Methanol Oxidation to Formaldehyde Promoted at the Step Sites of Ultrathin ZnO

Abstract

Adsorption and oxidation of methanol on ultrathin ZnO layers supported on Au(111) have been investigated using temperature programmed reaction spectroscopy (TPRS) and density functional theory (DFT) calculations. In the TPRS experiments, following adsorption of methanol-18O at T = 100 K, only molecular methanol-18O desorbed from the planar ZnO bilayer surface at T = 220 and 260 K, whereas a partial oxidation product, formaldehyde-18O (~ 95% selectivity), and a small amount of carbon dioxide (C16O18O) were produced at T = 580 K at the bilayer–trilayer step sites. The DFT calculations were used to identify the adsorption configurations of methanol on the planar ZnO surface and at the step sites, as well as the reaction pathways to gaseous formaldehyde. The most stable adsorption configuration corresponds to methanol molecule adsorbed at the bilayer–trilayer step sites with its C–O axis parallel to the upper terrace edge, forming a bond between its O atom and a Zn site on the lower terrace, and also a hydrogen bond between its H atom in the OH group and a lattice O anion at the upper terrace edge. Starting from the most stable adsorption configuration at the step sites, formation of gaseous formaldehyde was found to take place preferentially via a methoxy (CH3O(ad)) intermediate. This process follows the pathways CH3OH(ad) → CH3O(ad) + H(ad) → CH2O(g) + 2H(ad) and has an overall barrier of 19.0 kcal/mol. The reaction pathway to produce a lattice O-bonded formaldehyde (H2COOlattice(ad)), the proposed precursor leading to CO2, was found to be energetically less favorable with a barrier of ~ 38 kcal/mol. The preference to produce gaseous formaldehyde from the DFT calculations agrees well with the high selectivity toward formaldehyde observed in the TPRS experiments.