Magnetoelectrochemistry

Last updated

Magnetoelectrochemistry is a branch of electrochemistry dealing with magnetic effects in electrochemistry.

Contents

History

These effects have been supposed to exist since the time of Michael Faraday. There have also been observations on the existence of Hall effect in electrolytes. Until these observations, magnetoelectrochemistry was an esoteric curiosity, though this field has had a rapid development in the past years and is now an active area of research. Other scientific fields which contributed to the development of magnetoelectrochemistry are magnetohydrodynamics and convective diffusion theory. [ citation needed ]

Effects of magnetic field

There are three types of magnetic effects in electrochemistry:

Notes

    See also


    Related Research Articles

    Electrochemistry Branch of chemistry

    Electrochemistry is the branch of physical chemistry concerned with the relationship between electrical potential difference, as a measurable and quantitative phenomenon, and identifiable chemical change, with the potential difference as an outcome of a particular chemical change, or vice versa. These reactions involve electrons moving via an electronically-conducting phase between electrodes separated by an ionically conducting and electronically insulating electrolyte.

    Voltaic pile First electrical battery that could continuously provide an electric current to a circuit

    The voltaic pile was the first electrical battery that could continuously provide an electric current to a circuit. It was invented by Italian physicist Alessandro Volta, who published his experiments in 1799. The voltaic pile then enabled a rapid series of other discoveries including the electrical decomposition (electrolysis) of water into oxygen and hydrogen by William Nicholson and Anthony Carlisle (1800) and the discovery or isolation of the chemical elements sodium (1807), potassium (1807), calcium (1808), boron (1808), barium (1808), strontium (1808), and magnesium (1808) by Humphry Davy.

    Magnetohydrodynamics Study of electrically conducting fluids

    Magnetohydrodynamics is the study of the magnetic properties and behaviour of electrically conducting fluids. Examples of such magneto­fluids include plasmas, liquid metals, salt water, and electrolytes. The word "magneto­hydro­dynamics" is derived from magneto- meaning magnetic field, hydro- meaning water, and dynamics meaning movement. The field of MHD was initiated by Hannes Alfvén, for which he received the Nobel Prize in Physics in 1970.

    In electrochemistry, a half-cell is a structure that contains a conductive electrode and a surrounding conductive electrolyte separated by a naturally occurring Helmholtz double layer. Chemical reactions within this layer momentarily pump electric charges between the electrode and the electrolyte, resulting in a potential difference between the electrode and the electrolyte. The typical anode reaction involves a metal atom in the electrode dissolved and transported as a positive ion across the double layer, causing the electrolyte to acquire a net positive charge while the electrode acquires a net negative charge. The growing potential difference creates an intense electric field within the double layer, and the potential rises in value until the field halts the net charge-pumping reactions. This self-limiting action occurs almost instantly in an isolated half-cell; in applications two dissimilar half-cells are appropriately connected to constitute a Galvanic cell.

    Cyclic voltammetry

    Cyclic voltammetry (CV) is a type of potentiodynamic electrochemical 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.

    Magnetic flow meter

    A magnetic flow meter is a transducer that measures fluid flow by the voltage induced across the liquid by its flow through a magnetic field. A magnetic field is applied to the metering tube, which results in a potential difference proportional to the flow velocity perpendicular to the flux lines. The physical principle at work is electromagnetic induction. The magnetic flow meter requires a conducting fluid, for example, water that contains ions, and an electrical insulating pipe surface, for example, a rubber-lined steel tube.

    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.

    Electrochemistry, a branch of chemistry, went through several changes during its evolution from early principles related to magnets in the early 16th and 17th centuries, to complex theories involving conductivity, electric charge and mathematical methods. The term electrochemistry was used to describe electrical phenomena in the late 19th and 20th centuries. In recent decades, electrochemistry has become an area of current research, including research in batteries and fuel cells, preventing corrosion of metals, the use of electrochemical cells to remove refractory organics and similar contaminants in wastewater electrocoagulation and improving techniques in refining chemicals with electrolysis and electrophoresis.

    The Electrochemical Society is a learned society based in the United States that supports scientific inquiry in the field of electrochemistry and solid-state science and related technology. The Society membership comprises more than 8,000 scientists and engineers in over 85 countries at all degree levels and in all fields of electrochemistry, solid state science and related technologies. Additional support is provided by institutional members including corporations and laboratories.

    Non-faradaic electrochemical modification of catalytic activity (NEMCA effect), also known as electrochemical promotion of catalysis (EPOC), is used to describe the increase in catalytic activity (up to 90-fold) and selectivity of a gas exposed electrode on a solid electrolyte cell upon application of a potential. This phenomenon is well documented and has been observed on various surfaces (Ni, Au, Pt, Pd, IrO2, RuO2) supported by O2−, Na+ and proton conducting solid electrolytes.

    In electrochemistry, polarization is a collective term for certain mechanical side-effects by which isolating barriers develop at the interface between electrode and electrolyte. These side-effects influence the reaction mechanisms, as well as the chemical kinetics of corrosion and metal deposition. In a reaction we can displace the bonding electrons by attacking reagents. The electronic displacement in turn may be due to certain effects, some of which are permanent, and the others are temporary. Those effects which are permanently operating in the molecule are known as polarization effects, and those effects which are brought into play by attacking reagent are known as polarisability effects.

    Electrochemical engineering is the branch of chemical engineering dealing with the technological applications of electrochemical phenomena, such as electrosynthesis of chemicals, electrowinning and refining of metals, flow batteries and fuel cells, surface modification by electrodeposition, electrochemical separations and corrosion. This discipline is an overlap between electrochemistry and chemical engineering.

    Electrochemical kinetics is the field of electrochemistry that studies the rate of electrochemical processes. This includes the study of how process conditions such as concentration and electric potential influence the rate of oxidation and reduction reactions that occur at the surface of an electrode, as well as an investigation into electrochemical reaction mechanisms. Due to electrochemical phenomena unfolding at the interface between an electrode and an electrolyte, there are accompanying phenomena to electrochemical reactions which contribute to the overall reaction rate.

    A supporting electrolyte, in electrochemistry, according to an IUPAC definition, is an electrolyte containing chemical species that are not electroactive and which has an ionic strength and conductivity much larger than those due to the electroactive species added to the electrolyte. Supporting electrolyte is also sometimes referred to as inert electrolyte or inactive electrolyte.

    Double-layer capacitance is the important characteristic of the electrical double layer which appears, for example, at the interface between a conductive electrode and an adjacent liquid electrolyte. At this boundary two layers of charge with opposing polarity form, one at the surface of the electrode, and one in the electrolyte. These two layers, electrons on the electrode and ions in the electrolyte, are typically separated by a single layer of solvent molecules that adhere to the surface of the electrode and act like a dielectric in a conventional capacitor. The amount of electric charge stored in double-layer capacitor depends on the applied voltage. The unit of capacitance is the farad.

    Thermogalvanic cell

    A thermogalvanic cell is a kind of galvanic cell in which heat is employed to provide electrical power directly. These cells are electrochemical cells in which the two electrodes are deliberately maintained at different temperatures. This temperature difference generates a potential difference between the electrodes. The electrodes can be of identical composition and the electrolyte solution homogeneous. This is usually the case in these cells. This is in contrast to galvanic cells in which electrodes and/or solutions of different composition provide the electromotive potential. As long as there is a difference in temperature between the electrodes a current will flow through the circuit. A thermogalvanic cell can be seen as analogous to a concentration cell but instead of running on differences in the concentration/pressure of the reactants they make use of differences in the "concentrations" of thermal energy. The principal application of thermogalvanic cells is the production of electricity from low-temperature heat sources. Their energetic efficiency is low, in the range of 0.1% to 1% for conversion of heat into electricity.

    Sonoelectrochemistry is the application of ultrasound in electrochemistry. Like sonochemistry, sonoelectrochemistry was discovered in the early 20th century. The effects of power ultrasound on electrochemical systems and important electrochemical parameters were originally demonstrated by Moriguchi and then by Schmid and Ehert when the researchers investigated the influence of ultrasound on concentration polarisation, metal passivation and the production of electrolytic gases in aqueous solutions. In the late 1950s, Kolb and Nyborg showed that the electrochemical solution hydrodynamics in an electrochemical cell was greatly increased in the presence of ultrasound and described this phenomenon as acoustic streaming. In 1959, Penn et al. demonstrated that sonication had a great effect on the electrode surface activity and electroanalyte species concentration profile throughout the solution. In the early 1960s, the electrochemist Allen J. Bard showed in controlled potential coulometry experiments that ultrasound significantly enhances mass transport of electrochemical species from the bulk solution to the electroactive surface. In the range of ultrasonic frequencies [20 kHz – 2 MHz], ultrasound has been applied to many electrochemical systems, processes and areas of electrochemistry both in academia and industry, as this technology offers several benefits over traditional technologies. The advantages are as follows: significant thinning of the diffusion layer thickness (δ) at the electrode surface; increase in electrodeposit/electroplating thickness; increase in electrochemical rates, yields and efficiencies; increase in electrodeposit porosity and hardness; increase in gas removal from electrochemical solutions; increase in electrode cleanliness and hence electrode surface activation; lowering in electrode overpotentials ; and suppression in electrode fouling.

    The electrochemical promotion of catalysis (EPOC) effect in the realm of chemistry refers to the pronounced enhancement of catalytic reactions or significant changes in the catalytic properties of a conductive catalyst in the presence of electrical currents or interfacial potentials. Additionally, the EPOC effect can be utilized in a reverse manner in order to influence the selectivity of versatile heterogeneous catalytic reactions. In most cases, the electronically conductive catalyst is in metallic or metal oxide states in the form of a porous film deposited on a solid electrolyte. The EPOC effect was firstly discovered by M. Stoukides and C. Vayenas in the early 1980s and have been widely studied by various research groups for more than 100 heterogeneous catalytic reactions of mostly gaseous molecules. The EPOC effect has been evaluated as an important phenomenon which can closely link electrocatalysis and thermal catalysis.

    Doron Aurbach Israeli electrochemist, materials and surface scientist

    Doron Aurbach is an Israeli electrochemist, materials and surface scientist.

    Electrochemical quartz crystal microbalance

    Electrochemical quartz crystal microbalance (EQCM) is the combination of electrochemistry and quartz crystal microbalance, which was generated in the eighties. Typically, an EQCM device contains an electrochemical cells part and a QCM part. Two electrodes on both sides of the quartz crystal serve two purposes. Firstly, an alternating electric field is generated between the two electrodes for making up the oscillator. Secondly, the electrode contacting electrolyte is used as a working electrode (WE), together with a counter electrode (CE) and a reference electrode (RE), in the potentiostatic circuit constituting the electrochemistry cell. Thus, the working electrode of electrochemistry cell is the sensor of QCM.