JP3112796B2 - Chemical vapor deposition method - Google Patents

Chemical vapor deposition method

Info

Publication number
JP3112796B2
JP3112796B2 JP06154538A JP15453894A JP3112796B2 JP 3112796 B2 JP3112796 B2 JP 3112796B2 JP 06154538 A JP06154538 A JP 06154538A JP 15453894 A JP15453894 A JP 15453894A JP 3112796 B2 JP3112796 B2 JP 3112796B2
Authority
JP
Japan
Prior art keywords
layer
gas
substrate
vapor deposition
thickness
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 - Lifetime
Application number
JP06154538A
Other languages
Japanese (ja)
Other versions
JPH0822959A (en
Inventor
俊和 宮本
Original Assignee
徳山東芝セラミックス株式会社
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 徳山東芝セラミックス株式会社 filed Critical 徳山東芝セラミックス株式会社
Priority to JP06154538A priority Critical patent/JP3112796B2/en
Publication of JPH0822959A publication Critical patent/JPH0822959A/en
Application granted granted Critical
Publication of JP3112796B2 publication Critical patent/JP3112796B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Crystals, And After-Treatments Of Crystals (AREA)
  • Chemical Vapour Deposition (AREA)
  • Physical Deposition Of Substances That Are Components Of Semiconductor Devices (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、単結晶シリコンウエハ
等にエピタキシャル成長により結晶膜を形成する化学気
相成長方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a chemical vapor deposition method for forming a crystal film on a single crystal silicon wafer or the like by epitaxial growth.

【0002】[0002]

【従来の技術】従来から、半導体デバイスの製造工程等
においては、単結晶シリコンウエハ等にエピタキシャル
成長により結晶膜を形成することが行われている。この
ような結晶膜を形成する量産型の気相成長装置として
は、例えば、特開平5−47680号公報に示されるよ
うないわゆるベルジヤー型のもの、あるいは、いわゆる
シリンダ型のもの等が知られている。
2. Description of the Related Art Conventionally, in a semiconductor device manufacturing process, a crystal film is formed on a single crystal silicon wafer or the like by epitaxial growth. As a mass-production type vapor phase growth apparatus for forming such a crystal film, for example, a so-called bell-jar type or a so-called cylinder type as disclosed in JP-A-5-47680 is known. I have.

【0003】また、例えば、特開平4−245419号
公報等に示されるように、従来から上記エピタキシャル
成長による成膜技術を利用して、半導体デバイスを製造
することが行われている。
Further, as shown in, for example, Japanese Patent Application Laid-Open No. 4-245419, a semiconductor device has been conventionally manufactured by utilizing the above-mentioned film forming technique by epitaxial growth.

【0004】このような2層構造のエピタキシャル膜を
形成する場合、従来はSi原として比較的成長速度の速
いSiHCl3 ガスを使用している。
In forming such an epitaxial film having a two-layer structure, a SiHCl 3 gas having a relatively high growth rate is conventionally used as a Si source.

【0005】なお、このようにSiHCl3 ガスを使用
している理由は、第2層の膜厚が厚く、抵抗が高いた
め、成長速度の速いガスの方が条件が出し易く、スルー
プットも向上させることができるためである。
The reason why the SiHCl 3 gas is used is that the second layer has a large thickness and a high resistance, so that a gas having a high growth rate is more likely to provide conditions and improve the throughput. This is because you can do it.

【0006】[0006]

【発明が解決しようとする課題】しかしながら、このよ
うな従来の方法では、1層目のエピタキシャル膜を形成
する際、SiHCl3 ガスの流量を低く設定するため、
ガスの流れが悪くなり、第1層の膜厚のばらつきが大き
くなるという問題があった。このため、歩留まりが低下
し、生産性を向上させることが困難であった。
However, in such a conventional method, the flow rate of the SiHCl 3 gas is set low when the first epitaxial film is formed.
There has been a problem that the gas flow becomes worse and the thickness of the first layer varies greatly. For this reason, the yield has decreased, and it has been difficult to improve the productivity.

【0007】本発明は、かかる従来の事情に対処してな
されたもので、第1層、第2層ともにばらつきの少ない
均一な膜厚の所望のエピタキシャル膜を形成することが
でき、従来に比べて歩留まりを向上させて生産性の向上
を図ることのできる化学気相成長方法を提供しようとす
るものである。
The present invention has been made in view of such a conventional situation, and it is possible to form a desired epitaxial film having a uniform thickness with little variation in both the first layer and the second layer. It is an object of the present invention to provide a chemical vapor deposition method capable of improving the yield and improving the productivity.

【0008】[0008]

【課題を解決するための手段】請求項1記載の化学気相
成長方法は、基板を所定温度に加熱しつつ原料ガスを供
給し、当該基板上にエピタキシャル膜を形成するにあた
り、SiCl 4 ガスを供給して、前記基板に所定膜厚で
所定電気抵抗の第1層を成長させ、この後、SiHCl
3 ガスを供給して、前記基板に前記第1層より膜厚が厚
く前記第1層より電気抵抗の高い第2層を連続的に成長
させて2層構造のエピタキシャル膜を形成することを特
徴とする。
Chemical vapor deposition method according to claim 1, wherein Means for Solving the Problems], on the occasion of the raw material gas was supplied while heating the substrate to a predetermined temperature, to form an epitaxial film on the substrate, the SiCl 4 gas And supply the substrate with a predetermined thickness.
A first layer having a predetermined electrical resistance is grown, followed by SiHCl.
Supply 3 gases and make the substrate thicker than the first layer.
Continuously growing a second layer having a higher electrical resistance than the first layer
Thus, an epitaxial film having a two-layer structure is formed .

【0009】[0009]

【0010】[0010]

【0011】[0011]

【作用】上記構成の本発明の化学気相成長方法では、例
えば比較的成長速度の遅いSiCl4 ガスで電気抵抗が
低く膜厚の薄い第1層を成長させ、この後、ガスを比較
的成長速度の速いSiHCl3 ガスに切り換え、SiH
Cl3 ガスで、電気抵抗が高く膜厚の厚い第2層を成長
させる。
In the chemical vapor deposition method of the present invention having the above-mentioned structure, for example, a first layer having a low electric resistance and a small film thickness is grown by using a SiCl 4 gas having a relatively low growth rate, and thereafter, the gas is relatively grown. Switch to fast SiHCl 3 gas,
A second layer having a high electric resistance and a large thickness is grown with Cl 3 gas.

【0012】これによって、第1層、第2層ともにばら
つきの少ない均一な膜厚の所望のエピタキシャル膜を形
成することができる。
As a result, a desired epitaxial film having a uniform thickness with little variation can be formed in both the first and second layers.

【0013】[0013]

【実施例】以下、本発明の一実施例について図面を参照
して説明する。
An embodiment of the present invention will be described below with reference to the drawings.

【0014】図1は、本発明の一実施例に用いた装置の
概略構成を示すもので、同図に示すように、ベルジャー
型の反応管1内には、上面に複数枚のウエハ2を保持可
能に構成されたサセプタ3が設けられており、このサセ
プタ3は図中矢印で示すように、その中心を回転軸とし
て回転可能に構成されている。
FIG. 1 shows a schematic structure of an apparatus used in one embodiment of the present invention. As shown in FIG. 1, a plurality of wafers 2 are placed on a top surface in a bell-jar type reaction tube 1. A susceptor 3 configured to be able to be held is provided, and this susceptor 3 is configured to be rotatable around its center as a rotation axis, as indicated by an arrow in the figure.

【0015】また、サセプタ3の上部には、所定のガス
を反応管1内に導入するためのガス導入ノズル4が設け
られており、反応管1の下部には排気を行うための排気
管5が設けられていて、反応管1内部を所定のガス雰囲
気とすることができるよう構成されている。
A gas introduction nozzle 4 for introducing a predetermined gas into the reaction tube 1 is provided above the susceptor 3, and an exhaust pipe 5 for exhausting gas is provided below the reaction tube 1. Is provided so that the inside of the reaction tube 1 can be set to a predetermined gas atmosphere.

【0016】さらに、サセプタ3の下部には、高周波コ
イル6が配設され、サセプタ3を介してウエハ2を所望
の温度に加熱することができるようになっている。
Further, a high frequency coil 6 is provided below the susceptor 3 so that the wafer 2 can be heated to a desired temperature via the susceptor 3.

【0017】上記構成の装置を用いて、本実施例では、
サセプタ3に保持されたウエハ2を1100〜1120℃の所定
温度に加熱し、まず、ガス導入ノズル4から、原料ガス
として比較的成長速度の遅いSiCl4 ガスと不純物ガ
スとしてホスフィン(PH3)とキャリアガスとして水
素ガスの混合ガスを流量250 l/min で供給して約10分
間第1層の成膜を行い、続いて、原料ガスを比較的成長
速度の速いSiHCl3 ガスに切り換え、SiHCl3
ガスとホスフィンとキャリアガスとして水素ガスの混合
ガスを流量250 l/min で供給して約30分間第2層の成
膜を連続的に行った。
In the present embodiment, using the apparatus having the above configuration,
The wafer 2 held on the susceptor 3 is heated to a predetermined temperature of 1100 to 1120 ° C. First, a gas introduction nozzle 4 is used to supply SiCl 4 gas having a relatively low growth rate as a source gas and phosphine (PH 3 ) as an impurity gas. perform deposition of approximately the first layer 10 min the mixture gas of hydrogen gas was supplied at a flow rate of 250 l / min as a carrier gas, followed by switching the material gas to a relatively growth rate fast SiHCl 3 gas, SiHCl 3
A mixed gas of gas, phosphine, and hydrogen gas as a carrier gas was supplied at a flow rate of 250 l / min, and the second layer was continuously formed for about 30 minutes.

【0018】これによって、第1層(膜厚約10μm、比
抵抗約0.05Ω-cm )、第2層(膜厚約100 μm、比抵抗
約100 Ω-cm )ともに膜厚にばらつきの少ない均一な膜
厚のエピタキシャル膜を形成することができた。
As a result, the first layer (thickness of about 10 μm, specific resistance of about 0.05 Ω-cm) and the second layer (thickness of about 100 μm, specific resistance of about 100 Ω-cm) have uniform thickness with little variation in thickness. It was possible to form an epitaxial film having a large thickness.

【0019】なお、第1層のウエハ2面内における膜厚
の面内ばらつきは、従来の40%以下に抑制され、歩留
まりは従来の1.1〜1.2倍となった。
The in-plane variation of the film thickness of the first layer on the surface of the wafer 2 was suppressed to 40% or less of the conventional one, and the yield was 1.1 to 1.2 times that of the conventional one.

【0020】以上のように、本実施例によれば、第1
層、第2層ともにばらつきの少ない均一な膜厚のリンド
ープシリコン単結晶膜を形成することができ、従来に比
べて歩留まりを向上させて生産性の向上を図ることがで
きる。
As described above, according to the present embodiment, the first
It is possible to form a phosphorus-doped silicon single crystal film having a uniform thickness with little variation in both the layer and the second layer, and it is possible to improve the yield and the productivity as compared with the conventional case.

【0021】[0021]

【発明の効果】以上説明したように、本発明の化学気相
成長方法によれば、例えば、第1層に膜厚が薄く低抵抗
(膜厚1〜30μm、比抵抗0.01〜0.2 Ω-cm )で第2層
の膜厚が厚く高抵抗(膜厚30〜300 μm、比抵抗1〜30
0 Ω-cm )のIGBT用又はスイッチング・ダイオード
用エピウエハの製造において、第1層、第2層ともにば
らつきの少ない均一な膜厚の所望のエピタキシャル膜を
形成することができ、従来に比べて歩留まりを向上させ
て生産性の向上を図ることができる。
As described above, according to the chemical vapor deposition method of the present invention, for example, the first layer has a small film thickness and low resistance (film thickness 1 to 30 μm, specific resistance 0.01 to 0.2 Ω-cm). ), The thickness of the second layer is large and the resistance is high (thickness: 30 to 300 μm, specific resistance: 1 to 30).
In the manufacture of IGBT or switching diode epiwafers of 0 Ω-cm), a desired epitaxial film having a uniform thickness with little variation can be formed in both the first layer and the second layer. And the productivity can be improved.

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

【図1】本発明の一実施例の化学気相成長方法に用いる
装置の構成を示す図。
FIG. 1 is a diagram showing a configuration of an apparatus used in a chemical vapor deposition method according to one embodiment of the present invention.

【符号の説明】[Explanation of symbols]

1 反応管 2 ウエハ 3 サセプタ 4 原料ガス導入ノズル 5 排気管 6 高周波コイル DESCRIPTION OF SYMBOLS 1 Reaction tube 2 Wafer 3 Susceptor 4 Source gas introduction nozzle 5 Exhaust tube 6 High frequency coil

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) H01L 21/205 H01L 21/31 C23C 16/00 C30B 25/00 ──────────────────────────────────────────────────続 き Continued on the front page (58) Field surveyed (Int. Cl. 7 , DB name) H01L 21/205 H01L 21/31 C23C 16/00 C30B 25/00

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 基板を所定温度に加熱しつつ原料ガスを
供給し、当該基板上にエピタキシャル膜を形成するにあ
たり、 SiCl4 ガスを供給して、前記基板に所定膜厚で所定
電気抵抗の第1層を成長させ、この後、SiHCl3
スを供給して、前記基板に前記第1層より膜厚が厚く前
記第1層より電気抵抗の高い第2層を連続的に成長させ
て2層構造のエピタキシャル膜を形成することを特徴と
する化学気相成長方法。
1. A source gas is supplied while heating a substrate to a predetermined temperature, and in forming an epitaxial film on the substrate, a SiCl 4 gas is supplied to the substrate so that the substrate has a predetermined thickness and a predetermined electric resistance. One layer is grown, and thereafter, a SiHCl 3 gas is supplied to continuously grow a second layer having a thickness greater than that of the first layer and a higher electrical resistance than the first layer on the substrate, thereby forming two layers. A chemical vapor deposition method comprising forming an epitaxial film having a structure.
JP06154538A 1994-07-06 1994-07-06 Chemical vapor deposition method Expired - Lifetime JP3112796B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP06154538A JP3112796B2 (en) 1994-07-06 1994-07-06 Chemical vapor deposition method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP06154538A JP3112796B2 (en) 1994-07-06 1994-07-06 Chemical vapor deposition method

Publications (2)

Publication Number Publication Date
JPH0822959A JPH0822959A (en) 1996-01-23
JP3112796B2 true JP3112796B2 (en) 2000-11-27

Family

ID=15586452

Family Applications (1)

Application Number Title Priority Date Filing Date
JP06154538A Expired - Lifetime JP3112796B2 (en) 1994-07-06 1994-07-06 Chemical vapor deposition method

Country Status (1)

Country Link
JP (1) JP3112796B2 (en)

Also Published As

Publication number Publication date
JPH0822959A (en) 1996-01-23

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