Wöll , C.  / Yu, X. / Roth, J.P. / Wang, J. / Nefedov, A. / Heißler, S. / Pacchioni, G. / Wang, Y. / Sauter, E. (2020)

ChemPhysChem, 2020, doi.org/10.1002/cphc.202000747

Abstract

The growth of ZnO clusters supported by ZnO‐bilayers on Ag(111) and the interaction of these oxide nanostructures with water have been studied by a multi‐technique approach combining temperature‐dependent infrared reflection absorption spectroscopy, grazing‐emission X‐ray photoelectron spectroscopy, and density functional theory calculations. Our results reveal that the ZnO bilayers exhibiting graphitic‐like structure are chemically inactive for water dissociation, whereas small ZnO clusters formed on top of these well‐defined, yet chemically passive supports show extremely high reactivity, water is dissociated without apparent activation barrier. Systematic isotopic substitution experiments using H 2 16 O/ D 2 16 O/D 2 18 O allow identifying various types of acidic hydroxyl groups. We demonstrate that a reliable characterization of these OH‐species is possible via coadsorption of CO, which leads to a red shift of the OD frequency due to the weak interaction via hydrogen bonding. The theoretical results provide atomic‐level insight into the surface structure and chemical activity of the supported ZnO clusters and allow identifying the presence of under‐coordinated Zn and O atoms at the edges and corners of the ZnO‐clusters as the active sites for H 2 O dissociation.

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