Электрохимия: Химия мен Электр арасындағы Қарым-қатынас

Branch of chemistry

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 (typically an external electrical circuit, but not necessarily, as in electroless plating) between electrodes separated by an ionically conducting and electronically insulating electrolyte (or ionic species in a solution). When a chemical reaction is driven by an electrical potential difference, as in electrolysis, or if a potential difference results from a chemical reaction as in an electric battery or fuel cell, it is called an electrochemical reaction. Unlike in other chemical reactions, in electrochemical reactions electrons are not transferred directly between atoms, ions, or molecules, but via the aforementioned electronically conducting circuit. This phenomenon is what distinguishes an electrochemical reaction from a conventional chemical reaction.

Understanding of electrical matters began in the sixteenth century. During this century, the English scientist William Gilbert spent 17 years experimenting with magnetism and, to a lesser extent, electricity. For his work on magnets, Gilbert became known as the "Father of Magnetism." He discovered various methods for producing and strengthening magnets. In 1663, the German physicist Otto von Guericke created the first electric generator, which produced static electricity by applying friction in the machine. The generator was made of a large sulfur ball cast inside a glass globe, mounted on a shaft. The ball was rotated by means of a crank and an electric spark was produced when a pad was rubbed against the ball as it rotated. The globe could be removed and used as source for experiments with electricity. By the mid 18th century the French chemist Charles François de Cisternay du Fay had discovered two types of static electricity, and that like charges repel each other whilst unlike charges attract. Du Fay announced that electricity consisted of two fluids: "vitreous" (from the Latin for "glass"), or positive, electricity; and "resinous," or negative, electricity. This was the two fluid theory of electricity, which was to be opposed by Benjamin Franklin's one fluid theory later in the century. In 1785, Charles Augustin de Coulomb developed the law of electrostatic attraction as an outgrowth of his attempt to investigate the law of electrical repulsions as stated by Joseph Priestley in England. In the late 18th century the Italian physician and anatomist Luigi Galvani marked the birth of electrochemistry by establishing a bridge between chemical reactions and electricity on his essay "De Viribus Electricitatis in Motu Musculari Commentarius" (Latin for Commentary on the Effect of Electricity on Muscular Motion) in 1791 where he proposed a "nerveo electrical substance" on biological life forms. In his essay Galvani concluded that animal tissue contained a here to fore neglected innate, vital force, which he termed "animal electricity," which activated nerves and muscles spanned by metal probes. He believed that this new force was a form of electricity in addition to the "natural" form produced by lightning or by the electric eel and torpedo ray as well as the "artificial" form produced by friction (i. e., static electricity). Galvani's scientific colleagues generally accepted his views, but Alessandro Volta rejected the idea of an "animal electric fluid," replying that the frog's legs responded to differences in metal temper, composition, and bulk. By the 1810s, William Hyde Wollaston made improvements to the galvanic cell. Sir Humphry Davy's work with electrolysis led to the conclusion that the production of electricity in simple electrolytic cells resulted from chemical action and that chemical combination occurred between substances of opposite charge. This work led directly to the isolation of metallic sodium and potassium by electrolysis of their molten salts, and of the alkaline earth metals from theirs, in 1808. Hans Christian Ørsted's discovery of the magnetic effect of electric currents in 1820 was immediately recognized as an epoch making advance, although he left further work on electromagnetism to others. André Marie Ampère quickly repeated Ørsted's experiment, and formulated them mathematically. In 1821, Estonian German physicist Thomas Johann Seebeck demonstrated the electrical potential between the juncture points of two dissimilar metals when there is a temperature difference between the joints. In 1827, the German scientist Georg Ohm expressed his law in this famous book "Die galvanische Kette, mathematisch bearbeitet" (The Galvanic Circuit Investigated Mathematically) in which he gave his complete theory of electricity. Svante Arrhenius published his thesis in 1884 on Recherches sur la conductibilité galvanique des électrolytes (Investigations on the galvanic conductivity of electrolytes). From his results the author concluded that electrolytes, when dissolved in water, become to varying degrees split or dissociated into electrically opposite positive and negative ions. In 1886, Paul Héroult and Charles M. Hall developed an efficient method (the Hall–Héroult process) to obtain aluminium using electrolysis of molten alumina. In 1894, Friedrich Ostwald concluded important studies of the conductivity and electrolytic dissociation of organic acids. Walther Hermann Nernst developed the theory of the electromotive force of the voltaic cell in 1888. In 1889, he showed how the characteristics of the voltage produced could be used to calculate the free energy change in the chemical reaction producing the voltage. He constructed an equation, known as Nernst equation, which related the voltage of a cell to its properties. In 1898, Fritz Haber showed that definite reduction products can result from electrolytic processes if the potential at the cathode is kept constant. In 1898, he explained the reduction of nitrobenzene in stages at the cathode and this became the model for other similar reduction processes.

In 1902, The Electrochemical Society (ECS) was founded. In 1909, Robert Andrews Millikan began a series of experiments (see oil drop experiment) to determine the electric charge carried by a single electron. In 1911, Harvey Fletcher, working with Millikan, was successful in measuring the charge on the electron, by replacing the water droplets used by Millikan, which quickly evaporated, with oil droplets. Within one day Fletcher measured the charge of an electron within several decimal places. In 1923, Johannes Nicolaus Brønsted and Martin Lowry published essentially the same theory about how acids and bases behave, using an electrochemical basis. In 1937, Arne Tiselius developed the first sophisticated electrophoretic apparatus. Some years later, he was awarded the 1948 Nobel Prize for his work in protein electrophoresis. A year later, in 1949, the International Society of Electrochemistry (ISE) was founded. By the 1960s–1970s quantum electrochemistry was developed by Revaz Dogonadze and his students.

The term "redox" stands for reduction oxidation. It refers to electrochemical processes involving electron transfer to or from a molecule or ion, changing its oxidation state. This reaction can occur through the application of an external voltage or through the release of chemical energy. Oxidation and reduction describe the change of oxidation state that takes place in the atoms, ions or molecules involved in an electrochemical reaction. Formally, oxidation state is the hypothetical charge that an atom would have if all bonds to atoms of different elements were 100% ionic. An atom or ion that gives up an electron to another atom or ion has its oxidation state increase, and the recipient of the negatively charged electron has its oxidation state decrease. For example, when atomic sodium reacts with atomic chlorine, sodium donates one electron and attains an oxidation state of +1. Chlorine accepts the electron and its oxidation state is reduced to −1. The sign of the oxidation state (positive/negative) actually corresponds to the value of each ion's electronic charge. The attraction of the differently charged sodium and chlorine ions is the reason they then form an ionic bond. The loss of electrons from an atom or molecule is called oxidation, and the gain of electrons is reduction. This can be easily remembered through the use of mnemonic devices. Two of the most popular are "OIL RIG" (Oxidation Is Loss, Reduction Is Gain) and "LEO" the lion says "GER" (Lose Electrons: Oxidation, Gain Electrons: Reduction). Oxidation and reduction always occur in a paired fashion such that one species is oxidized when another is reduced. For cases where electrons are shared (covalent bonds) between atoms with large differences in electronegativity, the electron is assigned to the atom with the largest electronegativity in determining the oxidation state. The atom or molecule which loses electrons is known as the reducing agent, or reductant, and the substance which accepts the electrons is called the oxidizing agent, or oxidant. Thus, the oxidizing agent is always being reduced in a reaction; the reducing agent is always being oxidized. Oxygen is a common oxidizing agent, but not the only one. Despite the name, an oxidation reaction does not necessarily need to involve oxygen. In fact, a fire can be fed by an oxidant other than oxygen; fluorine fires are often unquenchable, as fluorine is an even stronger oxidant (it has a weaker bond and higher electronegativity, and thus accepts electrons even better) than oxygen. For reactions involving oxygen, the gain of oxygen implies the oxidation of the atom or molecule to which the oxygen is added (and the oxygen is reduced). In organic compounds, such as butane or ethanol, the loss of hydrogen implies oxidation of the molecule from which it is lost (and the hydrogen is reduced). This follows because the hydrogen donates its electron in covalent bonds with non metals but it takes the electron along when it is lost. Conversely, loss of oxygen or gain of hydrogen implies reduction.

Electrochemical reactions in water are better analyzed by using the ion electron method, where H+, OH− ion, H2O and electrons (to compensate the oxidation changes) are added to the cell's half reactions for oxidation and reduction.

Many types of battery have been commercialized and represent an important practical application of electrochemistry. Early wet cells powered the first telegraph and telephone systems, and were the source of current for electroplating. The zinc manganese dioxide dry cell was the first portable, non spillable battery type that made flashlights and other portable devices practical. The mercury battery using zinc and mercuric oxide provided higher levels of power and capacity than the original dry cell for early electronic devices, but has been phased out of common use due to the danger of mercury pollution from discarded cells. The lead–acid battery was the first practical secondary (rechargeable) battery that could have its capacity replenished from an external source. The electrochemical reaction that produced current was (to a useful degree) reversible, allowing electrical energy and chemical energy to be interchanged as needed. Common lead acid batteries contain a mixture of sulfuric acid and water, as well as lead plates. The most common mixture used today is 30% acid. One problem, however, is if left uncharged acid will crystallize within the lead plates of the battery rendering it useless. These batteries last an average of 3 years with daily use but it is not unheard of for a lead acid battery to still be functional after 7–10 years. Lead acid cells continue to be widely used in automobiles. All the preceding types have water based electrolytes, which limits the maximum voltage per cell. The freezing of water limits low temperature performance. The lithium metal battery, which does not (and cannot) use water in the electrolyte, provides improved performance over other types; a rechargeable lithium ion battery is an essential part of many mobile devices. The flow battery, an experimental type, offers the option of vastly larger energy capacity because its reactants can be replenished from external reservoirs. The fuel cell can turn the chemical energy bound in hydrocarbon gases or hydrogen and oxygen directly into electrical energy with a much higher efficiency than any combustion process; such devices have powered many spacecraft and are being applied to grid energy storage for the public power system.

Corrosion is an electrochemical process, which reveals itself as rust or tarnish on metals like iron or copper and their respective alloys, steel and brass.

Coinage metals, such as copper and silver, slowly corrode through use. A patina of green blue copper carbonate forms on the surface of copper with exposure to the water and carbon dioxide in the air. Silver coins or cutlery that are exposed to high sulfur foods such as eggs or the low levels of sulfur species in the air develop a layer of black silver sulfide. Gold and platinum are extremely difficult to oxidize under normal circumstances, and require exposure to a powerful chemical oxidizing agent such as aqua regia. Some common metals oxidize extremely rapidly in air. Titanium and aluminium oxidize instantaneously in contact with the oxygen in the air. These metals form an extremely thin layer of oxidized metal on the surface, which bonds with the underlying metal. This thin oxide layer protects the underlying bulk of the metal from the air preventing the entire metal from oxidizing. These metals are used in applications where corrosion resistance is important. Iron, in contrast, has an oxide that forms in air and water, called rust, that does not bond with the iron and therefore does not stop the further oxidation of the iron. Thus iron left exposed to air and water will continue to rust until all of the iron is oxidized.

Attempts to save a metal from becoming anodic are of two general types. Anodic regions dissolve and destroy the structural integrity of the metal. While it is almost impossible to prevent anode/cathode formation, if a non conducting material covers the metal, contact with the electrolyte is not possible and corrosion will not occur.

Metals can be coated with paint or other less conductive metals (passivation). This prevents the metal surface from being exposed to electrolytes. Scratches exposing the metal substrate will result in corrosion. The region under the coating adjacent to the scratch acts as the anode of the reaction.

A method commonly used to protect a structural metal is to attach a metal which is more anodic than the metal to be protected. This forces the structural metal to be cathodic, thus spared corrosion. It is called "sacrificial" because the anode dissolves and has to be replaced periodically. Zinc bars are attached to various locations on steel ship hulls to render the ship hull cathodic. The zinc bars are replaced periodically. Other metals, such as magnesium, would work very well but zinc is the least expensive useful metal. To protect pipelines, an ingot of buried or exposed magnesium (or zinc) is buried beside the pipeline and is connected electrically to the pipe above ground. The pipeline is forced to be a cathode and is protected from being oxidized and rusting. The magnesium anode is sacrificed. At intervals new ingots are buried to replace those dissolved.

The spontaneous redox reactions of a conventional battery produce electricity through the different reduction potentials of the cathode and anode in the electrolyte. However, electrolysis requires an external source of electrical energy to induce a chemical reaction, and this process takes place in a compartment called an electrolytic cell.

Electrolysis in an aqueous solution is a similar process as mentioned in electrolysis of water. However, it is considered to be a complex process because the contents in solution have to be analyzed in half reactions, whether reduced or oxidized.

Faraday devised the laws of chemical electrodeposition of metals from solutions in 1857. He formulated the second law of electrolysis stating "the amounts of bodies which are equivalent to each other in their ordinary chemical action have equal quantities of electricity naturally associated with them." In other words, the quantities of different elements deposited by a given amount of electricity are in the ratio of their chemical equivalent weights. An important aspect of the second law of electrolysis is electroplating, which together with the first law of electrolysis has a significant number of applications in industry, as when used to protectively coat metals to avoid corrosion.

There are various important electrochemical processes in both nature and industry, like the coating of objects with metals or metal oxides through electrodeposition, the addition (electroplating) or removal (electropolishing) of thin layers of metal from an object's surface, and the detection of alcohol in drunk drivers through the redox reaction of ethanol. The generation of chemical energy through photosynthesis is inherently an electrochemical process, as is production of metals like aluminum and titanium from their ores. Certain diabetes blood sugar meters measure the amount of glucose in the blood through its redox potential. In addition to established electrochemical technologies (like deep cycle lead acid batteries) there is also a wide range of new emerging technologies such as fuel cells, large format lithium ion batteries, electrochemical reactors and super capacitors that are becoming increasingly commercial. Electrochemical or coulometric titrations were introduced for quantitative analysis of minute quantities in 1938 by the Hungarian chemists László Szebellédy and Zoltan Somogyi. Electrochemistry also has important applications in the food industry, like the assessment of food/package interactions, the analysis of milk composition, the characterization and the determination of the freezing end point of ice cream mixes, or the determination of free acidity in olive oil.