The electrochemical reduction of CO2 is widely studied as a sustainable alternative for the production of fuels and chemicals. The electrolyte’s bulk pH and composition play an important role in... Show moreThe electrochemical reduction of CO2 is widely studied as a sustainable alternative for the production of fuels and chemicals. The electrolyte’s bulk pH and composition play an important role in the reaction activity and selectivity and can affect the extent of the buildup of pH gradients between the electrode surface and the bulk of the electrolyte. Quantifying the local pH and how it is affected by the solution species is desirable to gain a better understanding of the CO2 reduction reaction. Local pH measurements can be realized using Scanning Electrochemical Microscopy (SECM); however, finding a pH probe that is stable and selective under CO2 reduction reaction conditions is challenging. Here, we have used our recently developed voltammetric pH sensor to perform pH measurements in the diffusion layer during CO2 reduction using SECM, with high time resolution. Using a 4-hydroxylaminothiophenol (4-HATP)/4-nitrosothiophenol (4-NSTP) functionalized gold ultramicroelectrode, we compare the local pH developed above a gold substrate in an argon atmosphere, when only hydrogen evolution is taking place, to the pH developed in a CO2 atmosphere. The pH is monitored at a fixed distance from the surface, and the sample potential is varied in time. In argon, we observe a gradual increase of pH, while a plateau region is present in CO2 atmosphere due to the formation of HCO3– buffering the reaction interface. By analyzing the diffusion layer dynamics once the sample reaction is turned “off”, we gain insightful information on the time scale of the homogeneous reactions happening in solution and on the time required for the diffusion layer to fully recover to the initial bulk concentration of species. In order to account for the effect of the presence of the SECM tip on the measured pH, we performed finite element method simulations of the fluid and reaction dynamics. The results show the significant localized diffusion hindrance caused by the tip, so that in its absence, the pH values are more acidic than when the tip is present. Nonetheless, through the simulation, we can account for this effect and estimate the real local pH values across the diffusion layer. Show less
Electrode degradation under oxidizing conditions is a major drawback for large-scale applications of platinum electrocatalysts. Subjecting Pt(111) to oxidation-reduction cycles is known to lead to... Show moreElectrode degradation under oxidizing conditions is a major drawback for large-scale applications of platinum electrocatalysts. Subjecting Pt(111) to oxidation-reduction cycles is known to lead to the growth of nanoislands. We study this phenomenon using a combination of simultaneous in situ electrochemical scanning tunneling microscopy and cyclic voltammetry. Here, we present a detailed analysis of the formed islands, deriving the (evolution of the) average island growth shape. From the island shapes, we determine the densities of atomic-scale defect sites, e.g., steps and facets, which show an excellent correlation with the different voltammetric hydrogen adsorption peaks. Based on this combination of electrochemical scanning tunneling microscopy (EC-STM) and CV data, we derive a detailed atomistic picture of the nanoisland evolution during potential cycling, delivering new insights into the initial stages of platinum electrode degradation. Show less
Probing pH gradients during electrochemical reactions is important to better understand reaction mechanisms and to separate the influence of pH and pH gradients from intrinsic electrolyte effects.... Show moreProbing pH gradients during electrochemical reactions is important to better understand reaction mechanisms and to separate the influence of pH and pH gradients from intrinsic electrolyte effects. Here, we develop a pH sensor to measure pH changes in the diffusion layer during hydrogen evolution. The probe was synthesized by functionalizing a gold ultramicroelectrode with a self-assembled monolayer of 4-nitrothiophenol (4-NTP) and further converting it to form a hydroxylaminothiophenol (4-HATP)/4-nitrosothiophenol (4-NSTP) redox couple. The pH sensing is realized by recording the tip cyclic voltammetry and monitoring the Nernstian shift of the midpeak potential. We employ a capacitive approach technique in our home-built Scanning Electrochemical Microscope (SECM) setup in which an AC potential is applied to the sample and the capacitive current generated at the tip is recorded as a function of distance. This method allows for an approach of the tip to the electrode that is electrolyte-free and consequently also mediator-free. Hydrogen evolution on gold in a neutral electrolyte was studied as a model system. The pH was measured with the probe at a constant distance from the electrode (ca. 75 μm), while the electrode potential was varied in time. In the nonbuffered electrolyte used (0.1 M Li2SO4), even at relatively low current densities, a pH difference of three units is measured between the location of the probe and the bulk electrolyte. The time scale of the diffusion layer transient is captured, due to the high time resolution that can be achieved with this probe. The sensor has high sensitivity, measuring differences of more than 8 pH units with a resolution better than 0.1 pH unit. Show less
In homoepitaxial crystal growth, four basic growth morphologies (idealized growth modes) have been established that describe the deposition of atoms on single crystal surfaces: step-flow, layer-by... Show moreIn homoepitaxial crystal growth, four basic growth morphologies (idealized growth modes) have been established that describe the deposition of atoms on single crystal surfaces: step-flow, layer-by-layer, mound formation, and random/self-affine growth. Mound formation leads to nano-scale surface patterning. However, the formation of (nano)-islands, patterns, and roughness occurs also during ion bombardment, electrochemical etching and oxidation/ reduction cycling. Here we show, in analogy to many particle/anti-particle formalisms in physics, the existence of the dualism between individual adatom and single vacancy growth modes. We predict that all standard adatom growth modes do exist also in their counter, vacancy version. For the particular case of mound formation, we derive the theoretical equations and show the inverse similarity of the solution. We furthermore treat simultaneous growth by adatoms and vacancies, and derive the analytical solution of the growth shape evolution of the mounds. Finally, we present an experimental verification, in which both adatom and vacancy mound formation are active. The theoretically predicted mound shape nicely fits the experimental observation. 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
