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Probing the Nature of Active Centers in Pt–Cu/TiO2 Catalysts for Selective Ammonia Oxidation Full article

Journal The Journal of Physical Chemistry C
ISSN: 1932-7447 , E-ISSN: 1932-7455
Output data Year: 2024, Volume: 128, Number: 44, DOI: 10.1021/acs.jpcc.4c06021
Tags Bioremediation; Catalytic oxidation; Copper; High resolution transmission electron microscopy; Platinum; Platinum compounds; Redox reactions; X ray diffraction analysis
Authors Kibis Lidiya S. 1 , Ovsyuk Ivan Yu 1,2 , Popov Anton A. 3 , Svintsitskiy Dmitry A. 1 , Slavinskaya Elena M. 1 , Stonkus Olga A. 1 , Korenev Sergey V. 3 , Boronin Andrei I. 1
Affiliations
1 Boreskov Institute of Catalysis, Novosibirsk 630090, Russia
2 Novosibirsk State University, Novosibirsk 630090, Russia
3 Nikolaev Institute of Inorganic Chemistry, Novosibirsk 630090, Russia

Funding (1)

1 Russian Science Foundation 23-23-00322

Abstract: The activity and selectivity of catalytic systems are influenced by many important factors, such as the composition of the surface, the size and structure of the active sites, as well as the oxidation state of the active components. In this study, we investigated the nature of the active components in Pt/TiO2 catalysts for selective ammonia oxidation upon their modification with copper. Analysis using X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM) revealed that an increase in copper content led to a significant dispersion of platinum particles due to the formation of subnanoscale Pt(Cu)Ox species. Application of temperature-programmed reduction (TPR-H2) and X-ray photoelectron spectroscopy (XPS) techniques provided valuable data on the redox properties of the catalysts. The introduction of copper resulted in a notable increase in the fraction of oxidized platinum. Once reduced, platinum in the composition of the Pt–Cu/TiO2 catalysts was easily reoxidized upon subsequent exposure to oxygen already at room temperature. The Pt–Cu/TiO2 catalysts comprised oxidized copper species, which demonstrated more labile redox behavior at lower temperatures compared to the Cu/TiO2 catalyst. The facilitated redox transitions of the active components contributed to the enhanced selectivity of the Pt–Cu/TiO2 samples toward N2 by affecting the reaction mechanism. The obtained results provide new insights into key aspects governing the effective oxidation of slip ammonia at low temperatures.
Cite: Kibis L.S. , Ovsyuk I.Y. , Popov A.A. , Svintsitskiy D.A. , Slavinskaya E.M. , Stonkus O.A. , Korenev S.V. , Boronin A.I.
Probing the Nature of Active Centers in Pt–Cu/TiO2 Catalysts for Selective Ammonia Oxidation
The Journal of Physical Chemistry C. 2024. V.128. N44. DOI: 10.1021/acs.jpcc.4c06021 WOS Scopus РИНЦ OpenAlex
Dates:
Submitted: Sep 5, 2024
Accepted: Oct 22, 2024
Published online: Oct 29, 2024
Published print: Nov 7, 2024
Identifiers:
Web of science: WOS:001347186800001
Scopus: 2-s2.0-85208278042
Elibrary: 79165011
OpenAlex: W4403855236
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