Many polyols are abundant and cheap molecules highly spread in the biomass. These molecules have an enormous potential to be used in electrochemical devices to generate energy and/or value-added... Show moreMany polyols are abundant and cheap molecules highly spread in the biomass. These molecules have an enormous potential to be used in electrochemical devices to generate energy and/or value-added molecules. The electrooxidation of polyols can produce different substances of interest in the chemical industry concomitantly to high purity hydrogen in electrolyzers. The cost in the production of all these chemicals depends, among other factors, on the develop of more active and selective catalysts. However, in order to search for these materials using computational experiments, it is mandatory to have a better understanding of the fundamental aspect of the reactions, which permit to base the search on the adsorption energies of one or more key reaction intermediates. To contribute to this task, we performed (spectro)-electrochemical and computational experiments to study the electrooxidation of C-4 polyols. We show that the electrooxidation of polyols does not depend on the relative orientation of their OH groups. Besides, using Pt single crystals, we demonstrate that the trend for the oxidation of the primary carbon (relative to the secondary) increases in the order Pt(111) < Pt(100) < Pt(110) and that this result can be extended to polyols with longer carbon chains. Finally, computational experiments permit us to rationalize these trends looking at the relative stability of double dehydrogenated intermediates on the Pt basal planes. Show less
With the energy transition toward a renewable energy supply and a CO2-neutral economy, electrification of the energy system is rising in importance, which leads to the challenge of long-term... Show moreWith the energy transition toward a renewable energy supply and a CO2-neutral economy, electrification of the energy system is rising in importance, which leads to the challenge of long-term storage of renewable electricity. A promising option is the electrochemical conversion of biomass or carbon dioxide in chemicals as energy carrier. In this research, catalysis of the electrochemical CO2 reduction was studied to obtain liquid fuels. In this fundamental study we discovered that so-called disproportionation reactions may occur simultaneously with the CO2 reduction reaction influencing the product spectrum. Moreover, we focused on metalloprotoporphyrins immobilized on a graphite surface. We found that the selectivity can be steered toward formic acid with rhodium, tin or indium metal centers. Apart from intrinsic catalyst parameters, we studied the influence of parameters related to the immobilization and the composition of the electrolyte. We showed that the substrate and its pretreatment as well as encapsulation of the catalyst in polymers can have a signifcant influence on the electrocatalysis of CO2 reduction. The results obtained in this thesis provide insight in the energy efficiency, reaction rate and selectivity of the CO2 reduction reaction, and play an important role for the development of an industrially viable process. Show less
