Fingerprint imaging by scanning electrochemical microscopy

An efficient strategy for visualizing human fingerprints on a poly(vinylidene difluoride) membrane (PVDF) by scanning electrochemical microscopy (SECM) has been developed. Compared to a classical ink fingerprint image, here the ink is replaced by an aqueous solution of bovine serum albumin (BSA). After placing the “inked” finger on a PVDF membrane, the latent image is stained by silver nitrate and the fingerprint is imaged electrochemically using potassium hexachloroiridate (III) (K₃IrCl₆) as a redox mediator. SECM images with an area of 5 mm × 3 mm have been recorded with a high-resolution using a 25-μm-diameter Pt disk-shaped microelectrode. Pores in the skin (40–120 μm in diameter) and relative locations of ridges were clearly observed. The factors relevant to the quality of fingerprint images are discussed.     

Electrochemical studies of guanosine in DMF and detection of its radical cation in a scanning electrochemical microscopy nanogap experiment

This communication reports the findings of the investigation of the electrochemical (EC) oxidation of the important bimolecular guanosine (Gs) by scanning electrochemical microscopy (SECM) using carbon fiber ultramicroelectrodes (CF-UMEs) as the probe and substrate. The first attempt is to try to gain a steady-state voltammogram for EC oxidation of Gs at the CF-UME probe in aqueous buffer solutions with three different pH values. Experimental results indicate that due to serious adsorption of Gs on the CF-UME surface, an "S-shaped" steady-state voltammetric curve, which is required for SECM studies, cannot be obtained in aqueous solutions. To solve this adsorption problem, a series of experiments for studying the EC behavior of Gs in DMF are carried out. A well-defined "S-shaped" steady-state cyclic voltammogram (CV) could be achieved at the CF-UME in DMF containing 0.1M TBAPF6 as the supporting electrolyte. By combining several EC techniques, including cyclic voltammetry at glassy carbon (GC) macroelectrode and CF-UMEs, and chronoamperometry, the general chemical characteristics and EC behavior of Gs in DMF solution are studied. Furthermore, SECM detection of Gs*+, the radical cation of Gs electrogenerated in its first oxidation, is carried out by using feedback and tip generation/substrate collection modes in a nanogap configuration. Gs*+ has been electrochemically detected for the first time, with an estimated lifetime of 相似文献   

Photosystem I patterning imaged by scanning electrochemical microscopy

We report the first directed adsorption of Photosystem I (PSI) on patterned surfaces containing discrete regions of methyl- and hydroxyl-terminated self-assembled monolayers (SAMs) on gold. SAM and PSI patterns are characterized by scanning electrochemical microscopy (SECM). The insulating protein complex layer blocks the electron transfer of the SECM mediator, thereby reducing the electrochemical current significantly. Uniformly and densely packed adsorbed protein layers are observed with SECM. Pattern images correlate with our previous studies where we showed that low-energy surfaces (e.g., CH3-terminated) inhibit PSI adsorption in the presence of Triton X-100, whereas high-energy surfaces (e.g., OH-terminated) enable adsorption. Therefore, a SAM pattern with alternating methyl and hydroxyl surface regions allows PSI adsorption only on the hydroxyl surface, and this is demonstrated in the resulting SECM images.     

Electrochemical investigation of thin PEDOT film above an insulating substrate using scanning electrochemical microscopy

Thin layer of conducting polymer, poly(3,4-ethylenedioxythiophene) PEDOT, deposited on insulating substrates was electrochemically investigated. This study was performed through the reaction with a series of electrogenerated mediators at a microelectrode operating in the configuration of a scanning electrochemical microscope (SECM). The method proves to be a convenient tool for investigating redox properties of the electroactive materials onto insulating substrate and the occurrence of electron transfers across the modified substrate. The SECM results demonstrate the possibility of the regeneration of the mediator at the modified surface even if the used substrate is an insulator. The regeneration rate depends on the standard redox potential of the mediator, on the switching potential of the polymer and on its initial oxidation state. In addition, the obtained data could be analyzed through the construction of the steady state voltammograms allowing the extraction of the electrochemical properties of the thin organic layer deposited onto insulating surface.     

Simultaneous detection of uric acid and glucose on a dual-enzyme chip using scanning electrochemical microscopy/scanning chemiluminescence microscopy

Scanning electrochemical microscopy (SECM) and scanning chemiluminescence microscopy (SCLM) were used for imaging an enzyme chip with spatially-addressed spots for glucose oxidase (GOD) and uricase microspots. For the SECM imaging, hydrogen peroxide generated from the GOD and/or uricase spots was directly oxidized at the tip microelectrode in a solution containing glucose and/or uric acid (electrochemical (EC) detection). For the SCLM imaging, a tapered glass capillary (i.d. of 1∼2 μm) filled with luminol and horseradish peroxidase (HRP) was used as the scanning probe for generating the chemiluminescence (CL). The inner solution was injected from the capillary tip at 78 pl s⁻¹ while scanning above the enzyme-immobilized chip. The CL generated when the capillary tip was scanned above the enzyme spots was detected using a photon-counter (CL detection). Two-dimensional mapping of the oxidation current and photon-counting intensity against the tip position affords images of which their contrast reflects the activity of the immobilized GOD and uricase. For both the EC and CL detections, the signal responses were plotted as a function of the glucose and uric acid concentrations in solution. The sensitivities for the EC and CL detection were found to be comparable.     

Generation and detection of single metal nanoparticles using scanning electrochemical microscopy techniques

Different pathways towards the generation and detection of a single metal nanoparticle (MNP) on a conductive carbon support for testing as an electrocatalyst are described. Various approaches were investigated including interparticle distance enhancement, electrochemical and mechanical tip-substrate MNP transfer onto macroscopic surfaces, scanning electrochemical microscopy (SECM)-controlled electrodeposition, and the use of selective binding monolayers on carbon fiber electrodes (CFEs) for solution-phase-selective adsorption. A novel SECM technique for electrodepositing MNPs on CFE tips immersed 100-200 nm below the electrolyte level was developed and used to generate single Pt and Ni nanoparticles. Following their generation, we demonstrate electrocatalytic detection of Fe3+ on individual Pt particles with the CFE in a Fe3+/H2SO4 solution. We also describe an approach of attaching MNPs to CFEs by controlling the composition of monolayers bonded to the CFE. By employing a monolayer with a low ratio of binding (e.g., 4-aminopyridine) to nonbinding molecules (e.g., aniline) and controlling the position of the CFE in a colloidal Pt solution with a SECM, we attached a single 15 nm radius Pt nanoparticle to the CFE. Such chemisorbed Pt particles exhibited a stronger adhesion on surface-modified CFEs and better mechanical stability during proton reduction than MNPs electrodeposited directly on the CFE.     

Localization of proteins in paint cross-sections by scanning electrochemical microscopy as an alternative immunochemical detection technique

The qualitative identification of proteinaceous substances, as well as their location within a complex paint stratigraphy, is one of the most challenging issues in the characterization of painting materials. Nevertheless, information on paint components represent a crucial task for studies concerning both the ancient painting techniques adopted and the state of conservation, being fundamental investigations for the selection of appropriate conservation actions. The present research was aimed at developing a new detection approach for the immunochemical localization of ovalbumin in paint cross-sections based on the use of scanning electrochemical microscopy (SECM). The immunochemical analyses were performed using an anti-ovalbumin primary antibody and a secondary antibody labelled with horseradish peroxidase (HRP). SECM measurements were performed in feedback mode using benzoquinone (BQ)/hydroquinone (H₂Q) redox couple. In presence of hydrogen peroxide (H₂O₂), HRP catalyzes the re-oxidation of H₂Q to BQ and the increment of BQ concentration in correspondence of the target protein was detected by SECM through the electrochemical reduction of the regenerated BQ at the microelectrode. Indeed, the localization of ovalbumin was possible thanks to a clear discrimination of SECM currents, achieved by the comparison of the measurements recorded before and after H₂O₂ administration, based on the HRP on/off approach. The method was evaluated both on samples from standard mocks-up and on a historical sample, collected from a Renaissance wood painting. The obtained results were promising, foreseeing a wider application of SECM on cultural heritage researches.     

Interfacial reactivity of monolayer-protected clusters studied by scanning electrochemical microscopy

Solutions of monodisperse monolayer-protected clusters (MPCs) of gold can be used as multivalent redox mediators in electrochemical experiments due to their quantized double-layer charging properties. We demonstrate their use in scanning electrochemical microscopy (SECM) experiments wherein the species of interest (up to 2-electron reduction or 4-electron oxidation from the native charge-state of the MPCs) is generated at the tip electrode, providing a simple means to adjust the driving force of the electron transfer (ET). Approach curves to perfectly insulating (Teflon) and conducting (Pt) substrates are obtained. Subsequently, heterogeneous ET between MPCs in 1,2-dichloroethane and an aqueous redox couple (Ce(IV), Fe(CN)63-/4-, Ru(NH3)63+, and Ru(CN)64-) is probed with both feedback and potentiometric mode of SECM operation. Depending on the charge-state of the MPCs, they can accept/donate charge heterogeneously at the liquid-liquid interface. However, this reaction is very slow in contrast to ET involving MPCs at the metal-electrolyte interface.     

Nanostructuring and nanoanalysis by scanning electrochemical microscopy (SECM)

The generation and application of nanodes in SECM experiments are described. Nanodes are ultramicroelectrodes with an active disk diameter in the submicrometer range. We investigated the behaviour of these electrodes by testing their properties with SECM applications which were previously performed at the micrometer scale. The active diameter of the nanodes was determined using cyclic voltammetry and SECM. The nanoanalysis was conducted at two nano interdigitated arrays. The nanostructuring was demonstrated by galvanic and electroless silver deposition from solution and from the surface, respectively. Experiments with nanodes illustrate that they exhibit the same behaviour as ultramicroelectrodes, but are more sensitive to adsorption and dirt particles in the electrolyte solution.     

Electrochemical concept of scanning tunnel microscopy and scanning tunnel spectroscopy

The history of investigation, development and application of electrochemical scanning tunneling microscopy (ESTM) are reviewed.     

Electron transfer at self-assembled monolayers measured by scanning electrochemical microscopy

New approaches have been developed for measuring the rates of electron transfer (ET) across self-assembled molecular monolayers by scanning electrochemical microscopy (SECM). The developed models can be used to independently measure the rates of ET mediated by monolayer-attached redox moieties and direct ET through the film as well as the rate of a bimolecular ET reaction between the attached and dissolved redox species. By using a high concentration of redox mediator in solution, very fast heterogeneous (10(8) s(-1)) and bimolecular (10(11) mol(-1) cm(3) s(-1)) ET rate constants can be measured. The ET rate constants measured for ferrocene/alkanethiol on gold were in agreement with previously published data. The rates of bimolecular heterogeneous electron transfer between the monolayer-bound ferrocene and water-soluble redox species were measured. SECM was also used to measure the rate of ET through nonelectroactive alkanethiol molecules between substrate gold electrodes and a redox probe (Ru(NH(3))(6)(3+)) freely diffusing in the solution, yielding a tunneling decay constant, beta, of 1.0 per methylene group.     

Mapping peroxidase in plant tissues by scanning electrochemical microscopy.

Scanning electrochemical microscopy has been firstly used to map the enzymatic activity in natural plant tissues. The peroxidase (POD) was maintained in its original state in the celery (Apium graveolens L.) tissues and electrochemically visualized under its native environment. Ferrocenemethanol (FMA) was selected as a mediator to probe the POD in celery tissues based on the fact that POD catalyzed the oxidation of FMA by H(2)O(2) to increase FMA(+) concentration. Two-dimensional reduction current profiles for FMA(+) produced images indicating the distribution and activity of the POD at the surface of the celery tissues. These images showed that the POD was widely distributed in the celery tissues, and larger amounts were found in some special regions such as the center of celery stem and around some vascular bundles.     

Characterization of carboxylic acid-terminated self-assembled monolayers by electrochemical impedance spectroscopy and scanning electrochemical microscopy

Electrochemical impedance spectroscopy (EIS) and scanning electrochemical microscopy (SECM) are used to monitor changes in the ionization of monolayers of 11-mercaptoundecanoic acid. When using an anionic redox probe, Fe(CN)6(-4), the charge-transfer resistance of the 11-mercaptoundecanoic acid monolayer-modified interface increases in a sigmoidal fashion as the solution is made basic. The opposite effect is observed when using a cationic redox probe. The inflection points of these two titration curves, however, differ when using the different redox probes. This result is taken as being characteristic of the influence that applied potential has on the ionization of the monolayer. The role of substrate potential on the ionization of the monolayer is further investigated by SECM. The SECM measurement monitors the concentration of Ru(NH3)6(+3) as the potential of the substrate is varied about the potential of zero charge. For monolayers of 11-mercaptoundecanoic acid in solutions buffered near the pKa of the terminal carboxylic acid, potential excursions positive of the PZC cause an increase in the concentration of Ru(NH3)6(+3) local to the interface, and potential excursions negative of the PZC cause a decrease in the local concentration of Ru(NH3)6(+3). Similar experiments conducted with an interface modified with 11-undecanethiol had no impact on the local concentration of Ru(NH3)6(+3). These results are interpreted in terms of the influence that applied potential has on the pH of the solution local to the interface and the impact that this has on the ionization of the monolayer.     

Recent advances of scanning electrochemical microscopy and scanning ion conductance microscopy for single-cell analysis

Single-cell analysis is important for understanding fundamental biological processes and mechanisms. Scanning electrochemical microscopy and scanning ion conductance microscopy as two kinds of scanning probe microscopy, with high temporal and spatial resolutions as well as in situ and noninvasive characterization capabilities, emerge as strong tools for single-cell analysis. In this review, we introduce the latest advances of scanning electrochemical microscopy and scanning ion conductance microscopy for single-cell analysis, including characterizations of cell morphology dynamics, membrane properties and mechanics, and monitoring cell surface charge, extracellular pH, and intracellular substances.     

Visualization of DNA microarrays by scanning electrochemical microscopy (SECM)

DNA duplex regions of the spots on a DNA microarray were successfully visualized by scanning electrochemical microscopy (SECM) in the electrolyte containing ferrocenyl naphthalene diimide as a hybridization indicator.     

Application of scanning electrochemical microscopy and scanning electron microscopy for the characterization of carbon-spray modified electrodes

Different gold surfaces modified by carbon-spray have been investigated by scanning electron microscopy (SEM) and scanning electrochemical microscopy (SECM). A transformation of the SECM image to a distance-location profile is proposed which assists the correlation of both images. The structures found in the transformed SECM images of carbon-spray layers on gold substrates can be explained by the topographic features visible in the SEM pictures. Tempering the carbon spray results in an increased density of electrochemically reactive carbon particles which could be confirmed by cyclic voltammetric investigations. Gold minigrids modified with carbon spray expose some areas of especially large currents which could not be predicted from their SEM images. This effect may result from particles located at the edge of a wire intersection having relatively large active surfaces per particle. They contribute significantly to the total current of the minigrid.     

Nanoscale surface modification via scanning electrochemical probe microscopy

Micro- and nanoscale surface modification using scanning probe microscopy techniques in combination with electrochemically induced surface structuring provides a maskless in situ fabrication strategy enabling deposition or etching of three-dimensional nanostructures. This current opinion article focuses on scanning electrochemical probe microscopy techniques highlighting recent progress in nanoscale 3D surface modification along with a spotlight on approaches of practical relevance.     

Local amperometric detection of K+ in aqueous solution using scanning electrochemical microscopy ion-transfer voltammetry

A robust ultramicroelectrode (UME) probe is described for the amperometric determination of K⁺ ions in aqueous solution. The approach is based on ion-transfer voltammetry at the interface between two immiscible electrolyte solutions (ITIES), with a liquid ¦ liquid interface formed between a 1,2-dichloroethane solution, containing dibenzo-18-crown-6, in a glass capillary, which is placed in an aqueous K⁺ salt solution of interest (KCl in this study). The ITIES is externally polarised by applying a potential between silver electrodes in each phase. The UME probe has an inlaid disk geometry, making conventional ultramicroelectrode and scanning electrochemical microscopy (SECM) mass transport models applicable. Limiting current measurements of K⁺ in aqueous solution show a linear dependence on KCl concentration between 1 × 10⁴ and 2.5 × 10³ mol dm³. The K⁺ microprobe is shown to be particularly suitable for use in SECM, for both approach curve and imaging applications.     

Accurately measuring respiratory activity of single living cells by scanning electrochemical microscopy

Scanning electrochemical microscopy (SECM) is a powerful tool to examine the respiratory activity of living cells. However, in SECM measurements of cell respiratory activity, the signal recorded usually also includes the signal corresponding to the cell topography. Therefore, measurements of cell respiratory activity using conventional SECM techniques are not accurate. In the present work, we develop a method for accurate measurement of the respiratory activity of single living cells using SECM. First, cells are immobilized on a glass substrate modified with collagen. Then, a Pt ultramicroelectrode tip of SECM held at −0.50 V is scanned along the central line across a living cell and a SECM scan curve, i.e., the relationship of the tip current versus the displacement (the first scan curve) is recorded with a negative peak. The peak current i_p on this first scan curve is composed of i_p1, which corresponds to the cell respiratory activity and i_p2, which corresponds to the cell topography. In order to isolate the i_p2 component, the cell is killed by exposing it to 1.0 × 10⁻³ mol/L KCN for 10 min. The tip is then scanned again with the same trace over the dead cell, and a second SECM scan curve is recorded. Noting that the topography of the dead cell is the same as that of the living cell, this second scan curve with a negative peak corresponds now only to the cell topography. Thus, i_p2 is obtained from the second SECM scan curve. Finally, i_p1 corresponding to the respiratory activity of the living cell can be accurately calculated using i_p1 = i_p − i_p2. This method can be used to monitor real-time change in the respiratory activity of single cells after exposing them to KBr, NaN₃ and KCN.