The technical relevance of Rh, Pd, and Pt as catalysts used to reduce (Formula presented) pollutants has stimulated great interest in a detailed understanding of the chemisorption process of these systems. While experiment indicates Rh to be a better catalyst than the other transition metals, theory still does not give a satisfying explanation for this behavior. We have examined the c(2×2) atop chemisorption of NO on Rh, Pd, and Pt substrates with our full-potential linearized augmented-plane-wave method for thin films. Simultaneous relaxation of the NO bond length and the distance between the metal and N, as well as surface relaxation of the metal, was performed. Various vibration frequencies were determined from the dynamical matrix of the system. The analysis of the dynamical matrix shows stronger bonding of NO to Pd and Pt compared to the Rh surface. We find the metal surface to be strongly affected by NO chemisorption, including a buckling that is about 50% larger on Pd and Pt than on the Rh surface. While the calculated electronic properties, such as density of states, give very similar results for the three systems the geometric and dynamical properties may explain the observed higher efficiency of Rh as a catalyst.
|Original language||English (US)|
|Number of pages||6|
|Journal||Physical Review B - Condensed Matter and Materials Physics|
|State||Published - Jan 1 1997|
ASJC Scopus subject areas
- Electronic, Optical and Magnetic Materials
- Condensed Matter Physics