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Size and composition dependence in CO oxidation reaction on small free gold, silver, and binary silver–gold cluster anions
- Source :
-
Applied Catalysis A: General . Sep2005, Vol. 291 Issue 1/2, p170-178. 9p. - Publication Year :
- 2005
-
Abstract
- Abstract: Gas phase kinetics experiments with mass-selected gold, silver, and binary silver–gold cluster ions in a radio frequency (rf)-ion trap reactor are presented. For the catalytic CO combustion reaction, the adsorption of molecular oxygen onto the free clusters is identified as the first reaction step. A comparison of the measured O2 adsorption reaction rate constants for the investigated Ag n Au m − (n + m =1, 2, 3) clusters reveals a pronounced size and composition dependence. Favorable activation of the oxygen molecular bond is only expected in the case of Au2 −. In the reaction of the gold dimer with O2 and CO, a coadsorption complex is identified at cryogenic temperatures as decisive reaction intermediate in the observed CO oxidation reaction. Through detailed reaction kinetics measurements in combination with first-principles calculations, a comprehensive understanding of the molecular details of the catalytic reaction cycle emerges. The obtained data also permit the determination of the CO2 formation rate and the catalytic turn-over-frequency in the rf-ion trap reactor. In contrast to gold, odd size silver cluster anions are found to adsorb two oxygen molecules. These Ag n O4 − complexes are proposed to be key intermediates in oxidation reactions with silver clusters involved, and first experimental indications for catalytic activity of selected cluster sizes are presented. [Copyright &y& Elsevier]
- Subjects :
- *OXIDATION
*CHEMICAL kinetics
*SILVER ions
*CATALYSIS
Subjects
Details
- Language :
- English
- ISSN :
- 0926860X
- Volume :
- 291
- Issue :
- 1/2
- Database :
- Academic Search Index
- Journal :
- Applied Catalysis A: General
- Publication Type :
- Academic Journal
- Accession number :
- 18234062
- Full Text :
- https://doi.org/10.1016/j.apcata.2005.02.041