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The electrochemical carbon dioxide reduction reaction (CO2RR) over carbon-supported gold nanoparticles (AuNP) was investigated using a broad variety of (electro)analytical methods, including linear sweep voltammetry with a rotating disk electrode (LSV-RDE), sample-generation tip-collection mode of scanning electrochemical microscopy (SG/TC-SECM), as well as full cell tests with highly sensitive online gas chromatography (GC). In contrast to most other studies, this work focuses on the low-overpotential region (0 to -0.4 V vs RHE) where initial product formation is already detected and addresses micro- to macro-sized electrodes. The sub-10 nm AuNPs supported on three different carbon supports (CNTs and carbon blacks) were pretreated in H 2 /Ar to remove the stabilizer used during AuNP synthesis. LSV-RDE points toward different CO2RR mechanisms at the samples, additionally confirmed by the SG/TC-SECM and full cell tests with online GC. Besides H 2 and CO, the AuNP supported on carbon nanotubes showed significant evolution of H 2 CO in contrast to the other two samples, which was additionally confirmed by accumulating the product during chronoamperometric RDE experiments followed by mass spectroscopic analysis. Surface analysis indicated a complete removal of residual thiolate stabilizer molecules exclusively at the AuNPs supported on carbon nanotubes, which may result in a change in the adsorption geometry or reaction mechanism at this sample. The results demonstrate the effectiveness of the combination of these multiple methods to investigate the CO2RR in the low-overpotential region.

We present a spectroelectrochemical setup, in which Raman microscopy is combined with scanning electrochemical microscopy (SECM) in order to provide both spectroscopic and electrochemical information on the very same location of an electrode at the same time. The setup is applied to a subject of high academic and practical interest, namely, the oxygen evolution reaction at Ni and Ni/Fe electrodes. It comprises a transparent substrate electrode, onto which Ni and Ni/Fe thin films are deposited. An ultramicroelectrode (UME) is placed closely above the substrate to obtain electrochemical information, while a Raman microscope probes the same sample spot from below. To obtain information on oxygen evolution activity and structural changes, increasingly positive potentials from 0.1 up to 0.7 V vs Hg|HgO|1 M KOH were applied to the Ni/Fe-electrodes in 0.1 M KOH solution. Evolved oxygen is detected by reduction at a Pt UME, allowing for the determination of onset potentials, while the substrate current, which is recorded in parallel, is due to both overlapping oxygen evolution and the oxidation of Ni(OH) 2 to NiOOH. An optimum of 15% Fe in Ni/Fe films with respect to oxygen evolution activity was determined. At the same time, the potential-dependent formation of γ-NiOOH characterized by the Raman double band at 475 and 557 cm -1 allows for the conclusion that a certain amount of disorder introduced by Fe atoms is necessary to obtain high oxygen evolution reaction (OER) activity.

Scanning electrochemical microscopy (SECM) has been used to detect and visualize the local electrocatalytic activity of dimensionally stable anodes (DSA) for Cl(2) evolution from brine. The sample generation-tip collection (SG-TC) mode of SECM shows limitations arising from complications connected with the reduction of Cl(2) at the SECM tip due to the presence of a significant amount of nondissolved Cl(2) gas. Because only dissolved Cl(2) can be electrochemically reduced at the tip, a large amount of the Cl(2) gas which is produced at active spots of the DSA is not detected. Additionally, a decrease of the cathodic current at the tip may occur owing to the adhesion of gas bubbles and blocking of the electrode surface. To overcome this limitation, the redox competition mode of SECM was extended and applied to the local visualization of Cl(2) evolution from highly concentrated brine solutions. High concentrations of Cl(2) produced at the sample can cause inhibition of the same reaction at the tip by accumulation of Cl(2) in the proximity of the SECM tip. In this way the tip current is decreased, which can be used as a measure for the catalytic activity of the sample underneath the tip., (© 2011 American Chemical Society)

Pt-Ag nanoparticles were prepared on a glassy carbon (GC) surface by pulsed electrodeposition and tested using cyclic voltammetry and scanning electrochemical microscopy (SECM) with respect to their possible use as catalyst material for oxygen reduction in 400 mM HCl solution. For comparison, a Pt catalyst was investigated under similar conditions. The redox competition mode of scanning electrochemical microscopy (RC-SECM) was adapted to the specific conditions caused by the presence of Cl(-) ions and used to visualize the local catalytic activity of the Pt-Ag deposits. Similarly prepared Pt deposits were shown to dissolve underneath the SECM tip. Pt-Ag composites showed improved long-term stability toward oxygen reduction as compared with Pt even under multiple switching off to open-circuit potential in 400 mM HCl.

A strategy for the screening of the electrocatalytic activity of electrocatalysts for possible application in fuel cells and other devices is presented. In this approach, metal nanoclusters (Pt, Au, Ru, and Rh and their codeposits) were prepared using a capillary-based droplet-cell by pulsed electrodeposition in a diffusion-restricted viscous solution. A glassy carbon surface was modified with carbon nanotubes (CNTs) by electrophoretic accumulation and was used as substrate for metal nanoparticle deposition. The formed catalyst spots on the CNT-modified glassy carbon surface were investigated toward their catalytic activity for oxygen reduction as a test reaction employing the redox competition mode of scanning electrochemical microscopy (RC-SECM). Qualitative information on the electrocatalytic activity of the catalysts was obtained by varying the potential applied to the substrate; semiquantitative evaluation was based on the determination of the electrochemically deposited catalyst loading by means of the charge transferred during the metal nanoparticle deposition. Qualitatively, Au showed the highest electrocatalytic activity toward the oxygen reduction reaction (ORR) in phosphate buffer among all investigated single metal catalysts which was attributed to the much higher loading of Au achieved during electrodeposition. Coelectrodeposited Au-Pt catalysts showed a more positive onset potential (-150 mV in RC-SECM experiments) of the ORR in phosphate buffer at pH 6.7. After normalizing the SECM image by the charge during the metal nanocluster deposition which represents the mass loading of the catalyst, Ru showed a higher electrocatalytic activity toward the ORR than Au.

Carbon nanotubes (CNT) supported platinum-ruthenium (Pt-Ru) catalysts were prepared by impregnation-reduction using an ethanolic solution of H2PtCl6 and RuCl3. The effect of reduction temperatures on particle size, surface area and their relationship to the electrocatalytic activity for methanol oxidation were investigated. Thermogravimetric analysis, scanning electron microscopy, transmission electron microscopy, X-ray diffraction (XRD) as well as X-ray photoelectron spectroscopy (XPS) were used for the catalyst characterization. XRD analysis showed that the PtRu/ CNT catalysts possibly consist of separate Pt and Ru phases. XPS analysis showed that the catalysts contain hydrous ruthenium oxide in addition to Pt and Ru metal and oxide species. The electrocatalytic activities of the catalysts were investigated in half-cell experiments using cyclic voltammetry, CO stripping voltammetry, chronoamperometry, and impedance spectroscopy. The results showed that the catalyst reduced at a temperature of 350 degrees C had the largest electrochemical surface area, lowest charge transfer resistance and the highest electrocatalytic activity for methanol oxidation. The superior catalytic activity is discussed based on the presence of appropriate amount of hydrated Ru oxide.