Abstract

Using high resolution and ambient pressure X-ray photoelectron spectroscopy we show that the catalytically active FeO $$_{2}$$ trilayer films grown on Pt(111) are very active for water dissociation, in contrast to inert FeO(111) bilayer films. The FeO $$_{2}$$ trilayer is so active for water dissociation that it becomes hydroxylated upon formation, regardless of the applied preparation method. FeO $$_{2}$$ trilayers were grown by oxidation of FeO(111) bilayer films either with molecular oxygen in the mbar regime, or by NO $$_2$$ and atomic oxygen exposures, respectively, in the ultrahigh vacuum regime. Because it was impossible to prepare clean FeO $$_{2}$$ without any hydroxyls we propose that catalytically highly active FeO $$_{2}$$ trilayer films are generally hydroxylated. In addition, we provide spectroscopic fingerprints both for Pt(111)-supported FeO(111) and FeO $$_2$$ films that can serve as reference for future in situ studies.

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