Kinetics and Dynamics of Photocatalyzed Dissociation of Ethanol on TiO2(110)

Abstract

The kinetics and dynamics of photocatalyzed dissociation of ethanol on TiO 2 (110) surface have been studied using the time-dependent and time-resolved femtosecond two-photon photoemission spectroscopy respectively, in order to unravel the photochemical properties of ethanol on this prototypical metal oxide surface. By monitoring the time evolution of the photoinduced excited state which is associated with the photocatalyzed dissociation of ethanol on Ti 5c sites of TiO 2 (110), the fractal-like kinetics of this surface photocatalytic reaction has been obtained. The measured photocatalytic dissociation rate on reduced TiO 2 (110) is faster than that on the oxidized surface. This is attributed to the larger defect density on the reduced surface which lowers the reaction barrier of the photocatalytic reaction at least methodologically. Possible reasons associated with the defect electrons for the acceleration have been discussed. By performing the interferometric two-pulse correlation on ethanol/TiO 2 (110) interface, the ultrafast electron dynamics of the excited state has been measured. The analyzed lifetime (24 fs) of the excited state is similar to that on methanol/TiO 2 (110). The appearance of the excited state provides a channel to mediate the electron transfer between the TiO 2 substrate and its environment. Therefore studying its ultrafast electron dynamics may lead to the understanding of the microscopic mechanism of photocatalysis and photoelectrochemical energy conversion on TiO 2 .

Photocatalytic Dissociation of Ethanol on TiO2(110) by Near-Band-Gap Excitation

“…With the increase in light exposure, the excited resonance signal becomes more and more intense, indicating on the BBO sites that there are more and more hydroxyl groups that are likely due to photocatalytic dissociation of ethanol on TiO 2 (110). We have studied the effect of extent of the substrate reduction on the photochemistry of ethanol on TiO 2 (110), 41 and find that the apparent photoinduced phenomena are similar except the reaction rate. This is also similar to methanol.…”