Abstract

The electronic structure of multimetal, amorphous oxides can be varied across a wide range of elemental compositions. Bulk properties such as conductivity, work function, and absorption can thus be tailored to suit a range of applications spanning from carrier-selective contacts to catalysis. Missing, however, is an understanding of how the surface reactivity is impacted in mixed metal-oxide amorphous films. Here we investigate the propensity of Al(1–x)M(x)Oy (M = Fe, Mn) amorphous oxide films to dissociate water into hydroxyl groups in a humid environment and find comparable hydroxylation at the low relative humidity (∼0.3% RH) probed by ambient pressure X-ray photoelectron spectroscopy. In contrast, films with both Al and Fe show an increased formation of methoxy groups upon methanol exposure compared to pure Al- and Fe-oxide end members, indicating that the coordination environment of the amorphous oxide network impacts the acidity and redox character of surface metal and oxygen sites. These results pr...

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