We determine absolute reactivities for dissociation at low coordinated Pt sites. Two curved Pt(111) single-crystal surfaces allow us to probe either straight or highly kinked step edges with... Show moreWe determine absolute reactivities for dissociation at low coordinated Pt sites. Two curved Pt(111) single-crystal surfaces allow us to probe either straight or highly kinked step edges with molecules impinging at a low impact energy. A model extracts the average reactivity of inner and outer kink atoms, which is compared to the reactivity of straight A- and B-type steps. Local surface coordination numbers do not adequately capture reactivity trends for H(2)dissociation. We utilize the increase of reactivity with step density to determine the area over which a step causes increased dissociation. This step-type specific reactive area extends beyond the step edge onto the (111) terrace. It defines the reaction cross-section for H(2)dissociation at the step, bypassing assumptions about contributions of individual types of surface atoms. Our results stress the non-local nature of H(2)interaction with a surface and provide insight into reactivity differences for nearly identical step sites. Show less
Heterogeneous catalysis is essential to many industrial applications. These catalysts are often comprised of supported nanoparticles, which contain various different surface sites. For some... Show moreHeterogeneous catalysis is essential to many industrial applications. These catalysts are often comprised of supported nanoparticles, which contain various different surface sites. For some reactions, the presence of specific surface sights dominates the overall reactivity. Fundamental insight into the influence of different surface sites on the surface reaction dynamics may lead to better catalyst design in the future. In this thesis, we combine ultra-high vacuum techniques and (curved) single crystal surfaces to study surface structure effects relevant to heterogeneous catalysis. We study how step edges on a platinum surface affect (elementary) reactions that occur in oxygen reduction: hydrogen dissociation, hydrogen recombination, and oxygen reduction. Show less
Laan, P.C.M.; Franke, M.C.; Lent, R. van; Juurlink, L.B.F. 2019
A well-known demonstration is adapted to simplify the illustration of heterogeneous catalytic oxidation of ammonia. Various metal catalyst wires are placed above the liquid level in a flask... Show moreA well-known demonstration is adapted to simplify the illustration of heterogeneous catalytic oxidation of ammonia. Various metal catalyst wires are placed above the liquid level in a flask containing concentrated ammonia. After brief preheating, some metal wires continue to glow, providing visual evidence of an overall exothermic reaction taking place at the catalyst surface. Thermal heating by a butane flame prior to insertion and in situ resistive heating using a power supply yield identical results. Active catalysts are the group 9 and 10 elements Rh, Ir, Pd, and Pt. Besides the illustration of the Sabatier principle, the effect of the ammonia-to-oxygen ratio can also be visualized, and active metals vary in the production of a grayish smoke. These observations provide a starting point to discuss catalytic selectivity, a topic of great relevance to industrial catalytic oxidation of ammonia. Show less
