CO Oxidation on Technological Pd-Al2O3 Catalysts: Oxidation State and Activity
Artikel i vetenskaplig tidskrift, 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

Författare

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, Teknisk fysik, Kemisk fysik

Kompetenscentrum katalys (KCK)

G. Rupprechter

Technische Universitat Wien

Journal of Physical Chemistry C

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

Vol. 115 4 1103-1111

Styrkeområden

Nanovetenskap och nanoteknik

Energi

Materialvetenskap

Fundament

Grundläggande vetenskaper

Ämneskategorier (SSIF 2011)

Atom- och molekylfysik och optik

Kemi

DOI

10.1021/jp106235x

Mer information

Skapat

2017-10-07