Abstract
Monometallic gold and iridium, and bimetallic gold–iridium on ceria catalysts were synthesized by deposition–precipitation with urea. The activity of these ceria supported catalysts for CO oxidation was: Au–Ir ≫ Au > Ir. The bimetallic catalyst was highly active and stable during the carbon monoxide oxidation reaction, showing synergism between both metals. The catalysts were thoroughly characterized chemical and structurally. High-resolution electron microscopy coupled with energy dispersive spectroscopy and X-ray photoelectron spectroscopy showed evidences of iridium–gold intimacy. In situ infrared spectroscopy in the diffuse reflectance mode was used to investigate the reactivity of the active sites. Concentration-modulation excitation spectroscopy allowed selective identification of intermediates and ‘spectator’ species. CO chemisorbed onto iridium sites (2096, 2060 and 2012 cm−1) was found inactive, whereas carbon monoxide on metallic gold sites (Au0–CO, 2110 cm−1) exhibited reactivity for CO oxidation. In the bimetallic catalyst, new active sites (Auδ−–CO, 2095 and 2026 cm−1) together with Au0–CO species were observed, most likely produced by the isolation and stabilization of gold atoms by iridium.
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Acknowledgments
The authors acknowledge the financial support from CAI + D 0100/11 (UNL), CONACYT 130407, PAPIIT 103513 and the bi-national project CONICET‐CONACYT (2013) and project SECTEI- Santa Fe No 2010-067-13. We thank V. Maturano-Rojas for technical assistance. We would also like to thank ANPCyT for the facilities of PME8-2003 and PME-2006-311. Antonio Aguilar Tapia gratefully acknowledges CONACYT for his PhD Scholarship.
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Aguirre, A., Barrios, C.E., Aguilar-Tapia, A. et al. In-Situ DRIFT Study of Au–Ir/Ceria Catalysts: Activity and Stability for CO Oxidation. Top Catal 59, 347–356 (2016). https://doi.org/10.1007/s11244-015-0425-6
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DOI: https://doi.org/10.1007/s11244-015-0425-6