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Ambient Pressure Photoemission Spectroscopy Reveals the Mechanism of Carbon Soot Oxidation in Ceria‐Based Catalysts
Author(s) -
Soler Lluís,
Casanovas Albert,
Escudero Carlos,
PérezDieste Virginia,
Aneggi Eleonora,
Trovarelli Alessandro,
Llorca Jordi
Publication year - 2016
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201600615
Subject(s) - soot , x ray photoelectron spectroscopy , catalysis , oxygen , carbon fibers , combustion , chemical engineering , materials science , phase (matter) , oxygen storage , cubic zirconia , nox , chemistry , inorganic chemistry , organic chemistry , metallurgy , composite material , ceramic , composite number , engineering
Removing soot is one of the most important challenges in minimizing the impact of combustion engines on the environment. Catalysts based on CeO 2 have proved suitable to oxidize soot owing to their capacity to store and release oxygen easily while maintaining structural integrity, although their mode of operation in a complex environment involving two solid phases (catalyst and soot) and a gas phase (oxygen) is not yet fully understood. Herein, we provide a study of the surface/subsurface of ceria–soot and ceria–zirconia–soot mixtures under working conditions by means of near‐ambient‐pressure photoelectron spectroscopy. Soot abatement involves two cooperative routes: one occurring at the ceria–soot interface with formation of oxygen vacancies and Ce III and the other at the surface of soot, mediated by active superoxide species, which result from the reaction between gas‐phase O 2 and oxygen vacancies. The two routes occur simultaneously and mutually reinforce each other.