JP2001089293A - Epitaxial wafer and method of producing the same - Google Patents

Epitaxial wafer and method of producing the same

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Publication number
JP2001089293A
JP2001089293A JP25853099A JP25853099A JP2001089293A JP 2001089293 A JP2001089293 A JP 2001089293A JP 25853099 A JP25853099 A JP 25853099A JP 25853099 A JP25853099 A JP 25853099A JP 2001089293 A JP2001089293 A JP 2001089293A
Authority
JP
Japan
Prior art keywords
epitaxial
wafer
oxide film
epitaxial wafer
film
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
JP25853099A
Other languages
Japanese (ja)
Inventor
Mariko Takeshita
真理子 竹下
Susumu Suenaga
享 末永
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.)
Nippon Steel Corp
Original Assignee
Sumitomo Metal Industries 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 Sumitomo Metal Industries Ltd filed Critical Sumitomo Metal Industries Ltd
Priority to JP25853099A priority Critical patent/JP2001089293A/en
Publication of JP2001089293A publication Critical patent/JP2001089293A/en
Pending legal-status Critical Current

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  • Crystals, And After-Treatments Of Crystals (AREA)
  • Weting (AREA)
  • Formation Of Insulating Films (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a method of producing an epitaxial wafer, in which a particular device such as a oxidation furnace directly connected to an epitaxially growing reactor is not used and a particular treatment for cleaning or oxidizing the surface after epitaxially growing is not needed, thereby the production process is made simple, and by which an epitaxial wafer good in surface smoothness is produced. SOLUTION: When a wafer is taken out from an epitaxial reactor and taken into a carrying part, an oxide thin film having a thickness of <=1 nm is formed by introducing a small amount of oxygen into the inert gas in a carrying chamber and taking the wafer into the carrying chamber at >=600 deg.C immediately after forming an epitaxial film.

Description

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

【0001】[0001]

【発明の属する技術分野】この発明は、シリコン等の半
導体ウェーハに高品質かつ変質し難いエピタキシャル薄
膜を形成するエピタキシャルウェーハの製造方法に係
り、エピタキシャル成長後に洗浄や表面酸化のための特
別な処理を施すことなく、簡単な処理で、表面の平坦性
や清浄性が保持可能なエピタキシャルウェーハとその製
造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method of manufacturing an epitaxial wafer for forming an epitaxial thin film of high quality and hardly deteriorated on a semiconductor wafer such as silicon, and performing a special treatment for cleaning and surface oxidation after epitaxial growth. The present invention relates to an epitaxial wafer capable of maintaining surface flatness and cleanliness with a simple process without any processing, and a method for manufacturing the same.

【0002】[0002]

【従来の技術】シリコン半導体ウェーハにエピタキシャ
ル成長によるシリコン薄膜を設けた、いわゆるエピタキ
シャルウェーハは、水素で終端された面であるため、表
面は負に帯電しかつ接触角が大きく、表面に塵挨等が付
着し易い状態となっている。(J.J.A.P.,Vol.32(1993),p
p.L1489〜L1491)
2. Description of the Related Art A so-called epitaxial wafer in which a silicon semiconductor wafer is provided with a silicon thin film formed by epitaxial growth, is a surface terminated with hydrogen. Therefore, the surface is negatively charged and has a large contact angle. It is in a state where it easily adheres. (JJAP, Vol.32 (1993), p
(p.L1489 ~ L1491)

【0003】従来、エピタキシャルウェーハにおいて、酸化
された表面のほうが安定であることと、搬送時の付着粒
子などの汚染除去の効果を狙って、エピタキシャル成長
後に、RCA洗浄などのウェット洗浄後、エピタキシャル
表面に洗浄による酸化膜を形成させてから製品の出荷が
行われている。
[0003] Conventionally, in an epitaxial wafer, the oxidized surface is more stable, and the effect of removing contamination such as adhered particles during transportation is aimed at, after the epitaxial growth, wet cleaning such as RCA cleaning, and the like. Products are shipped after an oxide film is formed by cleaning.

【0004】しかし、エピタキシャル成長後の表面は、結晶
方位に依存し分子レベルで平担な面であるのに、ウェッ
ト洗浄をすることにより表面の平坦性をむしろ悪くして
しまうことが知られている。
[0004] However, it is known that the surface after epitaxial growth is flat at the molecular level depending on the crystal orientation, but the surface flatness is rather deteriorated by wet cleaning. .

【0005】また、反応後のエピタキシャル層をウェット洗
浄することにより、高清浄度のエピタキシャル炉でエピ
タキシャル成長を行ったものを、逆に汚染してしまう場
合もあるという問題があった。
[0005] In addition, there has been a problem that, by performing wet cleaning of the epitaxial layer after the reaction, the epitaxial layer grown in a high-purity epitaxial furnace may be contaminated.

【0006】そこで、エピタキシャル炉でエピタキシャル成
長を行った後、雰囲気を置換して熱酸化処理にて酸化膜
を形成してから反応炉より搬出する方法が採用されてい
る(例えば特開平4-196119号、特許2540690号)。あるい
はエピタキシャル成長後にオゾン酸化処理を行うことに
よってエピタキシャル表面に5nm以上の酸化膜を形成す
る方法が提案されている。
Therefore, a method has been adopted in which after epitaxial growth is performed in an epitaxial furnace, an atmosphere is replaced, an oxide film is formed by thermal oxidation treatment, and then an oxide film is carried out from the reaction furnace (for example, Japanese Patent Laid-Open No. 4-196119). , Patent No. 2540690). Alternatively, there has been proposed a method of forming an oxide film having a thickness of 5 nm or more on an epitaxial surface by performing an ozone oxidation treatment after epitaxial growth.

【0007】[0007]

【発明が解決しようとする課題】上記問題を解決するた
めに、エピタキシャル成長後に熱酸化処理またはオゾン
酸化処理を行うには、エピタキシャル反応炉に直結した
酸化炉が必要であること、また処理時間が長いことか
ら、工程が煩雑で製造コストが極めて高くつくという問
題があった。
In order to solve the above-mentioned problems, in order to perform the thermal oxidation treatment or the ozone oxidation treatment after the epitaxial growth, an oxidation furnace directly connected to the epitaxial reactor is required, and the processing time is long. Therefore, there is a problem that the process is complicated and the production cost is extremely high.

【0008】この発明は、前述の表面の平坦性や清浄性を保
持させるための酸化膜を形成する際、反応炉に直結した
酸化炉などの特別の装置を用いることなく、また、エピ
成長後洗浄または表面酸化のための特別な処理が必要で
なく、従来の製造工程を簡略化でき、かつ表面の平坦性
が良好であるエピタキシャルウェーハと、これを安価に
提供可能な製造方法の提供を目的とする。
[0008] According to the present invention, when forming an oxide film for maintaining the flatness and cleanliness of the above-mentioned surface, a special device such as an oxidation furnace directly connected to a reaction furnace is not used, and after the epitaxial growth, An object of the present invention is to provide an epitaxial wafer that does not require special treatment for cleaning or surface oxidation, can simplify the conventional manufacturing process, and has good surface flatness, and a manufacturing method that can provide the same at low cost. And

【0009】[0009]

【課題を解決するための手段】発明者らは、ウェーハ表
面形状をより平坦に保ちかつ変質や塵挨の付着を防ぐ手
段について、種々検討した結果、エピタキシャル薄膜上
に1nm以下の極薄い酸化膜を形成すれば、接触角が全面
水素終端された面よりも接触角が小さくなり、塵挨等の
付着も少なくなることを知見した。
Means for Solving the Problems The inventors of the present invention have conducted various studies on means for keeping the wafer surface shape more flat and preventing deterioration and adhesion of dust, and as a result, an extremely thin oxide film of 1 nm or less was formed on the epitaxial thin film. It has been found that the formation of a contact angle makes the contact angle smaller than that of the surface completely terminated with hydrogen, and reduces the adhesion of dust and the like.

【0010】また、発明者らは、エピタキシャル薄膜上に1n
m以下の極薄い酸化膜を簡単に設ける手段について、種
々検討した結果、エピタキシャル反応室から搬送部に取
り出す時に、搬送室内の不活性ガス中に僅かに酸素を存
在させ、エピタキシャル膜形成直後に600℃以上でウェ
ーハを搬送室に取り出すだけで、表面に1nm以下の薄い
酸化膜を形成させることができることを知見した。
[0010] Further, the inventors have proposed that 1n
As a result of various studies on means for easily providing an extremely thin oxide film of m or less, when taking out from the epitaxial reaction chamber to the transfer section, a slight amount of oxygen was present in the inert gas in the transfer chamber, and immediately after forming the epitaxial film, 600 It was found that a thin oxide film with a thickness of 1 nm or less can be formed on the surface simply by taking the wafer into the transfer chamber at a temperature of at least ° C.

【0011】また、発明者らは、上記の1nm以下の薄い酸化
膜を形成する条件として、温度は600〜900℃が望ましい
こと、酸素含有雰囲気として、純度99.99〜99.999%のN2
ガスまたはArガス、あるいは酸素を5〜1000ppm含むN2
スまたはArガス分意図することにより、エピタキシャル
成長直後に特別な酸化工程を設けることなく、表面に1n
m以下の薄い酸化膜を形成できることを知見し、この発
明を完成した。
[0011] Further, the inventors have set that the temperature is desirably 600 to 900 ° C as conditions for forming the thin oxide film having a thickness of 1 nm or less, and that N 2 having a purity of 99.99 to 99.999% is used as an oxygen-containing atmosphere.
Gas or Ar gas, or by oxygen intended N 2 gas or Ar gas partial comprises 5 to 1000 ppm, without providing a special oxidation process after epitaxial growth, 1n the surface
The inventors have found that a thin oxide film having a thickness of m or less can be formed, and have completed the present invention.

【0012】さらに、発明者らは、この発明によるエピタキ
シャルウェーハは、デバイスプロセス投入直前に、RCA
洗浄法の少なくとも1つの洗浄液、あるいはHF含有洗浄
液で洗浄することにより、容易に酸化膜を除去できるこ
とを知見した。
[0012] Further, the inventors have found that an epitaxial wafer according to the present invention can be used for RCA immediately before device process introduction.
It has been found that an oxide film can be easily removed by cleaning with at least one cleaning solution of the cleaning method or a cleaning solution containing HF.

【0013】[0013]

【発明の実施の形態】この発明は、エピタキシャル反応
室から搬送部に取り出す際に、例えば、搬送室内の不活
性ガス中の僅かな酸素を利用するか、あるいは僅かに存
在させて、エピタキシャル反応完了後に600℃以上でウ
ェーハを搬送室に取り出すだけで、表面に1nm以下の薄
い酸化膜を形成させることを特徴とする。
DESCRIPTION OF THE PREFERRED EMBODIMENTS In the present invention, when taking out from an epitaxial reaction chamber to a transfer section, for example, a small amount of oxygen in an inert gas in the transfer chamber is used or slightly present to complete the epitaxial reaction. It is characterized in that a thin oxide film of 1 nm or less is formed on the surface by simply taking out the wafer to a transfer chamber at 600 ° C. or higher.

【0014】すなわち、エピタキシャル反応室から取り出さ
れたウェーハが、表面に存在する水素の脱離温度450℃
よりも高く、しかもウェーハ全体が酸化される温度で、
反応室から若干の酸素を含む不活性雰囲気中に取り出す
ことにより、酸化膜を表面に形成させるというものであ
る。この際、500℃以下の温度で取り出すと、表面は水
素で終端されている。また、500℃を超え、600℃未満の
場合はできる膜が均一でなく実用的でない。
That is, the wafer taken out of the epitaxial reaction chamber has a desorption temperature of 450 ° C. of hydrogen existing on the surface.
Higher than the temperature at which the whole wafer is oxidized,
The oxide film is formed on the surface by taking out from the reaction chamber into an inert atmosphere containing some oxygen. At this time, when taken out at a temperature of 500 ° C. or less, the surface is terminated with hydrogen. If the temperature is higher than 500 ° C. and lower than 600 ° C., the resulting film is not uniform and is not practical.

【0015】この発明において、酸化膜厚みの測定は次のと
おりである。酸化膜厚doxは、x線をもちいた表面分析法
であるESCA(Electron Spectrosopy for Chemical Analy
sis)の測定から求めた。酸化によって化学シフトしたSi
2pスペクトルの光電子数Noxと、基板SiのSi2pスペクト
ルの光電子数NSiの比から、doxox・cosθ・In[k・N
ox/NSi)+1] の式で算出した。ここで、λoxは酸化膜中
のSi2p光電子の脱出深さであり、2.5nmである。kは定数
で2.086である。
In the present invention, the measurement of the thickness of the oxide film is as follows. Oxide film thickness d ox is an ESCA (Electron Spectrosopy for Chemical Analy
sis). Si chemically shifted by oxidation
A photoelectron number N ox of 2p spectrum, the ratio of the number of photoelectrons N Si of Si 2p spectrum of the substrate Si, d ox = λ ox · cosθ · In [k · N
ox / N Si ) +1]. Here, λ ox is the escape depth of Si 2p photoelectrons in the oxide film, which is 2.5 nm. k is a constant which is 2.086.

【0016】この発明において、酸化膜を形成するための雰
囲気中の酸素濃度については、少なくとも5ppmは必要で
あるが、安全面から1000ppm以下であることが望まし
い。また900℃を超える温度で搬送室へ取り出すと、エ
ピタキシャル膜の品質の劣化を生じるため、900℃以下
であることが望ましい。
In the present invention, the oxygen concentration in the atmosphere for forming the oxide film is required to be at least 5 ppm, but is preferably 1000 ppm or less from the viewpoint of safety. If the epitaxial film is taken out to the transfer chamber at a temperature exceeding 900 ° C., the quality of the epitaxial film is deteriorated.

【0017】また、工業的には、当該雰囲気を純度99.99〜9
9.999%のN2ガスまたはArガス中にすることで、前記の微
量酸素含有雰囲気と同等の作用効果を得ることが可能で
ある。
In addition, industrially, the atmosphere should be 99.99-9 purity.
By setting it in 9.999% N 2 gas or Ar gas, it is possible to obtain the same operation and effect as in the above-mentioned trace oxygen-containing atmosphere.

【0018】エピタキシャ反応直後の表面に薄い酸化膜を形
成させることによって、水素で終端された面に比べて塵
挨付着などは少なくなる利点がある。また、操作とし
て、反応炉からの取り出し温度を600℃以上にして雰囲
気中に5〜1000ppmの酸素を含有させるだけで、酸化膜を
形成できるため、工程を増やす必要なく簡単にウェーハ
を製造できる。さらに、その後の洗浄工程が不要にな
り、工程的に省力化できる利点がある。
By forming a thin oxide film on the surface immediately after the epitaxy reaction, there is an advantage that dust adhesion and the like are reduced as compared with the surface terminated with hydrogen. In addition, as an operation, an oxide film can be formed only by setting the temperature of taking out from the reaction furnace to 600 ° C. or higher and containing 5 to 1000 ppm of oxygen in the atmosphere, so that a wafer can be easily manufactured without increasing the number of steps. Further, there is an advantage that the subsequent cleaning step becomes unnecessary, and labor can be saved in the step.

【0019】この発明において、1nm以下の酸化膜を除去す
るには、いわゆるRCA法と呼ばれる最も標準的な化学的
洗浄法で容易に除去することが可能である。例えば、過
酸化水素(H2O2)をベースにした、高pHのアルカリ混合
液、低pHの酸混合液による2段階洗浄で利用される、一
般的にSC-1とよばれるH2O‐H2O2‐NH4OHやSC-2組成の洗
浄液を適宜選定利用できる。また、HFやHF/O3などのHF
含有洗浄液を用いることもできる。
In the present invention, an oxide film having a thickness of 1 nm or less can be easily removed by the most standard chemical cleaning method called a so-called RCA method. For example, to hydrogen peroxide (H 2 O 2) to the base, a high pH alkaline mixture is used in two stages washed with an acid mixture of low pH, generally H 2 called SC-1 O -H 2 O 2 -NH 4 OH or SC-2 composition cleaning solution can be appropriately selected and used. HF such as HF and HF / O 3
Containing cleaning liquids can also be used.

【0020】[0020]

【実施例】一般的な縦型気相成長装置を用いて、シリコ
ンウェーハにエピタキシャル成長による薄膜を設け、エ
ピタキシャル反応完了直後にウェーハを反応室から隣接
するロボット搬送により搬送室に取り出した。搬送室雰
囲気は、温度800℃、酸素100ppm含有のN2ガス雰囲気で
ある。
EXAMPLE A thin film was formed on a silicon wafer by epitaxial growth using a general vertical vapor phase epitaxy apparatus. Immediately after the completion of the epitaxial reaction, the wafer was taken out of the reaction chamber by an adjacent robot transfer to a transfer chamber. The atmosphere in the transfer chamber is a N 2 gas atmosphere at a temperature of 800 ° C. and containing 100 ppm of oxygen.

【0021】ウェーハの取出の際、300℃、500℃、600℃、7
00℃、750℃、800℃、900℃各種温度で取り出し、搬送
室からロボット搬送により搬送用カセットに収納される
間、搬送室雰囲気中にあった。
When taking out a wafer, 300 ° C, 500 ° C, 600 ° C, 7
It was taken out at various temperatures of 00 ° C., 750 ° C., 800 ° C., and 900 ° C., and was in a transfer room atmosphere while being stored in a transfer cassette by a robot transfer from the transfer room.

【0022】上記操作の後、取り出した各エピタキシャルウ
ェーハの表面状態を、ATR赤外吸収スペクトルにて測定
した。図1に300℃と700℃で取り出した試料の赤外吸収
スペクトルを示す。700℃取り出しのものにはウェーハ
全面に酸化膜が見られた。300℃取り出しのものには酸
化膜は見られなかった。なお、図1の1250〜1000cm -1
ピークは、Si‐Oの吸収に起因する酸化膜の吸収であ
る。
After the above operation, each epitaxial wafer taken out
Measure the surface condition of wafer by ATR infrared absorption spectrum
did. Figure 1 shows the infrared absorption of the samples taken at 300 ° C and 700 ° C.
The spectrum is shown. Wafer at 700 ° C
An oxide film was found on the entire surface. Acid at 300 ° C
No converted film was found. In addition, 1250-1000cm of FIG. -1of
The peak is the absorption of the oxide film due to the absorption of Si-O.
You.

【0023】図2に上記の各取り出し温度と酸化膜厚みとの
関係を示す。取り出し温度が600℃以上ではウェーハ全
面に酸化膜が得られた。また、N2ガス雰囲気中の酸素が
5ppm以下の場合は、どの温度で取り出してもエピ表面に
酸化膜は得られなかった。
FIG. 2 shows the relationship between each of the above-mentioned removal temperatures and the thickness of the oxide film. When the removal temperature was 600 ° C. or higher, an oxide film was obtained on the entire surface of the wafer. Also, oxygen in the N 2 gas atmosphere
In the case of 5 ppm or less, no oxide film was obtained on the epi surface regardless of the temperature taken out.

【0024】[0024]

【発明の効果】この発明によるウェーハは、エピタキシ
ャル反応直後の表面、すなわち、デバイスに実際用いら
れるSi表面層を、1nm以下の薄い酸化膜によって保護す
ることが可能であり、その後の工程での塵挨の付着及び
汚染から保護され、安定した品質を長期間保つことがで
きる。
According to the wafer of the present invention, the surface immediately after the epitaxial reaction, that is, the Si surface layer actually used for the device can be protected by a thin oxide film of 1 nm or less. It is protected from the attachment and contamination of greetings and can maintain stable quality for a long time.

【0025】また、この発明によるエピタキシャルウェーハ
は、デバイスプロセスに供する前に酸化膜を簡単に洗
浄、除去することが可能であり、当該酸化膜中及び酸化
膜上の汚染等の影響を受けることなく、使用できる。
In the epitaxial wafer according to the present invention, the oxide film can be easily washed and removed before the device is subjected to a device process, and is not affected by contamination in the oxide film and on the oxide film. , Available.

【0026】この発明は、一般的なエピタキシャル反応炉に
おいて、反応室から搬送室への取り出し温度を特定温度
にすることと、雰囲気中に微量の酸素を含有させるだけ
の簡単な操作で、所要厚みの酸化膜を形成でき、エピタ
キシャル形成の工程に関して何らの増工程もなく、簡単
に実施できる。また、この発明は、従来では必要であっ
たエピタキシャル成膜後の洗浄工程を省くことが可能
で、工程の簡略化が実現できる。
According to the present invention, in a general epitaxial reactor, the temperature required for taking out from the reaction chamber to the transfer chamber is set to a specific temperature, and the required thickness can be reduced by a simple operation of only containing a small amount of oxygen in the atmosphere. The oxide film can be easily formed without any additional step in the epitaxial formation step. Further, according to the present invention, it is possible to omit the cleaning step after the epitaxial film formation, which is conventionally required, and to simplify the steps.

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

【図1】エピタキシャルウェーハ表面の赤外吸収スペク
トルを示すグラフである。
FIG. 1 is a graph showing an infrared absorption spectrum of an epitaxial wafer surface.

【図2】エピタキシャル反応室からの取り出し温度と酸
化膜厚みとの関係を示すグラフである。
FIG. 2 is a graph showing a relationship between an extraction temperature from an epitaxial reaction chamber and an oxide film thickness.

───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4G077 AA02 BB03 FE04 5F043 AA02 AA32 BB22 DD12 GG10 5F058 BA05 BC02 BE01 BF55 BF62 BH11 BJ01  ──────────────────────────────────────────────────続 き Continued on the front page F term (reference) 4G077 AA02 BB03 FE04 5F043 AA02 AA32 BB22 DD12 GG10 5F058 BA05 BC02 BE01 BF55 BF62 BH11 BJ01

Claims (7)

【特許請求の範囲】[Claims] 【請求項1】 エピタキシャル成長膜の上に厚み1nm以下
の酸化膜を有するエピタキシャルウェーハ。
1. An epitaxial wafer having an oxide film having a thickness of 1 nm or less on an epitaxially grown film.
【請求項2】 エピタキシャル成長膜の上に厚み1nm以下
の酸化膜を形成する工程を含むエピタキシャルウェーハ
の製造方法。
2. A method for manufacturing an epitaxial wafer, comprising a step of forming an oxide film having a thickness of 1 nm or less on an epitaxial growth film.
【請求項3】 エピタキシャル成長後に反応室より、高
温保持されたウェーハを酸素含有雰囲気中に取り出し、
同雰囲気中でエピタキシャル成長膜の上に厚み1nm以下
の酸化膜を形成するエピタキシャルウェーハの製造方
法。
3. After the epitaxial growth, a wafer kept at a high temperature is taken out of the reaction chamber into an oxygen-containing atmosphere,
A method for manufacturing an epitaxial wafer in which an oxide film having a thickness of 1 nm or less is formed on an epitaxially grown film in the same atmosphere.
【請求項4】 高温保持温度が600〜900℃である請求項3
に記載のエピタキシャルウェーハの製造方法。
4. The high temperature holding temperature is 600 to 900 ° C.
3. The method for producing an epitaxial wafer according to item 1.
【請求項5】 酸素含有雰囲気は、酸素を5〜1000ppm含
むN2ガスまたはArガス中である請求項3に記載のエピタ
キシャルウェーハの製造方法
5. The method for producing an epitaxial wafer according to claim 3, wherein the oxygen-containing atmosphere is in an N 2 gas or an Ar gas containing 5 to 1000 ppm of oxygen.
【請求項6】 酸素含有雰囲気は、純度99.99〜99.999%
のN2ガスまたはArガス中である請求項3に記載のエピタ
キシャルウェーハの製造方法。
6. The oxygen-containing atmosphere has a purity of 99.99 to 99.999%.
4. The method for producing an epitaxial wafer according to claim 3, wherein the method is in an N 2 gas or an Ar gas.
【請求項7】 エピタキシャル成長膜の上に厚み1nm以下
の酸化膜を有するエピタキシャルウェーハを、RCA洗浄
法の少なくとも1つの洗浄液、あるいはHF含有洗浄液で
洗浄する工程を含むエピタキシャルウェーハの製造方
法。
7. A method for manufacturing an epitaxial wafer, comprising a step of cleaning an epitaxial wafer having an oxide film having a thickness of 1 nm or less on an epitaxial growth film with at least one cleaning liquid of RCA cleaning method or a cleaning liquid containing HF.
JP25853099A 1999-09-13 1999-09-13 Epitaxial wafer and method of producing the same Pending JP2001089293A (en)

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JP2001089293A true JP2001089293A (en) 2001-04-03

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Country Link
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009302125A (en) * 2008-06-10 2009-12-24 Fujitsu Microelectronics Ltd Method of manufacturing semiconductor device

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009302125A (en) * 2008-06-10 2009-12-24 Fujitsu Microelectronics Ltd Method of manufacturing semiconductor device

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