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Reaction selectivity in heterogeneous catalysis

An invited review

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Abstract

The understanding of selectivity in heterogeneous catalysis is of paramount importance to our society today. In this review we outline the current state of the art in research on selectivity in heterogeneous catalysis. Current in-situ surface science techniques have revealed several important features of catalytic selectivity. Sum frequency generation vibrational spectroscopy has shown us the importance of understanding the reaction intermediates and mechanism of a heterogeneous reaction, and can readily yield information as to the effect of temperature, pressure, catalyst geometry, surface promoters, and catalyst composition on the reaction mechanism. DFT calculations are quickly approaching the ability to assist in the interpretation of observed surface spectra, thereby making surface spectroscopy an even more powerful tool. HP-STM has revealed three vitally important parameters in heterogeneous selectivity: adsorbate mobility, catalyst mobility and selective site-blocking. The development of size controlled nanoparticles from 0.8 to 10 nm, of controlled shape, and of controlled bimetallic composition has revealed several important variables for catalytic selectivity. Lastly, DFT calculations may be paving the way to guiding the composition choice for multi-metallic heterogeneous catalysis for the intelligent design of catalysts incorporating the many factors of selectivity we have learned.

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Authors and Affiliations

  1. Department of Chemistry, University of California, Berkeley, California, 94720, USA

    Gabor A. Somorjai & Christopher J. Kliewer

  2. Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, 94720, USA

    Gabor A. Somorjai & Christopher J. Kliewer

Authors
  1. Gabor A. Somorjai
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  2. Christopher J. Kliewer
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Correspondence to Gabor A. Somorjai.

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Somorjai, G.A., Kliewer, C.J. Reaction selectivity in heterogeneous catalysis. React Kinet Catal Lett 96, 191–208 (2009). https://doi.org/10.1007/s11144-009-5531-7

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  • DOI: https://doi.org/10.1007/s11144-009-5531-7

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