CO Oxidation on Technological Pd-Al2O3 Catalysts: Oxidation State and Activity
Journal article, 2011

The specific CO oxidation activity of palladium versus palladium oxide is still controversially discussed. In this study, 5 wt. % Pd-gamma-Al2O3 catalysts were utilized to investigate the effect of the palladium oxidation state on the CO oxidation activity. Comprehensive in situ and ex situ characterization of different alumina supported PdOx (x = 0-1) phases (by HR-TEM, XRD, and FTIR spectroscopy), combined with kinetic measurements and DFT calculations of CO adsorption, allowed us to assess the catalytic activity of the different PdOx (x = 0-1) species: Supported Pd-0 and substoichiometric PdOx<1 exhibited comparable high activities, due to a rapid reduction of PdOx<1 to Pd upon CO exposure. PdO nanoparticles showed a lower catalytic activity resulting from their higher stability against reduction by CO. The limited extent of oxidation of Pd under typical reaction conditions together with the facile reduction of substoichiometric PdOx<1 suggest that the active phase present under the current reaction conditions is oxygen-covered metallic Pd.

reflection-absorption spectroscopy

ultrahigh-vacuum

single-crystal surfaces

sum-frequency generation

scanning-tunneling-microscopy

supported palladium catalysts

pd nanoparticles

functional theory calculations

model catalysts

metals

pt-group

Author

K. Zorn

Technische Universitat Wien

S. Giorgio

CNRS Centre National de la Recherche Scientifique

E. Halwax

Technische Universitat Wien

C. R. Henry

CNRS Centre National de la Recherche Scientifique

Henrik Grönbeck

Chalmers, Applied Physics, Chemical Physics

Competence Centre for Catalysis (KCK)

G. Rupprechter

Technische Universitat Wien

Journal of Physical Chemistry C

1932-7447 (ISSN) 1932-7455 (eISSN)

Vol. 115 4 1103-1111

Areas of Advance

Nanoscience and Nanotechnology

Energy

Materials Science

Roots

Basic sciences

Subject Categories (SSIF 2011)

Atom and Molecular Physics and Optics

Chemical Sciences

DOI

10.1021/jp106235x

More information

Created

10/7/2017