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Schottky Defects
A Schottky defect is an excitation of the site occupations in a crystal lattice leading to point defects named after Walter H. Schottky. In ionic crystals, this defect forms when oppositely charged ions leave their lattice sites and become incorporated for instance at the surface, creating oppositely charged vacancies. These vacancies are formed in stoichiometric units, to maintain an overall neutral charge in the ionic solid. Definition Schottky defects consist of unoccupied anion and cation sites in a stoichiometric ratio. For a simple ionic crystal of type A−B+, a Schottky defect consists of a single anion vacancy (A) and a single cation vacancy (B), or v + v following Kröger–Vink notation. For a more general crystal with formula AxBy, a Schottky cluster is formed of x vacancies of A and y vacancies of B, thus the overall stoichiometry and charge neutrality are conserved. Conceptually, a Schottky defect is generated if the crystal is expanded by one unit cell, whose ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Schottky Effect
The Schottky effect or field enhanced thermionic emission is a phenomenon in condensed matter physics named after Walter H. Schottky. In electron emission devices, especially electron guns, the thermionic electron emitter will be biased negative relative to its surroundings. This creates an electric field of magnitude ''F'' at the emitter surface. Without the field, the surface barrier seen by an escaping Fermi-level electron has height ''W'' equal to the local work-function. The electric field lowers the surface barrier by an amount Δ''W'', and increases the emission current. It can be modeled by a simple modification of the Richardson equation, by replacing ''W'' by (''W'' − Δ''W''). This gives the equation :J (F,T,W) = A_ T^2 e^ :\Delta W = \sqrt, where ''J'' is the emission current density, ''T'' is the temperature of the metal, ''W'' is the work function of the metal, ''k'' is the Boltzmann constant, ''q''e is the Elementary charge, ''ε''0 is the vacuum perm ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Nuclear Fuel
Nuclear fuel refers to any substance, typically fissile material, which is used by nuclear power stations or other atomic nucleus, nuclear devices to generate energy. Oxide fuel For fission reactors, the fuel (typically based on uranium) is usually based on the metal oxide; the oxides are used rather than the metals themselves because the oxide melting point is much higher than that of the metal and because it cannot burn, being already in the oxidized state. Uranium dioxide Uranium dioxide is a black semiconductor, semiconducting solid. It can be made by heating uranyl nitrate to form . : This is then converted by heating with hydrogen to form UO2. It can be made from Enriched uranium, enriched uranium hexafluoride by reacting with ammonia to form a solid called ammonium diuranate, . This is then heated (Calcination, calcined) to form and U3O8 which is then converted by heating with hydrogen or ammonia to form UO2. The UO2 is mixed with an organic binder and pressed in ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Plutonium Dioxide
Plutonium(IV) oxide, or plutonia, is a chemical compound with the chemical formula, formula plutonium, Puoxygen, O2. This high melting-point solid is a principal compound of plutonium. It can vary in color from yellow to olive green, depending on the particle size, temperature and method of production. Structure PuO2 crystallizes in the fluorite motif, with the Pu4+ centers organized in a face-centered cubic array and oxide ions occupying tetrahedral holes. PuO2 owes its utility as a nuclear fuel to the fact that vacancies in the octahedral holes allows room for fission products. In nuclear fission, one atom of plutonium splits into two. The vacancy of the octahedral holes provides room for the new product and allows the PuO2 monolith to retain its structural integrity. At high temperatures PuO2 tends to lose oxygen, becoming sub-stoichiometric PuO2−x, with the introduction of lower valence Pu3+. This continues into the molten liquid state where the local Pu-O coordination numbe ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Thorium Dioxide
Thorium dioxide (ThO2), also called thorium(IV) oxide, is a crystalline solid, often white or yellow in colour. Also known as thoria, it is mainly a by-product of lanthanide and uranium production. Thorianite is the name of the mineralogical form of thorium dioxide. It is moderately rare and crystallizes in an isometric system. The melting point of thorium oxide is 3300 °C – the highest of all known oxides. Only a few elements (including tungsten and carbon) and a few compounds (including tantalum carbide) have higher melting points. All thorium compounds, including the dioxide, are radioactive because there are no stable isotopes of thorium. Structure and reactions Thoria exists as two polymorphs. One has a fluorite crystal structure. This is uncommon among binary dioxides. (Other binary oxides with fluorite structure include cerium dioxide, uranium dioxide and plutonium dioxide.) The band gap of thoria is about 6 eV. A tetragonal form of thoria is also known. ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Uranium Dioxide
Uranium dioxide or uranium(IV) oxide (), also known as urania or uranous oxide, is an oxide of uranium, and is a black, radioactive, crystalline powder that naturally occurs in the mineral uraninite. It is used in nuclear fuel rods in nuclear reactors. A mixture of uranium and plutonium dioxides is used as MOX fuel. It has been used as an orange, yellow, green, and black color in ceramic glazes and glass. Production Uranium dioxide is produced by reducing uranium trioxide with hydrogen. This reaction often creates triuranium octoxide as an intermediate. :UO3 + H2 → UO2 + H2O at 700 °C (973 K) This reaction plays an important part in the creation of nuclear fuel through nuclear reprocessing and uranium enrichment. Chemistry Structure The solid is isostructural with (has the same structure as) fluorite ( calcium fluoride), where each U is surrounded by eight O nearest neighbors in a cubic arrangement. In addition, the dioxides of cerium, thorium, and the tran ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Zirconia
Zirconium dioxide (), sometimes known as zirconia (not to be confused with zirconium silicate or zircon), is a white crystalline oxide of zirconium. Its most naturally occurring form, with a monoclinic crystalline structure, is the mineral baddeleyite. A dopant stabilized cubic structured zirconia, cubic zirconia, is synthesized in various colours for use as a gemstone and a diamond simulant. Production, chemical properties, occurrence Zirconia is produced by calcining zirconium compounds, exploiting its high thermostability.Ralph Nielsen "Zirconium and Zirconium Compounds" in Ullmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim. Structure Three phases are known: monoclinic below 1170 °C, tetragonal between 1170 °C and 2370 °C, and cubic above 2370 °C. The trend is for higher symmetry at higher temperatures, as is usually the case. A small percentage of the oxides of calcium or yttrium stabilize in the cubic phase. The very ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Ceria
Cerium(IV) oxide, also known as ceric oxide, ceric dioxide, ceria, cerium oxide or cerium dioxide, is an oxide of the rare-earth metal cerium. It is a pale yellow-white powder with the chemical formula CeO2. It is an important commercial product and an intermediate in the purification of the element from the ores. The distinctive property of this material is its reversible conversion to a non-stoichiometric oxide. Production Cerium occurs naturally as oxides, always as a mixture with other rare-earth elements. Its principal ores are bastnaesite and monazite. After extraction of the metal ions into aqueous base, Ce is separated from that mixture by addition of an oxidant followed by adjustment of the pH. This step exploits the low solubility of CeO2 and the fact that other rare-earth elements resist oxidation.. Cerium(IV) oxide is formed by the calcination of cerium oxalate or cerium hydroxide. Cerium also forms cerium(III) oxide, , which is unstable and will oxidize t ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Calcium Fluoride
Calcium fluoride is the inorganic compound of the elements calcium and fluorine with the formula CaF2. It is a white solid that is practically insoluble in water. It occurs as the mineral fluorite (also called fluorspar), which is often deeply coloured owing to impurities. Chemical structure The compound crystallizes in a cubic motif called the fluorite structure. Ca2+ centres are eight-coordinate, being centred in a cube of eight F− centres. Each F− centre is coordinated to four Ca2+ centres in the shape of a tetrahedron. Although perfectly packed crystalline samples are colorless, the mineral is often deeply colored due to the presence of F-centers. The same crystal structure is found in numerous ionic compounds with formula AB2, such as CeO2, cubic ZrO2, UO2, ThO2, and PuO2. In the corresponding anti-structure, called the antifluorite structure, anions and cations are swapped, such as Be2C. Gas phase The gas phase is noteworthy for failing the predictions of VSEP ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Silver Bromide
Silver bromide (AgBr), a soft, pale-yellow, water-insoluble salt well known (along with other silver halides) for its unusual sensitivity to light. This property has allowed silver halides to become the basis of modern photographic materials. AgBr is widely used in photographic films and is believed by some to have been used for faking the Shroud of Turin. The salt can be found naturally as the mineral bromargyrite (bromyrite). Preparation Although the compound can be found in mineral form, AgBr is typically prepared by the reaction of silver nitrate with an alkali bromide, typically potassium bromide: :AgNO3(aq) + KBr(aq) → AgBr(s)+ KNO3(aq) Although less convenient, the salt can also be prepared directly from its elements. Modern preparation of a simple, light-sensitive surface involves forming an emulsion of silver halide crystals in a gelatine, which is then coated onto a film or other support. The crystals are formed by precipitation in a controlled environment to prod ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Caesium Chloride
Caesium chloride or cesium chloride is the inorganic compound with the formula Caesium, CsChloride, Cl. This colorless salt is an important source of caesium ions in a variety of niche applications. Its crystal structure forms a major structural type where each caesium ion is coordinated by 8 chloride ions. Caesium chloride dissolves in water. CsCl changes to NaCl structure on heating. Caesium chloride occurs naturally as impurities in carnallite (up to 0.002%), sylvite and kainite. Less than 20 tonnes of CsCl is produced annually worldwide, mostly from a caesium-bearing mineral pollucite. Caesium chloride is widely used in isopycnic centrifugation for separating various types of DNA. It is a reagent in analytical chemistry, where it is used to identify ions by the color and morphology of the precipitate. When enriched in radionuclide, radioisotopes, such as 137CsCl or 131CsCl, caesium chloride is used in nuclear medicine applications such as treatment of cancer and diagnosis of m ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Potassium Bromide
Potassium bromide ( K Br) is a salt, widely used as an anticonvulsant and a sedative in the late 19th and early 20th centuries, with over-the-counter use extending to 1975 in the US. Its action is due to the bromide ion ( sodium bromide is equally effective). Potassium bromide is used as a veterinary drug, in antiepileptic medication for dogs. Under standard conditions, potassium bromide is a white crystalline powder. It is freely soluble in water; it is not soluble in acetonitrile. In a dilute aqueous solution, potassium bromide tastes sweet, at higher concentrations it tastes bitter, and tastes salty when the concentration is even higher. These effects are mainly due to the properties of the potassium ion—sodium bromide tastes salty at any concentration. In high concentration, potassium bromide strongly irritates the gastric mucous membrane, causing nausea and sometimes vomiting (a typical effect of all soluble potassium salts). Chemical properties Potassium bromide, a typ ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Potassium Chloride
Potassium chloride (KCl, or potassium salt) is a metal halide salt composed of potassium and chlorine. It is odorless and has a white or colorless vitreous crystal appearance. The solid dissolves readily in water, and its solutions have a salt-like taste. Potassium chloride can be obtained from ancient dried lake deposits. KCl is used as a salt substitute for table salt (NaCl), a fertilizer, as a medication, in scientific applications, in domestic water softeners (as a substitute for sodium chloride salt), as a feedstock, and in food processing, where it may be known as E number additive E508. It occurs naturally as the mineral sylvite, which is named after salt's historical designations ''sal degistivum Sylvii'' and ''sal febrifugum Sylvii'', and in combination with sodium chloride as sylvinite. Uses Fertilizer The majority of the potassium chloride produced is used for making fertilizer, called potash, since the growth of many plants is limited by potassium availabil ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
