JPS6074534A - Method and equipment for forming thin film - Google Patents
Method and equipment for forming thin filmInfo
- Publication number
- JPS6074534A JPS6074534A JP18023683A JP18023683A JPS6074534A JP S6074534 A JPS6074534 A JP S6074534A JP 18023683 A JP18023683 A JP 18023683A JP 18023683 A JP18023683 A JP 18023683A JP S6074534 A JPS6074534 A JP S6074534A
- Authority
- JP
- Japan
- Prior art keywords
- substrate
- film
- ion source
- thin film
- microwave
- 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.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/22—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
- C23C16/30—Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
- C23C16/40—Oxides
- C23C16/401—Oxides containing silicon
- C23C16/402—Silicon dioxide
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/448—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for generating reactive gas streams, e.g. by evaporation or sublimation of precursor materials
- C23C16/452—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for generating reactive gas streams, e.g. by evaporation or sublimation of precursor materials by activating reactive gas streams before their introduction into the reaction chamber, e.g. by ionisation or addition of reactive species
Abstract
Description
【発明の詳細な説明】
〔発明の利用分野〕
本発明は薄膜形成方法および薄膜形成装置に関し、詳し
くは、たとえばSム02膜など、絶縁膜の形成にとくに
好適な薄膜形成方法および薄膜形成装置に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Application of the Invention] The present invention relates to a thin film forming method and a thin film forming apparatus, and more specifically, a thin film forming method and a thin film forming apparatus particularly suitable for forming an insulating film such as an Smu02 film. Regarding.
被処理物にバイアス電圧を印加しつつ、スパッタリング
を行なうバイアススパッタ法は、たとえばSiO,など
の膜の堆積と膜表面の平坦化を、同時に達成できるとい
う特長を有している。The bias sputtering method, in which sputtering is performed while applying a bias voltage to the object to be processed, has the advantage that it can simultaneously deposit a film of, for example, SiO, and flatten the surface of the film.
バイアススパッタ法は、SiO2などの堆積を行ないな
がら、堆積した5fOzなどの一部を同時にエッチして
、5IO2などの膜を形成する方法であシ、膜表面の平
坦化は、膜形成中に行なわれるエツチングの速度が、下
地の形状に依存することによって起る。The bias sputtering method is a method in which a part of the deposited 5fOz etc. is simultaneously etched while depositing SiO2 etc. to form a film of 5IO2 etc. The film surface is flattened during film formation. This occurs because the rate of etching depends on the shape of the underlying material.
すなわち、バイアススパッタ法においては、下地が傾斜
している部分のエツチング速度が、平坦である部分のエ
ツチング速度よシ大きいため、下地の突起に起因する堆
積膜表面の突起は、エツチングの進行とともに小さくな
シ、ついには表面平坦化が達成される。In other words, in the bias sputtering method, the etching rate on the sloped part of the base is higher than the etching rate on the flat part, so the protrusions on the surface of the deposited film caused by the protrusions on the base become smaller as etching progresses. Finally, surface flattening is achieved.
バイアススパッタ法において、膜表面を十分に平坦化す
るためには、膜形成中における上記エツチングの割合を
、再スパツタ率で30〜80チにする必要があシ、その
ためには、その上に膜を形成すべき基板に印加する高周
波電力を、ターゲット電力の15〜40チとする必要が
ある。In the bias sputtering method, in order to sufficiently flatten the film surface, it is necessary to increase the etching rate during film formation to a re-sputtering rate of 30 to 80 inches. It is necessary to set the high frequency power applied to the substrate on which the target power is to be 15 to 40 inches higher than the target power.
その結果、上記基板は、グロー放電に直接さらされるこ
とになり、S!02の凝縮エネルギや、入射する荷電粒
子の衝突エネルギのみではなく、グロー放電からのふく
射によっても温度が上昇する、という問題がある。As a result, the substrate is directly exposed to glow discharge and S! There is a problem in that the temperature rises not only due to the condensation energy of 0.02 and the collision energy of incident charged particles, but also due to radiation from the glow discharge.
しかも、SiO□など絶縁膜は、金属膜にくらべてスパ
ッタ率が小さいため、十分な形成速度を得るためには、
さらに大きな高周波電力を、ターゲットに印加しなけれ
ばならず、基板温度は、このターゲットからふく射によ
っても上昇してしまう。Moreover, insulating films such as SiO□ have a lower sputtering rate than metal films, so in order to obtain a sufficient formation rate,
Even greater high-frequency power must be applied to the target, and the substrate temperature also increases due to radiation from the target.
また、膜の形成をスパッタリングによって行なっている
ため、膜の堆積速度が遅いという問題があシ、解決が望
まれていた。Furthermore, since the film is formed by sputtering, there is a problem that the film deposition rate is slow, and a solution has been desired.
本発明の目的は、上記従来の問題を解決し、表面が平坦
な膜を、基板に対する大きな影響なしに形成することの
できる薄膜形成方法および薄膜形成装置を提供すること
でおる。SUMMARY OF THE INVENTION An object of the present invention is to provide a thin film forming method and a thin film forming apparatus that can solve the above-mentioned conventional problems and form a film with a flat surface without greatly affecting the substrate.
上記目的を達成するため、本発明は、薄膜を堆積する手
段とエツチングする手段をそれぞれ独立させ、両者を同
時または交互に使用することによって、表面が平坦な薄
膜を基板上に形成するものである。In order to achieve the above object, the present invention forms a thin film with a flat surface on a substrate by using independent means for depositing a thin film and means for etching, and using both simultaneously or alternately. .
本発明において、上記薄膜を堆積する手段や上記エツチ
ング手段から発生するプラズマやグロー放電を、それぞ
れ上記手段の近傍に局在させれば、上記プラズマやグロ
ー放電の、基板に対する影響を減少させ、基板温度の上
昇を少なくすることができる。In the present invention, if the plasma and glow discharge generated from the thin film depositing means and the etching means are localized in the vicinity of the means, the influence of the plasma and glow discharge on the substrate can be reduced, and The rise in temperature can be reduced.
また、上記プラズマやグロー放電の上記局在を行なわな
い場合は、基板の温度上昇を抑制することはできないが
、膜の堆積速度が極めて大きい、という利点が生ずる。Furthermore, if the plasma or glow discharge is not localized, the temperature rise of the substrate cannot be suppressed, but there is an advantage that the film deposition rate is extremely high.
以下、実施例を参照して本発明の詳細な説明する。 Hereinafter, the present invention will be described in detail with reference to Examples.
実施例1
第1図は、本発明の一実施例を説明するための図である
。Embodiment 1 FIG. 1 is a diagram for explaining an embodiment of the present invention.
反応容器となる真空槽5は、ガス導入口1.2゜3、排
気口4をそなえ、さらに、基板6上に膜を堆積するため
の、マイクロ波イオン源7および上記基板60表面をエ
ツチングするためのホットフィラメント型イオン源8を
それぞれ独立しつ有している。なお上記基板6は、石英
12によって回転可能なサセプタ9上に保持されている
。A vacuum chamber 5 serving as a reaction vessel is equipped with a gas inlet 1.2° 3 and an exhaust port 4, and is further provided with a microwave ion source 7 for depositing a film on a substrate 6 and for etching the surface of the substrate 60. Each of the hot filament ion sources 8 has an independent hot filament type ion source 8 for the purpose. Note that the substrate 6 is held on a rotatable susceptor 9 by quartz 12.
5loz膜を基板6上に形成する場合を例に用いて説明
すると、まず、排気口4を介して真空槽5内を排気し、
内部の空気圧をほぼ101〜1O−5paとする。To explain the case of forming a 5LOZ film on the substrate 6 as an example, first, the inside of the vacuum chamber 5 is evacuated through the exhaust port 4,
The internal air pressure is approximately 101 to 1 O-5 pa.
つぎに、上記マイクロ波イオン源7に周波数2、.45
GHZのマイクロ波電力を印加し、さらに、上記ガス
導入口2,3からモノシラン(SiH4)と酸素(02
)を導入するとともに、マイクロ波放電を発生してSi
H4と02を反応させ、CvD(Chemical V
apor Deposition )によって基板6上
に810z膜を堆積した。Next, the microwave ion source 7 is supplied with a frequency of 2, . 45
GHZ microwave power is applied, and monosilane (SiH4) and oxygen (02
) and generates microwave discharge to
By reacting H4 and 02, CvD (Chemical V
An 810z film was deposited on the substrate 6 by apor deposition.
一方、上記ガス導入口1からは、アルゴン(At)を導
入し、ホットフィラメント型イオン源8に電力を印加し
てArイオンを発生させ、グリッド13によって加速し
て得られたArイオンビームを、基板6を照射して、基
板6に堆積された810g膜をエツチングして表面の平
坦化を行なった。On the other hand, argon (At) is introduced from the gas inlet 1, power is applied to the hot filament ion source 8 to generate Ar ions, and the resulting Ar ion beam is accelerated by the grid 13. The substrate 6 was irradiated to etch the 810 g film deposited on the substrate 6 to flatten the surface.
なお、基板6は、内部を水冷されているサセプタ7/9
に静電チャックによって吸着させ、サセプタ9とともに
回転させた。Note that the substrate 6 includes a susceptor 7/9 whose interior is water-cooled.
was adsorbed by an electrostatic chuck and rotated together with the susceptor 9.
このようにすると、基板6に対するマイクロ波イオン源
8からの荷電粒子による衝撃は、グリッド14によって
防止させ、その結果、基板6の温度上昇は著るしく抑制
される。In this way, the impact of charged particles from the microwave ion source 8 on the substrate 6 is prevented by the grid 14, and as a result, the temperature rise of the substrate 6 is significantly suppressed.
すなわち、第2図は5iHz膜の形成速度と基板温度の
関係を示す曲線図であシ、曲線aおよびbは、それぞれ
従来のバイアススパッタ法および本発明によって得られ
た結果を示す。That is, FIG. 2 is a curve diagram showing the relationship between the formation rate of a 5iHz film and the substrate temperature, and curves a and b show the results obtained by the conventional bias sputtering method and the present invention, respectively.
ここに、上記曲線すは、真空槽5内の圧力を6.7 X
10−” pa、基板6の中心とマイクロ波イオン源
7およびホットフィラメント型イオン源8との間隙を、
いずれも15crnとし、膜形成中における薄膜の堆積
量に対するエツチング量の割合を、30鋒とした場合に
得られた結果を示す。Here, the above curve shows that the pressure inside the vacuum chamber 5 is 6.7
10-" pa, the gap between the center of the substrate 6 and the microwave ion source 7 and hot filament type ion source 8,
The results are shown when the etching amount was 15 crn and the ratio of the etching amount to the thin film deposition amount during film formation was 30 crn.
第2図から明らかなように、本発明によっての
5fOz膜!形成を行なうと、バイアススパッタ法を用
いた場合よシも、基板の温度上昇ははるかに少なく、た
とえば8i02膜の形成速度50■/分の場合の基板温
度の上昇は、本発明を用いると、バイアススパッタ法の
1/2以下となることがわかる。As is clear from FIG. 2, the 5fOz film according to the present invention! When forming the substrate, the temperature rise of the substrate is much smaller than when using the bias sputtering method. It can be seen that the amount is less than 1/2 that of the bias sputtering method.
また、許容される基板温度の上昇を250Cとすると、
バイアススパッタ法を用いたときよシも、5fOz膜の
形成速度が3倍以上になる。Also, assuming that the allowable increase in substrate temperature is 250C,
Even when bias sputtering is used, the formation rate of the 5fOz film is more than tripled.
このような基板温度上昇における改善は、プラズマ源を
基板から離間させたために基板への熱ふく射が減少し、
加えて、グリッド14によって、荷電粒子による基板へ
の衝撃が抑制されたためと考えられる。This improvement in substrate temperature rise is due to the fact that the plasma source is separated from the substrate, which reduces heat radiation to the substrate.
In addition, it is thought that this is because the grid 14 suppressed the impact of charged particles on the substrate.
実施例2 第3図に本発明の他の実施例を示す。Example 2 FIG. 3 shows another embodiment of the invention.
マイクロ波イオン源7とホットフィラメント型イオン源
8は、いずれも真空槽5の底面に設けられ、これら両イ
オン源7,8に対向した位置には、回転し得るサセプタ
9が設けられている。Both the microwave ion source 7 and the hot filament type ion source 8 are provided on the bottom surface of the vacuum chamber 5, and a rotatable susceptor 9 is provided at a position facing both of the ion sources 7 and 8.
上記サセプタ9上に、複数のf3i基板66′を固定し
て、サセプタ9を回転させながら、マイクロ波イオン源
7とホットフィラメント型イオン源8を動作させる。A plurality of f3i substrates 66' are fixed on the susceptor 9, and the microwave ion source 7 and the hot filament type ion source 8 are operated while the susceptor 9 is rotated.
このようにすると、基板6,6′がマイクロ波イオン源
7の上方に位置したときは、5io2膜の堆積が、実施
例と同様にCVDによって行なわれ、ホットフィラメン
ト型イオン源8の上方に達すると、堆積したSiQ、膜
のArイオンによるエツチングが行なわれるから、結局
、膜の堆積とエツチングが交互に行なわれる。その結果
、各基板6゜6′は、マイクロ波イオン源7またはポッ
トフィラメント型イオン源8に、対向した位置にあると
き以外は、上記両イオン源7,8からの熱ふく射を受け
ずに冷却され、基板温度上昇の抑制は、実施例の場合よ
シもさらに顕著になシ、基板温度の上昇を効果的に防止
しながら、膜の堆積と表面平坦化を達成できる。In this way, when the substrates 6, 6' are located above the microwave ion source 7, the 5io2 film is deposited by CVD as in the embodiment, and reaches above the hot filament type ion source 8. Then, since the deposited SiQ and the film are etched by Ar ions, the film deposition and etching are performed alternately. As a result, each substrate 6° 6' is cooled without being exposed to heat radiation from both the ion sources 7 and 8, except when it is in a position facing the microwave ion source 7 or the pot filament type ion source 8. The suppression of the substrate temperature rise is even more remarkable in the case of the embodiment, and film deposition and surface flattening can be achieved while effectively preventing the substrate temperature rise.
上記実施例は、SiH2と02を原料ガスとして用いて
、8102膜を形成する場合を示したが、例えばS l
s N4 膜やリンガラス膜などの他の絶縁膜あるい
は、金属膜、合金膜を形成する場合にも、本発明を用い
ることができる。The above example shows the case where an 8102 film is formed using SiH2 and 02 as raw material gases, but for example,
The present invention can also be used when forming other insulating films such as an s N4 film or a phosphorous glass film, a metal film, or an alloy film.
原料ガス間の気相反応を促進するためのプラズマは、上
記実施例ではマイクロ波イオン源を使用したが、他のプ
ラズマ発生手段を用いることも可能である。In the above embodiment, a microwave ion source was used as the plasma for promoting the gas phase reaction between the raw material gases, but it is also possible to use other plasma generation means.
堆積膜表面の平坦化には、上記実施例において使用した
Arイオン以外のイオン用いてもよいことは、いうまで
もないことであわ、たとえば中性ビームなどイオン以外
の種々を粒子線を照射してエツチングを行なうことも可
能である。It goes without saying that ions other than Ar ions used in the above embodiments may be used to flatten the surface of the deposited film. For example, various particle beams other than ions such as a neutral beam may be used. It is also possible to perform etching.
基板上に膜を堆積するため手段としては、上記(9)
CVDの他に、堆積速度は遅くなるが、スパッタリング
を用いることもできる。この場合、マイクロ波イオンに
はSJ烏と02などの反応性ガスのかわシに、不活性ガ
スを導入し、マイクロ波イオン源の開口側壁部に石英を
配置すれば、StO。As a means for depositing a film on a substrate, in addition to the above-mentioned (9) CVD, sputtering can also be used, although the deposition rate is slow. In this case, if an inert gas is introduced into the microwave ion source in addition to a reactive gas such as SJ02, and quartz is placed on the side wall of the opening of the microwave ion source, StO.
膜の堆積が行なわれる。Film deposition is performed.
また、マイクロ波イオン源やホットフィラメント型イオ
ン源と基板との間に、開閉可能なシャッタを設けるなど
、実施を円滑するための各種手段を付加してもよい。Further, various means may be added to facilitate the implementation, such as providing an openable/closable shutter between the microwave ion source or hot filament type ion source and the substrate.
上記のように、本発明は膜を堆積させる手段と、堆積し
た膜をエッチして表面を平坦化する手段を、互いに独立
して設けたものである。As described above, the present invention provides a means for depositing a film and a means for etching the deposited film to planarize the surface thereof, independently of each other.
そのため、従来のバイアススパッタ法にくらべて、基板
の温度上昇ははるかに少々くなり、また、膜の堆積手段
としてCVDを用いると、膜の堆積速度は極めて迅速に
なる。Therefore, compared to the conventional bias sputtering method, the temperature rise of the substrate is much smaller, and when CVD is used as a film deposition method, the film deposition rate becomes extremely rapid.
膜の堆積手段とエツチング手段を、それぞれ独立して制
御できるため、膜の堆積速度や表面の平(10)
坦度を所望の値に制御するのは容易である。Since the film deposition means and etching means can be controlled independently, it is easy to control the film deposition rate and surface flatness to desired values.
また、膜堆積手段がグリッドを有しているときは、膜の
堆積速度はやや小さくなるが、荷電粒子による衝撃が抑
制させて基板温度の上昇は極めて少ない。Furthermore, when the film deposition means has a grid, the film deposition rate is slightly lower, but the impact of charged particles is suppressed and the rise in substrate temperature is extremely small.
一方、上記グリッドを使用すると、荷電粒子の衝撃のた
め、基板温度抑制の効果はあ−1シ大きくないが、膜の
堆積速は極めて大きくなるので、グリッドを適宜使用す
ることによって、広範囲の目的に対応することができる
。On the other hand, when the above-mentioned grid is used, the effect of suppressing the substrate temperature is not very large due to the impact of charged particles, but the film deposition rate becomes extremely high. can correspond to
これらの特長は、いずれも従来の方法では不可能であっ
たものであり、表面が平坦な膜の形成に極めて有用であ
る。All of these features were not possible with conventional methods, and are extremely useful for forming a film with a flat surface.
施例を示す図である。
1.2.3・・・ガス導入口、4・・・排気口、5・・
・真空槽、6.6/・・・基板、7・・・マイクロ波イ
オン源、8・・・ホットフィラメント型イオン源、9・
・・サセプ(11)
り、10.11・・・電磁石、12・・・石英、13゜
(12)
第 1 目
第 2 図
5LO2膜#八遠度 (n鴫つ
第1頁の続き
0発 明 者 向 喜 −部 国分寺市東恋ケ窪央研究
所内It is a figure showing an example. 1.2.3...Gas inlet, 4...Exhaust port, 5...
・Vacuum chamber, 6.6/...Substrate, 7...Microwave ion source, 8...Hot filament type ion source, 9.
...Sasep (11) Ri, 10.11...Electromagnet, 12...Quartz, 13° (12) 1st item 2nd Figure 5 LO2 film #8 distance (Continued from 1st page 0 shots Akira Mukai - Department Kokubunji City Higashi Koigakubo Research Institute
Claims (1)
膜の堆積と、上記膜を堆積する手段とは独立して設けら
れた上記膜を粒子線によって照射する手段による上記膜
への粒子線の照射を、同時もしくは交互に行なうことに
よシ、上記基板上に所望の薄膜を形成することを特徴と
する段と、該膜を堆積する手段とは独立して設けられた
上記膜へ粒子を照射して上記膜をエッチする手段を少な
くともそなえたことを特徴とする薄膜形成装置。1. Deposition of the film on the substrate using a means for depositing a film on the substrate, and depositing the film on the substrate by means of irradiating the film with a particle beam, which is provided independently of the means for depositing the film. a step for forming a desired thin film on the substrate by simultaneously or alternately performing irradiation with particle beams; and the step provided independently of the means for depositing the film. A thin film forming apparatus comprising at least means for etching the film by irradiating the film with particles.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58180236A JPH067548B2 (en) | 1983-09-30 | 1983-09-30 | Thin film formation method |
US06/655,438 US4599135A (en) | 1983-09-30 | 1984-09-28 | Thin film deposition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58180236A JPH067548B2 (en) | 1983-09-30 | 1983-09-30 | Thin film formation method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6074534A true JPS6074534A (en) | 1985-04-26 |
JPH067548B2 JPH067548B2 (en) | 1994-01-26 |
Family
ID=16079746
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58180236A Expired - Lifetime JPH067548B2 (en) | 1983-09-30 | 1983-09-30 | Thin film formation method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH067548B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63233549A (en) * | 1987-03-20 | 1988-09-29 | Nippon Telegr & Teleph Corp <Ntt> | Thin film formation |
US5609691A (en) * | 1994-11-29 | 1997-03-11 | Nec Corporation | Plasma CVD apparatus for forming a thin film of uniform thickness |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS513875A (en) * | 1974-07-01 | 1976-01-13 | Hitachi Ltd | HAKUMAKUKEISEIHOHO |
JPS534778A (en) * | 1976-07-02 | 1978-01-17 | Matsushita Electric Ind Co Ltd | Crystal growth method with molecular beam |
JPS53125761A (en) * | 1977-04-08 | 1978-11-02 | Nec Corp | Manufacture for binary compound semiconductor thin film |
JPS583221A (en) * | 1981-06-29 | 1983-01-10 | Fujitsu Ltd | Ion beam accumulation |
-
1983
- 1983-09-30 JP JP58180236A patent/JPH067548B2/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS513875A (en) * | 1974-07-01 | 1976-01-13 | Hitachi Ltd | HAKUMAKUKEISEIHOHO |
JPS534778A (en) * | 1976-07-02 | 1978-01-17 | Matsushita Electric Ind Co Ltd | Crystal growth method with molecular beam |
JPS53125761A (en) * | 1977-04-08 | 1978-11-02 | Nec Corp | Manufacture for binary compound semiconductor thin film |
JPS583221A (en) * | 1981-06-29 | 1983-01-10 | Fujitsu Ltd | Ion beam accumulation |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63233549A (en) * | 1987-03-20 | 1988-09-29 | Nippon Telegr & Teleph Corp <Ntt> | Thin film formation |
US5609691A (en) * | 1994-11-29 | 1997-03-11 | Nec Corporation | Plasma CVD apparatus for forming a thin film of uniform thickness |
Also Published As
Publication number | Publication date |
---|---|
JPH067548B2 (en) | 1994-01-26 |
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