WO2017135272A1 - Procédé de fabrication d'un monocristal de sic et cristal de germe de sic - Google Patents

Procédé de fabrication d'un monocristal de sic et cristal de germe de sic Download PDF

Info

Publication number
WO2017135272A1
WO2017135272A1 PCT/JP2017/003519 JP2017003519W WO2017135272A1 WO 2017135272 A1 WO2017135272 A1 WO 2017135272A1 JP 2017003519 W JP2017003519 W JP 2017003519W WO 2017135272 A1 WO2017135272 A1 WO 2017135272A1
Authority
WO
WIPO (PCT)
Prior art keywords
crystal
sic
sic single
single crystal
crystal growth
Prior art date
Application number
PCT/JP2017/003519
Other languages
English (en)
Japanese (ja)
Inventor
楠 一彦
和明 関
寛典 大黒
幹尚 加渡
雅喜 土井
Original Assignee
新日鐵住金株式会社
トヨタ自動車株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 新日鐵住金株式会社, トヨタ自動車株式会社 filed Critical 新日鐵住金株式会社
Publication of WO2017135272A1 publication Critical patent/WO2017135272A1/fr

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B19/00Liquid-phase epitaxial-layer growth
    • C30B19/12Liquid-phase epitaxial-layer growth characterised by the substrate
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B29/00Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/10Inorganic compounds or compositions
    • C30B29/36Carbides

Definitions

  • the present invention relates to a method for producing a SiC single crystal and a SiC seed crystal, and more particularly to a method for producing a SiC single crystal by a solution growth method and a SiC seed crystal used in the solution growth method.
  • SiC single crystal is a thermally and chemically stable compound semiconductor.
  • the SiC single crystal has excellent physical properties as compared with the Si single crystal.
  • a SiC single crystal has a large band gap, a high breakdown voltage, and a high thermal conductivity, and has a high electron saturation rate compared to a Si single crystal. For this reason, SiC single crystals are attracting attention as next-generation semiconductor materials.
  • a sublimation recrystallization method (hereinafter also referred to as a sublimation method), a solution growth method (hereinafter also referred to as a solution method), and the like are known.
  • a SiC single crystal is grown by supplying a raw material on a SiC seed crystal in a gas phase state.
  • a SiC single crystal is grown on the SiC seed crystal by bringing the SiC seed crystal into contact with the Si—C solution.
  • a raw material containing Si is put in a crucible and melted to produce a Si—C solution.
  • a SiC single crystal is manufactured by bringing the SiC seed crystal into contact with the Si—C solution and supercooling the Si—C solution in the vicinity of the SiC seed crystal.
  • the Si—C solution refers to a solution in which carbon (C) is dissolved in a melt of Si or Si alloy.
  • Patent Document 1 JP 2004-323348 A (Patent Document 1), JP 2009-051701 A (Patent Document 2), JP 2010-254520 A (Patent Document 3), and JP 2013-087005 A (Patent Document 2).
  • Document 4 proposes a technique for obtaining a uniform SiC single crystal by adjusting the position of the facet region.
  • the SiC single crystal manufactured using the solution method has fewer defects such as micropipes and basal plane dislocations than the SiC single crystal manufactured using the sublimation method. Therefore, a method for producing a SiC single crystal by a solution method has been studied.
  • solvent inclusion refers to a defect caused by the Si—C solution being confined inside the SiC single crystal. If solvent inclusion occurs, the quality of the SiC single crystal is degraded.
  • Patent Document 5 proposes a technique for suppressing the occurrence of solvent inclusion in a solution method.
  • Patent Document 5 is characterized in that the Si—C solution is stirred by periodically changing the number of revolutions or the number of revolutions and the direction of rotation of the crucible.
  • Patent Document 5 describes that even if the diameter is 1 inch or more and the thickness is as large as 5 microns or more, a high-quality SiC single crystal without inclusion can be produced at a high crystal growth rate.
  • JP 2004-323348 A JP 2009-051701 A JP 2010-254520 A JP 2013-087005 A JP 2006-117441 A
  • An object of the present invention is to provide a method for producing a SiC single crystal by a solution growth method and a SiC seed crystal used for the solution growth method, which can suppress the occurrence of solvent inclusion.
  • the method for producing an SiC single crystal according to the present invention is a production method by a solution growth method in which an SiC single crystal is grown by bringing the crystal growth surface of an SiC seed crystal into contact with an Si—C solution.
  • the manufacturing method includes a preparation process and a growth process.
  • the preparation step the raw material is heated and melted to prepare a Si—C solution.
  • the growth step the crystal growth surface is brought into contact with the Si—C solution, and an SiC single crystal is grown on the crystal growth surface.
  • the crystal growth surface includes a facet region, and the offset angle of the crystal growth surface with respect to the ⁇ 0001 ⁇ plane is 0.5 ° or less.
  • the center of gravity of the facet region is arranged at a distance within 0.40 r from the center of gravity of the crystal growth surface.
  • the length of the longest line segment connecting the center of gravity of the crystal growth surface and the outer periphery of the crystal growth surface is r.
  • the SiC seed crystal according to the present invention is an SiC seed crystal used in a solution growth method in which a SiC single crystal is grown on an SiC seed crystal by bringing the SiC seed crystal into contact with an Si—C solution.
  • the SiC seed crystal has a crystal growth surface having an offset angle of 0.5 ° or less with respect to the ⁇ 0001 ⁇ plane.
  • the crystal growth surface includes a facet region.
  • the center of gravity of the facet region is arranged at a distance within 0.40 r from the center of gravity of the crystal growth surface.
  • the length of the longest line segment connecting the center of gravity of the crystal growth surface and the outer periphery of the crystal growth surface is r.
  • the method for producing a SiC single crystal and the SiC seed crystal according to the present invention can suppress the occurrence of solvent inclusion.
  • FIG. 1 is a schematic view of a manufacturing apparatus used in the method for manufacturing a SiC single crystal according to the present embodiment.
  • FIG. 2 is a bottom view (a diagram of a crystal growth surface) of the SiC seed crystal.
  • FIG. 3 is a bottom view of a SiC seed crystal according to another embodiment different from FIG.
  • the present inventors have made various studies on a method for producing an SiC single crystal by a solution method that can suppress the occurrence of solvent inclusion. As a result, the following knowledge was obtained.
  • the SiC single crystal is grown by bringing the crystal growth surface of the SiC seed crystal into contact with the Si-C solution.
  • the SiC seed crystal may include a facet region.
  • a facet region refers to a region having the same crystal structure as other regions and having a higher screw dislocation density and nitrogen concentration than other regions.
  • the screw dislocation has a small step at an atomic level called a step in which crystal growth easily proceeds.
  • the facet region is a source of steps during crystal growth because of the high screw dislocation density. That is, if a facet region is included in the crystal growth surface, crystal growth proceeds preferentially in the facet region compared to other regions.
  • step bunching promotes three-dimensional growth of SiC single crystal. If the SiC single crystal grows three-dimensionally, a part of the solvent is confined in the SiC single crystal, and solvent inclusion occurs.
  • the facet region is arranged at the center of the crystal growth surface. This reduces the distance between the facet area and the area farthest from the facet area. Therefore, the difference in crystal growth rate between the facet region and the region farthest from the facet region is reduced. That is, the variation in the crystal growth thickness is suppressed. This suppresses step bunching and three-dimensional growth of the SiC single crystal. As a result, solvent inclusion can be suppressed.
  • the SiC single crystal manufacturing method completed based on the above knowledge is a manufacturing method by a solution growth method in which the SiC single crystal is grown by bringing the crystal growth surface of the SiC seed crystal into contact with the Si-C solution.
  • the manufacturing method includes a preparation process and a growth process.
  • the preparation step the raw material is heated and melted to prepare a Si—C solution.
  • the growth step the crystal growth surface is brought into contact with the Si—C solution, and an SiC single crystal is grown on the crystal growth surface.
  • the crystal growth surface includes a facet region, and the offset angle of the crystal growth surface with respect to the ⁇ 0001 ⁇ plane is 0.5 ° or less.
  • the center of gravity of the facet region is arranged at a distance within 0.40 r from the center of gravity of the crystal growth surface.
  • the length of the longest line segment connecting the center of gravity of the crystal growth surface and the outer periphery of the crystal growth surface is r.
  • a SiC single crystal is manufactured using a SiC seed crystal in which the facet region is arranged in the center. Therefore, solvent inclusion can be suppressed.
  • the crystal growth surface is a single surface.
  • the center of gravity of the facet region is arranged at a distance within 0.25r from the center of gravity of the crystal growth surface.
  • the area ratio of the facet region to the crystal growth surface is 0.04 or more.
  • the area ratio of the facet region to the crystal growth surface is 0.10 or more.
  • a SiC single crystal may be grown by 2 mm or more.
  • the yield of the SiC single crystal can be increased.
  • the SiC seed crystal and the SiC single crystal may have a 4H polymorphic crystal structure.
  • the SiC seed crystal according to the present embodiment is an SiC seed crystal used in a solution growth method in which an SiC single crystal is grown on an SiC seed crystal by bringing the SiC seed crystal into contact with an Si—C solution.
  • the SiC seed crystal has a crystal growth surface having an offset angle of 0.5 ° or less with respect to the ⁇ 0001 ⁇ plane.
  • the crystal growth surface includes a facet region.
  • the center of gravity of the facet region is arranged at a distance within 0.40 r from the center of gravity of the crystal growth surface.
  • the length of the longest line segment connecting the center of gravity of the crystal growth surface and the outer periphery of the crystal growth surface is r.
  • the SiC single crystal produced using the seed crystal can suppress solvent inclusion.
  • the crystal growth surface is a single surface.
  • the area ratio of the facet region to the crystal growth surface is 0.04 or more.
  • FIG. 1 is a schematic diagram of an example of a manufacturing apparatus 1 used in the method for manufacturing a SiC single crystal according to the present embodiment.
  • the manufacturing apparatus 1 includes a chamber 2, a crucible 5, a heat insulating member 4, an induction heating device 3, a rotating device 20, and a seed shaft 6.
  • Chamber 2 is a casing.
  • the chamber 2 accommodates the heat insulating member 4 and the induction heating device 3.
  • the chamber 2 can further accommodate a crucible 5.
  • the chamber 2 is cooled with a cooling medium.
  • the crucible 5 is housed in a casing-shaped heat insulating member 4.
  • the crucible 5 is a housing whose upper end is open.
  • the crucible 5 may be provided with a top plate. In this case, evaporation of the Si—C solution 7 can be suppressed.
  • the crucible 5 accommodates the Si—C solution 7.
  • the Si-C solution 7 is produced by melting the raw material by heating.
  • the raw material may be only Si, or may contain Si and another metal element.
  • the metal element contained in the raw material of the Si-C solution 7 is selected from the group consisting of titanium (Ti), manganese (Mn), chromium (Cr), cobalt (Co), vanadium (V), and iron (Fe). 1 type, or 2 or more types.
  • the Si—C solution 7 is generated by further dissolving carbon (C) in these raw materials. When carbon is supplied to the Si—C solution 7 from the added carbon source, the raw material of the Si—C solution 7 contains carbon (C).
  • the crucible 5 When supplying carbon to the Si—C solution 7 by melting the crucible 5, the crucible 5 preferably contains carbon. More preferably, the material of the crucible 5 is graphite. When supplying carbon from the added carbon source to the Si—C solution 7, the crucible 5 may be any material that is stable at the crystal growth temperature. In this case, the material of the crucible 5 may be ceramics or a high melting point metal. When the crucible 5 is made of a material other than graphite, a film containing graphite may be formed on the inner surface of the crucible 5.
  • the heat insulating member 4 surrounds the crucible 5.
  • the heat insulating member 4 is made of a well-known heat insulating material.
  • the heat insulating material is, for example, a fiber-based or non-fiber-based molded heat insulating material.
  • the induction heating device 3 surrounds the heat insulating member 4.
  • the induction heating device 3 includes a high frequency coil.
  • the high frequency coil is disposed coaxially with the seed shaft 6.
  • the induction heating device 3 induction-heats the crucible 5 by electromagnetic induction and melts the raw material stored in the crucible 5 to generate the Si—C solution 7.
  • the induction heating device 3 further maintains the Si—C solution 7 at the crystal growth temperature.
  • Rotating device 20 is a shaft extending in the height direction of chamber 2.
  • the upper end of the rotating device 20 is disposed inside the chamber 2.
  • the crucible 5 is disposed on the upper surface of the rotating device 20.
  • the rotation device 20 is connected to a drive source 21 and rotates around the central axis of the rotation device 20 by the drive source 21. When the rotating device 20 rotates, the crucible 5 rotates.
  • the crucible 5 and the rotating device 20 may rotate or may not rotate.
  • the seed shaft 6 is a shaft extending in the height direction of the chamber 2.
  • the upper end of the seed shaft 6 is disposed outside the chamber 2.
  • the seed shaft 6 is attached to the drive source 9 outside the chamber 2.
  • the lower end of the seed shaft 6 is disposed inside the crucible 5.
  • An SiC seed crystal 8 is attached to the lower end of the seed shaft 6.
  • the seed shaft 6 can be moved up and down and rotated by a drive source 9.
  • the seed shaft 6 is lowered by the drive source 9, and the SiC seed crystal 8 comes into contact with the Si—C solution 7.
  • the seed shaft 6 is rotated by the drive source 9, and the SiC seed crystal 8 is rotated.
  • the rotation direction of the seed shaft 6 may be the same as the rotation direction of the crucible 5 or may be the opposite direction.
  • the seed shaft 6 may rotate or may not rotate.
  • the seed shaft 6 is graphite.
  • SiC seed crystal 8 has a plate shape and is made of a SiC single crystal.
  • SiC seed crystal 8 may be, for example, a SiC single crystal manufactured by a sublimation method.
  • the crystal structure of SiC seed crystal 8 is the same as the crystal structure of the SiC single crystal to be manufactured.
  • the surface on which the SiC single crystal grows on the Si-C solution 7 is called a crystal growth surface.
  • the offset angle of the crystal growth surface of the seed crystal of the present invention with respect to the ⁇ 0001 ⁇ plane is 0.5 ° or less.
  • the offset angle of the crystal growth surface with respect to the ⁇ 0001 ⁇ plane is also simply referred to as “offset angle”. If the offset angle is larger than 0.5 °, the step density is different between a region near the ⁇ 0001 ⁇ plane and a region far from the ⁇ 0001 ⁇ plane on the crystal growth surface.
  • the step density is higher in the region near the ⁇ 0001 ⁇ plane on the crystal growth surface than in the region far from the ⁇ 0001 ⁇ plane on the crystal growth surface.
  • step bunching is likely to occur in an area where the step density is high.
  • irregularities are generated on the surface of the grown crystal, and solvent inclusion may occur. Therefore, the offset angle of the crystal growth surface of the seed crystal of the present invention with respect to the ⁇ 0001 ⁇ plane is 0.5 ° or less.
  • the crystal growth surface is a ⁇ 0001 ⁇ plane. That is, the offset angle is 0.0 °.
  • the crystal growth plane is a (000-1) plane (carbon plane).
  • the fact that the offset angle of the crystal growth surface with respect to the ⁇ 0001 ⁇ plane is 0.5 ° or less is also referred to as “the crystal growth surface is on axis”.
  • the crystal growth surface of the seed crystal of the present invention is a single surface.
  • a single surface means a smooth surface having no ridgeline.
  • the crystal growth surface of the seed crystal of the present invention may have microscopic distortion as long as it does not have a ridgeline.
  • unevenness may occur in the ridge line portion of the grown crystal surface.
  • solvent inclusion may occur.
  • the crystal growth surface is a single plane.
  • FIG. 2 is a bottom view of the SiC seed crystal 8 (a diagram of a crystal growth surface).
  • crystal growth surface 80 includes a facet region 81.
  • the crystal growth surface 80 may be circular as shown in FIG. 2 or other shapes.
  • the shape of the crystal growth surface 80 is, for example, a hexagon shown in FIG.
  • the shape of the crystal growth surface 80 may be another polygon (such as a quadrangle and an octagon), or may be an ellipse.
  • the shape of the crystal growth surface 80 is not particularly limited.
  • the facet region 81 is a region having the same crystal structure as other regions and having a higher screw dislocation density and nitrogen concentration than the other regions.
  • the facet region 81 can be confirmed by measuring the screw dislocation density and the nitrogen concentration by a known method.
  • the facet area 81 can also be confirmed by the following method.
  • the SiC seed crystal 8 is cut to a thickness of 1 mm or less. The cut piece is placed in front of a light source such as an incandescent bulb to transmit light. A portion (facet region 81) that is more strongly colored than the other regions can be visually confirmed.
  • Facet region 81 is arranged at the center of crystal growth surface 80. Specifically, the centroid 82 of the facet region 81 is arranged at a distance within 0.40 r from the centroid 83 of the crystal growth surface 80. Here, the length of the longest line segment among the line segments connecting the center of gravity 83 of the crystal growth surface 80 and the outer periphery 84 of the crystal growth surface 80 is r.
  • facet region 81 By disposing facet region 81 in the center of crystal growth surface 80, the distance between facet region 81 and the region farthest from facet region 81 is reduced. Therefore, the difference in crystal growth rate between the facet region 81 and the region farthest from the facet region 81 is reduced. That is, the variation in the crystal growth thickness is suppressed. This suppresses the progress of step bunching during crystal growth. As a result, solvent inclusion can be suppressed.
  • the center of gravity 82 of the facet region 81 is arranged at a distance within 0.25 r from the center of gravity 83 of the crystal growth surface 80.
  • the area ratio of facet region 81 to crystal growth surface 80 is 0.04 or more, more preferably 0.10 or more.
  • the upper limit of the area ratio of facet region 81 to crystal growth surface 80 is not particularly limited.
  • the SiC seed crystal 8 including the crystal growth surface 80 including the facet region 81 in the center is manufactured by being cut out from a SiC single crystal ingot.
  • a well-known method can be adopted as a method for cutting the SiC single crystal ingot.
  • a blade saw method and a wire saw method are used as a method for cutting the SiC single crystal ingot.
  • the manufacturing method of the SiC single crystal according to the present embodiment includes a preparation process and a growth process.
  • the raw material is heated and melted to prepare the Si—C solution 7.
  • the raw material of the Si—C solution 7 having the above composition is stored in the crucible 5.
  • the crucible 5 containing the raw material is disposed on the upper surface of the rotating device 20 in the chamber 2.
  • the chamber 2 is filled with an inert gas, for example, helium gas.
  • the raw material of the crucible 5 and the Si—C solution 7 is heated by the induction heating device 3 to the melting point or higher of the raw material of the Si—C solution 7. If the crucible 5 containing carbon is heated, carbon melts from the crucible 5 into the melt.
  • a Si—C solution 7 is generated.
  • a solid-phase carbon source is charged into the Si—C solution 7 and dissolved.
  • the solid-phase carbon source is, for example, one or more selected from the group consisting of graphite, amorphous carbon raw material, SiC, and carbides of additive elements. These are added to the Si-C solution 7 in the form of blocks, rods, granules and powders.
  • the Si—C solution 7 is generated by heating the raw material containing carbon.
  • the heating is performed until the Si-C solution 7 reaches the crystal growth temperature. Heating may be continued up to the crystal growth temperature, or a period for holding at a constant temperature may be provided. When holding at a constant temperature, the holding temperature should just be more than the liquidus temperature of a raw material. In this case, the heating is performed until the SiC concentration in the Si—C solution 7 approaches a saturated state. When using a solid carbon source, it is preferable to heat until the carbon source is completely dissolved.
  • the heating time is, for example, 0.5 to 10 hours.
  • the crystal growth surface 80 of the SiC seed crystal 8 is brought into contact with the Si—C solution 7 to grow a SiC single crystal on the crystal growth surface 80 of the SiC seed crystal 8.
  • the crystal growth surface 80 of the SiC seed crystal 8 is brought into contact with the Si—C solution 7 (hereinafter also referred to as a landing liquid).
  • the crystal growth surface 80 is on axis and includes a facet region 81.
  • the facet region 81 includes a screw dislocation.
  • the steps (small steps at the atomic level) possessed by screw dislocations are structures depending on the crystal structure. Therefore, a crystal structure similar to SiC seed crystal 8 grows stably.
  • the output of the induction heating device 3 is adjusted to maintain the temperature of the Si—C solution 7 at the crystal growth temperature.
  • the crystal growth temperature is, for example, 1850 to 2050 ° C.
  • a SiC single crystal By applying a temperature gradient to the Si-C solution 7, a SiC single crystal can be produced efficiently. Specifically, a temperature gradient is applied so that the vicinity of the SiC seed crystal 8 in the Si—C solution 7 is lower in temperature than other portions. Thereby, the supersaturation degree of SiC in the vicinity of SiC seed crystal 8 can be increased. As a result, the growth rate of the SiC single crystal is increased.
  • the output of the induction heating device 3 is adjusted to give a temperature gradient so that the upper part of the Si—C solution 7 becomes a low temperature. Otherwise, the output of the induction heating device 3 is adjusted so that the temperature of the Si—C solution 7 is maintained by heat transfer from the crucible 5.
  • a temperature gradient is applied so that the center of the Si—C solution 7 has a low temperature.
  • the temperature gradient is preferably in the range of 5 to 50 ° C./cm regardless of the vertical direction or the horizontal direction. If the temperature gradient is 5 ° C./cm or more, the growth rate of the SiC single crystal is increased. If the temperature gradient is 50 ° C./cm or less, spontaneous generation of SiC nuclei in the Si—C solution 7 can be suppressed.
  • the growth step may be performed while maintaining the temperature of the Si—C solution 7 constant or may be performed while the temperature is increased.
  • the degree of supersaturation of the carbon (C) concentration in the Si—C solution 7 can be adjusted to an appropriate range. Therefore, spiral growth proceeds predominantly. As a result, mixing of different crystal polymorphs due to two-dimensional nucleus growth can be further suppressed.
  • the growth step is performed while raising the temperature of the Si—C solution 7, if the rate of temperature rise is within a certain range, the two-dimensional nucleus growth can be stably suppressed without dissolving the SiC single crystal.
  • a meniscus may be formed after the landing.
  • the SiC seed crystal 8 in contact with the Si—C solution 7 is pulled upward from the liquid level of the Si—C solution 7.
  • the meniscus height is, for example, 0.1 to 4.0 mm.
  • FIG. 1 the example of the manufacturing apparatus 1 using the crucible 5 is shown.
  • a levitation method in which the raw material is levitated and melted by electromagnetic force without using the crucible 5 may be employed.
  • a cold crucible method for generating the Si—C solution 7 levitated by magnetic repulsion in a water-cooled metal crucible may be employed.
  • the SiC single crystal of this embodiment can be manufactured through the above steps.
  • the manufacturing apparatus 1 shown in FIG. 1 was used.
  • the crucible 5 was a graphite crucible
  • the induction heating device 3 was a high frequency coil
  • the seed shaft 6 was graphite
  • the chamber 2 was a water-cooled stainless steel chamber.
  • the inside of the production apparatus was replaced with helium gas.
  • the raw material of the graphite crucible and the Si—C solution was heated by a high frequency coil to prepare an Si—C solution.
  • a temperature gradient was formed so that the upper part of the Si-C solution had a low temperature.
  • the temperature gradient was formed by controlling the positional relationship between the graphite crucible and the high frequency coil. Specifically, the temperature gradient was formed by arranging the Si—C solution so that the center portion is located above the center of the high-frequency coil (heat generation center). The temperature gradient was confirmed by inserting a thermocouple into the Si—C solution in advance and measuring the temperature separately from this example. The temperature gradient in the vicinity of the SiC seed crystal was about 12 ° C./cm. The temperature of the Si-C solution near the SiC seed crystal during crystal growth was measured. The measurement was performed by measuring the temperature of the graphite on the back surface of the SiC seed crystal with an optical thermometer using a seed shaft provided with a temperature measuring hole. The crystal growth temperature was 1940 ° C.
  • the seed shaft was lowered to allow the SiC seed crystal to land on the Si-C solution.
  • the SiC seed crystal was manufactured by a sublimation recrystallization method and had a circular crystal growth surface with a radius of 37.5 mm.
  • the crystal structure of the SiC seed crystal was 4H—SiC.
  • the crystal growth surface was a single plane and was a (000-1) plane on axis. That is, the offset angle of the crystal growth surface was 0.3 °.
  • the facet region was visually confirmed.
  • the facet area was circular. Table 1 shows the position of the center of gravity of the facet region, the area of the facet region, and the area ratio of the facet region to the crystal growth surface.
  • the position of the center of gravity of the facet region indicates the distance between the center of gravity of the crystal growth surface and the center of gravity of the facet region.
  • the length of the longest line segment among the line segments connecting the center of gravity of the crystal growth surface and the outer periphery of the crystal growth surface is described as r (mm).
  • the seed shaft After landing, the seed shaft was pulled up to form a meniscus. The meniscus height was 0.5 mm. Crystal growth was performed while keeping the temperature of the Si-C solution constant. The crucible and the seed shaft were rotated at 10 rpm in the opposite direction. The time from the landing to the end of crystal growth was 50 hours. After completion of crystal growth, the seed shaft was raised to separate the SiC single crystal from the Si—C solution. After slowly cooling the graphite crucible to room temperature, the SiC single crystal was separated from the seed shaft and collected.
  • the SiC seed crystals of Test No. 1 to Test No. 3 had a center of gravity position of the facet region of 0.25 r or less. Therefore, the SiC single crystals of Test No. 1 to Test No. 3 had a larger inclusion-free thickness than the SiC single crystals of Test No. having the same facet area ratio. Specifically, the inclusion-free thickness of the SiC single crystal of test number 1 was larger than that of the SiC single crystal of test number 4. The SiC single crystal of test number 2 had a larger inclusion-free thickness than the SiC single crystal of test number 5. The SiC single crystal of test number 3 had a larger inclusion-free thickness than the SiC single crystal of test number 6.
  • SiC single crystals having the same test number with the same center of gravity of the facet region solvent inclusion was suppressed as the area ratio of the facet region to the crystal growth surface was larger.
  • the SiC seed crystals of test numbers 2 and 3 had an area ratio of 0.04 or more. Therefore, the SiC single crystals of test numbers 2 and 3 had a larger inclusion-free thickness than the single crystal of test number 1.
  • the SiC seed crystals of test numbers 5 and 6 had an area ratio of 0.04 or more. Therefore, the SiC single crystals of test numbers 5 and 6 had a larger inclusion-free thickness than the SiC single crystal of test number 4.
  • the area ratio of the SiC seed crystal of test number 3 was 0.10 or more. Therefore, the SiC single crystal of test number 3 had a larger inclusion-free thickness than the SiC single crystals of test numbers 1 and 2.
  • the SiC seed crystal of test number 6 had an area ratio of 0.10 or more. Therefore, the SiC single crystal of test number 6 had a larger inclusion-free thickness than the SiC single crystals of test numbers 4 and 5.
  • the SiC seed crystals of Test No. 7 to Test No. 9 had a center of gravity position of the facet region larger than 0.40r. For this reason, the SiC single crystals of Test No. 7 to Test No. 9 had an inclusion free thickness of less than 2.0 mm.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Crystals, And After-Treatments Of Crystals (AREA)

Abstract

La présente invention concerne un procédé de fabrication d'un monocristal de SiC avec un procédé de croissance en solution, permettant la suppression de l'inclusion de solvant, et un cristal de germe de SiC. Le procédé de fabrication d'un monocristal de SiC selon le présent mode de réalisation est un procédé de fabrication basé sur un procédé de croissance en solution pour faire croître un monocristal de SiC, par mise en contact d'une face de croissance cristalline (80) d'un cristal de germe de SiC (8) avec une solution de Si-C (7). Le procédé de fabrication comprend une étape de préparation et une étape de croissance. Dans l'étape de préparation, un matériau de départ est chauffé et fondu pour préparer la solution de Si-C (7). Dans l'étape de croissance, la face de croissance cristalline (80) est mise en contact avec la solution de Si-C (7), et un monocristal de SiC est formé sur la face de croissance cristalline (80). La face de croissance cristalline (80) comprend une région de facette (81) et l'angle de décalage de la face croissance de cristal (80) est de 0,5° ou moins. Le centre de gravité (82) de la région de facette (81) est agencé à une distance d'au plus 0,40 r du centre de gravité (83) de la face de croissance cristalline (80). La longueur maximale d'un segment linéaire reliant le centre de gravité (83) et la périphérie externe (84) de la face de croissance cristalline (80) est r.
PCT/JP2017/003519 2016-02-04 2017-02-01 Procédé de fabrication d'un monocristal de sic et cristal de germe de sic WO2017135272A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2016019550 2016-02-04
JP2016-019550 2016-02-04

Publications (1)

Publication Number Publication Date
WO2017135272A1 true WO2017135272A1 (fr) 2017-08-10

Family

ID=59500825

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2017/003519 WO2017135272A1 (fr) 2016-02-04 2017-02-01 Procédé de fabrication d'un monocristal de sic et cristal de germe de sic

Country Status (1)

Country Link
WO (1) WO2017135272A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110911268A (zh) * 2018-09-14 2020-03-24 株式会社迪思科 晶片的生成方法和激光加工装置
CN111162017A (zh) * 2018-11-08 2020-05-15 株式会社迪思科 小面区域的检测方法和检测装置以及晶片的生成方法和激光加工装置

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010126380A (ja) * 2008-11-26 2010-06-10 Bridgestone Corp 炭化珪素単結晶の製造方法
JP2013100217A (ja) * 2011-10-17 2013-05-23 Sumitomo Electric Ind Ltd 炭化珪素インゴットおよび炭化珪素基板、ならびにこれらの製造方法
JP2014043369A (ja) * 2012-08-26 2014-03-13 Nagoya Univ SiC単結晶の製造方法およびSiC単結晶
JP2016204196A (ja) * 2015-04-21 2016-12-08 昭和電工株式会社 SiC単結晶シード、SiCインゴット、SiC単結晶シードの製造方法及びSiC単結晶インゴットの製造方法

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010126380A (ja) * 2008-11-26 2010-06-10 Bridgestone Corp 炭化珪素単結晶の製造方法
JP2013100217A (ja) * 2011-10-17 2013-05-23 Sumitomo Electric Ind Ltd 炭化珪素インゴットおよび炭化珪素基板、ならびにこれらの製造方法
JP2014043369A (ja) * 2012-08-26 2014-03-13 Nagoya Univ SiC単結晶の製造方法およびSiC単結晶
JP2016204196A (ja) * 2015-04-21 2016-12-08 昭和電工株式会社 SiC単結晶シード、SiCインゴット、SiC単結晶シードの製造方法及びSiC単結晶インゴットの製造方法

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110911268A (zh) * 2018-09-14 2020-03-24 株式会社迪思科 晶片的生成方法和激光加工装置
CN110911268B (zh) * 2018-09-14 2024-03-19 株式会社迪思科 晶片的生成方法和激光加工装置
CN111162017A (zh) * 2018-11-08 2020-05-15 株式会社迪思科 小面区域的检测方法和检测装置以及晶片的生成方法和激光加工装置
JP2020077783A (ja) * 2018-11-08 2020-05-21 株式会社ディスコ Facet領域の検出方法および検出装置ならびにウエーハの生成方法およびレーザー加工装置
JP7229729B2 (ja) 2018-11-08 2023-02-28 株式会社ディスコ Facet領域の検出方法および検出装置ならびにウエーハの生成方法およびレーザー加工装置
TWI831862B (zh) * 2018-11-08 2024-02-11 日商迪思科股份有限公司 Facet區域之檢測方法及檢測裝置和晶圓之生成方法及雷射加工裝置

Similar Documents

Publication Publication Date Title
JP5517913B2 (ja) SiC単結晶の製造装置、製造装置に用いられる治具、及びSiC単結晶の製造方法
JP5434801B2 (ja) SiC単結晶の製造方法
WO2016059788A1 (fr) PROCÉDÉ DE PRODUCTION DE MONOCRISTAL DE SiC ET DISPOSITIF DE PRODUCTION DE MONOCRISTAL DE SiC
US20150167196A1 (en) Sic single crystal ingot and production method therefor
US9530642B2 (en) Method for producing SiC single crystal
WO2015137439A1 (fr) PROCÉDÉ DE PRODUCTION DE SiC MONOCRISTALLIN
US10450671B2 (en) SiC single crystal and method for producing same
WO2017135272A1 (fr) Procédé de fabrication d'un monocristal de sic et cristal de germe de sic
WO2018062224A1 (fr) PROCÉDÉ DE PRODUCTION D'UN MONOCRISTAL DE SiC, ET GERME DE SiC
JP5828810B2 (ja) 溶液成長法に用いられるSiC単結晶の製造装置、当該製造装置に用いられる坩堝及び当該製造装置を用いたSiC単結晶の製造方法
JP6354615B2 (ja) SiC単結晶の製造方法
KR101983491B1 (ko) SiC 단결정의 제조 방법
JP2013112553A (ja) SiC単結晶の製造方法及びSiC単結晶の製造装置
JP6409955B2 (ja) SiC単結晶の製造方法
US9822468B2 (en) Method for producing SiC single crystal
WO2014192573A1 (fr) DISPOSITIF DE FABRICATION DE MONOCRISTAL SiC, ET PROCÉDÉ DE FABRICATION DE MONOCRISTAL SiC QUI UTILISE LEDIT DISPOSITIF DE FABRICATION
JP6104414B2 (ja) シードシャフト、単結晶の製造装置及び単結晶の製造方法
JP2010248003A (ja) SiC単結晶の製造方法
US10260167B2 (en) Method for producing silicon carbide single crystal in a solution process using a seed crystal having a bottom face with a circular shape and at least a partially removed section
JP6030525B2 (ja) SiC単結晶の製造方法
JP6627984B2 (ja) SiC単結晶の製造方法及び製造装置、並びにSiC単結晶の製造に用いるシードシャフト
WO2017086449A1 (fr) PROCÉDÉ DE PRODUCTION DE MONOCRISTAL DE SiC ET LINGOT DE MONOCRISTAL DE SiC
JP2018048044A (ja) SiC単結晶の製造方法

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 17747428

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 17747428

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: JP