Identification of active sites in CO oxidation and water-gas shift over supported Pt catalysts

Author:

Ding Kunlun1,Gulec Ahmet2,Johnson Alexis M.1,Schweitzer Neil M.3,Stucky Galen D.4,Marks Laurence D.2,Stair Peter C.15

Affiliation:

1. Department of Chemistry, Northwestern University, Evanston, IL 60208, USA.

2. Department of Materials Science and Engineering, Northwestern University, Evanston, IL 60208, USA.

3. Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL 60208, USA.

4. Department of Chemistry and Biochemistry, University of California, Santa Barbara, CA 93106, USA.

5. Chemical Sciences and Engineering Division, Argonne National Laboratory, Argonne, IL 60439, USA.

Abstract

Comparing active site reactivity Noble metal nanoparticles often exhibit behaviors distinct from atomic and bulk versions of the same material. Gold and platinum dispersed on metal oxide supports, for example, show remarkable low-temperature reactivity for carbon monoxide (CO) oxidation by oxygen or water. Ding et al. used infrared spectroscopy to identify CO adsorbed on isolated platinum atoms or nanoparticles dispersed on zeolite and oxide supports. Temperature-programmed desorption studies showed that CO reacted at much lower temperatures when adsorbed on nanoparticles versus on isolated metal atoms. Science , this issue p. 189

Funder

U.S. National Science Foundation

National Science Foundation

Northwestern University Institute for Catalysis in Energy Processes (ICEP)

Materials Research and Engineering Center

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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