TY - JOUR
T1 - Influence of gold particle size on the aqueous-phase oxidation of carbon monoxide and glycerol
AU - Ketchie, William C.
AU - Fang, Yu Lun
AU - Wong, Michael S.
AU - Murayama, Mitsuhiro
AU - Davis, Robert J.
N1 - Funding Information:
This work was supported by the National Science Foundation (grants CTS-0313484, CTS-0624608, EEC-0118007, and EEC-0647452) and a 3M Nontenured Faculty Award. Partial support also was provided from the U.S. Department of Energy, Office of Basic Energy Sciences (grant DE-FG02-95ER14549).
PY - 2007/8/15
Y1 - 2007/8/15
N2 - Carbon-supported Au particles with mean sizes ranging from 5 to 42 nm and unsupported Au powder were evaluated as catalysts in the aqueous-phase oxidation of CO and glycerol. For the aqueous-phase oxidation of CO at pH 14 and 300 K, the turnover frequency (TOF) for the 5-nm Au particles was 5 s-1, whereas the TOF for large supported Au (42 nm) and bulk Au were only 0.5 and 0.4 s-1, respectively. The observed rate of peroxide formation during CO oxidation also was much higher on the small Au particles. Oxidation of glycerol in the aqueous phase at 333 K and elevated pH over the same catalysts revealed a similar influence of particle size, with the 5-nm Au particles giving a TOF of 17 s-1 at pH 13.8 and the larger particles and bulk Au nearly an order of magnitude less active. However, large Au particles (>20 nm) were more selective to glyceric acid. The lower selectivity of small Au particles is attributed to a higher formation rate of H2O2 during glycerol oxidation, because peroxide promotes C{single bond}C cleavage reaction.
AB - Carbon-supported Au particles with mean sizes ranging from 5 to 42 nm and unsupported Au powder were evaluated as catalysts in the aqueous-phase oxidation of CO and glycerol. For the aqueous-phase oxidation of CO at pH 14 and 300 K, the turnover frequency (TOF) for the 5-nm Au particles was 5 s-1, whereas the TOF for large supported Au (42 nm) and bulk Au were only 0.5 and 0.4 s-1, respectively. The observed rate of peroxide formation during CO oxidation also was much higher on the small Au particles. Oxidation of glycerol in the aqueous phase at 333 K and elevated pH over the same catalysts revealed a similar influence of particle size, with the 5-nm Au particles giving a TOF of 17 s-1 at pH 13.8 and the larger particles and bulk Au nearly an order of magnitude less active. However, large Au particles (>20 nm) were more selective to glyceric acid. The lower selectivity of small Au particles is attributed to a higher formation rate of H2O2 during glycerol oxidation, because peroxide promotes C{single bond}C cleavage reaction.
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U2 - 10.1016/j.jcat.2007.06.001
DO - 10.1016/j.jcat.2007.06.001
M3 - Article
AN - SCOPUS:34447638327
SN - 0021-9517
VL - 250
SP - 94
EP - 101
JO - Journal of Catalysis
JF - Journal of Catalysis
IS - 1
ER -