Nanoscale scanning electrochemical microscopy (SECM) is a powerful scanning probe technique that enables high-resolution imaging of chemical processes at single nanometer-sized objects. However, it has been a challenging task to quantitatively understand nanoscale SECM images, which requires to accurately characterize the size and geometry of nanoelectrode tips. Herein, we address this challenge through transmission electron microscopy (TEM) of quartz nanopipets for SECM imaging of single solid-state nanopores by using nanopipet-supported interfaces between two immiscible electrolyte solutions (ITIES) as tips. We take advantage of the high resolution of TEM to demonstrate that laser-pulled quartz nanopipets reproducibly yield not only an extremely small tip diameter of ~30 nm, but also a substantial tip roughness of ~5 nm. The size and roughness of a nanopipet can be reliably determined by optimizing the intensity of the electron beam not to melt or deform the quartz nanotip without metal coating. Electrochemically, the nanoscale ITIES supported by a rough nanotip gives higher amperometric responses to tetrabutylammonium than expected for a 30 nm-diameter disk tip. The finite element simulation of sphere-cap ITIES tips accounts for the high current responses and also reveals that the SECM images of 100 nm-diameter Si3N4 nanopores are enlarged along the direction of the tip scan. Nevertheless, spatial resolution is not significantly compromised by a sphere-cap tip, which can be scanned in closer proximity to the substrate. This finding augments the utility of a protruded tip, which can be fabricated and miniaturized more readily to facilitate nanoscale SECM imaging.
The fabrication of a gold microelectrode modified with iridium oxide film (IrOx) and its use as tip with a dual function in SECM experiments is reported. The defective structure of the coating onto the microelectrode surface was used as strategy to combine the advantages of both amperometric (for current‐distance determination) and potentiometric (for pH sensing) SECM operation modes. Approach curves, using oxygen and hexaammineruthenium(III) as redox mediators, were obtained without significant loss of the performance and reproducibility of the potentiometric pH response. This allowed the precise positioning of the proposed tip above a substrate in SECM experiments and, subsequently, to monitor pH at the substrate surface. The IrOx modified microelectrode was applied successfully in SECM experiments involving the local proton consumption during the nitrate reduction at a copper cathode surface.
In this work, the EC' mechanism involving ascorbate (AA À ) and the oxidized form of ferrocenemethanol (FcMeOH) was explored as an analytical strategy to monitor AA À at low concentration levels. The feasibility of this approach was investigated at different mass transport regimes utilizing macro-(glassy carbon) and ultramicroelectrodes (5 μm radius carbon disk). Cyclic voltammograms (CV) were recorded in acetate buffer solution (pH 3.7) using a glassy carbon electrode, and an expressive increase in the anodic peak current (and decrease in the cathodic peak) was noticed in the CV in a solution containing both FcMeOH and ascorbate, con-firming the presence of an electrocatalytic process (EC'). The current increase was more pronounced when the reactants and products were confined in a thin solution layer, which was created by approaching an ultramicroelectrode close to an insulator surface. At optimized experimental conditions, a correlation between ascorbate concentration and the steady-state current measured at the ultramicroelectrode was established, allowing the development of an analytical method for ascorbate detection in the micromolar range. The proposed approach was used to quantify ascorbate in a commercial juice sample.
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