Controlling Ethylene Hydrogenation Reactivity on Pt13 Clusters by Varying the Stoichiometry of the Amorphous Silica Support
Abstract
Ethylene hydrogenation was investigated on size‐selected Pt13 clusters supported on three amorphous silica (a‐SiO2) thin films with different stoichiometries. Activity measurements of the reaction at 300 K revealed that on a silicon‐rich and a stoichiometric film, Pt13 exhibits a similar activity to that of Pt(111), in line with the known structure insensitivity of the reaction. On an oxygen‐rich film, a threefold increased rate was measured. Pulsing ethylene at 400 K, then measuring the activity at 300 K, resulted in complete loss of activity on the silicon‐rich surface compared to only marginal losses on the other surfaces. The measured reactivity trends correlate with charging characteristics of a Pt13 cluster on the SiO2 films, predicted through first‐principle calculations. The results reveal that the stoichiometry‐dependent charging by the support can be used to tune the selectivity of reaction pathways during a catalytic hydrogenation reaction.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Jun 29, 2016
- Source ID
- 10.1002/ange.201603332
Entities
People
- Andrew S. Crampton
- Bokwon Yoon
- Florian F. Schweinberger
- Marian D. Rötzer
- Ueli Heiz
- Uzi Landman
Organizations
- Air Force Office of Scientific Research
- Georgia Tech
- German Research Foundation
- Harvard University
- Office of Basic Energy Sciences
- Technical University of Munich