Abstract
The surface science of heterogeneous metal catalysis uses model systems ranging from single crystals to monodispersed nanoparticles in the 1–10 nm range. Molecular studies reveal that bond activation (C–H, H–H, C–C, C O) occurs at 300 K or below as the active metal sites simultaneously restructure. The strongly adsorbed molecules must be mobile to free up these sites for continued turnover of reaction. Oxide–metal interfaces are also active for catalytic turnover. Examples using C–H and C O activation are described to demonstrate these properties. Future directions include synthesis, characterization, and reaction studies with 2D and 3D monodispersed metal nanoclusters to obtain 100% selectivity in multipath reactions. Investigations of the unique structural, dynamic, and electronic properties of nanoparticles are likely to have major impact in surface technologies. The fields of heterogeneous, enzyme, and homogeneous catalysis are likely to merge for the benefit of all three.
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Dates
Type | When |
---|---|
Created | 19 years, 2 months ago (June 1, 2006, 8:57 p.m.) |
Deposited | 3 years, 4 months ago (April 12, 2022, 1:57 p.m.) |
Indexed | 2 days, 6 hours ago (Aug. 23, 2025, 9:31 p.m.) |
Issued | 19 years, 1 month ago (July 11, 2006) |
Published | 19 years, 1 month ago (July 11, 2006) |
Published Online | 19 years, 1 month ago (July 11, 2006) |
Published Print | 19 years, 1 month ago (July 11, 2006) |
@article{Somorjai_2006, title={Clusters, surfaces, and catalysis}, volume={103}, ISSN={1091-6490}, url={http://dx.doi.org/10.1073/pnas.0507691103}, DOI={10.1073/pnas.0507691103}, number={28}, journal={Proceedings of the National Academy of Sciences}, publisher={Proceedings of the National Academy of Sciences}, author={Somorjai, Gabor A. and Contreras, Anthony M. and Montano, Max and Rioux, Robert M.}, year={2006}, month=jul, pages={10577–10583} }