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Structure-Dependent CO and NO Oxidation over Bimetallic PtPd/Al$_{2}$O$_{3}$ Catalysts: Impact of Pt–Pd Mixing and Alloying on Activity and Stability

Czechowsky, Joachim ORCID iD icon 1; Dolcet, Paolo 1; Maliakkal, Carina B. 2,3; Popescu, Radian 4; Kübel, Christian ORCID iD icon 2,3; Behrens, Silke 5; Türk, Michael ORCID iD icon 6; Wolf, Moritz ORCID iD icon 5,7; Gross, Silvia 1; Grunwaldt, Jan-Dierk ORCID iD icon 1,5; Casapu, Maria ORCID iD icon 1
1 Institut für Technische Chemie und Polymerchemie (ITCP), Karlsruher Institut für Technologie (KIT)
2 Institut für Nanotechnologie (INT), Karlsruher Institut für Technologie (KIT)
3 Karlsruhe Nano Micro Facility (KNMF), Karlsruher Institut für Technologie (KIT)
4 Laboratorium für Elektronenmikroskopie (LEM), Karlsruher Institut für Technologie (KIT)
5 Institut für Katalyseforschung und -technologie (IKFT), Karlsruher Institut für Technologie (KIT)
6 Institut für Technische Thermodynamik und Kältetechnik (TTK), Karlsruher Institut für Technologie (KIT)
7 Engler-Bunte-Institut (EBI), Karlsruher Institut für Technologie (KIT)

Abstract:

The influence of the noble metal nanoparticle structure on the activity and stability of bimetallic PtPd/Al$_2$O$_3$ catalysts was systematically investigated. Various conventional and advanced synthesis methods were used to tune the initial Pt–Pd mixing/alloying extent. By using complementary characterization techniques, pronounced differences in the CO and NO oxidation activity could be correlated with variations in the noble metal oxidation state, particle size, and composition. The beneficial effect of Pt–Pd mixing/alloying in catalysts predominantly containing noble metal nanoparticles with a surface-averaged size smaller than ∼5 nm was revealed for the CO, NO, and combined CO/NO oxidation reactions. In this regard, colloidal methods enabled the formation of homogeneously alloyed PtPd particles with a narrow size distribution and superior catalytic activity at low temperatures. However, the presence of uniform PtPd bimetallic particles did not prevent catalyst deactivation, as pronounced noble metal sintering and segregation phenomena still occurred during hydrothermal aging. In contrast, for applications operating at temperatures exceeding 600 °C, catalysts with a less uniform initial structure exhibited improved stability.


Verlagsausgabe §
DOI: 10.5445/IR/1000198265
Veröffentlicht am 22.10.2026
Cover der Publikation
Zugehörige Institution(en) am KIT Engler-Bunte-Institut (EBI)
Institut für Katalyseforschung und -technologie (IKFT)
Institut für Nanotechnologie (INT)
Institut für Technische Chemie und Polymerchemie (ITCP)
Institut für Technische Thermodynamik und Kältetechnik (TTK)
Karlsruhe Nano Micro Facility (KNMF)
Laboratorium für Elektronenmikroskopie (LEM)
Publikationstyp Zeitschriftenaufsatz
Publikationsdatum 05.11.2026
Sprache Englisch
Identifikator ISSN: 1932-7447, 1932-7455
KITopen-ID: 1000198265
HGF-Programm 38.03.04 (POF IV, LK 01) Technical Fuel Assessment
Erschienen in The Journal of Physical Chemistry C
Verlag American Chemical Society (ACS)
Band 130
Heft 44
Seiten 15242–15264
Vorab online veröffentlicht am 21.10.2026
Nachgewiesen in Scopus
OpenAlex
Web of Science
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