DFT studies on the heterogeneous oxidation of SO2 by oxygen functional groups on graphene

Abstract

The heterogeneous oxidation of SO₂ has been the subject of intense scrutiny in atmospheric chemistry because of the adverse effects of sulfate particles. Although it has been found that the soot particles with a graphene-like structure play an important role in the oxidation of SO₂, little is known about the atomic-level mechanism involved. Here, we studied the oxidation of SO₂ on oxygen-functionalized graphene using density functional theory (DFT) calculation. The results showed that SO₂ is oxidized by the epoxide group via a two-step mechanism, where the C–O bond away from the SO₂ is broken first, followed by the breaking of the other C–O bond and the synchronous formation of a new S–O bond. The energy barriers are significantly decreased when solvation free energies are involved, suggesting that humidity is favorable for promoting the oxidation by reducing the reaction barrier. The energy barriers for H₂SO₃ oxidation are much higher than that for SO₂ oxidation, indicating that the direct conversion of SO₂ to SO₃ is the main pathway for the oxidation of SO₂ by oxygen-functionalized graphene sheets in both the gas phase and solution. The reduced density gradient (RDG) analysis showed that the hydrogen bond formed between H₂SO₃ and epoxide groups enhances the stability of the reaction complex, and is responsible for the high energy barrier that has to be overcome for the reaction to proceed. These atomistic studies proposed a two-step mechanism for the oxidation of SO₂ on the oxygen-functionalized graphene-like carbonaceous surfaces under ambient conditions.