Carbon in palladium catalysts: A metastable carbide

Author(s)
Nicola Seriani, Florian Mittendorfer, Georg Kresse
Abstract

The catalytic activity of palladium toward selective hydrogenation of hydrocarbons depends on the partial pressure of hydrogen. It has been suggested that the reaction proceeds selectively toward partial hydrogenation only when a carbon-rich film is present at the metal surface. On the basis of first-principles simulations, we show that carbon can dissolve into the metal because graphite formation is delayed by the large critical nucleus necessary for graphite nucleation. A bulk carbide Pd6C with a hexagonal six-layer fcc-like supercell forms. The structure is characterized by core level shifts of 0.66-0.70 eV in the core states of Pd, in agreement with experimental x-ray photoemission spectra. Moreover, this phase traps bulk-dissolved hydrogen, suppressing the total hydrogenation reaction channel and fostering partial hydrogenation.

Organisation(s)
Computational Materials Physics
Journal
Journal of Chemical Physics
Volume
132
No. of pages
8
ISSN
0021-9606
DOI
https://doi.org/10.1063/1.3290813
Publication date
2010
Peer reviewed
Yes
Austrian Fields of Science 2012
103009 Solid state physics, 103015 Condensed matter, 103025 Quantum mechanics, 103036 Theoretical physics
Portal url
https://ucrisportal.univie.ac.at/en/publications/ac1e7c45-0385-46ac-8b43-156cf1f2ecc2