Silicon carbide

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"Carborundum" redirects here. It is not to be confused with Corundum.
Silicon carbide
Sample of silicon carbide as a boule
Identifiers
CAS number 409-21-2 YesY
PubChem 9863
ChemSpider 9479 YesY
EC number 206-991-8
MeSH Silicon+carbide
ChEBI CHEBI:29390 YesY
RTECS number VW0450000
Gmelin Reference 13642
Jmol-3D images Image 1
Properties
Molecular formula CSi
Molar mass 40.10 g mol−1
Appearance Colorless crystals
Density 3.21 g·cm−3 (all polytypes)[1]
Melting point 2,730 °C (4,950 °F; 3,000 K) (decomposes)
Electron mobility ~900 cm2/V·s (all polytypes)
Refractive index (nD) 2.55 (infrared; all polytypes)[2]
Hazards
EU classification Not listed
NFPA 704
Flammability code 0: Will not burn. E.g., water Health code 1: Exposure would cause irritation but only minor residual injury. E.g., turpentine Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 YesY (verify) (what is: YesY/N?)
Infobox references

Silicon carbide (SiC), also known as carborundum /kɑrbəˈrʌndəm/, is a compound of silicon and carbon with chemical formula SiC. It occurs in nature as the extremely rare mineral moissanite. Silicon carbide powder has been mass-produced since 1893 for use as an abrasive. Grains of silicon carbide can be bonded together by sintering to form very hard ceramics that are widely used in applications requiring high endurance, such as car brakes, car clutches and ceramic plates in bulletproof vests. Electronic applications of silicon carbide as light-emitting diodes (LEDs) and detectors in early radios were first demonstrated around 1907, and today SiC is widely used in high-temperature/high-voltage semiconductor electronics. Large single crystals of silicon carbide can be grown by the Lely method; they can be cut into gems known as synthetic moissanite. Silicon carbide with high surface area can be produced from SiO2 contained in plant material.

Discovery and early production[edit]

Early experiments[edit]

Non-systematic, less-recognized, and often unverified syntheses of silicon carbide include

  • J. J. Berzelius's reduction of potassium fluorosilicate by potassium (1810)
  • César-Mansuète Despretz's passing an electric current through a carbon rod embedded in sand (1849)
  • Robert Sydney Marsden's (1856–1919) dissolution of silica in molten silver in a graphite crucible (1881)
  • Albert Colson's heating of silicon under a stream of ethylene (1882)
  • Paul Schuetzenberger's heating of a mixture of silicon and silica in a graphite crucible (1881).[3]
A replication of H.J. Round's LED experiments

Wide scale production[edit]

Wide-scale production is credited to Edward Goodrich Acheson in 1890.[4] Acheson was attempting to prepare artificial diamonds when he heated a mixture of clay (aluminum silicate) and powdered coke (carbon) in an iron bowl. He called the blue crystals that formed Carborundum, believing it to be a new compound of carbon and aluminum, similar to corundum. In 1893, Henri Moissan discovered the very rare naturally-occurring SiC mineral while examining rock samples found in the Canyon Diablo meteorite in Arizona. The mineral was named moissanite in his honor. Moissan also synthesized SiC by several routes, including dissolution of carbon in molten silicon, melting a mixture of calcium carbide and silica, and by reducing silica with carbon in an electric furnace.

Acheson patented the method for making silicon carbide powder on February 28, 1893.[5] Acheson also developed the electric batch furnace by which SiC is still made today and formed The Carborundum Company to manufacture bulk SiC, initially for use as an abrasive.[6] In 1900 the company settled with the Electric Smelting and Aluminum Company when a judge's decision gave "priority broadly" to its founders "for reducing ores and other substances by the incandescent method".[7] It is said that Acheson was trying to dissolve carbon in molten corundum (alumina) and discovered the presence of hard, blue-black crystals which he believed to be a compound of carbon and corundum: hence carborundum. It may be that he named the material "carborundum" by analogy to corundum, which is another very hard substance (9 on the Mohs scale).

The first use of SiC was as an abrasive. This was followed by electronic applications. In the beginning of the 20th century, silicon carbide was used as a detector in the first radios,[8] and in 1907 Henry Joseph Round produced the first LED by applying a voltage to a SiC crystal and observing yellow, green and orange emission at the cathode. Those experiments were later repeated by O. V. Losev in the Soviet Union in 1923.[9]

Natural occurrence[edit]

Moissanite single crystal (≈1 mm in size)

Naturally occurring moissanite is found in only minute quantities in certain types of meteorite and in corundum deposits and kimberlite. Virtually all the silicon carbide sold in the world, including moissanite jewels, is synthetic. Natural moissanite was first found in 1893 as a small component of the Canyon Diablo meteorite in Arizona by Dr. Ferdinand Henri Moissan, after whom the material was named in 1905.[10] Moissan's discovery of naturally occurring SiC was initially disputed because his sample may have been contaminated by silicon carbide saw blades that were already on the market at that time.[11]

While rare on Earth, silicon carbide is remarkably common in space. It is a common form of stardust found around carbon-rich stars, and examples of this stardust have been found in pristine condition in primitive (unaltered) meteorites. The silicon carbide found in space and in meteorites is almost exclusively the beta-polymorph. Analysis of SiC grains found in the Murchison meteorite, a carbonaceous chondrite meteorite, has revealed anomalous isotopic ratios of carbon and silicon, indicating an origin from outside the solar system; 99% of these SiC grains originate around carbon-rich asymptotic giant branch stars.[12] SiC is commonly found around these stars as deduced from their infrared spectra.[13]

Production[edit]

Because of the rarity of natural moissanite, most silicon carbide is synthetic. It is used as an abrasive, and more recently as a semiconductor and diamond simulant of gem quality. The simplest manufacturing process is to combine silica sand and carbon in an Acheson graphite electric resistance furnace at a high temperature, between 1,600 °C (2,910 °F) and 2,500 °C (4,530 °F). Fine SiO2 particles in plant material (e.g. rice husks) can be converted to SiC by heating in the excess carbon from the organic material.[14] The silica fume, which is a byproduct of producing silicon metal and ferrosilicon alloys, also can be converted to SiC by heating with graphite at 1,500 °C (2,730 °F).[15]

Synthetic SiC crystals ~3 mm in diameter
Synthetic SiC Lely crystals

The material formed in the Acheson furnace varies in purity, according to its distance from the graphite resistor heat source. Colorless, pale yellow and green crystals have the highest purity and are found closest to the resistor. The color changes to blue and black at greater distance from the resistor, and these darker crystals are less pure. Nitrogen and aluminium are common impurities, and they affect the electrical conductivity of SiC.[16]

Pure silicon carbide can be made by the so-called Lely process,[17] in which SiC powder is sublimated into high-temperature species of silicon, carbon, silicon dicarbide (SiC2), and disilicon carbide (Si2C) in an argon gas ambient at 2500 °C and redeposited into flake-like single crystals,[18] sized up to 2×2 cm, at a slightly colder substrate. This process yields high-quality single crystals, mostly of 6H-SiC phase (because of high growth temperature). A modified Lely process involving induction heating in graphite crucibles yields even larger single crystals of 4 inches (10 cm) in diameter, having a section 81 times larger compared to the conventional Lely process.[19] Cubic SiC is usually grown by the more expensive process of chemical vapor deposition (CVD).[16][20] Homoepitaxial and heteroepitaxial SiC layers can be grown employing both gas and liquid phase approaches.[21] Pure silicon carbide can also be prepared by the thermal decomposition of a polymer, poly(methylsilyne), under an inert atmosphere at low temperatures. Relative to the CVD process, the pyrolysis method is advantageous because the polymer can be formed into various shapes prior to thermalization into the ceramic.[21][22][23][24]

Structure and properties[edit]

Structure of major SiC polytypes.
SiC3Cstructure.jpg
SiC4Hstructure.jpg
SiC6Hstructure.jpg
(β)3C-SiC 4H-SiC (α)6H-SiC

Silicon carbide exists in about 250 crystalline forms.[25] The polymorphism of SiC is characterized by a large family of similar crystalline structures called polytypes. They are variations of the same chemical compound that are identical in two dimensions and differ in the third. Thus, they can be viewed as layers stacked in a certain sequence.[26]

Alpha silicon carbide (α-SiC) is the most commonly encountered polymorph; it is formed at temperatures greater than 1700 °C and has a hexagonal crystal structure (similar to Wurtzite). The beta modification (β-SiC), with a zinc blende crystal structure (similar to diamond), is formed at temperatures below 1700 °C.[27] Until recently, the beta form has had relatively few commercial uses, although there is now increasing interest in its use as a support for heterogeneous catalysts, owing to its higher surface area compared to the alpha form.

Properties of major SiC polytypes[2][21]
Polytype 3C (β) 4H 6H (α)
Crystal structure Zinc blende (cubic) Hexagonal Hexagonal
Space group T2d-F43m C46v-P63mc C46v-P63mc
Pearson symbol cF8 hP8 hP12
Lattice constants (Å) 4.3596 3.0730; 10.053 3.0810; 15.12
Density (g/cm3) 3.21 3.21 3.21
Bandgap (eV) 2.36 3.23 3.05
Bulk modulus (GPa) 250 220 220
Thermal conductivity (W cm−1K−1)

@ 300K (see [28] for temp. dependence)

3.6 3.7 4.9

Pure SiC is colorless. The brown to black color of industrial product results from iron impurities. The rainbow-like luster of the crystals is caused by a passivation layer of silicon dioxide that forms on the surface.

The high sublimation temperature of SiC (approximately 2700 °C) makes it useful for bearings and furnace parts. Silicon carbide does not melt at any known pressure. It is also highly inert chemically. There is currently much interest in its use as a semiconductor material in electronics, where its high thermal conductivity, high electric field breakdown strength and high maximum current density make it more promising than silicon for high-powered devices.[29] SiC also has a very low coefficient of thermal expansion (4.0 × 10−6/K) and experiences no phase transitions that would cause discontinuities in thermal expansion.[16]

Electrical conductivity[edit]

Silicon carbide is a semiconductor, which can be doped n-type by nitrogen or phosphorus and p-type by aluminium, boron, gallium or beryllium.[2] Metallic conductivity has been achieved by heavy doping with boron, aluminium or nitrogen. Superconductivity has been detected in 3C-SiC:Al, 3C-SiC:B and 6H-SiC:B at the same temperature of 1.5 K.[27][30] A crucial difference is however observed for the magnetic field behavior between aluminium and boron doping: SiC:Al is type-II, same as Si:B. On the contrary, SiC:B is type-I. In attempt to explain this difference, it was noted that Si sites are more important than carbon sites for superconductivity in SiC. Whereas boron substitutes carbon in SiC, Al substitutes Si sites. Therefore, Al and B "see" different environment that might explain different properties of SiC:Al and SiC:B.[31]

Uses[edit]

Abrasive and cutting tools[edit]

Cutting disks made of SiC

In the arts, silicon carbide is a popular abrasive in modern lapidary due to the durability and low cost of the material. In manufacturing, it is used for its hardness in abrasive machining processes such as grinding, honing, water-jet cutting and sandblasting. Particles of silicon carbide are laminated to paper to create sandpapers and the grip tape on skateboards.[32]

In 1982 an exceptionally strong composite of aluminium oxide and silicon carbide whiskers was discovered. Development of this laboratory-produced composite to a commercial product took only three years. In 1985, the first commercial cutting tools made from this alumina and silicon carbide whisker-reinforced composite were introduced by the Advanced Composite Materials Corporation (ACMC) and Greenleaf Corporation.[33]

Structural material[edit]

Silicon carbide is used for trauma plates of ballistic vests

In the 1980s and 1990s, silicon carbide was studied in several research programs for high-temperature gas turbines in Europe, Japan and the United States. The components were intended to replace nickel superalloy turbine blades or nozzle vanes. However, none of these projects resulted in a production quantity, mainly because of its low impact resistance and its low fracture toughness.[34]

Like other hard ceramics (namely alumina and boron carbide), silicon carbide is used in composite armor (e.g. Chobham armor), and in ceramic plates in bulletproof vests. Dragon Skin, which is produced by Pinnacle Armor, uses disks of silicon carbide.[35]

Silicon carbide is used as a support and shelving material in high temperature kilns such as for firing ceramics, glass fusing, or glass casting. SiC kiln shelves are considerably lighter and more durable than traditional alumina shelves.[36]

Automobile parts[edit]

The Porsche Carrera GT's carbon-ceramic (silicon carbide) disc brake

Silicon-infiltrated carbon-carbon composite is used for high performance "ceramic" brake discs, as it is able to withstand extreme temperatures. The silicon reacts with the graphite in the carbon-carbon composite to become carbon-fiber-reinforced silicon carbide (C/SiC). These discs are used on some road-going sports cars, supercars, as well as other performance cars including the Porsche Carrera GT, the Bugatti Veyron, the Chevrolet Corvette ZR1, Bentleys, Ferraris, Lamborghinis, some specific high performance Audis, and the McLaren P1.[37] Silicon carbide is also used in a sintered form for diesel particulate filters.[38] SiC is also used as an oil additive to reduce friction, emissions, and harmonics.[39]

Electric systems[edit]

The earliest electrical application of SiC was in lightning arresters in electric power systems. These devices must exhibit high resistance until the voltage across them reaches a certain threshold VT, at which point their resistance must drop to a lower level and maintain this level until the applied voltage drops below VT.[40]

It was recognized early on that SiC had such a voltage-dependent resistance, and so columns of SiC pellets were connected between high-voltage power lines and the earth. When a lightning strike to the line raises the line voltage sufficiently, the SiC column will conduct, allowing strike current to pass harmlessly to the earth instead of along the power line. Such SiC columns proved to conduct significantly at normal power-line operating voltages and thus had to be placed in series with a spark gap. This spark gap is ionized and rendered conductive when lightning raises the voltage of the power line conductor, thus effectively connecting the SiC column between the power conductor and the earth. Spark gaps used in lightning arresters are unreliable, either failing to strike an arc when needed or failing to turn off afterwards, in the latter case due to material failure or contamination by dust or salt. Usage of SiC columns was originally intended to eliminate the need for the spark gap in a lightning arrester. Gapped SiC lightning arresters were used as lightning-protection tool and sold under GE and Westinghouse brand names, among others. The gapped SiC arrester has been largely displaced by no-gap varistors that use columns of zinc oxide pellets.[41]

Electronic circuit elements[edit]

Ultraviolet LED

Power electronic devices[edit]

Silicon carbide is a semiconductor in research and early mass-production providing advantages for fast, high-temperature and/or high-voltage devices. First devices available were Schottky diodes, followed by Junction-gate FETs and MOSFETs for high-power switching. Bipolar transistors and thyristors are currently developed.[29] A major problem for SiC commercialization has been the elimination of defects: edge dislocations, screw dislocations (both hollow and closed core), triangular defects and basal plane dislocations.[42] As a result, devices made of SiC crystals initially displayed poor reverse blocking performance though researchers have been tentatively finding solutions to improving the breakdown performance.[43] Apart from crystal quality, problems with the interface of SiC with silicon dioxide have hampered the development of SiC-based power MOSFETs and insulated-gate bipolar transistors. Although the mechanism is still unclear, nitridation has dramatically reduced the defects causing the interface problems.[44] In 2008, the first commercial JFETs rated at 1200 V were introduced to the market, followed in 2011 by the first commercial MOSFETs rated at 1200 V.[citation needed] Beside SiC switches and SiC Schottky diodes (also Schottky barrier diode – SBD) in the popular TO-247 package, companies started even earlier to implement the bare chips into their power modules. SiC SBD diodes found wide market spread being used in PFC circuits and IGBT power modules. Conferences such as the International Conference on Integrated Power Electronics Systems (CIPS) report regularly about the technological progress of SIC power devices. Major challenges for fully unleashing the capabilities of SiC power devices are:

  • gate drive: SiC devices often require gate drive voltage levels that are different from their silicon counterparts and may be even unsymmetic, e.g. +20V and -5V.
  • packaging: SiC chips (Die (integrated circuit)) may have a higher power density that silicon power devices and are able to handle higher temperatures exceeding the silicon limit of 150°C. New die attach technologies as sintering are required to efficiently get the heat out of the devices and ensure a reliable interconnection.

LEDs[edit]

The first LED action was demonstrated in 1907 using SiC and the first commercial LEDs were again based on SiC. Yellow LEDs made from 3C-SiC were manufactured in the Soviet Union in the 1970s,[45] and blue ones (6H-SiC) worldwide in the 1980s.[46] The production was soon stopped because gallium nitride showed 10–100 times brighter emission. This difference in efficiency is due to the unfavorable indirect bandgap of SiC, whereas GaN has a direct bandgap which favors light emission. However, SiC is still one of the important LED components – it is a popular substrate for growing GaN devices, and it also serves as a heat spreader in high-power LEDs.[46]

Astronomy[edit]

The low thermal expansion coefficient, high hardness, rigidity and thermal conductivity make silicon carbide a desirable mirror material for astronomical telescopes. The growth technology (chemical vapor deposition) has been scaled up to produce disks of polycrystalline silicon carbide up to 3.5 meters in diameter, and several telescopes (like the Herschel Space Telescope) are already equipped with SiC optics.[47][48]

Thin filament pyrometry[edit]

Image of the test flame and glowing SiC fibers. The flame is about 7 cm tall.

Silicon carbide fibers are used to measure gas temperatures in an optical technique called thin filament pyrometry. It involves the placement of a thin filament in a hot gas stream. Radiative emissions from the filament can be correlated with filament temperature. Filaments are SiC fibers with a diameter of 15 micrometers; about one fifth that of a human hair. Because the fibers are so thin, they do little to disturb the flame and their temperature remains close to that of the local gas. Temperatures of about 800–2500 K can be measured.[49][50]

Heating elements[edit]

References to silicon carbide heating elements exist from the early 20th century when they were produced by Acheson's Carborundum Co. in the U.S. and EKL in Berlin. Silicon carbide offered increased operating temperatures compared with metallic heaters. Silicon carbide elements are used today in the melting of glass and non-ferrous metal, heat treatment of metals, float glass production, production of ceramics and electronics components, igniters in pilot lights for gas heaters, etc.[51]

Nuclear fuel particles[edit]

Silicon carbide is an important material in TRISO-coated fuel particles, the type of nuclear fuel found in high temperature gas cooled reactors (such as the Pebble Bed Reactor). A layer of silicon carbide gives coated fuel particles structural support and is the main diffusion barrier to the release of fission products.[52]

Nuclear fuel cladding[edit]

Silicon carbide composite material has been investigated for use as a replacement for Zircaloy cladding in light water reactors. The composite consists of SiC fibers wrapped around a SiC inner layer and surrounded by an SiC outer layer.[53] Problems have been reported with the ability to join the pieces of the SiC composite.[54]

Jewelry[edit]

A moissanite ring

As a gemstone used in jewelry, silicon carbide is called "synthetic moissanite" or just "moissanite" after the mineral name. Moissanite is similar to diamond in several important respects: it is transparent and hard (9–9.5 on the Mohs scale, compared to 10 for diamond), with a refractive index between 2.65 and 2.69 (compared to 2.42 for diamond). Moissanite is somewhat harder than common cubic zirconia. Unlike diamond, moissanite can be strongly birefringent. For this reason, moissanite jewels are cut along the optic axis of the crystal to minimize birefringent effects. It is lighter (density 3.21 g/cm3 vs. 3.53 g/cm3), and much more resistant to heat than diamond. This results in a stone of higher luster, sharper facets and good resilience. Loose moissanite stones may be placed directly into wax ring moulds for lost-wax casting, as can diamond,[55] as moissanite remains undamaged by temperatures up to 1800 °C. Moissanite has become popular as a diamond substitute, and may be misidentified as diamond, since its thermal conductivity is closer to diamond than any other substitute. Many thermal diamond-testing devices cannot distinguish moissanite from diamond, but the gem is distinct in its birefringence and a very slight green or yellow fluorescence under ultraviolet light. Some moissanite stones also have curved, string-like inclusions, which diamonds never have.[56]

Steel production[edit]

Piece of silicon carbide used in steel making

Silicon carbide, dissolved in a basic oxygen furnace used for making steel, acts as a fuel. The additional energy liberated allows the furnace to process more scrap with the same charge of hot metal. It can also be used to raise tap temperatures and adjust the carbon and silicon content. Silicon carbide is cheaper than a combination of ferrosilicon and carbon, produces cleaner steel and less emissions due to low levels of trace elements, has a low gas content, and does not lower the temperature of steel.[57]

Catalyst support[edit]

The natural resistance to oxidation exhibited by silicon carbide, as well as the discovery of new ways to synthesize the cubic β-SiC form, with its larger surface area, has led to significant interest in its use as a heterogeneous catalyst support. This form has already been employed as a catalyst support for the oxidation of hydrocarbons, such as n-butane, to maleic anhydride.[58][59]

Carborundum printmaking[edit]

Silicon carbide is used in carborundum printmaking – a collagraph printmaking technique. Carborundum grit is applied in a paste to the surface of an aluminium plate. When the paste is dry, ink is applied and trapped in its granular surface, then wiped from the bare areas of the plate. The ink plate is then printed onto paper in a rolling-bed press used for intaglio printmaking. The result is a print of painted marks embossed into the paper.[60]

Graphene production[edit]

Silicon carbide is used to produce epitaxial graphene by graphitization at high temperatures. This is considered as one of the promising methods to synthesize graphene at large scale for practical applications.[61][62]

See also[edit]

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