Rare-earth-doped ceria nanostructures for oxidation of soot with different reactivities: Role of catalyst restructuring and surface acidity in soot-catalyst contact renewal

Catalytic soot oxidation is a key process for particulate filter regeneration, yet catalyst performance is often evaluated using a single soot type, overlooking the strong influence of soot physicochemical properties on oxidation behavior. In this work, the impact of intrinsic soot reactivity on catalytic oxidation was systematically investigated using soot samples with distinct structural, textural, and chemical characteristics. Model flame soots and commercial carbon blacks with different initial reactivity were oxidized over three ceria-based nanostructured catalysts, i.e. pure ceria, equimolar ceria–praseodymia, and equimolar ceria-lanthana. Catalytic activity was assessed under loose and tight contact conditions by temperature-programmed oxidation, complemented by kinetic analysis and stepwise oxidation experiments combined with high-resolution transmission electron microscopy. Regardless of the catalyst, soot reactivity was primarily governed by nanostructural order, as reflected by fringe length, primary particle size, and C/H ratio. Rare earth-doped ceria catalysts exhibited enhanced activity compared to pure ceria, with ceria-lanthana showing the lowest oxidation temperatures in all conditions and the smallest sensitivity to contact degree. This behavior mainly arises from its higher surface acidity, combined with highly abundant surface oxygen species, improved oxygen storage and release capacity, and morphology-induced contact enhancement. HRTEM observations revealed that Ce50La50 dynamically restructures during oxidation, continuously generating new soot-catalyst contact sites that sustain activity under limited-contact conditions. These results highlight the critical interplay between soot properties, catalyst surface chemistry and contact dynamics, thus providing guidance for the rational design of soot oxidation catalysts combining high activity with robustness under operating conditions. • Six soot samples with different origins, properties, and reactivities were compared • Three ceria-based catalysts were employed to oxidize soot in tight and loose contact • Equimolar ceria-lanthana always outperformed ceria-praseodymia and pure ceria • Activity was mainly linked to the presence of active oxygen species and acid sites • Catalyst restructuring and continuous renewal of soot contact points were observed

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Journal
Journal of environmental chemical engineering
Published
2026-05-01
DOI
https://doi.org/10.1016/j.jece.2026.123057
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
0.00

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article

Rare-earth-doped ceria nanostructures for oxidation of soot with different reactivities: Role of catalyst restructuring and surface acidity in soot-catalyst contact renewal

Samir Bensaid, Dimosthenis Trimis, H. Bockhorn, Enrico Sartoretti et al.
Journal of environmental chemical engineering
Catalytic Processes in Materials Science
article

Rare-earth-doped ceria nanostructures for oxidation of soot with different reactivities: Role of catalyst restructuring and surface acidity in soot-catalyst contact renewal

Samir Bensaid, Dimosthenis Trimis, H. Bockhorn, Enrico Sartoretti, Fabian P. Hagen, Chiara Novara, Marco Piumetti
article en

Abstract

Catalytic soot oxidation is a key process for particulate filter regeneration, yet catalyst performance is often evaluated using a single soot type, overlooking the strong influence of soot physicochemical properties on oxidation behavior. In this work, the impact of intrinsic soot reactivity on catalytic oxidation was systematically investigated using soot samples with distinct structural, textural, and chemical characteristics. Model flame soots and commercial carbon blacks with different initial reactivity were oxidized over three ceria-based nanostructured catalysts, i.e. pure ceria, equimolar ceria–praseodymia, and equimolar ceria-lanthana. Catalytic activity was assessed under loose and tight contact conditions by temperature-programmed oxidation, complemented by kinetic analysis and stepwise oxidation experiments combined with high-resolution transmission electron microscopy. Regardless of the catalyst, soot reactivity was primarily governed by nanostructural order, as reflected by fringe length, primary particle size, and C/H ratio. Rare earth-doped ceria catalysts exhibited enhanced activity compared to pure ceria, with ceria-lanthana showing the lowest oxidation temperatures in all conditions and the smallest sensitivity to contact degree. This behavior mainly arises from its higher surface acidity, combined with highly abundant surface oxygen species, improved oxygen storage and release capacity, and morphology-induced contact enhancement. HRTEM observations revealed that Ce50La50 dynamically restructures during oxidation, continuously generating new soot-catalyst contact sites that sustain activity under limited-contact conditions. These results highlight the critical interplay between soot properties, catalyst surface chemistry and contact dynamics, thus providing guidance for the rational design of soot oxidation catalysts combining high activity with robustness under operating conditions. • Six soot samples with different origins, properties, and reactivities were compared • Three ceria-based catalysts were employed to oxidize soot in tight and loose contact • Equimolar ceria-lanthana always outperformed ceria-praseodymia and pure ceria • Activity was mainly linked to the presence of active oxygen species and acid sites • Catalyst restructuring and continuous renewal of soot contact points were observed

Journal of environmental chemical engineering
Politecnico di Torino (IT), DVGW-Forschungsstelle am Engler-Bunte-Institut des Karlsruher Instituts für Technologie (DE)
Forschungsvereinigung Verbrennungskraftmaschinen
Openalex Percentile: Top 11%
Catalytic Processes in Materials Science
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