4.6 Article

Microstructure of Bimetallic PtPd Catalysts under Oxidizing Conditions

期刊

CHEMCATCHEM
卷 5, 期 9, 页码 2636-2645

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cctc.201300181

关键词

EXAFS spectroscopy; bimetallic catalysts; palladium; platinum; structure elucidation

资金

  1. NSF [GOALI CBET-1067803, IGERT DGE-0504276, PIRE OISE-0730277, CBET 0960256]
  2. Department of Energy
  3. MRCAT
  4. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
  5. Institute for Atom-Efficient Chemical Transformations (IACT), an Energy Frontier Research Center
  6. U.S. Department of Energy, Office of Basic Energy Sciences [DE-AC02-98CH10886]
  7. Directorate For Engineering
  8. Div Of Chem, Bioeng, Env, & Transp Sys [1067803] Funding Source: National Science Foundation

向作者/读者索取更多资源

Diesel oxidation catalysts (DOCs), which decrease the amount of harmful carbon monoxide (CO), nitrogen oxide (NO), and hydrocarbon (HC) emissions in engine exhaust, typically utilize Pt and Pd in the active phase. There is universal agreement that the addition of Pd improves both the catalytic performance and the durability of Pt catalysts. However, the mechanisms by which Pd improves the performance of Pt are less clear. Because these catalysts operate under oxidizing conditions, it is important to understand these catalysts in their working state. Herein, we report the microstructure of PtPd catalysts that are aged in air at 750 degrees C. After 10h of aging, EXAFS and XANES analysis show that the Pt is fully reduced but that almost 30% of the Pd species are present as an oxide. HRTEM images show no evidence of surface oxides on the metallic PtPd particles. Instead, the PdO is present as a separate phase that is dispersed over the alumina support. Within the metallic particles, Pt and Pd are uniformly distributed and there is no evidence of core-shell structures. Therefore, the improved catalytic performance is likely associated with the co-existence of metallic Pt and Pd on the catalyst surface.

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