AVS 65th International Symposium & Exhibition | |
Surface Science Division | Tuesday Sessions |
Session SS+HC+NS+PS-TuM |
Session: | Controlling Mechanisms of Surface Chemical Reactions |
Presenter: | Dipna Patel, Tufts University |
Authors: | D.A. Patel, Tufts University E.C.H. Sykes, Tufts University |
Correspondent: | Click to Email |
Ni is one of the most extensively used industrial catalytic metals. Utilized for steam reforming of hydrocarbons, Ni atom ensembles detrimentally catalyze the formation of graphitic carbon which leads to coking and deactivation of the catalyst. By alloying Ni into Cu, a catalytically less active host metal, our single-atom alloy approach has the potential to greatly enhance catalytic selectivity and reduce poisoning, analogous to other systems such as Pt-Cu and Pd-Cu. First, we report characterization of the atomic-scale surface structure and local geometry of low coverages of Ni deposited on a Cu(111) single crystal, using scanning tunneling microscopy. Near room temperature, Ni preferentially alloys into the Cu host by forming Ni rich brims along ascending step edges. Next, temperature programmed desorption studies reveal that CO binds more weakly to single Ni atoms in Cu compared to larger Ni ensembles in Ni(111) which is promising for catalytic applications in which CO poisoning is an issue. This characterization of Ni-Cu surface alloys the catalytic activity and selectivity of the surface to be correlated with the atomic-scale structure of the alloy. Using this approach, the catalytic selectivity and resilience to poisoning can be tuned via both ligand and ensemble effects.