum is explained by a linear-chain Zundel isomer, alone or in a mixture with the Eigen cation. Recently, hole-burning experiments suggested a single isomer, with a second-order vibrational perturbation theory (VPT2) spectrum agreeing with the Eigen cation. To resolve this discrepancy, we have extended both calculations to more advanced DFT functionals, better basis sets, and dispersion correction. For Zundel-isomers, we find VPT2 anharmonic frequencies for four low-frequency modes involving the excess proton unreliable, including the 1750 cm-1 band that is pivotal for differentiating between Zundel and Eigen isomers. Because the analogous bands of the H5O2+ cation show little effect of anharmonicity, we utilize the harmonic frequencies for these modes. With this caveat, both AIMD and VPT2 agree on the spectrum as originating from a Zundel isomer. VPT2 also shows that both isomers have the same spectrum in the high frequency region, so that the hole burning experiments should be extended to lower frequencies.