WO2016051890A1 - 窒化ガリウム自立基板、発光素子及びそれらの製造方法 - Google Patents
窒化ガリウム自立基板、発光素子及びそれらの製造方法 Download PDFInfo
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- WO2016051890A1 WO2016051890A1 PCT/JP2015/068391 JP2015068391W WO2016051890A1 WO 2016051890 A1 WO2016051890 A1 WO 2016051890A1 JP 2015068391 W JP2015068391 W JP 2015068391W WO 2016051890 A1 WO2016051890 A1 WO 2016051890A1
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- WIPO (PCT)
- Prior art keywords
- gallium nitride
- substrate
- standing substrate
- single crystal
- crystal
- Prior art date
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- 239000000758 substrate Substances 0.000 title claims abstract description 537
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- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 162
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- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
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Images
Classifications
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- 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
- C30B29/10—Inorganic compounds or compositions
- C30B29/38—Nitrides
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L33/00—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L33/02—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the semiconductor bodies
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L33/00—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L33/005—Processes
- H01L33/0062—Processes for devices with an active region comprising only III-V compounds
- H01L33/0066—Processes for devices with an active region comprising only III-V compounds with a substrate not being a III-V compound
- H01L33/007—Processes for devices with an active region comprising only III-V compounds with a substrate not being a III-V compound comprising nitride compounds
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L33/00—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L33/02—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the semiconductor bodies
- H01L33/04—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the semiconductor bodies with a quantum effect structure or superlattice, e.g. tunnel junction
- H01L33/06—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the semiconductor bodies with a quantum effect structure or superlattice, e.g. tunnel junction within the light emitting region, e.g. quantum confinement structure or tunnel barrier
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L33/00—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L33/02—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the semiconductor bodies
- H01L33/16—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the semiconductor bodies with a particular crystal structure or orientation, e.g. polycrystalline, amorphous or porous
- H01L33/18—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the semiconductor bodies with a particular crystal structure or orientation, e.g. polycrystalline, amorphous or porous within the light emitting region
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/10—Details of semiconductor or other solid state devices to be connected
- H01L2924/11—Device type
- H01L2924/12—Passive devices, e.g. 2 terminal devices
- H01L2924/1204—Optical Diode
- H01L2924/12041—LED
Definitions
- the present invention relates to a gallium nitride free-standing substrate, a light emitting device, and a method for manufacturing the same.
- GaN gallium nitride
- MQW multi-quantum well layer
- a gallium nitride crystal multilayer substrate including a sapphire base substrate and a gallium nitride crystal layer formed by crystal growth on the substrate. Yes.
- GaN gallium nitride
- Patent Document 2 Japanese Patent Application Laid-Open No. 2010-1325566 discloses a self-supporting n-type gallium nitride single crystal substrate having a thickness of 200 ⁇ m or more.
- single crystal substrates are generally small in area and expensive.
- cost reduction of LED manufacturing using a large area substrate has been demanded, but it is not easy to mass-produce a large area single crystal substrate, and the manufacturing cost is further increased. Therefore, an inexpensive material that can be used as a substitute material for a single crystal substrate such as gallium nitride is desired.
- the present inventors have now obtained the knowledge that a gallium nitride free-standing substrate that is inexpensive and suitable for an increase in area can be produced as an alternative material for a gallium nitride single crystal substrate.
- an object of the present invention is to provide a gallium nitride free-standing substrate that is inexpensive and suitable for an increase in area and is useful as an alternative material for a gallium nitride single crystal substrate.
- a gallium nitride free-standing substrate comprising a plate composed of a plurality of gallium nitride-based single crystal particles having a single crystal structure in a substantially normal direction.
- a gallium nitride free-standing substrate according to the invention, A light emitting functional layer formed on the substrate and having at least one layer composed of a plurality of semiconductor single crystal particles having a single crystal structure in a substantially normal direction; A light-emitting element is provided.
- a step of preparing an oriented polycrystalline sintered body Forming a seed crystal layer made of gallium nitride on the oriented polycrystalline sintered body so as to have a crystal orientation substantially following the crystal orientation of the oriented polycrystalline sintered body; Forming a layer composed of a gallium nitride-based crystal having a thickness of 20 ⁇ m or more on the seed crystal layer so as to have a crystal orientation substantially following the crystal orientation of the seed crystal layer; Removing the oriented polycrystalline sintered body to obtain a gallium nitride free-standing substrate; A method for manufacturing a gallium nitride free-standing substrate is provided.
- a gallium nitride free-standing substrate according to the present invention or preparing the gallium nitride free-standing substrate by the method of the present invention;
- a gallium nitride free-standing substrate comprising a plate composed of a plurality of gallium nitride-based single crystal particles having a single crystal structure in a substantially normal direction, the gallium nitride-based single substrate exposed on a surface of the gallium nitride free-standing substrate.
- the crystal grains communicate with the back surface of the gallium nitride free-standing substrate without a grain boundary, and the cross-sectional average diameter D B at the outermost surface of the gallium nitride-based single crystal particles exposed on the back surface of the gallium nitride free-standing substrate
- the gallium nitride free-standing substrate according to Item 1 wherein an average cross-sectional diameter of the gallium nitride-based single crystal particles on the outermost surface of the substrate is 0.3 ⁇ m or more.
- Item 3 The gallium nitride free-standing substrate according to Item 2, wherein the average cross-sectional diameter is 3 ⁇ m or more.
- Claim 4 Item 3. The gallium nitride free-standing substrate according to Item 2, wherein the average cross-sectional diameter is 20 ⁇ m or more.
- Sitem 5 Item 5. The gallium nitride free-standing substrate according to any one of Items 1 to 4, having a thickness of 20 ⁇ m or more.
- [Section 8] Item 8 The gallium nitride free-standing substrate according to any one of Items 1 to 7, wherein the gallium nitride-based single crystal particles are doped with an n-type dopant or a p-type dopant.
- the aspect ratio T / D defined as the ratio of the thickness T of the gallium nitride free-standing substrate to the average cross-sectional diameter DT of the outermost surface of the gallium nitride-based single crystal particles exposed on the surface of the gallium nitride free-standing substrate Item 12.
- the gallium nitride free-standing substrate according to any one of Items 1 to 11, wherein T is 0.7 or more.
- the light emitting functional layer is composed of a gallium nitride material.
- [Section 23] Preparing the gallium nitride free-standing substrate according to any one of items 1 to 12, or preparing the gallium nitride free-standing substrate by the method according to any one of items 18 to 22, One or more layers composed of a plurality of semiconductor single crystal particles having a single crystal structure in a substantially normal direction so that the gallium nitride free-standing substrate has a crystal orientation that substantially follows the crystal orientation of the gallium nitride substrate.
- a gallium nitride free-standing substrate comprising a plate composed of a plurality of gallium nitride-based single crystal particles having a single crystal structure in a substantially normal direction, the gallium nitride-based single substrate exposed on a surface of the gallium nitride free-standing substrate. Crystal grains are connected to the back surface of the gallium nitride free-standing substrate without a grain boundary, and the average cross-sectional diameter of the gallium nitride single crystal particles on the outermost surface of the substrate is 20 ⁇ m or more and 1000 ⁇ m or less. Free-standing board. [Claim 26] Item 26.
- the gallium nitride free-standing substrate according to Item 25 wherein the average cross-sectional diameter is 50 ⁇ m or more and 500 ⁇ m or less.
- [Section 27] Item 27.
- [Claim 28] Item 28.
- Item 29 Item 29.
- the aspect ratio T / D defined as the ratio of the thickness T of the gallium nitride free-standing substrate to the average cross-sectional diameter DT of the outermost surface of the gallium nitride-based single crystal particles exposed on the surface of the gallium nitride free-standing substrate Item 34.
- the gallium nitride free-standing substrate according to any one of Items 25 to 33, wherein T is 0.7 or more.
- [Claim 35] The gallium nitride free-standing substrate according to any one of Items 25 to 34, A light emitting functional layer formed on the substrate and having at least one layer composed of a plurality of semiconductor single crystal particles having a single crystal structure in a substantially normal direction; A light emitting device comprising: [Claim 36] Item 36. The self-supporting light-emitting element according to Item 35, wherein an average cross-sectional diameter of the semiconductor single crystal particles on the outermost surface of the light-emitting functional layer is 20 ⁇ m or more. [Section 37] Item 37. The light-emitting device according to Item 36, wherein the cross-sectional average diameter is 50 ⁇ m or more. [Section 38] Item 38.
- the light emitting device according to any one of items 35 to 37, wherein the semiconductor single crystal particles have a structure grown substantially following the crystal orientation of the gallium nitride free-standing substrate.
- the light emitting functional layer is made of a gallium nitride material.
- [Claim 40] Preparing an oriented polycrystalline sintered body; Forming a seed crystal layer made of gallium nitride on the oriented polycrystalline sintered body so as to have a crystal orientation substantially following the crystal orientation of the oriented polycrystalline sintered body; Forming a layer composed of a gallium nitride-based crystal having a thickness of 20 ⁇ m or more on the seed crystal layer so as to have a crystal orientation substantially following the crystal orientation of the seed crystal layer; Removing the oriented polycrystalline sintered body to obtain a gallium nitride free-standing substrate; And the gallium nitride single crystal particles exposed on the surface of the gallium nitride free-standing substrate communicate with the back surface of the gallium nitride free-standing substrate without passing through a grain boundary, and are nitrided on the outermost surface of the substrate A method for producing a gallium nitride free-standing substrate, wherein the gallium single crystal particles have a cross-sectional average diameter of
- [Section 45] A step of preparing the gallium nitride free-standing substrate according to any one of Items 25 to 34, or preparing the gallium nitride free-standing substrate by the method according to any one of Items 40 to 44; One or more layers composed of a plurality of semiconductor single crystal particles having a single crystal structure in a substantially normal direction so that the gallium nitride free-standing substrate has a crystal orientation that substantially follows the crystal orientation of the gallium nitride substrate.
- Forming and providing a light emitting functional layer A method for manufacturing a light emitting device, comprising: [Claim 46] Item 46. The method according to Item 45, wherein the light emitting functional layer is composed of a gallium nitride-based material.
- FIG. 6 is an inverted pole figure orientation mapping of a cross section of a gallium nitride crystal measured in Example 4.
- FIG. 6 is an inverted pole figure orientation mapping of a plate surface (surface) of a gallium nitride crystal measured in Example 4.
- FIG. 6 is a crystal grain mapping near the interface between a gallium nitride crystal and an oriented alumina substrate measured in Example 4.
- FIG. 6 is a conceptual diagram of the growth behavior of gallium nitride crystals considered in Examples 4 and 5.
- FIG. 6 is an inverted pole figure orientation mapping of a cross section of a gallium nitride crystal measured in Example 5.
- the gallium nitride substrate of the present invention can have the form of a freestanding substrate.
- the “self-supporting substrate” means a substrate that can be handled as a solid material without being deformed or damaged by its own weight when handled.
- the gallium nitride free-standing substrate of the present invention can be used as a substrate for various semiconductor devices such as light-emitting elements, but in addition to this, an electrode (which may be a p-type electrode or an n-type electrode), a p-type layer, an n-type layer It can be used as a member or layer other than the substrate such as.
- the advantages of the present invention may be described by taking a light emitting element which is one of the main applications as an example. However, similar or similar advantages are not limited to the technical consistency. The same applies to semiconductor devices.
- the gallium nitride free-standing substrate of the present invention comprises a plate composed of a plurality of gallium nitride-based single crystal particles having a single crystal structure in a substantially normal direction. That is, the gallium nitride free-standing substrate is composed of a plurality of semiconductor single crystal particles that are two-dimensionally connected in the horizontal plane direction, and thus has a single crystal structure in a substantially normal direction. Therefore, although the gallium nitride free-standing substrate is not a single crystal as a whole, the gallium nitride free-standing substrate has a single crystal structure in a local domain unit, and therefore has a sufficiently high crystallinity to ensure device characteristics such as a light emitting function. it can.
- the gallium nitride free-standing substrate of the present invention is not a single crystal substrate.
- the single crystal substrate generally has a small area and is expensive.
- mass production of a large area single crystal substrate is not easy, and the manufacturing cost is further increased.
- These drawbacks are eliminated by the gallium nitride free-standing substrate of the present invention. That is, according to the present invention, it is possible to provide a gallium nitride free-standing substrate useful as an alternative material for a gallium nitride single crystal substrate that is inexpensive and suitable for increasing the area.
- gallium nitride imparted with conductivity by introducing a p-type or n-type dopant as a substrate, a light-emitting element having a vertical structure can be realized, whereby luminance can be increased.
- a large-area surface light-emitting element used for surface-emitting illumination or the like can be realized at low cost.
- a vertical LED structure is fabricated using the gallium nitride free-standing substrate of the present invention, a plurality of gallium nitride single crystal particles constituting the free-standing substrate have a single crystal structure in a substantially normal direction. High-resistance grain boundaries do not exist, and as a result, preferable luminous efficiency is expected.
- the gallium nitride free-standing substrate of the present invention can be preferably used for a vertical LED structure.
- the plurality of gallium nitride single crystal particles constituting the self-supporting substrate have crystal orientations substantially aligned in a substantially normal direction.
- Crystal orientation that is generally aligned in the normal direction is not necessarily a crystal orientation that is perfectly aligned in the normal direction, as long as a device such as a light-emitting element using a self-supporting substrate can ensure desired device characteristics. This means that the crystal orientation may be aligned to some extent in the normal or similar direction.
- the gallium nitride-based single crystal particles have a structure grown substantially following the crystal orientation of the oriented polycrystalline sintered body used as the base material during the production of the gallium nitride free-standing substrate.
- the “structure grown substantially following the crystal orientation of the oriented polycrystalline sintered body” means a structure brought about by crystal growth affected by the crystal orientation of the oriented polycrystalline sintered body, and is not necessarily oriented.
- the crystal of the oriented polycrystalline sintered body is not necessarily a structure that has grown completely following the crystal orientation of the crystalline sintered body, as long as a device such as a light-emitting element using a self-supporting substrate can ensure the desired device characteristics. It may be a structure grown to some extent along the direction. That is, this structure includes a structure that grows in a different crystal orientation from the oriented polycrystalline sintered body.
- the expression “a structure grown substantially following the crystal orientation” can also be rephrased as “a structure grown substantially derived from the crystal orientation”. This paraphrase and the above meaning are similar to those in this specification. The same applies to expression. Therefore, although such crystal growth is preferably by epitaxial growth, it is not limited to this, and various forms of crystal growth similar thereto may be used. In any case, by growing in this way, the gallium nitride free-standing substrate can have a structure in which crystal orientations are substantially aligned with respect to a substantially normal direction.
- a gallium nitride free-standing substrate is an aggregate of columnar-structured gallium nitride single crystal particles that are observed as single crystals when viewed in the normal direction and grain boundaries are observed when viewed in the cut plane in the horizontal plane direction. It is also possible to grasp that.
- the “columnar structure” does not mean only a typical vertically long column shape, but includes various shapes such as a horizontally long shape, a trapezoidal shape, and a shape in which the trapezoid is inverted. Defined as meaning.
- the gallium nitride free-standing substrate may be a structure having a crystal orientation that is aligned to some extent in the normal or similar direction, and does not necessarily have a columnar structure in a strict sense.
- the cause of the columnar structure is considered to be that the gallium nitride single crystal particles grow under the influence of the crystal orientation of the oriented polycrystalline sintered body used in the manufacture of the gallium nitride free-standing substrate as described above.
- the average particle diameter of the cross section of gallium nitride single crystal particles which can be said to be a columnar structure (hereinafter referred to as the average diameter of the cross section), depends not only on the film forming conditions but also on the average particle diameter of the plate surface of the oriented polycrystalline sintered body It is thought to do.
- the gallium nitride free-standing substrate is used as a part of the light emitting functional layer of the light emitting element, the light transmittance in the cross-sectional direction is poor due to the grain boundary, and the light is scattered or reflected. For this reason, in the case of a light-emitting element having a structure in which light is extracted in the normal direction, an effect of increasing luminance due to scattered light from the grain boundary is expected.
- the free-standing substrate surface on which the light emitting functional layer is formed and the free-standing substrate back surface on which the electrode is formed are It is preferable to communicate without passing through a grain boundary. That is, it is preferable that the gallium nitride single crystal particles exposed on the surface of the gallium nitride free-standing substrate communicate with the back surface of the gallium nitride free-standing substrate without passing through the grain boundary. If there is a grain boundary, resistance is caused during energization, which causes a decrease in luminous efficiency.
- the growth occurs not only in the normal direction but also in the horizontal direction, depending on the film forming conditions.
- the growth rate of each gallium nitride crystal is different.
- the growing particles cover the slow growing particles.
- the slow-growing crystal stops growing in the middle, and when observed in a certain section, grain boundaries can be observed in the normal direction.
- the particles exposed on the surface of the substrate communicate with the back surface of the substrate without passing through the grain boundary, and there is no resistance phase in flowing current.
- the particles exposed on the front surface side of the substrate are not back through the grain boundary. Therefore, it is preferable to form a light emitting functional layer on the substrate surface side from the viewpoint of increasing the light emission efficiency of the LED having a vertical structure.
- the substrate surface side (the side opposite to the side that was in contact with the oriented polycrystalline alumina sintered body at the time of manufacture) is gallium.
- the substrate back surface side (the side in contact with the oriented polycrystalline alumina sintered body which is the base substrate at the time of manufacture) is the nitrogen surface.
- the gallium surface of the gallium nitride free-standing substrate is dominated by particles communicating with the back surface without passing through the grain boundary. For this reason, it is preferable to produce a light emitting functional layer on the gallium surface side (substrate surface side) from the viewpoint of increasing the light emission efficiency of the vertically structured LED.
- the average cross-sectional diameter of the gallium nitride single crystal particles exposed on the substrate surface is It is preferable that the cross-sectional average diameter of the exposed gallium nitride-based single crystal particles is larger because the luminous efficiency increases (this is because the number of gallium nitride-based single crystal particles exposed on the substrate surface is reduced on the back surface of the substrate). In other words, it is preferable that the number is smaller than the number of exposed gallium nitride single crystal particles).
- cross-sectional average of the outermost surface of the gallium nitride single crystal particles exposed on the back surface of the gallium nitride free-standing substrate diameter (hereinafter, cross an average diameter D B of the substrate back surface) with respect to the surface of the gallium nitride free-standing substrate
- the ratio D T / D B of the cross-sectional average diameter (hereinafter referred to as the cross-sectional average diameter D T of the substrate surface) at the outermost surface of the gallium nitride-based single crystal particles exposed to is larger than 1.0.
- it is 1.5 or more, More preferably, it is 2.0 or more, Especially preferably, it is 3.0 or more, Most preferably, it is 5.0 or more.
- the ratio D T / D B is preferably 20 or less, and more preferably 10 or less.
- CAUSE luminous efficiency changes is not clear, but the grain boundary area is high the ratio D T / D B does not contribute to light emission by large grain size is decreased, or the crystal defects by large grain size This is considered to be reduced.
- the cause of the decrease in crystal defects is not clear, but it is also considered that particles containing defects grow slowly and particles with few defects grow at high speed.
- the ratio D T / D B is too high, particles communicating between the substrate surface and the substrate back surface (that is, particles exposed on the substrate surface side) have a small cross-sectional diameter in the vicinity of the substrate back surface side. As a result, it is considered that a sufficient current path cannot be obtained and the light emission efficiency may be reduced, but the details are not clear.
- the cross-sectional average diameter of the semiconductor single crystal particles on the outermost surface of the gallium nitride free-standing substrate is 0.3 ⁇ m or more, more preferably 3 ⁇ m or more, still more preferably 20 ⁇ m or more, particularly preferably 50 ⁇ m or more, and most preferably 70 ⁇ m or more. It is.
- the upper limit of the cross-sectional average diameter of the semiconductor single crystal particles on the outermost surface of the gallium nitride free-standing substrate is not particularly limited, but is practically 1000 ⁇ m or less, more realistically 500 ⁇ m or less, and more realistically 200 ⁇ m or less. is there.
- the sintered particle size on the plate surface of the particles constituting the oriented polycrystalline sintered body used for the production of the gallium nitride free-standing substrate is set to 0.
- the thickness is desirably 3 ⁇ m to 1000 ⁇ m, more desirably 3 ⁇ m to 1000 ⁇ m, still more desirably 10 ⁇ m to 200 ⁇ m, and particularly desirably 14 ⁇ m to 200 ⁇ m.
- the cross-sectional average diameter of the semiconductor single crystal particles on the outermost surface of the gallium nitride free-standing substrate is larger than the cross-sectional average diameter of the back surface of the free-standing substrate, the particles constituting the oriented polycrystalline sintered body
- the sintered grain size on the plate surface is preferably 10 ⁇ m to 100 ⁇ m, more preferably 14 ⁇ m to 70 ⁇ m.
- the gallium nitride single crystal particles constituting the gallium nitride free-standing substrate may not contain a dopant.
- dopant means that an element added for the purpose of imparting some function or characteristic is not contained, and it is needless to say that inclusion of inevitable impurities is allowed.
- the gallium nitride-based single crystal particles constituting the gallium nitride free-standing substrate may be doped with an n-type dopant or a p-type dopant.
- the gallium nitride free-standing substrate is formed by using a p-type electrode, an n-type electrode, p It can be used as a member or layer other than a substrate, such as a mold layer and an n-type layer.
- a p-type dopant include one or more selected from the group consisting of beryllium (Be), magnesium (Mg), calcium (Ca), strontium (Sr), zinc (Zn), and cadmium (Cd). It is done.
- the n-type dopant include one or more selected from the group consisting of silicon (Si), germanium (Ge), tin (Sn), and oxygen (O).
- the gallium nitride single crystal particles constituting the gallium nitride free-standing substrate may be mixed crystal for controlling the band gap.
- the gallium nitride single crystal particles may be composed of gallium nitride mixed with at least one crystal selected from the group consisting of AlN and InN, and may be p-type gallium nitride and / or n.
- the mixed gallium nitride may be doped with a p-type dopant or an n-type dopant.
- Al x Ga 1-x N which is a mixed crystal of gallium nitride and AlN, is used as a p-type substrate by doping Mg
- Al x Ga 1-x N is used as an n-type substrate by doping Si. be able to.
- the band gap is widened by mixing gallium nitride with AlN, and the emission wavelength can be shifted to a higher energy side.
- gallium nitride may be mixed with InN, whereby the band gap is narrowed and the emission wavelength can be shifted to a lower energy side.
- the gallium nitride free-standing substrate preferably has a diameter of 50.8 mm (2 inches) or more, more preferably has a diameter of 100 mm (4 inches) or more, and more preferably has a diameter of 200 mm (8 inches) or more.
- the gallium nitride free-standing substrate is larger, the number of devices that can be manufactured increases, which is preferable from the viewpoint of manufacturing cost. From the viewpoint of a surface light emitting device, the degree of freedom of the device area is increased and the use for surface light emitting lighting is expanded. The upper limit should not be prescribed
- the gallium nitride free-standing substrate is preferably circular or substantially circular when viewed from above, but is not limited thereto.
- the area is preferably at 2026Mm 2 or more, more preferably 7850mm 2 or more, further preferably 31400Mm 2 or more.
- the area may be smaller than the above range, for example, a diameter of 50.8 mm (2 inches) or less, and 2026 mm 2 or less in terms of area.
- the thickness of the gallium nitride free-standing substrate needs to be capable of imparting self-supporting properties to the substrate, and is preferably 20 ⁇ m or more, more preferably 100 ⁇ m or more, and further preferably 300 ⁇ m or more. An upper limit should not be defined for the thickness of the gallium nitride free-standing substrate, but 3000 ⁇ m or less is realistic from the viewpoint of manufacturing cost.
- an aspect ratio T / D T which is defined as the ratio of the thickness T of the GaN free-standing substrate 0 0.7 or more, more preferably 1.0 or more, and even more preferably 3.0 or more.
- this aspect ratio is an LED, it is preferable from the viewpoint of increasing luminous efficiency.
- the reason why the luminous efficiency is increased may be that the defect density in the gallium nitride is lower in the high aspect ratio particles and the light extraction efficiency is increased, but the details are not clear.
- the light emitting functional layer is formed on the free-standing substrate surface side (the side opposite to the side in contact with the oriented polycrystalline sintered body that is the base substrate at the time of manufacture).
- Write good (2) well of the ratio D T / D B sectional average diameter D T of the substrate surface takes an appropriate value for the free-standing substrate back surface of the cross-sectional average diameter D B, constitute a (3) self-supporting substrate good a larger cross-sectional average diameter of the substrate outermost surface of the particles, (4) the aspect ratio T / D T of the particles constituting the free-standing substrate is larger is better.
- the cross-sectional average diameter is large and the aspect ratio is large.
- a gallium nitride crystal having a large cross-sectional average diameter on the substrate surface side and a large thickness is preferable.
- the thickness of the gallium nitride free-standing substrate is preferably 20 ⁇ m or more, more preferably 100 ⁇ m or more, and further preferably 300 ⁇ m or more.
- the gallium nitride crystal is thin as long as it is independent.
- the thickness of the gallium nitride free-standing substrate is realistically 3000 ⁇ m or less, preferably 600 ⁇ m or less, and preferably 300 ⁇ m or less. Accordingly, the thickness that achieves both a self-supporting and high luminous efficiency and a cost viewpoint is preferably about 50 to 500 ⁇ m, and more preferably about 50 to 300 ⁇ m.
- the gallium nitride free-standing substrate of the present invention is prepared by (1) preparing an oriented polycrystalline sintered body, and (2) arranging a seed crystal layer made of gallium nitride on the oriented polycrystalline sintered body. (3) a layer composed of a gallium nitride-based crystal having a thickness of 20 ⁇ m or more on the seed crystal layer is approximately aligned with the crystal orientation of the seed crystal layer.
- the gallium nitride free-standing substrate can be manufactured by removing the oriented polycrystalline sintered body by forming it so as to have a crystal orientation that has been copied.
- An oriented polycrystalline sintered body is prepared as a base substrate for producing a gallium nitride free-standing substrate.
- the composition of the oriented polycrystalline sintered body is not particularly limited, but is preferably one selected from an oriented polycrystalline alumina sintered body, an oriented polycrystalline zinc oxide sintered body, and an oriented polycrystalline aluminum nitride sintered body.
- An oriented polycrystalline sintered body can be efficiently manufactured through molding and firing using commercially available plate-like powder, so it can be manufactured at a low cost, but also because it is easy to mold, it can also increase the area. Suitable.
- a large-area light-emitting element is manufactured at low cost by using an oriented polycrystalline sintered body as a base substrate and growing a plurality of semiconductor single crystal particles thereon. Can be produced. As a result, the gallium nitride free-standing substrate is extremely suitable for manufacturing a large-area light emitting device at low cost.
- the oriented polycrystalline sintered body is composed of a sintered body including a large number of single crystal particles, and a large number of single crystal particles are oriented to some extent or highly in a certain direction.
- a highly oriented gallium nitride free-standing substrate when such a highly oriented gallium nitride free-standing substrate is used as a substrate for a light emitting device, a light emitting functional layer can be formed in a state where crystal orientations are substantially aligned in a substantially normal direction. High luminous efficiency equivalent to that when a substrate is used can be realized. Alternatively, even when this highly oriented gallium nitride free-standing substrate is used as a light-emitting functional layer of a light-emitting element, high light emission efficiency equivalent to that when a single crystal substrate is used can be realized. In any case, in order to produce such a highly oriented gallium nitride free-standing substrate, it is necessary to use an oriented polycrystalline sintered body as a base substrate.
- the oriented polycrystalline sintered body preferably has translucency, but is not limited thereto.
- translucency a technique such as laser lift-off can be used when removing the oriented polycrystalline plate.
- a manufacturing method for obtaining an oriented polycrystalline sintered body in addition to a normal atmospheric pressure sintering method using an air furnace, a nitrogen atmosphere furnace, a hydrogen atmosphere furnace, etc., a hot isostatic pressing method (HIP), a hot press method (HP), pressure sintering methods such as spark plasma sintering (SPS), and a combination thereof can be used.
- HIP hot isostatic pressing method
- HP hot press method
- SPS spark plasma sintering
- the oriented polycrystalline sintered body preferably has a diameter of 50.8 mm (2 inches) or more, more preferably has a diameter of 100 mm (4 inches) or more, and more preferably has a diameter of 200 mm (8 inches) or more. .
- the gallium nitride free-standing substrate is preferably circular or substantially circular when viewed from above, but is not limited thereto. If not a circular or substantially circular shape, as the area is preferably at 2026Mm 2 or more, more preferably 7850mm 2 or more, further preferably 31400Mm 2 or more. However, for applications that do not require a large area, the area may be smaller than the above range, for example, a diameter of 50.8 mm (2 inches) or less, and 2026 mm 2 or less in terms of area.
- the thickness of the oriented polycrystalline sintered body is not particularly limited as long as it is self-supporting, but if it is too thick, it is not preferable from the viewpoint of production cost.
- the thickness is preferably 20 ⁇ m or more, more preferably 100 ⁇ m or more, and further preferably 100 to 1000 ⁇ m.
- the gallium nitride film is formed, the entire substrate is warped due to the stress caused by the difference in thermal expansion between alumina and gallium nitride, which may hinder subsequent processes.
- the stress varies depending on the gallium nitride film forming method and conditions, the material of the oriented polycrystalline sintered body, the film thickness, the substrate diameter, etc.
- the substrate is thickly oriented.
- a polycrystalline sintered body may be used.
- a gallium nitride free-standing substrate having a diameter of 50.8 mm (2 inches) and a thickness of 300 ⁇ m is produced.
- the thickness of the body may be 900 ⁇ m or more, or 1300 ⁇ m or more, or 2000 ⁇ m or more. In this way, the thickness of the oriented polycrystalline sintered body may be appropriately selected in consideration of the manufacturing cost viewpoint and the warp suppression viewpoint.
- the average particle size on the plate surface of the particles constituting the oriented polycrystalline sintered body is preferably 0.3 to 1000 ⁇ m, more preferably 3 to 1000 ⁇ m, still more preferably 10 ⁇ m to 200 ⁇ m, and particularly preferably 14 ⁇ m to 200 ⁇ m. It is.
- the oriented polycrystalline sintered body The sintered particle diameter of the particles constituting the particles is preferably 10 ⁇ m to 100 ⁇ m, more preferably 14 ⁇ m to 70 ⁇ m.
- the average grain size of the entire oriented polycrystalline sintered body has a correlation with the average grain size of the plate surface, and within these ranges, the sintered body is excellent in mechanical strength and easy to handle.
- the light-emitting functional layer is also excellent in light emission efficiency.
- grains in this invention is measured with the following method. That is, the plate surface of the plate-like sintered body is polished and an image is taken with a scanning electron microscope.
- the visual field range is a visual field range in which a straight line intersecting 10 to 30 particles can be drawn when a straight line is drawn on the diagonal line of the obtained image. Two straight lines are drawn on the diagonal line of the obtained image, and the value obtained by multiplying the average of the length of the inner line segment of each particle by 1.5 for all the particles that intersect the line.
- the average particle size of is performed after performing a process of making the interface stand out by thermal etching (for example, 1550 ° C. for 45 minutes) or chemical etching. You may go.
- a particularly preferred oriented polycrystalline sintered body is an oriented polycrystalline alumina sintered body.
- Alumina is aluminum oxide (Al 2 O 3 ), which is typically ⁇ -alumina having the same corundum type structure as single crystal sapphire, and the oriented polycrystalline alumina sintered body has innumerable alumina crystal particles oriented. Solids that are bonded together by sintering.
- the alumina crystal particles are particles composed of alumina, and may include a dopant and inevitable impurities as other elements, or may be composed of alumina and inevitable impurities.
- the oriented polycrystalline alumina sintered body may contain an additive as a sintering aid as a grain boundary phase.
- the oriented polycrystalline alumina sintered body may also contain other phases or other elements as described above in addition to the alumina crystal particles, but preferably comprises alumina crystal particles and inevitable impurities.
- the orientation plane of the oriented polycrystalline alumina sintered body is not particularly limited, and may be a c-plane, a-plane, r-plane, m-plane, or the like.
- the oriented crystal orientation of the oriented polycrystalline alumina sintered body is not particularly limited and may be a c-plane, a-plane, r-plane, m-plane, etc., from the viewpoint of lattice constant matching with a gallium nitride free-standing substrate. It is preferably oriented in the c-plane.
- the degree of orientation on the plate surface is preferably 50% or more, more preferably 65% or more, still more preferably 75% or more, particularly preferably 85%, and particularly preferably. 90% or more, and most preferably 95% or more.
- This degree of orientation is calculated by the following formula by measuring the XRD profile when X-rays are irradiated to the plate surface of plate-like alumina using an XRD apparatus (for example, RINT-TTR III, manufactured by Rigaku Corporation). It is obtained by doing.
- the crystallinity of the constituent particles of the gallium nitride free-standing substrate tends to be high, and the density of defects such as dislocations can be kept low.
- the gallium nitride free-standing substrate can even be preferably used as compared with the gallium nitride single crystal substrate in certain applications such as a light emitting device.
- the functional layer grows substantially following the underlying gallium nitride free-standing substrate and becomes an aggregate of columnar structures.
- one of the particles constituting the outermost surface of the oriented polycrystalline sintered body serving as a base substrate is used. It is more preferable that all or all of the portions are arranged in a form that is slightly inclined slightly from a certain orientation (for example, a reference orientation such as c-plane or a-plane).
- the inclined particles may be inclined almost entirely or in a certain amount at a substantially constant angle, or at various angles having a distribution within a certain range (preferably 0.01 to 20 °) and / or various. It may be inclined in any direction.
- inclined particles and non-inclined particles may be mixed in a desired ratio.
- the plate surface of the oriented polycrystalline alumina sintered body may be polished obliquely with respect to the reference surface, and the exposed surface of the particles may be inclined in a certain direction, or the surface of the particles on the outermost surface may be processed into a wavy shape or the like. A surface slightly inclined from the reference orientation may be exposed.
- some or all of the alumina single crystal particles constituting the outermost surface of the oriented polycrystalline alumina sintered body oriented in the reference orientation such as the c-plane, a-plane, etc. have their reference orientation determined by the substrate method. It is preferable to be arranged so as to be inclined so as to be displaced within a range of 0.5 to 20 ° from the line direction.
- An oriented polycrystalline alumina sintered body can be produced by molding and sintering using a plate-like alumina powder as a raw material.
- Plate-like alumina powder is commercially available and is commercially available.
- the type and shape of the plate-like alumina powder are not particularly limited as long as a dense oriented polycrystalline alumina sintered body can be obtained, but the average particle diameter may be 0.4 to 15 ⁇ m and the thickness may be 0.05 to 1 ⁇ m. It is good also as what mixed 2 or more types of raw materials of different average particle diameter.
- the plate-like alumina powder can be oriented by a technique using shearing force to obtain an oriented molded body.
- the technique using shearing force include tape molding, extrusion molding, doctor blade method, and any combination thereof.
- the orientation method using the shearing force is made into a slurry by appropriately adding additives such as a binder, a plasticizer, a dispersing agent, and a dispersion medium to the plate-like alumina powder. It is preferable to discharge and form the sheet on the substrate by passing through a thin discharge port.
- the slit width of the discharge port is preferably 10 to 400 ⁇ m.
- the amount of the dispersion medium is preferably such that the slurry viscosity is 5000 to 100,000 cP, more preferably 20000 to 60000 cP.
- the thickness of the oriented molded body formed into a sheet is preferably 5 to 500 ⁇ m, more preferably 10 to 200 ⁇ m. It is preferable to stack a large number of oriented molded bodies formed in this sheet shape to form a precursor laminate having a desired thickness, and press-mold the precursor laminate.
- This press molding can be preferably performed by isostatic pressing at a pressure of 10 to 2000 kgf / cm 2 in warm water at 50 to 95 ° C. by packaging the precursor laminate with a vacuum pack or the like.
- the sheet-shaped molded body is integrated and laminated in the mold after passing through a narrow discharge port in the mold due to the design of the flow path in the mold.
- the molded body may be discharged.
- the obtained molded body is preferably degreased according to known conditions.
- the oriented molded body obtained as described above is subjected to hot isostatic pressing (HIP), hot pressing (HP ), A pressure sintering method such as spark plasma sintering (SPS), and a combination thereof, and an alumina sintered body comprising oriented alumina crystal particles is formed.
- the firing temperature and firing time in the firing vary depending on the firing method
- the firing temperature is 1000 to 1950 ° C., preferably 1100 to 1900 ° C., more preferably 1500 to 1800 ° C.
- the firing time is 1 minute to 10 hours, preferably 30 minutes to 5 hours.
- a first firing step of firing at 1500 to 1800 ° C. for 2 to 5 hours under a surface pressure of 100 to 200 kgf / cm 2 in a hot press, More preferably, it is carried out through a second firing step in which firing is performed again at 1500 to 1800 ° C. for 30 minutes to 5 hours under a gas pressure of 1000 to 2000 kgf / cm 2 by an isotropic pressure method (HIP).
- HIP isotropic pressure method
- the firing time at the above-mentioned firing temperature is not particularly limited, but is preferably 1 to 10 hours, and more preferably 2 to 5 hours.
- a method is used in which a high-purity plate-like alumina powder is used as a raw material and calcined at 1100 to 1800 ° C. for 1 minute to 10 hours in an air furnace, a hydrogen atmosphere furnace, a nitrogen atmosphere furnace or the like. Is preferably exemplified.
- the obtained sintered body is again subjected to hot isostatic pressing (HIP) at 1200 to 1400 ° C. or 1400 to 1950 ° C. for 30 minutes to 5 hours under a gas pressure of 300 to 2000 kgf / cm 2.
- a method of firing may be used.
- the plate-like alumina powder is preferably highly pure, more preferably 98% or more, further preferably 99% or more, particularly preferably 99.9% or more, most preferably Preferably it is 99.99% or more.
- the firing conditions are not limited to the above.
- the second firing step by hot isostatic pressing (HIP) may be omitted as long as both densification and high orientation are possible.
- a very small amount of additives may be added to the raw material as a sintering aid. Although the addition of the sintering aid goes against the reduction of the grain boundary phase, the purpose is to improve the translucency as a result by reducing pores, which is one of the light scattering factors.
- oxides such as MgO, ZrO 2 , Y 2 O 3 , CaO, SiO 2 , TiO 2 , Fe 2 O 3 , Mn 2 O 3 , La 2 O 3 , AlF 3 , MgF 2 and at least one selected from fluorides such as YbF 3 .
- MgO, CaO, SiO 2 and La 2 O 3 are preferred, and MgO is particularly preferred.
- the amount of additive should be kept to a minimum, preferably 5000 ppm or less, more preferably 1000 ppm or less, and even more preferably 700 ppm or less.
- An oriented polycrystalline alumina sintered body can also be produced by molding and sintering using a mixed powder obtained by appropriately adding a plate-like alumina powder to a fine alumina powder and / or a transition alumina powder. it can.
- the plate-like alumina powder becomes a seed crystal (template)
- the fine alumina powder and / or the transition alumina powder becomes a matrix
- the template undergoes a so-called TGG (Tempered Grain Growth) process in which homoepitaxial growth is performed while incorporating the matrix. This causes crystal growth and densification.
- TGG Tempored Grain Growth
- the average particle size of the template is 0.5 to 15 ⁇ m
- the average particle size of the matrix is 0.4 ⁇ m or less. Is preferably 0.2 ⁇ m or less, and more preferably 0.1 ⁇ m or less.
- the mixing ratio of the template and matrix varies depending on the particle size ratio, firing conditions, and the presence or absence of additives. For example, a plate-like alumina powder with an average particle size of 2 ⁇ m is used as the template, and a fine alumina powder with an average particle size of 0.1 ⁇ m is used as the matrix In such a case, the template / matrix ratio may be 50/50 to 1/99 wt%.
- oxides such as MgO, ZrO 2 , Y 2 O 3 , CaO, SiO 2 , TiO 2 , Fe 2 O 3 , Mn 2 O 3 , and La 2 O 3 are used as sintering aids.
- fluorides such as AlF 3 , MgF 2 and YbF 3 may be added, MgO, CaO, SiO 2 and La 2 O 3 are preferable, and MgO is particularly preferable.
- a high-quality oriented polycrystalline alumina sintered body can be obtained by a pressure sintering method such as sintering (SPS) or a combination thereof.
- a pressure sintering method such as sintering (SPS) or a combination thereof.
- the alumina sintered body thus obtained becomes a polycrystalline alumina sintered body oriented in a desired plane such as the c-plane depending on the kind of the plate-like alumina powder used as the raw material. It is preferable that the oriented polycrystalline alumina sintered body thus obtained is ground with a grindstone to flatten the plate surface, and then the plate surface is smoothed by lapping using diamond abrasive grains to obtain an oriented alumina substrate.
- a seed crystal layer made of gallium nitride is formed on the oriented polycrystalline sintered body so as to have a crystal orientation that substantially follows the crystal orientation of the oriented polycrystalline sintered body.
- Forming so as to have a crystal orientation generally following the crystal orientation of the oriented polycrystalline sintered body means that the structure is brought about by crystal growth affected by the crystal orientation of the oriented polycrystalline sintered body. This means that the structure does not necessarily grow completely following the crystal orientation of the oriented polycrystalline sintered body, but also includes a structure that grows in a different crystal orientation from the oriented polycrystalline sintered body.
- the method for producing the seed crystal layer is not particularly limited, but MOCVD (metal organic vapor phase epitaxy), MBE (molecular beam epitaxy), HVPE (halide vapor phase epitaxy), gas phase methods such as sputtering, Na flux method, Preferred examples include liquid phase methods such as ammonothermal method, hydrothermal method, sol-gel method, powder method utilizing solid phase growth of powder, and combinations thereof.
- MOCVD metal organic vapor phase epitaxy
- MBE molecular beam epitaxy
- HVPE halide vapor phase epitaxy
- gas phase methods such as sputtering, Na flux method
- liquid phase methods such as ammonothermal method, hydrothermal method, sol-gel method, powder method utilizing solid phase growth of powder, and combinations thereof.
- the formation of a seed crystal layer by MOCVD is performed by depositing a 20 to 50 nm low-temperature GaN layer at 450 to 550 ° C. and then laminating a GaN film having a
- a melt composition containing a dopant or a p-type dopant such as beryllium (Be), magnesium (Mg), calcium (Ca), strontium (Sr), zinc (Zn), cadmium (Cd), etc.
- a nitrogen atmosphere Among them, it is preferable to carry out the heating and pressurizing to 830 to 910 ° C. and 3.5 to 4.5 MPa, and then rotating while maintaining the temperature and pressure.
- the holding time varies depending on the target film thickness, but may be about 10 to 100 hours.
- the gallium nitride crystal thus obtained by the Na flux method is ground with a grindstone to flatten the plate surface, and then the plate surface is smoothed by lapping using diamond abrasive grains.
- the oriented polycrystalline sintered body can be removed to obtain a gallium nitride free-standing substrate.
- the method for removing the oriented polycrystalline sintered body is not particularly limited, but is spontaneous, utilizing grinding, chemical etching, interfacial heating (laser lift-off) by laser irradiation from the oriented sintered body side, and thermal expansion difference during temperature rise Exfoliation and the like.
- a high-quality light-emitting element can be manufactured using the above-described gallium nitride free-standing substrate according to the present invention.
- a light-emitting element is manufactured by providing a light-emitting functional layer on a gallium nitride free-standing substrate, and the light-emitting functional layer is formed so that the crystal orientation approximately follows the crystal orientation of the gallium nitride substrate. It is preferable to form one or more layers composed of a plurality of semiconductor single crystal particles having a single crystal structure in the normal direction.
- a light-emitting element may be manufactured using a gallium nitride free-standing substrate as a member or layer other than a substrate such as an electrode (which may be a p-type electrode or an n-type electrode), a p-type layer, or an n-type layer.
- the element size is not particularly limited, and may be a small element of 5 mm ⁇ 5 mm or less, or a surface light emitting element of 10 cm ⁇ 10 cm or more.
- FIG. 1 schematically shows a layer structure of a light-emitting element according to one embodiment of the present invention.
- a light-emitting element 10 shown in FIG. 1 includes a gallium nitride free-standing substrate 12 and a light-emitting functional layer 14 formed on the substrate.
- the light emitting functional layer 14 has one or more layers composed of a plurality of semiconductor single crystal particles having a single crystal structure in a substantially normal direction.
- the light-emitting functional layer 14 emits light based on the principle of a light-emitting element such as an LED by appropriately providing electrodes and applying a voltage.
- gallium nitride free-standing substrate 12 of the present invention it can be expected to obtain a light-emitting element having a light emission efficiency equivalent to that when a gallium nitride single crystal substrate is used, and a significant cost reduction can be realized.
- gallium nitride imparted with conductivity by introducing a p-type or n-type dopant as a substrate, a light-emitting element having a vertical structure can be realized, whereby luminance can be increased.
- a large area surface light emitting device can be realized at low cost.
- a light emitting functional layer 14 is formed on the substrate 12.
- the light emitting functional layer 14 may be provided on the entire surface or a part of the substrate 12, or may be provided on the entire surface or a part of the buffer layer when a buffer layer described later is formed on the substrate 12. Good.
- the light-emitting functional layer 14 has one or more layers composed of a plurality of semiconductor single crystal particles having a single crystal structure in a substantially normal direction, and is appropriately provided with electrodes and / or phosphors to apply a voltage. Therefore, it is possible to adopt various known layer configurations that cause light emission based on the principle of a light emitting element typified by an LED. Therefore, the light emitting functional layer 14 may emit visible light such as blue and red, or may emit ultraviolet light without visible light or with visible light.
- the light emitting functional layer 14 preferably constitutes at least a part of a light emitting element using a pn junction, and the pn junction includes a p-type layer 14a and an n-type layer 14c as shown in FIG.
- the active layer 14b may be included in between.
- a double heterojunction or a single heterojunction (hereinafter collectively referred to as a heterojunction) using a layer having a smaller band gap than the p-type layer and / or the n-type layer as the active layer may be used.
- a quantum well structure in which the active layer is thin can be adopted as one form of the p-type layer-active layer-n-type layer.
- the light emitting functional layer 14 preferably includes a pn junction and / or a heterojunction and / or a quantum well junction having a light emitting function.
- At least one layer constituting the light emitting functional layer 14 is at least selected from the group consisting of an n-type layer doped with an n-type dopant, a p-type layer doped with a p-type dopant, and an active layer.
- an n-type layer, the p-type layer, and the active layer may be composed of the same material as the main component, or may be composed of materials whose main components are different from each other.
- each layer constituting the light emitting functional layer 14 is not particularly limited as long as it grows substantially following the crystal orientation of the gallium nitride free-standing substrate and has a light emitting function, but gallium nitride (GaN) based material, zinc oxide ( It is preferably composed of a material mainly composed of at least one selected from a ZnO) -based material and an aluminum nitride (AlN) -based material, and appropriately contains a dopant for controlling p-type or n-type. It may be.
- a particularly preferable material is a gallium nitride (GaN) -based material, which is the same material as the gallium nitride free-standing substrate.
- the material constituting the light emitting functional layer 14 may be a mixed crystal in which, for example, AlN, InN or the like is dissolved in GaN in order to control the band gap.
- the light emitting functional layer 14 may be a heterojunction made of a plurality of types of materials. For example, a gallium nitride (GaN) -based material may be used for the p-type layer, and a zinc oxide (ZnO) -based material may be used for the n-type layer.
- GaN gallium nitride
- ZnO zinc oxide
- a structure grown substantially following the crystal orientation of a gallium nitride free-standing substrate means a structure brought about by crystal growth affected by the crystal orientation of the gallium nitride free-standing substrate, and is not necessarily a crystal of the gallium nitride free-standing substrate.
- the structure does not necessarily grow perfectly following the orientation, and may be a structure grown somewhat following the crystal orientation of the gallium nitride free-standing substrate as long as a desired light emitting function can be secured. That is, this structure includes a structure that grows in a different crystal orientation from the oriented polycrystalline sintered body. In that sense, the expression “a structure grown substantially following the crystal orientation” can be rephrased as “a structure grown substantially derived from the crystal orientation”.
- crystal growth is preferably by epitaxial growth, it is not limited to this, and various forms of crystal growth similar thereto may be used.
- the crystal in the substantially normal direction is also observed in each layer of the light emitting functional layer from the gallium nitride free-standing substrate.
- a structure in which the orientation is substantially uniform can be obtained, and good light emission characteristics can be obtained. That is, when the light emitting functional layer 14 also grows substantially following the crystal orientation of the gallium nitride free-standing substrate 12, the orientation is substantially constant in the vertical direction of the substrate.
- the normal direction is the same as that of a single crystal, and when a gallium nitride free-standing substrate to which an n-type dopant is added is used, a light-emitting element having a vertical structure using the gallium nitride free-standing substrate as a cathode can be obtained.
- a gallium nitride free-standing substrate to which a p-type dopant is added is used, a vertical structure light-emitting element using the gallium nitride free-standing substrate as an anode can be obtained.
- each layer only needs to have a structure grown to some extent along the crystal orientation of the gallium nitride free-standing substrate, and does not necessarily have a columnar structure in a strict sense.
- the cause of the columnar structure is considered to be that the semiconductor single crystal particles grow under the influence of the crystal orientation of the gallium nitride free-standing substrate as the substrate 12 as described above.
- the average particle diameter of the cross section of the semiconductor single crystal particles which can be said to be a columnar structure (hereinafter referred to as the average cross section diameter), depends not only on the film formation conditions but also on the average particle diameter of the plate surface of the gallium nitride free-standing substrate. Conceivable.
- the interface of the columnar structure constituting the light emitting functional layer affects the light emission efficiency and the light emission wavelength, but due to the presence of the grain boundary, the light transmittance in the cross-sectional direction is poor, and the light is scattered or reflected. For this reason, in the case of a structure in which light is extracted in the normal direction, an effect of increasing the luminance due to scattered light from the grain boundary is also expected.
- the cross-sectional average diameter of the columnar structure is larger.
- the cross-sectional average diameter of the semiconductor single crystal particles on the outermost surface of the light emitting functional layer 14 is 0.3 ⁇ m or more, more preferably 3 ⁇ m or more, still more preferably 20 ⁇ m or more, particularly preferably 50 ⁇ m or more, and most preferably 70 ⁇ m or more. It is.
- a buffer layer for suppressing the reaction is provided between the gallium nitride free-standing substrate 12 and the light emitting functional layer 14. Also good.
- the main component of such a buffer layer is not particularly limited, but it is preferably composed of a material mainly containing at least one selected from a zinc oxide (ZnO) -based material and an aluminum nitride (AlN) -based material. , A dopant for controlling p-type to n-type may be included as appropriate.
- Each layer constituting the light emitting functional layer 14 is preferably made of a gallium nitride material.
- a gallium nitride material For example, an n-type gallium nitride layer and a p-type gallium nitride layer may be grown in order on the gallium nitride free-standing substrate 12, and the stacking order of the p-type gallium nitride layer and the n-type gallium nitride layer may be reversed.
- the p-type dopant used for the p-type gallium nitride layer include a group consisting of beryllium (Be), magnesium (Mg), calcium (Ca), strontium (Sr), zinc (Zn), and cadmium (Cd).
- n-type dopant used for the n-type gallium nitride layer at least one selected from the group consisting of silicon (Si), germanium (Ge), tin (Sn), and oxygen (O) is used.
- Si silicon
- Ge germanium
- Sn tin
- O oxygen
- the p-type gallium nitride layer and / or the n-type gallium nitride layer may be made of gallium nitride mixed with one or more kinds of crystals selected from the group consisting of AlN and InN.
- the mixed gallium nitride may be doped with a p-type dopant or an n-type dopant.
- a p-type dopant for example, Al x Ga 1-x N, which is a mixed crystal of gallium nitride and AlN, is used as a p-type layer by doping Mg, and Al x Ga 1-x N is used as an n-type layer by doping Si. be able to.
- gallium nitride is mixed with AlN, the band gap is widened, and the emission wavelength can be shifted to a higher energy side.
- the active layer may be made of a mixed crystal of GaN having one or more selected from the group consisting of GaN or AlN and InN having a smaller band gap than either one of the two layers. Even in such a single heterojunction, the luminous efficiency can be further increased.
- the gallium nitride buffer layer may be made of non-doped GaN, n-type or p-type doped GaN, and selected from the group consisting of AlN, InN, or GaN, AlN, and InN having a close lattice constant. It may be mixed with one or more kinds of crystals.
- the light emitting functional layer 14 may be composed of a plurality of material systems selected from gallium nitride (GaN) -based materials, zinc oxide (ZnO) -based materials, and aluminum nitride (AlN) -based materials.
- GaN gallium nitride
- ZnO zinc oxide
- AlN aluminum nitride
- a p-type gallium nitride layer and an n-type zinc oxide layer may be grown on the gallium nitride free-standing substrate 12, and the stacking order of the p-type gallium nitride layer and the n-type zinc oxide layer may be reversed.
- an n-type or p-type zinc oxide layer may be formed.
- Preferable examples of the p-type dopant used for the p-type zinc oxide layer include nitrogen (N), phosphorus (P), arsenic (As), carbon (C), lithium (Li), sodium (Na), potassium ( K), one or more selected from the group consisting of silver (Ag) and copper (Cu).
- Preferred examples of the n-type dopant used for the n-type zinc oxide layer include aluminum (Al), gallium (Ga), indium (In), boron (B), fluorine (F), chlorine (Cl), One or more selected from the group consisting of bromine (Br), iodine (I), and silicon (Si) may be mentioned.
- the film formation method of the light emitting functional layer 14 and the buffer layer is not particularly limited as long as it grows substantially following the crystal orientation of the gallium nitride free-standing substrate, but a vapor phase method such as MOCVD, MBE, HVPE, sputtering, Na flux, etc.
- a vapor phase method such as MOCVD, MBE, HVPE, sputtering, Na flux, etc.
- Preferred examples include a liquid phase method such as a method, an ammonothermal method, a hydrothermal method, a sol-gel method, a powder method utilizing solid phase growth of powder, and a combination thereof.
- a gas for example, ammonia
- an organometallic gas for example, trimethyl gallium
- gallium (Ga) and nitrogen (N) On the substrate as a raw material and grown in a temperature range of about 300 to 1200 ° C. in an atmosphere containing hydrogen, nitrogen, or both.
- organometallic gases containing indium (In), aluminum (Al), silicon (Si) and magnesium (Mg) as n-type and p-type dopants for example, trimethylindium, trimethylaluminum, monosilane, disilane) Bis-cyclopentadienylmagnesium
- n-type and p-type dopants for example, trimethylindium, trimethylaluminum, monosilane, disilane
- Bis-cyclopentadienylmagnesium may be appropriately introduced to form a film.
- a seed crystal layer may be formed on the gallium nitride free-standing substrate.
- any method may be used as long as it promotes crystal growth substantially following the crystal orientation.
- a zinc oxide-based material is used for a part or all of the light emitting functional layer 14
- an ultrathin zinc oxide seed crystal is prepared by vapor phase growth methods such as MOCVD, MBE, HVPE, and sputtering. May be.
- the electrode layer 16 and / or the phosphor layer may be further provided on the light emitting functional layer 14.
- an electrode layer 18 is provided on the back surface of the gallium nitride free-standing substrate 12 as shown in FIG.
- the gallium nitride free-standing substrate 12 may be used as the electrode itself. In that case, it is preferable that an n-type dopant is added to the gallium nitride free-standing substrate 12.
- the electrode layers 16 and 18 may be made of a known electrode material.
- the electrode layer 16 on the light emitting functional layer 14 is a transparent conductive film such as ITO, or a metal electrode having a high aperture ratio such as a lattice structure, This is preferable in that the extraction efficiency of light generated in the light emitting functional layer 14 can be increased.
- a phosphor layer for converting ultraviolet light into visible light may be provided outside the electrode layer.
- the phosphor layer is not particularly limited as long as it includes a known fluorescent component capable of converting ultraviolet light into visible light.
- a fluorescent component that emits blue light when excited by ultraviolet light, a fluorescent component that emits blue to green light when excited by ultraviolet light, and a fluorescent component that emits red light when excited by ultraviolet light are mixed. It is preferable that the white color is obtained as a mixed color.
- Preferred combinations of such fluorescent components include (Ca, Sr) 5 (PO 4 ) 3 Cl: Eu, BaMgAl 10 O 17 : Eu, and Mn, Y 2 O 3 S: Eu, and these components Is preferably dispersed in a resin such as a silicone resin to form a phosphor layer.
- a fluorescent component is not limited to the above-exemplified substances, but may be a combination of other ultraviolet light-excited phosphors such as yttrium aluminum garnet (YAG), silicate phosphors, and oxynitride phosphors. .
- a phosphor layer for converting blue light into yellow light may be provided outside the electrode layer.
- the phosphor layer is not particularly limited as long as it includes a known fluorescent component capable of converting blue light into yellow light. For example, it may be combined with a phosphor emitting yellow light such as YAG. By doing in this way, since blue light emission which permeate
- the phosphor layer includes both a fluorescent component that converts blue light into yellow and a fluorescent component that converts ultraviolet light into visible light, thereby converting ultraviolet light into visible light and blue light yellow. It is good also as a structure which performs both conversion to light.
- gallium nitride self-supporting substrate of the present invention can be preferably used for various applications such as various electronic devices, power devices, light receiving elements, solar cell wafers as well as the above-described light emitting elements.
- Example 1 Production of c-plane oriented alumina sintered body As a raw material, a plate-like alumina powder (manufactured by Kinsei Matech Co., Ltd., grade 0700) was prepared. 7 parts by weight of a binder (polyvinyl butyral: product number BM-2, manufactured by Sekisui Chemical Co., Ltd.) and a plasticizer (DOP: di (2-ethylhexyl) phthalate, Kurokin Kasei Co., Ltd.) per 100 parts by weight of the plate-like alumina particles 3.5 parts by weight), 2 parts by weight of a dispersant (Rheidol SP-O30, manufactured by Kao Corporation), and a dispersion medium (2-ethylhexanol) were mixed.
- a binder polyvinyl butyral: product number BM-2, manufactured by Sekisui Chemical Co., Ltd.
- DOP di (2-ethylhexyl)
- the amount of the dispersion medium was adjusted so that the slurry viscosity was 20000 cP.
- the slurry prepared as described above was formed into a sheet shape on a PET film by a doctor blade method so that the thickness after drying was 20 ⁇ m.
- the obtained tape was cut into a circular shape having a diameter of 50.8 mm (2 inches), 150 sheets were laminated, placed on an Al plate having a thickness of 10 mm, and then vacuum-packed. This vacuum pack was hydrostatically pressed in warm water at 85 ° C. at a pressure of 100 kgf / cm 2 to obtain a disk-shaped molded body.
- the obtained molded body was placed in a degreasing furnace and degreased at 600 ° C. for 10 hours.
- the obtained degreased body was fired in a nitrogen atmosphere at 1600 ° C. for 4 hours under a surface pressure of 200 kgf / cm 2 using a graphite mold.
- the obtained sintered body was fired again at 1700 ° C. for 2 hours in argon at a gas pressure of 1500 kgf / cm 2 by a hot one-pressure method (HIP).
- HIP hot one-pressure method
- the sintered body thus obtained was fixed to a ceramic surface plate and ground to # 2000 using a grindstone to flatten the plate surface.
- the surface of the plate was smoothed by lapping using diamond abrasive grains, and an oriented alumina sintered body having a diameter of 50.8 mm (2 inches) and a thickness of 1 mm was obtained as an oriented alumina substrate.
- the flatness was improved while gradually reducing the size of the abrasive grains from 3 ⁇ m to 0.5 ⁇ m.
- the average roughness Ra after processing was 1 nm.
- the average particle diameter of the plate surface was measured with the following method.
- the plate surface of the obtained oriented alumina substrate was polished and subjected to thermal etching at 1550 ° C. for 45 minutes, and then an image was taken with a scanning electron microscope.
- the visual field range was such that a straight line intersecting 10 to 30 particles could be drawn when a straight line was drawn on the diagonal line of the obtained image.
- the average particle size of the plate surface was 100 ⁇ m.
- a seed crystal layer was formed on the processed oriented alumina substrate by MOCVD. Specifically, after depositing a low-temperature GaN layer of 40 nm at 530 ° C., a GaN film having a thickness of 3 ⁇ m was laminated at 1050 ° C. to obtain a seed crystal substrate.
- volume resistivity The in-plane volume resistivity of the gallium nitride free-standing substrate was measured using a Hall effect measuring device. As a result, the volume resistivity was 1 ⁇ 10 ⁇ 2 ⁇ ⁇ cm.
- the visual field range was such that a straight line intersecting with 10 to 30 columnar structures could be drawn when a straight line was drawn on the diagonal line of the obtained image.
- Two straight lines are arbitrarily drawn on the diagonal line of the obtained image, and the value obtained by multiplying the average length of the line segments inside each particle by 1.5 for all the particles intersecting the straight line,
- the average cross-sectional diameter of the single crystal particles on the outermost surface of the light emitting functional layer was used. As a result, the average cross-sectional diameter was about 100 ⁇ m.
- a Ni / Au film was patterned on the p-type layer as a light-transmitting anode electrode to a thickness of 6 nm and 12 nm, respectively. Thereafter, a heat treatment at 500 ° C. was performed for 30 seconds in a nitrogen atmosphere in order to improve the ohmic contact characteristics. Further, by using a photolithography process and a vacuum deposition method, a Ni / Au film serving as an anode electrode pad is formed to a thickness of 5 nm and 60 nm on a partial region of the upper surface of the Ni / Au film serving as a light-transmitting anode electrode, respectively. Patterned. The wafer thus obtained was cut into chips and further mounted on a lead frame to obtain a light emitting device having a vertical structure.
- an Mg-doped gallium nitride crystal was grown on the entire surface of a 50.8 mm (2 inch) seed crystal substrate, and the thickness of the crystal was about 0.5 mm. Cracks were not confirmed. Moreover, Mg density
- the oriented alumina substrate portion of the sample thus obtained was removed by grinding with a grindstone to obtain a simple Mg-doped gallium nitride.
- the plate surface of this Mg-doped gallium nitride crystal is ground with a # 600 and # 2000 grindstone to flatten the plate surface, and then smoothed by lapping using diamond abrasive grains, and a Mg surface having a thickness of about 150 ⁇ m.
- a doped gallium nitride free-standing substrate was obtained.
- the flatness was improved while gradually reducing the size of the abrasive grains from 3 ⁇ m to 0.1 ⁇ m.
- the average roughness Ra after processing of the surface of the Mg-doped gallium nitride free-standing substrate was 0.2 nm.
- the cross-sectional average diameter of the Mg-doped gallium nitride free-standing substrate was measured by the same method as in Example 1 (3b), the cross-sectional average diameter was about 100 ⁇ m.
- a gallium nitride free-standing substrate on which a seed crystal layer was formed was suspended and placed in 1 liter in an aqueous solution for growth.
- a waterproof ceramic heater and a magnetic stirrer were placed in an aqueous solution, placed in an autoclave and subjected to hydrothermal treatment at 270 ° C. for 3 hours to deposit a ZnO layer on the seed crystal layer.
- the gallium nitride free-standing substrate on which the ZnO layer was deposited was washed with pure water and then annealed at 500 ° C. in the atmosphere to form an n-ZnO layer doped with Al having a thickness of about 3 ⁇ m.
- the cross-sectional average diameter of the light emitting functional layer was about 100 ⁇ m.
- Example 3 (1) Fabrication of light-emitting device using Mg-doped gallium nitride free-standing substrate (1a) Formation of active layer by RS-MBE method Mg-doped gallium nitride free-standing substrate by the same method as (2) in Example 2 And p-GaN was added to the substrate as a p-type layer at a volume of 200 nm. Next, using a RS-MBE (radical source molecular beam growth) apparatus, zinc (Zn) and cadmium (Cd), which are metal materials, were irradiated with a Knudsen cell and supplied onto the p-type layer.
- RS-MBE radio source molecular beam growth
- Oxygen (O) which is a gas material, was supplied as oxygen radicals using O 2 gas as a raw material in an RF radical generator.
- the purity of various raw materials was Zn, Cd 7N, and O 2 6N.
- the substrate was heated to 700 ° C. using a resistance heater, and an active layer having a thickness of 1.5 nm was formed while controlling the flux of various gas sources so as to be a Cd 0.2 Zn 0.8 O layer.
- a Ni / Au film having a thickness of 5 nm and 100 nm is formed as an anode electrode on the surface opposite to the p-GaN layer and the n-ZnO layer of the gallium nitride free-standing substrate, respectively. Patterned. Thereafter, a heat treatment at 500 ° C. was performed for 30 seconds in a nitrogen atmosphere in order to improve the ohmic contact characteristics. The wafer thus obtained was cut into chips and further mounted on a lead frame to obtain a light emitting device having a vertical structure.
- Example 4 Preparation of c-plane oriented alumina sintered body A disk-shaped molded body was obtained in the same manner as in Example 1 (1). The obtained molded body was placed in a degreasing furnace and degreased at 600 ° C. for 10 hours. The obtained degreased body was fired in a nitrogen atmosphere at 1700 ° C. for 4 hours under a surface pressure of 200 kgf / cm 2 using a graphite mold.
- the sintered body thus obtained was fixed to a ceramic surface plate and ground to # 2000 using a grindstone to flatten the plate surface.
- the surface of the plate was smoothed by lapping using diamond abrasive grains, and an oriented alumina sintered body having a diameter of 50.8 mm (2 inches) and a thickness of 1 mm was obtained as an oriented alumina substrate.
- the flatness was improved while gradually reducing the size of the abrasive grains from 3 ⁇ m to 0.5 ⁇ m.
- the average roughness Ra after processing was 4 nm.
- the c-plane orientation degree and the average grain size of the plate surface were evaluated in the same manner as in Example 1, the c-plane orientation degree was 99% and the average grain size was 18 ⁇ m.
- a seed crystal substrate was produced by laminating a GaN film having a thickness of 3 ⁇ m on an oriented alumina substrate in the same manner as in (1a) of Example 1. On this seed crystal substrate, a Ge-doped GaN film was formed in the same manner as (3b) of Example 1 except that the holding time was 20 hours. In the obtained sample, a Ge-doped gallium nitride crystal was grown on the entire surface of a 50.8 mm (2 inch) seed crystal substrate, and the thickness of the crystal was about 0.2 mm. Cracks were not confirmed.
- the plate surface (surface) of the Ge-doped gallium nitride crystal of the sample thus obtained was ground and flattened using a # 600 and # 2000 grindstone until the thickness of the gallium nitride crystal was about 50 ⁇ m, and then diamond abrasive grains The plate surface was smoothed by lapping using.
- the sample was cut to expose a surface perpendicular to the plate surface, polished using a CP polishing machine (IB-09010CP, manufactured by JEOL Ltd.), and then backscattered with an electron beam (EBSD) (EBSD) ( Reverse pole figure orientation mapping of the cross section of the gallium nitride crystal was performed by TSL Solutions.
- FIG. 2 shows the reverse pole figure orientation mapping.
- FIG. 2 shows the reverse pole figure orientation mapping. Also, FIG.
- FIG. 3 shows a reverse pole figure orientation mapping measured on the plate surface (surface) of the gallium nitride crystal
- FIG. 4 shows a crystal grain mapping image in which the interface between the oriented alumina substrate and the gallium nitride crystal is enlarged.
- the gallium nitride crystal has a larger particle size on the surface side (the side opposite to the oriented alumina substrate) than the oriented alumina substrate side, and the shape of the gallium nitride crystal is not a perfect columnar shape such as a trapezoid or a triangle on the cross-sectional image. I understand that. Further, it can be seen that there are particles that grow as the film thickness increases and grow to the surface, and particles that do not grow to the surface.
- FIG. 1 shows a reverse pole figure orientation mapping measured on the plate surface (surface) of the gallium nitride crystal
- FIG. 4 shows a crystal grain mapping image in which the interface between the oriented alumina substrate and the gallium nitride
- FIG. 3 shows that the c-plane of each particle constituting the gallium nitride crystal is generally oriented in the normal direction.
- FIG. 4 shows that the gallium nitride crystal particles grow from the crystal particles constituting the oriented alumina substrate as the base.
- the cause of the growth behavior in which the particle size increases as the film thickness increases is not clear, but as shown conceptually in FIG. 5, the growth is performed by covering the slow-growing particles with the fast-growing particles. It is thought that this is because of progress. Therefore, among the gallium nitride particles that make up the gallium nitride crystal, the particles exposed on the front side communicate with the back surface without going through the grain boundary, but some of the particles exposed on the back side grow on the way. This includes those that stopped.
- the oriented alumina substrate portion of the sample was removed by grinding with a grindstone to obtain a Ge-doped gallium nitride simple substance.
- the back surface of the Ge-doped gallium nitride crystal (the surface on the side in contact with the oriented alumina substrate) was lapped with diamond abrasive grains, and the plate surface (the side opposite to the side in contact with the oriented alumina substrate) and the back surface (oriented alumina)
- a gallium nitride free-standing substrate having a smoothed surface on the side in contact with the substrate was obtained.
- the average roughness Ra after processing of the front surface and the back surface of the gallium nitride free-standing substrate was 0.2 nm.
- the volume resistivity was 1 ⁇ 10 ⁇ 2 ⁇ ⁇ cm.
- the cross-sectional average diameter of the GaN single crystal particles on the front and back surfaces of the gallium nitride free-standing substrate was measured using the same method as in Example 1 (3). The diameter was about 18 ⁇ m. Sectional average diameter in this way it is larger than the back side of the surface, the ratio D T / D B sectional average diameter D T of the substrate surface to its section average diameter D B of the substrate back surface was about 2.8.
- the aspect ratio of the GaN single crystal particles calculated as the ratio of the thickness of the GaN crystal to the average cross-sectional diameter of the surface was about 1.0.
- a free-standing substrate having a thickness of 20 ⁇ m was prepared by grinding the surface side of the free-standing gallium nitride substrate manufactured in the same manner as in the above (1) and (2).
- the cross-sectional average diameter of the single crystal particles on the outermost surface is about 35 ⁇ m
- the ratio D T / D B of the cross-sectional average diameter D T of the substrate surface to the cross-sectional average diameter D B of the back surface of the substrate is 1.9, and the aspect ratio was about 0.6.
- a binder polyvinyl butyral: product number BM-2, manufactured by Sekisui Chemical Co., Ltd.
- a plasticizer DOP: di (2-ethylhexyl) phthalate, black metal chemical stock
- a dispersant Rosui Chemical Co., Ltd.
- a dispersion medium a mixture of xylene and 1-butanol at a weight ratio of 1: 1
- the slurry prepared as described above was formed into a sheet shape on a PET film by a doctor blade method so that the thickness after drying was 100 ⁇ m.
- the obtained tape was cut into a circular shape having a diameter of 50.8 mm (2 inches), then laminated in 30 sheets, placed on an Al plate having a thickness of 10 mm, and then vacuum-packed. This vacuum pack was hydrostatically pressed in warm water at 85 ° C. at a pressure of 100 kgf / cm 2 to obtain a disk-shaped molded body.
- the obtained molded body was placed in a degreasing furnace and degreased at 600 ° C. for 10 hours.
- the obtained degreased body was fired in a nitrogen atmosphere at 1800 ° C. for 4 hours under a surface pressure of 200 kgf / cm 2 using a graphite mold.
- a seed crystal substrate was produced by laminating a GaN film having a thickness of 3 ⁇ m on an oriented alumina substrate in the same manner as in (1a) of Example 1. On this seed crystal substrate, a Ge-doped GaN film was formed in the same manner as (3b) of Example 1 except that the holding time was 30 hours. In the obtained sample, a Ge-doped gallium nitride crystal was grown on the entire surface of a 50.8 mm (2 inch) seed crystal substrate, and the thickness of the crystal was about 0.3 mm. Cracks were not confirmed.
- the plate surface (surface) of the Ge-doped gallium nitride crystal of the sample thus obtained was ground and flattened using a # 600 and # 2000 grindstone until the thickness of the gallium nitride crystal was about 180 ⁇ m, and then the diamond abrasive grains were The plate surface was smoothed by the lapping used.
- the sample was cut to expose a surface perpendicular to the plate surface, polished using a CP polishing machine (IB-09010CP, manufactured by JEOL Ltd.), and then backscattered with an electron beam (EBSD) (EBSD) ( Reverse pole figure orientation mapping of the cross section of the gallium nitride crystal was performed by TSL Solutions.
- FIG. 6 shows the reverse pole figure orientation mapping. From FIG.
- the gallium nitride crystal has a larger particle size on the surface side (the side opposite to the oriented alumina substrate) than the oriented alumina substrate side, and the shape of the gallium nitride crystal is not a perfect columnar shape such as a trapezoid or a triangle on the cross-sectional image. I understand that. Further, it can be seen that there are particles that grow as the film thickness increases and grow to the surface, and particles that do not grow to the surface. The cause of this behavior is not clear, but it is thought to be the result of the growth progressing as shown in FIG.
- the oriented alumina substrate portion of the sample was removed by grinding with a grindstone to obtain a Ge-doped gallium nitride simple substance.
- the back surface of the Ge-doped gallium nitride crystal (the surface on the side in contact with the oriented alumina substrate) was lapped with diamond abrasive grains, and the plate surface (the side opposite to the side in contact with the oriented alumina substrate) and the back surface (oriented alumina)
- a gallium nitride free-standing substrate having a thickness of about 180 ⁇ m with a smoothed surface on the side in contact with the substrate was obtained.
- the average roughness Ra after processing of the front surface and the back surface of the gallium nitride free-standing substrate was 0.2 nm.
- a self-standing substrate having a thickness of 50 ⁇ m and a self-standing substrate having a thickness of 20 ⁇ m were prepared by grinding the surface side of a gallium nitride free-standing substrate manufactured in the same manner as in the above (1) and (2).
- Sectional average diameter of the single crystal grains in the outermost surface of the free-standing substrate having a thickness of 50 ⁇ m is about 63 .mu.m
- the ratio D T / D B sectional average diameter D T of the substrate surface to its section average diameter D B of the substrate back surface 3. 2 and the aspect ratio was about 0.8.
- Example 6 (1) Production of Ge-doped gallium nitride free-standing substrate A c-plane oriented alumina substrate was produced in the same manner as in Example 5 to produce a seed crystal substrate in which a GaN film having a thickness of 3 ⁇ m was laminated. On this seed crystal substrate, a Ge-doped GaN film was formed in the same manner as (3b) of Example 1 except that the holding time was 40 hours. In the obtained sample, a Ge-doped gallium nitride crystal was grown on the entire surface of a 50.8 mm (2 inch) seed crystal substrate, and the thickness of the crystal was about 0.4 mm. Cracks were not confirmed.
- Example 7 (1) Production of c-plane oriented alumina sintered body A c-plane oriented alumina substrate was produced in the same manner as in Example 5 except that the firing temperature in the hot press was 1750 ° C. The sintered body thus obtained was fixed to a ceramic surface plate and ground to # 2000 using a grindstone to flatten the plate surface. Next, the surface of the plate was smoothed by lapping using diamond abrasive grains, and an oriented alumina sintered body having a diameter of 50.8 mm (2 inches) and a thickness of 1 mm was obtained as an oriented alumina substrate. The flatness was improved while gradually reducing the size of the abrasive grains from 3 ⁇ m to 0.5 ⁇ m.
- the average roughness Ra after processing was 4 nm. Further, when the c-plane orientation degree and the average grain size of the plate surface were evaluated in the same manner as in Example 1, the c-plane orientation degree was 96% and the average grain size was 14 ⁇ m.
- the grain size was larger, and the shape of the gallium nitride crystal was not a perfect columnar shape such as a trapezoid or a triangle on the cross-sectional image. Further, it has been found that there are particles that grow as the film thickness increases and grow to the surface, and particles that do not grow to the surface. The cause of this behavior is not clear, but it is thought to be the result of the growth progressing as shown in FIG. Therefore, among the gallium nitride particles that make up the gallium nitride crystal, the particles exposed on the front side communicate with the back surface without going through the grain boundary, but some of the particles exposed on the back side grow on the way. This includes those that stopped.
- the oriented alumina substrate portion of the sample was removed by grinding with a grindstone to obtain a Ge-doped gallium nitride simple substance.
- the back surface of the Ge-doped gallium nitride crystal (the surface on the side in contact with the oriented alumina substrate) was lapped with diamond abrasive grains, and the plate surface (the side opposite to the side in contact with the oriented alumina substrate) and the back surface (oriented alumina)
- a gallium nitride free-standing substrate having a thickness of about 90 ⁇ m and a smooth surface (the surface on the side in contact with the substrate) was obtained (Example 7-1).
- the average roughness Ra after processing of the front surface and the back surface of the gallium nitride free-standing substrate was 0.2 nm.
- a Ge-doped gallium nitride crystal is prepared in the same manner as described above, and the plate surface (surface) is ground using a # 600 and # 2000 grindstone, and the thickness of the gallium nitride crystal is 70, 50, 30 and 20 ⁇ m.
- Each sample was prepared, and the plate surface was smoothed by lapping using diamond abrasive grains.
- the alumina substrate portion is removed in the same manner as described above, and the back surface of the Ge-doped gallium nitride crystal (the surface on the side in contact with the oriented alumina substrate) is lapped with diamond abrasive grains to obtain the plate surface (the oriented alumina substrate).
- Gallium nitride free-standing substrate having smoothed thicknesses of 70, 50, 30 and 20 ⁇ m respectively on the side opposite to the side in contact with the surface and the back surface (the surface on the side in contact with the oriented alumina substrate) was obtained (Example 7). -2 to Example 7-5). The average roughness Ra after processing of the front and back surfaces of each sample was 0.2 nm.
- the volume resistivity of each sample was measured by the same method as in Example 1, (3), the volume resistivity was 1 ⁇ 10 ⁇ 2 ⁇ ⁇ cm.
- the thickness of the gallium nitride free-standing substrate and the cross-sectional average diameter of the surface The average cross-sectional diameter of the back surface, the ratio D T / D B of the cross-sectional average diameter D T of the substrate surface to the cross-sectional average diameter D B of the back surface of the substrate, and the ratio of the GaN crystal thickness to the cross-sectional average diameter of the front surface Table 1 shows the aspect ratio of the crystal grains.
- Example 8 (1) Production of c-plane oriented alumina sintered body As raw materials, plate-like alumina powder (Kinsei Matec Co., Ltd., Grade 02025), fine alumina powder (Daimei Chemical Industry Co., Ltd., Grade TM-DAR), aluminum fluoride (Manufactured by Kanto Chemical) and magnesium oxide powder (Ube Materials Co., Ltd., grade 500A), 5 parts by weight of plate-like alumina powder, 95 parts by weight of fine alumina powder, 0.05 part by weight of aluminum fluoride powder, oxidation 0.025 parts by weight of magnesium powder was mixed to obtain an alumina raw material.
- plate-like alumina powder Karlinsei Matec Co., Ltd., Grade 02025
- fine alumina powder Daimei Chemical Industry Co., Ltd., Grade TM-DAR
- aluminum fluoride Manufactured by Kanto Chemical
- magnesium oxide powder Ube Materials Co., Ltd., grade 500A
- a binder polyvinyl butyral: product number BM-2, manufactured by Sekisui Chemical Co., Ltd.
- a plasticizer DOP: di (2-ethylhexyl) phthalate, black metal chemical stock
- a dispersant Rosui Chemical Co., Ltd.
- a dispersion medium a mixture of xylene and 1-butanol at a weight ratio of 1: 1
- the slurry prepared as described above was formed into a sheet shape on a PET film by a doctor blade method so that the thickness after drying was 100 ⁇ m.
- the obtained tape was cut into a circular shape having a diameter of 50.8 mm (2 inches), then laminated in 30 sheets, placed on an Al plate having a thickness of 10 mm, and then vacuum-packed. This vacuum pack was hydrostatically pressed in warm water at 85 ° C. at a pressure of 100 kgf / cm 2 to obtain a disk-shaped molded body.
- the obtained molded body was placed in a degreasing furnace and degreased at 600 ° C. for 10 hours.
- the obtained degreased body was fired in a nitrogen atmosphere at 1800 ° C. for 4 hours under a surface pressure of 200 kgf / cm 2 using a graphite mold.
- the sintered body thus obtained was fixed to a ceramic surface plate and ground to # 2000 using a grindstone to flatten the plate surface.
- the surface of the plate was smoothed by lapping using diamond abrasive grains, and an oriented alumina sintered body having a diameter of 50.8 mm (2 inches) and a thickness of 1 mm was obtained as an oriented alumina substrate.
- the flatness was improved while gradually reducing the size of the abrasive grains from 3 ⁇ m to 0.5 ⁇ m.
- the average roughness Ra after processing was 4 nm.
- the c-plane orientation degree and the average grain size of the plate surface were evaluated in the same manner as in Example 1, the c-plane orientation degree was 92% and the average grain size was about 64 ⁇ m.
- a seed crystal substrate was produced by laminating a GaN film having a thickness of 3 ⁇ m on an oriented alumina substrate in the same manner as in (1a) of Example 1. On this seed crystal substrate, a Ge-doped GaN film was formed in the same manner as (3b) of Example 1 except that the holding time was 30 hours. In the obtained sample, a Ge-doped gallium nitride crystal was grown on the entire surface of a 50.8 mm (2 inch) seed crystal substrate, and the thickness of the crystal was about 0.3 mm. Cracks were not confirmed.
- the surface (surface) of the Ge-doped gallium nitride crystal of the sample thus obtained was ground and flattened using a # 600 and # 2000 grindstone until the thickness of the gallium nitride crystal was about 90 ⁇ m, and then the diamond abrasive grains were The plate surface was smoothed by the lapping used.
- reverse pole figure orientation mapping of the cross section of the gallium nitride crystal was performed using the same method as in Examples 4 to 7. As a result, the gallium nitride crystal was closer to the surface side than the oriented alumina substrate side (opposite to the oriented alumina substrate).
- the grain size was larger, and the shape of the gallium nitride crystal was not a perfect columnar shape such as a trapezoid or a triangle on the cross-sectional image. Further, it has been found that there are particles that grow as the film thickness increases and grow to the surface, and particles that do not grow to the surface. The cause of this behavior is not clear, but it is thought to be the result of the growth progressing as shown in FIG. Therefore, among the gallium nitride particles that make up the gallium nitride crystal, the particles exposed on the front side communicate with the back surface without going through the grain boundary, but some of the particles exposed on the back side grow on the way. This includes those that stopped.
- the oriented alumina substrate portion of the sample was removed by grinding with a grindstone to obtain a Ge-doped gallium nitride simple substance.
- the back surface of the Ge-doped gallium nitride crystal (the surface that was in contact with the oriented alumina substrate) was lapped with diamond abrasive grains to smooth the plate surface and the back surface (the surface that was in contact with the oriented alumina substrate).
- a gallium nitride free-standing substrate having a thickness of about 90 ⁇ m was obtained.
- the average roughness Ra after processing of the front surface and the back surface of the gallium nitride free-standing substrate was 0.2 nm.
- the volume resistivity was 1 ⁇ 10 ⁇ 2 ⁇ ⁇ cm.
- the cross-sectional average diameter of the GaN single crystal particles on the front and back surfaces of the gallium nitride free-standing substrate was measured using the same method as in Example 1 (3). The diameter was about 64 ⁇ m. Sectional average diameter in this way it is larger than the back side of the surface, the ratio D T / D B sectional average diameter D T of the substrate surface to its section average diameter D B of the substrate back surface was about 1.3.
- the aspect ratio of the GaN single crystal particles calculated as the ratio of the thickness of the GaN crystal to the average cross-sectional diameter of the surface was about 1.1.
- Example 9 (1) Production of c-plane oriented alumina sintered body A c-plane oriented alumina substrate was produced in the same manner as in Example 8 except that the amount of aluminum fluoride powder was 0.02 part by weight. The sintered body thus obtained was fixed to a ceramic surface plate and ground to # 2000 using a grindstone to flatten the plate surface. Next, the surface of the plate was smoothed by lapping using diamond abrasive grains, and an oriented alumina sintered body having a diameter of 50.8 mm (2 inches) and a thickness of 1 mm was obtained as an oriented alumina substrate. The flatness was improved while gradually reducing the size of the abrasive grains from 3 ⁇ m to 0.5 ⁇ m.
- the average roughness Ra after processing was 4 nm. Further, when the c-plane orientation degree and the average grain size of the plate surface were evaluated in the same manner as in Example 1, the c-plane orientation degree was 94% and the average grain size was 41 ⁇ m.
- a seed crystal substrate was produced by laminating a GaN film having a thickness of 3 ⁇ m on an oriented alumina substrate in the same manner as in (1a) of Example 1. On this seed crystal substrate, a Ge-doped GaN film was formed in the same manner as (3b) of Example 1 except that the holding time was 30 hours. In the obtained sample, a Ge-doped gallium nitride crystal was grown on the entire surface of a 50.8 mm (2 inch) seed crystal substrate, and the thickness of the crystal was about 0.3 mm. Cracks were not confirmed.
- the particles exposed on the front side communicate with the back surface without going through the grain boundary, but some of the particles exposed on the back side grow on the way. This includes those that stopped.
- the volume resistivity was 1 ⁇ 10 ⁇ 2 ⁇ ⁇ cm.
- the cross-sectional average diameter of the GaN single crystal particles on the front and back surfaces of the gallium nitride free-standing substrate was measured using the same method as in Example 1 (3). The diameter was about 61 ⁇ m. Sectional average diameter in this way it is larger than the back side of the surface, the ratio D T / D B sectional average diameter D T of the substrate surface to its section average diameter D B of the substrate back surface was about 1.3.
- the aspect ratio of the GaN single crystal particles calculated as the ratio of the thickness of the GaN crystal to the average cross-sectional diameter of the surface was about 0.7.
- Example 3 Production of light-emitting element using Ge-doped gallium nitride free-standing substrate A light-emitting functional layer was produced on a gallium nitride free-standing substrate in the same manner as in Example 1 (4a), and the average cross-sectional diameter of single crystal particles on the outermost surface was determined. When measured, the average cross-sectional diameter was about 81 ⁇ m. Further, as a result of fabricating a vertical light emitting device in the same manner as in Example 4 (4b), rectification was confirmed by IV measurement between the cathode electrode and the anode electrode, and light emission at a wavelength of 450 nm was confirmed by forward current application. It was done. However, the emission luminance was somewhat high, but was found to be weaker than Example 8.
- Example 10 (1) Production of c-plane oriented alumina sintered body As raw materials, plate-like alumina powder (Kinsei Matec Co., Ltd., grade 10030), fine alumina powder (Daimei Chemical Co., Ltd. grade TM-DAR), and magnesium oxide Powder (Ube Materials Co., Ltd., grade 500A) was prepared, and 5 parts by weight of plate-like alumina powder, 95 parts by weight of fine alumina powder, and 0.025 part by weight of magnesium oxide powder were mixed to obtain an alumina raw material.
- plate-like alumina powder Karlinsei Matec Co., Ltd., grade 10030
- fine alumina powder Daimei Chemical Co., Ltd. grade TM-DAR
- magnesium oxide Powder Ube Materials Co., Ltd., grade 500A
- a binder polyvinyl butyral: product number BM-2, manufactured by Sekisui Chemical Co., Ltd.
- a plasticizer DOP: di (2-ethylhexyl) phthalate, black metal chemical stock
- a dispersant Rosui Chemical Co., Ltd.
- a dispersion medium a mixture of xylene and 1-butanol at a weight ratio of 1: 1
- the slurry prepared as described above was formed into a sheet shape on a PET film by a doctor blade method so that the thickness after drying was 100 ⁇ m.
- the obtained tape was cut into a circular shape having a diameter of 50.8 mm (2 inches), then laminated in 30 sheets, placed on an Al plate having a thickness of 10 mm, and then vacuum-packed. This vacuum pack was hydrostatically pressed in warm water at 85 ° C. at a pressure of 100 kgf / cm 2 to obtain a disk-shaped molded body.
- the obtained molded body was placed in a degreasing furnace and degreased at 600 ° C. for 10 hours.
- the obtained degreased body was fired in a nitrogen atmosphere at 1800 ° C. for 4 hours under a surface pressure of 200 kgf / cm 2 using a graphite mold.
- the sintered body thus obtained was fixed to a ceramic surface plate and ground to # 2000 using a grindstone to flatten the plate surface.
- the surface of the plate was smoothed by lapping using diamond abrasive grains, and an oriented alumina sintered body having a diameter of 50.8 mm (2 inches) and a thickness of 1 mm was obtained as an oriented alumina substrate.
- the flatness was improved while gradually reducing the size of the abrasive grains from 3 ⁇ m to 0.5 ⁇ m.
- the average roughness Ra after processing was 4 nm.
- the c-plane orientation degree and the average grain size of the plate surface were evaluated in the same manner as in Example 1, the c-plane orientation degree was 99% and the average grain size was about 24 ⁇ m.
- a seed crystal substrate was produced by laminating a GaN film having a thickness of 3 ⁇ m on an oriented alumina substrate in the same manner as in (1a) of Example 1. On this seed crystal substrate, a Ge-doped GaN film was formed in the same manner as (3b) of Example 1 except that the holding time was 30 hours. In the obtained sample, a Ge-doped gallium nitride crystal was grown on the entire surface of a 50.8 mm (2 inch) seed crystal substrate, and the thickness of the crystal was about 0.3 mm. Cracks were not confirmed.
- the oriented alumina substrate portion of the sample thus obtained was removed by grinding with a grindstone to obtain a Ge-doped gallium nitride simple substance.
- the back surface of the Ge-doped gallium nitride crystal (the surface that was in contact with the oriented alumina substrate) was cut by about 90 ⁇ m using a # 600 and # 2000 grindstone.
- the plate surface (front surface) is ground and flattened until the thickness of the gallium nitride crystal becomes about 40 ⁇ m, and then the front and back surfaces are smoothed by lapping using diamond abrasive grains, and the gallium nitride freestanding about 40 ⁇ m thick.
- a substrate was obtained.
- the average roughness Ra after processing of the front surface and the back surface of the gallium nitride free-standing substrate was 0.2 nm.
- the particles exposed on the front side communicate with the back surface without going through the grain boundary, but some of the particles exposed on the back side grow on the way. This includes those that stopped.
- the volume resistivity was 1 ⁇ 10 ⁇ 2 ⁇ ⁇ cm.
- the cross-sectional average diameter of the GaN single crystal particles on the front and back surfaces of the gallium nitride free-standing substrate was measured using the same method as in Example 1 (3). The diameter was about 60 ⁇ m. Sectional average diameter in this way it is larger than the back side of the surface, the ratio D T / D B sectional average diameter D T of the substrate surface to its section average diameter D B of the substrate back surface was about 1.3.
- the aspect ratio of the GaN single crystal particles calculated as the ratio of the thickness of the GaN crystal to the average cross-sectional diameter of the surface was about 0.5.
- Example 11 A verification experiment was conducted in order to more clearly confirm that setting the average cross-sectional diameter of the gallium nitride single crystal particles to 20 ⁇ m or more significantly improves the luminous efficiency.
- gallium nitride single crystal particles having various cross-sectional average diameters DT of 2, 3, 13, 16, 20, 35, 42, 50, 72, 90 and 110 ⁇ m were prepared. Then, a light emitting element was produced using this, and the light emission luminance at 200 A / cm 2 (chip size: 1 mm square, forward current: 2 A) was measured using LED Tester LX4681A manufactured by Technolog Co., Ltd. The results were as shown in Table 2.
- a gallium nitride free-standing substrate comprising a plate composed of a plurality of gallium nitride-based single crystal particles having a single crystal structure in a substantially normal direction.
- the gallium nitride free-standing substrate according to Item 1, wherein an average cross-sectional diameter of the gallium nitride-based single crystal particles on the outermost surface of the substrate is 0.3 ⁇ m or more.
- a gallium nitride free-standing substrate according to Item 2 wherein the average cross-sectional diameter is 3 ⁇ m or more.
- the gallium nitride free-standing substrate according to Item 2 wherein the average cross-sectional diameter is 20 ⁇ m or more.
- the gallium nitride free-standing substrate according to any one of Items 1 to 4 having a thickness of 20 ⁇ m or more.
- the gallium nitride free-standing substrate according to any one of Items 1 to 5 which has a diameter of 100 mm or more.
- the gallium nitride-based single crystal particles have a crystal orientation substantially aligned in a substantially normal direction.
- the gallium nitride single crystal particles exposed on the surface of the gallium nitride free-standing substrate are communicated with the back surface of the gallium nitride free-standing substrate without a grain boundary.
- the gallium nitride free-standing substrate as described.
- D B For sectional average diameter D B at the outermost surface of the gallium nitride single crystal particles exposed on the back surface of the gallium nitride free-standing substrate, cross-section at the outermost surface of the gallium nitride single crystal particles exposed on the surface of the gallium nitride free-standing substrate Item 12.
- the gallium nitride self-supporting substrate according to any one of Items 1 to 11, wherein the ratio D T / D B of the average diameter D T is larger than 1.0.
- the aspect ratio T / D defined as the ratio of the thickness T of the gallium nitride free-standing substrate to the average cross-sectional diameter DT of the outermost surface of the gallium nitride-based single crystal particles exposed on the surface of the gallium nitride free-standing substrate Item 13.
- the gallium nitride free-standing substrate according to any one of Items 1 to 12, wherein T is 0.7 or more.
- [Section 14] The gallium nitride free-standing substrate according to any one of Items 1 to 13, A light emitting functional layer formed on the substrate and having at least one layer composed of a plurality of semiconductor single crystal particles having a single crystal structure in a substantially normal direction; A light emitting device comprising: [Section 15] Item 15. The self-supporting light-emitting element according to Item 14, wherein the semiconductor single crystal particle has an average cross-sectional diameter of 0.3 ⁇ m or more on the outermost surface of the light-emitting functional layer. [Section 16] Item 16. The light-emitting element according to Item 15, wherein the cross-sectional average diameter is 3 ⁇ m or more. [Section 17] Item 17.
- the light-emitting device according to any one of Items 14 to 16, wherein the semiconductor single crystal particles have a structure grown substantially following the crystal orientation of the gallium nitride free-standing substrate.
- the light emitting functional layer is composed of a gallium nitride material.
- [Section 19] Preparing an oriented polycrystalline sintered body; Forming a seed crystal layer made of gallium nitride on the oriented polycrystalline sintered body so as to have a crystal orientation substantially following the crystal orientation of the oriented polycrystalline sintered body; Forming a layer composed of a gallium nitride-based crystal having a thickness of 20 ⁇ m or more on the seed crystal layer so as to have a crystal orientation substantially following the crystal orientation of the seed crystal layer; Removing the oriented polycrystalline sintered body to obtain a gallium nitride free-standing substrate; A method for manufacturing a gallium nitride free-standing substrate. [Section 20] Item 20.
- [Claim 24] Preparing the gallium nitride free-standing substrate according to any one of Items 1 to 13, or preparing the gallium nitride free-standing substrate by the method according to any one of Items 19 to 23; One or more layers composed of a plurality of semiconductor single crystal particles having a single crystal structure in a substantially normal direction so that the gallium nitride free-standing substrate has a crystal orientation that substantially follows the crystal orientation of the gallium nitride substrate.
- a method for manufacturing a light emitting device comprising: [Claim 25] Item 25. The method according to Item 24, wherein the light emitting functional layer is composed of a gallium nitride-based material.
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Abstract
Description
該基板上に形成され、略法線方向に単結晶構造を有する複数の半導体単結晶粒子で構成される層を一以上有する発光機能層と、
を備えた、発光素子が提供される。
前記配向多結晶焼結体上に、窒化ガリウムからなる種結晶層を、前記配向多結晶焼結体の結晶方位に概ね倣った結晶方位を有するように形成する工程と、
前記種結晶層上に、厚さ20μm以上の窒化ガリウム系結晶から構成される層を、前記種結晶層の結晶方位に概ね倣った結晶方位を有するように形成する工程と、
前記配向多結晶焼結体を除去して、窒化ガリウム自立基板を得る工程と、
を含む、窒化ガリウム自立基板の製造方法が提供される。
前記窒化ガリウム自立基板に、前記窒化ガリウム基板の結晶方位に概ね倣った結晶方位を有するように、略法線方向に単結晶構造を有する複数の半導体単結晶粒子で構成される層を一つ以上形成して発光機能層を設ける工程と、
を含む、発光素子の製造方法が提供される。
[項1]
略法線方向に単結晶構造を有する複数の窒化ガリウム系単結晶粒子で構成される板からなる窒化ガリウム自立基板であって、前記窒化ガリウム自立基板の表面に露出している前記窒化ガリウム系単結晶粒子が、該窒化ガリウム自立基板の裏面に粒界を介さずに連通してなり、前記窒化ガリウム自立基板の裏面に露出している窒化ガリウム系単結晶粒子の最表面における断面平均径DBに対する、前記窒化ガリウム自立基板の表面に露出している窒化ガリウム系単結晶粒子の最表面における断面平均径DTの比DT/DBが1.0よりも大きい、窒化ガリウム自立基板。
[項2]
前記基板の最表面における前記窒化ガリウム系単結晶粒子の断面平均径が0.3μm以上である、項1に記載の窒化ガリウム自立基板。
[項3]
前記断面平均径が3μm以上である、項2に記載の窒化ガリウム自立基板。
[項4]
前記断面平均径が20μm以上である、項2に記載の窒化ガリウム自立基板。
[項5]
20μm以上の厚さを有する、項1~4のいずれか一項に記載の窒化ガリウム自立基板。
[項6]
直径100mm以上の大きさを有する、項1~5のいずれか一項に記載の窒化ガリウム自立基板。
[項7]
前記窒化ガリウム系単結晶粒子が、略法線方向に概ね揃った結晶方位を有する、項1~6のいずれか一項に記載の窒化ガリウム自立基板。
[項8]
前記窒化ガリウム系単結晶粒子がn型ドーパント又はp型ドーパントでドープされている、項1~7のいずれか一項に記載の窒化ガリウム自立基板。
[項9]
前記窒化ガリウム系単結晶粒子がドーパントを含まない、項1~7のいずれか一項に記載の窒化ガリウム自立基板。
[項10]
前記窒化ガリウム系単結晶粒子が混晶化されている、項1~9のいずれか一項に記載の窒化ガリウム自立基板。
[項11]
前記比DT/DBが1.5以上である、項1~10のいずれか一項に記載の窒化ガリウム自立基板。
[項12]
前記窒化ガリウム自立基板の表面に露出している前記窒化ガリウム系単結晶粒子の最表面における断面平均径DTに対する、前記窒化ガリウム自立基板の厚さTの比として規定されるアスペクト比T/DTが0.7以上である、項1~11のいずれか一項に記載の窒化ガリウム自立基板。
[項13]
項1~12のいずれか一項に記載の窒化ガリウム自立基板と、
該基板上に形成され、略法線方向に単結晶構造を有する複数の半導体単結晶粒子で構成される層を一以上有する発光機能層と、
を備えた、発光素子。
[項14]
前記発光機能層の最表面における前記半導体単結晶粒子の断面平均径が0.3μm以上である、項13に記載の自立した発光素子。
[項15]
前記断面平均径が3μm以上である、項14に記載の発光素子。
[項16]
前記半導体単結晶粒子が、前記窒化ガリウム自立基板の結晶方位に概ね倣って成長した構造を有する、項13~15のいずれか一項に記載の発光素子。
[項17]
前記発光機能層が窒化ガリウム系材料で構成される、項13~16のいずれか一項に記載の発光素子。
[項18]
配向多結晶焼結体を用意する工程と、
前記配向多結晶焼結体上に、窒化ガリウムからなる種結晶層を、前記配向多結晶焼結体の結晶方位に概ね倣った結晶方位を有するように形成する工程と、
前記種結晶層上に、厚さ20μm以上の窒化ガリウム系結晶から構成される層を、前記種結晶層の結晶方位に概ね倣った結晶方位を有するように形成する工程と、
前記配向多結晶焼結体を除去して、窒化ガリウム自立基板を得る工程と、
を含み、前記窒化ガリウム自立基板の表面に露出している前記窒化ガリウム系単結晶粒子が、該窒化ガリウム自立基板の裏面に粒界を介さずに連通してなり、前記窒化ガリウム自立基板の裏面に露出している窒化ガリウム系単結晶粒子の最表面における断面平均径DBに対する、前記窒化ガリウム自立基板の表面に露出している窒化ガリウム系単結晶粒子の最表面における断面平均径DTの比DT/DBが1.0よりも大きい、窒化ガリウム自立基板の製造方法。
[項19]
前記配向多結晶焼結体が配向多結晶アルミナ焼結体である、項18に記載の方法。
[項20]
前記配向多結晶焼結体を構成する粒子の板面における平均粒径が0.3~1000μmである、項18又は19に記載の方法。
[項21]
前記窒化ガリウム系結晶から構成される層の形成がNaフラックス法により行われる、項18~20のいずれか一項に記載の方法。
[項22]
前記配向多結晶焼結体が透光性を有する、項18~21のいずれか一項に記載の方法。
[項23]
項1~12のいずれか一項に記載の窒化ガリウム自立基板を用意する、又は項18~22のいずれか一項に記載の方法により前記窒化ガリウム自立基板を用意する工程と、
前記窒化ガリウム自立基板に、前記窒化ガリウム基板の結晶方位に概ね倣った結晶方位を有するように、略法線方向に単結晶構造を有する複数の半導体単結晶粒子で構成される層を一つ以上形成して発光機能層を設ける工程と、
を含む、発光素子の製造方法。
[項24]
前記発光機能層が窒化ガリウム系材料で構成される、項23に記載の方法。
[項25]
略法線方向に単結晶構造を有する複数の窒化ガリウム系単結晶粒子で構成される板からなる窒化ガリウム自立基板であって、前記窒化ガリウム自立基板の表面に露出している前記窒化ガリウム系単結晶粒子が、該窒化ガリウム自立基板の裏面に粒界を介さずに連通してなり、前記基板の最表面における前記窒化ガリウム系単結晶粒子の断面平均径が20μm以上1000μm以下である、窒化ガリウム自立基板。
[項26]
前記断面平均径が50μm以上500μm以下である、項25に記載の窒化ガリウム自立基板。
[項27]
20μm以上の厚さを有する、項25又は26に記載の窒化ガリウム自立基板。
[項28]
直径100mm以上の大きさを有する、項25~27のいずれか一項に記載の窒化ガリウム自立基板。
[項29]
前記窒化ガリウム系単結晶粒子が、略法線方向に概ね揃った結晶方位を有する、項25~28のいずれか一項に記載の窒化ガリウム自立基板。
[項30]
前記窒化ガリウム系単結晶粒子がn型ドーパント又はp型ドーパントでドープされている、項25~29のいずれか一項に記載の窒化ガリウム自立基板。
[項31]
前記窒化ガリウム系単結晶粒子がドーパントを含まない、項25~29のいずれか一項に記載の窒化ガリウム自立基板。
[項32]
前記窒化ガリウム系単結晶粒子が混晶化されている、項25~31のいずれか一項に記載の窒化ガリウム自立基板。
[項33]
窒化ガリウム自立基板の裏面に露出している窒化ガリウム系単結晶粒子の最表面における断面平均径DBに対する、窒化ガリウム自立基板の表面に露出している窒化ガリウム系単結晶粒子の最表面における断面平均径DTの比DT/DBが1.0よりも大きい、項25~32のいずれか一項に記載の窒化ガリウム自立基板。
[項34]
前記窒化ガリウム自立基板の表面に露出している前記窒化ガリウム系単結晶粒子の最表面における断面平均径DTに対する、前記窒化ガリウム自立基板の厚さTの比として規定されるアスペクト比T/DTが0.7以上である、項25~33のいずれか一項に記載の窒化ガリウム自立基板。
[項35]
項25~34のいずれか一項に記載の窒化ガリウム自立基板と、
該基板上に形成され、略法線方向に単結晶構造を有する複数の半導体単結晶粒子で構成される層を一以上有する発光機能層と、
を備えた、発光素子。
[項36]
前記発光機能層の最表面における前記半導体単結晶粒子の断面平均径が20μm以上である、項35に記載の自立した発光素子。
[項37]
前記断面平均径が50μm以上である、項36に記載の発光素子。
[項38]
前記半導体単結晶粒子が、前記窒化ガリウム自立基板の結晶方位に概ね倣って成長した構造を有する、項35~37のいずれか一項に記載の発光素子。
[項39]
前記発光機能層が窒化ガリウム系材料で構成される、項35~38のいずれか一項に記載の発光素子。
[項40]
配向多結晶焼結体を用意する工程と、
前記配向多結晶焼結体上に、窒化ガリウムからなる種結晶層を、前記配向多結晶焼結体の結晶方位に概ね倣った結晶方位を有するように形成する工程と、
前記種結晶層上に、厚さ20μm以上の窒化ガリウム系結晶から構成される層を、前記種結晶層の結晶方位に概ね倣った結晶方位を有するように形成する工程と、
前記配向多結晶焼結体を除去して、窒化ガリウム自立基板を得る工程と、
を含み、前記窒化ガリウム自立基板の表面に露出している前記窒化ガリウム系単結晶粒子が、該窒化ガリウム自立基板の裏面に粒界を介さずに連通してなり、前記基板の最表面における窒化ガリウム系単結晶粒子の断面平均径が20μm以上1000μm以下である、窒化ガリウム自立基板の製造方法。
[項41]
前記配向多結晶焼結体が配向多結晶アルミナ焼結体である、項40に記載の方法。
[項42]
前記配向多結晶焼結体を構成する粒子の板面における平均粒径が0.3~1000μmである、項40又は41に記載の方法。
[項43]
前記窒化ガリウム系結晶から構成される層の形成がNaフラックス法により行われる、項40~42のいずれか一項に記載の方法。
[項44]
前記配向多結晶焼結体が透光性を有する、項40~43のいずれか一項に記載の方法。
[項45]
項25~34のいずれか一項に記載の窒化ガリウム自立基板を用意する、又は項40~44のいずれか一項に記載の方法により前記窒化ガリウム自立基板を用意する工程と、
前記窒化ガリウム自立基板に、前記窒化ガリウム基板の結晶方位に概ね倣った結晶方位を有するように、略法線方向に単結晶構造を有する複数の半導体単結晶粒子で構成される層を一つ以上形成して発光機能層を設ける工程と、
を含む、発光素子の製造方法。
[項46]
前記発光機能層が窒化ガリウム系材料で構成される、項45に記載の方法。
本発明の窒化ガリウム基板は自立基板の形態を有しうる。本発明において「自立基板」とは、取り扱う際に自重で変形又は破損せず、固形物として取り扱うことのできる基板を意味する。本発明の窒化ガリウム自立基板は発光素子等の各種半導体デバイスの基板として使用可能であるが、それ以外にも、電極(p型電極又はn型電極でありうる)、p型層、n型層等の基材以外の部材又は層として使用可能なものである。なお、以下の説明においては、主たる用途の一つである発光素子を例に本発明の利点を記述することがあるが、同様ないし類似の利点は技術的整合性を損なわない範囲内で他の半導体デバイスにも当てはまる。
本発明の窒化ガリウム自立基板は、(1)配向多結晶焼結体を用意し、(2)配向多結晶焼結体上に、窒化ガリウムからなる種結晶層を、配向多結晶焼結体の結晶方位に概ね倣った結晶方位を有するように形成し、(3)種結晶層上に、厚さ20μm以上の窒化ガリウム系結晶から構成される層を、種結晶層の結晶方位に概ね倣った結晶方位を有するように形成し、(4)配向多結晶焼結体を除去して、窒化ガリウム自立基板を得ることにより製造することができる。
窒化ガリウム自立基板を作製するための下地基板として、配向多結晶焼結体を用意する。配向多結晶焼結体の組成は特に限定されないが、配向多結晶アルミナ焼結体、配向多結晶酸化亜鉛焼結体、配向多結晶窒化アルミニウム焼結体から選ばれる1種であるのが好ましい。配向多結晶焼結体は、商業的に入手可能な板状粉末を用いて成形及び焼成を経て効率的に製造できるため、低コストで製造できるだけでなく、成形しやすいが故に大面積化にも適する。そして、本発明者らの知見によれば、配向多結晶焼結体を下地基板として用い、その上に複数の半導体単結晶粒子を成長させることで、大面積の発光素子を低コストで製造するのに適した窒化ガリウム自立基板を製造できる。その結果、窒化ガリウム自立基板は、大面積の発光素子を低コストで製造するのに極めて適するものとなる。
配向多結晶焼結体上に、窒化ガリウムからなる種結晶層を、配向多結晶焼結体の結晶方位に概ね倣った結晶方位を有するように形成する。なお、「配向多結晶焼結体の結晶方位に概ね倣った結晶方位を有するように形成する」とは、配向多結晶焼結体の結晶方位の影響を受けた結晶成長によりもたらされた構造を意味し、必ずしも配向多結晶焼結体の結晶方位に完全に倣って成長した構造であるとは限らず、配向多結晶焼結体と異なる結晶方位に成長する構造も含む。種結晶層の作製方法は特に限定されないが、MOCVD(有機金属気相成長法)、MBE(分子線エピタキシー法)、HVPE(ハライド気相成長法)、スパッタリング等の気相法、Naフラックス法、アモノサーマル法、水熱法、ゾルゲル法等の液相法、粉末の固相成長を利用した粉末法、及びこれらの組み合わせが好ましく例示される。例えば、MOCVD法による種結晶層の形成は、450~550℃にて低温GaN層を20~50nm堆積させた後に、1000~1200℃にて厚さ2~4μmのGaN膜を積層させることにより行うのが好ましい。
種結晶層上に、厚さ20μm以上の窒化ガリウム系結晶から構成される層を、種結晶層の結晶方位に概ね倣った結晶方位を有するように形成する。窒化ガリウム系結晶から構成される層の形成方法は配向多結晶焼結体及び/又は種結晶層の結晶方位に概ね倣った結晶方位を有する限り特に限定がなく、MOCVD、HVPE等の気相法、Naフラックス法、アモノサーマル法、水熱法、ゾルゲル法等の液相法、粉末の固相成長を利用した粉末法、及びこれらの組み合わせが好ましく例示されるが、Naフラックス法により行われるのが特に好ましい。Naフラックス法によれば結晶性の高い厚肉の窒化ガリウム結晶層を種結晶層上に効率良く作製できる。Naフラックス法による窒化ガリウム系結晶層の形成は、種結晶基板を設置した坩堝に金属Ga、金属Na及び所望によりドーパント(例えばゲルマニウム(Ge)、シリコン(Si)、酸素(O)等のn型ドーパント、又はベリリウム(Be)、マグネシウム(Mg)、カルシウム(Ca)、ストロンチウム(Sr)、亜鉛(Zn)、カドミウム(Cd)等のp型ドーパント)を含む融液組成物を充填し、窒素雰囲気中で830~910℃、3.5~4.5MPaまで昇温加圧した後、温度及び圧力を保持しつつ回転することにより行うのが好ましい。保持時間は目的の膜厚によって異なるが、10~100時間程度としてもよい。また、こうしてNaフラックス法により得られた窒化ガリウム結晶を砥石で研削して板面を平坦にした後、ダイヤモンド砥粒を用いたラップ加工により板面を平滑化するのが好ましい。
配向多結晶焼結体を除去して、窒化ガリウム自立基板を得ることができる。配向多結晶焼結体を除去する方法は、特に限定されないが、研削加工、ケミカルエッチング、配向焼結体側からのレーザー照射による界面加熱(レーザーリフトオフ)、昇温時の熱膨張差を利用した自発剥離等が挙げられる。
上述した本発明による窒化ガリウム自立基板を用いて高品質の発光素子を作製することができる。本発明の窒化ガリウム自立基板を用いた発光素子の構造やその作製方法は特に限定されるものではない。典型的には、発光素子は、窒化ガリウム自立基板に発光機能層を設けることにより作製され、この発光機能層の形成は、窒化ガリウム基板の結晶方位に概ね倣った結晶方位を有するように、略法線方向に単結晶構造を有する複数の半導体単結晶粒子で構成される層を一つ以上形成することに行われるのが好ましい。もっとも、窒化ガリウム自立基板を電極(p型電極又はn型電極でありうる)、p型層、n型層等の基材以外の部材又は層として利用して発光素子を作製してもよい。素子サイズに特に規定はなく、5mm×5mm以下の小素子としてもよいし、10cm×10cm以上の面発光素子としてもよい。
本発明の窒化ガリウム自立基板は、上述した発光素子のみならず、各種電子デバイス、パワーデバイス、受光素子、太陽電池用ウェハー等の種々の用途に好ましく利用することができる。
(1)c面配向アルミナ焼結体の作製
原料として、板状アルミナ粉末(キンセイマテック株式会社製、グレード00610)を用意した。板状アルミナ粒子100重量部に対し、バインダー(ポリビニルブチラール:品番BM-2、積水化学工業株式会社製)7重量部と、可塑剤(DOP:ジ(2-エチルヘキシル)フタレート、黒金化成株式会社製)3.5重量部と、分散剤(レオドールSP-O30、花王株式会社製)2重量部と、分散媒(2-エチルヘキサノール)を混合した。分散媒の量は、スラリー粘度が20000cPとなるように調整した。上記のようにして調製されたスラリーを、ドクターブレード法によって、PETフィルムの上に、乾燥後の厚さが20μmとなるように、シート状に成形した。得られたテープを口径50.8mm(2インチ)の円形に切断した後150枚積層し、厚さ10mmのAl板の上に載置した後、真空パックを行った。この真空パックを85℃の温水中で、100kgf/cm2の圧力にて静水圧プレスを行い、円盤状の成形体を得た。
(配向度の評価)
得られた配向アルミナ基板の配向度を確認するため、XRDにより本実験例における測定対象とする結晶面であるc面の配向度を測定した。XRD装置(株式会社リガク製、RINT-TTR III)を用い、配向アルミナ基板の板面に対してX線を照射したときの2θ=20~70°の範囲でXRDプロファイルを測定した。c面配向度は、以下の式により算出した。この結果、本実験例におけるc面配向度の値は97%であった。
配向アルミナ基板の焼結体粒子について、板面の平均粒径を以下の方法により測定した。得られた配向アルミナ基板の板面を研磨し、1550℃で45分間サーマルエッチングを行った後、走査電子顕微鏡にて画像を撮影した。視野範囲は、得られる画像の対角線に直線を引いた場合に、いずれの直線も10個から30個の粒子と交わるような直線が引けるような視野範囲とした。得られた画像の対角線に引いた2本の直線において、直線が交わる全ての粒子に対し、個々の粒子の内側の線分の長さを平均したものに1.5を乗じた値を板面の平均粒径とした。この結果、板面の平均粒径は100μmであった。
(3a)種結晶層の成膜
次に、加工した配向アルミナ基板の上に、MOCVD法を用いて種結晶層を形成した。具体的には、530℃にて低温GaN層を40nm堆積させた後に、1050℃にて厚さ3μmのGaN膜を積層させて種結晶基板を得た。
上記工程で作製した種結晶基板を、内径80mm、高さ45mmの円筒平底のアルミナ坩堝の底部分に設置し、次いで融液組成物をグローブボックス内で坩堝内に充填した。融液組成物の組成は以下のとおりである。
・金属Ga:60g
・金属Na:60g
・四塩化ゲルマニウム:1.85g
ホール効果測定装置を用い、窒化ガリウム自立基板の面内の体積抵抗率を測定した。その結果、体積抵抗率は1×10-2Ω・cmであった。
窒化ガリウム自立基板の最表面におけるGaN単結晶粒子の断面平均径を測定するため、自立基板の表面を走査電子顕微鏡にて画像を撮影した。視野範囲は、得られる画像の対角線に直線を引いた場合に、10個から30個の柱状組織と交わるような直線が引けるような視野範囲とした。得られた画像の対角線に2本の直線を任意に引き、直線が交わる全ての粒子に対し、個々の粒子の内側の線分の長さを平均したものに1.5を乗じた値を、窒化ガリウム自立基板の最表面におけるGaN単結晶粒子の断面平均径とした。この結果、断面平均径は約100μmであった。なお、本例では表面の走査顕微鏡像で明瞭に界面を判別できたが、サーマルエッチングやケミカルエッチングによって界面を際立たせる処理を施した後に上記の評価を行ってもよい。
(4a)MOCVD法による発光機能層の成膜
MOCVD法を用いて、窒化ガリウム自立基板上にn型層として1050℃でSi原子濃度が5×1018/cm3になるようにドーピングしたn-GaN層を1μm堆積した。次に発光層として750℃で多重量子井戸層を堆積した。具体的にはInGaNによる2.5nmの井戸層を5層、GaNによる10nmの障壁層を6層にて交互に積層した。次にp型層として950℃でMg原子濃度が1×1019/cm3になるようにドーピングしたp-GaNを200nm堆積した。その後、MOCVD装置から取り出し、p型層のMgイオンの活性化処理として、窒素雰囲気中で800℃の熱処理を10分間行った。発光機能層の再表面における単結晶粒子の断面平均径を測定するため、発光機能層の表面を走査電子顕微鏡にて画像を撮影した。視野範囲は、得られる画像の対角線に直線を引いた場合に、10個から30個の柱状組織と交わるような直線が引けるような視野範囲とした。得られた画像の対角線に2本の直線を任意に引き、直線が交わる全ての粒子に対し、個々の粒子の内側の線分の長さを平均したものに1.5を乗じた値を、発光機能層の最表面における単結晶粒子の断面平均径とした。この結果、断面平均径は約100μmであった。
フォトリソグラフィープロセスと真空蒸着法とを用いて、窒化ガリウム自立基板のn-GaN層及びp-GaN層とは反対側の面にカソード電極としてのTi/Al/Ni/Au膜をそれぞれ15nm、70nm、12nm、60nmの厚みでパターニングした。その後、オーム性接触特性を良好なものとするために、窒素雰囲気中での700℃の熱処理を30秒間行った。さらに、フォトリソグラフィープロセスと真空蒸着法とを用いて、p型層に透光性アノード電極としてNi/Au膜をそれぞれ6nm、12nmの厚みにパターニングした。その後、オーム性接触特性を良好なものとするために窒素雰囲気中で500℃の熱処理を30秒間行った。さらに、フォトリソグラフィープロセスと真空蒸着法とを用いて、透光性アノード電極としてのNi/Au膜の上面の一部領域に、アノード電極パッドとなるNi/Au膜をそれぞれ5nm、60nmの厚みにパターニングした。こうして得られたウェハーを切断してチップ化し、さらにリードフレームに実装して、縦型構造の発光素子を得た。
カソード電極とアノード電極間に通電し、I-V測定を行ったところ、整流性が確認された。また、順方向の電流を流したところ、波長450nmの発光が確認された。
(1)Mgドープ窒化ガリウム自立基板の作製
例1の(1)~(3)と同様の方法で配向アルミナ基板の上に厚さ3μmのGaN膜を積層させた種結晶基板を作製した。この種結晶基板上に、融液組成物を下記組成としたこと以外は例1の(3b)と同様にしてMgドープGaN膜を成膜した。
・金属Ga:60g
・金属Na:60g
・金属Mg:0.02g
(2a)MOCVD法によるp型層の成膜
MOCVD法を用いて、基板上にp型層として950℃でMg原子濃度が1×1019/cm3になるようにドーピングしたp-GaNを200nm堆積した。その後、MOCVD装置から取り出し、p型層のMgイオンの活性化処理として、窒素雰囲気中で800℃の熱処理を10分間行った。
(2b-1)RS-MBE法による種結晶層の成膜
RS-MBE(ラジカルソース分子線成長)装置にて、金属材料である亜鉛(Zn)とアルミニウム(Al)をクヌーセンセルで照射し、p型層上に供給した。ガス材料である酸素(O)は、RFラジカル発生装置にてそれぞれO2ガスを原料とし、酸素ラジカルとして供給した。各種原料の純度はZnが7N、O2が6Nのものを用いた。基板は抵抗加熱ヒーターを用いて700℃に加熱し、膜中のAl濃度が2×1018/cm3となり、ZnとO原子濃度の比が1対1となるように各種ガスソースのフラックスを制御しながら厚さ20nmのAlがドープされたn-ZnOからなる種結晶層を成膜した。
硝酸亜鉛を純水中に0.1Mとなるように溶解させて溶液Aとした。次に1Mのアンモニア水を準備し、溶液Bとした。次に硫酸アルミニウムを純水中に0.1Mとなるように溶解させて溶液Cとした。これらの溶液を容積比で、溶液A:溶液B:溶液C=1:1:0.01となるように混合及び撹拌して、育成用水溶液を得た。
フォトリソグラフィープロセスと真空蒸着法とを用いて、n型層にカソード電極としてTi/Al/Ni/Au膜をそれぞれ15nm、70nm、12nm、60nmの厚みでパターニングした。カソード電極のパターンは、電極が形成されていない箇所から光が取り出せるように開口部を有する形状とした。その後、オーム性接触特性を良好なものとするために、窒素雰囲気中での700℃の熱処理を30秒間行った。さらに、フォトリソグラフィープロセスと真空蒸着法とを用いて、窒化ガリウム自立基板のp-GaN層及びn-ZnO層とは反対側の面にアノード電極として、Ni/Au膜をそれぞれ50nm、100nmの厚みにパターニングした。その後、オーム性接触特性を良好なものとするために窒素雰囲気中で500℃の熱処理を30秒間行った。こうして得られたウェハーを切断してチップ化し、さらにリードフレームに実装して、縦型構造の発光素子を得た。
カソード電極とアノード電極間に通電し、I-V測定を行ったところ、整流性が確認された。また、順方向の電流を流したところ、波長約380nmの発光が確認された。
(1)Mgドープ窒化ガリウム自立基板を用いた発光素子の作製
(1a)RS-MBE法による活性層の成膜
例2の(1)及び(2a)と同様の方法でMgドープ窒化ガリウム自立基板を作製し、基板上にp型層としてp-GaNを200nm体積した。次にRS-MBE(ラジカルソース分子線成長)装置にて、金属材料である亜鉛(Zn)、カドミウム(Cd)をクヌーセンセルで照射し、p型層上に供給した。ガス材料である酸素(O)は、RFラジカル発生装置にてそれぞれO2ガスを原料とし、酸素ラジカルとして供給した。各種原料の純度はZn、Cdが7N、O2が6Nのものを用いた。基板は抵抗加熱ヒーターを用いて700℃に加熱し、Cd0.2Zn0.8O層となるように各種ガスソースのフラックスを制御しながら厚さ1.5nmの活性層を成膜した。
次にRFマグネトロンスパッタ法を用いて、活性層上にn型ZnO層を500nm成膜した。成膜にはAlが2重量部添加されたZnOターゲットを使用し、成膜条件は純Ar雰囲気、圧力0.5Pa、投入電力150W、成膜時間5分間とした。また、例1の(4a)と同様の方法を用いて発光機能層の断面平均径を評価した結果、発光機能層の板面の平均粒径は約100μmであった。
フォトリソグラフィープロセスと真空蒸着法とを用いて、n型層にカソード電極としてTi/Al/Ni/Au膜をそれぞれ15nm、70nm、12nm、60nmの厚みでパターニングした。カソード電極のパターンは、電極が形成されていない箇所から光が取り出せるように開口部を有する形状とした。その後、オーム性接触特性を良好なものとするために、窒素雰囲気中での700℃の熱処理を30秒間行った。さらに、フォトリソグラフィープロセスと真空蒸着法とを用いて、窒化ガリウム自立基板のp-GaN層及びn-ZnO層とは反対側の面にアノード電極として、Ni/Au膜をそれぞれ5nm、100nmの厚みにパターニングした。その後、オーム性接触特性を良好なものとするために窒素雰囲気中で500℃の熱処理を30秒間行った。こうして得られたウェハーを切断してチップ化し、さらにリードフレームに実装して、縦型構造の発光素子を得た。
カソード電極とアノード電極間に通電し、I-V測定を行ったところ、整流性が確認された。また、順方向の電流を流したところ、波長約400nmの発光が確認された。
(1)c面配向アルミナ焼結体の作製
例1の(1)と同様にして円盤状の成形体を得た。得られた成形体を脱脂炉中に配置し、600℃で10時間の条件で脱脂を行った。得られた脱脂体を黒鉛製の型を用い、ホットプレスにて窒素中1700℃で4時間、面圧200kgf/cm2の条件で焼成した。
例1の(3a)と同様にして配向アルミナ基板の上に厚さ3μmのGaN膜を積層させた種結晶基板を作製した。この種結晶基板上に、保持時間を20時間とした以外は例1の(3b)と同様にしてGeドープGaN膜を成膜した。得られた試料は、50.8mm(2インチ)の種結晶基板の全面上にGeドープ窒化ガリウム結晶が成長しており、結晶の厚さは約0.2mmであった。クラックは確認されなかった。
例1の(4a)と同様にして窒化ガリウム自立基板上に発光機能層を作製し、最表面における単結晶粒子の断面平均径を測定したところ、断面平均径は約50μmであった。また例1の(4b)と同様にして縦型の発光素子を作製した結果、カソード電極とアノード電極間のI-V測定より整流性が確認され、順方向の通電により波長450nmの発光が確認された。
(1)c面配向アルミナ焼結体の作製
原料として、板状アルミナ粉末(キンセイマテック株式会社製、グレード02025)、微細アルミナ粉末(大明化学工業株式会社製、グレードTM-DAR)、及び酸化マグネシウム粉末(宇部マテリアルズ株式会社、グレード500A)を用意し、板状アルミナ粉末5重量部、微細アルミナ粉末95重量部、酸化マグネシウム粉末0.025重量部を混合してアルミナ原料を得た。次に、アルミナ原料100重量部に対し、バインダー(ポリビニルブチラール:品番BM-2、積水化学工業株式会社製)8重量部と、可塑剤(DOP:ジ(2-エチルヘキシル)フタレート、黒金化成株式会社製)4重量部と、分散剤(レオドールSP-O30、花王株式会社製)2重量部と、分散媒(キシレンと1-ブタノールを重量比1:1で混合したもの)を混合した。分散媒の量は、スラリー粘度が20000cPとなるように調整した。上記のようにして調製されたスラリーを、ドクターブレード法によって、PETフィルムの上に、乾燥後の厚さが100μmとなるように、シート状に成形した。得られたテープを口径50.8mm(2インチ)の円形に切断した後30枚積層し、厚さ10mmのAl板の上に載置した後、真空パックを行った。この真空パックを85℃の温水中で、100kgf/cm2の圧力にて静水圧プレスを行い、円盤状の成形体を得た。
例1の(3a)と同様にして配向アルミナ基板の上に厚さ3μmのGaN膜を積層させた種結晶基板を作製した。この種結晶基板上に、保持時間を30時間とした以外は例1の(3b)と同様にしてGeドープGaN膜を成膜した。得られた試料は、50.8mm(2インチ)の種結晶基板の全面上にGeドープ窒化ガリウム結晶が成長しており、結晶の厚さは約0.3mmであった。クラックは確認されなかった。
例1の(4a)と同様にして窒化ガリウム自立基板上に発光機能層を作製し、最表面における単結晶粒子の断面平均径を測定したところ、断面平均径は約150μmであった。また例1の(4b)と同様にして縦型の発光素子を作製した結果、カソード電極とアノード電極間のI-V測定より整流性が確認され、順方向の通電により波長450nmの発光が確認された。
(1)Geドープ窒化ガリウム自立基板の作製
例5と同様にしてc面配向アルミナ基板を作製し、厚さ3μmのGaN膜を積層させた種結晶基板を作製した。この種結晶基板上に、保持時間を40時間とした以外は例1の(3b)と同様にしてGeドープGaN膜を成膜した。得られた試料は、50.8mm(2インチ)の種結晶基板の全面上にGeドープ窒化ガリウム結晶が成長しており、結晶の厚さは約0.4mmであった。クラックは確認されなかった。
例1の(4a)と同様にして窒化ガリウム自立基板上に発光機能層を作製し、最表面における単結晶粒子の断面平均径を測定したところ、断面平均径は約220μmであった。また例1の(4b)と同様にして縦型の発光素子を作製した結果、カソード電極とアノード電極間のI-V測定より整流性が確認され、順方向の通電により波長450nmの発光が確認された。発光輝度はある程度高かったが、例5の素子より低いことがわかった。
(1)c面配向アルミナ焼結体の作製
ホットプレスでの焼成温度を1750℃とした以外は例5と同様にしてc面配向アルミナ基板を作製した。このようにして得た焼結体をセラミックスの定盤に固定し、砥石を用いて#2000まで研削して板面を平坦にした。次いで、ダイヤモンド砥粒を用いたラップ加工により、板面を平滑化し、口径50.8mm(2インチ)、厚さ1mmの配向アルミナ焼結体を配向アルミナ基板として得た。砥粒のサイズを3μmから0.5μmまで段階的に小さくしつつ、平坦性を高めた。加工後の平均粗さRaは4nmであった。また、例1と同様の方法でc面配向度と板面の平均粒径を評価したところ、c面配向度は96%、平均粒径は14μmであった。
例1の(3a)と同様にして配向アルミナ基板の上に厚さ3μmのGaN膜を積層させた種結晶基板を作製した。この種結晶基板上に、保持時間を30時間とした以外は例1の(3b)と同様にしてGeドープGaN膜を成膜した。得られた試料は、50.8mm(2インチ)の種結晶基板の全面上にGeドープ窒化ガリウム結晶が成長しており、結晶の厚さは約0.3mmであった。クラックは確認されなかった。
例1の(4a)と同様にして窒化ガリウム自立基板上に発光機能層を作製し、最表面における単結晶粒子の断面平均径を測定した結果を表1に示す。また例1の(4b)と同様にして縦型の発光素子を作製した結果、いずれの試料もカソード電極とアノード電極間のI-V測定より整流性が確認され、順方向の通電により波長450nmの発光が確認された。発光輝度はいずれもある程度高かったが、例7-1>例7-2>例7-3>例7-4>例7-5の関係であった。
(1)c面配向アルミナ焼結体の作製
原料として、板状アルミナ粉末(キンセイマテック株式会社製、グレード02025)、微細アルミナ粉末(大明化学工業株式会社製、グレードTM-DAR)、フッ化アルミニウム(関東化学製)、及び酸化マグネシウム粉末(宇部マテリアルズ株式会社、グレード500A)を用意し、板状アルミナ粉末5重量部、微細アルミナ粉末95重量部、フッ化アルミニウム粉末0.05重量部、酸化マグネシウム粉末0.025重量部を混合してアルミナ原料を得た。次に、アルミナ原料100重量部に対し、バインダー(ポリビニルブチラール:品番BM-2、積水化学工業株式会社製)8重量部と、可塑剤(DOP:ジ(2-エチルヘキシル)フタレート、黒金化成株式会社製)4重量部と、分散剤(レオドールSP-O30、花王株式会社製)2重量部と、分散媒(キシレンと1-ブタノールを重量比1:1で混合したもの)を混合した。分散媒の量は、スラリー粘度が20000cPとなるように調整した。上記のようにして調製されたスラリーを、ドクターブレード法によって、PETフィルムの上に、乾燥後の厚さが100μmとなるように、シート状に成形した。得られたテープを口径50.8mm(2インチ)の円形に切断した後30枚積層し、厚さ10mmのAl板の上に載置した後、真空パックを行った。この真空パックを85℃の温水中で、100kgf/cm2の圧力にて静水圧プレスを行い、円盤状の成形体を得た。
例1の(3a)と同様にして配向アルミナ基板の上に厚さ3μmのGaN膜を積層させた種結晶基板を作製した。この種結晶基板上に、保持時間を30時間とした以外は例1の(3b)と同様にしてGeドープGaN膜を成膜した。得られた試料は、50.8mm(2インチ)の種結晶基板の全面上にGeドープ窒化ガリウム結晶が成長しており、結晶の厚さは約0.3mmであった。クラックは確認されなかった。
例1の(4a)と同様にして窒化ガリウム自立基板上に発光機能層を作製し、最表面における単結晶粒子の断面平均径を測定したところ、断面平均径は約80μmであった。また例1の(4b)と同様にして縦型の発光素子を作製した結果、カソード電極とアノード電極間のI-V測定より整流性が確認され、順方向の通電により波長450nmの発光が確認された。
(1)c面配向アルミナ焼結体の作製
フッ化アルミニウム粉末の量を0.02重量部とした以外は例8と同様にしてc面配向アルミナ基板を作製した。このようにして得た焼結体をセラミックスの定盤に固定し、砥石を用いて#2000まで研削して板面を平坦にした。次いで、ダイヤモンド砥粒を用いたラップ加工により、板面を平滑化し、口径50.8mm(2インチ)、厚さ1mmの配向アルミナ焼結体を配向アルミナ基板として得た。砥粒のサイズを3μmから0.5μmまで段階的に小さくしつつ、平坦性を高めた。加工後の平均粗さRaは4nmであった。また、例1と同様の方法でc面配向度と板面の平均粒径を評価したところ、c面配向度は94%、平均粒径は41μmであった。
例1の(3a)と同様にして配向アルミナ基板の上に厚さ3μmのGaN膜を積層させた種結晶基板を作製した。この種結晶基板上に、保持時間を30時間とした以外は例1の(3b)と同様にしてGeドープGaN膜を成膜した。得られた試料は、50.8mm(2インチ)の種結晶基板の全面上にGeドープ窒化ガリウム結晶が成長しており、結晶の厚さは約0.3mmであった。クラックは確認されなかった。
例1の(4a)と同様にして窒化ガリウム自立基板上に発光機能層を作製し、最表面における単結晶粒子の断面平均径を測定したところ、断面平均径は約81μmであった。また例1の(4b)と同様にして縦型の発光素子を作製した結果、カソード電極とアノード電極間のI-V測定より整流性が確認され、順方向の通電により波長450nmの発光が確認された。しかし、発光輝度はある程度高かったが、例8より弱いことがわかった。
(1)c面配向アルミナ焼結体の作製
原料として、板状アルミナ粉末(キンセイマテック株式会社製、グレード10030)、微細アルミナ粉末(大明化学工業株式会社製、グレードTM-DAR)、及び酸化マグネシウム粉末(宇部マテリアルズ株式会社、グレード500A)を用意し、板状アルミナ粉末5重量部、微細アルミナ粉末95重量部、酸化マグネシウム粉末0.025重量部を混合してアルミナ原料を得た。次に、アルミナ原料100重量部に対し、バインダー(ポリビニルブチラール:品番BM-2、積水化学工業株式会社製)8重量部と、可塑剤(DOP:ジ(2-エチルヘキシル)フタレート、黒金化成株式会社製)4重量部と、分散剤(レオドールSP-O30、花王株式会社製)2重量部と、分散媒(キシレンと1-ブタノールを重量比1:1で混合したもの)を混合した。分散媒の量は、スラリー粘度が20000cPとなるように調整した。上記のようにして調製されたスラリーを、ドクターブレード法によって、PETフィルムの上に、乾燥後の厚さが100μmとなるように、シート状に成形した。得られたテープを口径50.8mm(2インチ)の円形に切断した後30枚積層し、厚さ10mmのAl板の上に載置した後、真空パックを行った。この真空パックを85℃の温水中で、100kgf/cm2の圧力にて静水圧プレスを行い、円盤状の成形体を得た。
例1の(3a)と同様にして配向アルミナ基板の上に厚さ3μmのGaN膜を積層させた種結晶基板を作製した。この種結晶基板上に、保持時間を30時間とした以外は例1の(3b)と同様にしてGeドープGaN膜を成膜した。得られた試料は、50.8mm(2インチ)の種結晶基板の全面上にGeドープ窒化ガリウム結晶が成長しており、結晶の厚さは約0.3mmであった。クラックは確認されなかった。
例1の(4a)と同様にして窒化ガリウム自立基板上に発光機能層を作製し、最表面における単結晶粒子の断面平均径を測定したところ、断面平均径は約75μmであった。また例1の(4b)と同様にして縦型の発光素子を作製した結果、カソード電極とアノード電極間のI-V測定より整流性が確認され、順方向の通電により波長450nmの発光が確認された。但し、発光輝度はある程度高かったが、例8及び9より弱いことが分かった。
窒化ガリウム系単結晶粒子の断面平均径を20μm以上にすることが発光効率を顕著に向上させる点をより明確に確認すべく、検証実験を行った。この検証実験においては、窒化ガリウム系単結晶粒子の断面平均径DTが2、3、13、16、20、35、42、50、72、90及び110μmである各種窒化ガリウム自立基板を作製して、これを用いて発光素子を作製し、株式会社テクノローグ製LEDテスターLX4681Aを使用して、200A/cm2(チップサイズ:1mm角、順方向電流:2A)における発光輝度を測定した。その結果は表2に示されるとおりであった。そして、表2に示される発光輝度の結果から明らかなように、断面平均径DTが3~16μmである窒化ガリウム自立基板を用いた場合には発光輝度が0.40~0.42(a.u.)であったに対し、断面平均径DTが20μm以上である窒化ガリウム自立基板を用いると、発光輝度が0.91以上(a.u.)と顕著に増加することが確認された。これらの結果は、20μmなる断面平均径を境に発光効率が顕著に向上することを示すものに他ならない。
[項1]
略法線方向に単結晶構造を有する複数の窒化ガリウム系単結晶粒子で構成される板からなる、窒化ガリウム自立基板。
[項2]
前記基板の最表面における前記窒化ガリウム系単結晶粒子の断面平均径が0.3μm以上である、項1に記載の窒化ガリウム自立基板。
[項3]
前記断面平均径が3μm以上である、項2に記載の窒化ガリウム自立基板。
[項4]
前記断面平均径が20μm以上である、項2に記載の窒化ガリウム自立基板。
[項5]
20μm以上の厚さを有する、項1~4のいずれか一項に記載の窒化ガリウム自立基板。
[項6]
直径100mm以上の大きさを有する、項1~5のいずれか一項に記載の窒化ガリウム自立基板。
[項7]
前記窒化ガリウム系単結晶粒子が、略法線方向に概ね揃った結晶方位を有する、項1~6のいずれか一項に記載の窒化ガリウム自立基板。
[項8]
前記窒化ガリウム系単結晶粒子がn型ドーパント又はp型ドーパントでドープされている、項1~7のいずれか一項に記載の窒化ガリウム自立基板。
[項9]
前記窒化ガリウム系単結晶粒子がドーパントを含まない、項1~7のいずれか一項に記載の窒化ガリウム自立基板。
[項10]
前記窒化ガリウム系単結晶粒子が混晶化されている、項1~9のいずれか一項に記載の窒化ガリウム自立基板。
[項11]
前記窒化ガリウム自立基板の表面に露出している前記窒化ガリウム系単結晶粒子が、該窒化ガリウム自立基板の裏面に粒界を介さずに連通してなる、項1~10のいずれか一項に記載の窒化ガリウム自立基板。
[項12]
窒化ガリウム自立基板の裏面に露出している窒化ガリウム系単結晶粒子の最表面における断面平均径DBに対する、窒化ガリウム自立基板の表面に露出している窒化ガリウム系単結晶粒子の最表面における断面平均径DTの比DT/DBが1.0よりも大きい、項1~11のいずれか一項に記載の窒化ガリウム自立基板。
[項13]
前記窒化ガリウム自立基板の表面に露出している前記窒化ガリウム系単結晶粒子の最表面における断面平均径DTに対する、前記窒化ガリウム自立基板の厚さTの比として規定されるアスペクト比T/DTが0.7以上である、項1~12のいずれか一項に記載の窒化ガリウム自立基板。
[項14]
項1~13のいずれか一項に記載の窒化ガリウム自立基板と、
該基板上に形成され、略法線方向に単結晶構造を有する複数の半導体単結晶粒子で構成される層を一以上有する発光機能層と、
を備えた、発光素子。
[項15]
前記発光機能層の最表面における前記半導体単結晶粒子の断面平均径が0.3μm以上である、項14に記載の自立した発光素子。
[項16]
前記断面平均径が3μm以上である、項15に記載の発光素子。
[項17]
前記半導体単結晶粒子が、前記窒化ガリウム自立基板の結晶方位に概ね倣って成長した構造を有する、項14~16のいずれか一項に記載の発光素子。
[項18]
前記発光機能層が窒化ガリウム系材料で構成される、項14~17のいずれか一項に記載の発光素子。
[項19]
配向多結晶焼結体を用意する工程と、
前記配向多結晶焼結体上に、窒化ガリウムからなる種結晶層を、前記配向多結晶焼結体の結晶方位に概ね倣った結晶方位を有するように形成する工程と、
前記種結晶層上に、厚さ20μm以上の窒化ガリウム系結晶から構成される層を、前記種結晶層の結晶方位に概ね倣った結晶方位を有するように形成する工程と、
前記配向多結晶焼結体を除去して、窒化ガリウム自立基板を得る工程と、
を含む、窒化ガリウム自立基板の製造方法。
[項20]
前記配向多結晶焼結体が配向多結晶アルミナ焼結体である、項19に記載の方法。
[項21]
前記配向多結晶焼結体を構成する粒子の板面における平均粒径が0.3~1000μmである、項19又は20に記載の方法。
[項22]
前記窒化ガリウム系結晶から構成される層の形成がNaフラックス法により行われる、項19~21のいずれか一項に記載の方法。
[項23]
前記配向多結晶焼結体が透光性を有する、項19~22のいずれか一項に記載の方法。
[項24]
項1~13のいずれか一項に記載の窒化ガリウム自立基板を用意する、又は項19~23のいずれか一項に記載の方法により前記窒化ガリウム自立基板を用意する工程と、
前記窒化ガリウム自立基板に、前記窒化ガリウム基板の結晶方位に概ね倣った結晶方位を有するように、略法線方向に単結晶構造を有する複数の半導体単結晶粒子で構成される層を一つ以上形成して発光機能層を設ける工程と、
を含む、発光素子の製造方法。
[項25]
前記発光機能層が窒化ガリウム系材料で構成される、項24に記載の方法。
Claims (22)
- 略法線方向に単結晶構造を有する複数の窒化ガリウム系単結晶粒子で構成される板からなる、窒化ガリウム自立基板。
- 前記基板の最表面における前記窒化ガリウム系単結晶粒子の断面平均径が0.3μm以上である、請求項1に記載の窒化ガリウム自立基板。
- 前記断面平均径が3μm以上である、請求項2に記載の窒化ガリウム自立基板。
- 20μm以上の厚さを有する、請求項1~3のいずれか一項に記載の窒化ガリウム自立基板。
- 直径100mm以上の大きさを有する、請求項1~4のいずれか一項に記載の窒化ガリウム自立基板。
- 前記窒化ガリウム系単結晶粒子が、略法線方向に概ね揃った結晶方位を有する、請求項1~5のいずれか一項に記載の窒化ガリウム自立基板。
- 前記窒化ガリウム系単結晶粒子がn型ドーパント又はp型ドーパントでドープされている、請求項1~6のいずれか一項に記載の窒化ガリウム自立基板。
- 前記窒化ガリウム系単結晶粒子がドーパントを含まない、請求項1~6のいずれか一項に記載の窒化ガリウム自立基板。
- 前記窒化ガリウム系単結晶粒子が混晶化されている、請求項1~8のいずれか一項に記載の窒化ガリウム自立基板。
- 前記窒化ガリウム自立基板の表面に露出している前記窒化ガリウム系単結晶粒子の最表面における断面平均径DTに対する、前記窒化ガリウム自立基板の厚さTの比として規定されるアスペクト比T/DTが0.7以上である、請求項1~9のいずれか一項に記載の窒化ガリウム自立基板。
- 請求項1~10のいずれか一項に記載の窒化ガリウム自立基板と、
該基板上に形成され、略法線方向に単結晶構造を有する複数の半導体単結晶粒子で構成される層を一以上有する発光機能層と、
を備えた、発光素子。 - 前記発光機能層の最表面における前記半導体単結晶粒子の断面平均径が0.3μm以上である、請求項11に記載の自立した発光素子。
- 前記断面平均径が3μm以上である、請求項12に記載の発光素子。
- 前記半導体単結晶粒子が、前記窒化ガリウム自立基板の結晶方位に概ね倣って成長した構造を有する、請求項11~13のいずれか一項に記載の発光素子。
- 前記発光機能層が窒化ガリウム系材料で構成される、請求項11~14のいずれか一項に記載の発光素子。
- 配向多結晶焼結体を用意する工程と、
前記配向多結晶焼結体上に、窒化ガリウムからなる種結晶層を、前記配向多結晶焼結体の結晶方位に概ね倣った結晶方位を有するように形成する工程と、
前記種結晶層上に、厚さ20μm以上の窒化ガリウム系結晶から構成される層を、前記種結晶層の結晶方位に概ね倣った結晶方位を有するように形成する工程と、
前記配向多結晶焼結体を除去して、窒化ガリウム自立基板を得る工程と、
を含む、窒化ガリウム自立基板の製造方法。 - 前記配向多結晶焼結体が配向多結晶アルミナ焼結体である、請求項16に記載の方法。
- 前記配向多結晶焼結体を構成する粒子の板面における平均粒径が0.3~1000μmである、請求項16又は17に記載の方法。
- 前記窒化ガリウム系結晶から構成される層の形成がNaフラックス法により行われる、請求項16~18のいずれか一項に記載の方法。
- 前記配向多結晶焼結体が透光性を有する、請求項16~19のいずれか一項に記載の方法。
- 請求項1~10のいずれか一項に記載の窒化ガリウム自立基板を用意する、又は請求項16~20のいずれか一項に記載の方法により前記窒化ガリウム自立基板を用意する工程と、
前記窒化ガリウム自立基板に、前記窒化ガリウム基板の結晶方位に概ね倣った結晶方位を有するように、略法線方向に単結晶構造を有する複数の半導体単結晶粒子で構成される層を一つ以上形成して発光機能層を設ける工程と、
を含む、発光素子の製造方法。 - 前記発光機能層が窒化ガリウム系材料で構成される、請求項21に記載の方法。
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JP2018078232A (ja) * | 2016-11-11 | 2018-05-17 | 日本碍子株式会社 | 広波長域発光素子および広波長域発光素子の作製方法 |
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0927636A (ja) * | 1995-07-12 | 1997-01-28 | Toshiba Corp | 化合物半導体装置及び化合物半導体発光装置 |
JP2004359495A (ja) * | 2003-06-04 | 2004-12-24 | Ngk Insulators Ltd | エピタキシャル膜用アルミナ基板 |
WO2009044638A1 (ja) * | 2007-10-04 | 2009-04-09 | Sumitomo Electric Industries, Ltd. | GaNエピタキシャル基板、半導体デバイス、GaNエピタキシャル基板及び半導体デバイスの製造方法 |
JP2009073710A (ja) * | 2007-09-25 | 2009-04-09 | Panasonic Corp | 窒化ガリウム基板の製造方法、および窒化ガリウム基板ならびに半導体装置 |
WO2014192911A1 (ja) * | 2013-05-31 | 2014-12-04 | 日本碍子株式会社 | 窒化ガリウム自立基板、発光素子及びそれらの製造方法 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW428331B (en) | 1998-05-28 | 2001-04-01 | Sumitomo Electric Industries | Gallium nitride single crystal substrate and method of producing the same |
WO2007010645A1 (ja) * | 2005-07-21 | 2007-01-25 | Sumitomo Electric Industries, Ltd. | 窒化ガリウムウエハ |
JP2007056164A (ja) * | 2005-08-25 | 2007-03-08 | Univ Nagoya | 発光層形成用基材、発光体及び発光物質 |
JP4341702B2 (ja) * | 2007-06-21 | 2009-10-07 | 住友電気工業株式会社 | Iii族窒化物系半導体発光素子 |
JP2011121815A (ja) * | 2009-12-10 | 2011-06-23 | Sumitomo Electric Ind Ltd | 単結晶の製造方法 |
JP2012184144A (ja) | 2011-03-07 | 2012-09-27 | Tokuyama Corp | 窒化ガリウム結晶積層基板及びその製造方法 |
CN102208331B (zh) * | 2011-04-11 | 2012-09-19 | 青岛铝镓光电半导体有限公司 | 晶体生长方法及衬底的制作方法 |
JP6144630B2 (ja) * | 2012-08-30 | 2017-06-07 | 日本碍子株式会社 | 複合基板の製造方法、13族元素窒化物からなる機能層の製造方法 |
-
2015
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Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0927636A (ja) * | 1995-07-12 | 1997-01-28 | Toshiba Corp | 化合物半導体装置及び化合物半導体発光装置 |
JP2004359495A (ja) * | 2003-06-04 | 2004-12-24 | Ngk Insulators Ltd | エピタキシャル膜用アルミナ基板 |
JP2009073710A (ja) * | 2007-09-25 | 2009-04-09 | Panasonic Corp | 窒化ガリウム基板の製造方法、および窒化ガリウム基板ならびに半導体装置 |
WO2009044638A1 (ja) * | 2007-10-04 | 2009-04-09 | Sumitomo Electric Industries, Ltd. | GaNエピタキシャル基板、半導体デバイス、GaNエピタキシャル基板及び半導体デバイスの製造方法 |
WO2014192911A1 (ja) * | 2013-05-31 | 2014-12-04 | 日本碍子株式会社 | 窒化ガリウム自立基板、発光素子及びそれらの製造方法 |
Non-Patent Citations (3)
Title |
---|
F.R. HU ET AL.: "Molecular beam epitaxial growth of GaN thin film on Si substrate with InN as interlayer", JOURNAL OF CRYSTAL GROWTH, vol. 294, pages 197 - 201, XP028016898, DOI: doi:10.1016/j.jcrysgro.2006.07.009 * |
P. R. HAGEMAN ET AL.: "GaN growth on single- crystal diamond substrates by metalorganic chemical vapour deposition and hydride vapour deposition", THIN SOLID FILMS, vol. 443, 2003, pages 9 - 13, XP004458334, DOI: doi:10.1016/S0040-6090(03)00906-4 * |
TSUTOMU ARAKI ET AL.: "Crystal Growth and Characterization of Polycrystalline GaN on Silica Glass by ECR-MBE", JOURNAL OF THE JAPANESE ASSOCIATION OF CRYSTAL GROWTH, vol. 30, no. 2, 2003, pages 73 - 81 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2018078232A (ja) * | 2016-11-11 | 2018-05-17 | 日本碍子株式会社 | 広波長域発光素子および広波長域発光素子の作製方法 |
WO2018179240A1 (ja) * | 2017-03-30 | 2018-10-04 | 日本碍子株式会社 | アルミナ結晶及びその製法 |
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