Magnetron sputtering of gold nanoparticles onto WO3 and activated carbon

Gabriel M. Veith, Andrew R. Lupini, Stephen J. Pennycook, Alberto Villa, Laura Prati, Nancy J. Dudney

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Abstract

In this paper we describe the production and investigation of two supported gold catalyst systems prepared by magnetron sputtering: Au on WO3 and Au on activated carbon. The magnetron sputtering technique entails using an argon plasma to sputter a high purity gold target producing a flux of gold atoms which are deposited onto a constantly tumbling support material. This technique offers a number of advantages over conventional chemical preparation methods. One advantage is the ability to create gold nanoparticles (diameters <3 nm) on unusual support materials, such as WO3 and carbon, which are generally not accessible using the ubiquitous deposition-precipitation technique. We present data demonstrating the formation of catalytic gold nanoparticles with average diameters of 1.7 nm (Au/C) and 2.1 nm (Au/WO3), as well as a substantial number of single atom species on the Au/C sample. Prototypical carbon monoxide oxidation (Au/WO3) and glycerol oxidation (Au/C) reactions were performed in order to gauge the activity of these catalysts. The WO3 supported catalyst exhibits substantial catalytic activity from room temperature to 135 °C (0.0018-0.082 mol CO/mol Au s) with an activation energy near 23 kJ/mol. The activity of the Au/C catalyst was compared to a Au/C catalyst prepared from a poly(vinyl alcohol) (PVA) sol. The smaller catalysts prepared by sputtering are more active than the large gold particles prepared using the PVA sol, however the larger gold nanoparticles are substantially more selective towards the production of intermediate products from the oxidation of glycerol.

Original languageEnglish
Pages (from-to)248-253
Number of pages6
JournalCatalysis Today
Volume122
Issue number3-4
DOIs
StatePublished - Apr 30 2007

Funding

The authors would like to thank Mrs. Tamara Keever of Oak Ridge National Laboratories Chemical Sciences Division for assistance with ICP. The WO 3 support material was graciously provided by the H. C. Stark Chemical company. LP and AV are grateful for financial support from the Auricat EU network (HPRN-CT-2002-00174). The research performed at Oak Ridge National Laboratory was sponsored by the U.S. Department of Energy's Office of Basic Energy Sciences, Division of Materials Science and Engineering, under contract DE-AC05-00OR22725, with ORNL, managed & operated by UT-Battelle, LLC.

FundersFunder number
Auricat EU networkHPRN-CT-2002-00174
Division of Materials Science and EngineeringDE-AC05-00OR22725
Office of Basic Energy Sciences
U.S. Department of Energy
Oak Ridge National Laboratory

    Keywords

    • Aberration corrected
    • Acidic support
    • Glycerol oxidation
    • Gold catalyst
    • Scanning Transmission Electron Microscopy
    • Sputtering

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