4.8 Article

Regenerative trapping: How Pd improves the durability of Pt diesel oxidation catalysts

期刊

APPLIED CATALYSIS B-ENVIRONMENTAL
卷 218, 期 -, 页码 581-590

出版社

ELSEVIER
DOI: 10.1016/j.apcatb.2017.06.085

关键词

Catalyst sintering; Pt-Pd; Diesel oxidation catalysts; Accelerated aging; Ostwald ripening

资金

  1. NSF GOALI [CBET-1438765]
  2. Chemical and Materials Systems Lab at GM Global RD
  3. U.S. Department of Energy's National Nuclear Security Administration [DE-AC04-94AL85000]
  4. Div Of Chem, Bioeng, Env, & Transp Sys
  5. Directorate For Engineering [1438765] Funding Source: National Science Foundation

向作者/读者索取更多资源

Pt is an active component in diesel oxidation catalysts (DOCs) but it ripens to form large particles at elevated temperatures due to significant vapor phase transport of PtO2. Adding Pd improves the durability of the catalyst but there is no clear consensus in the literature for the responsible mechanism. In this study, we examined the role of PtO2 vapor pressure on sintering. The vapor pressure of PtO2 was determined by measuring the emission of Pt using planar model catalysts and electron probe microanalysis (EPMA). Significant emission of Pt to the vapor phase was observed in a Pt/SiO2 model catalyst that was aged in flowing air at 800 degrees C. Adding Pd lowered the rate of emission, and so did decreasing the oxygen concentration. Lowering of the vapor pressure of PtO2 led to a decreased rate of sintering. However, the most significant decrease in sintering rate was observed in the presence of excess PdO. The excess PdO serves to trap mobile Pt species, resulting in significantly smaller Pt-Pd particles after aging in air at 800 degrees C for 10 h. When PtO2 is emitted from a metallic Pt-Pd particle it can result in the formation of a separate PdO phase. Hence, in these catalysts the PdO is regenerated in the course of catalyst sintering. We propose that regenerative trapping of mobile Pt species by PdO plays an important role in improving the durability of Pt-Pd bimetallic catalysts. (C) 2017 Elsevier B.V. All rights reserved.

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