Adsorption and isomerization of glyoxal and methylglyoxal at the air/hydroxylated silica surface.

We present results from molecular dynamics simulations coupled with enhanced sampling techniques on the adsorption and isomerization of glyoxal (GL) and methylglyoxal (MG) at the air/hydroxylated silica (α-Quartz) interface. GL and MG are two organic compounds present in the atmosphere as oxidation products of both biogenic and anthropogenic precursors. By adsorption and hydration on liquid droplets or wetted dust particles, they can enable aerosol growth in the atmosphere. Moreover, thanks to the different polar characters of their trans and cis conformers, GL and MG have been suggested as possible molecular switches capable of responding to changes in solvent polarity. Here, we show that the hydroxylated silica surface does not significantly catalyze the trans-to-cis isomerization, but it stabilizes the cis-isomers, indicating a higher interfacial cis/trans relative concentration compared to the gas phase. Moreover, adsorbed GL prefers to lie parallel on the silica surface, while adsorbed MG shows a tilted orientation. In particular, we report the aldehyde group pointing upward (downward) to the gas phase (to the silica surface) in trans-MG (cis-MG). These results will help in the rationalization of upcoming experimental and modeling work on the adsorption of ketonic compounds on dust aerosols, while it clarifies the catalytic role of the solid substrate surface in promoting conformational changes.