ISSN:
1572-879X
Keywords:
Concepts of catalysis
;
activity trends
;
surface restructuring
;
cluster-like bonding
;
rough surface reactivity
;
building complex catalyst systems
;
bimetallic systems
;
oxide-metal interfaces
Source:
Springer Online Journal Archives 1860-2000
Topics:
Chemistry and Pharmacology
Notes:
Abstract The roles of the atomic structure and the electronic structure of the active surface sites in bonding of reactants and causing bond breaking or bond formation have been the focus of theoretical studies. In addition to calculations on static systems, usually clusters, modelling of the transition states and the dynamics of elementary reaction steps (adsorption, dissociation, surface diffusion, desorption) have been performed. Variations of electronic structure of elements across the periodic table have been shown to be responsible for the unique importance of transition metals in catalysis. Experimental studies utilize catalysts with well-characterized structure (zeolites, crystal surfaces) and information about surface structure, composition and chemical bonding of adsorbates becomes available on the molecular level. Deliberate alteration of catalyst structure, surface composition by alloying and electronic structure by addition of electron donor and electron acceptor promoters have been utilized to modify reaction rates and selectivity. This way many of the molecular ingredients of heterogeneous catalytic reactions have been identified. In recent years evidence has been accumulating that indicates periodic and long term restructuring of the catalyst surface as necessary for chemical change and reaction turnover. These findings point to the need of time resolved studies and in-situ investigations of both the substrate and the adsorbate sides of the surface chemical bonds simultaneously on a time scale shorter than the reaction turnover frequency. Close collaboration between theorists and experimentalists is essential if we are to succeed in designing heterogeneous catalysts.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF00773188
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