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1	Studium oxidace CO a metanolu za vysokého tlaku na katalyzátorech ve formě nanoprášků oxidů kovů vzácných zemin a tenkých vrstev na bázi platiny / High pressure CO and methanol oxidation study over nanopowders Rare Earth Oxides and platinum thin film catalysts Rednyk, Andrii January 2016 (has links) Title: High pressure CO and methanol oxidation study over nanopowder Rare Earth Oxides and platinum thin film catalysts Author: Mgr. Andrii Rednyk Department: Department of Surface and Plasma Science Supervisor: Prof. RNDr. Vladimír Matolín, DrSc. matolin@mbox.troja.mff.cuni.cz Abstract: This doctoral thesis focuses on reactivity study of nanopowder rare earth oxides (REOs) and platinum based thin film catalysts using microreactor with high pressure reaction cell. REOs nanoparticles were prepared by new approach based on sol-gel chemistry. Magnetron sputtering technique was used for preparation of thin film samples. In the first part of the thesis CO oxidation on REOs and on Pt, PtOx thin films were performed. Among prepared REOs catalyst better activity exhibited alumina stabilized ceria, due to higher surface area. Both Pt and PtOx deposited on silicon substrate exhibited similar activity. When carbon (G-foil or C interlayer) is used as support, activity of Pt thin film decreases while PtOx preserves high activity. In the second part of the thesis steam reforming of methanol (SRM) and partial oxidation of methanol (POM) were performed on Pt thin films. It was shown that PtOx thin film exhibited superior activity compared to other samples with the same thickness. It is due to the reduction of platinum...
2	First-principles simulations of the oxidation of methane and CO on platinum oxide surfaces and thin films Seriani, Nicola 10 November 2006 (has links) (PDF) The catalytic oxidation activity of platinum particles in automobile catalysts is thought to originate from the presence of highly reactive superficial oxide phases which form under oxygen-rich reaction conditions. The thermodynamic stability of platinum oxide surfaces and thin films was studied, as well as their reactivities towards oxidation of carbon compounds by means of first-principles atomistic thermodynamics calculations and molecular dynamics simulations based on density functional theory. On the Pt(111) surface the most stable superficial oxide phase is found to be a thin layer of alpha-PtO2, which appears not to be reactive towards either methane dissociation or carbon monoxide oxidation. A PtO-like structure is most stable on the Pt(100) surface at oxygen coverages of one monolayer, while the formation of a coherent and stress-free Pt3O4 film is favoured at higher coverages. Bulk Pt3O4 is found to be thermodynamically stable in a region around 900 K at atmospheric pressure. The computed net driving force for the dissociation of methane on the Pt3O4(100) surface is much larger than on all other metallic and oxide surfaces investigated. Moreover, the enthalpy barrier for the adsorption of CO molecules on oxygen atoms of this surface is as low as 0.34 eV, and desorption of CO2 is observed to occur without any appreciable energy barrier in molecular dynamics simulations. These results, combined, indicate a high catalytic oxidation activity of Pt3O4 phases that can be relevant in the contexts of Pt-based automobile catalysts and gas sensors. Catalysis carbon monoxide methane platinum oxide first-principles molecular dynamics thermodynamics computer simulation Katalyse Kohlenmonoxid Methan Platinoxid Ab-initio Molekulardynamik Thermodynamik Computersimulation ddc:620 rvk:VE 7047 Katalyse Oxidation Methan Kohlenmonoxid Platin Oberfläche Computersimulation
3	First-principles simulations of the oxidation of methane and CO on platinum oxide surfaces and thin films Seriani, Nicola 20 July 2006 (has links) The catalytic oxidation activity of platinum particles in automobile catalysts is thought to originate from the presence of highly reactive superficial oxide phases which form under oxygen-rich reaction conditions. The thermodynamic stability of platinum oxide surfaces and thin films was studied, as well as their reactivities towards oxidation of carbon compounds by means of first-principles atomistic thermodynamics calculations and molecular dynamics simulations based on density functional theory. On the Pt(111) surface the most stable superficial oxide phase is found to be a thin layer of alpha-PtO2, which appears not to be reactive towards either methane dissociation or carbon monoxide oxidation. A PtO-like structure is most stable on the Pt(100) surface at oxygen coverages of one monolayer, while the formation of a coherent and stress-free Pt3O4 film is favoured at higher coverages. Bulk Pt3O4 is found to be thermodynamically stable in a region around 900 K at atmospheric pressure. The computed net driving force for the dissociation of methane on the Pt3O4(100) surface is much larger than on all other metallic and oxide surfaces investigated. Moreover, the enthalpy barrier for the adsorption of CO molecules on oxygen atoms of this surface is as low as 0.34 eV, and desorption of CO2 is observed to occur without any appreciable energy barrier in molecular dynamics simulations. These results, combined, indicate a high catalytic oxidation activity of Pt3O4 phases that can be relevant in the contexts of Pt-based automobile catalysts and gas sensors. info:eu-repo/classification/ddc/620 ddc:620

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