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JPS5837388B2 - Kisouseichiyouhouhou - Google Patents
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JPS5837388B2 - Kisouseichiyouhouhou - Google Patents

Kisouseichiyouhouhou

Info

Publication number
JPS5837388B2
JPS5837388B2 JP50013335A JP1333575A JPS5837388B2 JP S5837388 B2 JPS5837388 B2 JP S5837388B2 JP 50013335 A JP50013335 A JP 50013335A JP 1333575 A JP1333575 A JP 1333575A JP S5837388 B2 JPS5837388 B2 JP S5837388B2
Authority
JP
Japan
Prior art keywords
substrate
aluminum
plasma generation
temperature
hydrogen
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
JP50013335A
Other languages
Japanese (ja)
Other versions
JPS5189384A (en
Inventor
清勝 神野
巌 東中川
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.)
Toshiba Corp
Original Assignee
Tokyo Shibaura Electric 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 Tokyo Shibaura Electric Co Ltd filed Critical Tokyo Shibaura Electric Co Ltd
Priority to JP50013335A priority Critical patent/JPS5837388B2/en
Publication of JPS5189384A publication Critical patent/JPS5189384A/ja
Publication of JPS5837388B2 publication Critical patent/JPS5837388B2/en
Expired legal-status Critical Current

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  • Electrodes Of Semiconductors (AREA)
  • Chemical Vapour Deposition (AREA)

Description

【発明の詳細な説明】 本発明は、気相,戊長方法に関する。[Detailed description of the invention] The present invention relates to a gas phase, elongation method.

エレクトロニクス工業の分野において、気相成長方法に
よる膜の形膚が広く用いられている。
In the field of electronics industry, the formation of films by vapor phase growth methods is widely used.

この方法は通常の蒸着法、スパッタリング法、メッキ法
などに比して膜の純度、基板に対する相傷の有無、段差
部における段切れの点等ですぐれた方法である。
This method is superior to the usual vapor deposition method, sputtering method, plating method, etc. in terms of the purity of the film, the presence or absence of mutual damage to the substrate, and the fact that there is no step breakage at the step portion.

例えば、モリブデン(MO)を戒長させる場合MoCl
!,を水素中で還元することにより行う。
For example, when molybdenum (MO) is precipitated, MoCl
! , by reducing it in hydrogen.

この場合、ハロゲ゛ン化物の還元温度は非常に高いため
成長基板の温度を上げなくてはならず、基板の劣化を生
じ易い欠点がある。
In this case, since the reduction temperature of the halide is very high, it is necessary to raise the temperature of the growth substrate, which has the drawback of easily causing deterioration of the substrate.

このことは、例えばアルミニウムの気相成長方法などに
ついてはさらに問題となる。
This becomes a further problem when it comes to vapor phase growth methods for aluminum, for example.

即ち、従来行われているアルミニウムの有機化合物熱分
解法は、炭素などの混入のため半導体工業にとり入れる
ことは難かしいので、ハロゲン化物例えばAlCl3を
水素還元する方法が考えられるが、AI!CI!3が1
?に変換される反応温度は、AI!の融点よりはるかに
高温であり、成長は困難なためである。
In other words, it is difficult to apply the conventional thermal decomposition method of organic compounds of aluminum to the semiconductor industry due to the contamination of carbon, etc., so a method of reducing a halide such as AlCl3 with hydrogen may be considered, but AI! CI! 3 is 1
? The reaction temperature converted to AI! This is because the temperature is much higher than the melting point of , making it difficult to grow.

本発明は、上記点に鑑みなされたもので気相成長方法に
新たなプラズマ反応を加えることにより単体や化合物膜
の戒長を容易ならしめる方法を提供するものである。
The present invention has been devised in view of the above points, and provides a method that facilitates the lengthening of single or compound films by adding a new plasma reaction to the vapor phase growth method.

以下、本発明を一実施例により図面を用いて説明する。DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below by way of an example with reference to the drawings.

反応装置は反応容器本体1とふた2及びプラズマ生成用
高周波コイル3、基板加熱ヒータ4とを備えている。
The reaction apparatus includes a reaction vessel main body 1, a lid 2, a high frequency coil 3 for plasma generation, and a substrate heater 4.

反応容器本体1は石英製管であり、この内部の基板設置
部に成長用基板5,6・・・・・・が支持台7で保持さ
れている。
The reaction vessel main body 1 is a quartz tube, and growth substrates 5, 6, .

支持台7はシリコンカーバイト或いはグラファイト等で
構成されており、外部の加熱ヒータ4例えば高周波コイ
ルに電力を加えることにより、加熱される。
The support base 7 is made of silicon carbide, graphite, or the like, and is heated by applying power to an external heater 4, such as a high-frequency coil.

本実施例では基板を300℃に保った。In this example, the substrate was kept at 300°C.

又、前記ふた2は着脱自在で、前記成長基板5,6・・
・・・・の取り入れ取り出しが行えるとともに、排気口
8を介して真空ポンプ(図示せず)に連結されている。
Further, the lid 2 is removable and covers the growth substrates 5, 6...
... can be taken in and taken out, and is connected to a vacuum pump (not shown) via an exhaust port 8.

ふた2と反応容器本体1とは密封性よく構成してある。The lid 2 and the reaction vessel body 1 are configured to have good sealing properties.

一方、前記反応容器本体1には、ガス導入口9が設けら
れ、ここから水素ガス及びAlCl3ガスが導入される
On the other hand, the reaction vessel main body 1 is provided with a gas inlet 9, through which hydrogen gas and AlCl3 gas are introduced.

この反応容器本体1内部は10 Torr程度に減
圧してある。
The pressure inside this reaction vessel main body 1 is reduced to about 10 Torr.

これは、後述するプラズマ生成を良好にするためであり
、前記真空ポンプによって真空度調整が行える。
This is to improve plasma generation, which will be described later, and the degree of vacuum can be adjusted by the vacuum pump.

又、AICII3ガスは、溶液中にガスを通してバブル
して供給する。
Further, the AICII3 gas is supplied in the form of bubbling through the solution.

このようにして、反応容器本体1内に水素ガス、AlC
l3ガスを導入し、前記高周波コイルにプラズマを生或
するに十分な電力例えば300Wを加える。
In this way, hydrogen gas, AlC
13 gas is introduced, and sufficient power, for example 300 W, to generate plasma is applied to the high frequency coil.

この結果、前記成長基板5,6・・・・・・上には、A
lが成長する。
As a result, A
l grows.

この時、基板温度は300℃であり、融点以下で良好な
Al膜が形成できた。
At this time, the substrate temperature was 300° C., and a good Al film could be formed at a temperature below the melting point.

プラズマ生或部と基板設置部とを離隔してもAlの成長
が行えることが確認された。
It was confirmed that Al could be grown even if the plasma generation part and the substrate installation part were separated.

プラズマ生戊部と基板設置部とが離隔していると、基板
がプラズマによる損傷を受けることがなく、またアルミ
ニウム膜の成長状況を良好に観察することができその実
用的価値は太きい。
If the plasma generation part and the substrate installation part are separated, the substrate will not be damaged by the plasma, and the growth status of the aluminum film can be observed well, which has great practical value.

なお、装置の小型化のためには、基板設置部にプラズマ
を生成するようにしてもよい。
Note that in order to downsize the device, plasma may be generated in the substrate installation portion.

上記実施例では単体膜の形或を例にとって説明したが、
気相成長源ガス内に2種類以上の戒長物質を含ませてお
き、化合物膜を形成することも出来る。
In the above embodiment, the shape of a single film was explained as an example.
It is also possible to form a compound film by including two or more types of chemical substances in the vapor phase growth source gas.

,本発明の効果としては、基板温度を十分低温にしてし
かも成長が行えることが挙げられる。
An advantage of the present invention is that growth can be performed while keeping the substrate temperature sufficiently low.

このため特に低融点物質の成長に本発明方法を適用する
ことは有効である。
Therefore, it is particularly effective to apply the method of the present invention to the growth of low-melting-point substances.

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

図は本発明の一実施例方法を説明するための断面図であ
る。
The figure is a sectional view for explaining a method according to an embodiment of the present invention.

Claims (1)

【特許請求の範囲】[Claims] 1 塩化アルミニウムと水素を含むガスを減圧されたプ
ラズマ生戊領域に導入する段階と、前記プラズマ生或領
域内で水素により還元された成長物質を含むガスを前記
プラズマ生或領域とは離隔した位置に配置された加熱さ
れた基板に導ひき、アルミニウムの融点温度以下で前記
基板上にアルミニウム膜を或長させる段階とから成る気
相或長方法。
1. Introducing a gas containing aluminum chloride and hydrogen into a reduced pressure plasma generation region, and introducing the gas containing a growth substance reduced by hydrogen within the plasma generation region at a location separated from the plasma generation region. a heated substrate disposed at a temperature below the melting point temperature of aluminum, and growing an aluminum film on the substrate at a temperature below the melting point temperature of aluminum.
JP50013335A 1975-02-03 1975-02-03 Kisouseichiyouhouhou Expired JPS5837388B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP50013335A JPS5837388B2 (en) 1975-02-03 1975-02-03 Kisouseichiyouhouhou

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP50013335A JPS5837388B2 (en) 1975-02-03 1975-02-03 Kisouseichiyouhouhou

Publications (2)

Publication Number Publication Date
JPS5189384A JPS5189384A (en) 1976-08-05
JPS5837388B2 true JPS5837388B2 (en) 1983-08-16

Family

ID=11830246

Family Applications (1)

Application Number Title Priority Date Filing Date
JP50013335A Expired JPS5837388B2 (en) 1975-02-03 1975-02-03 Kisouseichiyouhouhou

Country Status (1)

Country Link
JP (1) JPS5837388B2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57123969A (en) * 1981-01-26 1982-08-02 Semiconductor Energy Lab Co Ltd Formation of zinc oxide film by vapor phase method using plasma
JPS58158916A (en) * 1982-03-16 1983-09-21 Fujitsu Ltd Preparation of semiconductor device
JPS58161763A (en) * 1982-03-17 1983-09-26 Nippon Telegr & Teleph Corp <Ntt> Vacuum deposition method
JPS62274072A (en) * 1986-05-21 1987-11-28 Canon Inc Improved method for forming tin oxide thin films
JPS62260065A (en) * 1986-04-04 1987-11-12 Canon Inc Formation of thin tin oxide film

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5525493B2 (en) * 1971-10-04 1980-07-07
JPS496168A (en) * 1972-04-10 1974-01-19

Also Published As

Publication number Publication date
JPS5189384A (en) 1976-08-05

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