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Titlebook: Construction and Reactivity of Pt-Based Bi-component Catalytic Systems; Rentao Mu Book 2017 Springer-Verlag GmbH Germany 2017 Bi-component

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楼主: 自治
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,Construction and Reactivity of Pt–Ni Catalysts,t the high reduction in temperature can induce more Ni diffuse inward. Upon the reduction at 523 K, the sandwich-like structure with half Ni on the surface and another half Ni inside the nanoparticle can be formed, which shows high CO oxidation reactivity.
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2190-5053 ates the correlation between the surface structure and reactIn 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 ef
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Reactivity of Graphene-Confined Pt(111) Surface, K. DFT calculations show the adsorption energy of CO on Pt(111) is decreased by the confinement effect of graphene on top. Furthermore, the dynamic process of CO oxidation is also studied. We find that the graphene wrinkles act as the reaction channels for CO desorption and CO oxidation processes.
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Book 2017om 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
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https://doi.org/10.1007/978-3-476-05780-8 Pt-skin surface is observed. The catalysts pretreated at low temperatures show high CO oxidation reactivity due to the formation of the sandwich-like structure with surface and subsurface Ni species.
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,Modulating the Structure and Reactivity of Pt–Ni Catalysts, Pt-skin surface is observed. The catalysts pretreated at low temperatures show high CO oxidation reactivity due to the formation of the sandwich-like structure with surface and subsurface Ni species.
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,Construction and Reactivity of Pt–Ni Catalysts,O. and subsurface Ni performs best CO oxidation reactivity. The surface NiO. provides active sites for O. dissociative adsorption. The subsurface Ni lowers the barrier for CO + O elemental reaction. As thus, the synergetic effect of surface NiO. and subsurface Ni promotes CO oxidation on Pt. The eff
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