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Use of the Differential Charging Effect in XPS to Determine the Nature of Surface Compounds Resulting from the Interaction of a Pt/(BaCO3 + CeO2) Model Catalyst with SOx Full article

Journal Kinetics and Catalysis
ISSN: 0023-1584 , E-ISSN: 1608-3210
Output data Year: 2011, Volume: 52, Number: 4, Pages: 595-604 Pages count : 10 DOI: 10.1134/S0023158411040161
Tags Barium Sulfate; Cerium Dioxide; Barium Carbonate; Tantalum Foil; Electron Photoemission
Authors Smirnov M.Y. 1 , Kalinkin A.V. 1 , Dubkov A.A. 2 , Vovk E.I. 1 , Sorokin A.M. 1 , Nizovskii A.I. 1 , Carberry B.P. 2 , Bukhtiyarov V.I. 1,3
Affiliations
1 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090, Russia
2 Ford Forschungszentrum Aachen GmbH, Aachen, D-52072, Germany
3 Novosibirsk State University, Novosibirsk, 630090, Russia

Abstract: Changes in the chemical composition of the surface of a Pt/(BaCO3 + CeO2) model NO x storage-reduction catalyst upon its interaction with SO x (SO2 (260 Pa) + O2 (2600 Pa) + H2O (525 Pa)) followed by regeneration in a mixture of CO (2100 Pa) with H2O (525 Pa) were studied by X-ray photoelectron spectroscopy (XPS). Model catalyst samples were prepared as a thin film (about several hundreds of angstrom units in thickness) on the surface of tantalum foil coated with a layer of aluminum oxide (∼100 Å). It was found that the Pt/BaCO3 and Pt/CeO2 catalyst constituents acquired different surface charges (differential charging) in the course of photoelectron emission; because of this, it was possible to determine the nature of surface compounds formed as a result of the interaction of the catalyst with a reaction atmosphere. It was found that barium carbonate was converted into barium sulfate as a result of reaction with SO x on the surface of BaCO3 at 150°C. As the treatment temperature in SO x was increased to 300°C, the formation of sulfate on the surface of CeO2 was observed. The sulfatization of CeO2 was accompanied by the reduction of Ce(IV) to Ce(III). The regeneration reaction of the catalyst treated in SO x at 300°C resulted in the consecutive decomposition of cerium(III) sulfate at ≤500°C and then barium sulfate at 600–700°C. Upon the decomposition of BaSO4, a portion of sulfur was converted into a sulfide state, probably, because of the formation of BaS.
Cite: Smirnov M.Y. , Kalinkin A.V. , Dubkov A.A. , Vovk E.I. , Sorokin A.M. , Nizovskii A.I. , Carberry B.P. , Bukhtiyarov V.I.
Use of the Differential Charging Effect in XPS to Determine the Nature of Surface Compounds Resulting from the Interaction of a Pt/(BaCO3 + CeO2) Model Catalyst with SOx
Kinetics and Catalysis. 2011. V.52. N4. P.595-604. DOI: 10.1134/S0023158411040161 WOS Scopus РИНЦ ANCAN OpenAlex
Original: Смирнов М.Ю. , Калинкин А.В. , Дубков А.А. , Вовк Е.И. , Сорокин А.М. , Низовский А.И. , Карберри Б. , Бухтияров В.И.
Использование эффекта дифференциальной зарядки в методе РФЭС для установления природы поверхностных соединений, образующихся при взаимодействии с SOx модельного катализатора Pt/(BaCO3+ CeO2)
Кинетика и катализ. 2011. Т.52. №4. С.605-614. РИНЦ
Dates:
Submitted: Nov 9, 2010
Published print: Jul 1, 2011
Published online: Aug 7, 2011
Identifiers:
Web of science: WOS:000293639300019
Scopus: 2-s2.0-80051625242
Elibrary: 18058802
Chemical Abstracts: 2011:985796
Chemical Abstracts (print): 155:570206
OpenAlex: W1996225335
Citing:
DB Citing
Web of science 9
Scopus 7
Elibrary 7
OpenAlex 8
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