Researchers Find Controls To Gold Nanocatalysis
Researchers at the Georgia Institute of Technology have made a discovery that could allow scientists to exercise more control over the catalytic activity of gold nanoclusters.
The finding – that the dimensionality and structure, and thus the catalytic activity, of gold nanoclusters changes as the thickness of their supporting metal-oxide films is varied – is an important one in the rapidly developing field of nanotechnology.
This and further advances in nanocatalysis may lead to lowering the cost of manufacturing materials from plastics to fertilizers.
The research appeared in the July 21, 2006 issue of the journal Physical Review Letters.
"We've been searching for methods for controlling and tuning the nanocatalytic activity of gold nanoclusters," said Uzi Landman, director of the Center for Computational Materials Science and Regents' professor and Callaway chair of physics at Georgia Tech. "I believe the effect we discovered, whereby the structure and dimensionality of supported gold nanoclusters can be influenced and varied by the thickness of the underlying magnesium-oxide film may open new avenues for controlled nanocatalytic activity," he said.
Landman's research group has been exploring the catalytic properties of gold, which is inert in its bulk form, for about seven years. In 1999, along with the experimental group of Ueli Heiz and Wolf-Dieter Schneider at the University of Lausanne, Landman's group showed that gold exhibits remarkable catalytic capabilities to speed the rate of chemical reactions if it is clustered in groups of eight to about two dozen atoms in size.
Last year in the journal Science, the teams of Landman and Heiz (now at the Technical University of Munich) showed that this catalytic activity involves defects, in the form of missing oxygen atoms, in the catalytic bed on which the gold clusters rest. These defect sites, referred to as F-centers, serve as sites for the gold to anchor itself, giving the gold clusters a slight negative charge.
The charged gold transfers an electron to the reacting molecules, weakening the chemical bonds that keep them together. Once the bond is sufficiently weakened, it may be broken, allowing reactions to occur between the adsorbed reactants.
Now Landman's group has found that by using a thin catalytic bed with a thickness of up to 1 nanometer (nm), or 4-5 layers, of magnesium oxide, one may activate the gold nanoclusters which may act then as catalysts even if the bed is defect-free.
A model reaction tested in these studies is one where carbon monoxide and molecular oxygen combine to form carbon dioxide, even at low temperatures. In these reactions, the bond connecting the two atoms in the adsorbed oxygen molecule weakens, thus, promoting the reaction with CO.
"Structures of a gold cluster (depicted by yellow spheres) containing 20 atoms, adsorbed on a magnesium oxide bed ( magnesium in green and oxygen in red) which is itself supported on top of a molybdenum substrate (blue spheres). The excess electronic charge at the interface is depicted in pink and the charge depletion is shown in light blue. Credit: Uzi Landman/Georgia Tech"
Source: Georgia Institute of Technology
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