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Nanoelectrochemistry is a branch of electrochemistry that investigates the electrical and electrochemical properties of materials at the nanometer size regime. Nanoelectrochemistry plays significant role in the fabrication of various sensors, and devices for detecting molecules at very low concentrations.
Two transport mechanisms are fundamental for nanoelectrochemistry: electron transfer and mass transport. The formulation of theoretical models allows to understand the role of the different species involved in the electrochemical reactions.
The electron transfer between the reactant and the nanoelectrode can be explained by the combination of various theories based on the Marcus theory.
Mass transport, that is the diffusion of the reactant molecules from the electrolyte bulk to the nanoelectrode, is influenced by the formation of a double electric layer at the electrode/electrolyte interface. At the nanoscale it is necessary to theorize a dynamic double electric layer which takes into account an overlap of the Stern layer and the diffuse layer. [1]
Knowledge of the mechanisms involved allows to build computational models that combine the density functional theory with electron transfer theories and the dynamic double electric layer. [2] In the field of molecular modelling, accurate models could predict the behaviour of the system as reactants, electrolyte or electrode change.
The role of the surface is strongly reaction-specific: in fact, one site can catalyze certain reactions and inhibit other ones.
According to TSK model, surface atoms in nanocrystals can occupy terrace, step or kink positions: each site has a different tendency to adsorb reactants and to let them move along the surface. Generally, sites having lower coordination number (steps and kinks) are more reactive due to their high free energy. High energy sites, however, are less thermodynamically stable and nanocrystals have a tendency to transform to their equilibrium shape.
Thanks to the progress in nanoparticles synthesis it is now possible to have a single-crystal approach to surface science, allowing more precise research on the effect of a given surface. Studies have been conducted on nanoelectrodes exposing a (100), (110) or (111) plane to a solution containing the reactants, in order to define the surface effect on reaction rate and selectivity of the most common electrochemical reactions. [3]
Nanoelectrodes are tiny electrodes made of metals or semiconducting materials having typical dimensions of 1-100 nm. Various forms of nanoelectrodes have been developed taking advantage of the different possible fabrication techniques: among the most studied are the nanoband, disk, hemispherical, nanopore geometries as well as the different forms of carbon nanostructures. [4] [5]
It is necessary to characterize each produced electrode: size and shape determine its behavior. The most used characterization techniques are: [4] [6]
There are mainly two properties that distinguish nanoelectrodes from electrodes: smaller RC constant and faster mass transfer. The former allows measurements to be made in high-resistance solutions because they offer less resistance, the latter, due to radial diffusion, allows much faster voltammetry responses. Due to these and other properties, nanoelectrodes are used in various applications: [1] [4]
The main advantages of using nanoelectrodes and arrays of nanoelectrodes include enhanced mass transport, lower capacitance, ability to work in smaller volumes and smaller overall device footprints. [7]
The electrical current generated at an electrode is proportional to the electrode's geometric area. A disadvantage of using a single nanoelectrode is that it generates a small current output, which puts pressure on the instrumentation, and in turn, the reliability of the measurements recorded. One way to overcome this is the use an array of nanoelectrodes. The arrays produce a current, which is proportional with the number of electrodes in the array. This method has been used extensively in electroanalysis. Through the careful and accurate fabrication of arrays of nanoelectrodes, the electrochemical instrumentation is more reliable for sensitive measurement that enables implementation of a range of electroanalytical techniques. [8]
There are two main types of arrangements; nanoelectrode arrays (NEAs) where the nanoelectrodes are spaced in an ordered arrangement and nanoelectrode ensembles (NEEs), where the individual nanoelectrodes are distributed randomly.
Electrochemistry is the branch of physical chemistry concerned with the relationship between electrical potential difference and identifiable chemical change. These reactions involve electrons moving via an electronically conducting phase between electrodes separated by an ionically conducting and electronically insulating electrolyte.
Surface science is the study of physical and chemical phenomena that occur at the interface of two phases, including solid–liquid interfaces, solid–gas interfaces, solid–vacuum interfaces, and liquid–gas interfaces. It includes the fields of surface chemistry and surface physics. Some related practical applications are classed as surface engineering. The science encompasses concepts such as heterogeneous catalysis, semiconductor device fabrication, fuel cells, self-assembled monolayers, and adhesives. Surface science is closely related to interface and colloid science. Interfacial chemistry and physics are common subjects for both. The methods are different. In addition, interface and colloid science studies macroscopic phenomena that occur in heterogeneous systems due to peculiarities of interfaces.
Proton-exchange membrane fuel cells (PEMFC), also known as polymer electrolyte membrane (PEM) fuel cells, are a type of fuel cell being developed mainly for transport applications, as well as for stationary fuel-cell applications and portable fuel-cell applications. Their distinguishing features include lower temperature/pressure ranges and a special proton-conducting polymer electrolyte membrane. PEMFCs generate electricity and operate on the opposite principle to PEM electrolysis, which consumes electricity. They are a leading candidate to replace the aging alkaline fuel-cell technology, which was used in the Space Shuttle.
In electrochemistry, cyclic voltammetry (CV) is a type of potentiodynamic measurement. In a cyclic voltammetry experiment, the working electrode potential is ramped linearly versus time. Unlike in linear sweep voltammetry, after the set potential is reached in a CV experiment, the working electrode's potential is ramped in the opposite direction to return to the initial potential. These cycles of ramps in potential may be repeated as many times as needed. The current at the working electrode is plotted versus the applied voltage to give the cyclic voltammogram trace. Cyclic voltammetry is generally used to study the electrochemical properties of an analyte in solution or of a molecule that is adsorbed onto the electrode.
Voltammetry is a category of electroanalytical methods used in analytical chemistry and various industrial processes. In voltammetry, information about an analyte is obtained by measuring the current as the potential is varied. The analytical data for a voltammetric experiment comes in the form of a voltammogram, which plots the current produced by the analyte versus the potential of the working electrode.
Nanobatteries are fabricated batteries employing technology at the nanoscale, particles that measure less than 100 nanometers or 10−7 meters. These batteries may be nano in size or may use nanotechnology in a macro scale battery. Nanoscale batteries can be combined to function as a macrobattery such as within a nanopore battery.
The Fritz Haber Institute of the Max Planck Society (FHI) is a science research institute located at the heart of the academic district of Dahlem, in Berlin, Germany.
Electroanalytical methods are a class of techniques in analytical chemistry which study an analyte by measuring the potential (volts) and/or current (amperes) in an electrochemical cell containing the analyte. These methods can be broken down into several categories depending on which aspects of the cell are controlled and which are measured. The three main categories are potentiometry, amperometry, coulometry.
In surface science, a double layer is a structure that appears on the surface of an object when it is exposed to a fluid. The object might be a solid particle, a gas bubble, a liquid droplet, or a porous body. The DL refers to two parallel layers of charge surrounding the object. The first layer, the surface charge, consists of ions which are adsorbed onto the object due to chemical interactions. The second layer is composed of ions attracted to the surface charge via the Coulomb force, electrically screening the first layer. This second layer is loosely associated with the object. It is made of free ions that move in the fluid under the influence of electric attraction and thermal motion rather than being firmly anchored. It is thus called the "diffuse layer".
In analytical chemistry, linear sweep voltammetry is a method of voltammetry where the current at a working electrode is measured while the potential between the working electrode and a reference electrode is swept linearly in time. Oxidation or reduction of species is registered as a peak or trough in the current signal at the potential at which the species begins to be oxidized or reduced.
In analytical chemistry, a rotating disk electrode (RDE) is a working electrode used in three-electrode systems for hydrodynamic voltammetry. The electrode rotates during experiments, inducing a flux of analyte to the electrode. These working electrodes are used in electrochemical studies when investigating reaction mechanisms related to redox chemistry, among other chemical phenomena. The more complex rotating ring-disk electrode can be used as a rotating disk electrode if the ring is left inactive during the experiment.
An ultramicroelectrode (UME) is a working electrode with a low surface area primarily used in voltammetry experiments. The small size of UMEs limits mass transfer, which give them large diffusion layers and small overall currents at typical electrochemical potentials. These features allow UMEs to achieve useful cyclic steady-state conditions at fast scan rates (V/s) with limited current distortion. UMEs were developed independently by Wightman and Fleischmann around 1980. UMEs enable electrochemical measurements in electrolytes with high solution resistance, such as organic solvents. The low current at an UME limits the Ohmic drop, which conventional electrodes do not limit. Furthermore, the low Ohmic drop at UMEs lead to low voltage distortions at the electrode-electrolyte interface, allowing for the use of two electrodes in a voltammetric experiment instead of the conventional three electrodes.
An electrocatalyst is a catalyst that participates in electrochemical reactions. Electrocatalysts are a specific form of catalysts that function at electrode surfaces or, most commonly, may be the electrode surface itself. An electrocatalyst can be heterogeneous such as a platinized electrode. Homogeneous electrocatalysts, which are soluble, assist in transferring electrons between the electrode and reactants, and/or facilitate an intermediate chemical transformation described by an overall half reaction. Major challenges in electrocatalysts focus on fuel cells.
Scanning electrochemical microscopy (SECM) is a technique within the broader class of scanning probe microscopy (SPM) that is used to measure the local electrochemical behavior of liquid/solid, liquid/gas and liquid/liquid interfaces. Initial characterization of the technique was credited to University of Texas electrochemist, Allen J. Bard, in 1989. Since then, the theoretical underpinnings have matured to allow widespread use of the technique in chemistry, biology and materials science. Spatially resolved electrochemical signals can be acquired by measuring the current at an ultramicroelectrode (UME) tip as a function of precise tip position over a substrate region of interest. Interpretation of the SECM signal is based on the concept of diffusion-limited current. Two-dimensional raster scan information can be compiled to generate images of surface reactivity and chemical kinetics.
A chemically modified electrode is an electrical conductor that has its surface modified for different electrochemical functions. Chemically modified electrodes are made using advanced approaches to electrode systems by adding a thin film or layer of certain chemicals to change properties of the conductor according to its targeted function.
Pseudocapacitance is the electrochemical storage of electricity in an electrochemical capacitor known as a pseudocapacitor. This faradaic charge transfer originates by a very fast sequence of reversible faradaic redox, electrosorption or intercalation processes on the surface of suitable electrodes. Pseudocapacitance is accompanied by an electron charge-transfer between electrolyte and electrode coming from a de-solvated and adsorbed ion. One electron per charge unit is involved. The adsorbed ion has no chemical reaction with the atoms of the electrode since only a charge-transfer takes place.
Electrochemical AFM (EC-AFM) is a particular type of Scanning probe microscopy (SPM), which combines the classical Atomic force microscopy (AFM) together with electrochemical measurements. EC-AFM allows to perform in-situ AFM measurements in an electrochemical cell, in order to investigate the actual changes in the electrode surface morphology during electrochemical reactions. The solid-liquid interface is thus investigated. This technique was developed for the first time in 1996 by Kouzeki et al., who studied amorphous and polycrystalline thin films of Naphthalocyanine on Indium tin oxide in a solution of 0.1 M Potassium chloride (KCl). Unlike the Electrochemical scanning tunneling microscope, previously developed by Itaya and Tomita in 1988, the tip is non-conductive and it is easily steered in a liquid environment.
Single-Entity Electrochemistry (SEE) refers to the electroanalysis of an individual unit of interest. A unique feature of SEE is that it unifies multiple different branches of electrochemistry. Single-Entity Electrochemistry pushes the bounds of the field as it can measure entities on a scale of 100 microns to angstroms. Single-Entity Electrochemistry is important because it gives the ability to view how a single molecule, or cell, or "thing" affects the bulk response, and thus the chemistry that might have gone unknown otherwise. The ability to monitor the movement of one electron or ion from one unit to another is valuable, as many vital reactions and mechanisms undergo this process. Electrochemistry is well suited for this measurement due to its incredible sensitivity. Single-Entity Electrochemistry can be used to investigate nanoparticles, wires, vesicles, nanobubbles, nanotubes, cells, and viruses, and other small molecules and ions. Single-entity electrochemistry has been successfully used to determine the size distribution of particles as well as the number of particles present inside a vesicle or other similar structures
Spectroelectrochemistry (SEC) is a set of multi-response analytical techniques in which complementary chemical information is obtained in a single experiment. Spectroelectrochemistry provides a whole vision of the phenomena that take place in the electrode process. The first spectroelectrochemical experiment was carried out by Theodore Kuwana, PhD, in 1964.
Raman spectroelectrochemistry (Raman-SEC) is a technique that studies the inelastic scattering or Raman scattering of monochromatic light related to chemical compounds involved in an electrode process. This technique provides information about vibrational energy transitions of molecules, using a monochromatic light source, usually from a laser that belongs to the UV, Vis or NIR region. Raman spectroelectrochemistry provides specific information about structural changes, composition and orientation of the molecules on the electrode surface involved in an electrochemical reaction, being the Raman spectra registered a real fingerprint of the compounds.