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Ultrafast Probing of CO Reactions on Metal Surfaces : Changes in the molecular orbitals during the catalysis process

Gladh, Jörgen, 1964- (author)
Stockholms universitet,Fysikum,Kemisk fysik
Öström, Henrik, Doktor (thesis advisor)
Stockholms universitet,Fysikum
Mårtensson, Nils, Professor (opponent)
Uppsala University
 (creator_code:org_t)
ISBN 9789176494417
Stockholm : Department of Physics, Stockholm University, 2017
English 54 s.
  • Doctoral thesis (other academic/artistic)
Abstract Subject headings
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  • This thesis presents experimental studies of three different chemical reaction steps relevant for heterogeneous catalysis: dissociation, desorption, and oxidation. CO on single-crystal metal surfaces was chosen as the model systems.X-ray absorption spectroscopy (XAS) and x-ray emission spectroscopy (XES) provide information about the electronic structure, and were performed on CO/Fe to measure both a non-dissociative, and a pre-dissociative state. The measurement on the pre-dissociative state showed a π →  π* excitation, which implies a partly broken internal π bond in the molecule.Ultrafast laser-induced reactions were used to examine the dynamic properties of desorption and oxidation. Here CO/Ru and CO/O/Ru were used as model systems. Desorption of CO from a Ru surface involve both hot electrons and phonons. In the case of CO oxidation from CO/O/Ru a pronounced wavelength dependence of the branching ratio between desorption and oxidation was observed. Excitation with 400 nm showed a factor of 3-4 higher selectivity towards oxidation than 800 nm. This was attributed to coupling to transiently excited, non-thermalized electrons.Finally, by performing optical pump/x-ray probe XAS and XES changes in the electronic structure during the reaction could be followed, both for desorption and oxidation. In the CO/Ru experiment, two different transient excitation paths were observed, one leading to a precursor state, and one where CO moves into a more highly coordinated site. Using selective excitation in XES, these were shown to coexist on the surface. In the oxidation experiment, probing the reacting species located near the transition state region in an associative catalytic surface reaction was demonstrated for the very first time.

Subject headings

NATURVETENSKAP  -- Fysik -- Atom- och molekylfysik och optik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Atom and Molecular Physics and Optics (hsv//eng)

Keyword

Hetrogenous catalysis
CO
transition metals
Ultrafast probing
oxidation
desorption
dissociation
kemisk fysik
Chemical Physics

Publication and Content Type

vet (subject category)
dok (subject category)

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