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Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
Published on: November 9, 2019
Reduction of NO by CO on unsupported Ir: bridging the materials gap
Wenhua Chen1, Quantong Shen, Robert A Bartynski
1Department of Physics and Astronomy and Laboratory for Surface Modification, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854, USA. wchen@physics.rutgers.edu
Abstract:
Temperature programmed desorption (TPD) and density functional theory (DFT) are used to investigate adsorption sites and reaction of coadsorbed NO and CO on planar Ir(210) and faceted Ir(210) with tailored sizes of three-sided nanopyramids exposing (311), (31 1) and (110) faces. Both planar and faceted Ir(210) are highly active for reduction of NO by CO with high selectivity to N(2), which is accompanied by simultaneous oxidation of CO. Evidence is found for structure sensitivity in adsorption sites and reaction of coadsorbed NO and CO on faceted Ir(210) versus planar Ir(210). Strong interaction between NO and CO at high NO exposure and one-monolayer CO pre-coverage results in "explosive" evolution of N(2) and CO(2) on planar Ir(210) and size effects in reduction of NO by CO on faceted Ir(210) for average facet size ranging from 5 to 14 nm without change in facet structure.
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