Abstract
Supported gold nanoparticles have generated an immense interest in the field of catalysis due to their extremely high reactivity and selectivity. Recently, alloy nanoparticles of gold have received a lot of attention due to their enhanced catalytic properties. Here we report the synthesis of silica supported AuCu nanoparticles through the conversion of supported Au nanoparticles in a solution of Cu(C2H3O2) 2 at 300 °C. The AuCu alloy structure was confirmed through powder XRD (which indicated a weakly ordered alloy phase), XANES, and EXAFS. It was also shown that heating the AuCu/SiO2 in an O2 atmosphere segregated the catalyst into a Au-CuOx heterostructure between 150 °C to 240 °C. Heating the catalyst in H2 at 300 °C reduced the CuOx back to Cu0 to reform the AuCu alloy phase. It was found that the AuCu/SiO2 catalysts were inactive for CO oxidation. However, various pretreatment conditions were required to form a highly active and stable Au-CuOx/SiO2 catalyst to achieve 100% CO conversion below room-temperature. This is explained by the in situ FTIR result, which shows that CO molecules can be chemisorbed and activated only on the Au-CuOx/SiO2 catalyst but not on the AuCu/SiO2 catalyst.
Original language | English |
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Pages (from-to) | 2571-2581 |
Number of pages | 11 |
Journal | Physical Chemistry Chemical Physics |
Volume | 13 |
Issue number | 7 |
DOIs | |
State | Published - Feb 21 2011 |