Bimetallic Au–Pt Nanocomposites in the CO Oxidation Reaction: New Synthetic Approach and Evolution in the Course of Catalysis
- Авторлар: Budnikov A.1, Naumkin A.1, Said-Galiev E.1, Tret’yakov V.2, Vasil’kov A.1
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Мекемелер:
- Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
- Topchiev Institute of Petrochemical Synthesis, Russian Academy of Science
- Шығарылым: Том 483, № 1 (2018)
- Беттер: 251-255
- Бөлім: Chemistry
- URL: https://journals.rcsi.science/0012-5008/article/view/154123
- DOI: https://doi.org/10.1134/S0012500818110010
- ID: 154123
Дәйексөз келтіру
Аннотация
A combination of two green chemistry methods—fluid (supercritical carbon dioxide) and metal vapor synthesis—has afforded γ-Al2O3-based systems modified with Au, Pt, Au–Pt, and Pt–Au nanoparticles. It has been shown that bimetallic nanocomposites in the CO oxidation reaction are more efficient catalysts than monometallic systems. The composition of the Au–Pt/Al2O3 intermetallic compound and its evolution in the course of catalysis have been studied by X-ray photoelectron spectroscopy. It has been demonstrated that the increase in system activity during catalysis is accompanied by a significant rearrangement of the structure and composition of the nanocomposite surface.
Авторлар туралы
A. Budnikov
Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Email: alexandervasilkov@yandex.ru
Ресей, Moscow, 119991
A. Naumkin
Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Email: alexandervasilkov@yandex.ru
Ресей, Moscow, 119991
E. Said-Galiev
Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Email: alexandervasilkov@yandex.ru
Ресей, Moscow, 119991
V. Tret’yakov
Topchiev Institute of Petrochemical Synthesis, Russian Academy of Science
Email: alexandervasilkov@yandex.ru
Ресей, Moscow, 119991
A. Vasil’kov
Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Хат алмасуға жауапты Автор.
Email: alexandervasilkov@yandex.ru
Ресей, Moscow, 119991