Abstract
We have studied the reforming reaction of ethanol co-adsorbed with atomic oxygen (O*, * denotes adspecies) and deuterated water (D(2)O*) on a Rh(111) surface, with varied surface probe techniques under UHV conditions and with density-functional-theory calculations. Adsorbed ethanol molecules were found to penetrate readily through pre-adsorbed water, even up to eight overlayers, to react at the Rh surface; they decomposed at a probability promoted by the water overlayers. The production probabilities of H(2), CO, CH(2)CH(2) and CH(4) continued to increase with co-adsorbed D(2)O*, up to two D(2)O overlayers, despite separate increasing rates; above two D(2)O overlayers, those of H(2), CO and CH(2)CH(2) were approximately saturated while that of CH(4) decreased. The increased (or saturated) production probabilities are rationalized with an increased (saturated) concentration of surface hydroxyl (OD*, formed by O* abstracting D from D(2)O*), whose intermolecular hydrogen bonding with adsorbed ethanol facilitates proton transfer from ethanol to OD* and thus enhances the reaction probability. The decreasing behavior of CH(4) could also involve the competition for H* with the formation of H(2) and HDO.