Jeyavel Velmurugan

Adsorption/Desorption of Hydrogen on Pt Nanoelectrodes: Evidence of Surface Diffusion and Spillover

Nanoelectrochemical approaches were used to investigate adsorption/desorption of hydrogen on Pt electrodes. These processes, which have been extensively studied over the last century, remain of current interest because of their applications in energy storage systems. The effective surface area of a nanoelectrode was found to be much larger than its geometric surface area due to surface diffusion of adsorbed redox species at the Pt/glass interface. An additional peak of hydrogen desorption was observed and attributed to the spillover of hydrogen from the Pt surface into glass. The results were compared to those obtained for underpotential deposition of copper on Pt nanoelectrodes.

Nanoelectrodes for determination of reactive oxygen and nitrogen species inside murine macrophages.

Reactive oxygen and nitrogen species (ROS and RNS) produced by macrophages are essential for protecting a human body against bacteria and viruses. Micrometer-sized electrodes coated with Pt black have previously been used for selective and sensitive detection of ROS and RNS in biological systems. To determine ROS and RNS inside macrophages, one needs smaller (i.e., nanometer-sized) sensors. In this article, the methodologies have been extended to the fabrication and characterization of Pt/Pt black nanoelectrodes. Electrodes with the metal surface flush with glass insulator, most suitable for quantitative voltammetric experiments, were fabricated by electrodeposition of Pt black inside an etched nanocavity under the atomic force microscope control. Despite a nanometer-scale radius, the true surface area of Pt electrodes was sufficiently large to yield stable and reproducible responses to ROS and RNS in vitro. The prepared nanoprobes were used to penetrate cells and detect ROS and RNS inside macrophages. Weak and very short leaks of ROS/RNS from the vacuoles into the cytoplasm were detected, which a macrophage is equipped to clean within a couple of seconds, while higher intensity oxidative bursts due to the emptying of vacuoles outside persist on the time scale of tens of seconds.

Nanoscale imaging of surface topography and reactivity with the scanning electrochemical microscope.

Over the last 2 decades, scanning electrochemical microscopy (SECM) has been extensively employed for topographic imaging and mapping surface reactivity on the micrometer scale. We used flat, polished nanoelectrodes as SECM tips to carry out feedback mode imaging of various substrates with nanoscale resolution. Constant-height and constant-current images of plastic and Au compact disc surfaces and more complicated objects (computer chips and wafers) were obtained. The possibility of simultaneous imaging of surface topography and electrochemical reactivity was demonstrated. Very fast mass transfer at nanoelectrodes allowed us to obtain high-quality electrochemical images in viscous media under steady-state conditions, e.g., in 1-methyl-3-octylimidazolium-bis(tetrafluoromethylsulfonyl)imide (C(8)mimC(1)C(1)N) ionic liquid. Ion-transfer-based imaging was also performed using nanopipets as SECM tips.

Kinetic study of rapid transfer of tetraethylammonium at the 1,2-dichloroethane/water interface by nanopipet voltammetry of common ions.

Steady-state voltammetry at the pipet-supported liquid/liquid interface has previously been used to measure kinetics of simple and facilitated ion transfer (IT) processes. Recently, we showed that the conventional experimental protocol and data analysis produce large uncertainties in kinetic parameters of rapid IT processes extracted from pipet voltammograms. Here, we used a new mode of nanopipet voltammetry, in which a transferable ion is initially present as a common ion in both liquid phases, and improved methodology for silanization of the outer pipet wall to investigate the kinetics of the rapid transfer of tetraethylammonium (TEA(+)) at the 1,2-dichloroethane/water interface. This reaction was often employed as a model system to check the IT theory. The determined standard rate constant and transfer coefficient of the TEA(+) transfer are compared with previously reported values to demonstrate limitations of conventional nanopipet voltammetry with a transferrable ion present only in one liquid phase.

Atomic Force Microscopy of Electrochemical Nanoelectrodes

Nanometer-sized electrodes have recently been used to investigate important chemical and biological systems on the nanoscale. Although nanoelectrodes offer a number of advantages over macroscopic electrochemical probes, visualization of their surfaces remains challenging. Thus, the interpretation of the electrochemical response relies on assumptions about the electrode shape and size prior to the experiment and the changes induced by surface reactions (e.g., electrodeposition). In this paper, we present first AFM images of nanoelectrodes, which provide detailed and unambiguous information about the electrode geometry. The effects of polishing and cleaning nanoelectrodes are investigated, and AFM results are compared to those obtained by voltammetry and SEM. In situ AFM is potentially useful for monitoring surface reactions at nanoelectrodes.

Polished Nanopipets: New Probes for High-Resolution Scanning Electrochemical Microscopy

Nanometer-sized pipets pulled from glass or quartz capillaries have been extensively used as probes for scanning electrochemical microscopy (SECM) and scanning ion conductance microscopy (SICM). A small separation distance between such a probe and the sample, which is required for high-resolution SECM measurements, may be hard to attain because of considerable roughness of the pipet tip. In this Letter, we report the preparation and characterization of polished nanopipet SECM probes with a much smoother tip edge. Using polished pipets, quantitative SECM measurements were performed at extremely short tip/substrate distances (e.g., d ≈ 1 nm).

Electrochemistry through glass

In this Article we have used new approaches to investigate a well-known chemical process, the propagation of electrochemical signals through a thin glass membrane. This process, which has been extensively studied over the last century, is the basis of the response of a potentiometric glass pH sensor; however, no amperometric glass sensors have yet been reported because of its high ohmic resistance. Voltammetry at nanoelectrodes has revealed that water molecules can diffuse through nanometre-thick layers of dry glass and undergo oxidation/reduction at the buried platinum surface. After soaking for a few hours in an aqueous solution, voltammetric waves of other redox couples, such as Ru(NH(3))(6)(3+/2+), could also be obtained at the glass-covered platinum nanoelectrodes. This behaviour suggests that the nanometre-thick insulating glass sheath surrounding the platinum core can be largely converted to hydrated gel, and electrochemical processes occur at the platinum/hydrogel interface. Potential applications range from use in nanometre-sized solid-state pH probes and determination of the water content in organic solvents to glass-modified voltammetric sensors and electrocatalysts.

Nucleation and growth of metal on nanoelectrodes

Three-dimensional nucleation and growth on active surface sites are fundamentally important initial stages of the electrodeposition of metals. Electrochemical studies of these processes are greatly complicated by the formation of multiple crystals interacting with each other. We investigated Ag electrodeposition on the surface of well-characterized, nanometer-sized Pt electrodes and measured the nucleation/growth kinetics of individual Ag crystals by a combination of nanoelectrochemistry and atomic force microscopy (AFM). Basic parameters, including the number of surface active sites, the kinetic time lag and the number of growing nuclei, were directly accessed from current transients and in situ AFM imaging. The existence of a single nucleation site on the surface of a 50 nm electrode persisting through several deposition/stripping cycles has been demonstrated.

Fabrication of Nanoelectrodes and Metal Clusters by Electrodeposition

Most nanometer-sized electrodes reported to date are made from either Pt or Au. For technical reasons, it is difficult to make nanoelectrodes from many other metals (e.g. Hg) by heat-sealing microwires into glass capillaries or by other established techniques. Such nanoelectrodes can be useful for a wide range of analytical and physicochemical applications from high sensitivity stripping analysis (Hg) to pH nano-sensors to studies of electrocatalysis. In this paper, nanometer-sized metal electrodes are prepared by electrodeposition of Hg or Pt on disk-type, polished or recessed nanoelectrodes. The deposition of Hg is monitored chronoamperometrically to produce near-hemispherical electrodes, which are characterized by voltammetry and scanning electrochemical microscopy (SECM). The well-shaped deposits of a solid metal (Pt) at Au nanoelectrodes are prepared and imaged by scanning electron microscopy (SEM). Catalytic metal clusters can also be prepared using this methodology. Electrodes with the metal surface flush with glass insulator, most suitable for quantitative voltammetric and SECM experiments are fabricated by electrodeposition of a metal inside an etched nanocavity.

Electron transfer/ion transfer mode of scanning electrochemical microscopy (SECM): a new tool for imaging and kinetic studies

A new mode of the scanning electrochemical microscope (SECM) operation was developed that combines reagent delivery from the nanopipette with electron transfer at the conductive substrate and ion transfer across the liquid/liquid interface supported at the nanopipette tip. This approach offers potential advantages for measurements of heterogeneous electron transfer kinetics and reaction rate imaging by enabling straightforward separation of the contributions of surface topography and reactivity features to the tip current. It addresses some other long-standing technical issues, including sensitive probing of low signal sources (e.g., immobilized enzymes or catalyst particles) without diffusional broadening and the elimination of the elevated background signal in generation/collection-type experiments. The high spatial resolution attainable in electron transfer/ion transfer mode experiments and the absence of redox mediator species in the bulk solution are advantageous for studies of biological cells.