JP2019156659A - MANUFACTURING METHOD OF SiC INGOT MANUFACTURING SUBSTRATE, AND SiC INGOT MANUFACTURING SUBSTRATE - Google Patents
MANUFACTURING METHOD OF SiC INGOT MANUFACTURING SUBSTRATE, AND SiC INGOT MANUFACTURING SUBSTRATE Download PDFInfo
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- 238000003825 pressing Methods 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 25
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- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 18
- 239000012298 atmosphere Substances 0.000 claims description 16
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 14
- 239000007789 gas Substances 0.000 claims description 14
- 239000011261 inert gas Substances 0.000 claims description 14
- 229910002804 graphite Inorganic materials 0.000 claims description 13
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- 230000004913 activation Effects 0.000 claims description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 229910052786 argon Inorganic materials 0.000 claims description 9
- 230000001678 irradiating effect Effects 0.000 claims description 6
- 230000003213 activating effect Effects 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 238000000151 deposition Methods 0.000 claims description 3
- 239000000853 adhesive Substances 0.000 abstract description 6
- 230000001070 adhesive effect Effects 0.000 abstract description 5
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- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 129
- 229910010271 silicon carbide Inorganic materials 0.000 description 129
- 239000010410 layer Substances 0.000 description 31
- 238000001994 activation Methods 0.000 description 15
- 239000002344 surface layer Substances 0.000 description 7
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- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 3
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Abstract
Description
本発明は、SiCインゴット製造用基板の製造方法、及び、SiCインゴット製造用基板に関する。 The present invention relates to a method for manufacturing a substrate for manufacturing a SiC ingot and a substrate for manufacturing a SiC ingot.
通常、母材となるSiC(炭化ケイ素)基板とグラファイト(黒鉛)基板を接着した後、チャンバーの中でSiC基板の表面に気化したSiC分子を蒸着させてSiCのインゴットを製造している。例えば、特許文献1には、グラファイト基板が接着されたSiCからなる種結晶基板上にSiC結晶を成長させることにより、SiCのインゴットを製造する方法が開示されている。 Usually, after a SiC (silicon carbide) substrate and a graphite (graphite) substrate as a base material are bonded together, vaporized SiC molecules are vapor-deposited on the surface of the SiC substrate in a chamber to manufacture a SiC ingot. For example, Patent Document 1 discloses a method of manufacturing an SiC ingot by growing an SiC crystal on a seed crystal substrate made of SiC to which a graphite substrate is bonded.
SiCのインゴットが製造された後、SiC基板とグラファイト基板は剥離される。一般的に、SiCのインゴットを製造する際のチャンバー内の温度は2300℃以上あり、さらに、SiCのインゴットが完成するまで200時間以上かかっている。通常、SiC基板とグラファイト基板の接着には耐熱性に優れる接着剤を用いているが、インゴット製造に必要な温度を長時間に亘ってかけると、接着剤の物性が変化するという問題がある。 After the SiC ingot is manufactured, the SiC substrate and the graphite substrate are peeled off. Generally, the temperature in the chamber when manufacturing the SiC ingot is 2300 ° C. or higher, and it takes 200 hours or more to complete the SiC ingot. Usually, an adhesive having excellent heat resistance is used for bonding the SiC substrate and the graphite substrate. However, if the temperature required for manufacturing the ingot is applied for a long time, there is a problem that the physical properties of the adhesive change.
また、接着剤による接着時にSiC基板とグラファイト基板との間にピンホール状の欠陥が存在する場合、インゴット製造時の高温により、ピンホール内部のガス残渣が熱により膨張し、SiC基板とグラファイト基板が剥離する恐れもある。 In addition, when there is a pinhole-like defect between the SiC substrate and the graphite substrate during bonding with the adhesive, the gas residue inside the pinhole expands due to heat due to the high temperature during ingot production, and the SiC substrate and the graphite substrate May peel off.
本発明は、上記に鑑みてなされたものであって、SiCインゴットが蒸着されるSiC基板と、SiC基板が接着される支持基板とを接着剤を用いずに接着することができる、SiCインゴット製造用基板の製造方法、及び、SiCインゴット製造用基板を提供することを目的とする。 This invention is made in view of the above, Comprising: The SiC ingot manufacture which can adhere | attach the SiC substrate in which a SiC ingot is vapor-deposited, and the support substrate to which a SiC substrate is adhere | attached, without using an adhesive agent An object of the present invention is to provide a method for manufacturing a substrate and a substrate for manufacturing a SiC ingot.
上述した課題を解決し、目的を達成するために、本発明におけるSiCインゴット製造用基板の製造方法は、SiC結晶が形成されるSiC基板とSiC基板を支持する支持基板とが接合される接合予定面の少なくとも一方に、SiC中間層を形成する形成工程と、SiC基板と支持基板とを互いに押し付けて、SiC中間層を介してSiC基板と支持基板とを接合する接合工程と、を備えることを特徴とする。 In order to solve the above-described problems and achieve the object, a manufacturing method of a substrate for manufacturing an SiC ingot according to the present invention is a bonding plan in which an SiC substrate on which an SiC crystal is formed and a support substrate that supports the SiC substrate are bonded Forming a SiC intermediate layer on at least one of the surfaces; and a bonding step of pressing the SiC substrate and the support substrate together to bond the SiC substrate and the support substrate through the SiC intermediate layer. Features.
また、本発明の一態様によれば、SiC基板と支持基板とを剥離する剥離工程をさらに備えることを特徴とする。 Moreover, according to one aspect of the present invention, the method further includes a peeling step of peeling the SiC substrate and the support substrate.
また、本発明の一態様によれば、接合工程の後、かつ剥離工程の前に、SiC基板上にSiC分子を蒸着させてSiCのインゴットを形成するインゴット形成工程を備えることを特徴とする。 Moreover, according to one aspect of the present invention, an ingot forming step of forming SiC ingots by depositing SiC molecules on a SiC substrate after the bonding step and before the peeling step is provided.
また、本発明の一態様によれば、上記製造方法において、支持基板がグラファイト(黒鉛)基板、または、SiC基板であることを特徴とする。 According to another aspect of the present invention, in the above manufacturing method, the support substrate is a graphite (graphite) substrate or a SiC substrate.
また、本発明の一態様によれば、上記製造方法において、形成工程において、SiC中間層を複数形成することを特徴とする。 Moreover, according to one aspect of the present invention, in the manufacturing method, a plurality of SiC intermediate layers are formed in the forming step.
また、本発明の一態様によれば、上記製造方法において、接合工程の前に、SiC基板か支持基板の少なくとも一方の接合予定面を、所定の運動エネルギーを備える粒子を照射することで活性化させる表面活性化工程をさらに備える。 Moreover, according to one aspect of the present invention, in the above manufacturing method, before the bonding step, at least one of the planned bonding surfaces of the SiC substrate or the support substrate is activated by irradiating particles having predetermined kinetic energy. And a surface activation step.
また、本発明の一態様によれば、上記製造方法において、接合工程の前に、SiC中間層の表面を、所定の運動エネルギーを備える粒子を照射することで活性化させる表面活性化工程をさらに備える。 Moreover, according to one aspect of the present invention, in the above manufacturing method, a surface activation step of activating the surface of the SiC intermediate layer by irradiating particles having a predetermined kinetic energy before the bonding step is further performed. Prepare.
また、本発明の一態様によれば、上記製造方法において、接合工程の前に、基板接合予定面の一部を選択的に表面活性化する。 Moreover, according to one aspect of the present invention, in the manufacturing method described above, a part of the substrate bonding planned surface is selectively surface activated before the bonding step.
また、本発明の一態様によれば、上記製造方法において、接合工程の前に、SiC基板と支持基板の接合予定面の少なくとも一方を不活性ガスを含むガス雰囲気中に晒す。 Moreover, according to one aspect of the present invention, in the above manufacturing method, at least one of the planned bonding surfaces of the SiC substrate and the support substrate is exposed to a gas atmosphere containing an inert gas before the bonding step.
また、本発明の一態様によれば、上記製造方法において、不活性ガスが窒素、アルゴン、またはこれらの混合ガスである。 According to one embodiment of the present invention, in the manufacturing method, the inert gas is nitrogen, argon, or a mixed gas thereof.
また、本発明の一態様によれば、上記製造方法において、接合工程が、真空雰囲気中または不活性ガス雰囲気中で行われる。 According to one embodiment of the present invention, in the above manufacturing method, the joining step is performed in a vacuum atmosphere or an inert gas atmosphere.
また、本発明の一態様によれば、上記製造方法において、接合工程が行われる不活性ガス雰囲気中の不活性ガスは窒素、アルゴン、またはこれらの混合ガスである。 According to one embodiment of the present invention, in the above manufacturing method, the inert gas in the inert gas atmosphere in which the bonding step is performed is nitrogen, argon, or a mixed gas thereof.
また、本発明の一態様によれば、上記製造方法において、接合工程が、バックグラウンド圧力が1×10−8Pa以上大気圧未満である、真空ないしは減圧雰囲気中で行われる。 According to one embodiment of the present invention, in the above manufacturing method, the joining step is performed in a vacuum or a reduced pressure atmosphere in which the background pressure is 1 × 10 −8 Pa or more and less than atmospheric pressure.
また、本発明の一態様によれば、上記の製造方法によって製造されるSiCインゴット製造用基板が提供される。 Moreover, according to 1 aspect of this invention, the board | substrate for SiC ingot manufacture manufactured by said manufacturing method is provided.
本発明によれば、SiCインゴットが蒸着されるSiC基板と、SiC基板が接着される支持基板とを接着剤を用いずに接着することができるので、SiCインゴット製造に必要な高温に長時間さらされても、SiC基板と支持基板との接合面にボイドの発生などの劣化がなく、SiC基板と支持基板と剥離の恐れがないという効果を奏する。 According to the present invention, since the SiC substrate on which the SiC ingot is deposited and the support substrate to which the SiC substrate is bonded can be bonded without using an adhesive, the SiC substrate is exposed to a high temperature required for manufacturing the SiC ingot for a long time. However, there is no deterioration such as generation of voids in the joint surface between the SiC substrate and the support substrate, and there is an effect that there is no fear of peeling between the SiC substrate and the support substrate.
以下に、実施形態を挙げて本発明を説明するが、本発明がこれらの具体的な実施形態に限定されないことは自明である。 Hereinafter, the present invention will be described with reference to embodiments, but it is obvious that the present invention is not limited to these specific embodiments.
[実施形態1]
本実施形態の製造方法は、SiCインゴット製造用基板の製造方法であって、SiC結晶が形成されるSiC基板とSiC基板を支持する支持基板とが接合される接合予定面の少なくとも一方に、SiC中間層を形成する形成工程と、SiC基板と支持基板とを互いに押し付けて、SiC中間層を介してSiC基板と支持基板とを接合する接合工程と、を備える。
[Embodiment 1]
The manufacturing method of the present embodiment is a manufacturing method of a substrate for manufacturing an SiC ingot, and an SiC substrate on which SiC substrates on which an SiC crystal is formed and a support substrate that supports the SiC substrate are bonded to at least one of the surfaces to be bonded. A forming step of forming the intermediate layer, and a bonding step of pressing the SiC substrate and the support substrate together to bond the SiC substrate and the support substrate through the SiC intermediate layer.
上記構成からなる製造方法では、SiC中間層を介してSiC基板と支持基板とを接合することにより、基板接合後の工程において、2300℃以上の加熱処理などを行っても、接合面が劣化せず、後に基板と支持基板とを容易に剥離することができる。または、材料や条件によってはさらなる高温で加熱処理を行ってもSiC基板と支持基板は容易に剥離できる可能性がある。 In the manufacturing method having the above-described configuration, the bonding surface is deteriorated even when heat treatment at 2300 ° C. or higher is performed in the process after bonding the substrate by bonding the SiC substrate and the support substrate through the SiC intermediate layer. In addition, the substrate and the supporting substrate can be easily peeled later. Alternatively, depending on the material and conditions, there is a possibility that the SiC substrate and the support substrate can be easily peeled even if heat treatment is performed at a higher temperature.
図1は、本実施形態に係るSiCインゴット製造用基板の製造方法の一例を説明する図である。この例では、SiC結晶が形成されるSiC基板1と、SiC基板1を支持する支持基板2とが、支持基板2上に形成されたSiC中間層3を介して接合されることにより、SiCインゴット製造用基板が製造される形態を示している。 FIG. 1 is a view for explaining an example of a method for producing a substrate for producing an SiC ingot according to the present embodiment. In this example, a SiC substrate 1 on which a SiC crystal is formed and a support substrate 2 that supports the SiC substrate 1 are bonded together via a SiC intermediate layer 3 formed on the support substrate 2, so that a SiC ingot is obtained. The form by which the board | substrate for manufacture is manufactured is shown.
(a)SiC基板および支持基板の準備工程
SiC結晶が形成されるSiC基板1と、該基板を支持する支持基板2とを用意する。
(b)SiC中間層形成工程
SiC基板1が接合される支持基板2の接合予定面に、SiC中間層3を形成する。
(c)基板接合工程
SiC基板1と支持基板2とを互いに押し付けて、SiC中間層3を介してSiC基板と支持基板とを接合して、基板接合体を形成する。この結果、SiCインゴット製造用基板が製造される。
(A) SiC substrate and supporting substrate preparation step An SiC substrate 1 on which an SiC crystal is formed and a supporting substrate 2 that supports the substrate are prepared.
(B) SiC intermediate layer forming step The SiC intermediate layer 3 is formed on the planned bonding surface of the support substrate 2 to which the SiC substrate 1 is bonded.
(C) Substrate Bonding Step The SiC substrate 1 and the support substrate 2 are pressed against each other, and the SiC substrate and the support substrate are bonded via the SiC intermediate layer 3 to form a substrate bonded body. As a result, an SiC ingot manufacturing substrate is manufactured.
図2は、SiCインゴット製造用基板にSiC結晶を成長させる工程の一例を説明する図である。 FIG. 2 is a diagram for explaining an example of a process for growing a SiC crystal on a SiC ingot manufacturing substrate.
(d)SiCエピタキシャル成長工程
支持基板2との接合面とは反対の面にエピタキシャル成長のためのSiC含有原料ガス4を接触流通させる。
(e)SiCインゴットの形成
SiC基板1上にSiCがエピタキシャル成長により形成され、SiC基板1とエピタキシャル成長により形成されたSiCからなるSiCインゴット5が形成される。
(D) SiC epitaxial growth process The SiC-containing source gas 4 for epitaxial growth is made to contact and flow on the surface opposite to the joint surface with the support substrate 2.
(E) Formation of SiC Ingot SiC is formed on the SiC substrate 1 by epitaxial growth, and a SiC ingot 5 made of SiC formed by the SiC substrate 1 and epitaxial growth is formed.
上記の製造方法において、支持基板2はグラファイト(黒鉛)基板、または、SiC基板であってよい。 In the above manufacturing method, the support substrate 2 may be a graphite (graphite) substrate or a SiC substrate.
上記の製造方法において、工程(b)と工程(c)との間に、後述する表面活性化工程をさらに備えてもよい。 In the above manufacturing method, a surface activation step described later may be further provided between the step (b) and the step (c).
上記製造方法において、接合工程の前に、SiC基板1か支持基板2の少なくとも一方の接合予定面を、所定の運動エネルギーを備える粒子を照射することで活性化させる表面活性化工程をさらに備えてもよい。 The manufacturing method further includes a surface activation step of activating at least one of the planned bonding surfaces of the SiC substrate 1 or the support substrate 2 by irradiating particles having a predetermined kinetic energy before the bonding step. Also good.
あるいは、上記製造方法において、接合工程の前に、SiC中間層3の表面を、所定の運動エネルギーを備える粒子を照射することで活性化させる表面活性化工程をさらに備えてもよい。 Or in the said manufacturing method, you may further provide the surface activation process of activating the surface of SiC intermediate layer 3 by irradiating the particle | grains provided with predetermined | prescribed kinetic energy before a joining process.
表面活性化工程における表面活性化処理により、基板接合工程において、SiC基板1、又は、支持基板2上に形成されたSiC中間層3のいずれか同士の接合界面の接合強度を増すことができる。 By the surface activation process in the surface activation process, the bonding strength at the bonding interface between the SiC substrate 1 or the SiC intermediate layer 3 formed on the support substrate 2 can be increased in the substrate bonding process.
所定の運動エネルギーを有する粒子を衝突させて、接合面を形成する物質を物理的に弾き飛ばす現象(スパッタリング現象)を生じさせることで、酸化物や汚染物など表面層を除去し、表面エネルギーの高い、すなわち活性な無機材料の新生表面を露出させることができる。 By causing particles having a predetermined kinetic energy to collide and causing the material that forms the bonding surface to physically repel (sputtering phenomenon), the surface layer such as oxides and contaminants is removed, and the surface energy An emerging surface of high or active inorganic material can be exposed.
表面活性化処理に用いる粒子として、たとえば、ネオン(Ne)、アルゴン(Ar)、クリプトン(Kr)、キセノン(Xe)、ヘリウム(He)などの希ガスまたは不活性ガスを採用することができる。これらの希ガスは、衝突される接合面を形成する物質と化学反応を起こしにくいので、化合物を形成するなどして、接合面の化学的性質を大きく変化させることはない。 As particles used for the surface activation treatment, for example, a rare gas or an inert gas such as neon (Ne), argon (Ar), krypton (Kr), xenon (Xe), or helium (He) can be employed. These rare gases are unlikely to cause a chemical reaction with a substance that forms a collision surface to be collided, so that a chemical property of the bonding surface is not greatly changed by forming a compound or the like.
表面活性化される接合面に衝突させる粒子には、粒子ビーム源やプラズマ発生装置を用いて、粒子を接合面に向けて加速することで所定の運動エネルギーを与えることができる。 Particles that collide with the surface to be surface activated can be given a predetermined kinetic energy by accelerating the particles toward the surface using a particle beam source or a plasma generator.
表面活性化される接合面に衝突させる粒子の運動エネルギーは、1eVから2keVであることが好ましい。上記の運動エネルギーにより、効率的に表面層におけるスパッタリング現象が生じると考えられる。除去すべき表面層の厚さ、材質などの性質、新生表面の材質などに応じて、上記運動エネルギーの範囲から所望の運動エネルギーの値を設定することもできる。 It is preferable that the kinetic energy of the particles colliding with the surface to be surface activated is 1 eV to 2 keV. It is considered that the above kinetic energy efficiently causes a sputtering phenomenon in the surface layer. A desired value of kinetic energy can also be set from the above kinetic energy range according to the thickness of the surface layer to be removed, the properties such as the material, the material of the new surface, and the like.
粒子ビーム源を用いて、粒子に所定の運動エネルギーを与えることもできる。粒子ビーム源は、たとえばバックグラウンド圧力が1×10−8Pa(パスカル)以下などの、比較的高い真空中で作動する。比較的高い真空に引くために真空ポンプの作動により、金属領域の表面から除去された物質が効率よく雰囲気外へ排気される。 A particle beam source can also be used to impart a predetermined kinetic energy to the particles. The particle beam source operates in a relatively high vacuum, such as a background pressure of 1 × 10 −8 Pa (pascal) or less. The substance removed from the surface of the metal region is efficiently exhausted out of the atmosphere by the operation of the vacuum pump to draw a relatively high vacuum.
これにより、露出された新生表面への望ましくない物質の付着を抑制することができる。さらに、粒子ビーム源は、比較的高い加速電圧を印加することができるので、高い運動エネルギーを粒子に付与することができる。したがって、効率よく表面層の除去および新生表面の活性化を行うことができると考えられる。 Thereby, adhesion of the undesirable substance to the exposed new surface can be suppressed. Furthermore, since the particle beam source can apply a relatively high acceleration voltage, high kinetic energy can be imparted to the particles. Therefore, it is considered that the surface layer can be efficiently removed and the nascent surface can be activated.
あるいは、バックグラウンド圧力が1×10−8Pa以上大気圧未満である、真空ないしは減圧雰囲気中で表面活性化処理を行ってもよい。 Alternatively, the surface activation treatment may be performed in a vacuum or reduced pressure atmosphere in which the background pressure is 1 × 10 −8 Pa or more and less than atmospheric pressure.
粒子ビーム源として、イオンビームを放射するイオンビーム源や中性原子ビームを放射する中性原子ビーム源を用いることができる。イオンビーム源としては、コールドカソード型イオン源を用いることができる。 As the particle beam source, an ion beam source that emits an ion beam or a neutral atom beam source that emits a neutral atom beam can be used. As the ion beam source, a cold cathode ion source can be used.
中性原子ビーム源としては、高速原子ビーム源(FAB,Fast Atom Beam)を用いることができる。高速原子ビーム源(FAB)は、表面層を剥がすための典型的なプラズマを発生させ、このプラズマに電界を掛けて、プラズマから電離した粒子の陽イオンを摘出し電子雲の中を通過させて中性化する構成を有している。 As the neutral atom beam source, a fast atom beam source (FAB, Fast Atom Beam) can be used. A fast atom beam source (FAB) generates a typical plasma for peeling off a surface layer, applies an electric field to the plasma, extracts positive ions of particles ionized from the plasma, and passes them through an electron cloud. It has a structure that is neutralized.
この場合、たとえば、希ガスとしてアルゴン(Ar)の場合、高速原子ビーム源(FAB)への供給電力を、1.5kV(キロボルト)、15mA(ミリアンペア)に設定してもよく、あるいは0.1から500W(ワット)の間の値に設定してもよい。たとえば、高速原子ビーム源(FAB)を100W(ワット)から200W(ワット)で稼動してアルゴン(Ar)の高速原子ビームを2分ほど照射すると、接合面の上記酸化物、汚染物など(表面層)は除去され、新生表面を露出させることができる。 In this case, for example, when argon (Ar) is used as the rare gas, the power supplied to the fast atom beam source (FAB) may be set to 1.5 kV (kilovolt), 15 mA (milliampere), or 0.1 To a value between 500 W (watts). For example, when a fast atom beam source (FAB) is operated from 100 W (watts) to 200 W (watts) and irradiated with a fast atom beam of argon (Ar) for about 2 minutes, the oxide, contaminants, etc. (surface) Layer) can be removed to expose the nascent surface.
本発明において、表面活性化に用いられる粒子は、中性原子またはイオンでもよく、さらには、ラジカル種でもよく、またさらには、これらが混合した粒子群でもよい。 In the present invention, the particles used for surface activation may be neutral atoms or ions, may be radical species, and may be a particle group in which these are mixed.
各プラズマまたはビーム源の稼動条件、または粒子の運動エネルギーに応じて、表面層の除去速度は変化しえる。そこで、表面活性化処理に必要な処理時間を調節する必要がある。 Depending on the operating conditions of each plasma or beam source, or the kinetic energy of the particles, the removal rate of the surface layer can vary. Therefore, it is necessary to adjust the treatment time required for the surface activation treatment.
たとえば、オージェ電子分光法(AES,Auger Electron Spectroscopy)やX線光電子分光法(XPS,X−ray Photo Electron Spectroscopy)などの表面分析法を用いて、表面層に含まれる酸素や炭素の存在が確認できなくなる時間またはそれより長い時間を、表面活性化処理の処理時間として採用してもよい。 For example, the presence of oxygen and carbon contained in the surface layer is confirmed using surface analysis methods such as Auger Electron Spectroscopy (AES) and X-ray Photoelectron Spectroscopy (XPS). You may employ | adopt the time which becomes impossible or longer than it as the processing time of a surface activation process.
プラズマ発生装置を用いて、粒子に所定の運動エネルギーを与えることもできる。基板の接合面に対して、交番電圧を印加することで、接合面の周りに粒子を含むプラズマを発生させ、プラズマ中の電離した粒子の陽イオンを、上記電圧により接合面に向けて加速させることで、所定の運動エネルギーを与える。
プラズマは数パスカル(Pa)程度の低真空度の雰囲気で発生させることができるので、真空システムを簡易化でき、かつ真空引きなどの工程を短縮化することができる。
A predetermined kinetic energy can also be given to particles using a plasma generator. By applying an alternating voltage to the bonding surface of the substrate, a plasma containing particles is generated around the bonding surface, and the cations of the ionized particles in the plasma are accelerated toward the bonding surface by the voltage. Thus, given kinetic energy is given.
Since the plasma can be generated in an atmosphere with a low degree of vacuum of about several pascals (Pa), the vacuum system can be simplified and the steps such as evacuation can be shortened.
上記製造方法において、SiC基板1と支持基板2とを接合する接合工程の前に、基板表面へ選択的に表面活性化処理を施してもよい。また接合工程の前に、SiC中間層3の一部へ選択的に表面活性化を施してもよい。 In the above manufacturing method, a surface activation process may be selectively performed on the substrate surface before the bonding step of bonding the SiC substrate 1 and the support substrate 2. Moreover, you may selectively surface-activate to a part of SiC intermediate | middle layer 3 before a joining process.
SiC中間層3の一部とは、たとえば、SiC基板1の外周部であり、外周部のみ表面活性化処理を施すことにより、SiC基板1の中央部に対して外周部の接合力が高くなり好ましい。 Part of SiC intermediate layer 3 is, for example, the outer peripheral portion of SiC substrate 1, and the surface activation treatment is performed only on the outer peripheral portion, so that the bonding force of the outer peripheral portion is increased with respect to the central portion of SiC substrate 1. preferable.
支持基板2は、既設の設備を使えるという観点から、厚みが0.1mm以上1.1mm以下であることが好ましい。 The support substrate 2 preferably has a thickness of 0.1 mm or more and 1.1 mm or less from the viewpoint that an existing facility can be used.
SiC中間層3は、プラズマ促進化学気相成長法(PECVD)やスパッタ蒸着、イオンビームスパッタなどの堆積方法で形成されることが好ましいが、これに限られない。SiC中間層3を形成する際に、所定のマスクを用いることで、所定の領域にのみ形成することができる。 The SiC intermediate layer 3 is preferably formed by a deposition method such as plasma enhanced chemical vapor deposition (PECVD), sputter deposition, or ion beam sputtering, but is not limited thereto. When the SiC intermediate layer 3 is formed, it can be formed only in a predetermined region by using a predetermined mask.
SiC基板1と支持基板2との接合のために用いられるSiC中間層3は、加熱工程や洗浄工程などを経た後、容易に剥がれる状態に膜厚、膜質が調整されることが好ましい。 It is preferable that the film thickness and film quality of SiC intermediate layer 3 used for bonding SiC substrate 1 and support substrate 2 are adjusted so that they can be easily peeled off after a heating process, a cleaning process, and the like.
SiC基板1の厚みは、0.5μm以上0.5mm以下であることが好ましく、0.5μm以上0.2mm以下であることがより好ましい。 The thickness of SiC substrate 1 is preferably not less than 0.5 μm and not more than 0.5 mm, and more preferably not less than 0.5 μm and not more than 0.2 mm.
上記の実施形態に係る製造方法において、基板接合工程は、真空雰囲気中または不活性ガス雰囲気中で行われてもよい。これにより、SiC基板1と支持基板2との接合強度が容易にコントロールできる。不活性ガスは窒素(N2)、ヘリウム(He)、ネオン(Ne)、アルゴン(Ar)、等を単体で、または、これらのいずれかを組み合わせた混合ガスであってよい。 In the manufacturing method according to the above-described embodiment, the substrate bonding step may be performed in a vacuum atmosphere or an inert gas atmosphere. Thereby, the joining strength between SiC substrate 1 and support substrate 2 can be easily controlled. The inert gas may be nitrogen (N 2 ), helium (He), neon (Ne), argon (Ar), or the like alone or a mixed gas in which any of these is combined.
上記の実施形態に係る製造方法において、基板接合工程の前に、SiC基板1と支持基板2の接合面を不活性ガス雰囲気中に晒す。これにより、加熱による、SiC基板1と支持基板2との接合強度の変化が生じ難い。不活性ガスは窒素(N2)、ヘリウム(He)、ネオン(Ne)、アルゴン(Ar)、等を単体で、または、これらのいずれかを組み合わせた混合ガスであってよい。 In the manufacturing method according to the above embodiment, before the substrate bonding step, the bonding surface between the SiC substrate 1 and the support substrate 2 is exposed to an inert gas atmosphere. Thereby, the change in the bonding strength between SiC substrate 1 and support substrate 2 due to heating is unlikely to occur. The inert gas may be nitrogen (N 2 ), helium (He), neon (Ne), argon (Ar), or the like alone or a mixed gas in which any of these is combined.
上記実施形態に係る製造方法において、基板接合工程が、バックグラウンド圧力が1×10−8Pa以上大気圧未満である、真空ないしは減圧雰囲気中で行われてもよい。 In the manufacturing method according to the embodiment, the substrate bonding step may be performed in a vacuum or a reduced pressure atmosphere in which the background pressure is 1 × 10 −8 Pa or more and less than atmospheric pressure.
基礎真空度をコントロールする事により、SiC中間層3中に含まれる水分、酸素を適正にコントロ―ルできる。適正にコントロールされた水分、酸素量を有するSiC中間層3は加熱時にも接合強度が増すことがなく、剥離も容易である。 By controlling the basic vacuum, moisture and oxygen contained in the SiC intermediate layer 3 can be controlled appropriately. The SiC intermediate layer 3 having appropriately controlled moisture and oxygen amounts does not increase the bonding strength even during heating, and is easy to peel off.
また、たとえば、先述の表面活性工程を経ずに、基板同士の接合を行ってもよい。たとえば真空中で蒸着などにより形成されたSiC中間層3は、表面において酸化や不純物による汚染などが進んでおらず、表面エネルギーが高い状態にある。このようなSiC中間層3の表面同士を接触させることで、比較的強度の高い接合界面を形成することができる。 Further, for example, the substrates may be joined without going through the above-described surface activation process. For example, the SiC intermediate layer 3 formed by vapor deposition or the like in a vacuum is in a state where the surface energy is high because oxidation or contamination due to impurities does not proceed on the surface. By bringing the surfaces of the SiC intermediate layer 3 into contact with each other, a relatively strong bonding interface can be formed.
[他の実施形態1]
図3を参照して、他の実施形態1を示す。本実施形態は、実施形態1の図1(b)のSiC中間層形成工程において、図3(f)のように、SiC基板1と支持基板2の両方の接合面にSiC中間層3が形成されている点のみ異なっており、その他は実施形態1と同一の工程である。
[Other embodiment 1]
With reference to FIG. 3, another embodiment 1 is shown. In the present embodiment, the SiC intermediate layer 3 is formed on the bonding surfaces of both the SiC substrate 1 and the support substrate 2 as shown in FIG. Only the points described above are different, and the other steps are the same as those in the first embodiment.
[他の実施形態2]
図4を参照して、他の実施形態2を示す。本実施形態は、実施形態2の図3(f)のSiC中間層形成工程において、図4(g)のように、SiC基板1と支持基板2の両方の接合面に複数のSiC中間層3が形成されている点のみ異なっており、その他は実施形態1と同一の工程である。なお、本図では、SiC中間層3はそれぞれ2層形成されているが、何層形成されてもよい。
[Other embodiment 2]
Another embodiment 2 is shown with reference to FIG. In this embodiment, in the SiC intermediate layer forming step of FIG. 3F of the second embodiment, a plurality of SiC intermediate layers 3 are formed on the bonding surfaces of both the SiC substrate 1 and the support substrate 2 as shown in FIG. However, the other steps are the same as those in the first embodiment. In this figure, two SiC intermediate layers 3 are formed, but any number of layers may be formed.
以上、本発明の実施形態を説明したが、これらの実施形態の各構成を組み合わせることも本発明に含まれることは自明である。 Although the embodiments of the present invention have been described above, it is obvious that the present invention includes combinations of the configurations of these embodiments.
以下に、実施例を示す。 Examples are shown below.
[実施例]
実施例の試験は、以下の手順で行った。
(1)SiC基板(支持基板)の準備
支持基板と仮定して、厚みが0.5mmであるSiC基板を用意した。
[Example]
The test of the Example was performed in the following procedures.
(1) Preparation of SiC substrate (support substrate) Assuming a support substrate, an SiC substrate having a thickness of 0.5 mm was prepared.
(2)SiC基板(SiCエピタキシャル成長用基板)の準備
SiC基板として、厚みが0.5mmであるSiC基板を用意した。
(2) Preparation of SiC substrate (SiC epitaxial growth substrate) An SiC substrate having a thickness of 0.5 mm was prepared as the SiC substrate.
(3)SiC中間層の形成
イオンビームスパッタを使用して、SiC中間層を、支持基板とSiC基板の接合がおこなわれる表面の両面に形成した。このときのイオンビームの入力値は、1.3Kv/400mAであった。
(3) Formation of SiC intermediate layer Using ion beam sputtering, the SiC intermediate layer was formed on both surfaces of the surface on which the support substrate and the SiC substrate are bonded. The input value of the ion beam at this time was 1.3 Kv / 400 mA.
(4)常温接合処理
下記条件で、常温接合処理を行った。
(常温接合条件)
5.0kN、5min
(4) Room temperature bonding treatment Room temperature bonding treatment was performed under the following conditions.
(Normal temperature bonding conditions)
5.0kN, 5min
上記条件で問題なく接合できた。(図5) It was able to join without any problem under the above conditions. (Fig. 5)
以上、本発明の様々な実施形態を説明したが、上記の説明は本発明を限定するものではなく、本発明の技術的範囲において、構成要素の削除、追加、置換を含む様々な変形例が考えられる。 Although various embodiments of the present invention have been described above, the above description is not intended to limit the present invention, and various modifications including deletion, addition, and replacement of components are included in the technical scope of the present invention. Conceivable.
1 支持基板
2 SiC基板
3 SiC中間層
4 SiC含有のエピタキシャル成長原料ガス
5 SiCインゴット(エピタキシャル成長後)
DESCRIPTION OF SYMBOLS 1 Support substrate 2 SiC substrate 3 SiC intermediate layer 4 SiC containing epitaxial growth source gas 5 SiC ingot (after epitaxial growth)
Claims (14)
SiC基板と支持基板とを互いに押し付けて、SiC中間層を介してSiC基板と支持基板とを接合する接合工程と、
を備えることを特徴とするSiCインゴット製造用基板の製造方法。 A forming step of forming a SiC intermediate layer on at least one of bonding planned surfaces where a SiC substrate on which a SiC crystal is formed and a support substrate that supports the SiC substrate are bonded;
A bonding step of pressing the SiC substrate and the support substrate together to bond the SiC substrate and the support substrate via the SiC intermediate layer;
A method for manufacturing a substrate for manufacturing a SiC ingot, comprising:
A SiC ingot manufacturing substrate manufactured by the manufacturing method according to claim 1.
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