Implications of coverage-dependent O adsorption for catalytic NO oxidation on the late transition metals
Author:
Affiliation:
1. Department of Chemical and Biomolecular Engineering
2. University of Notre Dame
3. Notre Dame, USA
4. Department of Materials Science and Engineering
5. Northwestern University
6. Evanston, USA
7. Department of Chemistry and Biochemistry
Abstract
Cluster-expansion-based kinetic model reveals that adsorbate interactions both promote and inhibit NO oxidation on the late transition metals.
Funder
National Science Foundation
U.S. Department of Energy
Publisher
Royal Society of Chemistry (RSC)
Subject
Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2014/CY/C4CY00763H
Reference38 articles.
1. Reactivity Theory of Transition-Metal Surfaces: A Brønsted−Evans−Polanyi Linear Activation Energy−Free-Energy Analysis
2. Configurational correlations in the coverage dependent adsorption energies of oxygen atoms on late transition metal fcc(111) surfaces
3. Understanding Trends in Catalytic Activity: The Effect of Adsorbate–Adsorbate Interactions for CO Oxidation Over Transition Metals
4. First-principles reaction site model for coverage-sensitive surface reactions: Pt(111)–O temperature programmed desorption
5. DFT-Based Coverage-Dependent Model of Pt-Catalyzed NO Oxidation
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