Surface diffusion and entrapment of simple molecules on porous silica

Abstract

Interactions of simple molecules with the surface of porous silica have been investigated using time-of-flight secondary ion mass spectrometry and temperature programmed desorption. A monolayer of water diffuses into pores at temperatures higher than 110K. Multilayers of water are also incorporated in pores via sequential surface diffusion. In contrast, a methanol monolayer tends to stay on the surface up to 150K, and carbon dioxide diffuses into pores rather gradually. Results can be explained as the contribution of hydrogen bonds between the adsorbate–substrate and adsorbate–adsorbate interactions. The predominance of the former (latter) might be responsible for single-molecule migration of methanol and carbon-dioxide (collective diffusion of water molecules) on the surface. These molecules are entrapped at higher coordination sites in pores, as revealed from thermal desorption peaks appearing at higher temperatures than those from non-porous silica. However, no significant difference is observed in desorption kinetics of CF2Cl2, Kr, CH4, and N2 molecules between the porous and non-porous silica substrates.