Theoretical studies on the coupling interactions in H2SO4⋯HOO˙⋯(H2O)n (n = 0–2) clusters: toward understanding the role of water molecules in the uptake of HOO˙ radical by sulfuric acid aerosols

Abstract

A detailed knowledge of coupling interactions among sulfuric acid (H₂SO₄), the hydroperoxyl radical (HOO˙), and water molecules (H₂O) is crucial for the better understanding of the uptake of HOO˙ radicals by sulfuric acid aerosols at different atmospheric humidities. In the present study, the equilibrium structures, binding energies, equilibrium distributions, and the nature of the coupling interactions in H₂SO₄⋯HOO˙⋯(H₂O)_n (n = 0–2) clusters have been systematically investigated at the B3LYP/6-311++G(3df,3pd) level of theory in combination with the atoms in molecules (AIM) theory, natural bond orbital (NBO) method, energy decomposition analyses, and ab initio molecular dynamics. Two binary, five ternary, and twelve tetramer clusters possessing multiple intermolecular H-bonds have been located on their potential energy surfaces. Two different modes for water molecules have been observed to influence the coupling interactions between H₂SO₄ and HOO˙ through the formations of intermolecular H-bonds with or without breaking the original intermolecular H-bonds in the binary H₂SO₄⋯HOO˙ cluster. It was found that the introduction of one or two water molecules can efficiently enhance the interactions between H₂SO₄ and HOO˙, implying the positive role of water molecules in the uptake of the HOO˙ radical by sulfuric acid aerosols. Additionally, the coupling interaction modes of the most stable clusters under study have been verified by the ab initio molecular dynamics.