| Autor: |
Wagner J; The James Franck Institute and Department of Chemistry, The University of Chicago, 929 East 57th Street, Chicago, Illinois 60637, United States., Grabnic T; The James Franck Institute and Department of Chemistry, The University of Chicago, 929 East 57th Street, Chicago, Illinois 60637, United States., Sibener SJ; The James Franck Institute and Department of Chemistry, The University of Chicago, 929 East 57th Street, Chicago, Illinois 60637, United States. |
| Abstrakt: |
This paper examines the reactive surface dynamics of energy- and angle-selected N 2 dissociation on a clean Ru(0001) surface. Presented herein are the first STM images of highly energetic N 2 dissociation on terrace sites utilizing a novel UHV instrument that combines a supersonic molecular beam with an in situ STM that is in-line with the molecular beam. Atomically resolved visualization of individual N 2 dissociation events elucidates the fundamental reactive dynamics of the N 2 /Ru(0001) system by providing a detailed understanding of the on-surface dissociation dynamics: the distance and angle between nitrogen atoms from the same dissociated N 2 molecule, site specificity and coordination of binding on terrace sites, and the local evolution of surrounding nanoscopic areas. These properties are precisely measured over a range of impinging N 2 kinetic energies and angles, revealing previously unattainable information about the energy dissipation channels that govern the reactivity of the system. The experimental results presented in this paper provide insight into the fundamental N 2 dissociation mechanism that, in conjunction with ongoing theoretical modeling, will help determine the role of dynamical processes such as energy transfer to surface phonons and nonadiabatic excitation of electron-hole pairs (ehps). These results will not only help uncover the underlying chemistry and physics that give rise to the unique behavior of this activated dissociative chemisorption system but also represent an exciting approach to studying reaction dynamics by pairing the angstrom-level spatiotemporal resolution of an in situ STM with nonequilibrium fluxes of reactive gases generated in a supersonic molecular beam to access highly activated chemical dynamics and observe the results of individual reaction events.
Competing Interests: The authors declare no competing financial interest.
(© 2022 The Authors. Published by American Chemical Society.) |
