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Methanol Oxidation on a Copper Catalyst Investigated Using in Situ X-ray Photoelectron Spectroscopy Научная публикация

Общее Язык: Английский, Жанр: Статья (Full article),
Статус опубликования: Опубликована, Оригинальность: Оригинальная
Журнал The Journal of Physical Chemistry B
ISSN: 1520-6106 , E-ISSN: 1520-5207
Вых. Данные Год: 2004, Том: 108, Номер: 38, Страницы: 14340-14347 Страниц : 8 DOI: 10.1021/jp040080j
Авторы Bluhm Hendrik 1 , Hävecker Michael 1 , Knop-Gericke Axel 1 , Kleimenov Evgueni 1 , Schlögl Robert 1 , Teschner Detre 2 , Bukhtiyarov Valerii I. 3 , Ogletree D.Frank 4 , Salmeron Miquel 4
Организации
1 Abteilung Anorganische Chemie, Fritz-Haber-Institut der Max-Planck-Gesellschaft, Faradayweg 4-6, D-14195 Berlin, Germany
2 Institute of Isotope & Surface Chemistry, CRC, Hungarian Academy of Sciences, P.O. Box 77, Budapest, H-1525 Hungary
3 Boreskov Institute of Catalysis, 6300090 Novosibirsk, Russia
4 Materials Sciences DiVision, Lawrence Berkeley National Laboratory, One Cyclotron Road, Berkeley, California 94720

Информация о финансировании (2)

1 United States Department of Energy DE-AC03-76SF00098
2 German Research Foundation Schl. 332/4-1

Реферат: The surface and near-surface regions of an active catalyst and the adjacent gas-phase reactants were investigated simultaneously under reaction conditions using in situ X-ray photoelectron spectroscopy (XPS). This investigation of methanol oxidation on a copper catalyst showed that there was a linear correlation between the catalytic activity of the sample and the presence of a subsurface oxygen species that can only be observed in situ. The concentration profile of the subsurface oxygen species within the first few nanometers below the surface was determined using photon-energy-dependent depth-profiling. The chemical composition of the surface and the near-surface regions varied strongly with the oxygen-to-methanol ratio in the reactant stream. The experiments show that the pure metal is not an active catalyst for the methanol oxidation reaction, but that a certain amount of oxygen has to be present in the subsurface region to activate the catalytic reaction. Oxide formation was found to be detrimental to formaldehyde production. Our results demonstrate also that for an understanding of heterogeneous catalysts a characterization of the surface alone may not be sufficient, and that subsurface characterization is essential.
Библиографическая ссылка: Bluhm H. , Hävecker M. , Knop-Gericke A. , Kleimenov E. , Schlögl R. , Teschner D. , Bukhtiyarov V.I. , Ogletree D.F. , Salmeron M.
Methanol Oxidation on a Copper Catalyst Investigated Using in Situ X-ray Photoelectron Spectroscopy
The Journal of Physical Chemistry B. 2004. V.108. N38. P.14340-14347. DOI: 10.1021/jp040080j WOS Scopus РИНЦ
Файлы: Полный текст от издателя
Даты:
Поступила в редакцию: 28 янв. 2004 г.
Принята к публикации: 25 мар. 2004 г.
Опубликована online: 14 мая 2004 г.
Опубликована в печати: 1 сент. 2004 г.
Идентификаторы:
Web of science WOS:000223922500018
Scopus 2-s2.0-4944266771
РИНЦ 13460171
Chemical Abstracts 2004:390665
Chemical Abstracts (print) 141:190414
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