Electronic and Structural Properties of Thin Iron Oxide Films on CeO 2 .

Modification of CeO 2 (ceria) with 3d transition metals, particularly iron, has been proven to significantly enhance its catalytic efficiency in oxidation or combustion reactions. Although this phenomenon is widely reported, the nature of the iron-ceria interaction responsible for this improvement remains debated. To address this issue, we prepared well-defined model FeO x /CeO 2 (111) catalytic systems and studied their structure and interfacial electronic properties using photoelectron spectroscopy, scanning tunneling microscopy, and low-energy electron diffraction, coupled with density functional theory (DFT) calculations. Our results show that under ultrahigh vacuum conditions, Fe deposition leads to the formation of small FeO x clusters on the ceria surface. Subsequent annealing results in the growth of large amorphous FeO x particles and a 2D FeO x layer. Annealing in an oxygen-rich atmosphere further oxidizes iron up to the Fe 3+ state and improves the crystallinity of both the 2D layer and the 3D particles. Our DFT calculations indicate that the 2D FeO x layer interacts strongly with the ceria surface, exhibiting structural corrugations and transferred electrons between Fe 2+ /Fe 3+ and Ce 4+ /Ce 3+ redox pairs. The novel 2D FeO x /CeO 2 (111) phase may explain the enhancement of the catalytic properties of CeO 2 by iron. Moreover, the corrugated 2D FeO x layer can serve as a template for the ordered nucleation of other catalytically active metals, in which the redox properties of the 2D FeO x /CeO 2 (111) system are exploited to modulate the charge of the supported metals.