Methane oxidation over alumina supported platinum investigated by time-resolved in situ XANES spectroscopy
Artikel i vetenskaplig tidskrift, 2007

In situ time-resolved X-ray absorption spectroscopy and mass spectrometry were used to correlate changes in catalyst surface composition with catalytic activity for methane oxidation over alumina supported Pt. Different transient experiments (i.e., pulsing of oxygen or hydrogen to an otherwise constant gas composition) were performed to study the methane oxidation kinetics. Changes in the surface O/Pt ratio were monitored by the introduction of a new analysis method of the white line area corresponding to the Pt L-III-edge XANES spectra. The relevance of the method was confirmed by first-principles calculations demonstrating how hydrogen and oxygen adsorbates modify the electronic structure of Pt. The experimental results show that during the gas-phase transients, the surface O/Pt ratio changes, which in turn affects the methane oxidation rate. Activity maxima are observed for an intermediate surface O/Pt ratio. An oxygen-rich surface seems to hinder the dissociative adsorption of methane, leading to low methane oxidation activity at oxygen excess.

transient methods

platinum oxide

dissociative adsorption

Pt

heterogeneous catalysis

CH4

X-ray absorption spectroscopy

Pt/Al2O3

Författare

Elin Becker

Kompetenscentrum katalys (KCK)

Chalmers, Kemi- och bioteknik, Teknisk ytkemi

Per-Anders Carlsson

Chalmers, Kemi- och bioteknik

Kompetenscentrum katalys (KCK)

Henrik Grönbeck

Chalmers, Teknisk fysik, Kemisk fysik

Kompetenscentrum katalys (KCK)

Magnus Skoglundh

Kompetenscentrum katalys (KCK)

Chalmers, Kemi- och bioteknik

Journal of Catalysis

0021-9517 (ISSN) 1090-2694 (eISSN)

Vol. 252 11-17

Drivkrafter

Hållbar utveckling

Styrkeområden

Nanovetenskap och nanoteknik

Transport

Energi

Materialvetenskap

Ämneskategorier

Fysikalisk kemi

Kemiteknik

DOI

10.1016/j.jcat.2007.09.004