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TiO2 Supported RuRe Nanocatalysts for Soot Oxidation: Effect of Re and the Support Nature

  • Katarzyna Adamska
  • , Szymon Smykała
  • , Sebastian Zieliński
  • , Damian Szymański
  • , Paweł Stelmachowski
  • , Andrzej Kotarba
  • , Janina Okal
  • , Leszek Kępiński
  • Polish Academy of Sciences
  • Jagiellonian University in Kraków

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

Catalytic combustion of hazardous particulate matter (soot) generated by automobile engines is a primary method of their elimination. Ruthenium-based catalysts are a promising alternative for traditional noble metal (Pt, Pd) based systems; however, their relatively poor thermal stability hinders wide applications. In this study, we synthesized a novel, highly active, and stable catalyst for soot oxidation containing bimetallic RuRe nanoparticles supported on TiO2. The RuRe NPs were synthesized by colloidal, microwave-assisted polyol method and deposited on rutile or anatase TiO2. The effect of rhenium content and the nature of TiO2 support on the performance of RuRe nanoparticles (NPs) in the soot oxidation under air atmosphere was investigated. Bimetallic RuRe/TiO2 nanocatalysts exhibited higher activity in the soot oxidation than Ru/TiO2 systems, and the rutile supported 2 wt% Ru–0.4 wt% Re nanocatalyst (Ru/Re atomic ratio of 9:1) showed the best catalytic performance (T50 = 340 °C and T90 < 400 °C). All studied nanocatalysts were stable under reaction conditions in the consecutive catalytic tests. The exceptional catalytic performance of bimetallic RuRe NPs is explained by the synergy effect between ruthenium, rhenium, and TiO2. Graphical Abstract: [Figure not available: see fulltext.]

Original languageEnglish
Pages (from-to)1372-1389
Number of pages18
JournalCatalysis Letters
Volume153
Issue number5
DOIs
Publication statusPublished - May 2023

Keywords

  • Anatase
  • Bimetallic RuRe NPs
  • Rutile
  • Soot oxidation
  • Synergetic effect
  • TiO nature

ASJC Scopus subject areas

  • Catalysis
  • General Chemistry

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