WO2012050122A1 - Soi substrate - Google Patents
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- WO2012050122A1 WO2012050122A1 PCT/JP2011/073412 JP2011073412W WO2012050122A1 WO 2012050122 A1 WO2012050122 A1 WO 2012050122A1 JP 2011073412 W JP2011073412 W JP 2011073412W WO 2012050122 A1 WO2012050122 A1 WO 2012050122A1
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- film
- soi substrate
- carbon film
- substrate
- silicon
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- 239000000758 substrate Substances 0.000 title claims abstract description 154
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 94
- 229910003460 diamond Inorganic materials 0.000 claims abstract description 92
- 239000010432 diamond Substances 0.000 claims abstract description 92
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 82
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 63
- 239000010703 silicon Substances 0.000 claims abstract description 63
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 63
- 238000000034 method Methods 0.000 claims abstract description 49
- 238000004050 hot filament vapor deposition Methods 0.000 claims abstract description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229910052814 silicon oxide Inorganic materials 0.000 claims abstract description 14
- 150000001721 carbon Chemical class 0.000 claims description 13
- 238000007740 vapor deposition Methods 0.000 claims description 12
- 238000001947 vapour-phase growth Methods 0.000 claims description 12
- 239000004065 semiconductor Substances 0.000 abstract description 29
- 230000015572 biosynthetic process Effects 0.000 abstract description 17
- 238000001816 cooling Methods 0.000 abstract description 11
- 230000007246 mechanism Effects 0.000 abstract description 5
- 238000003786 synthesis reaction Methods 0.000 abstract description 5
- 229910052751 metal Inorganic materials 0.000 abstract description 2
- 239000002184 metal Substances 0.000 abstract description 2
- 229910052681 coesite Inorganic materials 0.000 abstract 1
- 238000010276 construction Methods 0.000 abstract 1
- 229910052906 cristobalite Inorganic materials 0.000 abstract 1
- 150000002739 metals Chemical class 0.000 abstract 1
- 239000000377 silicon dioxide Substances 0.000 abstract 1
- 229910052682 stishovite Inorganic materials 0.000 abstract 1
- 229910052905 tridymite Inorganic materials 0.000 abstract 1
- 239000010408 film Substances 0.000 description 178
- 230000005684 electric field Effects 0.000 description 19
- 238000004519 manufacturing process Methods 0.000 description 12
- 229910052721 tungsten Inorganic materials 0.000 description 12
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 11
- 239000010937 tungsten Substances 0.000 description 11
- 238000009413 insulation Methods 0.000 description 10
- 239000002245 particle Substances 0.000 description 10
- 238000011156 evaluation Methods 0.000 description 9
- 239000012535 impurity Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 7
- 230000007547 defect Effects 0.000 description 7
- 230000017525 heat dissipation Effects 0.000 description 7
- 230000015556 catabolic process Effects 0.000 description 6
- 238000010292 electrical insulation Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000005498 polishing Methods 0.000 description 4
- 239000010409 thin film Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229910002601 GaN Inorganic materials 0.000 description 3
- 229910004298 SiO 2 Inorganic materials 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000002159 nanocrystal Substances 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 229910052715 tantalum Inorganic materials 0.000 description 3
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- JMASRVWKEDWRBT-UHFFFAOYSA-N Gallium nitride Chemical compound [Ga]#N JMASRVWKEDWRBT-UHFFFAOYSA-N 0.000 description 2
- ORILYTVJVMAKLC-UHFFFAOYSA-N adamantane Chemical compound C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 2
- SBYXRAKIOMOBFF-UHFFFAOYSA-N copper tungsten Chemical compound [Cu].[W] SBYXRAKIOMOBFF-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000012212 insulator Substances 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 229910010271 silicon carbide Inorganic materials 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- RNQKDQAVIXDKAG-UHFFFAOYSA-N aluminum gallium Chemical compound [Al].[Ga] RNQKDQAVIXDKAG-UHFFFAOYSA-N 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- WUUZKBJEUBFVMV-UHFFFAOYSA-N copper molybdenum Chemical compound [Cu].[Mo] WUUZKBJEUBFVMV-UHFFFAOYSA-N 0.000 description 1
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000005669 field effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000010884 ion-beam technique Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 238000000259 microwave plasma-assisted chemical vapour deposition Methods 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910021392 nanocarbon Inorganic materials 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 238000001004 secondary ion mass spectrometry Methods 0.000 description 1
- 238000005389 semiconductor device fabrication Methods 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 238000004506 ultrasonic cleaning Methods 0.000 description 1
- 238000000927 vapour-phase epitaxy Methods 0.000 description 1
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/76—Making of isolation regions between components
- H01L21/762—Dielectric regions, e.g. EPIC dielectric isolation, LOCOS; Trench refilling techniques, SOI technology, use of channel stoppers
- H01L21/7624—Dielectric regions, e.g. EPIC dielectric isolation, LOCOS; Trench refilling techniques, SOI technology, use of channel stoppers using semiconductor on insulator [SOI] technology
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- H—ELECTRICITY
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- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02109—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
- H01L21/02112—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer
- H01L21/02115—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material being carbon, e.g. alpha-C, diamond or hydrogen doped carbon
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- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02225—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer
- H01L21/0226—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process
- H01L21/02263—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase
- H01L21/02271—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase deposition by decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition
- H01L21/02277—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase deposition by decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition the reactions being activated by other means than plasma or thermal, e.g. photo-CVD
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- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02367—Substrates
- H01L21/0237—Materials
- H01L21/02373—Group 14 semiconducting materials
- H01L21/02381—Silicon, silicon germanium, germanium
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- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
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- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02367—Substrates
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- H01L21/02422—Non-crystalline insulating materials, e.g. glass, polymers
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- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
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- H01L21/02444—Carbon, e.g. diamond-like carbon
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- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02436—Intermediate layers between substrates and deposited layers
- H01L21/02439—Materials
- H01L21/02488—Insulating materials
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- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02436—Intermediate layers between substrates and deposited layers
- H01L21/02494—Structure
- H01L21/02496—Layer structure
- H01L21/02502—Layer structure consisting of two layers
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- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02436—Intermediate layers between substrates and deposited layers
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- H01L21/02513—Microstructure
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- H01L21/02612—Formation types
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- H01L29/00—Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
- H01L29/66—Types of semiconductor device ; Multistep manufacturing processes therefor
- H01L29/68—Types of semiconductor device ; Multistep manufacturing processes therefor controllable by only the electric current supplied, or only the electric potential applied, to an electrode which does not carry the current to be rectified, amplified or switched
- H01L29/76—Unipolar devices, e.g. field effect transistors
- H01L29/772—Field effect transistors
- H01L29/78—Field effect transistors with field effect produced by an insulated gate
- H01L29/786—Thin film transistors, i.e. transistors with a channel being at least partly a thin film
- H01L29/78603—Thin film transistors, i.e. transistors with a channel being at least partly a thin film characterised by the insulating substrate or support
Definitions
- the present invention relates to a silicon-on-insulator (SOI) substrate for use in a power semiconductor device or the like, and more particularly to an SOI substrate having high insulation and high thermal conductivity.
- SOI silicon-on-insulator
- the power consumption of the CPU of the computer has been reduced.
- the insulating property of a silicon oxide film (SiO 2 ) layer used as an insulating layer (hereinafter referred to as “I layer”) of an existing SOI substrate is low, low power consumption for power converters and car electronics and It cannot be used as a low-loss power semiconductor device substrate.
- Non-Patent Document 1 Non-Patent Document 2
- MPCVD microwave plasma vapor deposition
- Patent Document 1 and Patent Document 2 disclose a technique for forming a uniform carbon film in an area of about 30 cm in diameter by surface wave plasma vapor deposition.
- a field effect transistor intended for an integrated circuit (LSI) application has been prototyped on an SOI substrate created using this method, and its operation has been confirmed (Non-patent Document 3).
- HFCVD hot filament vapor deposition
- tungsten (W) or tantalum (Ta) used as a filament during synthesis is mixed into the silicon substrate.
- the device characteristics may be affected, such as by forming defects at the silicon / diamond interface.
- a film thickness of 100 ⁇ m or more is required, so cracking or breakage due to thermal stress is a problem due to thick film formation.
- the carbon film formed by the surface wave plasma vapor deposition method has excellent characteristics such as high thermal conductivity and high insulation, and a power semiconductor device is formed on an SOI substrate using the carbon film as an I layer.
- a rare metal-free device having no cooling mechanism is realized. Since the carbon film synthesized by the surface wave plasma vapor deposition method is as thin as several hundred nm, the thermal conductivity is several tens W / mK. However, it is not sufficient and is difficult to apply to power semiconductor devices.
- the present invention has been made in view of the above circumstances, and solves the conventional problem in a SOI substrate using a carbon-based material for the I layer and free of rare metal and having no cooling mechanism. It is an object of the present invention to provide an SOI substrate with high thermal conductivity and high insulation that can be applied to an SOI substrate for devices.
- the inventors of the present invention have made a hybrid structure of a carbon film and a microcrystalline diamond film as the I layer, whereby an SOI using a carbon film as a conventional I layer. It has been found that an SOI substrate having high thermal conductivity and high insulation can be obtained by simultaneously solving both the problem of the substrate and the problem of diamond synthesis in the HFCVD method.
- the present invention has been completed based on these findings, and is as follows.
- An SOI substrate wherein the insulating layer of the SOI substrate has a hybrid structure of a carbon film and a microcrystalline diamond film.
- the hybrid structure is composed of carbon film / microcrystalline diamond film / carbon film.
- the microcrystalline diamond film is a film formed by a hot filament vapor deposition method.
- an SOI substrate having high thermal conductivity and high insulation which is a problem of a conventional SOI substrate, can be obtained, and can be used as a power semiconductor device substrate.
- FIG. 5 shows current-electric field characteristics of an SOI substrate obtained in Example 1.
- FIG. 11 shows current-electric field characteristics of an SOI substrate obtained in Example 2.
- silicone of the SOI substrate obtained by the comparative example 1 The figure which shows the electric current electric field characteristic of the SOI substrate obtained by the comparative example 1
- the SOI substrate of the present invention is characterized in that the I layer has a hybrid structure composed of a carbon film and a microcrystalline diamond film.
- 1 to 4 schematically show some embodiments of an SOI substrate of the present invention, in which 1 is a silicon substrate, 2 is a carbon film, and 3 is a microcrystalline diamond film. Reference numerals 4 denote silicon oxide films, respectively. That is, FIG. 1 shows an SOI substrate in which the I layer is composed of the carbon film 2 and the microcrystalline diamond film 3.
- FIG. 2 shows the SOI substrate shown in FIG. 1 between the silicon substrate 1 and the carbon film 2. 1 having a silicon oxide film 4 is shown.
- 3 shows an SOI substrate in which the I layer is composed of the carbon film 2, the microcrystalline diamond film 3, and the carbon film 2.
- FIG. 4 shows the silicon substrate 1 and the carbon film in the SOI substrate shown in FIG. A film having a silicon oxide film 4 between 2 is shown.
- a carbon film is formed on a silicon substrate having a diameter of 30 cm or more by using the surface wave plasma vapor deposition method in order to adapt to the manufacturing process of an existing silicon semiconductor device.
- a homogeneous microcrystalline diamond film having a diameter of 30 cm or more on a formed substrate hereinafter, also referred to as “carbon film / silicon substrate”
- high thermal conductivity is achieved.
- W tungsten
- Ta tantalum
- the film can prevent a defect from being formed in silicon as a device manufacturing layer, and can reduce a leakage current.
- the microcrystalline diamond film has a thick film structure of 100 ⁇ m or more in order to increase the breakdown voltage.
- a microcrystalline diamond film is formed by hot filament vapor deposition on a carbon film having a high thermal conductivity and high withstand voltage function formed by surface wave plasma vapor deposition.
- the carbon film As a film having a function of preventing the filament material from being mixed into silicon and having a high pressure resistance and high thermal conductivity, the carbon film has a flat surface and also has a high pressure resistance and high thermal conductivity function. Although it is the most suitable film, in addition to the carbon film, a silicon oxide film, an aluminum nitride film, a silicon nitride film, or the like can also be used as having the same function.
- one of the methods for manufacturing an SOI substrate of the present invention is to form a carbon film having a flat surface at an atomic level and a function of preventing entry into silicon, high pressure resistance, and high thermal conductivity on a silicon substrate.
- This is a method comprising a step of forming a film and a step of forming a microcrystalline diamond on the carbon film / silicon substrate obtained in the previous step by a hot filament vapor phase growth method. (See FIG. 1).
- the method for forming the silicon oxide film can be selected from the formation by a thermal oxidation method, a known film formation method such as a vapor phase growth method and a sputtering method.
- a carbon film having a flat surface at the atomic level and a function of high pressure resistance and high thermal conductivity after the above-described microcrystalline diamond film forming step is used.
- an SOI substrate having a hybrid structure (carbon film / microcrystalline diamond film / carbon film) of a carbon film and a microcrystalline diamond film having a high withstand voltage and high thermal conductivity can be produced (FIGS. 3 and 4). reference).
- a homogeneous microcrystalline diamond film with a diameter of 30 cm or more is laminated on the silicon / carbon film substrate with a diameter of 30 cm or more. It is also possible by the method.
- a mechanical polishing method is used to flatten the diamond surface. When this mechanical polishing is used on the carbon film surface of the silicon / carbon film substrate, defects and strains are generated in the silicon substrate for manufacturing the device. For this reason, it is necessary to form a carbon film formed on the silicon substrate by a surface wave plasma vapor deposition method that can form a flat surface at the atomic level in a self-organized manner.
- the microcrystalline diamond film requires an area of 30 cm or more in diameter
- synthesis by a hot filament vapor phase growth method can be used.
- the interface side of the microcrystalline diamond film with the substrate can be used as a bonding surface.
- an SOI substrate having a hybrid structure of carbon film / microcrystalline diamond film by the bonding method described above will be specifically described.
- a carbon film having a flat surface at an atomic level is formed on a silicon substrate by surface wave plasma vapor deposition to produce a carbon film / silicon substrate.
- a microcrystalline diamond film is formed on another silicon substrate by hot filament vapor deposition, and the silicon substrate is removed to form atoms formed at the interface between silicon and microcrystalline diamond. A level microcrystalline diamond surface is obtained.
- the obtained flat surface at the atomic level is bonded to the carbon film surface of the carbon film / silicon substrate.
- the carbon film surface and the microcrystalline diamond surface can be cleaned using an ion beam or plasma, and the carbon film surface and the microcrystalline diamond surface can be bonded together by a vacuum pressure bonding method.
- yet another method for manufacturing an SOI substrate according to the present invention includes (1) a step of first forming a carbon film having a flat surface at an atomic level on a silicon substrate by surface wave plasma vapor deposition.
- a method comprising a step of bonding a flat surface at an atomic level to the surface of the carbon film, and the method has a hybrid structure of a carbon film / microcrystalline diamond film having a high breakdown voltage and high thermal conductivity.
- An SOI substrate can be created.
- a carbon film / silicon substrate is bonded to a silicon substrate and a carbon substrate by bonding a microcrystalline diamond film formed by a hot filament vapor deposition method or a hot filament vapor deposition method.
- An SOI substrate for power semiconductors having no heat active defects and impurities and having excellent heat dissipation characteristics is produced at the interface of the film.
- the SOI substrate of the present invention has a hybrid structure of a carbon film and a microcrystalline diamond film.
- the hybrid structure of the carbon film and the microcrystalline diamond film is a diamond thin film formed by CVD, such as tungsten or tantalum. Therefore, it is possible to combine with power semiconductor devices (silicon carbide, gallium nitride, aluminum gallium nitride) other than silicon semiconductor.
- power semiconductor devices silicon carbide, gallium nitride, aluminum gallium nitride
- a hybrid structure of a carbon film and a microcrystalline diamond film can be directly formed on a semiconductor material such as silicon carbide or gallium nitride. As in the case of, it can be realized by a bonding technique used in a semiconductor process.
- ⁇ Electrical insulation> As a sample used for evaluation of electrical insulation, a sample in which an electrode having a diameter of 30 ⁇ m was formed on a microcrystalline diamond film of an SOI substrate of the present invention was used. The silicon of the SOI substrate was placed in a copper sample holder using a conductive silver paste. The measurement was performed by measuring current-voltage characteristics in a vacuum of 5 ⁇ 10 ⁇ 7 Torr. The value obtained by dividing the applied voltage by the total thickness of the microcrystalline diamond film and the carbon film was defined as the electric field, and the electric insulation was evaluated using the current-electric field characteristics. The larger the electric field where current is observed, the higher the electrical insulation.
- the thermal conductivity was measured by a thermoreflectance method.
- the silicon substrate of the SOI substrate was removed with a mixed solution of hydrofluoric acid and nitric acid to produce a self-stereoscopic structure of a microcrystalline diamond film / carbon film.
- a molybdenum thin film having a thickness of 100 nm was formed on the microcrystalline diamond surface and the carbon film surface by sputtering.
- the thermal conductivity in the direction perpendicular to the laminating direction and the laminating direction (in-plane direction) of the laminate was evaluated.
- Example 1 A 4-inch diameter wafer-like silicon substrate was used as the substrate. In order to increase the nucleation density of the carbon particles and form a uniform film, a pretreatment (nanocrystal diamond particle adhesion treatment) was performed on the substrate before the film formation.
- a colloidal solution (product name: Nanoamand, manufactured by Nano Carbon Laboratory Co., Ltd.) in which nanocrystal diamond particles having an average particle size of 5 nm are dispersed in pure water, or nanocrystal diamond particles having an average particle size of 30 nm or 40 nm (Tomei) Diamond Co., Ltd., product names MD30 and MD40) dispersed in pure water, or cluster diamond particles or graphite cluster diamond particles (Tokyo Diamond Tool Co., Ltd., product names CD and GCD, respectively), or Adamantane or a derivative thereof or a derivative thereof (each made by Idemitsu Kosan Co., Ltd.) solution was used, and the substrate was immersed in an ultrasonic cleaner.
- nanoamand manufactured by Nano Carbon Laboratory Co., Ltd.
- the substrate is immersed in ethanol for ultrasonic cleaning and dried, or these solutions are uniformly applied on the substrate by spin coating and dried.
- the uniformity of this pretreatment affects the uniformity of the carbon film after film formation.
- the number of diamond particles adhering on the substrate was 10 10 to 10 11 per cm 2 .
- the source gas a mixed gas of CH 4 , CO 2 and H 2 was used, and the concentrations of CH 4 and CO 2 were each 1 mol%.
- the gas pressure in the reaction vessel is 1.0 to 1.2 ⁇ 10 2 Pa (1.0 to 1.2 mbar), which is lower than the pressure (10 3 to 10 4 Pa) usually used for CVD synthesis of diamond, and a total of 20 A large area and uniform plasma was generated in a region wider than the substrate area by applying a microwave of ⁇ 24 kW.
- the substrate temperature during film formation can be maintained at 450 ° C. or less by adjusting the distance between the substrate and the antenna by closely contacting the Mo sample stage and the cooling stage.
- Film formation was performed for 6 hours under the above film formation conditions. A uniform and transparent carbon film was formed on the glass substrate after film formation. The film thickness was 200 nm.
- a microcrystalline diamond film was formed on the surface of the carbon film by a hot filament vapor deposition method.
- a hot filament vapor phase growth apparatus a large-area HFCVD apparatus (Sp3 Model 650) was used. Tungsten (W) was used as the filament, and the film was formed for 6 hours at a filament temperature of 2000 ° C. and a substrate temperature of 800 ° C. The film thickness was about 10 ⁇ m.
- the SOI substrate obtained in Example 1 has the structure shown in FIG.
- FIG. 5 shows the evaluation results of impurities in the silicon of the SOI substrate obtained in Example 1. Tungsten was not observed in the carbon film and the silicon substrate, and it was found that the carbon film has a role to prevent tungsten from being mixed during the formation of the microcrystalline diamond film.
- Example 1 the current-electric field characteristics of the SOI substrate obtained in Example 1 are shown in FIG. Assuming that the electric field at which the current rapidly increases is the threshold electric field, the threshold electric field was 85 V / ⁇ m. This value is almost the same as the dielectric breakdown electric field (1 MV / cm) of single crystal diamond.
- the thermal conductivity of the SOI substrate obtained in Example 1 was 250 W / mK in the stacking direction and 110 W / mK in the direction perpendicular to the stacking direction. This value is almost the same as the reported value of microcrystalline diamond, which is one digit higher than the previously reported carbon film.
- Example 2 An SOI substrate was fabricated in the same manner as in Example 1 except that a silicon substrate on which a silicon oxide film (SiO 2 film) (thickness 20 nm) was formed was used. The structure of the SOI substrate obtained in Example 2 is shown in FIG.
- FIG. 7 shows the result of evaluating impurities in the silicon of the SOI substrate obtained in Example 2. Tungsten was not observed in the carbon film, silicon oxide film (SiO 2 film), or silicon substrate, and it was found that the carbon film has a role of preventing the entry of tungsten during the formation of the microcrystalline diamond film.
- Example 2 the current-electric field characteristics of the SOI substrate obtained in Example 2 are shown in FIG. Assuming that the electric field at which the current rapidly increases is the threshold electric field, the threshold electric field was 92 V / ⁇ m. This value is almost the same as the dielectric breakdown electric field (1 MV / cm) of single crystal diamond.
- An excellent SOI substrate for power semiconductor devices can be manufactured.
- FIG. 9 shows the results of impurity evaluation in silicon of the SOI substrate obtained in Comparative Example 1. Tungsten was observed at the interface between the microcrystalline diamond film and the silicon substrate, and was detected in the silicon substrate to a depth of 0.5 ⁇ m from the interface.
- FIG. 10 shows the current-electric field characteristics of the SOI substrate obtained in Comparative Example 1. Assuming that the electric field at which the current rapidly increases is the threshold electric field, the threshold electric field was 40 V / ⁇ m. This value was half of the dielectric breakdown electric field (100 V / ⁇ m) of single crystal diamond.
- the electric field where the leakage current of the SOI substrate of Example 1 is observed is that the SOI substrate having a hybrid structure of a carbon film and a microcrystalline diamond hybrid film as an I layer is Comparative Example 1. Compared with SOI using only the microcrystalline diamond film as an insulating layer, the electric field in which leakage current was observed increased twice. Therefore, it can be seen that an SOI substrate having a hybrid structure of a carbon film and a microcrystalline diamond film as an I layer can ensure insulation with a thickness half that of a microcrystalline diamond film alone. .
- Example 3 In Example 1 and Example 2, by forming a similar 200 nm carbon film on the microcrystalline diamond film, the electric field at which leakage current was observed was doubled. That is, it can be seen that by forming the structures of FIGS. 3 and 4, an SOI substrate having a leakage electric field of about 120 V / ⁇ m and about 130 V / ⁇ m can be manufactured. Further, the thermal conductivity was improved by 8 times in the film forming direction of the value of the carbon film and 3 times in the direction perpendicular to the film forming direction (in-plane direction).
- the SOI substrate having a hybrid structure of a carbon film and a microcrystalline diamond film or a film having a hybrid structure of a carbon film and a microcrystalline diamond film according to the present invention has a high insulating property and a high thermal conductivity. This is a very important technology because it can be used for all power semiconductor devices such as electric vehicles, hybrid vehicles, and inverters for motor control.
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Abstract
Description
一方、表面波プラズマ気相成長法により、直径30cm程度の面積に均一な炭素膜を形成する技術が、特許文献1および特許文献2に開示されている。この方法を用いて作成したSOI基板上に、集積回路(LSI)用途を目的とした電界効果トランジスタが試作され、動作が確認されている(非特許文献3)。 On the other hand, a microcrystalline diamond thin film can be formed on a large area having a diameter of 30 cm or more by a hot filament vapor deposition (HFCVD) method.
On the other hand,
一方、前述の表面波プラズマ気相成長法により形成された炭素膜は高熱伝導性かつ高絶縁性という優れた特性を有するもの、該炭素膜をI層として用いたSOI基板上にパワー半導体デバイスを作製することで、レアメタルフリーで冷却機構を有しないデバイス実現する場合、表面波プラズマ気相成長法で合成した炭素膜の膜厚が数100nmと薄いために熱伝導度が数10W/mKであって充分なものとはいえず、パワー半導体デバイスへの応用は難しいという課題がある。 However, when the microcrystalline diamond film formed by the above-mentioned hot filament vapor deposition (HFCVD) method is used as the I layer of the SOI substrate, tungsten (W) or tantalum (Ta) used as a filament during synthesis is mixed into the silicon substrate. There is a concern that the device characteristics may be affected, such as by forming defects at the silicon / diamond interface. Furthermore, for power device applications that require high insulation and high thermal conductivity, a film thickness of 100 μm or more is required, so cracking or breakage due to thermal stress is a problem due to thick film formation.
On the other hand, the carbon film formed by the surface wave plasma vapor deposition method has excellent characteristics such as high thermal conductivity and high insulation, and a power semiconductor device is formed on an SOI substrate using the carbon film as an I layer. By fabricating the device, a rare metal-free device having no cooling mechanism is realized. Since the carbon film synthesized by the surface wave plasma vapor deposition method is as thin as several hundred nm, the thermal conductivity is several tens W / mK. However, it is not sufficient and is difficult to apply to power semiconductor devices.
本発明は、これらの知見に基づいて完成するに至ったものであり、以下のとおりのものである。 As a result of intensive studies to achieve the above object, the inventors of the present invention have made a hybrid structure of a carbon film and a microcrystalline diamond film as the I layer, whereby an SOI using a carbon film as a conventional I layer. It has been found that an SOI substrate having high thermal conductivity and high insulation can be obtained by simultaneously solving both the problem of the substrate and the problem of diamond synthesis in the HFCVD method.
The present invention has been completed based on these findings, and is as follows.
[2]前記ハイブリット構造が、炭素膜/マイクロ結晶ダイヤモンド膜で構成されていることを特徴とする前記[1]のSOI基板。
[3]前記ハイブリット構造が、炭素膜/マイクロ結晶ダイヤモンド膜/炭素膜で構成されていることを特徴とする前記[1]のSOI基板。
[4]前記炭素膜が、表面波プラズマ気相成長法で形成された膜であることを特徴とする前記[1]~[3]のいずれかのSOI基板。
[5]前記マイクロ結晶ダイヤモンド膜が、熱フィラメント気相成長法で形成された膜であることを特徴とする前記[1]~[4]のいずれかのSOI基板。
[6]前記炭素膜上に、熱フィラメント気相成長法によりマイクロ結晶ダイヤモンド膜が形成されていることを特徴とする前記[1]~[5]のいずれかのSOI基板。
[7]前記炭素膜上に、熱フィラメント気相成長法で形成されたマイクロ結晶ダイヤモンド膜を張り合わせることにより形成されたことを特徴とする前記[5]のSOI基板。
[8]シリコン基板と炭素膜の界面にシリコン酸化膜を有することを特徴とする前記[1]~[7]のいずれかのSOI基板。 [1] An SOI substrate, wherein the insulating layer of the SOI substrate has a hybrid structure of a carbon film and a microcrystalline diamond film.
[2] The SOI substrate according to [1], wherein the hybrid structure is composed of a carbon film / microcrystalline diamond film.
[3] The SOI substrate according to the above [1], wherein the hybrid structure is composed of carbon film / microcrystalline diamond film / carbon film.
[4] The SOI substrate according to any one of [1] to [3], wherein the carbon film is a film formed by a surface wave plasma vapor deposition method.
[5] The SOI substrate according to any one of [1] to [4], wherein the microcrystalline diamond film is a film formed by a hot filament vapor deposition method.
[6] The SOI substrate according to any one of [1] to [5], wherein a microcrystalline diamond film is formed on the carbon film by a hot filament vapor deposition method.
[7] The SOI substrate according to [5], which is formed by bonding a microcrystalline diamond film formed by a hot filament vapor phase growth method on the carbon film.
[8] The SOI substrate according to any one of [1] to [7], wherein a silicon oxide film is provided at an interface between the silicon substrate and the carbon film.
図1~図4は、本発明のSOI基板の実施形態の幾つかを模式的に示すものであって、図中、1は、シリコン基板、2は、炭素膜、3は、マイクロ結晶ダイヤモンド膜、4は、シリコン酸化膜、をそれぞれ示している。
すなわち、図1は、I層が、炭素膜2及びマイクロ結晶ダイヤモンド膜3からなるSOI基板を示しており、図2は、図1に示すSOI基板において、シリコン基板1と炭素膜2の間に、シリコン酸化膜4を有するものを示している。また、図3は、I層が、炭素膜2、マイクロ結晶ダイヤモンド膜3及び炭素膜2からなるSOI基板を示しており、図4は、図3に示すSOI基板において、シリコン基板1と炭素膜2の間に、シリコン酸化膜4を有するものを示している。 The SOI substrate of the present invention is characterized in that the I layer has a hybrid structure composed of a carbon film and a microcrystalline diamond film.
1 to 4 schematically show some embodiments of an SOI substrate of the present invention, in which 1 is a silicon substrate, 2 is a carbon film, and 3 is a microcrystalline diamond film.
That is, FIG. 1 shows an SOI substrate in which the I layer is composed of the
炭素膜とマイクロ結晶ダイヤモンド膜を張り合わせるためには、両膜の張り合わせ面が、原子レベルで平坦であることが必要条件である。一般的に、ダイヤモンド表面の平坦化には、機械的な研磨方法が用いられている。
この機械的研磨を、シリコン/炭素膜基板の炭素膜表面に用いた場合、デバイスを作製するシリコン基板に欠陥やひずみが生じてしまう。このため、原子レベルで平坦な表面が自己組織化的に形成できる表面波プラズマ気相成長法により成膜された炭素膜を、シリコン基板上に形成する必要がある。 In the development of SOI substrates for power semiconductor devices, in order to adapt to the manufacturing process of existing silicon semiconductor devices, a homogeneous microcrystalline diamond film with a diameter of 30 cm or more is laminated on the silicon / carbon film substrate with a diameter of 30 cm or more. It is also possible by the method.
In order to bond the carbon film and the microcrystalline diamond film, it is a necessary condition that the bonding surfaces of the two films are flat at the atomic level. In general, a mechanical polishing method is used to flatten the diamond surface.
When this mechanical polishing is used on the carbon film surface of the silicon / carbon film substrate, defects and strains are generated in the silicon substrate for manufacturing the device. For this reason, it is necessary to form a carbon film formed on the silicon substrate by a surface wave plasma vapor deposition method that can form a flat surface at the atomic level in a self-organized manner.
(1)まずシリコン基板に表面波プラズマ気相成長法で、原子レベルで平坦な表面を有する炭素膜を成膜し、炭素膜/シリコン基板を製造する。
(2)次に、熱フィラメント気相成長法で、別のシリコン基板上にマイクロ結晶ダイヤモンド膜を成膜し、シリコン基板を除去することで、シリコンとマイクロ結晶ダイヤモンドの界面に形成された、原子レベルで平坦なマイクロ結晶ダイヤモンド表面を得る。
(3)次いで、得られた原子レベルで平坦な表面を、前記炭素膜/シリコン基板の炭素膜表面に張り合わせる。張り合わせには、イオンビームやプラズマを用いて該炭素膜表面およびマイクロ結晶ダイヤモンド表面洗浄を行い、真空加圧貼付け方式で、炭素膜表面とマイクロ結晶ダイヤモンド表面とを張り合わせることができる。 Hereinafter, the production of an SOI substrate having a hybrid structure of carbon film / microcrystalline diamond film by the bonding method described above will be specifically described.
(1) First, a carbon film having a flat surface at an atomic level is formed on a silicon substrate by surface wave plasma vapor deposition to produce a carbon film / silicon substrate.
(2) Next, a microcrystalline diamond film is formed on another silicon substrate by hot filament vapor deposition, and the silicon substrate is removed to form atoms formed at the interface between silicon and microcrystalline diamond. A level microcrystalline diamond surface is obtained.
(3) Next, the obtained flat surface at the atomic level is bonded to the carbon film surface of the carbon film / silicon substrate. For the bonding, the carbon film surface and the microcrystalline diamond surface can be cleaned using an ion beam or plasma, and the carbon film surface and the microcrystalline diamond surface can be bonded together by a vacuum pressure bonding method.
したがって、本発明のSOI基板の作製方法のさらにもう1つは、(1)まずシリコン基板に表面波プラズマ気相成長法で、原子レベルで平坦な表面を有する炭素膜を成膜する工程と、(2)熱フィラメント気相成長法で、シリコン基板上にマイクロ結晶ダイヤモンド膜を成膜し、機械的研磨方法で、マイクロ結晶ダイヤモンド表面を原子レベルでの平坦化とシリコンの除去を行う工程と、(3)の原子レベルで平坦な表面を、前記炭素膜表面に張り合わせる工程とからなる方法であり、該方法により、高耐圧かつ高熱伝導性の炭素膜/マイクロ結晶ダイヤモンド膜のハイブリット構造を有するSOI基板が作成できる。 In addition, since the microcrystalline diamond film requires an area of 30 cm or more in diameter, synthesis by a hot filament vapor deposition method can be used. At this time, mechanical polishing is used to form a flat substrate surface at an atomic level. Can be used.
Therefore, yet another method for manufacturing an SOI substrate according to the present invention includes (1) a step of first forming a carbon film having a flat surface at an atomic level on a silicon substrate by surface wave plasma vapor deposition. (2) forming a microcrystalline diamond film on a silicon substrate by a hot filament vapor deposition method, planarizing the surface of the microcrystalline diamond at an atomic level and removing silicon by a mechanical polishing method; (3) A method comprising a step of bonding a flat surface at an atomic level to the surface of the carbon film, and the method has a hybrid structure of a carbon film / microcrystalline diamond film having a high breakdown voltage and high thermal conductivity. An SOI substrate can be created.
なお、実施例における炭素膜の製造方法は、特許文献1および特許文献2で開示されている方法を用いた。 EXAMPLES Hereinafter, although an Example etc. demonstrate this invention further more concretely, this invention is not limited at all by these Examples.
In addition, the method currently disclosed by
《不純物評価》
本発明のSOI基板のシリコン基板中のタングステンの評価は、二次イオン質量分析法により行った。測定は、一次イオンにO2 +を用い、加速電圧を3kVとした。測定時の真空度は3×10-9Torrである。 First, use and evaluation methods are described in the examples.
<Evaluation of impurities>
Evaluation of tungsten in the silicon substrate of the SOI substrate of the present invention was performed by secondary ion mass spectrometry. In the measurement, O 2 + was used as the primary ion, and the acceleration voltage was 3 kV. The degree of vacuum during the measurement is 3 × 10 −9 Torr.
電気絶縁性の評価に用いた試料として、本発明のSOI基板のマイクロ結晶ダイヤモンド膜上に直径30μmの電極を形成したものを用いた。SOI基板のシリコンは導電性の銀ペーストを用いて銅製の試料ホルダーに設置した。測定は、5×10-7Torrの真空中で、電流-電圧特性を測定した。印加電圧をマイクロ結晶ダイヤモンドの膜厚と炭素膜の膜厚の合計膜厚で割った値を電界とし、電流-電界特性を用いて、電気絶縁性を評価した。電流が観測される電界が大きい程電気絶縁性が高いことを意味する。 <Electrical insulation>
As a sample used for evaluation of electrical insulation, a sample in which an electrode having a diameter of 30 μm was formed on a microcrystalline diamond film of an SOI substrate of the present invention was used. The silicon of the SOI substrate was placed in a copper sample holder using a conductive silver paste. The measurement was performed by measuring current-voltage characteristics in a vacuum of 5 × 10 −7 Torr. The value obtained by dividing the applied voltage by the total thickness of the microcrystalline diamond film and the carbon film was defined as the electric field, and the electric insulation was evaluated using the current-electric field characteristics. The larger the electric field where current is observed, the higher the electrical insulation.
熱伝導度の測定は、サーモリフレクタンス法で評価した。試料は、SOI基板のシリコン基板をフッ酸と硝酸の混合液で除去し、マイクロ結晶ダイヤモンド膜/炭素膜の自立体構造を作製した。このマイクロ結晶ダイヤモンド/炭素膜自立体構造マイクロ結晶ダイヤモンド面と炭素膜面にスパッタリング法で厚さ100nmのモリブデン薄膜を形成した。
熱伝導度は、積層体の積層方向および積層方向に対して垂直方向(面内方向)の熱伝導度を評価した。 《Thermal conductivity》
The thermal conductivity was measured by a thermoreflectance method. As a sample, the silicon substrate of the SOI substrate was removed with a mixed solution of hydrofluoric acid and nitric acid to produce a self-stereoscopic structure of a microcrystalline diamond film / carbon film. A molybdenum thin film having a thickness of 100 nm was formed on the microcrystalline diamond surface and the carbon film surface by sputtering.
For the thermal conductivity, the thermal conductivity in the direction perpendicular to the laminating direction and the laminating direction (in-plane direction) of the laminate was evaluated.
基板として4インチ径のウェハ状のシリコン基板を用いた。炭素粒子の核形成密度を高め均一な成膜とするために、成膜前の基板に前処理(ナノクリスタルダイヤモンド粒子付着処理)を行った。
この前処理には平均粒径5nmのナノクリスタルダイヤモンド粒子を純水中に分散させたコロイド溶液(有限会社ナノ炭素研究所製 製品名ナノアマンド)または平均粒径30nm又は40nmのナノクリスタルダイヤモンド粒子(トーメイダイヤ株式会社製 製品名各々MD30およびMD40)を純水中に分散させた溶液、あるいはクラスターダイヤモンド粒子またはグラファイトクラスターダイヤモンド粒子(東京ダイヤモンド工具製作所製 製品名各々CDおよびGCD)を分散させたエタノール、あるいはアダマンタンまたはその誘導体あるいはそれらの誘導体(各々出光興産株式会社製)溶液を用い,これに基板を浸して超音波洗浄器にかけた。
その後、基板をエタノール中に浸して超音波洗浄を行い、乾燥させるか、またはこれらの溶液をスピンコートによって基板上に均一に塗布し、乾燥させる。この前処理の均一性が成膜後の炭素膜の均一性に影響する。この場合、基板上に付着するダイヤモンド粒子は、1cm2当たり、1010~1011個であった。 Example 1
A 4-inch diameter wafer-like silicon substrate was used as the substrate. In order to increase the nucleation density of the carbon particles and form a uniform film, a pretreatment (nanocrystal diamond particle adhesion treatment) was performed on the substrate before the film formation.
For this pretreatment, a colloidal solution (product name: Nanoamand, manufactured by Nano Carbon Laboratory Co., Ltd.) in which nanocrystal diamond particles having an average particle size of 5 nm are dispersed in pure water, or nanocrystal diamond particles having an average particle size of 30 nm or 40 nm (Tomei) Diamond Co., Ltd., product names MD30 and MD40) dispersed in pure water, or cluster diamond particles or graphite cluster diamond particles (Tokyo Diamond Tool Co., Ltd., product names CD and GCD, respectively), or Adamantane or a derivative thereof or a derivative thereof (each made by Idemitsu Kosan Co., Ltd.) solution was used, and the substrate was immersed in an ultrasonic cleaner.
Thereafter, the substrate is immersed in ethanol for ultrasonic cleaning and dried, or these solutions are uniformly applied on the substrate by spin coating and dried. The uniformity of this pretreatment affects the uniformity of the carbon film after film formation. In this case, the number of diamond particles adhering on the substrate was 10 10 to 10 11 per cm 2 .
以上の成膜条件の下、6時間成膜を行った。成膜後のガラス基板上には、均一かつ透明な炭素膜が形成された。この膜の膜厚は、200nmであった。 As the source gas, a mixed gas of CH 4 , CO 2 and H 2 was used, and the concentrations of CH 4 and CO 2 were each 1 mol%. The gas pressure in the reaction vessel is 1.0 to 1.2 × 10 2 Pa (1.0 to 1.2 mbar), which is lower than the pressure (10 3 to 10 4 Pa) usually used for CVD synthesis of diamond, and a total of 20 A large area and uniform plasma was generated in a region wider than the substrate area by applying a microwave of ˜24 kW. At that time, the substrate temperature during film formation can be maintained at 450 ° C. or less by adjusting the distance between the substrate and the antenna by closely contacting the Mo sample stage and the cooling stage.
Film formation was performed for 6 hours under the above film formation conditions. A uniform and transparent carbon film was formed on the glass substrate after film formation. The film thickness was 200 nm.
基板として、シリコン酸化膜(SiO2膜)(厚さ20nm)を形成したシリコン基板を用いた以外は、実施例1と同様にしてSOI基板を作製した。実施例2で得られたSOI基板の構造を図2に示す。 (Example 2)
An SOI substrate was fabricated in the same manner as in Example 1 except that a silicon substrate on which a silicon oxide film (SiO 2 film) (thickness 20 nm) was formed was used. The structure of the SOI substrate obtained in Example 2 is shown in FIG.
マイクロ結晶ダイヤモンドのみをI層(絶縁層)としたSOI基板を作製した。基板には、シリコン基板を用いた。
マイクロ結晶ダイヤモンド膜の成膜の前処理として、ダイヤモンド粒子でシリコン基板に傷付け処理をおこなった。熱フィラメント気相成長装置は、大面積HFCVD装置(sp3社製 Model 650)を用いた。フィラメントにはタングステン(W)を用い、フィラメント温度2000℃、基板温度800℃で、6時間の成膜をおこなった。この膜の膜厚は、約10μmであった。 (Comparative Example 1)
An SOI substrate using only microcrystalline diamond as an I layer (insulating layer) was manufactured. A silicon substrate was used as the substrate.
As a pretreatment for forming the microcrystalline diamond film, the silicon substrate was scratched with diamond particles. As the hot filament vapor phase growth apparatus, a large-area HFCVD apparatus (Model 650 manufactured by sp3) was used. Tungsten (W) was used as the filament, and the film was formed for 6 hours at a filament temperature of 2000 ° C. and a substrate temperature of 800 ° C. The film thickness was about 10 μm.
実施例1及び実施例2において、マイクロ結晶ダイヤモンド膜に、さらに同様の200nmの炭素膜を形成することで、リーク電流が観測される電界が2倍となった。つまり、図3および図4の構造を形成することで、リーク電界が約120V/μmおよび約130V/μmのSOI基板が作製できることがわかる。また、熱伝導性は、炭素膜の値の成膜方向は8倍、成膜方向と垂直方向(面内方向)は3倍と改善された。 Example 3
In Example 1 and Example 2, by forming a similar 200 nm carbon film on the microcrystalline diamond film, the electric field at which leakage current was observed was doubled. That is, it can be seen that by forming the structures of FIGS. 3 and 4, an SOI substrate having a leakage electric field of about 120 V / μm and about 130 V / μm can be manufactured. Further, the thermal conductivity was improved by 8 times in the film forming direction of the value of the carbon film and 3 times in the direction perpendicular to the film forming direction (in-plane direction).
2:炭素膜
3:マイクロ結晶ダイヤモンド膜
4:シリコン酸化膜 1: Silicon substrate 2: Carbon film 3: Microcrystalline diamond film 4: Silicon oxide film
Claims (8)
- SOI基板の絶縁層が、炭素膜とマイクロ結晶ダイヤモンド膜のハイブリット構造を有することを特徴とするSOI基板。 An SOI substrate, wherein the insulating layer of the SOI substrate has a hybrid structure of a carbon film and a microcrystalline diamond film.
- 前記ハイブリット構造が、炭素膜/マイクロ結晶ダイヤモンド膜で構成されていることを特徴とする請求項1に記載のSOI基板。 2. The SOI substrate according to claim 1, wherein the hybrid structure is composed of a carbon film / microcrystalline diamond film.
- 前記ハイブリット構造が、炭素膜/マイクロ結晶ダイヤモンド膜/炭素膜で構成されていることを特徴とする請求項1に記載のSOI基板。 2. The SOI substrate according to claim 1, wherein the hybrid structure is composed of a carbon film / microcrystalline diamond film / carbon film.
- 前記炭素膜が、表面波プラズマ気相成長法で形成された膜であることを特徴とする請求項1~3のいずれか1項に記載のSOI基板。 The SOI substrate according to any one of claims 1 to 3, wherein the carbon film is a film formed by a surface wave plasma vapor deposition method.
- 前記マイクロ結晶ダイヤモンド膜層が、熱フィラメント気相成長法で形成された膜であることを特徴とする請求項1~4のいずれか1項に記載のSOI基板。 The SOI substrate according to any one of claims 1 to 4, wherein the microcrystalline diamond film layer is a film formed by a hot filament vapor deposition method.
- 前記炭素膜上に、熱フィラメント気相成長法によりマイクロ結晶ダイヤモンド膜が形成されていることを特徴とする請求項1~5のいずれか1項に記載のSOI基板。 The SOI substrate according to any one of claims 1 to 5, wherein a microcrystalline diamond film is formed on the carbon film by a hot filament vapor deposition method.
- 前記炭素膜上に、熱フィラメント気相成長法で形成されたマイクロ結晶ダイヤモンド膜を張り合わせることにより形成されたことを特徴とする請求項5に記載のSOI基板。 6. The SOI substrate according to claim 5, wherein the SOI substrate is formed by bonding a microcrystalline diamond film formed by a hot filament vapor phase growth method on the carbon film.
- シリコン基板と炭素膜の界面にシリコン酸化膜を有することを特徴とする請求項1~7のいずれか1項に記載のSOI基板。 8. The SOI substrate according to claim 1, further comprising a silicon oxide film at an interface between the silicon substrate and the carbon film.
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DE112011103476T DE112011103476T5 (en) | 2010-10-14 | 2011-10-12 | SOI substrate |
JP2012538690A JP5665202B2 (en) | 2010-10-14 | 2011-10-12 | SOI substrate |
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WO2020250815A1 (en) * | 2019-06-14 | 2020-12-17 | Tdk株式会社 | Electronic-component-incorporating substrate and circuit module using the same |
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JPS63150926A (en) * | 1986-12-15 | 1988-06-23 | Ricoh Co Ltd | Film formation of diamond-shaped carbon film |
JP2006228963A (en) * | 2005-02-17 | 2006-08-31 | Kobe Steel Ltd | Method of manufacturing semiconductor wafer |
WO2008057055A1 (en) * | 2006-11-10 | 2008-05-15 | Agency For Science, Technology And Research | A micromechanical structure and a method of fabricating a micromechanical structure |
JP2010202911A (en) * | 2009-03-02 | 2010-09-16 | Mitsubishi Materials Corp | Carbon film, production method of carbon film, and cmp pad conditioner |
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CN1969058B (en) * | 2004-04-19 | 2010-04-14 | 独立行政法人产业技术总合研究所 | Carbon film |
WO2007004647A1 (en) * | 2005-07-04 | 2007-01-11 | National Institute Of Advanced Industrial Science And Technology | Carbon film |
JP2011241463A (en) * | 2010-05-20 | 2011-12-01 | Toyota Motor Corp | Layer structure having hard carbon film layer, and valve lifter having the layer structure on surface |
-
2011
- 2011-10-12 DE DE112011103476T patent/DE112011103476T5/en not_active Withdrawn
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JPS63150926A (en) * | 1986-12-15 | 1988-06-23 | Ricoh Co Ltd | Film formation of diamond-shaped carbon film |
JP2006228963A (en) * | 2005-02-17 | 2006-08-31 | Kobe Steel Ltd | Method of manufacturing semiconductor wafer |
WO2008057055A1 (en) * | 2006-11-10 | 2008-05-15 | Agency For Science, Technology And Research | A micromechanical structure and a method of fabricating a micromechanical structure |
JP2010202911A (en) * | 2009-03-02 | 2010-09-16 | Mitsubishi Materials Corp | Carbon film, production method of carbon film, and cmp pad conditioner |
Cited By (3)
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WO2020250815A1 (en) * | 2019-06-14 | 2020-12-17 | Tdk株式会社 | Electronic-component-incorporating substrate and circuit module using the same |
JPWO2020250815A1 (en) * | 2019-06-14 | 2020-12-17 | ||
JP7439833B2 (en) | 2019-06-14 | 2024-02-28 | Tdk株式会社 | Electronic component built-in board and circuit module using the same |
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JPWO2012050122A1 (en) | 2014-02-24 |
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