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A liquid metal electrode is an electrode that uses a liquid metal, such as mercury, Galinstan, and NaK.[ not verified in body ] They can be used in electrocapillarity, voltammetry, and impedance measurements. [1]
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A liquid metal electrode is an electrode that uses a liquid metal, such as mercury, Galinstan, and NaK.[ not verified in body ] They can be used in electrocapillarity, voltammetry, and impedance measurements. [1]
The dropping mercury electrode (DME) is a working electrode made of mercury and used in polarography. Experiments run with mercury electrodes are referred to as forms of polarography even if the experiments are identical or very similar to a corresponding voltammetry experiment which uses solid working electrodes. Like other working electrodes these electrodes are used in electrochemical studies using three electrode systems when investigating reaction mechanisms related to redox chemistry among other chemical phenomena. [2] [3] [4] [5] [6]
A flow of mercury passes through an insulating capillary producing a droplet which grows from the end of the capillary in a reproducible way. Each droplet grows until it reaches a diameter of about a millimeter and releases. The released droplet is no longer in contact with the working electrode whose contact is above the capillary. As the electrode is used mercury collects in the bottom of the cell. In some cell designs this mercury pool is connected to a lead and used as the cell's auxiliary electrode. Each released drop is immediately followed by the formation of another drop. The drops are generally produced at a rate of about 0.2 Hz.
A major advantage of the DME is that each drop has a smooth and uncontaminated surface free from any adsorbed analyte or impurity. The self-renewing electrode does not need to be cleaned or polished like a solid electrode. This advantage comes at the cost of a working electrode with a constantly changing surface area. Since the drops are produced predictably the changing surface area can be accounted for or even used advantageously. In addition, the drops' growth causes more and more addition of capacitive current to the faradaic current. These changing current effects combined with experiments where the potential is continuously changed can result in noisy traces. In some experiments the traces are continually sampled, showing all the current deviation resulting from the drop growth. Other sampling methods smooth the data by sampling the current at the electrode only once per drop at a specific size. The DME's periodic expansion into the solution and hemispherical shape also affects the way the analyte diffuses to the electrode surface. The DME consists of a fine capillary with a bore size of 20–50 μm.
The hanging mercury drop electrode (HMDE) is a working electrode variation on the dropping mercury electrode (DME). It was developed by Polish chemist Wiktor Kemula. [7] Experiments run with dropping mercury electrodes are referred to as forms of polarography. If the experiments are performed at an electrode with a constant surface (like the HMDE) it is referred as voltammetry.
Like other working electrodes these electrodes are used in electrochemical studies using three electrode systems when investigating reaction mechanisms related to redox chemistry among other chemical phenomenon. [8] [9] [10] [11]
The hanging mercury drop electrode produces a partial mercury drop of controlled geometry and surface area at the end of a capillary in contrast to the dropping mercury electrode which steadily releases drops of mercury during an experiment. The disadvantages a DME experiences due to a constantly changing surface are not experienced by the HMDE since it has static surface area during an experiment. The static surface of the HMDE means it is more likely to suffer from the surface adsorption phenomenon than a DME. Unlike solid electrodes which need to be cleaned and polished between most experiments, the self-renewing HMDE can simply release the contaminated drop and grow a clean drop between each experiment.
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.
Differential pulse voltammetry (DPV) is a voltammetry method used to make electrochemical measurements and a derivative of linear sweep voltammetry or staircase voltammetry, with a series of regular voltage pulses superimposed on the potential linear sweep or stairsteps. The current is measured immediately before each potential change, and the current difference is plotted as a function of potential. By sampling the current just before the potential is changed, the effect of the charging current can be decreased.
A reference electrode is an electrode that has a stable and well-known electrode potential. The overall chemical reaction taking place in a cell is made up of two independent half-reactions, which describe chemical changes at the two electrodes. To focus on the reaction at the working electrode, the reference electrode is standardized with constant concentrations of each participant of the redox reaction.
A potentiostat is the electronic hardware required to control a three electrode cell and run most electroanalytical experiments. A Bipotentiostat and polypotentiostat are potentiostats capable of controlling two working electrodes and more than two working electrodes, respectively.
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.
In electrochemistry, chronoamperometry is an analytical technique in which the electric potential of the working electrode is stepped and the resulting current from faradaic processes occurring at the electrode is monitored as a function of time. The functional relationship between current response and time is measured after applying single or double potential step to the working electrode of the electrochemical system. Limited information about the identity of the electrolyzed species can be obtained from the ratio of the peak oxidation current versus the peak reduction current. However, as with all pulsed techniques, chronoamperometry generates high charging currents, which decay exponentially with time as any RC circuit. The Faradaic current - which is due to electron transfer events and is most often the current component of interest - decays as described in the Cottrell equation. In most electrochemical cells, this decay is much slower than the charging decay-cells with no supporting electrolyte are notable exceptions. Most commonly a three-electrode system is used. Since the current is integrated over relatively longer time intervals, chronoamperometry gives a better signal-to-noise ratio in comparison to other amperometric techniques.
Wiktor Kemula was a Polish chemist, electrochemist, and polarographist. He greatly contributed to the development of electroanalytical chemistry, particularly polarography. He is known for developing the hanging mercury drop electrode (HMDE).
Polarography is a type of voltammetry where the working electrode is a dropping mercury electrode (DME) or a static mercury drop electrode (SMDE), which are useful for their wide cathodic ranges and renewable surfaces. It was invented in 1922 by Czechoslovak chemist Jaroslav Heyrovský, for which he won the Nobel prize in 1959. The main advantages of mercury as electrode material are as follows: 1) a large voltage window: ca. from +0.2 V to -1.8 V vs reversible hydrogen electrode (RHE). Hg electrode is particularly well-suited for studying electroreduction reactions. 2) very reproducible electrode surface, since mercury is liquid. 3) very easy cleaning of the electrode surface by making a new drop of mercury from a large Hg pool connected by a glass capillary.
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 four main categories are potentiometry, amperometry, coulometry, and voltammetry.
In electrochemistry, the working electrode is the electrode in an electrochemical system on which the reaction of interest is occurring. The working electrode is often used in conjunction with an auxiliary electrode, and a reference electrode in a three-electrode system. Depending on whether the reaction on the electrode is a reduction or an oxidation, the working electrode is called cathodic or anodic, respectively. Common working electrodes can consist of materials ranging from inert metals such as gold or platinum, to inert carbon such as glassy carbon, boron-doped diamond or pyrolytic carbon, and mercury drop and film electrodes. Chemically modified electrodes are employed for the analysis of both organic and inorganic samples.
Squarewave voltammetry (SWV) is a form of linear potential sweep voltammetry that uses a combined square wave and staircase potential applied to a stationary electrode. It has found numerous applications in various fields, including within medicinal and various sensing communities.
In electrochemistry, the auxiliary electrode, often also called the counter electrode, is an electrode used in a three-electrode electrochemical cell for voltammetric analysis or other reactions in which an electric current is expected to flow. The auxiliary electrode is distinct from the reference electrode, which establishes the electrical potential against which other potentials may be measured, and the working electrode, at which the cell reaction takes place.
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.
In analytical chemistry, a rotating ring-disk electrode (RRDE) is a double working electrode used in hydrodynamic voltammetry, very similar to a rotating disk electrode (RDE). The electrode rotates during experiments inducing a flux of analyte to the electrode. This system used in electrochemical studies when investigating reaction mechanisms related to redox chemistry and other chemical phenomena.
An ultramicroelectrode (UME) is a working electrode used in a voltammetry. The small size of UME give them large diffusion layers and small overall currents. These features allow UME to achieve useful steady-state conditions and very high scan rates (V/s) with limited distortion. UME were developed independently by Wightman and Fleischmann around 1980. Small current at UME enables electrochemical measurements in low conductive media, where voltage drop associated with high solution resistance makes these experiments difficult for conventional electrodes. Furthermore, small voltage drop at UME leads to a very small voltage distortion at the electrode-solution interface which allows using two-electrode setup in voltammetric experiment instead of conventional three-electrode setup.
In analytical chemistry, hydrodynamic voltammetry is a form of voltammetry in which the analyte solution flows relative to a working electrode. In many voltammetry techniques, the solution is intentionally left still to allow diffusion-controlled mass transfer. When a solution is made to flow, through stirring or some other physical mechanism, it is very important to the technique to achieve a very controlled flux or mass transfer in order to obtain predictable results. These methods are types of electrochemical studies which use potentiostats to investigate reaction mechanisms related to redox chemistry among other chemical phenomenon.
Bulk electrolysis is also known as potentiostatic coulometry or controlled potential coulometry. The experiment is a form of coulometry which generally employs a three electrode system controlled by a potentiostat. In the experiment the working electrode is held at a constant potential (volts) and current (amps) is monitored over time (seconds). In a properly run experiment an analyte is quantitatively converted from its original oxidation state to a new oxidation state, either reduced or oxidized. As the substrate is consumed, the current also decreases, approaching zero when the conversion nears completion.
If an electric field is applied parallel to the surface of a liquid and this surface has a net charge then the surface and so the liquid will move in response to the field. This is electrocapillary flow, an example of electrocapillarity. Electrocapillary phenomena are phenomena related to changes in the surface free energy of charged fluid interfaces, for example that of the dropping mercury electrode (DME), or in principle, any electrode, as the electrode potential changes or the electrolytic solution composition and concentration change.
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.
Electrochemical stripping analysis is a set of analytical chemistry methods based on voltammetry or potentiometry that are used for quantitative determination of ions in solution. Stripping voltammetry have been employed for analysis of organic molecules as well as metal ions. Carbon paste, glassy carbon paste, and glassy carbon electrodes when modified are termed as chemically modified electrodes and have been employed for the analysis of organic and inorganic compounds.