Pretreatment Effects on the Surface Chemistry of Small Oxygenates on Molybdenum Trioxide

Abstract

Understanding surface reactions of biomass-derived oxygenates on metal oxides is important for designing catalysts for valorization of biomass. This work elucidated the effect of different pretreatments on molybdenum trioxide (MoO3) to understand how surface reactivity is controlled by the surface oxidation state. The catalyst was pretreated in oxidative, inert, and reducing environments. The inert and reducing pretreatments created oxygen vacancies on the catalyst surface that acted as active sites for the adsorption of oxygenated molecules, with the reducing pretreatment yielding a higher density of these active sites. Exposing the catalyst to an alcoholic solvent such as methanol also led to a partial reduction similar to the inert pretreatment. After pretreatment, the catalyst was exposed to ethanol, acetaldehyde, and crotonaldehyde with subsequent characterization by diffuse reflectance infrared spectroscopy (DRIFTS), temperature-programmed desorption (TPD), X-ray absorption near edge spectroscopy (XANES), and X-ray photoelectron spectroscopy (XPS). Density functional theory (DFT) was also used to determine adsorption configurations and energies of ethanol, acetaldehyde, and crotonaldehyde. Reduced surfaces were shown to have a stronger affinity for carbonyls, leading to a higher activity for the aldol condensation of acetaldehyde and ethanol to C4 molecules. Catalysts pretreated in an oxidative environment were completely inactive toward chemisorption and reaction of acetaldehyde.