Evidence of charge transfer to atomic and molecular adsorbates on graphitic-like ZnO/X(111) (X = Cu, Ag, Au) ultrathin films

15 November 2017, Version 1
This content is a preprint and has not undergone peer review at the time of posting.


ZnO bilayers grown on Cu(111), Ag(111), and Au(111) surfaces form graphitic-like flat structures. They belong to the class of two-dimensional materials. We show, by means of density functional theory (DFT) calculations including dispersion, that Au, NO2, and O2 species adsorbed on ZnO/Cu(111) induce a spontaneous net charge transfer (CT) via electron tunneling from the Cu support through the insulating ZnO film, resulting in the formation of negatively charged atomic, Au-, or molecular, NO2- and O2-, adsorbates. We show for the case of gold that the CT is found also for ZnO/Ag(111) and ZnO/Au(111) interfaces. The stabilization of the anionic species is accompanied by a polaronic distortion of the ZnO lattice. Other molecules with low electron affinity such as NO and CO2, on the contrary, do not induce the CT. However, charge transfer and activation of two CO2 molecules to form an oxalate species, [C2O4]2-, is promoted by a single Au anion, and similar catalytic activity is expected for the negatively charged Au clusters. By comparing the properties of the metal supported ZnO films with those of the free-standing ZnO bilayer, we demonstrate the key role of the metal/oxide interface. These results are relevant in the field of methanol synthesis based on ZnO/Cu catalysts where ultrathin layers of ZnO supported on Cu are formed under reaction conditions.


graphitic-like ZnO
charge transfer
CO2 activation


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