1. Field of the Invention
The present invention relates to Physical Vapor Transport growth of SiC single crystals.
2. Description of Related Art
Wafers of silicon carbide of the 4H and 6H polytype serve as lattice-matched substrates to grow epitaxial layers of SiC and GaN, which are used for fabrication of SiC- and GaN-based semiconductor devices for power and RF applications.
Large, industrial-size SiC single crystals are grown by a sublimation technique commonly known as Physical Vapor Transport (PVT). PVT growth is usually carried out in a graphite crucible that includes solid SiC sublimation source material disposed, typically, at the crucible bottom and a SiC single crystal seed disposed, typically, at the crucible top. The sublimation source material is, usually, polycrystalline SiC grain synthesized separately. The loaded crucible is placed in a furnace and heated to the growth temperature, which is, generally, between 2000° C. and 2400° C. During growth, the source material temperature is maintained higher than that of the seed crystal, typically, by 10° to 200°.
Upon reaching a suitable high temperature, the sublimation source vaporizes and fills the interior of the crucible with vapor species, such as Si, Si2C and/or SiC2. The temperature difference between the sublimation source and the seed crystal forces the vapor species to migrate and condense on the seed crystal causing a SiC single crystal to grow on the seed crystal. In order to control the growth rate and thus facilitate good crystal quality, PVT growth is carried out under a small pressure of inert gas, typically, between 1 and 100 Torr.
Generally, SiC crystals grown using this basic PVT arrangement suffer from structural defects, such as inclusions, micropipes and dislocations. It is commonly believed that inclusions of carbon, silicon and foreign polytypes are caused by deviations in the vapor phase stoichiometry, which is conventionally expressed as the Si:C atomic ratio. It is well-known that SiC sublimes incongruently with the Si:C atomic ratio in the vapor larger than 1 Depending on the SiC source conditions (such as the grain structure and size, polytype composition, stoichiometry, temperature, etc.) the Si:C ratio in the vapor over the sublimation source material can be as high as 1.5 or even higher. When the Si:C ratio in the vapor is too high, silicon inclusions form in the growing SiC crystal. Conversely, when the Si:C atomic ratio in the vapor is too low, carbon inclusions form in the growing SiC crystal.
It is also believed that stable growth of SiC single crystals of hexagonal 4H and 6H polytypes requires a carbon-rich vapor phase, whereas inclusions of foreign polytypes such as 15R are caused by deviations in the vapor stoichiometry.
Inclusions of metal carbides can appear in grown SiC single crystals when the SiC sublimation source material contains metallic contaminants.
Inclusions in a PVT grown SiC single crystal leads to local stress, which is relieved via generation, multiplication and movement of dislocations and micropipes. When SiC single crystal wafers are used as substrates in GaN or SiC epitaxy, the presence of inclusions, micropipes and dislocations in the substrate is harmful to the quality of the epilayers and the performance of semiconductor devices formed on said epilayers.
Since the inception of the PVT growth technique, a number of process modifications have been developed with the aim to improve the grown crystal quality and reduce defect densities.
For example, U.S. Pat. No. 5,858,086 to Hunter (hereinafter “the '086 patent”) discloses a system for the growth of AlN (aluminum nitride) crystals by sublimation. A schematic diagram of the system disclosed in the '086 Hunter patent is shown in
U.S. Pat. No. 5,985,024 to Balakrishna et al. discloses a system for the growth of high-purity SiC single crystals. A schematic diagram of the system disclosed in the Balakrishna et al. patent is shown in
U.S. Pat. No. 6,045,613 to Hunter (hereinafter “the '613 patent”) discloses the SiC crystal growth system shown in
U.S. Pat. No. 6,086,672 to Hunter discloses a system for the growth of AlN—SiC alloy crystals that is similar to the growth system disclosed in the '086 Hunter patent (
U.S. Pat. No. 7,323,052 to Tsvetkov et al. discloses sublimation growth of SiC single crystals containing reduced densities of point defects. The cause of such defects is believed to be vapor species that contain too much silicon. A schematic diagram of the apparatus disclosed in this patent is shown in
Generally, crucibles made of high-density, small-grain graphite are utilized in SiC sublimation crystal growth. Herein, high-density or dense graphite is graphite having a density between 1.70 and 1.85 g/cm3, grain sizes between several and tens of microns, and porosity on the order of 10%. Those skilled in the art recognize that such graphite is highly permeable to common gases, such as N2, Ar, He, CO, CO2, HCl, etc. However, dense graphite shows very low permeability to the vapors formed as a result of SiC sublimation: Si, Si2C and SiC2. Vapor losses from an enclosed crucible made of dense graphite incurred during SiC sublimation growth, typically, do not exceed several grams, and this is not enough to provide for sufficient or desirable removal of the vapor from the crucible. This low permeability of dense graphite to the Si-bearing vapors is the main reason why special holes or vents are made in the growth crucibles of the prior art discussed above for the purpose of venting.
It is also known that low-density, porous graphite can show higher permeability to the Si-containing vapor species formed as a result of SiC sublimation. Herein, low-density graphite is graphite having a density between 0.8 and 1.6 g/cm3; a porosity between 30% and 60%; and pore sizes between 1 and 100 microns. These properties of low-density graphite are utilized in U.S. Pat. No. 7,323,052 to Tsvetkov et al., where, alternatively to outlets 72 shown in
In summary, the aforementioned prior art teaches partial removal of vapor from the space surrounding the growing crystal by way of venting said vapor from inside the growth crucible to a space outside the growth crucible, e.g., into a chamber or space formed between the growth crucible and the outer wall of the furnace chamber where thermal insulation typically resides.
Venting the vapor into this chamber, however, has its problems. Specifically, the chamber or space surrounding the growth crucible is usually filled with thermal insulation made of purified, light-weight, fibrous graphite. The Si-containing vapor is very reactive toward graphite, especially when graphite is in such a light-weight form. Degradation of the thermal insulation caused by vapor erosion leads to uncontrollable changes in the temperatures of the crucible and, hence, the source and crystal. This has a negative effect on the growth process and crystal quality.
Another consequence of the escape of vapor into the chamber from the crucible is a reduced service time of the expensive thermal insulation. Utilization of a special gettering furnace for the disposal of the escaping vapor, as taught in the '613 patent, adds to the complexity and cost of the growth system.
The present invention is an improved SiC sublimation crystal growth process and apparatus for the growth of high quality SiC single crystals suitable for the fabrication of industrial size substrates, including substrates of 2″, 3″, 100 mm, 125 mm and 150 mm in diameter. The crystal growth crucible includes grains of SiC source material and a SiC seed crystal disposed inside a sealed graphite crucible in spaced relationship. During growth, the SiC source material vaporizes producing volatile vapor species, such as Si, Si2C and SiC2. Driven by a temperature gradient inside of the crucible, these vapor species migrate toward the seed crystal and precipitate on it causing the growth of a SiC single crystal on the seed crystal.
The SiC crystal growth crucible includes a baffle disposed around the seed crystal in the growth crucible, said baffle defining on a first side thereof in said growth crucible a growth zone where the SiC single crystal grows on the seed crystal, said baffle defining on a second side thereof in said growth crucible a vapor-capture trap around the seed crystal. The vapor-capture trap can be located at a position in the growth crucible where the temperature is lower than that of the seed crystal during the growth of the SiC single crystal on the seed crystal. The temperature within the vapor-capture trap can be lower than the temperature of the seed crystal by 3° C. to 20° C. The crucible design includes a pathway that enables the vapor to migrate toward the vapor-capture trap and enter it.
Upon reaching the vapor-capture trap, the Si-bearing vapor becomes supercooled and precipitates forming solid deposits of polycrystalline SiC within the vapor-capture trap. As a result of this process, part of the vapor is removed from the vicinity of the growing SiC single crystal, i.e., vapor is removed from the vicinity of the SiC single crystal growth interface. Simultaneously, unwanted vapor constituents harmful to the crystal quality are also removed. These harmful components include excessive silicon- or carbon-containing vapors as well as volatile contaminants.
The SiC crystal growth crucible can further include a porous vapor-absorbing member disposed in the vapor-capture trap and operative for absorbing vapor produced during sublimation growth of the SiC single crystal on the seed crystal.
The porous vapor-absorbing member can be disposed in the vapor-capture trap at a position where the vapor-absorbing member is at a temperature lower than that of the seed crystal during the growth of the SiC single crystal on the seed crystal. The temperature of the vapor-absorbing member during the growth of the SiC single crystal on the seed crystal can be lower than the temperature of the seed crystal by 3° C. to 20° C. The crucible design desirably includes a pathway that enables the vapor to migrate toward the porous vapor-absorbing member, permeate it, and react with it.
Upon reaching the vapor-absorbing member, the vapor permeates the pores of the vapor-absorbing member where it chemically reacts with the material of the member to form solid products. As a result of this process, part of the vapor is removed from the vicinity of the growing SiC single crystal. Simultaneously, unwanted vapor constituents harmful to the crystal quality are also removed. These harmful components include excessive silicon- or carbon-containing vapors as well as volatile contaminants.
In one embodiment, the vapor-absorbing member is made of purified porous graphite having a density, desirably, between 0.8 and 1.6 g/cm3; a porosity, desirably, between 30% and 60%; and pore sizes, desirably, between 1 and 100 microns.
The use of the vapor-absorbing member inside of the growth crucible facilitates growth of SiC single crystal boules with reduced densities of defects such as inclusions, micropipes and dislocations.
More specifically, the invention is an apparatus for sublimation growth of a SiC single crystal that includes a growth crucible operative for receiving a source material and a seed crystal in spaced relation and for substantially preventing the escape of vapor produced during sublimation growth of a SiC single crystal on the seed crystal from inside said growth crucible; and a baffle disposed around the seed crystal in the growth crucible, said baffle defining on a first side thereof in said growth crucible a growth zone where the SiC single crystal grows on the seed crystal, said baffle defining on a second side thereof in said growth crucible a vapor capture space, hereinafter a “vapor-capture trap”, around the seed crystal.
For substantially preventing the escape of vapor produced during sublimation growth of a SiC single crystal on the seed crystal, said growth crucible: can be made from a material that is substantially impermeable to the passage of the vapor produced during sublimation growth of a SiC single crystal on the seed crystal; and can include no intentional pathways or holes for escape of the vapor produced during sublimation growth of a SiC single crystal on the seed crystal from inside the growth crucible to outside the growth crucible.
The vapor-capture trap can be located at a position in the growth crucible where the temperature is lower than that of the seed crystal during the growth of the SiC single crystal on the seed crystal.
The apparatus can further include a vapor-absorbing member disposed in the vapor-capture trap and operative for absorbing vapor produced during sublimation growth of the SiC single crystal on the seed crystal.
The vapor-absorbing member can be disposed in the vapor-capture trap at a position where the vapor-absorbing member is at a temperature lower than that of the seed crystal during the growth of the SiC single crystal on the seed crystal.
The temperature of the vapor-absorbing member during the growth of the SiC single crystal on the seed crystal can be lower than the temperature of the seed crystal by 3° C. to 20° C.
The vapor-absorbing member can be made from porous graphite having a density between 0.8 and 1.6 g/cm3; a porosity between 30% and 60%; and pore sizes between 1 and 100 microns.
The baffle can define a pathway inside said growth crucible for the vapor to flow into the vapor-capture trap.
The growth crucible can include therein a pedestal for supporting the seed crystal intermediate a top of the growth crucible and the source material. The pedestal can have a height between 5 mm and 25 mm. The pathway can comprise a gap between an inner diameter of the baffle and an outer diameter of the pedestal. The gap can be between 1 mm and 8 mm wide. The pathway can comprise one or more holes in the baffle.
The invention is also a method of SiC sublimation crystal growth comprising: (a) providing a growth crucible charged with a source material and a seed crystal in spaced relation and a baffle disposed in the growth crucible around the seed crystal, said baffle defining on a first side thereof a growth zone where a single crystal grows on the seed crystal, said baffle defining on a second side thereof a vapor-capture trap around the seed crystal; and (b) heating the growth crucible of step (a) to a growth temperature whereupon a temperature gradient forms in the growth chamber that causes the source material to sublimate and form a vapor which is transported by the temperature gradient to the growth zone of the growth crucible where the single crystal grows by precipitation of the vapor on the seed crystal, wherein a fraction of the vapor enters the vapor-capture trap.
The vapor entering the vapor-capture trap can be removed during growth of the crystal from the growth zone by forming a deposit therein. One or more of the source material, the seed crystal, and the single crystal can be SiC.
The vapor-capture trap can be located at a position in the growth crucible where the temperature is lower than that of the seed crystal during the growth of the single crystal on the seed crystal.
A vapor-absorbing member can be disposed inside the vapor-capture trap. The vapor entering the vapor-capture trap can be removed during growth of the crystal from the growth zone by chemically reacting with the vapor-absorbing member, e.g., without limitation, to form a deposit.
The vapor-absorbing member can be at a lower temperature than the seed crystal during growth of the single crystal.
The vapor-absorbing member can be made from porous graphite with a density between 0.8 and 1.6 g/cm3; a porosity between 30% and 60%; and pore sizes between 1 and 100 microns.
The weight of the deposit formed in the vapor-capture trap can be between 5% and 20% of the weight of the grown crystal. Stated differently, the weight of the vapor absorbed by the vapor-absorbing member can be between 5% and 20% of the weight of the grown crystal.
The baffle can define a pathway for the vapor to flow to the vapor-capture trap. The growth crucible of step (a) can further include a pedestal for supporting the seed crystal intermediate a top of the growth crucible and the source material. The pathway can comprise a gap formed between an inner diameter of the baffle and an outer diameter of the pedestal.
The pathway can comprise at least one perforation in a wall of the baffle.
The present invention will now be described with reference to
With reference to
Driven by a vertical temperature gradient inside of crucible 102, vapor 110 migrates in the axial direction toward seed crystal 106 and condenses on seed crystal 106 causing growth of a SiC single crystal 112 thereon. The growing SiC crystal 112 is surrounded by a baffle 114 which delimits a space 116 adjacent growing SiC crystal 112. Space 116 is also known as the “growth zone”. During growth, growth zone 116 fills with volatile byproducts emerging as a result of vapor condensation, crystal growth and graphite erosion. These volatile byproducts can contain impurities as well as excessive silicon or carbon. Such uncontrollable changes in the vapor phase composition in growth zone 116 affect negatively the quality of growing SiC crystal 112.
Desirably, crucible 102 is formed from high density graphite that “substantially prevents” the escape of vapor 110 from the inside crucible 102. To “substantially prevent” the escape of vapor 110 from the interior of crucible 102, the high density graphite forming crucible 102 is “substantially impermeable” to vapors 110 and crucible 102 includes no intentional holes or vents for the escape of vapor 110 from the interior of crucible 102. Herein, crucible 102 “substantially preventing” the escape of vapor 110 from the interior thereof and crucible 102 being made from high density graphite that is “substantially impermeable” to vapors 110 means that the loss of vapor 110 from the interior of crucible 102 during the growth of SiC single crystal 112 on seed crystal 106 occurs via diffusion of vapor 110 across the wall of crucible 102 and lid 108, and the total of such loss of vapor 110 from the interior of crucible 102 during the growth of SiC single crystal 112 on seed crystal 106 is between 1% and 5% of the initial weight of SiC source material 104.
A vapor-capture trap 117 is provided in the interior of the crucible 102 in order to reduce the aforementioned uncontrollable changes in the vapor phase composition in the growth zone. The thermal field in the crucible is tuned such that vapor-capture trap 117 has the lowest temperature in the crucible interior. In particular, the temperature in vapor-capture trap 117 is desirably lower than the temperature of the seed 106. A common approach to tuning the temperature field inside the SiC growth crucible is by using finite-element thermal modeling. Driven by the temperature and pressure gradients, vapor 110 migrates toward the crucible top, reaches vapor-capture trap 117, and precipitates in vapor-capture trap 117 forming a solid polycrystalline SiC deposit 126 in vapor-capture trap 117, e.g., without limitation, on the interior surface of the wall of crucible 102 adjacent lid 108 and, optionally, on the interior surface of lid 108 adjacent the wall of crucible 102. As a result of the formation of solid polycrystalline SiC deposit 126, a fraction of vapor 110 is removed from growth zone 116. The shape of vapor-capture trap 117 in
A vapor-capture member 117a (shown in phantom in
Two possible vapor flows from growth zone 116 toward vapor-capture trap 117 and, if provided, member 117a are shown in
Desirably, vapor-absorbing member 117a is made of purified porous graphite having a density, desirably, between 0.8 and 1.6 g/cm3; a porosity, desirably, between 30% and 60%; and pore sizes, desirably, between 1 and 100 microns, i.e., a low-density graphite. Chemical reaction between vapor 110 and the carbon of the member 117a leads to the formation of solid polycrystalline SiC deposit 128 on or inside the pores of the member 117a. As a result of this reaction and the formation of the SiC deposits 128, a fraction of vapor 110 is removed from growth zone 116. Simultaneously, excessive silicon- or carbon-containing vapors, as well as volatile contaminants, are also removed from growth zone 116.
With continuing reference to
Two extremes are desirably avoided in order for vapor-capture trap 117 and, if provided, vapor-absorbing member 117a in vapor-capture trap 117 to be beneficial to the growth of SiC crystal 112 and the quality of the grown SiC crystal 112. In one extreme, too much of vapor 110 is removed from growth zone 116, leading to a dramatic reduction in the growth rate of SiC crystal 112. Another extreme is when too little vapor 110 is removed from growth zone 116, whereupon the presence of the vapor-capture trap 117 and, if provided, vapor-absorbing member 117a in crucible 102 has no beneficial effect on the quality of the grown SiC crystal 112.
Experimental results show that in order to realize the beneficial effects of vapor-capture trap 117 and, if provided, vapor-absorbing member 117a in vapor-capture trap 117, the weight of SiC deposit 126 or 128 formed in vapor-capture trap 117 or, if provided, vapor-absorbing member 117a, respectively, is desirably between 5% and 20% of the weight of the grown SiC single crystal 112. For example, where only vapor-capture trap 117 is present (i.e., without vapor-absorbing member 117a in vapor-capture trap 117), the weight of SiC deposit 126 formed in vapor-capture trap 117 is desirably between 5% and 20% of the weight of the grown SiC single crystal 112. On the other hand, where vapor-absorbing member 117a is included in vapor-capture trap 117, the weight of SiC deposit 128 formed in vapor-absorbing member 117a is desirably between 5% and 20% of the weight of the grown SiC single crystal 112.
It is envisioned, that when vapor-absorbing member 117a is included in vapor-capture trap 117, that some SiC deposit 126 may also form on the wall of crucible 102, the interior of lid 108, or both, adjacent space 136. However, it is envisioned that the total of SiC deposits 126 and 128 will desirably be between 5% and 20% of the weight of the grown SiC single crystal 112.
Desirably, control over the amount of vapor 110 absorbed in vapor-capture trap 117 and, if provided, vapor-absorbing member 117a in vapor-capture trap 117 is achieved by controlling the temperature of vapor-capture trap 117 and, if provided, vapor-absorbing member 117a in vapor-capture trap 117, and by providing a pathway 118 and/or 120 of desired cross-section, length and geometry for vapor 110 to flow from growth zone 116 to vapor-capture trap 117 and, if provided, vapor-absorbing member 117a in vapor-capture trap 117.
In order for the SiC deposit to form reliably inside vapor-capture trap 117 and, if provided, vapor-absorbing member 117a in vapor-capture trap 117, the temperature of vapor-capture trap 117 and, if provided, vapor-absorbing member 117a in vapor-capture trap 117 is desirably the lowest inside of crucible 102 during the growth of SiC crystal 112. More specifically, the temperature of vapor-capture trap 117 and, if provided, vapor-absorbing member 117a in vapor-capture trap 117 is desirably lower than that of seed crystal 106. In one embodiment, the temperature of vapor-capture trap 117 and, if provided, vapor-absorbing member 117a in vapor-capture trap 117 is lower than that of seed crystal 106, desirably, by 3° C. to 20° C.
This difference between the temperatures of seed crystal 106 and vapor-capture trap 117 and, if provided, vapor-absorbing member 117a in vapor-capture trap 117 can be realized in a number of ways. In one embodiment, the desired temperature difference between seed 106 and vapor-absorbing member 117a in vapor-capture trap 117 is achieved by the following combination: (i) vapor-absorbing member 117a (included in vapor-capture trap 117) is shaped as a short cylinder, as shown in
The geometry of the vapor pathway(s) that vapor 110 traverses to reach vapor-capture trap 117 and, if provided, vapor-absorbing member 117a in vapor-capture trap 117, specifically the length and cross-section of such vapor pathway(s), is another factor that can be used to control the amount of removed vapor 110. Two exemplary vapor pathways are shown schematically in
In
Upon reaching vapor-absorbing member 117a′ disposed in vapor-capture trap 117′, vapor 110 permeates it, diffuses through its bulk and reacts with the carbon forming said member 117a′. As a result of such reaction, polycrystalline SiC deposit 134′ forms on the member 117a′ and/or inside said member 117a′ in its coldest spot. It is envisioned that a portion of SiC deposit 134′ may also form on the wall of vapor-capture trap 117′.
Smartly, upon reaching vapor-absorbing member 117a″ in vapor-capture trap 117″, vapor 110 permeates it, diffuses through its bulk and reacts with the carbon forming said member 117a″. As a result of such reaction, polycrystalline SiC deposit 134″ forms on the member 117a″ and/or inside said member 117a″ in its coldest spot. It is envisioned that a portion of SiC deposit 134″ may also form on the wall of vapor-capture trap 117″.
When vapor-capture trap 117′ in
This growth run was carried out in a growth furnace having the crucible, baffle, and vapor-absorbing member 117a′ arrangement like the one shown in
A 3.25″ diameter SiC wafer of the 6H polytype was used as the seed crystal 106. This wafer was oriented on-axis, with its faces parallel to the basal c-plane. The surface of the wafer where the growth of SiC crystal 112 was to occur was polished prior to the growth of SiC crystal 112 using a chemico-mechanical polishing (CMP) technique to remove scratches and sub-surface damage. This seed crystal 106 was attached to pedestal 124 of crucible lid 108 using a high-temperature carbon adhesive. Pedestal 124 had a height H of 12.5 mm.
Baffle 114′ was machined from dense, isostatically molded and halogen-purified graphite and had a 3 mm thick wall. The inner diameter of baffle 114′ was larger than the outer diameter of pedestal 124 to form a 2 mm wide annular gap 130 between pedestal 124 and baffle 114′.
Vapor-absorbing member 117a′, shaped as a cylinder in
Following this, the RF coil position and the RF power were adjusted to achieve a temperature of source material 104 of 2120° C. and a temperature of seed crystal 106 of 2090° C. The Ar pressure was then reduced to 10 Torr to start sublimation growth of SiC crystal 112 boule. Upon completion of the run, the growth furnace was cooled to room temperature over a period of 12 hours.
The grown 6H boule of SiC crystal 112 weighed 300 grams. The weight of the polycrystalline SiC deposit 134 formed inside vapor-absorbing member 117′ was about 20 grams. The grown boule of SiC crystal 112 contained neither carbon particles, nor Si droplets, nor foreign polytype inclusions. The micropipe density in this boule of SiC crystal 112 was about 0.9 cm−2 and the dislocation density was close to 1·104 cm−2.
The boule of SiC crystal 112 was fabricated into 25 standard 3″ diameter, 400 micron thick wafers, and their resistivity was measured and mapped using Corema, a contactless resistivity tool. The resistivity of all wafers was close to 1·1011 Ohm-cm, with a standard deviation below 10%.
This growth run gas was carried out in a growth furnace having the crucible, baffle, and vapor-absorbing member 117a″ arrangement like the one shown in
A 110 mm diameter SiC wafer of the 6H polytype oriented on-axis was used as the seed crystal 106. The surface of the wafer where SiC crystal 112 was to grow was CMP polished prior to growth. The seed crystal 106 was attached to pedestal 124 of crucible lid 108 using a high-temperature adhesive. Pedestal 124 had a height of 10 mm.
Baffle 114″ used in this run had the configuration shown in
Vapor-absorbing member 117″ had the configuration shown in
The growth conditions were as follows: the temperature of source material 104 was 2150° C.; the temperature of seed crystal 106 was 2100° C.; and the pressure of inert gas (Ar) was 20 Torr.
The grown 6H boule of SiC crystal 112 weighed 380 grams. The weight of the polycrystalline SiC deposit 134 formed inside vapor-absorbing member 117″ was about 35 grams. Upon inspection, no inclusions were detected in the boule bulk. The micropipe density in this boule was below 0.3 cm−2 and the dislocation density was about 9·103 cm−2.
The boule of SiC crystal 112 was fabricated into 23 standard 100 mm diameter, 400 microns thick wafers. The resistivity of all wafers was close to 1·1011 Ohm-cm, with the standard deviation below 10%.
As can be seen, sublimation growth of SiC single crystals in accordance with the present invention yields SiC boules with reduced densities of inclusions, such as foreign polytypes, silicon droplets and carbon particles. The invention also leads to reduced densities of micropipes and dislocations.
The invention has been described with reference to exemplary embodiments. Obvious modifications and alterations will occur to others upon reading and understanding the preceding detailed description. It is intended that the invention be construed as including all such modifications and alterations insofar as they come within the scope of the appended claims or the equivalents thereof.
Number | Date | Country | Kind |
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61242549 | Sep 2009 | US | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US10/48765 | 9/14/2010 | WO | 00 | 3/8/2012 |