Stabilization of Copper Catalysts for Liquid‐Phase Reactions by Atomic Layer Deposition1. (26th November 2013)

• Record Type: Journal Article
• Authors: O'Neill, Brandon J.; Jackson, David H. K.; Crisci, Anthony J.; Farberow, Carrie A.; Shi, Fengyuan; Alba‐Rubio, Ana C.; Lu, Junling; Dietrich, Paul J.; Gu, Xiangkui; Marshall, Christopher L.; Stair, Peter C.; Elam, Jeffrey W.; Miller, Jeffrey T.; Ribeiro, Fabio H.; Voyles, Paul M.; Greeley, Jeffrey; Mavrikakis, Manos; Scott, Susannah L.; Kuech, Thomas F.; Dumesic, James A.
• Is Part Of: Angewandte Chemie. Volume 125:Number 51(2013)
• Page Start: 14053
• Page End: 14057
• Publication Date: 2013-11-26
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201308245
• Languages: English
• ISSNs: 0044-8249

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Atomic layer deposition (ALD) of an alumina overcoat can stabilize a base metal catalyst (e.g., copper) for liquid‐phase catalytic reactions (e.g., hydrogenation of biomass‐derived furfural in alcoholic solvents or water), thereby eliminating the deactivation of conventional catalysts by sintering and leaching. This method of catalyst stabilization alleviates the need to employ precious metals (e.g., platinum) in liquid‐phase catalytic processing. The alumina overcoat initially covers the catalyst surface completely. By using solid state NMR spectroscopy, X‐ray diffraction, and electron microscopy, it was shown that high temperature treatment opens porosity in the overcoat by forming crystallites of γ‐Al₂O₃. Infrared spectroscopic measurements and scanning tunneling microscopy studies of trimethylaluminum ALD on copper show that the remarkable stability imparted to the nanoparticles arises from selective armoring of under‐coordinated copper atoms on the nanoparticle surface.</p> </abstract>