WO2004067812A1 - ダイヤモンド複合基板及びその製造方法 - Google Patents
ダイヤモンド複合基板及びその製造方法 Download PDFInfo
- Publication number
- WO2004067812A1 WO2004067812A1 PCT/JP2004/000532 JP2004000532W WO2004067812A1 WO 2004067812 A1 WO2004067812 A1 WO 2004067812A1 JP 2004000532 W JP2004000532 W JP 2004000532W WO 2004067812 A1 WO2004067812 A1 WO 2004067812A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- diamond
- composite substrate
- single crystal
- plane
- substrate according
- Prior art date
Links
- 239000010432 diamond Substances 0.000 title claims abstract description 302
- 229910003460 diamond Inorganic materials 0.000 title claims abstract description 300
- 239000000758 substrate Substances 0.000 title claims abstract description 212
- 239000002131 composite material Substances 0.000 title claims abstract description 93
- 238000000034 method Methods 0.000 title claims abstract description 21
- 239000013078 crystal Substances 0.000 claims abstract description 252
- 239000012808 vapor phase Substances 0.000 claims abstract description 35
- 238000005304 joining Methods 0.000 claims abstract description 4
- 238000004519 manufacturing process Methods 0.000 claims description 26
- 238000001308 synthesis method Methods 0.000 claims description 15
- 230000003746 surface roughness Effects 0.000 claims description 6
- 239000012071 phase Substances 0.000 claims description 5
- 230000002194 synthesizing effect Effects 0.000 claims 1
- 239000004065 semiconductor Substances 0.000 abstract description 10
- 230000015572 biosynthetic process Effects 0.000 abstract description 8
- 239000000463 material Substances 0.000 abstract description 7
- 238000003786 synthesis reaction Methods 0.000 abstract description 5
- 230000003287 optical effect Effects 0.000 abstract description 4
- 238000005498 polishing Methods 0.000 description 15
- 238000001947 vapour-phase growth Methods 0.000 description 13
- 238000012360 testing method Methods 0.000 description 9
- 238000005452 bending Methods 0.000 description 5
- 230000017525 heat dissipation Effects 0.000 description 5
- 238000005259 measurement Methods 0.000 description 4
- 238000000354 decomposition reaction Methods 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 2
- 230000002159 abnormal effect Effects 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 238000001069 Raman spectroscopy Methods 0.000 description 1
- 238000005162 X-ray Laue diffraction Methods 0.000 description 1
- 238000005219 brazing Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000005669 field effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000004093 laser heating Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000013001 point bending Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/22—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
- C23C16/26—Deposition of carbon only
- C23C16/27—Diamond only
- C23C16/279—Diamond only control of diamond crystallography
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/22—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
- C23C16/26—Deposition of carbon only
- C23C16/27—Diamond only
- C23C16/274—Diamond only using microwave discharges
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-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
- C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
- C30B29/02—Elements
- C30B29/04—Diamond
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-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
- C30B33/00—After-treatment of single crystals or homogeneous polycrystalline material with defined structure
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-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
- C30B33/00—After-treatment of single crystals or homogeneous polycrystalline material with defined structure
- C30B33/06—Joining of crystals
Definitions
- the present invention relates to a diamond composite substrate and a method for producing the same, and more particularly to a large-area, high-quality diamond composite substrate used for semiconductor materials, electronic components, optical components, and the like, and a method for producing the same.
- Diamond has many unique properties, unique to semiconductors, such as high thermal conductivity, high electron and hole mobility, high breakdown field strength, low dielectric loss, and wide band gap. . Particularly in recent years, ultraviolet light-emitting devices utilizing a wide band gap and field-effect transistors having excellent high-frequency characteristics are being developed.
- artificial diamond single crystals produced mainly by the high-temperature high-pressure synthesis method have a thermal conductivity 5 times or more that of copper at room temperature. Utilizing this, it is applied as a heat dissipation board that requires high performance and high reliability.
- the thermal conductivity of a diamond polycrystalline film mainly obtained by a vapor phase synthesis method is about half that of a diamond single crystal because of the influence of phonon scattering at grain boundaries.
- Diamond single crystals obtained by the high-temperature and high-pressure method are useful as substrates for semiconductors, because single crystals with good crystallinity can be obtained as compared with single crystals produced naturally.
- the ultrahigh-pressure synthesis equipment used in the high-temperature and high-pressure method has a large size and is expensive, so there is a limit in reducing the cost of producing a single crystal.
- the size of the obtained single crystal is proportional to the size of the apparatus, the size of 1 cm class is practically the limit. Therefore, as a method for obtaining a diamond single crystal substrate having a large area, for example, Japanese Patent Application Laid-Open No.
- Patent Document 1 discloses a method in which a plurality of high pressure A method is disclosed in which a phase substance is arranged to form a substrate serving as a nucleus for vapor phase growth, and a single crystal is grown thereon by a vapor phase synthesis method to obtain an integrated large single crystal.
- Japanese Patent Application Laid-Open No. 2-5141-13 discloses that a diamond surface with a gap is provided. And a method of bonding diamond to diamond by growing diamond or diamond-like bridges between the diamond surfaces by chemical vapor deposition (CVD).
- CVD chemical vapor deposition
- such a diamond bonded body cross-linked between two surfaces has a problem in that when the surface is polished, polishing stress concentrates on the bonded interface and the bonded portion is separated.
- Diamond is one of the materials with the lowest coefficient of thermal expansion.
- semiconductor materials typified by Si and GaAs have a coefficient of thermal expansion that is 1.5 to several times that of diamond. If they are heated by brazing or the like in order to join them, deformation and cracking will occur during cooling.
- diamond single crystal is a brittle material with low toughness because it has a large Young's modulus and is hard to deform. That is, when a force is applied to the diamond single crystal, the diamond single crystal has a disadvantage that it is easily cleaved along the ⁇ 111 ⁇ plane.
- a single-crystal substrate composed of a plurality of substrates serving as nuclei for vapor phase growth usually does not have completely the same plane orientation of the growth plane, but each has a slightly different plane orientation.
- single-crystal vapor phase growth is performed to integrate the single crystals, and the junction has a growth interface with a different angle called a small-angle grain boundary, that is, a defect in a broad sense. Does not basically disappear even if the single crystal growth is continued.
- the present inventors observed the vicinity of the small-angle grain boundaries in detail using a Raman scattering spectrometer, and as a result, measured a peak shift different from a normal diamond peak.
- 1 3 3 2 cm- instead of one near the normal of the diamond monocrystal peak in the vicinity of the single crystal connection interface exists microscopic regions to shift it from a few cm one 1 wavenumber or low wavenumber I found out.
- the single crystal growth was continued as it was, it was found that the single crystal was decomposed during the vapor phase growth at the boundary of the single crystal connection when the film thickness exceeded about 100 / m.
- the present invention has been made to overcome the problems in the prior art, and has a high toughness, a large area and a high quality diamond substrate used for semiconductor materials, electronic components, optical components and the like, and a method for producing the same.
- the purpose is to provide.
- the present invention is c having aspects of the following (1) to (23)
- a diamond composite substrate composed of a diamond single crystal substrate and a diamond polycrystalline film laminated thereon by a vapor phase synthesis method.
- the ratio of the thickness of the diamond single crystal substrate to the thickness of the diamond polycrystalline film is in the range of 1: 1 to 1: 4,
- the diamond composite substrate according to any one of (5) to (5).
- the single-crystal diamond substrate is composed of a plurality of single-crystal diamonds in which the principal plane having the largest area has the same plane orientation, and is formed on the single-crystal diamond by a vapor phase synthesis method.
- the diamond composite substrate according to any one of (1) to (6), wherein the plurality of diamond single crystals are joined by a diamond polycrystalline film.
- the difference between the orientation of the rotation direction with respect to the axis perpendicular to the principal plane of each of the plurality of diamond single crystals is within 0.2 degrees, and the plane orientation of each principal plane and the ⁇ 100 ⁇ plane The difference from the plane orientation is within 5 degrees.
- a diamond single crystal substrate is composed of a plurality of diamond single crystals each having a difference of less than 5 degrees from the plane orientation of the plane, and a vapor phase is formed on a facing surface parallel to a main surface of each of the plurality of diamond single crystals.
- Each diamond single crystal is joined by a diamond polycrystalline film formed by a synthesis method, and a gas-phase synthetic diamond single crystal grown on a diamond single crystal substrate as a seed crystal on the main surface.
- a diamond composite substrate integrated over the entire surface.
- the thickness of the diamond polycrystal film synthesized in a vapor phase on the diamond single crystal body is 0.1 mm or more and l mm or less, wherein (1 2) to (14) The diamond composite substrate according to any one of the above.
- the ratio of the thickness of the diamond single crystal body to the thickness of the diamond polycrystalline film is in the range of 1: 1 to 1: 4, wherein the above (1 2) to (1) 5)
- the surface roughness of the diamond polycrystalline film is Rmax 1 ⁇ m.
- a plurality of diamond single crystals having the same plane orientation are arranged side by side, a diamond polycrystal film is vapor-phase synthesized on the single crystal by a vapor phase synthesis method, and a plurality of diamond polycrystal films are formed by the diamond polycrystal film.
- Each of the plurality of diamond single crystals has a deviation of the orientation in the rotation direction with respect to the axis perpendicular to the principal plane having the largest area within 2 degrees, and the plane orientation of each principal plane is different from that of the principal plane.
- the thickness of the polycrystalline diamond film synthesized in a vapor phase on the diamond single crystal body is 0.1 mm or more and lmm or less, any one of the above (21) to (24). 3.
- the ratio of the thickness of the diamond single crystal body to the thickness of the diamond polycrystalline film is in the range of 1: 1 to 1: 4, wherein The method for producing a diamond composite substrate according to any one of the above.
- diamond single-crystal substrate means not only a substrate composed of a single single crystal but also a substrate composed of a plurality of single crystals.
- This diamond single crystal may be any of a natural diamond single crystal, a human diamond single crystal obtained by a high-temperature and high-pressure method, or a vapor-phase synthesized diamond single crystal, or a diamond single crystal manufactured by any other method. There may be.
- the single crystal surface on the opposite side where the diamond polycrystalline film is laminated will be used for actual applications such as semiconductor applications and connection surfaces as heat dissipation substrates. In that case, the application is easier if the single crystal surface is composed of ⁇ 100 ⁇ planes that are relatively soft and easy to process.
- the diamond composite substrate of the present invention the deviation of the plane orientation of the major surface of the diamond single crystal, when considered also good c applications be characterized by within 5 degrees from ⁇ 1 0 0 ⁇ , the single crystal
- the principal plane is desirably ⁇ 100 ⁇ , but the present inventors have conducted a detailed investigation on the deviation of the orientation of the principal plane, and found that the deviation from the ⁇ 100 ⁇ plane is within 5 degrees. If so, he clearly stated that there would be no problems with subsequent semiconductor applications or polishing calories.
- the thickness of the diamond single crystal is 0.1 mm or more and 1 mm or less, and the thickness of the diamond polycrystalline film laminated on the diamond single crystal is 0.1 mm or more.
- the thickness may be 1 mm or less, and the ratio of the thickness of the single crystal to the thickness of the diamond polycrystalline film may be in the range of 1: 1 to 1: 4.
- the thermal conductivity and toughness of the diamond composite substrate are in opposition to each other, so there is an optimum range for the thickness of the single crystal, the thickness of the polycrystalline layer, and the ratio. I do.
- the present inventors have clarified that by keeping these values within the above ranges, high toughness can be achieved while maintaining sufficient thermal conductivity.
- the diamond composite substrate of the present invention is composed of a plurality of diamond single crystals in which the plane orientation of the main surface of the diamond single crystal substrate is uniform, and the plurality of diamond single crystals are formed of the single crystal. It may be characterized in that it is joined by a diamond polycrystalline film formed thereon by a vapor phase synthesis method.
- a single crystal is directly vapor-phase grown from a single crystal substrate composed of a plurality of single crystal bodies, the substrate may be decomposed due to stress concentration at the interface.
- one or more single-crystal bodies are joined by a polycrystalline film, such a decomposition does not occur, and a large-sized composite substrate that is substantially integrated can be obtained.
- the diamond polycrystalline film does not necessarily need to be formed on the side surface of each single crystal body, as long as it is joined by the polycrystal formed on the main surface.
- the deviation of the azimuth in the rotation direction with respect to the axis perpendicular to the main surface of each of the plurality of diamond single crystal bodies constituting the diamond single crystal substrate is within 2 degrees, and
- the plane may be ⁇ 100 ⁇ , or the plane orientation of the main plane of the diamond single crystal may be shifted within 5 ° from ⁇ 100 ⁇ , respectively.
- the plane orientation shift exists two-dimensionally in the vertical and rotational directions.
- the physical properties such as the workability of the single crystal surface must match on each substrate, and there is an allowable range for the deviation of the plane orientation.
- Exists. The present inventors have made clear that the physical properties of the composite substrate can be stabilized by keeping the plane orientation of each single crystal within the above range. Aspects (10) and (11)>
- the difference in the thickness of each of the plurality of diamond single crystals constituting the diamond single crystal substrate is within 10 Atm, and the gap generated between the diamond single crystals is 5 mm. It may be characterized in that it is not more than 0 ⁇ m.
- the gap between the single crystals when they are integrated by the vapor phase synthesis method is difficult to arrange if it is too small, and there is a disadvantage in increasing the size of the composite substrate. It is desirable to have more than one.
- the present inventors have studied various application examples, and as a result, by keeping these values within the above numerical range, the diamond It has been clarified that there is no practical problem as a Mondo composite substrate. Modes (1 2) to (20)>
- the plane orientation of the principal plane of each diamond single crystal is ⁇ 100 ⁇ , or the difference between the plane orientation of each principal plane and the plane orientation of the ⁇ 100 ⁇ plane is:
- a diamond single-crystal substrate is composed of a plurality of diamond single-crystals having an angle of 5 degrees or more, and a diamond single-crystal is formed by a diamond polycrystalline film formed on a surface parallel to a main surface of each of the diamond single-crystals. They are joined to each other, and their main surface is entirely integrated with a vapor-phase synthesized diamond single crystal grown from a seed crystal diamond single crystal.
- the single crystal when a single crystal is directly grown from a plurality of diamond single crystals by vapor phase growth and bonded, the single crystal may be decomposed by stress. Therefore, a structure in which one side is joined by a polycrystalline film and the other side is made of a single crystal grown by vapor phase is unrelated to such a decomposition problem.
- This integrated gas-phase synthetic diamond single crystal can be applied as a large single crystal substrate.
- the thickness of the diamond single crystal is 0.1 mm or more and 1 mm or less, and the thickness of the diamond polycrystalline film vapor-phase synthesized on the diamond single crystal is 0.1 mm or more and 1 mm or less.
- the ratio of the thickness of the diamond single crystal body to the thickness of the diamond polycrystalline film is preferably in the range of 1: 1 to 1: 4. Further, it is desirable that the difference in plate thickness of the diamond single crystal composed of a plurality of pieces is within 10 zin, and the gap generated between the single crystals is 500 nm or less.
- the size and arrangement of the single crystal body and the polycrystalline layer within the above ranges, it can be used as a large-area, high-quality diamond substrate intended in the present invention. Further, if the surface of the polycrystalline film is polished and the surface roughness is 0.1 ⁇ m or less in R max, it is more preferable from the viewpoint of subsequent application.
- a plurality of diamond single crystals having a uniform plane orientation are arranged and arranged, and a diamond polycrystalline film is vapor-phase synthesized on the single crystal by a vapor phase synthesis method.
- the method is characterized in that a plurality of diamond single crystal bodies are joined by the generated polycrystalline diamond film.
- a manufacturing method for forming a polycrystalline film on a plurality of diamond single crystal substrates and bonding the single crystal with the polycrystalline film a diamond single crystal having a uniform plane orientation is prepared. Adopt a method to grow polycrystalline film by vapor phase synthesis on top
- the obtained diamond composite substrate can be applied as a large-area high-quality diamond composite substrate.
- the principal surface having the largest area is the ⁇ 100 ⁇ plane, and the deviation of the rotation direction of each single crystal relative to the axis perpendicular to the principal surface. It is preferable that the deviation of the orientation of the main surface be within 5 degrees from ⁇ 100 ⁇ .
- the plate thickness of the diamond single crystal body is 0.11 mm or more and 1 mm or less, and the thickness of the diamond polycrystalline film vapor-phase synthesized on the diamond single crystal body is 0.1 mm or more and 1 mm or less,
- the ratio of the thickness of the diamond single crystal body to the thickness of the diamond polycrystalline film is desirably in the range of 1: 1 to 1: 4. Further, it is desirable that the thickness difference between the diamond single crystals composed of a plurality of pieces is within 10 / im and the gap generated between the single crystals is below 500 ⁇ m.
- FIG. 1 is a schematic view of a diamond single crystal substrate used in the present invention.
- FIG. 2 is a schematic diagram of a heat conduction test using the diamond composite substrate of the present invention.
- FIG. 3 is an arrangement diagram of a diamond single crystal substrate for manufacturing a diamond composite substrate of the present invention.
- FIG. 4 is a schematic view of a large diamond composite substrate manufactured by the present invention.
- FIG. 5 is an example of producing a large diamond single crystal using the diamond composite substrate of the present invention.
- a configuration example of a diamond composite substrate in which a diamond polycrystalline film is laminated on a single crystal diamond single crystal substrate will be described.
- This single-crystal substrate is cut from a single-crystal ore of the so-called Ib type, which contains nitrogen as an impurity and is manufactured by a high-temperature high-pressure synthesis method.
- the X-ray Laue measurement of the deviation of the plane orientation (angle a in Fig. 1) from ⁇ 100 ⁇ of the main surface with the largest area was 1.9 degrees.
- a known microwave plasma CVD method is applied on this diamond single crystal substrate.
- the single crystal layer did not exist in the film formation region after the growth, and it was clearly divided into a single crystal substrate region and a polycrystal film formation region.
- the thickness of the polycrystalline layer was 0.5 mm.
- This substrate (substrate 1) was evaluated for toughness and thermal conductivity by the following method. First, toughness 1 "was evaluated by a three-point bending test in accordance with JISR 1601. The bending direction was the direction in which tensile stress was applied to the single crystal side. The evaluation conditions are shown in Table 2. Table 2. Conditions for evaluating toughness As a result of the measurement, the bending force of the substrate 1 was 124 OMPa.
- FIG. 1 shows a schematic diagram of the heat conduction test.
- Table 3 The evaluation conditions of the test are shown. Table 3. Thermal conductivity evaluation conditions As a result of measurement, the maximum temperature of the LD heating section was 75, and the laser output was normal.
- Table 4 summarizes the configuration of the diamond single crystal substrate and the test results.
- the size of the main surface of each of the diamond single crystal substrates was 10 mm square similar to that of substrate 1, the plane orientation was ⁇ 100 ⁇ , and the deviation of the orientation was within 2 degrees except substrate 9.
- the conditions for forming the polycrystalline film were the same as those in Table 1. Table 4. Test results
- Substrates 2 and 3 in Table 4 are a single-crystal diamond substrate and a polycrystalline diamond substrate, respectively. Table 4 shows the test results for these substrates. Since the substrate 2 is a single crystal alone, the heat conduction is improved and the temperature of the heating part is lowered. Flexural power is reduced to about 1 Z5 compared to the composite substrate of substrate 1. For this reason, it is difficult to use for applications requiring toughness. Since the substrate 3 is made of polycrystal alone, the bending strength is higher than that of the substrate 1, but the thermal conductivity is lowered and the temperature of the heat generating part is raised. As a result, a decrease in laser output was observed.
- Substrates up to 6 have different thicknesses (ratio) of single crystal and polycrystalline films, and compare their performance.
- the toughness and thermal conductivity of the diamond composite substrate are in conflict, and this is evident from Table 4.
- the bending power or the laser output was significantly deteriorated, and the superiority of the diamond substrate was reduced.
- the performance changes of the substrates 7 and 8 when the substrate thickness was changed were compared.
- both the single crystal and polycrystalline films are thinner than the preferable values.
- the transverse rupture strength is reduced and the substrate 7 cannot be used for applications requiring high toughness.
- both the single-crystal and polycrystalline films are thicker than desirable values, and the heat resistance is increased although the bending force is exerted.
- Another drawback is that the manufacturing cost increases because it is thicker than necessary.
- the effect when the main surface of the single crystal deviated from ⁇ 100 ⁇ by 5 degrees or more was investigated.
- the flexural strength was slightly lower than that of Substrate 1, it was a problematic value including the thermal conductivity.
- the polishing rate of the single crystal face was reduced to 2Z3 of the substrate 1, and there was a problem in workability.
- the diamond single crystal / polycrystalline film composite substrate represented by the substrate 1 is useful as a heat radiation substrate having both high toughness and high thermal conductivity.
- Example 2
- a diamond polycrystal film is laminated on a plurality of diamond single crystals having a uniform plane orientation and bonded together, and thereafter, a diamond single crystal is vapor-phased on a single crystal surface.
- a grown example will be described.
- the single crystal is 4 mm long and 0.5 mm thick and 0.5 mm thick, and its main surface is polished.
- the plane orientation of the main and side surfaces was ⁇ 100 ⁇ , and ⁇ indicating the deviation of the main plane was less than 2 degrees.
- These were arranged on the substrate holder so that the side surfaces coincided as shown in FIG.
- the azimuth deviation in the rotation direction with respect to the axis perpendicular to the main surface (; 3 in Fig. 3, the lower figure in Fig. 3 shows the circled part in the upper figure in FIG. ) was within 1 degree in each of all adjacent single crystals.
- the difference in plate thickness is a maximum of 1 ⁇ , and the maximum gap between single crystals is 90 ⁇ m.
- a diamond polycrystal film 4 was formed on the diamond single crystal substrate 1 composed of a plurality of single crystals by the microphone mouth-wave plasma CVD method under the same conditions as in Table 1 of Example 1.
- a diamond composite substrate 2 having a thickness of the polycrystalline layer 4 of 0.5 mm and 16 single crystals bonded together by a polycrystalline film (this Substrate 10) was obtained.
- the vapor-phase single-crystal films grown from the individual single-crystal bodies became 0.5 mm thick after growth, and were joined together to form one large single-crystal substrate (Fig. 5). After that, the polycrystalline film and the single crystal substrate portion composed of plural pieces were removed by polishing, and a large vapor-phase synthetic diamond single crystal of 16 mm square and 0.5 mm thickness was obtained.
- a gas-phase synthetic diamond single crystal was prepared on the single crystal face of the composite substrate 1 120 under the same conditions as the substrate 10. With respect to the substrates 11 and 12, the plane orientation of the different single crystal bodies was large, and abnormal growth frequently occurred at the connection interface of the vapor-phase single crystals, so that it was not possible to realize completely integrated single crystal growth.
- a diamond composite substrate similar to the substrate 10 could be obtained. Furthermore, when a single crystal is grown from the single crystal of the substrate 16 by vapor phase growth, the size of the single crystal becomes larger than that of the substrate 10 by the larger interval, and a large vapor phase synthesis of 16.5 mm square and 0.5 mm thick is performed. for large substrates 1 7 of diamond single crystal obtained c further substrate spacing, but cracks partially caused by stress concentration at the interface during polishing of the polycrystalline layer, degradation could be polished without. Sa Further, the substrate 18 having a larger interval was broken and broken during the polishing of the polycrystalline layer and could not be polished.
- the diamond composite substrate manufactured by the method typified by the substrate 10 is useful as a seed substrate for obtaining a diamond single crystal substrate having a large area and good crystallinity.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Inorganic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mechanical Engineering (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Carbon And Carbon Compounds (AREA)
- Chemical Vapour Deposition (AREA)
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/510,848 US7892356B2 (en) | 2003-01-28 | 2004-01-22 | Diamond composite substrate and process for producing the same |
JP2005504682A JP5160032B2 (ja) | 2003-01-28 | 2004-01-22 | ダイヤモンド複合基板及びその製造方法 |
EP04704342A EP1522611B1 (en) | 2003-01-28 | 2004-01-22 | Diamond composite substrate |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2003-018736 | 2003-01-28 | ||
JP2003018736 | 2003-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2004067812A1 true WO2004067812A1 (ja) | 2004-08-12 |
Family
ID=32820590
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2004/000532 WO2004067812A1 (ja) | 2003-01-28 | 2004-01-22 | ダイヤモンド複合基板及びその製造方法 |
Country Status (7)
Country | Link |
---|---|
US (1) | US7892356B2 (ja) |
EP (2) | EP1522611B1 (ja) |
JP (1) | JP5160032B2 (ja) |
KR (1) | KR100988104B1 (ja) |
CN (1) | CN100567592C (ja) |
TW (1) | TWI246173B (ja) |
WO (1) | WO2004067812A1 (ja) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012053254A1 (ja) * | 2010-10-18 | 2012-04-26 | 住友電気工業株式会社 | 炭化珪素基板を有する複合基板の製造方法 |
WO2012053252A1 (ja) * | 2010-10-18 | 2012-04-26 | 住友電気工業株式会社 | 炭化珪素基板を有する複合基板 |
JP2012516572A (ja) * | 2009-01-30 | 2012-07-19 | エイエムジー・アイデアルキャスト・ソーラー・コーポレーション | シード層及びシード層の製造方法 |
JP2013053051A (ja) * | 2011-09-06 | 2013-03-21 | Sumitomo Electric Ind Ltd | ダイヤモンド複合体およびそれから分離した単結晶ダイヤモンド、及びダイヤモンド複合体の製造方法 |
JP2016050139A (ja) * | 2014-08-29 | 2016-04-11 | 国立大学法人電気通信大学 | 単結晶ダイヤモンドの製造方法、単結晶ダイヤモンド、単結晶ダイヤモンド基板の製造方法、単結晶ダイヤモンド基板及び半導体デバイス |
RU2705518C1 (ru) * | 2018-12-27 | 2019-11-07 | федеральное государственное автономное образовательное учреждение высшего образования "Национальный исследовательский ядерный университет МИФИ" (НИЯУ МИФИ) | Способ сращивания диэлектрических пластин под действием сильного электрического поля |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPWO2010131572A1 (ja) * | 2009-05-11 | 2012-11-01 | 住友電気工業株式会社 | 半導体装置 |
GB201000768D0 (en) * | 2010-01-18 | 2010-03-03 | Element Six Ltd | CVD single crystal diamond material |
GB201107736D0 (en) | 2011-05-10 | 2011-06-22 | Element Six Holdings N V | Composite diamond assemblies |
US9966161B2 (en) * | 2015-09-21 | 2018-05-08 | Uchicago Argonne, Llc | Mechanical design of thin-film diamond crystal mounting apparatus with optimized thermal contact and crystal strain for coherence preservation x-ray optics |
RU2635612C1 (ru) * | 2016-11-29 | 2017-11-14 | Федеральное государственное бюджетное учреждение науки Институт общей физики им. А.М. Прохорова Российской академии наук (ИОФ РАН) | Способ сращивания изделий из поликристаллических алмазов в СВЧ-плазме |
WO2019222458A1 (en) * | 2018-05-18 | 2019-11-21 | Board Of Trustees Of Michigan State University | Methods for forming large area diamond substrates |
CN110857467A (zh) * | 2018-08-23 | 2020-03-03 | 中国科学院宁波材料技术与工程研究所 | 一种金刚石复合片及其制备方法 |
CN109355702B (zh) * | 2018-12-19 | 2022-03-18 | 长沙新材料产业研究院有限公司 | 一种用于降低cvd合成金刚石杂质含量的方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0375298A (ja) * | 1989-05-22 | 1991-03-29 | Sumitomo Electric Ind Ltd | 高圧相物質単結晶の製造方法 |
JPH0748198A (ja) * | 1993-08-05 | 1995-02-21 | Sumitomo Electric Ind Ltd | ダイヤモンドの合成法 |
JPH11145056A (ja) * | 1997-11-07 | 1999-05-28 | Sony Corp | 半導体材料 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01208397A (ja) | 1988-02-16 | 1989-08-22 | Asahi Daiyamondo Kogyo Kk | ダイヤモンド被覆体及びこれを用いた切削工具 |
GB8810113D0 (en) * | 1988-04-28 | 1988-06-02 | Jones B L | Bonded composite |
JPH0393695A (ja) | 1989-09-07 | 1991-04-18 | Sumitomo Electric Ind Ltd | 多結晶ダイヤモンド及びその製造法 |
JPH0799791B2 (ja) | 1992-04-15 | 1995-10-25 | インターナショナル・ビジネス・マシーンズ・コーポレイション | 透明基板上の回路ライン接続方法 |
JPH0672797A (ja) | 1992-08-24 | 1994-03-15 | Sumitomo Electric Ind Ltd | 高圧相物質の合成方法 |
JPH06107494A (ja) | 1992-09-24 | 1994-04-19 | Sumitomo Electric Ind Ltd | ダイヤモンドの気相成長法 |
JPH06172089A (ja) | 1992-12-08 | 1994-06-21 | Sumitomo Electric Ind Ltd | ダイヤモンドの合成法 |
US5474021A (en) * | 1992-09-24 | 1995-12-12 | Sumitomo Electric Industries, Ltd. | Epitaxial growth of diamond from vapor phase |
US5442199A (en) * | 1993-05-14 | 1995-08-15 | Kobe Steel Usa, Inc. | Diamond hetero-junction rectifying element |
JPH06345592A (ja) * | 1993-06-10 | 1994-12-20 | Kobe Steel Ltd | ダイヤモンド薄膜の形成方法 |
US5804321A (en) * | 1993-07-30 | 1998-09-08 | The United States Of America As Represented By The Secretary Of The Navy | Diamond brazed to a metal |
JPH08241942A (ja) * | 1994-12-28 | 1996-09-17 | Toyota Central Res & Dev Lab Inc | 薄膜積層体 |
US5803967A (en) * | 1995-05-31 | 1998-09-08 | Kobe Steel Usa Inc. | Method of forming diamond devices having textured and highly oriented diamond layers therein |
-
2004
- 2004-01-22 CN CNB2004800003220A patent/CN100567592C/zh not_active Expired - Fee Related
- 2004-01-22 EP EP04704342A patent/EP1522611B1/en not_active Expired - Fee Related
- 2004-01-22 EP EP09012562A patent/EP2135977B1/en not_active Expired - Fee Related
- 2004-01-22 KR KR1020047016807A patent/KR100988104B1/ko not_active IP Right Cessation
- 2004-01-22 JP JP2005504682A patent/JP5160032B2/ja not_active Expired - Fee Related
- 2004-01-22 WO PCT/JP2004/000532 patent/WO2004067812A1/ja active Application Filing
- 2004-01-22 US US10/510,848 patent/US7892356B2/en not_active Expired - Fee Related
- 2004-01-28 TW TW093101858A patent/TWI246173B/zh not_active IP Right Cessation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0375298A (ja) * | 1989-05-22 | 1991-03-29 | Sumitomo Electric Ind Ltd | 高圧相物質単結晶の製造方法 |
JPH0748198A (ja) * | 1993-08-05 | 1995-02-21 | Sumitomo Electric Ind Ltd | ダイヤモンドの合成法 |
JPH11145056A (ja) * | 1997-11-07 | 1999-05-28 | Sony Corp | 半導体材料 |
Non-Patent Citations (1)
Title |
---|
See also references of EP1522611A4 * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012516572A (ja) * | 2009-01-30 | 2012-07-19 | エイエムジー・アイデアルキャスト・ソーラー・コーポレーション | シード層及びシード層の製造方法 |
WO2012053254A1 (ja) * | 2010-10-18 | 2012-04-26 | 住友電気工業株式会社 | 炭化珪素基板を有する複合基板の製造方法 |
WO2012053252A1 (ja) * | 2010-10-18 | 2012-04-26 | 住友電気工業株式会社 | 炭化珪素基板を有する複合基板 |
JP2013053051A (ja) * | 2011-09-06 | 2013-03-21 | Sumitomo Electric Ind Ltd | ダイヤモンド複合体およびそれから分離した単結晶ダイヤモンド、及びダイヤモンド複合体の製造方法 |
JP2016050139A (ja) * | 2014-08-29 | 2016-04-11 | 国立大学法人電気通信大学 | 単結晶ダイヤモンドの製造方法、単結晶ダイヤモンド、単結晶ダイヤモンド基板の製造方法、単結晶ダイヤモンド基板及び半導体デバイス |
RU2705518C1 (ru) * | 2018-12-27 | 2019-11-07 | федеральное государственное автономное образовательное учреждение высшего образования "Национальный исследовательский ядерный университет МИФИ" (НИЯУ МИФИ) | Способ сращивания диэлектрических пластин под действием сильного электрического поля |
Also Published As
Publication number | Publication date |
---|---|
JPWO2004067812A1 (ja) | 2006-05-18 |
US20050160968A1 (en) | 2005-07-28 |
EP2135977A3 (en) | 2010-03-24 |
US7892356B2 (en) | 2011-02-22 |
EP2135977A2 (en) | 2009-12-23 |
KR20050094341A (ko) | 2005-09-27 |
EP1522611A1 (en) | 2005-04-13 |
TW200428622A (en) | 2004-12-16 |
CN1697894A (zh) | 2005-11-16 |
CN100567592C (zh) | 2009-12-09 |
JP5160032B2 (ja) | 2013-03-13 |
EP1522611A4 (en) | 2008-12-24 |
KR100988104B1 (ko) | 2010-10-18 |
EP2135977B1 (en) | 2012-03-07 |
TWI246173B (en) | 2005-12-21 |
EP1522611B1 (en) | 2012-03-07 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2004067812A1 (ja) | ダイヤモンド複合基板及びその製造方法 | |
JP2654232B2 (ja) | 高圧相物質単結晶の製造方法 | |
JP5163920B2 (ja) | ダイヤモンド単結晶基板の製造方法及びダイヤモンド単結晶基板 | |
JP3834314B2 (ja) | ダイヤモンド製造用装置及び方法 | |
JP6772711B2 (ja) | 半導体積層構造体および半導体デバイス | |
EP0567124B1 (en) | Bonding tool having diamond head and method of manufacturing the same | |
EP2072646A1 (en) | Process for producing single crystal of silicon carbide | |
TW200422446A (en) | Single crystal diamond | |
US9590046B2 (en) | Monocrystalline SiC substrate with a non-homogeneous lattice plane course | |
JP5162895B2 (ja) | 窒化アルミニウム結晶の製造方法、窒化アルミニウム結晶、窒化アルミニウム結晶基板および半導体デバイス | |
JP2008013390A (ja) | AlN結晶基板の製造方法、AlN結晶の成長方法およびAlN結晶基板 | |
JP4385764B2 (ja) | ダイヤモンド単結晶基板の製造方法 | |
JPH02273960A (ja) | ダイヤモンドヒートシンク | |
JP5003918B2 (ja) | ダイヤモンド単結晶基板 | |
JP2007161535A (ja) | 半導体結晶基板の製造方法 | |
CN116180222A (zh) | 一种单晶金刚石外延生长方法 | |
JP2000086391A (ja) | 単結晶ダイヤモンド合成用基板 | |
JPH0672797A (ja) | 高圧相物質の合成方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): BW GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2005504682 Country of ref document: JP |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 10510848 Country of ref document: US |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2004704342 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1020047016807 Country of ref document: KR |
|
WWE | Wipo information: entry into national phase |
Ref document number: 20048003220 Country of ref document: CN |
|
WWP | Wipo information: published in national office |
Ref document number: 2004704342 Country of ref document: EP |
|
WWP | Wipo information: published in national office |
Ref document number: 1020047016807 Country of ref document: KR |