JPH04297569A - Method and apparatus for forming film - Google Patents
Method and apparatus for forming filmInfo
- Publication number
- JPH04297569A JPH04297569A JP6045791A JP6045791A JPH04297569A JP H04297569 A JPH04297569 A JP H04297569A JP 6045791 A JP6045791 A JP 6045791A JP 6045791 A JP6045791 A JP 6045791A JP H04297569 A JPH04297569 A JP H04297569A
- Authority
- JP
- Japan
- Prior art keywords
- film
- treated
- forming
- ion beam
- vacuum
- 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.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims abstract description 17
- 239000000463 material Substances 0.000 claims abstract description 32
- 238000010884 ion-beam technique Methods 0.000 claims abstract description 11
- 239000010408 film Substances 0.000 claims description 49
- 230000015572 biosynthetic process Effects 0.000 claims description 11
- 238000005468 ion implantation Methods 0.000 claims description 10
- 238000001704 evaporation Methods 0.000 claims description 9
- 239000010409 thin film Substances 0.000 claims description 9
- 230000008020 evaporation Effects 0.000 claims description 8
- 238000007738 vacuum evaporation Methods 0.000 claims description 7
- 238000001771 vacuum deposition Methods 0.000 claims description 4
- 238000007740 vapor deposition Methods 0.000 abstract description 16
- 238000011109 contamination Methods 0.000 abstract description 5
- 239000007888 film coating Substances 0.000 abstract 2
- 238000009501 film coating Methods 0.000 abstract 2
- 239000012535 impurity Substances 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 239000007789 gas Substances 0.000 description 13
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 238000000151 deposition Methods 0.000 description 5
- 238000007796 conventional method Methods 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 239000000356 contaminant Substances 0.000 description 3
- 230000001678 irradiating effect Effects 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 238000001659 ion-beam spectroscopy Methods 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000004611 spectroscopical analysis Methods 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 206010021143 Hypoxia Diseases 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007737 ion beam deposition Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、イオン注入および真空
蒸着の併用によって材料の表層に耐摩耗性や耐食性等に
優れた皮膜を形成する方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for forming a film having excellent wear resistance and corrosion resistance on the surface layer of a material by using a combination of ion implantation and vacuum deposition.
【0002】0002
【従来の技術】従来のイオン注入および真空蒸着の併用
によって行う成膜装置では、イオン源や蒸着源などの直
前にシャッターを設け、被処理材の前にシャッターを設
けてなかった。これらの目的は、まずイオン源において
は、イオン源内のプラズマが安定し、イオンビームが安
定に引き出せるようになるまで被処理材に照射しないよ
うにするためであり、また、蒸着源においては、蒸着物
質がハース内で加熱・溶融され、安定な蒸着蒸気が得ら
れるまで被処理材に付着しないようにするためであった
。そしてイオンビームおよび蒸着蒸気が安定したときに
、両シャッターを開けて、成膜を開始していた。2. Description of the Related Art In a conventional film forming apparatus that uses both ion implantation and vacuum evaporation, a shutter is provided immediately before the ion source, vapor deposition source, etc., and no shutter is provided in front of the material to be processed. The purpose of these is to prevent the ion source from irradiating the material to be processed until the plasma within the ion source is stabilized and the ion beam can be stably extracted, and for the evaporation source to This was to prevent the substance from adhering to the material to be treated until it was heated and melted within the hearth and stable vapor deposition was obtained. When the ion beam and vapor deposition became stable, both shutters were opened and film formation started.
【0003】イオン注入および真空蒸着の併用によって
行う成膜方法の手順は、まず処理チャンバーを大気圧に
して被処理材を取り付け、真空排気を行い、所定の真空
度に達した後、イオン注入および真空蒸着の併用によっ
て皮膜を形成し、処理が終わると再び大気圧に戻して被
処理材を取り替えるという手順になる。このとき処理チ
ャンバー内面や試料ホルダーは、被処理材の交換の度に
大気に晒されるため、大気中の酸素や水分等の吸着ガス
や汚染が付着することになる。[0003] The procedure for a film forming method using a combination of ion implantation and vacuum evaporation is to first set the processing chamber at atmospheric pressure, attach the material to be processed, and evacuate the chamber.After reaching a predetermined degree of vacuum, ion implantation and vacuum evaporation are performed. A film is formed using vacuum evaporation, and once the treatment is finished, the pressure is returned to atmospheric pressure and the material to be treated is replaced. At this time, the inner surface of the processing chamber and the sample holder are exposed to the atmosphere each time the material to be processed is replaced, so that adsorbed gases such as oxygen and moisture in the atmosphere and contamination adhere to the inner surface of the processing chamber and the sample holder.
【0004】成膜において、イオンビーム照射を行うた
めに、付着した吸着ガスや汚染などがイオンビームスパ
ッタリングによって処理チャンバー内に再放出される。
これは特に成膜初期に多く放出される。この放出された
吸着ガスや汚染は、成膜中に皮膜に取り込まれて、皮膜
の純度を低下させる原因となっていた。[0004] During film formation, in order to perform ion beam irradiation, adhering gases, contaminants, etc. are re-released into the processing chamber by ion beam sputtering. A large amount of this is released especially in the initial stage of film formation. This released adsorbed gas and contamination are taken into the film during film formation, causing a decrease in the purity of the film.
【0005】これを避けるために被処理材の交換のとき
、乾燥窒素や不活性ガスを処理チャンバーに導入して大
気圧へ戻し、さらにこれらのガスを処理チャンバー内に
流しながら、できるだけ大気ガスが入らないようにして
交換することが行われるが、これでは十分に防ぎきれず
、さらに作業員の酸欠の危険や、運転費用がかかる等の
問題があった。また、交換作業においても汚染が付着し
ないように細心の注意を払う必要があった。In order to avoid this, when replacing the material to be processed, dry nitrogen or inert gas is introduced into the processing chamber to return it to atmospheric pressure, and these gases are flowed into the processing chamber to remove as much atmospheric gas as possible. Although it is common practice to replace the gas to prevent it from entering, this method is not sufficient to prevent the gas from entering, and there are further problems such as the danger of oxygen deficiency for workers and the high operating costs. In addition, great care had to be taken to avoid contamination during replacement work.
【0006】[0006]
【発明が解決しようとする課題】本発明の目的は、イオ
ン注入と真空蒸着を併用する薄膜形成方法において、処
理チャンバーなどに付着した吸着ガスや汚染などが成膜
時に放出されないように処理して、高純度の皮膜を形成
する方法および装置を提供するものである。[Problems to be Solved by the Invention] An object of the present invention is to prevent adsorbed gases and contaminants adhering to a processing chamber from being released during film formation in a thin film forming method that uses both ion implantation and vacuum evaporation. , provides a method and apparatus for forming a highly pure film.
【0007】[0007]
【課題を解決するための手段】上述の問題点を解決する
ために本発明はイオンビームの照射によって起こるスパ
ッタリングにより原子が放出されるのは避け得ないもの
であることから、成膜する皮膜と同じ材質のものを被処
理材以外の照射される部分に事前に蒸着しておくことに
より吸着ガスや汚染などが放出されないようにするもの
である。すなわち、この事前蒸着皮膜は、その後に成膜
する皮膜と同じ材質であるために、イオンビームスパッ
タリングにより処理チャンバー内に放出されたとしても
皮膜の純度に影響を及ぼさないのである。よって、本発
明の要旨は、イオン注入および真空蒸着の併用によって
行う薄膜形成方法において、あらかじめ被処理材以外の
イオンビームが照射される部分に蒸着膜を形成し、その
後被処理材にイオンビームを照射して成膜することによ
って高純度の皮膜を形成するところにある。[Means for Solving the Problems] In order to solve the above-mentioned problems, the present invention is designed to solve the problems described above, since it is inevitable that atoms are emitted by sputtering caused by irradiation with an ion beam. By pre-depositing the same material on the parts to be irradiated other than the treated material, adsorbed gases and contamination are prevented from being released. That is, since this pre-deposited film is made of the same material as the subsequently deposited film, even if it is released into the processing chamber by ion beam sputtering, it does not affect the purity of the film. Therefore, the gist of the present invention is to form a thin film in a method of forming a thin film using a combination of ion implantation and vacuum deposition, in which a vapor deposited film is formed in advance on a portion of the material other than the material to be irradiated with the ion beam, and then the material to be processed is irradiated with the ion beam. The purpose is to form a highly pure film by irradiating the film.
【0008】[0008]
【作用】本発明の内容を図面に基づき説明する。図1は
、装置構成の概略を示す。処理チャンバー1の中に試料
ホルダー2、イオン源3および蒸着源4が取り付けてあ
る。被処理材9を試料ホルダー2に取り付け、真空排気
を行う。所定の真空度に到達したところで、処理を開始
するが、このとき試料ホルダーシャッター5を閉じたま
ま(図示の状態)にしておく。まず蒸着源4を起動し、
蒸着が安定した時点で蒸着シャッター6を開け(仮想線
の位置迄移動)、蒸着源4より真空蒸着を行う。このと
き蒸着により形成する膜厚は、その後に被処理材に形成
する皮膜の膜厚により異なる。すなわち、形成膜厚が大
きいときは長時間のイオン照射を受けるために長時間の
事前蒸着を行い、蒸着膜を厚く付着させておく必要があ
り、また、形成膜厚が小さいときは短時間の事前蒸着に
よって蒸着膜を薄く形成する。この事前蒸着の時間は、
その後にイオン注入と真空蒸着の併用によって行うのに
必要な成膜時間の半分から3倍になるようにする。
この理由は、事前蒸着膜が薄すぎると、成膜中に膜がス
パッタリングによりすべて削られてしまい、吸着したガ
スや汚染が放出されることから、少なくとも成膜時間の
半分程度は必要であり、また、あまり多く蒸着すると蒸
着材料の無駄を生じることから、多くとも成膜時間の3
倍程度が適切である。この蒸着終了後、イオン源3を起
動し、イオンビームが安定したところで、試料ホルダー
2に設けた試料ホルダーシャッター駆動装置7を駆動し
て、試料ホルダーシャッター5が取り付けてある軸を軸
中心回転させることにより試料ホルダーシャッター5を
開け(仮想線位置に移動)、イオン注入と真空蒸着の併
用によって被処理材9の表面に成膜を行う。また成膜前
の蒸着が終了した後に、成膜の前処理としてイオンビー
ムのみを照射し、被処理材のクリーニングを行うことも
ある。このときは、蒸着源4を一旦停止し、試料ホルダ
ーシャッター5を開けてクリーニングを行うことになる
。[Operation] The contents of the present invention will be explained based on the drawings. FIG. 1 shows an outline of the device configuration. A sample holder 2, an ion source 3, and a vapor deposition source 4 are installed in a processing chamber 1. The material to be processed 9 is attached to the sample holder 2, and vacuum evacuation is performed. When a predetermined degree of vacuum is reached, processing is started, but at this time the sample holder shutter 5 is kept closed (state shown). First, start the vapor deposition source 4,
When the vapor deposition becomes stable, the vapor deposition shutter 6 is opened (moved to the position of the virtual line), and vacuum vapor deposition is performed from the vapor deposition source 4. The thickness of the film formed by vapor deposition at this time varies depending on the thickness of the film to be formed on the material to be treated afterwards. In other words, when the thickness of the film to be formed is large, it is necessary to perform long-term pre-evaporation to receive long-term ion irradiation to make the deposited film thick, and when the thickness of the film to be formed is small, a short-time A thin vapor deposited film is formed by pre-evaporation. The time of this pre-deposition is
After that, the film forming time is set to be half to three times the time required for the combined use of ion implantation and vacuum evaporation. The reason for this is that if the pre-deposited film is too thin, the film will be completely scraped away by sputtering during film formation, and the adsorbed gases and contaminants will be released, so at least half of the film formation time is required. In addition, if too much evaporation is performed, the evaporation material will be wasted, so at most 30% of the deposition time is required.
Approximately twice that amount is appropriate. After this vapor deposition is completed, the ion source 3 is started, and when the ion beam becomes stable, the sample holder shutter drive device 7 provided on the sample holder 2 is driven to rotate the shaft to which the sample holder shutter 5 is attached around the axis. As a result, the sample holder shutter 5 is opened (moved to the imaginary line position), and a film is formed on the surface of the material to be processed 9 by a combination of ion implantation and vacuum deposition. Further, after the vapor deposition prior to film formation is completed, the material to be processed may be cleaned by irradiating only an ion beam as a pretreatment for film formation. At this time, the vapor deposition source 4 is temporarily stopped and the sample holder shutter 5 is opened to perform cleaning.
【0009】[0009]
【実施例】鉄基板上に窒化チタン膜を従来法と本発明に
よる方法で成膜し、グロー放電分光法で分析し比較した
。窒化チタンの成膜条件は、どちらも窒素イオンの加速
電圧:20kV、ビーム電流密度:0.44mA/cm
2 、チタン蒸着レート:5.0A/s.、膜厚:1ミ
クロンであった。従来法では、被処理材の交換後、真空
度が、5×10−6torrに到達した後、そのまま窒
化チタンの成膜を行った。一方、本方法では、被処理材
の交換後、真空度が5×10−6torrに到達した後
、窒化チタンを成膜する前に試料ホルダーシャッターを
閉じて35分間、蒸着レート:5.0A/s.でチタン
を事前蒸着した後に窒化チタンを成膜したものである。
図2に、両皮膜のグロー放電分析結果を示す。図2から
判るように本発明法(同図(a))の方が、従来法(同
図(b))よりも炭素、酸素の取り込みが圧倒的に少な
かった。[Example] Titanium nitride films were formed on iron substrates using a conventional method and a method according to the present invention, and were analyzed and compared using glow discharge spectroscopy. The deposition conditions for titanium nitride are: nitrogen ion acceleration voltage: 20 kV, beam current density: 0.44 mA/cm.
2. Titanium deposition rate: 5.0A/s. , film thickness: 1 micron. In the conventional method, after the material to be treated was replaced and the degree of vacuum reached 5×10 −6 torr, titanium nitride film was directly formed. On the other hand, in this method, after replacing the material to be treated and after the degree of vacuum reaches 5 x 10-6 torr, the sample holder shutter is closed before forming the titanium nitride film, and the evaporation rate is 5.0 A/ s. After pre-evaporating titanium, a titanium nitride film was formed. Figure 2 shows the glow discharge analysis results for both films. As can be seen from FIG. 2, the method of the present invention (FIG. 2(a)) captured much less carbon and oxygen than the conventional method (FIG. 2(b)).
【0010】0010
【発明の効果】本発明によれば、大気ガスに影響されず
に被処理材を交換することができるので、乾燥窒素や不
活性ガスを処理チャンバーに導入して大気圧へ戻し、さ
らにこれらのガスを処理チャンバー内に流しながら、で
きるだけ大気ガスが入らないようにして被処理材を交換
するような繁雑な作業や、注意深いハンドリングを必要
とせずに、容易に高純度の薄膜が形成できる。[Effects of the Invention] According to the present invention, the material to be treated can be replaced without being affected by atmospheric gases, so dry nitrogen or inert gas is introduced into the processing chamber to return it to atmospheric pressure, and High-purity thin films can be easily formed without the need for complicated work such as replacing the material to be processed or careful handling while keeping gases flowing into the processing chamber while preventing atmospheric gases from entering as much as possible.
【図1】本発明による成膜装置の構成概略図である。FIG. 1 is a schematic diagram of the configuration of a film forming apparatus according to the present invention.
【図2】成膜した窒化チタン膜のグロー放電分光法によ
る分析結果を示す図で、(a)は本発明法、(b)は従
来法によって成膜した場合を示す。FIG. 2 is a diagram showing the analysis results of a titanium nitride film formed by glow discharge spectroscopy, in which (a) shows the case where the film was formed by the method of the present invention, and (b) shows the case where the film was formed by the conventional method.
1…処理チャンバー 2…試料ホルダー 3…イオン源 4…蒸着源 5…試料ホルダーシャッター 6…蒸着源シャッター 7…試料ホルダーシャッター駆動装置 8…蒸着膜 9…被処理材 1...Processing chamber 2...Sample holder 3...Ion source 4... Vapor deposition source 5...Sample holder shutter 6...Vapor deposition source shutter 7...Sample holder shutter drive device 8...Vapor deposited film 9...Material to be treated
Claims (3)
って行う薄膜形成方法において、被処理材に成膜を行う
前に、被処理材を除き、イオンビームが照射される部分
に蒸着膜を形成し、その後被処理材に成膜することによ
って高純度の皮膜を形成することを特徴とする薄膜形成
方法。1. A method for forming a thin film using a combination of ion implantation and vacuum deposition, in which, before forming a film on a material to be treated, a vapor deposited film is formed on a portion to be irradiated with an ion beam, excluding the material to be treated, A thin film forming method characterized by forming a highly pure film by subsequently forming a film on a material to be treated.
される部分に行う真空蒸着膜形成時間を、その後に成膜
するときに必要な成膜時間の半分から3倍とする請求項
1記載の薄膜形成方法。2. The method according to claim 1, wherein the time required to form the vacuum-deposited film on the part to be irradiated with the ion beam, excluding the material to be treated, is half to three times the time required for subsequent film formation. thin film formation method.
って行う薄膜形成装置において、蒸気を発生させる蒸着
源および被処理材を保持する試料ホルダーにそれぞれ独
立に動作し、かつ被処理材への蒸着を独立に制御できる
シャッターを設けたことを特徴とする薄膜形成装置。3. A thin film forming apparatus that uses ion implantation and vacuum evaporation in combination, wherein the evaporation source that generates vapor and the sample holder that holds the material to be processed each operate independently, and independently perform the evaporation on the material to be processed. A thin film forming apparatus characterized by being provided with a shutter that can be controlled.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6045791A JPH04297569A (en) | 1991-03-25 | 1991-03-25 | Method and apparatus for forming film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6045791A JPH04297569A (en) | 1991-03-25 | 1991-03-25 | Method and apparatus for forming film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04297569A true JPH04297569A (en) | 1992-10-21 |
Family
ID=13142819
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6045791A Withdrawn JPH04297569A (en) | 1991-03-25 | 1991-03-25 | Method and apparatus for forming film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04297569A (en) |
-
1991
- 1991-03-25 JP JP6045791A patent/JPH04297569A/en not_active Withdrawn
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Date | Code | Title | Description |
---|---|---|---|
A300 | Application deemed to be withdrawn because no request for examination was validly filed |
Free format text: JAPANESE INTERMEDIATE CODE: A300 Effective date: 19980514 |