The work in this thesis demonstrates how to obtain an atomic-scale picture of a diverse set of complex surface structures observed using STM, under disparate conditions. Chapters 4−6 each represent... Show moreThe work in this thesis demonstrates how to obtain an atomic-scale picture of a diverse set of complex surface structures observed using STM, under disparate conditions. Chapters 4−6 each represent a different approach to answer the same question: How can we find out what a surface looks like at the atomic scale? By employing appropriate theoretical tools that complement the experimental conditions and measurement techniques, it is possible to compare the results from theory and experiment in an intuitive manner to obtain additional insights. Additionally, Chapter 4 shows that theoretical studies, which do not take experimental conditions into account appropriately, can lead to wrong conclusions. Show less
This thesis focuses on the synthesis, characterization and performance towards CO2 electroreduction of mono and bi-metallic particles based on p-block metals. With an industrial perspective in mind... Show moreThis thesis focuses on the synthesis, characterization and performance towards CO2 electroreduction of mono and bi-metallic particles based on p-block metals. With an industrial perspective in mind, we try to synthesize particulate, high surface area materials with clean, scalable synthesis methods where possible and test their performance in H-Cell and gas diffusion electrode flow cell configurations. With a combination of characterization techniques, we find possible explanations for the catalytic behaviors. Show less
In surface science there is great effort to move from studying simple, flat model surfaces in vacuum to investigating more complex model catalysts in gas environments (in situ). This thesis gives... Show moreIn surface science there is great effort to move from studying simple, flat model surfaces in vacuum to investigating more complex model catalysts in gas environments (in situ). This thesis gives three examples of such studies using microscopy and spectroscopy.Exposure of ZnO(10-10) to moderate pressures of water in an in situ scanning tunneling microscope reveals that the surface roughens. The flat ZnO(10-10) is thus only conditionally suited as a model catalyst for reactions involving water.In the same microscope, surface gold oxide formation is observed on TiO2/Au(111) during CO oxidation at 1 bar pressure. Comparisons to the Au(111) surface suggest that the titania does not supply atomic oxygen to the Au(111) substrate as part of the reaction mechanism of the CO oxidation.Co(0001) is investigated as a model catalyst for Fischer-Tropsch synthesis, the reaction of CO and H2 to form hydrocarbons. In this thesis the oxidation behavior of the cobalt and the adsorption of carbon species during the reaction are investigated using near-ambient pressure X-ray photoelectron spectroscopy.Generally, this thesis exemplifies the significant influence that small concentrations of contaminants in gases and materials can have on the structure and behavior of surfaces in in situ studies. Show less
Organic molecules in interstellar space are important as they influence the structure of galaxies and star formations. Studying catalytic processes in space allows us to understand how molecular... Show moreOrganic molecules in interstellar space are important as they influence the structure of galaxies and star formations. Studying catalytic processes in space allows us to understand how molecular species are formed and chemically evolved in the interstellar medium and solar system objects. Quantum chemical methods, such as “Density Functional Theory” (DFT), can be employed to study the chemical pathways for the formation of molecular species, which is challenging with only observations and experiments. This thesis studies, with DFT methods, how polycyclic aromatic hydrocarbons (PAHs), the most abundant organic species in space, catalyze the formation of molecular hydrogen in the interstellar medium. Specifically, how linear PAHs become superhydrogenated and how the presence of Stone Wales defect in PAHs contributes to their catalytic activity for molecular hydrogen formation. In addition, this thesis reports the study of the catalytic activity of forsterite, a silicate mineral abundant in grains, asteroids, and meteorites. Specifically, the presence of Schottky MgO vacancy in forsterite can catalyze the C-H activation of PAHs as the first step to study the breakdown reaction of PAHs in asteroidal settings. The latter is indispensable to understand the formation of the so-called organic inventory of solar system objects. Show less
Molecular complexes can be used as electrocatalysts for oxygen reduction, water oxidation, and/or hydrogen peroxide production. However, in situ degradation of these catalyst is a major issue. This... Show moreMolecular complexes can be used as electrocatalysts for oxygen reduction, water oxidation, and/or hydrogen peroxide production. However, in situ degradation of these catalyst is a major issue. This dissertations describes the analysis of degradation processes as well as the performance of various molecular electrocatalysts. In addition, complexes have been structurally modified to perform structure-activity studies that could to mechanistic insight. In addition, it is described how molecular catalysts can be beneficial to heterogeneous electrocatalysis as well. Show less
In most applications, electrocatalysts exhibit a large surface area to volume ratio, for example using nanoparticles. To fully understand fundamental electrochemical processes at the length scale... Show moreIn most applications, electrocatalysts exhibit a large surface area to volume ratio, for example using nanoparticles. To fully understand fundamental electrochemical processes at the length scale of these nanoparticles, it is necessary to use specialized experimental techniques. In this thesis, the stability and activity of platinum electrode surfaces are studied at the nano- and micrometer scale using Electrochemical Scanning Probe Microscopy (EC-SPM) techniques. Chapters 2 and 3 describe the roughening of an atomically flat Pt(111) surface upon repetitive oxidation and reduction. These data were acquired using a combination of Electrochemical Scanning Tunneling Microscopy (EC-STM) and Cyclic Voltammetry (CV). Chapter 4 describes the development of a new technique to resolve small differences in local reactivity: voltammetric Scanning Electrochemical Cell Microscopy (SECCM). The power of this technique is demonstrated by studying the reactivity of a polycrystalline Pt sample towards hydrazine oxidation. Finally, Chapter 5 compares the reactivity of small Pt ultramicroelectrodes to that of conventional macroelectrodes. Show less
The thesis is focused on the investigation of the electron transfer mechanisms leading to solar fuel production and to the identification of engineering principles that can be used to design... Show moreThe thesis is focused on the investigation of the electron transfer mechanisms leading to solar fuel production and to the identification of engineering principles that can be used to design materials able to improve charge separation. Molecular systems composed of three or more subunits arranged in a Donor-Antenna-Acceptor design are required to achieve efficient photoinduced charge separation. It is shown how structural changes in the systems design can be used to systematically optimize the energy gradients and electronic coupling between the molecular subunits, necessary to achieve controlled unidirectional charge transfer. To gain insight into the mechanisms governing the charge transfer processes within a molecular system, the process of photoinduced heterogeneous electron injection is investigated through nonadiabatic dynamics simulations. Coherent electron-nuclear vibrational effects are found to drive the electron transfer process by promoting the coherent superposition of the exciton and the charge transfer quantum state. A photoanode for solar water splitting comprising the functions of light-harvesting, charge separation and catalysis is also investigated. It is observed that, following a fast heterogeneous electron injection, the system catalytic activity is driven by a proton-coupled electron transfer mechanism in which the role of the solvent is crucial. Show less
The primary goal of this thesis is to study the potential role of electrochemistry in finding new routes for sustainable chemicals from biomass in aqueous-phase solutions. In order to assess the... Show moreThe primary goal of this thesis is to study the potential role of electrochemistry in finding new routes for sustainable chemicals from biomass in aqueous-phase solutions. In order to assess the potential of electrochemistry in biomass conversion, we developed an online HPLC system by using a fraction collector with a micrometer-sized sampling tip placed close to the working electrode, with the collected sample fractions subsequently analyzed in an offline HPLC system. To demonstrate this method, we applied it to the poly-ols, i.e. glycerol (C3H8O3), electro-oxidation on Au and Pt electrodes at different pH conditions, visualizing the concentration changes of glycerol and its reaction products in correspondence with the current measured in voltammetry, which brought us a concept to co-generate hydrogen and valuable chemicals (i.e. glyceraldehyde, glyceric acid, dihydroxyacetone, formic acid) with high selectivity depending on the applied potential. In addition, we aimed at single-cell synthesis of sorbitol from cellulosic material by generating glucose as an intermediate species. This thesis has demonstrated the separate reactions of cellobiose hydrolysis to glucose by acid and hydroxyl radical on an anode and glucose hydrogenation to sorbitol on a cathode in an electrolysis cell. Show less
This thesis describes the development of a combined high-pressure/ultrahigh-vacuum flow reactor for the study of model catalysts by means of surface x-ray diffraction and grazing incidence small... Show moreThis thesis describes the development of a combined high-pressure/ultrahigh-vacuum flow reactor for the study of model catalysts by means of surface x-ray diffraction and grazing incidence small angle scattering. The system was used to measure a stability diagram for the different oxide phases (surface oxide, bulk-like oxides) that exist on Pd(100) during catalytic CO oxidation at near ambient pressures. As soon as an oxide was present the reactivity of the surface was found to be mass transfer limited by the flux of CO molecules reaching the surface. Experiments on spontaneous reaction oscillations of the CO oxidation rate on Pd(100) reveal that a high density of steps strongly alters the stability of the thin, catalytically active palladium oxide film. It is shown that stabilization of the metal, caused by the steps and consequent destabilization of the oxide, is at the heart of the well-known reaction rate oscillations exhibited during CO oxidation at atmospheric pressure. Lastly reaction oscillations on supported Pd nanoparticles are shown to be accompanied by shape changes of the particles consistent with the formation and removal of a thin palladium oxide film on the particles. Show less
This thesis describes the construction of a second generation high-pressure, high-temperature scanning tunneling microscope, the ReactorSTM, with which the surfaces of catalysts can be studied... Show moreThis thesis describes the construction of a second generation high-pressure, high-temperature scanning tunneling microscope, the ReactorSTM, with which the surfaces of catalysts can be studied under relevant reaction conditions. Furthermore, the thesis describes three separate catalytic systems at ~ 1 bar, and elevated temperatures. Firstly, NO reduction on Pt(100), in which a mathematical model for the reaction mechanism, following Langmuir-Hinshelwood kinetics, is proposed. Secondly, CO oxidation, in which the Pt(110) surface is atomically resolved at high p, T. Thirdly, the thesis describes a successful pilot experiment about the hydrodesulphurization of thiophene, which is catalytically activated by molybdenum disulphide nano-crystallites on an Au(111) support. Show less
An industrially applicable process was developed for the synthesis of epoxy resin components. A catalytic reaction was explored towards allyl phenyl ethers that prevents the use of chloride... Show moreAn industrially applicable process was developed for the synthesis of epoxy resin components. A catalytic reaction was explored towards allyl phenyl ethers that prevents the use of chloride-containing starting materials and thus formation of chloride-containing side products. The preferred allylating agent is allyl alcohol or its derivatives since this only produces water as a side product. Ruthenium and palladium complexes were used as catalysts and their structure proved to be of key importance for the outcome of the reaction. By fine-tuning the catalyst structure with phosphine ligands, the reaction could be performed highly selective. Besides the homogeneous catalytic system, also retrieval of the catalyst was studied and the scope of the reaction was explored. Show less
