JPH02224221A - Manufacture of semiconductor device, substrate treatment apparatus and semiconductor device manufacturing apparatus - Google Patents
Manufacture of semiconductor device, substrate treatment apparatus and semiconductor device manufacturing apparatusInfo
- Publication number
- JPH02224221A JPH02224221A JP4299589A JP4299589A JPH02224221A JP H02224221 A JPH02224221 A JP H02224221A JP 4299589 A JP4299589 A JP 4299589A JP 4299589 A JP4299589 A JP 4299589A JP H02224221 A JPH02224221 A JP H02224221A
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- Japan
- Prior art keywords
- substrate
- atmosphere
- processing
- semiconductor device
- film
- Prior art date
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Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、半導体装置の製造方法における、機能性薄膜
を連続して形成する方法に関し、特に薄膜界面の適正化
及び半導体装置の歩留り向上を図る方法に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a method of continuously forming functional thin films in a method of manufacturing semiconductor devices, and particularly to optimization of thin film interfaces and improvement of yield of semiconductor devices. Regarding how to achieve this.
従来の装置は、例えば特開昭62−131513号に記
載のように基板に機能性薄膜形成した後5大気雰囲気の
減圧状態の搬送通路を通して上記基板を次の機能性薄膜
形成室へ搬送するといった方法がとられていた。The conventional apparatus, for example, as described in Japanese Patent Application Laid-Open No. 131513/1984, forms a functional thin film on a substrate and then transports the substrate to the next functional thin film forming chamber through a transport passage under reduced pressure in an atmospheric atmosphere. A method was taken.
上記従来技術は、薄膜形成、特に機能性の高い半導体膜
を形成した後の、該薄膜表面の状態や、基板を搬送する
通路の雰囲気の点について配慮されておらず、製造した
半導体装置が所望通りの機能を示さないといった問題が
あった。The above conventional techniques do not take into consideration the condition of the thin film surface after forming a thin film, especially a highly functional semiconductor film, or the atmosphere of the passageway through which the substrate is transported, and the manufactured semiconductor device does not meet the desired expectations. There was a problem that it did not show the expected function.
本発明の目的は上記不都合を改善することにある。An object of the present invention is to improve the above-mentioned disadvantages.
上記目的を達成するために、機能性膜を形成した後、基
板を大気にさらさないのはもちろんのこと、減圧状態に
ある大気雰囲気やチッ素雰囲気にも基板をさらさないよ
うにし、次処理をするようにしたものである。7すなわ
ち、機能性薄膜を形成した後の基板の搬送は、薄膜表面
に影響を与えないガスの減圧雰囲気下例えば希ガスの減
圧雰囲気下や次処理のガスの減圧雰囲気下で行なうよう
にしたものである。さらに、処理室のガス雰囲気の影響
を避けるために、基板処理の少なくとも1工程以上を、
電子サイクロトロン(以後ECRと略す)共鳴を利用し
てプラズマを発生させ、該プラズマで基板を処理するよ
うにしたものである。In order to achieve the above purpose, after forming the functional film, the substrate should not be exposed to the atmosphere, but should also not be exposed to the atmospheric atmosphere under reduced pressure or a nitrogen atmosphere, and should not be exposed to the next process. It was designed to do so. 7. In other words, after the functional thin film has been formed, the substrate is transported under a reduced pressure atmosphere of a gas that does not affect the thin film surface, such as a reduced pressure atmosphere of a rare gas or a reduced pressure atmosphere of a gas for subsequent processing. It is. Furthermore, in order to avoid the influence of the gas atmosphere in the processing chamber, at least one step of substrate processing is
Plasma is generated using electron cyclotron (hereinafter abbreviated as ECR) resonance, and a substrate is treated with the plasma.
形成直後の機能性薄膜の表面には多数の未結合手が存在
する。この未結合手は化学反応性が高いため、例えば、
膜形成後、ただちに、別処理室へ搬入し、処理しても、
途中の基板搬送通路の雰囲気が大気の減圧状態であった
場合、ここを通過する間に、上記未結合手はチッ素や酸
素と反応し、薄膜表面にはチツ化物や酸化物が形成され
る。従って、次処理にて、機能性膜を連続して形成して
も、前形成膜との界面では適正な接合面の形成が不可能
になる。そこで、基板搬送通路の雰囲気を希ガスの減圧
雰囲気にすると、未結合手部には希ガス原子が付着する
が、化学反応は起きないため5表面状態が活性のまま次
処理を施すことができる。There are many dangling bonds on the surface of the functional thin film immediately after formation. This dangling bond has high chemical reactivity, so for example,
Even if the film is immediately transported to a separate processing room and processed,
If the atmosphere in the substrate transport passageway is at reduced pressure, the dangling bonds will react with nitrogen and oxygen while passing through this passage, and nitrides and oxides will be formed on the thin film surface. . Therefore, even if functional films are successively formed in the next process, it is impossible to form an appropriate bonding surface at the interface with the previously formed film. Therefore, if the atmosphere in the substrate transport path is made into a reduced pressure atmosphere of rare gas, rare gas atoms will adhere to the dangling bonds, but no chemical reaction will occur, so the next treatment can be performed while the surface state 5 remains active. .
希ガス雰囲気のかわりに1次処理に用いるガスの減圧雰
囲気下にしても良く、この場合には未結合手は次に形成
される膜の構成原子に覆われるため。Instead of the rare gas atmosphere, a reduced pressure atmosphere of the gas used for the primary treatment may be used, since in this case, the dangling bonds are covered by atoms constituting the film to be formed next.
次に形成される膜との場合は良好に取れる。Good results can be obtained with the next film.
また、基板をプラズマを用いて処理する場合、処理する
際の動作圧力が高いと、処理後に処理室内での基板への
被処理ガス種の吸着量が増え、この結果、次処理により
形成される膜との接合面の適正が図れない問題が生じる
。従って、動作圧力が低い、電子サイクロトロン共鳴を
利用したプラズマ処理を行なった方が接合面の適正化が
図れる。In addition, when processing a substrate using plasma, if the operating pressure during processing is high, the amount of adsorption of the gas species to be processed on the substrate in the processing chamber increases after processing, and as a result, the amount of gas species to be processed that is formed during the next processing increases. A problem arises in that the bonding surface with the membrane cannot be made properly. Therefore, the bonding surface can be made more suitable by performing plasma treatment using electron cyclotron resonance, which requires a lower operating pressure.
また、プラズマを用いて基板を処理すると、プラズマが
照射される面、例えば基板ホルダ面とはスパッタされる
。このため、被スパツタ材の原子が基板に取り込まれる
。従って、例えばシリコン膜を形成するような際には、
基板下にシリコン板を置くとかいった工夫を行なうと、
上記した接合面の適正等がさらに推進される。Furthermore, when a substrate is processed using plasma, a surface irradiated with plasma, for example, a substrate holder surface, is sputtered. Therefore, atoms of the material to be sputtered are incorporated into the substrate. Therefore, for example, when forming a silicon film,
If you try something like placing a silicon plate under the board,
The appropriateness of the joint surfaces described above will be further promoted.
(実施例〕 以下、本発明を実施例を用いて説明する。(Example〕 The present invention will be explained below using examples.
実施例1
第1図は本発明に基づくプラズマ処理装置の主要部の断
面を示す。装置は、試料室1,3室の第1.2,3.プ
ラズマ処理室2a、2b、2c、基板搬送室3、それぞ
れの処理室へガス導入するガス導入管4a、4b、4c
、5a、5b、5c排気口(図省略)、RF電源6.上
部RF組電極。Embodiment 1 FIG. 1 shows a cross section of the main parts of a plasma processing apparatus based on the present invention. The device is installed in sample chambers 1, 2, and 3 of sample chambers 1 and 3. Gas introduction pipes 4a, 4b, 4c for introducing gas into the plasma processing chambers 2a, 2b, 2c, the substrate transfer chamber 3, and the respective processing chambers
, 5a, 5b, 5c exhaust ports (not shown), RF power source 6. Upper RF group electrode.
下部アース電極8.ゲートバルブ9,10.試料取出し
室11.搬送室3ヘガスを送るノズル12゜搬送室3の
排気口13より成る。基板14として100(nn)角
のガラス板上にn型シリコン/ノンドープシリコン/チ
ツ化の積層膜を連続形成した。形成には試料室1あるい
は試料14をゲートバルブ9を開けて第1のプラズマ処
理室2aへ搬送し、2a内を5 X 10”−2(To
rr)まで排気後、ガスノズル4aより、アンモニア、
NHsを20Cm n /win)、5aよりモノシラ
ンSiSiH45(/win)導入し1 (Torr)
とし、RF電源よりRFを300(W)印加し、7)I
、tミf 、 A Q 203膜を被覆した上下電極7
と8の間に放電させてチツ化シリコン膜、SiN堆積さ
せた、この後、2a内を5 X 1.0−”[丁orr
)まで排気し、圧力がIX 10’−”(Torr)の
基板搬送室3内を経由してプラズマ処理室2bへ送った
。次に2b内を5X10−2(Torr)まで排気し、
次に4b、5bのガスノズルを通して水素、H2を20
(m Q /m1n)、 S i H4を5 (m
U /win)導入し、圧力1 (Torr)、RFバ
ク300(W〕にて、SiN膜上にアモルファスシリコ
ン(iJl)を堆積させた。堆積後、5×10−2(T
orr:lまで排気し、基板搬送室3を経由してプラズ
マ処理室2cへ送った。次に2c内を5X 10−2(
Torr)まで排気し、4c、5bのガスノズルを通し
て水素により5〔%〕に希釈されたホスフィン、PHa
を20 (m Q /+++in〕、及びS i H4
を5 [m Q /min]導入して、上記1層上にリ
ンドープのn型シリコン膜(n層)を堆積させた。次に
2c内を5 X 10 ”−”[Torr]まで減圧後
、試料取出し室11内に送った。上記膜形成の際、基板
搬送室内の雰囲気を、(A)ノズルによりチッ素N2を
導入後、減圧とした、減圧のチッ素雰囲気、(B)ノズ
ルによりヘリウム、Heを導入後減圧した、減圧の希ガ
ス雰囲気、とした時の形成膜をXPSにより元素分析し
た。(A)の場合、i層とn層の間に微量の酸素、水素
の他にチッ素が検出されたが、(B)の場合にはチッ素
は検出されなかった。Lower earth electrode 8. Gate valves 9, 10. Sample extraction chamber 11. It consists of a nozzle 12° for sending gas to the transfer chamber 3 and an exhaust port 13 of the transfer chamber 3. As a substrate 14, a laminated film of n-type silicon/non-doped silicon/nitride was continuously formed on a glass plate of 100 (nn) square. For formation, the sample chamber 1 or the sample 14 is transported to the first plasma processing chamber 2a by opening the gate valve 9, and the inside of the chamber 2a is placed in a 5×10”-2 (To
After exhausting to rr), ammonia,
NHs was introduced at 20 Cm n /win) and monosilane SiSiH45 (/win) was introduced from 5a to 1 (Torr).
Then, apply 300 (W) of RF from the RF power supply, and 7) I
, tmif, A Q 203 film-covered upper and lower electrodes 7
A silicon nitride film, SiN, was deposited by discharging between
), and sent to the plasma processing chamber 2b via the substrate transfer chamber 3 at a pressure of IX 10'-'' (Torr).Next, the inside of 2b was evacuated to 5X10-2 (Torr),
Next, 20% hydrogen, H2, is passed through the gas nozzles 4b and 5b.
(m Q /m1n), S i H4 is 5 (m
Amorphous silicon (iJl) was deposited on the SiN film at a pressure of 1 (Torr) and an RF energy of 300 (W). After deposition, 5 x 10-2 (T
It was evacuated to orr:l and sent to the plasma processing chamber 2c via the substrate transfer chamber 3. Next, 5X 10-2 (
Phosphine, PHa diluted to 5% with hydrogen through gas nozzles 4c and 5b.
20 (m Q /+++in), and S i H4
5 [m Q /min] was introduced to deposit a phosphorus-doped n-type silicon film (n layer) on the above-mentioned one layer. Next, the pressure inside 2c was reduced to 5×10 ”-” [Torr], and then the sample was sent into the sample extraction chamber 11 . During the above film formation, the atmosphere in the substrate transfer chamber was (A) a reduced pressure nitrogen atmosphere after introducing nitrogen N2 through a nozzle and then reduced pressure; (B) a reduced pressure after introducing helium and He through a nozzle. The formed film was subjected to elemental analysis by XPS in a rare gas atmosphere. In the case of (A), trace amounts of oxygen and hydrogen as well as nitrogen were detected between the i-layer and the n-layer, but in the case of (B), no nitrogen was detected.
上記(A)と(B)の場合で形成した上記積層膜を用い
、所定の工程を経て、トランジスタを形成した所、(A
)の場合には不良率が35〔%〕であった所が、(B)
の場合には10〔%〕以下であった。不良原因は1層と
n層の接合の不良によるものであった。先のxPS分析
と合わせて考えると、(A)の場合にはi層形成後、チ
ッ素雰囲気の基板搬送室を通過したため、形成面のダン
グリングボンドがチッ素と反応し、表面にSiN膜が形
成され、このため、上部n層との接合が旨くとれないた
めであることがわかる。一方(B)の場合のように、希
ガス雰囲気の搬送室を・基板が通過した際には、ダング
リングボンド部に希ガスは付着するが、希ガスは反応し
ないため、活性面が維持されたまま、次処理に移された
ため、適正な接合面が形成されたことがわかる。Using the laminated films formed in cases (A) and (B) above, a transistor was formed through predetermined steps.
), the defective rate was 35%, but in (B)
In this case, it was 10% or less. The cause of the defect was due to a defective bond between the first layer and the n layer. Considering this in conjunction with the previous xPS analysis, in the case of (A), after the i-layer was formed, it passed through a substrate transport chamber with a nitrogen atmosphere, so the dangling bonds on the formation surface reacted with nitrogen, and a SiN film was formed on the surface. It can be seen that this is because the bonding with the upper n-layer cannot be achieved properly. On the other hand, as in case (B), when the substrate passes through a transfer chamber with a rare gas atmosphere, the rare gas adheres to the dangling bond, but the active surface is maintained because the rare gas does not react. It can be seen that a proper bonding surface was formed because the bonding surface was transferred to the next process.
実施例2
上記(B)の変わりに水素雰囲気の減圧状態に搬送室を
して(C)、上記と同様に1−ランジスタを製作した。Example 2 Instead of (B) above, the transfer chamber was placed in a reduced pressure state of hydrogen atmosphere (C), and a 1-transistor was manufactured in the same manner as above.
不良率は(B)の時と同じ<10〔%〕以下であった。The defect rate was <10% or less, the same as in (B).
これらの結果より、基板搬送室の雰囲気は、希ガス雰囲
気や次処理に用いるガス種と似た雰囲気の減圧状態にす
ると、適正な半導体処理がなされることがわかる。These results show that proper semiconductor processing can be performed when the atmosphere in the substrate transfer chamber is reduced to a rare gas atmosphere or a reduced pressure atmosphere similar to the type of gas used in the subsequent processing.
実施例3
第2図は本発明に基づく一環式の処理断面図を示す。本
装置の特徴は、プラズマを生成するのに、RF放電では
なく、電子サイクロトロン共鳴(ECR)を利用してい
る点である。本装置では磁界コイル18によりECR条
件を満たす磁界強度を真空容器内に印加し、ガスを導入
後、μ波源波管17を通して、μ波16をμ波導入窓2
1よリプラズマ生成室19(a”c)に導入するとEC
Rによりプラズマが効率良く生成する。基板ホルダ15
としては石英製のホルダを用いた。該プラズマを磁力線
22により基板処理室20(a〜C)に導入して反応ガ
スと反応させると基板に所望の処理ができる。本装置を
用い、実施例と同一ガス流量で、μ波パワ300(W)
、反応圧力lX10″″’(Torrl 、処理前後圧
力を1×10一番(Torr) 、搬送室はHe雰囲気
のI×1O−5(Torr)の減圧状態として、同一積
層膜を形成した。処理後の界面分析を行なった所、i層
及びn層の界面で微量の酸素の他に、実施例1では検出
された水素は検出されなかった。この積層膜を用いたト
ランジスタの不良率は3〔%〕以下となった。これは、
ECRプラズマの動作圧力が低いため、処理直後のダン
グリングボンドと用いたガスの反応が低くおさえられた
ため、さらなる接合面の適正化がなされたためであるこ
とがわかる。Example 3 FIG. 2 shows a cross-sectional view of a one-shot process according to the present invention. A feature of this device is that it uses electron cyclotron resonance (ECR) rather than RF discharge to generate plasma. In this device, the magnetic field coil 18 applies a magnetic field strength that satisfies the ECR conditions into the vacuum vessel, and after introducing gas, the μ-waves 16 are passed through the μ-wave source tube 17 to the μ-wave introduction window 2.
1, when introduced into the replasma generation chamber 19 (a"c), EC
Plasma is efficiently generated by R. Board holder 15
A holder made of quartz was used. When the plasma is introduced into the substrate processing chambers 20 (a to C) by magnetic lines of force 22 and reacted with the reaction gas, the substrate can be subjected to desired processing. Using this device, the μ-wave power was 300 (W) at the same gas flow rate as in the example.
The same laminated film was formed under the following conditions: the reaction pressure was 1 x 10'''' (Torrl), the pressure before and after the treatment was 1 x 10 Torr, and the transfer chamber was under reduced pressure of I x 1 O-5 (Torr) in a He atmosphere. A subsequent interface analysis revealed that in addition to a trace amount of oxygen at the interface between the i-layer and n-layer, hydrogen, which was detected in Example 1, was not detected.The failure rate of the transistor using this laminated film was 3. [%] or less.This is
It can be seen that this is because the reaction between the dangling bond immediately after treatment and the gas used was suppressed to a low level due to the low operating pressure of the ECR plasma, which enabled further optimization of the bonding surface.
実施例4 上記i層とn層の界面にて検出された酸素は。Example 4 The oxygen detected at the interface between the i-layer and n-layer is as follows.
基板ホルダにプラズマが照射されることによりスパッタ
された石英が原因と考えられる。酸素が混入すると適正
な接合面が形成されずらくなる。これを防止するため、
基板ホルダ上にシリコン板を設置して実施例3と同一の
実験を行なった、この結果、先には検出された酸素が、
本実験では検出されなかった。また、トランジスタを作
製し、不良率を調べた所、不良率は0.5〔%〕以下と
なった。このことより、プラズマが照射される面は、素
子に影響を与えない物質、例えば、シリコン膜形成時に
は、シリコンにするといった工夫を行なうと、さらに半
導体製造における処理の適正化が図れることがわかる。The cause is thought to be quartz sputtered when the substrate holder is irradiated with plasma. If oxygen is mixed in, it becomes difficult to form a proper bonding surface. To prevent this,
The same experiment as in Example 3 was conducted with a silicon plate placed on the substrate holder. As a result, the previously detected oxygen was
It was not detected in this experiment. Further, when transistors were manufactured and the defective rate was examined, the defective rate was 0.5% or less. This shows that if the surface to which plasma is irradiated is made of a material that does not affect the device, for example, silicon when forming a silicon film, processing in semiconductor manufacturing can be further optimized.
本発明によれば、連続してプラズマ処理する方法におい
て、接合面の適正化等、デバイス特性を劣下させない処
理が可能となるため、歩留り良く形成できる効果がある
。According to the present invention, in a continuous plasma processing method, it is possible to perform processing without degrading device characteristics, such as optimizing the bonding surface, so that it is possible to form a device with a high yield.
第1図は本発明の一実施例を示すRFプラズマ処理装置
の断面図、第2図は本発明の一実施例を示すプラズマ処
理装置の断面図である。
2a、2b、2c・・・基板処理室、3・・・基板搬送
室、7・・・上部RF電極、8・・・下部基板設置電極
、15・・・基板ホルダ、16・・・マイクロ波、18
・・・磁界コイル、19 a 、 19 b 、 19
c−プラズマ生成室、20 a 、 20 b 、
20 c −処理室。
手
続
補
正
書(方式)
%式%
および半導体装置製造装置
補正をする者
・Iif’lとの関係 特許出願人
と、 伯+51L11体式会ll 日立
製
作
所
代
理
人
補正命令の日付
平成1年5月30日(発送臼)FIG. 1 is a sectional view of an RF plasma processing apparatus showing an embodiment of the present invention, and FIG. 2 is a sectional view of a plasma processing apparatus showing an embodiment of the invention. 2a, 2b, 2c...substrate processing chamber, 3...substrate transfer chamber, 7...upper RF electrode, 8...lower substrate installation electrode, 15...substrate holder, 16...microwave , 18
...Magnetic field coil, 19 a, 19 b, 19
c-plasma generation chamber, 20a, 20b,
20 c - processing chamber. Procedural amendment (method) Relationship between % formula % and the person/Iif'l who amends the semiconductor device manufacturing equipment Patent applicant and Haku+51L11 type association ll Date of Hitachi agent's amendment order May 30, 1999 (Shipping mortar)
Claims (1)
は減圧の大気雰囲気に処理基板をさらさずに、続けて次
処理を該基板上に施すことを特徴とした半導体装置製造
方法。 2、連続的に基板を処理する装置において、基板を搬送
する通過路の雰囲気を、次処理に用いるガス種のうち少
なくとも一種を含んだガス雰囲気、あるいは希ガス雰囲
気の減圧状態としたことを特徴とした特許請求の範囲第
1項に記載した半導体装置製造方法。 3、上記処理において、機能性薄膜の連続形成を含んだ
ことを特徴とした特許請求の範囲第1項及び第2項に記
載の半導体装置製造方法。 4、上記処理において、少なくともシリコンのi層の形
成後続けてシリコンのn層の形成をなす工程を含むこと
を特徴とした請求項第1項乃至第3項記載の半導体装置
製造方法。 5、上記処理において、少なくとも1つの処理に電子サ
イクロトロン共鳴を利用して発生させたプラズマを用い
、基板を処理することを特徴とした特許請求の範囲第1
項乃至第4項に記載の半導体装置製造方法。 6、基板を大気にさらさずに、少なくとも基板を処理す
る処理室と基板の搬送路を有し、基板を上記処理室と基
板搬送路の間で複数回移動させて、基板を連続的に処理
する装置において、基板搬送路の雰囲気を、次処理に用
いるガス種の少なくとも一種以上のガス雰囲気、あるい
は希ガス雰囲気の減圧状態にしてあることを特徴とした
基板処理装置。 7、上記、基板の処理において、電子サイクロトロン共
鳴を利用してプラズマを生成させ、該プラズマにより基
板を処理できるチャンバを少なくとも1つ有したことを
特徴とした特許請求の範囲第6項に記載した基板処理装
置。 8.(1)絶縁層を形成する、(2)半導体膜を形成す
る、(3)希ガス雰囲気の減圧下の基板搬送路を通す、
の3つの工程で、(1)−(3)−(2)−(3)−(
2)の順に工程手順を少なくとも含めた液晶ディスプレ
ーを製造することを特徴とした、特許請求の範囲第1項
乃至第5項に記載の半導体装置製造方法。 9、プラズマがふれる面に、形成膜と主成分が同じ材質
の物質をおくことを特徴とした特許請求の範囲第6項及
び第7項に記載の半導体装置製造装置。 10、シリコン膜をプラズマにて形成する際に、基板を
シリコン板あるいはシリコンを被覆させたホルダ上に置
いて処理することを特徴とした特許請求の範囲第1項乃
至第5項に記載の半導体装置製造方法。[Claims] 1. Semiconductor device manufacturing characterized in that after processing a substrate, subsequent processing is performed on the substrate without exposing the processed substrate to the air, a nitrogen atmosphere, or a reduced pressure atmosphere. Method. 2. An apparatus for continuously processing substrates, characterized in that the atmosphere in the path through which the substrates are transported is a gas atmosphere containing at least one type of gas used in the next processing, or a reduced pressure state of a rare gas atmosphere. A method for manufacturing a semiconductor device according to claim 1. 3. The semiconductor device manufacturing method according to claims 1 and 2, wherein the process includes continuous formation of a functional thin film. 4. The method of manufacturing a semiconductor device according to any one of claims 1 to 3, wherein the process includes at least the step of forming an n-layer of silicon subsequent to the formation of the i-layer of silicon. 5. Claim 1, characterized in that in the above treatment, at least one treatment uses plasma generated using electron cyclotron resonance to treat the substrate.
5. A method for manufacturing a semiconductor device according to items 4 to 4. 6. Having at least a processing chamber for processing the substrate and a substrate transport path without exposing the substrate to the atmosphere, and continuously processing the substrate by moving the substrate between the processing chamber and the substrate transport path multiple times. What is claimed is: 1. A substrate processing apparatus characterized in that the atmosphere in a substrate transport path is a reduced pressure state of at least one type of gas used in subsequent processing or a rare gas atmosphere. 7. In the above-mentioned substrate processing, plasma is generated using electron cyclotron resonance, and the method is characterized in that it has at least one chamber capable of processing the substrate with the plasma. Substrate processing equipment. 8. (1) Forming an insulating layer, (2) Forming a semiconductor film, (3) Passing a substrate transport path under reduced pressure in a rare gas atmosphere.
In the three steps, (1)-(3)-(2)-(3)-(
A semiconductor device manufacturing method according to any one of claims 1 to 5, characterized in that a liquid crystal display is manufactured including at least the process steps in the order of 2). 9. The semiconductor device manufacturing apparatus according to claims 6 and 7, characterized in that a substance whose main component is the same as that of the formed film is placed on a surface that is exposed to the plasma. 10. The semiconductor according to claims 1 to 5, characterized in that when forming a silicon film using plasma, the substrate is placed on a silicon plate or a holder coated with silicon. Device manufacturing method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4299589A JPH02224221A (en) | 1989-02-27 | 1989-02-27 | Manufacture of semiconductor device, substrate treatment apparatus and semiconductor device manufacturing apparatus |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4299589A JPH02224221A (en) | 1989-02-27 | 1989-02-27 | Manufacture of semiconductor device, substrate treatment apparatus and semiconductor device manufacturing apparatus |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH02224221A true JPH02224221A (en) | 1990-09-06 |
Family
ID=12651604
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4299589A Pending JPH02224221A (en) | 1989-02-27 | 1989-02-27 | Manufacture of semiconductor device, substrate treatment apparatus and semiconductor device manufacturing apparatus |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02224221A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7507991B2 (en) | 1991-06-19 | 2009-03-24 | Semiconductor Energy Laboratory Co., Ltd. | Electro-optical device and thin film transistor and method for forming the same |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5893321A (en) * | 1981-11-30 | 1983-06-03 | Semiconductor Energy Lab Co Ltd | Manufacturing apparatus for semiconductor device |
| JPS58169980A (en) * | 1982-03-19 | 1983-10-06 | Matsushita Electric Ind Co Ltd | Manufacture of photo voltaic element |
| JPS58196063A (en) * | 1982-05-10 | 1983-11-15 | Matsushita Electric Ind Co Ltd | Manufacture of photovoltaic element |
| JPS60211823A (en) * | 1984-04-06 | 1985-10-24 | Agency Of Ind Science & Technol | Forming apparatus for thin film semiconductor device |
| JPS6273707A (en) * | 1985-09-27 | 1987-04-04 | Hitachi Ltd | semiconductor manufacturing equipment |
| JPS62131513A (en) * | 1985-12-04 | 1987-06-13 | Hitachi Ltd | Multi-chamber separation type plasma CVD equipment |
| JPH01184928A (en) * | 1988-01-20 | 1989-07-24 | Toshiba Corp | Thin film formation |
-
1989
- 1989-02-27 JP JP4299589A patent/JPH02224221A/en active Pending
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5893321A (en) * | 1981-11-30 | 1983-06-03 | Semiconductor Energy Lab Co Ltd | Manufacturing apparatus for semiconductor device |
| JPS58169980A (en) * | 1982-03-19 | 1983-10-06 | Matsushita Electric Ind Co Ltd | Manufacture of photo voltaic element |
| JPS58196063A (en) * | 1982-05-10 | 1983-11-15 | Matsushita Electric Ind Co Ltd | Manufacture of photovoltaic element |
| JPS60211823A (en) * | 1984-04-06 | 1985-10-24 | Agency Of Ind Science & Technol | Forming apparatus for thin film semiconductor device |
| JPS6273707A (en) * | 1985-09-27 | 1987-04-04 | Hitachi Ltd | semiconductor manufacturing equipment |
| JPS62131513A (en) * | 1985-12-04 | 1987-06-13 | Hitachi Ltd | Multi-chamber separation type plasma CVD equipment |
| JPH01184928A (en) * | 1988-01-20 | 1989-07-24 | Toshiba Corp | Thin film formation |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7507991B2 (en) | 1991-06-19 | 2009-03-24 | Semiconductor Energy Laboratory Co., Ltd. | Electro-optical device and thin film transistor and method for forming the same |
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