Kinetic Study of a Direct Water Synthesis over Silica-Supported Gold Nanoparticles

Abstract

The reaction mechanism of water formation from H₂ and O₂ was studied over a series of silica-supported gold nanoparticles. The metal particle size distributions were estimated with TEM and XRD measurements. Hydrogen and oxygen adsorption calorimetry was used to probe the nature and properties of surface species formed by these molecules. DFT calculations with Au₅, Au₁₃, and Au₅₅ clusters and with Au(111) and Au(211) periodic slabs were performed to estimate the thermodynamic stability and reactivity of surface species. Kinetic measurements were performed by varying the reactant partial pressures at 433 K and by varying the temperature from 383 to 483 K at 2.5 kPa of O₂ and 5 kPa of H₂. The measured apparent power law kinetic parameters were similar for all catalysts in this study: hydrogen order of 0.7−0.8, oxygen order of 0.1−0.2, and activation energy of 37−41 kJ/mol. Catalysts with Si−MFI (Silicalite-1) and Ti−MFI (TS-1 with 1 wt % Ti) exhibited similar activities. The activities of these catalysts with the MFI crystalline supports were 60−70 times higher than that of an analogous catalyst with an amorphous silica support. Water addition in the inlet stream at 3 vol % did not affect the reaction rates. The mechanism of water formation over gold is proposed to proceed through the formation of OOH and H₂O₂ intermediates. A rate expression derived based on this mechanism accurately describes the experimental kinetic data. The higher activity of the MFI-supported catalysts is attributed to a higher concentration of gold particles comparable in size to Au₁₃, which can fit inside MFI pores. DFT results suggest that such intermediate-size gold particles are most reactive toward water formation. Smaller particles are proposed to be less reactive due to the instability of the OOH intermediate whereas larger particles are less reactive due to the instability of adsorbed oxygen.