Abstract
Photocatalytic oxidation of ethanol over rutile TiO2(1 1 0) in the presence of O-2 have been studied with scanning tunneling microscopy and on-line mass spectrometry to elucidate the reaction mechanisms. The O-2 partial pressure has a direct impact on C-C bond cleavage, resulting in a shift of selectivity in gas phase products from acetaldehyde (dehydrogenation) to methyl radicals (C-C bond dissociation) with increasing pressure. This differs from the behavior of anatase TiO2(1 0 1) single crystal, where at all investigated pressures negligible C-C bond dissociation occurs. The prevalence of the methyl radical species at high oxygen pressures is correlated with an increase in the surface population of an adsorbed species bound to Ti-5c after the reaction, which are identified as formate moieties. Parallel XPS Cl s, Ti2p and 01s further confirmed the assignment of surface population, by STM, to ethoxides at 300 K, in dark conditions (Cl s at 286.7 and 285.4 eV attributed to -CH2O- and -CH3 groups respectively). After photoreaction, a large fraction of the surface was covered by formates (XPS Cl at 289.7 eV). This also correlated with the STM assignment where species spaced by 6 angstrom along the [0 0 1] direction and with a height of ca. 1.1 angstrom attributed to formates. Moreover the profile for CH3 radical desorption in the gas phase as a function O-2 partial pressures correlated with the increasing surface population of formates. Analysis of the rate of methyl radical formation reveals fast and slow regimes, with photoreaction cross -sections between 10(-17) cm(2) and 10(-19) cm(2). The parallel channel of acetaldehyde production has a non -varying cross-section of ca. 2 x 10(-19) cm(2). A schematic description of the two different reaction channels (dehydrogenation and C-C bond dissociation) is given and discussed. (C) 2018 Elsevier Inc. All rights reserved.