Uptake and hydration of sulfur dioxide on dry and wet hydroxylated silica surfaces: a computational study

Ivan Gladich; Chen Lin; Alessandro Sinopoli; Joseph S Francisco

doi:10.1039/d1cp04747g

Uptake and hydration of sulfur dioxide on dry and wet hydroxylated silica surfaces: a computational study

Phys Chem Chem Phys. 2021 Dec 22;24(1):172-179. doi: 10.1039/d1cp04747g.

Authors

Ivan Gladich¹, Chen Lin², Alessandro Sinopoli¹, Joseph S Francisco³

Affiliations

¹ Qatar Environment and Energy Research Institute, Hamad Bin Khalifa University, P.O. Box 34410, Doha, Qatar. igladich@hbku.edu.qa.
² Department of Chemistry and Biochemistry, University of California Los Angeles, CA, USA.
³ Department of Earth and Environmental Science and Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA. frjoseph@sas.upenn.edu.

PMID: 34878450
DOI: 10.1039/d1cp04747g

Abstract

We present a first-principles molecular dynamics study on the uptake and hydration of sulfur dioxide on the dry and wet fully hydroxylated surfaces of (0001) α-quartz, which are a proxy for suspended silica dust in the atmosphere. The average adsorption energy for SO₂ is about -10 kcal mol^-1 on both dry and wet surfaces. The adsorption is driven by hydrogen bond formation between SO₂ and the interfacial hydroxyl groups (on dry silica), or with water molecules (in the wet case). In the dry system, we report an additional electrostatic interaction between the interfacial hydroxyl oxygen and the sulfur atom, which further stabilizes the adsorbate. On dry silica, the interfacial hydroxyl group coordinates to SO₂ yielding a surface bound bisulfite (Si-SO₃H) complex. On the wet surface, SO₂ reacts with water forming bisulfite (HSO₃^-), and the latter remains solvated inside the adsorbed water layer. The hydration barrier for sulfur dioxide is 1 kcal mol^-1 and 3 kcal mol^-1 on dry and wet silica, respectively, while for the backward reaction (i.e., bisulfite to SO₂) the barrier is 6 kcal mol^-1 on both surfaces. The modest backward barrier rationalizes earlier experimental findings showing no SO₂ uptake on silica. These results underline the importance of the surface hydroxylation and/or adsorbed water layers for the SO₂ uptake and its hydration on silica. Moreover, the hydration to bisulfite may prevent direct SO₂ photochemistry and be an additional source of sulfate; this is especially relevant in atmospheres subject to a high level of suspended mineral dust, intense solar radiation and atmospheric oxidizers.