Selectivity of Electrochemical Reactions Based on Adsorption at Nanoporous Electrodes.

Enhancing selectivity is a pivotal area of research when electrodes are utilized as catalysts or sensors. Nanoporous electrodes are representative electrode materials for diverse applications, such as catalysts and sensors. Selectivity arising from nanoporous structures has been applied to systems involving nonfaradaic reactions such as capacitive deionization, electrochemical supercapacitors, and conductometry. Since selectivity in faradaic reactions has primarily been explored based on reactivity and molecular charge and size, we propose that the surface adsorption of reactant molecules can be considered as another crucial factor in achieving selectivity. Our observations reveal that the nonadsorptive reaction of 2-propanol and 2-butanol experienced a more pronounced enhancement compared to the adsorptive reaction of 1-propanol and 1-butanol at nanoporous Pt electrodes, owing to the nanoconfinement effect. Even within the same molecule with a mixture of adsorptive and nonadsorptive reactions, the degree of influence of the nanostructure depends on the adsorptive capacity of the reaction, which affects the overall selectivity. Moreover, the size effect of the reactants in the nanoporous electrode is also dependent on the degree of adsorption. These findings provide valuable insights into the effective utilization of nanoporous materials as catalysts or sensors.

Surface-Charge Effects on Voltammetry in Carbon Nanocavities.

Ion transport controlled by electrostatic interactions is an important phenomenon in biological and artificial membranes, channels, and nanopores. Here, we employ carbon-coated nanopipets (CNPs) for studying permselective electrochemistry in a conductive nanopore. A significant accumulation (up to 2000-fold) of cationic redox species and anion depletion inside a CNP by diffuse-layer and surface-charge effects in a solution of low ionic strength were observed as well as the shift of the voltammetric midpeak potential. Finite-element simulations of electrostatic effects on CNP voltammograms show permselective ion transport in a single conducting nanopore and semiquantitatively explain our experimental data. The reported results are potentially useful for improving sensitivity and selectivity of CNP sensors for ionic analytes.

Photo-Scanning Electrochemical Microscopy on the Nanoscale with Through-Tip Illumination.

Scanning electrochemical microscopy (SECM) has previously been employed in probing photoelectrochemical processes at semiconductor surfaces. However, the spatial resolution of these studies has not yet matched the nanoscale SECM resolution attained without substrate illumination. Herein, we introduce nanoscale photo-SECM with a glass-sealed, polished tip simultaneously serving as a nanoelectrode and a light guide to produce a microscopic light spot on the substrate surface. The advantages of this approach are demonstrated by comparing current transients obtained using through-tip and global illumination of the sample. The spot of light on the substrate surface facing the nanotip was sufficiently bright to measure the diffusion-controlled positive feedback current in good agreement with the theory. We employed this approach for high-resolution photoelectrochemical mapping of ferrocenemethanol oxidation and oxygen evolution reactions at the Nb:TiO2 rutile (110) single crystal surface. The images obtained using 40-50 nm radius tips showed only minor and random variations in photoelectrochemical reactivity for both processes, pointing to essentially uniform distribution of the Nb dopant over the TiO2 surface and no measurable segregation on the ∼50 nm scale.

Ultrasensitive Detection of Dopamine with Carbon Nanopipets.

Carbon fiber micro- and nanoelectrodes have been extensively used to measure dopamine and other neurotransmitters in biological systems. Although the radii of some reported probes were ≪1 µm, the lengths of the exposed carbon were typically on the micrometer scale, thus limiting the spatial resolution of electroanalytical measurements. Recent attempts to determine neurotransmitters in single cells and vesicles have provided additional impetus for decreasing the probe dimensions. Here, we report two types of dopamine sensors based on carbon nanopipets (CNP) prepared by chemical vapor deposition of carbon into prepulled quartz capillaries. These include 10-200 nm radius CNPs with a cavity near the orifice and CNPs with an open path in the middle, in which the volume of sampled solution can be controlled by the applied pressure. Because of the relatively large surface area of carbon exposed to solution inside the pipet, both types of sensors yielded well-shaped voltammograms of dopamine down to ca. 1 nM concentrations, and the unprecedented voltammetric response to 100 pM dopamine was obtained with open CNPs. TEM tomography and numerical simulations were used to model CNP responses. The effect of dopamine adsorption on the CNP detection limit is discussed along with the possibilities of measuring other physiologically important analytes (e.g., serotonin) and eliminating anionic and electrochemically irreversible interferences (e.g., ascorbic acid).

Dissolution of Pt during Oxygen Reduction Reaction Produces Pt Nanoparticles.

The loss of Pt during the oxygen reduction reaction (ORR) affects the performance and economic viability of fuel cells and sensors. Our group previously observed the dissolution of Pt nanoelectrodes at moderately negative potentials during the ORR. Here we report a more detailed study of this process and identify its product. The nanoporous Pt surface formed during the ORR was visualized by AFM and high-resolution SEM, which also showed ∼5 nm sized Pt particles on the glass surface surrounding the electrode. The release of these nanoparticles into the solution was confirmed by monitoring their catalytically amplified collisions with a Hg-coated microelectrode used as the tip in the scanning electrochemical microscope (SECM).

Nonfaradaic nanoporous electrochemistry for conductometry at high electrolyte concentration.

Nanoporous electrified surfaces create a unique nonfaradaic electrochemical behavior that is sensitively influenced by pore size, morphology, ionic strength, and electric field modulation. Here, we report the contributions of ion concentration and applied ac frequency to the electrode impedance through an electrical double layer overlap and ion transport along the nanopores. Nanoporous Pt with uniform pore size and geometry (L2-ePt) responded more sensitively to conductivity changes in aqueous solutions than Pt black with poor uniformity despite similar real surface areas and enabled the previously difficult quantitative conductometry measurements at high electrolyte concentrations. The nanopores of L2-ePt were more effective in reducing the electrode impedance and exhibited superior linear responses to not only flat Pt but also Pt black, leading to successful conductometric detection in ion chromatography without ion suppressors and at high ionic strengths.

Operando spectroscopic characterization of formamidinium lead iodide perovskite quantum dots for tracking electrochemical reactions.

Multidimensional ABX3 hybrid perovskites three-dimensionally confined dot-shaped structure demonstrate versatile potential to photoelectrochemical cells for water splitting, hydrogen generation, solar cells, and light-emitting diodes. To apply perovskite quantum dots (PQDs) to solar-driven chemistry and optoelectronic devices, understanding the photoinduced charge carrier dynamics of PQDs under electrochemical conditions or applied bias are important. In this study, the detailed transformation mechanism of formamidinium lead iodide perovskite quantum dots under electrochemical conditions was studied by tracking the products of the reaction through cyclic voltammetry, X-ray photoemission spectroscopy, in-situ UV-visible spectroelectrochemistry, etc. Through comprehensive characterizations, the mechanism of irreversible oxidative transformation of perovskite quantum dots was presented. This study provides deeper insight into the electrochemical behavior of PQDs for successful solar-driven chemistry and optoelectronic device applications.

Enhanced electrochemical reactions of 1,4-benzoquinone at nanoporous electrodes.

We report that the proton-coupled electron transfer kinetics of 1,4-benzoquinone was significantly enhanced in electrified nanopores in aqueous media. At nanoporous Pt and Au electrodes, the voltammetric behaviour of 1,4-benzoquinone at nanoporous electrodes was clearly distinct from that at flat surfaces. Proton transfer as well as electron transfer kinetics were facilitated in the nanopores by the confinement effect, which indicates all factors originated from the geometric features of nano-scale concave space surrounded by inner walls, suggesting how to utilize nanoporous electrodes for electrocatalysis.

In-channel electrochemical detection in the middle of microchannel under high electric field.

We propose a new method for performing in-channel electrochemical detection under a high electric field using a polyelectrolytic gel salt bridge (PGSB) integrated in the middle of the electrophoretic separation channel. The finely tuned placement of a gold working electrode and the PGSB on an equipotential surface in the microchannel provided highly sensitive electrochemical detection without any deterioration in the separation efficiency or interference of the applied electric field. To assess the working principle, the open circuit potentials between gold working electrodes and the reference electrode at varying distances were measured in the microchannel under electrophoretic fields using an electrically isolated potentiostat. In addition, "in-channel" cyclic voltammetry confirmed the feasibility of electrochemical detection under various strengths of electric fields (∼400 V/cm). Effective separation on a microchip equipped with a PGSB under high electric fields was demonstrated for the electrochemical detection of biological compounds such as dopamine and catechol. The proposed "in-channel" electrochemical detection under a high electric field enables wider electrochemical detection applications in microchip electrophoresis.

Electrochemistry at nanoporous interfaces: new opportunity for electrocatalysis.

Physical and electrochemical features of nanoporous electrodes arising from their morphology are presented in this perspective. Although nanoporous electrodes have been used to enhance electrocatalysis for several decades, the origin of their capability was understood on the basis of enlarged surface area or crystalline facet. However, considerable attention should be paid to the fact that nano-confined space of nanoporous electrodes can significantly affect electrochemical efficiency. Molecular dynamics in nano-confined spaces is capable of offering much more chances of interaction between a redox molecule and an electrode surface. The mass transport in the nanoporous electrode depends on various pore characteristics such as size, shape, charge, connectivity, and symmetry as well as molecular properties such as size, charge, and kinetics. Moreover, when the pore size is comparable to the thickness of an electric double layer (EDL), the EDLs overlap in the porous structure so that electrochemically effective surface area is not the same as that of the real electrode surface. These unique properties come from simply nanoporous structure and suggest new opportunity to innovative electrocatalysts in the future.

Ion flow crossing over a polyelectrolyte diode on a microfluidic chip.

Key evidences are reported for the rectification mechanism of an aqueous ion diode based on polyelectrolytic plugs on a microfluidic chip by monitoring the ion flow crossing over the junction. The ion flow penetrating the polyelectrolyte junction is visualized by employing a fluorescent chemodosimeter, rhodamine B hydrazide and the pH-dependent dye, carboxy-fluorescein. How hysteresis phenomena, exhibited through the nonlinear behavior of the polyelectrolyte diode, are affected by a variety of parameters (e.g., switching potential, scan rate, and electrolyte concentration) is also investigated. The insights and knowledge from this study provide a crucial foundation for ion control at the iontronic diode in the aqueous phase, leading to more advanced aqueous organic computing devices and more diverse applications for microfluidic logic devices.

Oligonucleotide-Based Reusable Electrochemical Silver(I) Sensor and Its Optimization via Probe Packing Density.

We report herein a selective, sensitive, and reusable electrochemical sensor for the detection of silver(I) ions. This sensor detects Ag+ through a structure-switching electrode-bound DNA by measuring the changes in the electron-transfer efficiency. A single-stranded DNA, featuring a methylene blue (MB)-tagged DNA hairpin structure, strategically provides selective binding for the silver-mediated coordination of cytosine-Ag+-cytosine complexes. The DNA-modified electrode produces a change in the electrochemical signal due to the redox current of the surface-confined MB tag. The "turn-on" signaling upon silver(I) ion binding could be attributed to a conformational change in the MB-tagged DNA from an open structure to a target-induced folding structure. Differential pulse voltammetry of the DNA-modified electrode showed that the MB reduction signal increased linearly with an increase in Ag+ concentrations in a range of 10-200 nM, with a detection limit of 10 nM. The structure-switching silver(I) ion sensor was amenable to regeneration by simply unfolding the electrode-bound MB-tagged DNA in 100 mM ethylenediaminetetraacetic acid, and it could be regenerated with no loss in signal gain upon subsequent silver(I) ion binding. We also demonstrated that by controlling the probe packing density on the electrode surface, the fabrication parameters can be varied to achieve optimal sensor performance.

Light-Controlled Nanoparticle Collision Experiments.

Electrochemical monitoring of catalytically amplified collisions of individual metal nanoparticles (NP) with ultramicroelectrodes (UME) has been extensively used to study electrocatalysis, mass-transport, and charge-transfer processes at the single NP level. More recently, photoelectrochemical collision experiments were carried out with semiconductive NPs. Here, we introduce two new types of light-controlled nanoimpact experiments. The first experiment involves localized photodeposition of catalyst (Pt) on TiO2 NPs with a glass-sheathed carbon fiber simultaneously serving as the light guide and collector UME. The collisions of in situ prepared Pt@TiO2 NPs with the carbon surface produced blips of water oxidation current, while the activity of pristine TiO2 NPs was too low to yield measurable signal. In another experiment, collisions of catalytic (Ir oxide) NPs with the semiconductor (Nb doped n-type TiO2 rutile single crystal) electrode are monitored by measuring the photocurrent of water oxidation.

Practical model for imperfect conductometric molecular wire sensors.

We present a theoretical model for description of real polyreceptor molecular wire sensors (MWS), whose conductance signal may dramatically reduce upon analyte binding to one of the receptors coupled to the molecular wire but may not vanish as completely as assumed in the ideal MWS model. For the present nonideal MWS model, we establish the exact relationship between analyte concentration and the sensory signal intensity. It turns out that, whereas the Stern-Volmer curve of the ideal MWS always has a positive curvature, the Stern-Volmer curve of the imperfect MWS can have a negative curvature, consistent with experimental data. We find that the MWS still performs better than the corresponding ideal monoreceptor sensor, unless the nonideality of the imperfect MWS is egregiously large. We establish the conditions for the imperfect polyreceptor MWS to have a sensitivity and detection limit superior to the traditional monoreceptor sensor.

Excess grand potential for a system under an external field: effects of external field driven nonextensivity.

We report that an external field can drive inherently extensive systems into nonextensive ones. For the correct grand canonical description of nonextensive systems, it is necessary to take into account the excess grand potential, X, in addition to the conventional grand potential proportional to the thermodynamic pressure, which has long been overlooked in the literature in this field. We present the statistical mechanical expression for X of a system as a functional of the external field imposed on the system, from which we establish the criterion for the external field that drives an inherently extensive macroscopic system into a nonextensive one.

Mean first passage time for the contact between the ends of a chain polymer.

We investigate the first passage times for the contact between the ends of a Rouse chain, whose initial separation is greater than a predefined contact distance, sigma, and equilibrium-distributed. An approximate analytic expression for the mean first passage time is obtained and compared with the results of previous theories and Brownian dynamics simulations. We find that the results of the present theory are in better agreement with Brownian dynamics simulation results than those of previously reported theories.

Diffuse Layer Effect on Electron-Transfer Kinetics Measured by Scanning Electrochemical Microscopy (SECM).

Recent theoretical and experimental studies revealed strong effects of the electrical double layer (EDL) on mass transfer at nanometer-sized electrodes and in electrochemical nanogaps. Although the EDL effect is much stronger in weakly supported media, it can significantly influence the kinetics of electron-transfer processes involving multicharged ionic redox species, even at high concentrations of supporting electrolyte. We measured the kinetics of Fe(CN)64- oxidation in 1 M KCl solution at the Pt nanoelectrode used as a tip in the scanning electrochemical microscope. The apparent standard rate constant values extracted from tip voltammograms without double-layer correction increased markedly with the decreasing separation distance between the tip and substrate electrodes. The same steady-state voltammograms were fitted to the theory including the EDL effect and yielded the rate constant essentially independent of the separation distance.

Effects of adsorption and confinement on nanoporous electrochemistry.

Characteristic molecular dynamics of reactant molecules confined in the space of the nanometer scale augments the frequency of collisions with the electrified surface so that a given faradaic reaction can be enhanced at nanoporous electrodes, the so-called nano-confinement effect. Since this effect is grounded on diffusion inside nanopores, it is predicted that adsorption onto the surface will seriously affect the enhancement by nano-confinement. We experimentally explored the correlation between adsorption and the confinement effect by examining the oxidation of butanol isomers at platinum and gold nanoporous electrodes. The results showed that electrooxidation of 2-butanol, which is a non-adsorption reaction, was enhanced more than that of 1-butanol, which is an adsorption reaction, at nanoporous platinum in acidic media. In contrast, the nanoporous gold electrode, on which 1-butanol is less adsorptive than it is on platinum, enhanced the electrooxidation of 1-butanol greatly. Furthermore, the electrocatalytic activity of nanoporous gold for oxygen reduction reaction was improved so much as to be comparable with that of flat Pt. These findings show that the nano-confinement effect can be appreciable for electrocatalytic oxygen reduction as well as alcohol oxidation unless the adsorption is extensive, and suggests a new strategy in terms of material design for innovative non-noble metal electrocatalysts.

Hydrogen-atom-mediated electrochemistry.

Silicon dioxide thin films are widely used as dielectric layers in microelectronics and can also be engineered on silicon wafers. It seems counterintuitive that electrochemical reactions could occur on such an insulator without relying on tunnelling current. Here we report electrochemistry based on electron transfer through a thin insulating layer of thermally grown silicon dioxide on highly n-doped silicon. Under a negative electrical bias, protons in the silicon dioxide layer were reduced to hydrogen atoms, which served as electron mediators for electrochemical reduction. Palladium nanoparticles were preferentially formed on the dielectric layer and enabled another hydrogen-atom-mediated electrochemistry, as their surfaces retained many electrogenerated hydrogen atoms to act as a 'hydrogen-atom reservoir' for subsequent electrochemical reduction. By harnessing the precisely controlled electrochemical generation of hydrogen atoms, palladium-copper nanocrystals were synthesized without any surfactant or stabilizer on the silicon dioxide layer.

Gold microshell tip for in situ electrochemical Raman spectroscopy.

Tip fabrication by a new strategy is proposed for simultaneous acquisition of electrochemical (EC) signals from an ultramicroelectrode and spectroscopic information from surface-enhanced Raman scattering (SERS). The EC-SERS tip is prepared by carefully tuning a SERS-active gold microshell to maximize Raman scattering, mechanically attaching it to the end of a micropipet, and electrically connecting it to a ruthenium inner layer through electroless deposition.