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JPS5920381B2 - Gas phase reactor - Google Patents
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JPS5920381B2 - Gas phase reactor - Google Patents

Gas phase reactor

Info

Publication number
JPS5920381B2
JPS5920381B2 JP51125767A JP12576776A JPS5920381B2 JP S5920381 B2 JPS5920381 B2 JP S5920381B2 JP 51125767 A JP51125767 A JP 51125767A JP 12576776 A JP12576776 A JP 12576776A JP S5920381 B2 JPS5920381 B2 JP S5920381B2
Authority
JP
Japan
Prior art keywords
gas
reaction
injection device
reaction chamber
gas injection
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP51125767A
Other languages
Japanese (ja)
Other versions
JPS5350075A (en
Inventor
敦夫 西川
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP51125767A priority Critical patent/JPS5920381B2/en
Publication of JPS5350075A publication Critical patent/JPS5350075A/en
Publication of JPS5920381B2 publication Critical patent/JPS5920381B2/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/455Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
    • C23C16/45502Flow conditions in reaction chamber
    • C23C16/45508Radial flow
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/455Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/455Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
    • C23C16/45519Inert gas curtains

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Physical Or Chemical Processes And Apparatus (AREA)
  • Crystals, And After-Treatments Of Crystals (AREA)
  • Chemical Vapour Deposition (AREA)

Description

【発明の詳細な説明】 本発明は気相反応装置に関するものである。[Detailed description of the invention] The present invention relates to a gas phase reactor.

気相成長反応においては反応室に導入された反応物質を
含んだガスの流れる状態が反応効率や反応生成物の純度
あるいは反応生成物の膜厚や膜質の均一性に大きな影響
を与える。このため気相反応装置においては反応室内の
形状や導入ガスの噴出方向等を充分考慮して設計するこ
とが重要となつて来る。従来では、気相化学反応を用い
て反応生成物を形成対象物上に堆積被着させる場合、ベ
ースとなるキャリア−ガス中に反応成分を添加した混合
ガスを、形成対象物が設置され適当な反応温度に昇温さ
れたいる反応室内にガス噴射装置を介して導入すること
により行なつていた。
In a vapor phase growth reaction, the flow conditions of the gas containing the reactant introduced into the reaction chamber have a large effect on the reaction efficiency, the purity of the reaction product, and the uniformity of the film thickness and film quality of the reaction product. For this reason, it is important to design a gas phase reactor with sufficient consideration given to the internal shape of the reaction chamber, the ejection direction of the introduced gas, and the like. Conventionally, when a reaction product is deposited on an object to be formed using a gas phase chemical reaction, a mixed gas in which a reaction component is added to a carrier gas serving as a base is added to an appropriate place where the object to be formed is placed. This was carried out by introducing gas into the reaction chamber heated to the reaction temperature via a gas injection device.

第1図に従来の気相反応装置の断面概略図を示し、同図
を用いてガス噴射装置1から噴射されたガスの流れにつ
いて説明する。ガス噴射装置1の下方のガス導入口2よ
り導入された反応成分を含んだ混合ガスは、ガス導入口
2と反対側のガス噴出口3より反応室4内に噴出される
。ガス噴出口3の開口面積は、ガス導入口2の開口面積
よりも小さくなつているので、反応室4内に噴出される
ガスの噴射速度はガス導入口2に導入されるガスの速度
よりも大となる。反応室4内に噴出されたガスはペルシ
ャー5上部に到達した後反応室4下方に導びかれその一
部のガスは形成対象物6を載置し、且つ気相化学反応を
行なわしめる温度に高周波加熱装置7により昇温された
サセプター8上に達する。サセプター8はサセプター支
持台9により回転されると共に支持されている。反応成
分を含んだ混合ガスは形成対象物6およびサセプター8
上で反応を行ない反応生成物を堆積被着する。その後サ
セプター8の中心部方向に流れ再度中心部に位置してい
るガス噴射装置1から噴出されたガスに巻込まれた状態
となり再びペルシャー5上部へ導びかれる。すなわち従
来の気相成長装置における反応室4ノ 内のガスの流れ
は反応室4中心からペルシャー5の内壁に向つての対流
状態となつており、また反応室4内に導入された反応成
分を含んだ混合ガスの一部のみしか形成対象物6上に達
しないために以下の欠点を生じていた。’i(1)形成
対象物6上に到達する対流ガスの成分としては、導入さ
れた混合ガス成分とサセプター8上で既に気相反応によ
り生成した副生成ガスおよび反応室4内で発生する不純
物ガス、例えば高温に昇温されているサセプター8や形
成対象物6から発散した吸着ガスおよび混合ガス成分と
形成対象物6との反応により生じる成分、例えばSOS
(シリコン・オン・サファイア)結晶成長におけるアル
ミナの水素キャリヤーにおける還元作用で発生する酸化
アルミニウム(At2O,AtO)等、種々雑多な成分
を含むので形成対象物6上に堆積被着する反応生成物の
純度は必らずしも目的とした物質のみの清浄な物とは限
らない。
FIG. 1 shows a schematic cross-sectional view of a conventional gas phase reactor, and the flow of gas injected from a gas injection device 1 will be explained using the same figure. A mixed gas containing reaction components introduced from the gas inlet 2 at the lower part of the gas injection device 1 is ejected into the reaction chamber 4 from the gas outlet 3 on the opposite side to the gas inlet 2. Since the opening area of the gas outlet 3 is smaller than the opening area of the gas inlet 2, the injection velocity of the gas injected into the reaction chamber 4 is lower than the velocity of the gas introduced into the gas inlet 2. Becomes large. After the gas ejected into the reaction chamber 4 reaches the upper part of the Persian 5, it is guided to the lower part of the reaction chamber 4, and a part of the gas places the object 6 to be formed and reaches a temperature at which a gas phase chemical reaction can be carried out. It reaches onto the susceptor 8 whose temperature has been raised by the high frequency heating device 7. The susceptor 8 is rotated and supported by a susceptor support base 9. The mixed gas containing the reaction components is transferred to the formation target 6 and the susceptor 8.
The reaction is carried out on the surface and the reaction product is deposited. Thereafter, the gas flows toward the center of the susceptor 8 and is again engulfed by the gas ejected from the gas injection device 1 located at the center, and is again guided to the upper part of the persier 5. In other words, the flow of gas in the reaction chamber 4 in the conventional vapor phase growth apparatus is in a convection state from the center of the reaction chamber 4 toward the inner wall of the Persian 5, and the reaction components introduced into the reaction chamber 4 are Since only a part of the mixed gas contained reaches the formation target 6, the following drawbacks have occurred. 'i(1) The components of the convective gas that reaches the formation target 6 include the introduced mixed gas component, the by-product gas already generated by the gas phase reaction on the susceptor 8, and the impurities generated in the reaction chamber 4. Gas, for example, adsorbed gas and mixed gas components emitted from the susceptor 8 or the object to be formed 6 heated to a high temperature, and a component generated by the reaction between the object to be formed 6 and the object to be formed, such as SOS.
(Silicon on Sapphire) Contains various miscellaneous components such as aluminum oxide (At2O, AtO) generated by the reduction action of alumina's hydrogen carrier during crystal growth, so reaction products deposited on the formation target 6 are Purity does not necessarily mean that only the intended substance is clean.

(2)反応室4内に導入された混合ガスの一部は、ペル
シャー5の内壁とサセプター8の間隙を通り、気相成長
装置下方に配設されているガス排出口10から装置外に
排出される。
(2) A part of the mixed gas introduced into the reaction chamber 4 passes through the gap between the inner wall of the Persian 5 and the susceptor 8, and is discharged to the outside of the device from the gas exhaust port 10 provided below the vapor growth device. be done.

反応室4内における前記混合ガスの流れは形成対象物6
上への反応生成物の堆積被着には寄与しないため導入さ
れた混合ガスの利用効率が悪い。本発明はこれらの欠点
を解決することができる気相反応装置を提供するもので
、以下実施例を用いて図面と共に本発明を説明する。
The flow of the mixed gas in the reaction chamber 4 causes the object to be formed 6
Since it does not contribute to the deposition of reaction products on top, the efficiency of utilization of the introduced mixed gas is poor. The present invention provides a gas phase reactor capable of solving these drawbacks, and the present invention will be explained below using examples and drawings.

本発明の一実施例における気相反応装置の断面概略を第
2図に示す。
FIG. 2 shows a schematic cross-section of a gas phase reactor in one embodiment of the present invention.

第1のガス噴射装置11Aは、反応成分ガスとベースと
なるキヤリアーガスを含んだ混合ガスを噴射するもので
、反応装置底面の中心に配設されていて、ガス導入口1
2Aを有し、該ガス導入口12Aと反対の先端部には、
ガス遮蔽板22Aがガス導入方向と直交してガス噴射装
置11Aの一端を封じるように配設されている。また該
ガス遮蔽板22A近傍の該ガス噴射装置11Aの側面に
複数個のガス噴出口13Aを有している。該ガス噴出口
13Aは、その開口総面積が前記ガス導入口12Aの面
積よりも小となるように開口されていて、ガス噴出口1
3Aから噴射される混合ガスの噴射速度が、ガス導入口
12Aに導入されるガス速度より大となるように考慮さ
れている。該ガス噴出口13Aの位置よりも下方には基
台となるサセプター18が配設されており、該サセプタ
ー18は、回転機構を備えたサセプター支持台19に支
持されると共にガス噴射装置11Aを中心として水平に
回転する。サセプター18の下方には、サセプター18
を反応温度に昇温するための高周波加熱装置17が、サ
セプター18と平行し且つガス噴射装置11Aと同心と
なる様に配設されている。また反応室14の底面には、
ガスを排出するためのガス排出口20が配設されている
。ところで反応室14を構成するペルシャー15の側壁
には、前記ガス噴射装置11Aから噴射される混合ガス
中のキヤリアーガスと同種のガス、あるいはアルゴン、
ヘリウム等の不活性ガスの様に反応成分ガスを含まず、
直接的には反応そのものに寄与せず悪影響も与えないガ
ス(以下この様なガスを本説明においては非反応キヤリ
アーガスと称する)を噴射するための第2のガス噴射装
置11Bが配設されている。該ガス噴射装置11Bは、
反応室14外の先端にガス導入口12Bを有し、反応室
14内の他方の一端にはガス遮蔽板22Bを有しガス噴
射装置11Bの一端を封じている。ガス遮蔽板22Bは
ガス噴射装置11Aのガス遮蔽板22Aに対して対向す
ると共に平行な関係に配設されている。ガス遮蔽板22
Bの近傍のガス噴射装置11Bには複数個のガス噴出口
13Bが開口されている。ガス噴出口13Bの開口総面
積は、ガス導入口12Bの面積よりも小となるように開
口されていて、ガス噴出口13Bから噴射される非反応
キヤリアーガスの噴射速度が、ガス導入口12Bに導入
される時の速度より大となる様に考慮されている。ガス
噴射装置11A,11Bのガス噴射口13A,13B領
域をガス噴射管と称するならば、ガス噴射装置11Aと
ガス噴射装置11Bのガス噴射管は互いに同軸をなす様
に配設されている。この様な構成による気相反応装置の
反応室14内のガス流について説明する。
The first gas injection device 11A injects a mixed gas containing a reaction component gas and a base carrier gas, and is disposed at the center of the bottom of the reaction device.
2A, and at the tip opposite to the gas inlet 12A,
A gas shielding plate 22A is disposed perpendicular to the gas introduction direction to close one end of the gas injection device 11A. Further, a plurality of gas injection ports 13A are provided on the side surface of the gas injection device 11A near the gas shielding plate 22A. The gas outlet 13A is opened so that its total opening area is smaller than the area of the gas inlet 12A.
The injection velocity of the mixed gas injected from 3A is considered to be higher than the velocity of the gas introduced into the gas introduction port 12A. A susceptor 18 serving as a base is disposed below the position of the gas injection port 13A, and the susceptor 18 is supported by a susceptor support stand 19 equipped with a rotation mechanism and rotates around the gas injection device 11A. Rotate horizontally as . Below the susceptor 18, the susceptor 18
A high frequency heating device 17 for raising the temperature to the reaction temperature is arranged parallel to the susceptor 18 and concentrically with the gas injection device 11A. In addition, on the bottom of the reaction chamber 14,
A gas outlet 20 is provided for discharging gas. Incidentally, on the side wall of the Persian 15 constituting the reaction chamber 14, a gas similar to the carrier gas in the mixed gas injected from the gas injection device 11A, or argon,
Does not contain reactive gases like inert gases such as helium,
A second gas injection device 11B is provided for injecting a gas that does not directly contribute to the reaction itself and does not have any adverse effects (hereinafter such a gas will be referred to as a non-reactive carrier gas in this explanation). There is. The gas injection device 11B is
A gas inlet 12B is provided at the tip outside the reaction chamber 14, and a gas shielding plate 22B is provided at the other end inside the reaction chamber 14 to seal off one end of the gas injection device 11B. The gas shielding plate 22B is arranged to face and be parallel to the gas shielding plate 22A of the gas injection device 11A. Gas shielding plate 22
A plurality of gas ejection ports 13B are opened in the gas injection device 11B near B. The total opening area of the gas outlet 13B is smaller than the area of the gas inlet 12B, and the injection velocity of the non-reactive carrier gas injected from the gas outlet 13B is such that the It is designed to be faster than the speed at which it is introduced. If the regions of the gas injection ports 13A and 13B of the gas injection devices 11A and 11B are referred to as gas injection tubes, the gas injection tubes of the gas injection devices 11A and 11B are arranged coaxially with each other. The gas flow within the reaction chamber 14 of the gas phase reactor having such a configuration will be explained.

まず説明を簡単にするため第1のガス噴射装置11Aの
みにガスが導入された場合について説明する。ガス噴射
装置11Aのガス噴出口13Aから噴射される混合ガス
の噴射方向は、反応室14中心から外方向に向けての横
方向であるが、ガス噴射装置11A内のガス進行方向が
下方から上方向であるので慣性により若干水平より上向
きの流れとなつてサセプター18の上部を進行する。サ
セプター18は形成対象物16を載置し反応温度まで加
熱昇温されると共に回転しているガス噴射装置11Aか
ら噴射された混合ガス中の反応成分は、サセプター18
上で昇温されることにより反応を行ない、反応生成物を
形成対象物16やサセプター18上に堆積被着させる。
また混合ガスのガス流は昇温されることにより膨張し、
密度が小さくなつて反応室14内で対流をおこす方向に
作用すると共に、ガス噴射方向(若干水平よりも上向き
)等が原因となり、ペルシャー15内壁に衝突後ペルシ
ャー15内壁に沿つて上昇しペルシャー15最頂部から
下降する対流となる。反応室14の内容積が一定のため
ガス流は対流をおこしながらも導入ガス流量とほぼ等し
い流量のガスが反応室14からガス排出口20を通り装
置外に排出される。以上の如くガス噴射装置11Aのみ
にガスを導入した場合の反応室14内でガス流は対流を
おこすことが判る。
First, to simplify the explanation, a case will be described in which gas is introduced only into the first gas injection device 11A. The injection direction of the mixed gas injected from the gas injection port 13A of the gas injection device 11A is the horizontal direction outward from the center of the reaction chamber 14, but the gas traveling direction inside the gas injection device 11A is from the bottom to the top. Because of the direction, the flow flows slightly upward from the horizontal direction due to inertia and advances over the upper part of the susceptor 18. The susceptor 18 places the formation target 16 and is heated to the reaction temperature, and the reaction components in the mixed gas injected from the rotating gas injection device 11A are transferred to the susceptor 18.
The reaction is carried out by raising the temperature above, and the reaction product is deposited on the formation object 16 and the susceptor 18.
Also, the gas flow of the mixed gas expands as it is heated,
As the density decreases, it acts in the direction of causing convection within the reaction chamber 14, and due to the gas injection direction (slightly upwards than horizontal), etc., after colliding with the inner wall of the Persian 15, it rises along the inner wall of the Persian 15. Convection flows downward from the top. Since the internal volume of the reaction chamber 14 is constant, the gas flow causes convection, but a flow rate of gas substantially equal to the flow rate of the introduced gas is discharged from the reaction chamber 14 through the gas outlet 20 to the outside of the apparatus. As described above, it can be seen that the gas flow causes convection within the reaction chamber 14 when gas is introduced only into the gas injection device 11A.

次に、第1のガス噴射装置11Aにガスを導入すると共
に、第2のガス噴射装置11Bからも非反応キヤリアー
ガスを導入した場合の反応室14内のガス流について説
明する。
Next, a description will be given of the gas flow in the reaction chamber 14 when gas is introduced into the first gas injection device 11A and a non-reactive carrier gas is also introduced from the second gas injection device 11B.

ガス噴射装置11Bのガス導入口12Bから導入された
非反応キヤリアーガスは、反応室14内において上方か
ら下方に進行した後、複数個のガス噴出口13Bから反
応室14内に横方向のガス流となつて大きな速度で噴射
される。非反応キヤリアーガスのガス流はガス噴射装置
11Aから噴射される混合ガスのガス流と対向する様に
サセプター18上を流れると共に、反応室14内上部を
絶えず清浄な非反応キヤリアーガスで充満する様に流れ
る。その後ペルシャー15内壁に沿つて反応室14下方
に流れた後、ガス排出口20から装置外に排出される。
つまりガス噴射装置11Bから反応室14内に噴射され
るキヤリアーガスBの作用として、(1)混合ガスに対
するカーテンの作用(一般に見られるエアーカーテンと
同じ)と、(2)反応室14の内容積を実効的に小さく
することであり、以上の作用からガス噴射装置11Aか
ら噴射される反応成分を含んだ混合ガスのガス流れは、
対流が阻止されると共に、反応成分を含む混合ガスの流
れがサセプター18に対して平行で、且つ近接した状態
の流れとなる。本発明の気相反応装置により、反応室内
のガス流を混合ガス流量と非反応キヤリアーガスの流量
比あるいは総ガス流量により自由に制御することが可能
となる。
The non-reactive carrier gas introduced from the gas inlet 12B of the gas injection device 11B travels from above to below in the reaction chamber 14, and then flows into the reaction chamber 14 from a plurality of gas ejection ports 13B in a lateral gas flow. It is ejected at a high speed. The gas flow of the non-reactive carrier gas flows over the susceptor 18 so as to oppose the gas flow of the mixed gas injected from the gas injection device 11A, and the upper part of the reaction chamber 14 is constantly filled with clean non-reactive carrier gas. flows to Thereafter, the gas flows down the reaction chamber 14 along the inner wall of the gas chamber 15 and is then discharged from the gas outlet 20 to the outside of the apparatus.
In other words, the effects of the carrier gas B injected into the reaction chamber 14 from the gas injection device 11B are: (1) the effect of a curtain on the mixed gas (same as a commonly seen air curtain); and (2) the internal volume of the reaction chamber 14. The purpose of this is to effectively reduce
Convection is prevented, and the mixed gas containing the reaction components flows parallel to and close to the susceptor 18. The gas phase reaction apparatus of the present invention allows the gas flow within the reaction chamber to be freely controlled by the flow rate ratio of the mixed gas flow rate and the non-reactive carrier gas or the total gas flow rate.

実際には、第1のガス噴射装置11Aから噴射される混
合ガスと第2のガス噴射装置11Bから噴射される非反
応キヤリアーガスとの比率として、混合ガスに対して非
反応キヤリノC アーガスが1.5〜4倍の間が適当であつた。
Actually, as a ratio of the mixed gas injected from the first gas injection device 11A and the non-reactive carrier gas injected from the second gas injection device 11B, the non-reactive carrier gas is 1 to the mixed gas. A value between .5 and 4 times was appropriate.

また、混合ガスと非反応キヤリアーガスとのトータル流
量は、反応室14の内容積を1とした場合、1分間あた
りその2〜6倍のガス流量が反応生成物の均一性の点で
結果として良好であつた。以下に述べる本発明の効果に
より、本発明の気相反応装置は工業上、特に半導体工業
上非常に大きな価値を有するものである。
In addition, the total flow rate of the mixed gas and non-reactive carrier gas should be 2 to 6 times the internal volume of the reaction chamber 14 per minute in terms of uniformity of the reaction products. It was good and warm. Due to the effects of the present invention described below, the gas phase reactor of the present invention has great value industrially, particularly in the semiconductor industry.

(1)サセプターや形成対象物上を流れるガス流が平行
で且つ流速が大なるため膜厚や膜質の均一性の良い反応
生成物を再現性良く堆積被着形成することが可能である
(1) Since the gas flow flowing over the susceptor and the object to be formed is parallel and the flow velocity is high, it is possible to deposit and form a reaction product with good uniformity in film thickness and film quality with good reproducibility.

(2)サセプターや形成対象物上を流れる反応成分を含
有した混合ガスのガス流は対流とならないため、反応に
より生じる副生成ガスあるいは形成対象物やサセプター
から発散する吸着ガス中の不純物を反応生成物中に取り
込むことが少なくなる。
(2) Since the gas flow of the mixed gas containing the reaction components flowing over the susceptor and the object to be formed does not form convection, the by-product gas generated by the reaction or the impurities in the adsorbed gas emanating from the object to be formed or the susceptor are generated by the reaction. It is less likely to be incorporated into things.

即ち、オートピングやアウトデイフユージヨンの少ない
清浄な反応成性物を堆積被着することができるので、例
えばサフアイア基板上にシリコンを成長させるような基
板と異種物質を気相成長させる時には、不純物分布の急
峻な堆積層を得ることができるので特に効果的である。
That is, since it is possible to deposit and deposit a clean reaction product with little autoping or out-diffusion, when growing a substrate and a different material, such as growing silicon on a sapphire substrate, by vapor phase, This is particularly effective since it is possible to obtain a deposited layer with a steep impurity distribution.

(3)反応成分を含んだ混合ガスのガス流はサセプター
の上面に近接して流れるため、反応成分ガスの反応効率
が良くなり、反応成分の殆んどが反応に寄与することに
より堆積被着形成速度が従来と比して大となる。即ち、
堆積被着速度が大であるため、従来装置よりも堆積に要
する時間が短縮でき、反応温度に加熱するための電力、
反応物質およびキヤリアーガス等の資源節約が可能とな
る。(4)反応速度を従来と同一のものにして同一堆積
層を得ようとする場合、反応温度を下げる以外に、反応
成分を含んだ混合ガス濃度を稀くするととも可能である
ので、有毒物質や可燃性物質を用いた反応においては危
険性が減少する。
(3) Since the gas flow of the mixed gas containing the reactive components flows close to the upper surface of the susceptor, the reaction efficiency of the reactive component gas is improved, and most of the reactive components contribute to the reaction, resulting in deposition. The formation speed is faster than before. That is,
Because the deposition rate is high, the time required for deposition can be reduced compared to conventional equipment, and the electric power required to heat the reaction temperature can be reduced.
Resources such as reactants and carrier gas can be saved. (4) When trying to obtain the same deposited layer with the same reaction rate as before, in addition to lowering the reaction temperature, it is also possible to reduce the concentration of the mixed gas containing the reaction components, so it is possible to reduce the amount of toxic substances. The danger is reduced in reactions involving combustible materials or flammable materials.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は従来の気相反応装置の断面概略図、第2図は本
発明の気相反応装置の一実施例を示す断面概略図である
。 11A,11B・・・・・・ガス噴射装置、12A,1
2B・・・・・・ガス導入口、13A,13B・・・・
・・ガス噴出口、14・・・・・・反応室、15・・・
・・・ペルシャー、16・・・・・・形成対象物、17
・・・・・・高周波加熱装置、18・・・・・・サセプ
ター、19・・・・・・サセプター支持台、20・・・
・・・ガス排出口、22A,22B・・・・・・ガス遮
蔽板。
FIG. 1 is a schematic cross-sectional view of a conventional gas phase reactor, and FIG. 2 is a schematic cross-sectional view showing an embodiment of the gas phase reactor of the present invention. 11A, 11B... Gas injection device, 12A, 1
2B...Gas inlet, 13A, 13B...
...Gas outlet, 14...Reaction chamber, 15...
... Persian, 16 ... Formation object, 17
...High frequency heating device, 18 ... Susceptor, 19 ... Susceptor support base, 20 ...
...Gas exhaust port, 22A, 22B...Gas shielding plate.

Claims (1)

【特許請求の範囲】 1 気相成長すべき形成対象物が載置せられる基台と、
前記形成対象物に反応ガスを噴出するガス噴出口を有す
る第1のガス噴射装置と、前記第1のガス噴出装置の上
方に設置せられ、前記形成対象物の主面方向に非反応ガ
スを噴出する噴出口を設けた第2のガス噴射装置とが反
応室内に形成されたことを特徴とする気相反応装置。 2 第1、第2のガス噴射装置の噴出口を設けた部分は
管状体で構成されるとともに、互いに対抗配置され、前
記管状体の一端に、前記管状体の一端の開口面積より大
きな面積を有するガス遮蔽板を有することを特徴とする
特許請求の範囲第1項に記載の気相反応装置。
[Claims] 1. A base on which an object to be formed by vapor phase growth is placed;
a first gas injection device having a gas ejection port for ejecting a reactive gas to the object to be formed; and a first gas injection device installed above the first gas injection device to emit a non-reactive gas in the direction of the main surface of the object to be formed. A gas phase reaction device characterized in that a second gas injection device provided with an ejection port is formed in a reaction chamber. 2 The parts of the first and second gas injection devices provided with the ejection ports are formed of tubular bodies, are arranged opposite to each other, and have one end of the tubular body having an area larger than the opening area of one end of the tubular body. 2. The gas phase reactor according to claim 1, further comprising a gas shielding plate having a gas shielding plate.
JP51125767A 1976-10-19 1976-10-19 Gas phase reactor Expired JPS5920381B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP51125767A JPS5920381B2 (en) 1976-10-19 1976-10-19 Gas phase reactor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51125767A JPS5920381B2 (en) 1976-10-19 1976-10-19 Gas phase reactor

Publications (2)

Publication Number Publication Date
JPS5350075A JPS5350075A (en) 1978-05-08
JPS5920381B2 true JPS5920381B2 (en) 1984-05-12

Family

ID=14918313

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51125767A Expired JPS5920381B2 (en) 1976-10-19 1976-10-19 Gas phase reactor

Country Status (1)

Country Link
JP (1) JPS5920381B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59158328U (en) * 1983-04-11 1984-10-24 東芝機械株式会社 Vapor phase growth equipment

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4851255U (en) * 1971-10-15 1973-07-04

Also Published As

Publication number Publication date
JPS5350075A (en) 1978-05-08

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