Probing the propensity of perchlorate anions for surface solvation by infrared photodissociation spectroscopy

We investigate the perchlorate anion, ClO₄⁻, microhydrated with up to eight water molecules using infrared photodissociation (IRPD) spectroscopy aided by density functional theory computations. The features observed in the IRPD spectra of D₂-tagged ClO₄⁻(H₂O)_n with n = 0−8 in the O–H stretching (2800–3800 cm⁻¹) and fingerprint (800–1800 cm⁻¹) spectral ranges are assigned to vibrational modes of the solvent, i.e., free and hydrogen-bonded O–H stretching and H₂O bending modes, and of the solute, i.e., perchlorate stretching modes. The splitting of the triply degenerate antisymmetric stretching mode in the bare ClO₄⁻ (1102 cm⁻¹) upon microhydration directly reports on the symmetry of the local solvation network, while the red-shift of the hydrogen-bonded O–H stretching bands in comparison to those of free O–H oscillators (>3700 cm⁻¹) reflects the strength of the anion-water (3550–3650 cm⁻¹) and water-water (3240–3540 cm⁻¹) hydrogen bonds. The stronger water-water interaction leads to an early onset of water-water hydrogen bond formation (n = 2) and eventually asymmetric solvation of ClO₄⁻, evidenced by the population of the second and third hydration shells at n = 5 and n = 8, respectively, before the first hydration shell is completed. The present study provides a bottom-up view of the initial stages of hydrogen-bond network formation around a high surface propensity anion, and these insights are discussed in the context of recent results obtained for the water-vapor interface of perchlorate solutions.