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Construction and Reactivity of Pt-Based Bi-component Catalytic Systems
Title statement Construction and Reactivity of Pt-Based Bi-component Catalytic Systems [electronic resource] / by Rentao Mu. Publication Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer, 2017. Phys.des. XII, 90 p. 64 illus., 60 illus. in color. online resource. ISBN 9783662552445 Edition Springer Theses, Recognizing Outstanding Ph.D. Research, ISSN 2190-5053 Contents Introduction -- Experimental Methods -- Construction and Reactivity of Pt-Ni Catalysts -- Modulating the Structure and Reactivity of Pt-Ni Catalysts -- Comparison of Pt-Fe and Pt-Ni Catalysts -- Reactivity of Graphene-confined Pt(111) Surfaces -- Conclusions. Notes to Availability Přístup pouze pro oprávněné uživatele Another responsib. SpringerLink (Online service) Subj. Headings Chemistry. * Physical chemistry. * Catalysis. * Surfaces (Physics). * Interfaces (Physical sciences). * Thin films. * Materials - Surfaces. Form, Genre elektronické knihy electronic books Country Německo Language angličtina Document kind Electronic books URL Plný text pro studenty a zaměstnance UPOL book
In this thesis, the author outlines the construction of active structure and modulation of catalytic reactivity of Pt-based bi-component catalysts, from the model systems to real supported catalysts. The thesis investigates the promotion effect of the second components on catalytic performance of Pt catalysts, and presents the reversible generation of the “sandwich-like” structure of Pt-Ni catalysts, containing both surface NiO1-X and subsurface Ni by alternating redox treatments at medium temperature. With the aid of single layer graphene, the dynamic process of chemical reactions occurring on the Pt(111) surface can be visualized using in-situ LEEM and DUV-PEEM techniques, the results of which are included here. The author reveals that the graphene layer exhibits a strong confinement effect on the chemistry of molecules underneath and the intercalated CO can desorb from the Pt surface around room temperature and in UHV, which may promote the CO oxidation confined under graphene.
Introduction -- Experimental Methods -- Construction and Reactivity of Pt-Ni Catalysts -- Modulating the Structure and Reactivity of Pt-Ni Catalysts -- Comparison of Pt-Fe and Pt-Ni Catalysts -- Reactivity of Graphene-confined Pt(111) Surfaces -- Conclusions.
Number of the records: 1