4.8 Article

Surface Noble Metal Concentration on Ceria as a Key Descriptor for Efficient Catalytic CO Oxidation

Journal

ACS CATALYSIS
Volume 12, Issue 4, Pages 2473-2486

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.1c04565

Keywords

In situ characterization; nanoparticle formation; Raman spectroscopy; X-ray absorption spectroscopy; surface diffusion; proximity effect; surface noble metal concentration

Funding

  1. Fonds der Chemischen Industrie (FCI) of the Verband der Chemischen Industrie e.V. (VCI)
  2. state of Baden Wurttemberg [bwl17D011]
  3. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [SFB 1441 - Project-ID 426888090, INST 121384/16-1, INST 121384/73-1, BMWi: 19U15014B]
  4. French National Research Agency [ANR-14-CE22-0011-02]
  5. DESY (Hamburg, Germany)
  6. Karlsruhe Nano Micro Facility (KNMF)
  7. Helmholtz Research Infrastructure at KIT [I-20210886]
  8. Agence Nationale de la Recherche (ANR) [ANR-14-CE22-0011] Funding Source: Agence Nationale de la Recherche (ANR)

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Increasing the Pt surface concentration can decrease the ignition temperature of CO oxidation and enhance the stability of the Pt/CeO2 catalyst. The improved reaction rate at higher Pt surface concentrations is attributed to the formation of larger oxidized Pt clusters and the aggregation of highly dispersed Pt species. The influence of the Pt surface noble metal concentration on the reaction rate is temporarily diminished when Pt particle formation is forced.
During the CO oxidation over metallic Pt clusters and Pt nanoparticles in Pt/CeO2 catalysts, we found that the Pt surface concentration is a key descriptor for the reaction rate. By increasing the surface noble metal concentration (SNMC) of a Pt/CeO2 catalyst by a factor of similar to 4, while keeping the weight hourly space velocity constant, the ignition temperature of CO oxidation was decreased by similar to 200 degrees C in the as-prepared state. Moreover, the stability was enhanced at higher SNMC. Complementary characterization and theoretical calculations unraveled that the origin of this improved reaction rate at higher Pt surface concentrations can be traced back to the formation of larger oxidized Pt-clusters and the SNMC-dependent aggregation rate of highly dispersed Pt species. The Pt diffusion barriers for cluster formation were found to decrease with increasing SNMC, promoting more facile agglomeration of active, metallic Pt particles. In contrast, when Pt particle formation was forced with a reductive pretreatment, the influence of the SNMC was temporarily diminished, and all catalysts showed a similar CO oxidation activity. The work shows the general relevance of the proximity influence in the formation and stabilization of active centers in heterogeneous catalysis.

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