Growth and structural studies of In/Au(111) alloys and InOx/Au(111) inverse oxide/metal model catalysts

氧化物 反向 材料科学 金属 催化作用 冶金 化学 数学 几何学 有机化学
作者
Jindong Kang,Mausumi Mahapatra,Ning Rui,Ivan Orozco,Rui Shi,Sanjaya D. Senanayake,José A. Rodríguez
出处
期刊:Journal of Chemical Physics [American Institute of Physics]
卷期号:152 (5) 被引量:9
标识
DOI:10.1063/1.5139237
摘要

Indium oxide has received attention as an exciting candidate for catalyzing the CO2 hydrogenation to methanol due to its high selectivity (>80%). Compared to the extent of research on the activity of indium oxide-based powder catalysts, very little is known about the phenomena associated with the formation of surface alloys involving indium or the growth mechanism for indium oxide nanoparticles. In this report, scanning tunneling microscopy and X-ray photoelectron spectroscopy (XPS) were employed to elucidate the growth mode, structure, and chemical state of In/Au(111) alloys and InOx/Au(111) inverse model catalysts. Our study reveals distinct morphological differences between In/Au(111) and InOx/Au(111), and the InOx structure also depends strongly on the preparation conditions. In/Au surface alloy systems with extremely low coverage (0.02 ML) form islands preferentially on the elbow sites of reconstructed Au(111) herringbone, regardless of hexagonally closed packed and face centered cubic stacking. At higher coverage (0.1 ML), the In islands expand over the herringbone in the ⟨110⟩ direction and create two dimensional domain structures over the entire surfaces. Moreover, this 2D domain structure is disturbed by temperature with high dispersion of indium atoms observed during the annealing process. Oxidation of the In/Au(111) surface alloys with O2 at 550 K produces InOx/Au(111) systems which contain various sizes of InOx aggregates (from 0.7 nm to 10 nm). On the other hand, InOx/Au(111) surfaces prepared by vapor deposition of In at 550 K in an O2 background exhibit highly dispersed and uniformly small InOx particles (∼1 nm). Both InOx systems were confirmed to be partially oxidized by XPS.
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