390172 Speciation and Reactivity of Small Fe, Cu, or Co Oxide Clusters Supported on Ceria and Silica

Wednesday, November 19, 2014: 9:30 AM
303 (Hilton Atlanta)
Justin M. Notestein1, Dario Prieto-Centurion1, Fabian Schax2, Scott Nauert1, Louisa Savereide1, Charles A. Roberts3 and Christian Limberg2, (1)Chemical and Biological Engineering, Northwestern University, Evanston, IL, (2)Institute for Chemistry, Humbolt University of Berlin, (3)Toyota Motor Engineering & Manufacturing North America, Inc., Ann Arbor, MI

The redox activity of supported metal oxides determines their utility in emissions abatement and their role in activation of H2 or O2 for chemicals synthesis. This talk describes two routes to controlling the redox activity of dispersed metal oxides. In the first part, we support Fe(III), Co(II), and Cu(II) oxides by incipient wetness impregnation of aqueous EDTA complexes of Fe, Cu, and Co on neat and alkali-modified CeO2, followed by calcination to give small clusters, following prior work on SiO2. [1] The catalysts are characterized principally by TPR, in situ XANES, and diffuse reflectance UV-visible spectroscopy (DRS), and it is seen that a larger fraction of the oxide is redox active in reversible 1-electron cycles than compared to impregnation with more typical precursors. This improvement in activity is hypothesized to be due to the presence of more uniform interactions between CeO2 and the oxide afforded by the bulky, anionic precursor. These materials are active in crotonaldehyde hydrogenation and H2-SCR of NO, with rates of the latter quantitatively correlated to the fraction of redox active sites.

In a second example, we deposit pre-formed clusters of Cu(I) oxides onto SiO2. The LxCuy clusters were previously synthesized as potential models for active sites in Cu-exchanged zeolites and in oxidase enzymes, where L are bridging siloxane ligands. [2] The Cu(I) oxidation state and some degree of the cluster structure is stabilized by incipient wetness impregnation onto SiO2, such that they are resistant to oxidative decomposition into bulk CuO up to ~400°C. These Cu(I) materials activate O2 at lower temperatures, as we demonstrate through their ability to carry out oxidative dehydrogenation of cyclohexane.

[1] Prieto-Centurion, D.; Boston, A. M.; Notestein, J. M., Structural and electronic promotion with alkali cations of silica-supported Fe(III) sites for alkane oxidation. J. Catal. 2012, 296, 77-85.

[2] Schax, F.; Limberg, C.; Mugge, C., Copper(I) Siloxides - Aggregated Solid-State Structures, Cu-Cu Interactions and Dynamic Solution Behavior. Eur. J. Inorg. Chem. 2012, 4661-4668.

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See more of this Session: Fundamentals of Oxide Catalysis I
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