JPS63148617A - Molecular beam epitaxy apparatus - Google Patents

Molecular beam epitaxy apparatus

Info

Publication number
JPS63148617A
JPS63148617A JP29602986A JP29602986A JPS63148617A JP S63148617 A JPS63148617 A JP S63148617A JP 29602986 A JP29602986 A JP 29602986A JP 29602986 A JP29602986 A JP 29602986A JP S63148617 A JPS63148617 A JP S63148617A
Authority
JP
Japan
Prior art keywords
molecular beam
chamber
beam source
source
growth chamber
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.)
Pending
Application number
JP29602986A
Other languages
Japanese (ja)
Inventor
Kunihiro Takahashi
邦弘 高橋
Hideaki Kanbara
秀明 蒲原
Kazumasa Fujioka
藤岡 和正
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.)
Hitachi Ltd
Original Assignee
Hitachi 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 Hitachi Ltd filed Critical Hitachi Ltd
Priority to JP29602986A priority Critical patent/JPS63148617A/en
Publication of JPS63148617A publication Critical patent/JPS63148617A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To realize the miniaturization of a system by a method wherein a delivery mechanism of a molecular beam source is installed at the tip of a conveyance mechanism and on the side of a growth chamber and a reserve chamber is made detachable. CONSTITUTION:A molecular beam source 3 having a crucible 4 containing a source substance is installed in the air at a delivery mechanism 14 at the tip of a conveyance mechanism 7 inside a reserve chamber 6; the reverse chamber 6 is connected to a gate valve 8; after the inside of the reserve chamber 6 has been evacuated to produce a vacuum, the gate valve 8 is opened. Then, the molecular beam source 3 is shifted to the side of a growth chamber 1 by means of the conveyance mechanism 7, and the molecular beam source 3 is delivered to the delivery mechanism 14; the molecular beam source 3 is supported by a positioning device. After that, the conveyance mechanism 7 is returned to its initial position; after the gate valve 8 has been closed, the reserve chamber 6 is detached from the gate valve 8. It is possible to supply the source substance for the molecular beam source 3 without exposing the growth chamber 1 to the atmospheric pressure, to execute this operation in the single reserve chamber 6 and, furthermore, to detach the reserve chamber 6 during the growth of a film; as a result, it is possible to miniaturize a system.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は1分子線エピタキシー装置に係り、特に良質な
エピタキシ一層を高い生産性をもって成長させるための
蒸着材料であるソース物質の補給を、成長室を大気に解
放することなく、容易に行うことができるようにした分
子線エピタキシー装置に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a single-molecular beam epitaxy apparatus, and particularly relates to a single molecular beam epitaxy system that is capable of replenishing a source material, which is a vapor deposition material, for growing a high-quality epitaxy layer with high productivity. The present invention relates to a molecular beam epitaxy device that can easily perform epitaxy without opening a chamber to the atmosphere.

(従来の技術〕 従来一般に用いられている分子線エピタキシー装置とし
ては、その主要構成要素を第3図に示したように、排気
装置5により超高真空に保たれた成長室1の内部にウェ
ハ2を設置し、このウェハ2に対向する位置に薄膜の材
料となるソース物質を入れたルツボ4を有する複数の分
子線源3を設け、この分子線源3によってウェハ2の表
面に膜成長を行うようにしたものである。この膜成長を
ある期間続けると、ソース物質が枯渇するので、新たな
ソース物質を補給することが必要になる。
(Prior Art) As shown in FIG. 3, the main components of a commonly used molecular beam epitaxy apparatus are as follows: A wafer is placed inside a growth chamber 1 maintained at an ultra-high vacuum by an exhaust device 5. A plurality of molecular beam sources 3 each having a crucible 4 containing a source material to be a thin film material are provided at positions facing the wafer 2, and the molecular beam sources 3 grow a film on the surface of the wafer 2. If this film growth continues for a certain period of time, the source material will be depleted, and it will be necessary to supply new source material.

この基金には、成長室1を大気圧に解放し、分子線源3
を成長室1より取り外し、ルツボ4にソース物質を補給
する。その後再度膜成長を行うことができるようにする
ためには、ソース物質のベーキングを含め、大気圧に解
放した成長室1をベーキングして、壁面等に付着した不
純物質の除去を行うことが必要になる。この様に一度成
長室1を大気圧に解放すると、その立ち上げに多くの時
間を必要とし、また立ち上げ直後に成長させた数回の薄
膜は良質の膜ができないのが通例であった。
This fund includes opening growth chamber 1 to atmospheric pressure and molecular beam source 3.
is removed from the growth chamber 1 and the crucible 4 is replenished with the source material. In order to be able to perform film growth again after that, it is necessary to bake the growth chamber 1, which has been released to atmospheric pressure, including baking the source material, to remove impurities attached to the walls, etc. become. Once the growth chamber 1 is released to atmospheric pressure in this manner, it takes a long time to start up the chamber, and the thin films grown several times immediately after the start-up usually fail to produce a good quality film.

そこでソース物質が枯渇した場合、成長室を大気圧に解
放しないで、ソース物質を補給するものが提案されてい
る。この方法を大きく分けると、成長室を真空に保った
ままで、ソース物質だけまたはソース物質を入れたルツ
ボを補給する方法と、成長室を真空に保ったままで分子
線源を取り外してソース物質を補給する方法とがある。
Therefore, it has been proposed to replenish the source material without releasing the growth chamber to atmospheric pressure when the source material is depleted. This method can be broadly divided into two methods: one is to replenish only the source material or the crucible containing the source material while keeping the growth chamber in vacuum, and the other is to remove the molecular beam source and replenish the source material while keeping the growth chamber in vacuum. There is a way to do this.

以下、これらの方法を用いた従来装置を第4図〜第7図
により説明する。
Conventional devices using these methods will be explained below with reference to FIGS. 4 to 7.

第4図は、特開昭58−33825号公報に記載された
装置を示したもので、成長室1とは別個にゲートバルク
8を介して排気装置9を有する予備室6と該予備室6内
に搬送機構7を設け、前記搬送機構7を用いて予備室6
内よりソース物質を入れたルツボを成長室1内のルツボ
4の位置に補給するようになっている。
FIG. 4 shows an apparatus described in Japanese Patent Application Laid-open No. 58-33825, in which a preliminary chamber 6 is provided with an exhaust device 9 via a gate bulk 8 separately from the growth chamber 1, and the preliminary chamber 6 A transport mechanism 7 is provided inside the chamber, and the transport mechanism 7 is used to transport the preliminary chamber 6.
A crucible containing a source material is supplied to a crucible 4 in the growth chamber 1 from inside.

第5図は、特開昭58−194796号公報に記載され
た装置を示したもので、成長室1とは別個にゲートバル
ク8を介して排気装置i’19を有する予備室6を、設
け、該予備室6内にはソース物質だけをルツボ4に補給
する搬送機構7が設けられている。
FIG. 5 shows an apparatus described in Japanese Patent Application Laid-Open No. 58-194796, in which a preliminary chamber 6 having an exhaust device i'19 is installed separately from the growth chamber 1 via a gate bulk 8. A transport mechanism 7 for supplying only the source material to the crucible 4 is provided in the preliminary chamber 6.

第6図は、特開昭60−27118号公報に記載された
装置を示したもので、成長室1とは別個にゲートバルク
を介して排気口11を有する金)A管状体L3を設け、
該金属管状体13には分子線源3を移動させる伸縮iJ
能骨管状体0を接続し、分子線源3を前記金属管状体1
3内から伸縮可能管状体10内を通して外部に取り出す
ようになっている。
FIG. 6 shows the apparatus described in Japanese Unexamined Patent Publication No. 60-27118, in which a tubular body L3 having an exhaust port 11 is provided separately from the growth chamber 1 via a gate bulk.
The metal tubular body 13 has a telescopic iJ for moving the molecular beam source 3.
Connect the functional bone tubular body 0 and connect the molecular beam source 3 to the metal tubular body 1.
3 through the expandable tubular body 10 and taken out to the outside.

第7図に示した装置は、成長室1とゲートバルク8を介
して伸縮可能管状体10を設け、該伸縮可能管状体10
には排気口11と分子線源3を移動させる搬送機構7を
設けたものである。
The apparatus shown in FIG.
is provided with an exhaust port 11 and a transport mechanism 7 for moving the molecular beam source 3.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

上記従来技術においては、成長室にゲートバルクを介し
て取り付けられる予備室の構造について特に問題があっ
た。すなわち、第4図及び第5図に示した装置において
は、予備室が大きなスペースを占め、かつ複数の分子線
源にソース物質を補給するためには、複数個の予備室が
必要となる。
In the above-mentioned prior art, there was a particular problem with the structure of the preliminary chamber attached to the growth chamber via the gate bulk. That is, in the apparatus shown in FIGS. 4 and 5, the preliminary chamber occupies a large space, and a plurality of preliminary chambers are required in order to supply source materials to the plurality of molecular beam sources.

また、一つの予備室と搬送機構だけで、複数の分子線源
にソース物質を補給するためには、その搬送機構は大変
複雑なものになる。
Furthermore, in order to supply source material to a plurality of molecular beam sources using only one preparatory chamber and a transport mechanism, the transport mechanism becomes very complicated.

また第6図及び第7図に示した装置の場合でも同様で、
複数個の分子線源に対して複数個の伸縮可能管状体が必
要になり、かつ、それらの伸縮可能管状体は常に成長室
に接続されたままとなるので装置が大型、複雑化する等
の問題があった。
The same applies to the devices shown in FIGS. 6 and 7.
Multiple extensible tubular bodies are required for multiple molecular beam sources, and these extensible tubular bodies are always connected to the growth chamber, which increases the size and complexity of the device. There was a problem.

本発明の目的は、ソース物質の補給に当って、1個のp
備室を用いて分子線源の取り付け、取り外しができるよ
うにすると共に、補給作業が完了した際には、前記予備
室を取り外すことを可能にした分子線エピタキシー装置
を提供することにある。
The object of the present invention is to supply one p.
It is an object of the present invention to provide a molecular beam epitaxy apparatus in which a molecular beam source can be attached and removed using a preliminary chamber, and the preliminary chamber can be removed when replenishment work is completed.

〔問題点を解決するための手段〕[Means for solving problems]

上記の目的を達成するために1本発明の分子線エピタキ
シー装置は、超高真空に保たれた成長室内にウェハと、
該ウェハにソース物質の分子線を照射して、前記ウェハ
表面に薄膜を形成する分子線源と、前記成長室にゲート
バルクを介して接続した予備室と、該予備室の軸方向に
前記分子線源を移動し得る搬送機構とを備えた分子線エ
ピタキシー装置において、前記搬送機構の先端と成長室
側とに、それぞれ前記分子線源の受け渡し機構を設ける
と共に、前記予備室を着脱可能にしたものである。
In order to achieve the above object, the molecular beam epitaxy apparatus of the present invention has a wafer placed in a growth chamber kept in an ultra-high vacuum,
a molecular beam source that irradiates the wafer with a molecular beam of a source material to form a thin film on the wafer surface; a preliminary chamber connected to the growth chamber via a gate bulk; In a molecular beam epitaxy apparatus equipped with a transport mechanism capable of moving a radiation source, a delivery mechanism for the molecular beam source is provided at the tip of the transport mechanism and on the side of the growth chamber, and the preliminary chamber is made detachable. It is something.

〔作用〕 」二記の構成によると、ソース物質の補給は、まず大気
中において予備室内の搬送機構の先端に設けた受け渡し
機構に、ソース物質を有する分子線源を設置したのち、
前記予備室をゲートバルクに接続する0次いで予備室内
を真空排気したのちゲートバルクを開放する。次に搬送
機構により分子線源を軸方向に移動させ、前記分子線源
を成長室内の受け渡し機構に受け渡す。これにより分子
線源は成長室の所定の位置に設置される6その後搬送機
構を初期の位置に戻し、ゲートバルクを閉じたのち、予
備室をゲートバルクより取り外す。以上によりソース物
質の補給作業が完了する。
[Operation] According to the configuration described in Section 2, source material is supplied by first installing a molecular beam source containing the source material in the delivery mechanism installed at the tip of the transport mechanism in the preliminary chamber in the atmosphere.
The preliminary chamber is connected to the gate bulk.The preliminary chamber is then evacuated and the gate bulk is opened. Next, the molecular beam source is moved in the axial direction by a transport mechanism, and the molecular beam source is delivered to a delivery mechanism in the growth chamber. As a result, the molecular beam source is installed at a predetermined position in the growth chamber.6 Afterwards, the transport mechanism is returned to the initial position, the gate bulk is closed, and the preliminary chamber is removed from the gate bulk. With the above steps, the source material replenishment work is completed.

〔実施例〕〔Example〕

以下、本発明の実施例を図に従って説明する。 Embodiments of the present invention will be described below with reference to the drawings.

なお、公知の構成部材と同一機能を有する構成部材には
同一符号を付す。
Note that components having the same functions as known components are given the same reference numerals.

本発明の一実施例の全体構成を第1図に示したように、
成長室1にはゲートバルク8を介して、排気口11を有
する着脱可能な予備室6が設けられている。前記予備室
6内には分子線源3の搬送機構7が設置され、該搬送機
4i17の先端には、ルツボ4を有する分子線源3を保
持すると共に1分子線源3を成長室1側に受け渡すため
の受け渡し機構12が設けられている。一方、成長室1
側には、搬送機構7によって搬送された分子線源3を支
持並びに位置決めし、かつ受け取るための受け渡し機構
14と、分子線源3のソース物質の加熱用ヒータとその
温度測定用の熱電対のリード線の電流導入端子15が設
けられている。この場合の成長室1側における前記分子
線源3の位置決め並びに支持方法は、分子線源3の搬送
機構及び受け渡しの機構等と密接な関係をもち、ワンタ
ッチで真空の成長室内に支持される構造とする。また。
As shown in FIG. 1, the overall configuration of an embodiment of the present invention is as follows.
A removable preliminary chamber 6 having an exhaust port 11 is provided in the growth chamber 1 via a gate bulk 8 . A transport mechanism 7 for the molecular beam source 3 is installed in the preliminary chamber 6, and at the tip of the transport machine 4i17, the molecular beam source 3 having the crucible 4 is held, and the single molecular beam source 3 is moved to the growth chamber 1 side. A delivery mechanism 12 is provided for delivery to. On the other hand, growth chamber 1
On the side, there is a delivery mechanism 14 for supporting, positioning, and receiving the molecular beam source 3 transported by the transport mechanism 7, a heater for heating the source material of the molecular beam source 3, and a thermocouple for measuring its temperature. A current introduction terminal 15 for a lead wire is provided. In this case, the method of positioning and supporting the molecular beam source 3 on the side of the growth chamber 1 has a close relationship with the transport mechanism and delivery mechanism of the molecular beam source 3, and has a structure that can be supported in the vacuum growth chamber with one touch. shall be. Also.

分子線源3が成長室1側に支持された際には、ソース物
質の加熱用リード線と、その温度測定用の熱電対のリー
ド線の電流導入端子15を介しての装置外への取り出し
は1分子線源3側と成長室1側における分子線源3の支
持機構側とに、それぞれ電気的接触点を有し、押し付け
または回転機構等によって電気的接続が真空中で行なわ
れる構造とする。
When the molecular beam source 3 is supported on the side of the growth chamber 1, the lead wire for heating the source material and the lead wire for the thermocouple for measuring its temperature are taken out of the apparatus through the current introduction terminal 15. The structure has electrical contact points on the single molecule beam source 3 side and on the support mechanism side of the molecular beam source 3 in the growth chamber 1, respectively, and the electrical connection is made in vacuum by a pressing or rotating mechanism, etc. do.

つぎに、上記実施例の作用を説明する。ソース物質を補
給する場合について述べると、まず大気中で予備室6内
の搬送機構7の先端に有する受け渡し機構12に、ソー
ス物質を入れたルツボ4を有する分子線源3を設置した
のち、前記予備室6をゲートバルク8にボルト締め等に
より接続し、次いで排気口11から排気して予備室6内
を真空にした後、ゲートバルク8を開放する。次に搬送
機構7により分子線源3を成長室1側に移動させ、受け
渡し機構14に分子線源3を受け渡すことにより、該分
子線源3は受け渡し機構14により位置決め並びに支持
される。その後搬送機構7を初期の位置に戻し、次いで
ゲートバルク8を閉じた後、予備室6をゲートバルク8
より取り外し、補給作業は完了する。なお分子線VA3
は通常複数本必要とするが、本実施例によれば、1個の
予備室で複数本の分子線源のソース物質の補給が可能で
ある。
Next, the operation of the above embodiment will be explained. Regarding the case of replenishing the source material, first, the molecular beam source 3 having the crucible 4 containing the source material is installed in the delivery mechanism 12 provided at the tip of the transport mechanism 7 in the preliminary chamber 6 in the atmosphere. The preliminary chamber 6 is connected to the gate bulk 8 by bolting or the like, and then the preliminary chamber 6 is evacuated by exhausting air through the exhaust port 11, and then the gate bulk 8 is opened. Next, the molecular beam source 3 is moved to the growth chamber 1 side by the transport mechanism 7, and the molecular beam source 3 is delivered to the delivery mechanism 14, whereby the molecular beam source 3 is positioned and supported by the delivery mechanism 14. After that, the transport mechanism 7 is returned to the initial position, and then the gate bulk 8 is closed, and the preliminary chamber 6 is moved to the gate bulk 8.
Removal and replenishment work is complete. In addition, molecular beam VA3
Normally, a plurality of molecular beam sources are required, but according to this embodiment, source materials for a plurality of molecular beam sources can be supplied in one preliminary chamber.

第2図は本発明の他の実施例を示したもので、基本的構
成は第1図の場合と同じ構成であるが、異なるのは、予
備室6の周囲に加熱用のヒータ16を設けたことである
。本実施例によれば分子線源3を成長室1に搬送する前
に予備ベーキングすることができ、より良質の薄膜を成
長させることができる。
FIG. 2 shows another embodiment of the present invention, the basic configuration of which is the same as that of FIG. 1, except that a heater 16 for heating is provided around the preliminary chamber 6. That's what happened. According to this embodiment, the molecular beam source 3 can be prebaked before being transported to the growth chamber 1, and a thin film of better quality can be grown.

〔発明の効果〕〔Effect of the invention〕

以上本発明によれば、成長室を大気圧に解放することな
く1分子線源のソース物質を補給することができ、かう
これらの操作を1個の予備室で行うことができ、さらに
膜の成長時には予備室を取り外すことができるので、装
置を小型化することが可能となる。
As described above, according to the present invention, the source material for a single molecule beam source can be replenished without opening the growth chamber to atmospheric pressure, and these operations can be performed in one preparatory chamber. Since the preliminary chamber can be removed during growth, it is possible to downsize the device.

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

第1図は本発明の実施例の分子線エピタキシー装置の主
要構成要素を示す断面図、第2図は本発明の他の実施例
の主要要素を示す断面図、第3図乃至第7図は従来の分
子線エピタキシー装置の断面図である。 1・・・・・・成長室、  3・・・・・・分子線源、
4・・・・・・ルツボ、  6・・・・・・予備室、7
・・・・・・搬送機構、 8・・・・・・ゲートバルク
、11・・・・・・排気口、 12.14・・・・・・
受け渡し機構、15・・・・・・電流導入端子、 16・・・・・・加熱用ヒータ。
FIG. 1 is a cross-sectional view showing the main components of a molecular beam epitaxy apparatus according to an embodiment of the present invention, FIG. 2 is a cross-sectional view showing main components of another embodiment of the present invention, and FIGS. 3 to 7 are 1 is a cross-sectional view of a conventional molecular beam epitaxy apparatus. 1...Growth chamber, 3...Molecular beam source,
4... Crucible, 6... Preliminary room, 7
...Transport mechanism, 8...Gate bulk, 11...Exhaust port, 12.14...
Delivery mechanism, 15... Current introduction terminal, 16... Heater for heating.

Claims (2)

【特許請求の範囲】[Claims] (1)超高真空に保たれた成長室内にウェハと、該ウェ
ハにソース物質の分子線を照射して、前記ウェハ表面に
薄膜を形成する分子線源と、前記成長室にゲートバルク
を介して接続した予備室と、該予備室の軸方向に分子線
源を移動し得る搬送機構とを備えた分子線エピタキシー
装置において、前記搬送機構の先端と成長室側とに、そ
れぞれ分子線源の受け渡し機構を設けると共に、前記予
備室を着脱可能にしたことを特徴とする分子線エピタキ
シー装置。
(1) A wafer is placed in a growth chamber kept in an ultra-high vacuum, a molecular beam source that irradiates the wafer with a molecular beam of a source material to form a thin film on the wafer surface, and a gate bulk is placed in the growth chamber. In a molecular beam epitaxy apparatus equipped with a prechamber connected to the prechamber and a transport mechanism capable of moving a molecular beam source in the axial direction of the prechamber, a molecular beam source is provided at the tip of the transport mechanism and on the side of the growth chamber, respectively. A molecular beam epitaxy apparatus characterized in that a delivery mechanism is provided and the preliminary chamber is detachable.
(2)前記予備室の外周に加熱用ヒータを配設したこと
を特徴とする特許請求の範囲第1項記載の分子線エピタ
キシー装置。
(2) The molecular beam epitaxy apparatus according to claim 1, characterized in that a heater is disposed around the outer periphery of the preliminary chamber.
JP29602986A 1986-12-12 1986-12-12 Molecular beam epitaxy apparatus Pending JPS63148617A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP29602986A JPS63148617A (en) 1986-12-12 1986-12-12 Molecular beam epitaxy apparatus

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP29602986A JPS63148617A (en) 1986-12-12 1986-12-12 Molecular beam epitaxy apparatus

Publications (1)

Publication Number Publication Date
JPS63148617A true JPS63148617A (en) 1988-06-21

Family

ID=17828188

Family Applications (1)

Application Number Title Priority Date Filing Date
JP29602986A Pending JPS63148617A (en) 1986-12-12 1986-12-12 Molecular beam epitaxy apparatus

Country Status (1)

Country Link
JP (1) JPS63148617A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5989339A (en) * 1994-09-04 1999-11-23 Sony Corporation MBE system and semiconductor device fabricated, using same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5989339A (en) * 1994-09-04 1999-11-23 Sony Corporation MBE system and semiconductor device fabricated, using same

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