Abstract
Polyol conversion to value-added products is of great interest for the bio-diesel industry. Photocatalytic oxidation processes may offer a green approach for polyol conversion; however the lack of comprehensive mechanistic understanding from an interdisciplinary perspective limits or even misleads the design of highly selective and efficient photocatalysts for such process. Here we have studied the photocatalytic polyol conversion on pristine TiO2 and metal (Au, Pd, and Pt) nanoparticles (NPs) decorated TiO2 using ethylene glycol (EG) as the model compound. We have developed a mechanistic picture at molecular level by coupling in-situ surface science study on rutile (110) surface with in-situ vibrational-mass spectrometry study on TiO2 nanopowders. The CC bond cleavage was found to be the only pathway in EG photo-conversion under deaerated conditions, leading to the formation of formaldehyde and hydrogen. We rationalized that the desorption of the surface adsorbed H (Hads) to be the rate determining step (RDS), making pristine TiO2 a poor photocatalyst that only catalyze the EG conversion at very low surface coverages. The addition of metal NPs on TiO2 surface promotes the desorption of Hads significantly, thus leading to an enhanced CC bond cleavage performance at higher surface coverages that is more applicable.
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