| Autor: |
Molina DL; Department of Chemistry, University of Illinois at Chicago, 845 W Taylor St., Chicago, Illinois 60607, USA., Muir M; Department of Chemistry, University of Illinois at Chicago, 845 W Taylor St., Chicago, Illinois 60607, USA., Abdel-Rahman MK; Department of Chemistry, University of Illinois at Chicago, 845 W Taylor St., Chicago, Illinois 60607, USA., Trenary M; Department of Chemistry, University of Illinois at Chicago, 845 W Taylor St., Chicago, Illinois 60607, USA. |
| Abstrakt: |
We have used reflection absorption infrared spectroscopy (RAIRS) and temperature programmed reaction (TPR) to study the selective hydrogenation of acetylene on both a clean Ag(111) surface and on a Pd/Ag(111) single-atom-alloy surface. The partial hydrogenation of acetylene to ethylene is an important catalytic process that is often carried out using PdAg alloys. It is challenging to study the reaction with ultrahigh vacuum techniques because H 2 does not dissociate on Ag(111), and while H 2 will dissociate at Pd sites, H-atom spillover from Pd to Ag sites does not generally occur. We bypassed the H 2 dissociation step by exposing the surfaces to atomic hydrogen generated by the hot filament of an ion gauge. We find that hydrogen atoms react with acetylene to produce adsorbed ethylene at 85 K, the lowest temperature studied. This is revealed by the appearance of a RAIRS peak at 950 cm -1 due to the out-of-plane wagging mode of adsorbed ethylene when acetylene is exposed to a surface on which H atoms are pre-adsorbed. The formation of both ethylene and ethane are detected with TPR, but no acetylene coupling products, such as benzene, were found. From quantitative analysis of the TPR results, the percent conversion and selectivities to ethylene and ethane were determined. Low coverages of Pd enhance the conversion but do so mainly by increasing ethane formation. |
