The PhD project was aimed to understand the role of the solvent in the hydrogen oxidation and evolution reactions on platinum and gold. This approach sheds light on the molecular origins... Show more The PhD project was aimed to understand the role of the solvent in the hydrogen oxidation and evolution reactions on platinum and gold. This approach sheds light on the molecular origins affecting the kinetics of the hydrogen evolution reaction, as a promising source of energy in the era of sustainable energy production and storage. Ultimately, this work demonstrates the importance of the solvent in the hydrogen electrocatalysis, specifically, water, by settling its role as a solvent, as a proton donor, and by preferential proton solvation, clarifying a long-existing debate regarding the pH dependence of the hydrogen evolution, and setting a path for future exploration of solvent-electrode interfaces for the tailoring of electrocatalytic reactions. Show less
This thesis discusses the parameters affecting the catalysis for the electrochemical conversion of water into oxygen. The slow kinetics for the oxygen evolution reaction (OER) is one of the major... Show moreThis thesis discusses the parameters affecting the catalysis for the electrochemical conversion of water into oxygen. The slow kinetics for the oxygen evolution reaction (OER) is one of the major bottlenecks in the solar energy-to-fuels conversion process, which reduces the efficiency for the photo-electrochemical fuels generation (artificial photosynthesis). The work shows that to enhance the kinetics for the oxygen evolution reaction, one should not only look at the catalysts but also consider the synergy between catalyst and electrolyte. A more general approach that considers the electrochemical interface as a whole (electrode + electrolyte) is therefore the most promising route towards optimal activity. Show less
Nitrate reduction on Sn-modified polycrystalline Pt has been investigated. NO is the main product at high Sn coverage, whereas N2O is dominant at low Sn coverage. The N2O reduction on Sn-modified... Show moreNitrate reduction on Sn-modified polycrystalline Pt has been investigated. NO is the main product at high Sn coverage, whereas N2O is dominant at low Sn coverage. The N2O reduction on Sn-modified Pt electrodes indicates electrochemical formation of N2 is related to pristine Pt sites. Moreover, homogeneous chemical reactions of intermediates products also contribute to N2O and N2 formation of in solution. The p-block metals have been studied: Cd, In and Sn show a promoting effect; Ga shows a limited enhancement; Tl shows a special promoting effect in sulfuric acid; Pb shows a weak formation of N2O. Density Functional Theory calculations show that Sn and In enhance nitrate adsorption compared with pristine Pt. Moreover, ammonia is found as the only product on Pt. After modification by Sn, hydroxylamine is specifically found with nitrite, which supports that nitrate reduction to nitrite is enhanced by Sn and Sn could steer the hydrogenation of NOads. However, solution pH is an important factor. On Pt, nitrate reduction is only observed in acidic solution. On Rh, a higher activity is observed in wide pH, which suggests a mechanism that HNO3 molecule is the active species. However, Rh additionally shows a special ability to reduce NO3- directly. Show less
This project has dealt with the mechanistic study of the electrocatalytic nitrite reduction, the selectivity-determining step of nitrate reduction. Nitrate is a polluting ion targeted by wastewater... Show moreThis project has dealt with the mechanistic study of the electrocatalytic nitrite reduction, the selectivity-determining step of nitrate reduction. Nitrate is a polluting ion targeted by wastewater remediation; electrochemistry strives to achieve selectivity to harmless products (N2). A multi-pronged approach has been followed, aimed at establishing the influence of several variables (electrocatalyst material, surface structure, pH and electrode potential) on the catalytic activity and the product distribution, which has been determined with in situ analytical techniques (mass spectrometry and infrared spectroscopy). The molecular underpinnings of nitrite reduction have thereby been unravelled for transition metals, showing that an optimal catalytic performance is achieved when metals intermediate affinities to reaction intermediates (Sabatier Principle). The all-important concept of structure sensitivity also applies to nitrite reduction at Pt electrodes, although only in alkaline media: a Pt(100) single-crystal is the sole Pt surface able to achieve the desired direct conversion of nitrite into 100% N2. Such selectivity is unparalleled for a simple monometallic surface and is an outstanding finding. Additionally, the nitrite-reducing performance of bio-inspired catalysts, (electroactive metalloporphyrins) was investigated. A further side-project of this PhD thesis has also been the electrochemical characterization of preferentially-oriented cuboid Pt nanoparticles synthesized with the innovative __cathodic corrosion__. Show less
The thesis contains a discussion on the subject of the Oxygen Reduction Reaction (ORR) on Pt-alloy nanoparticle catalysts in the Rotating Disk Electrode (RDE) method. An insight in some of the... Show moreThe thesis contains a discussion on the subject of the Oxygen Reduction Reaction (ORR) on Pt-alloy nanoparticle catalysts in the Rotating Disk Electrode (RDE) method. An insight in some of the difficulties of this method is given with proper solutions and compensations for these problems. Pt3Co, Au-core Pt3Fe-shell catalysts dispersed on carbon support, as well as the 3M Nanostructured Thin Film (NSTF) catalyst are analyzed and the ORR activities measured. For the Pt3Co catalyst, the particle size effect and the effect of catalyst pretreatment is determined. The significant durability enhancement of the gold-core Pt3Fe-shell catalyst is discussed. A novel pretreatment method for the NSTF catalyst is shown, as well as the significant increase in mass activity for the ORR compared to carbon-supported catalysts. The thesis ends with an insight in the cyclic voltammetry of a Pt (100) single crystal electrodein alkaline media and the effect of the pretreatment of the catalyst. Show less
This thesis describes the results of the fundamental research on the electro-oxidation of ethanol. In addition, the oxidation of intermediates in the ethanol electro-oxidation reaction, such as... Show moreThis thesis describes the results of the fundamental research on the electro-oxidation of ethanol. In addition, the oxidation of intermediates in the ethanol electro-oxidation reaction, such as acetaldehyde and adsorbed CO, has also been studied. The goal of this research is to provide deeper insight into the molecular level understanding of the mechanism, and how various operational parameters affect this mechanism. With these insights, the development of low temperature direct ethanol fuel cells (DEFC) can be advanced, since, ultimately, the goal of fundamental catalysis research is the rational design of new catalysts, for which the understanding of molecular mechanisms is of essential importance. The mechanism of the electro-oxidation reaction is investigated using electrochemical techniques, such as cyclic voltammetry and chronoamperometry, as well as in situ characterization techniques, such as surface enhanced Raman spectroscopy (SERS), Fourier transform infrared spectroscopy (FTIR) and online electrochemical mass spectrometry (OLEMS). Show less
The main goal of the research presented in this thesis is the synthesis of suitable structural and functional models for the enzyme [NiFe] hydrogenase, which can reduce protons into dihydrogen. A... Show moreThe main goal of the research presented in this thesis is the synthesis of suitable structural and functional models for the enzyme [NiFe] hydrogenase, which can reduce protons into dihydrogen. A brief survey of the roles of all the known nickel containing enzymes in biological systems with a focus on the [NiFe] hydrogenases. Structure, function, physicochemical and catalytic properties of the [NiFe] hydrogenase itself and of the reported model complexes are presented. Many new Nickel, [NiFe], [NiRu] and [NiCu] complexes have been synthesized and studied in view of better catalysts for proton electroreduction into dihydrogen. Show less
