4.6 Article

Tuning the Placement of Pt Single Atoms on a Mixed CeO2-TiO2 Support

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume -, Issue -, Pages -

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.2c05198

Keywords

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Funding

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences ( U.S. DOE BES) [DE-SC0022199]
  2. U.S. DOE BES [DE-SC0012704]
  3. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division, Catalysis Science program
  4. U.S. DOE Early Career Award
  5. DOE Office of Science by Brookhaven National Laboratory [DE-SC0012704]
  6. Synchrotron Catalysis Consortium ( U.S. DOE, Office of Basic Energy Sciences) [DE-SC0012335]
  7. U.S. DOE Office of Science Facility, at Brookhaven National Laboratory [DE-SC0012704]
  8. U.S. Department of Energy (DOE) [DE-SC0022199] Funding Source: U.S. Department of Energy (DOE)

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This study successfully created and controlled unique sites for Pt SACs on CeO2 support by designing anchoring sites. By changing the Pt weight loading, the placement of Pt atoms on the mixed oxide surface can be tuned.
Defect sites on the oxide supports can be used to anchor and activate single-atom catalysts (SACs). By engineering the anchoring sites for supporting SACs, one can alter their electronic and atomic structures which, in turn, define their activity, selectivity, and stability for catalytic reactions. To create and tune unique sites for Pt SACs on CeO2 support, in this work, we synthesized a system consisting of CeO2 decorated on TiO2 nano-oxides for supporting the Pt SACs and investigated the effect of Pt weight loading. A combination of multiple structural characterization methods including diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), X-ray photoelectron spectroscopy (XPS), and X-ray absorption spectroscopy (XAS) was employed to characterize the distribution of charge states of single atoms and evaluate the heterogeneity of their binding sites. We have found that the placement of Pt atoms can be tuned on a mixed oxide surface by changing the weight loading of Pt.

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