JP3634461B2 - Coating film excellent in halogen-based gas corrosion resistance and halogen-based plasma corrosion resistance, and laminated structure provided with the coating film - Google Patents

Coating film excellent in halogen-based gas corrosion resistance and halogen-based plasma corrosion resistance, and laminated structure provided with the coating film Download PDF

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JP3634461B2
JP3634461B2 JP25658395A JP25658395A JP3634461B2 JP 3634461 B2 JP3634461 B2 JP 3634461B2 JP 25658395 A JP25658395 A JP 25658395A JP 25658395 A JP25658395 A JP 25658395A JP 3634461 B2 JP3634461 B2 JP 3634461B2
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Prior art keywords
corrosion resistance
halogen
coating film
film
laminated structure
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JPH0995766A (en
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貢基 池田
淳 久本
隆 大西
正剛 山本
克広 板山
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Kobe Steel Ltd
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Kobe Steel Ltd
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Priority to JP25658395A priority Critical patent/JP3634461B2/en
Priority to PCT/JP1996/002887 priority patent/WO2004076711A1/en
Priority to US08/849,123 priority patent/US6027792A/en
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【0001】
【発明の属する技術分野】
本発明は腐食性の強いガスまたはプラズマに対して強い抵抗性を示すコーティング膜及び積層構造体に関し、詳細には、塩素,臭素,弗素等のハロゲンまたは該ハロゲン含有化合物ガス(以下ハロゲン系ガスと言う)、更には該ハロゲン系ガス雰囲気で形成されたハロゲン系プラズマに対して優れた耐食性を示すコーティング膜及びこのコーティング膜を施した積層構造体に関するものである。
【0002】
【従来の技術】
半導体製造装置においては素子の高集積化が進み、配線間隔はサブミクロン単位の高精度化が要求される様になってきた。一方この様な素子では微粒子や細菌が付着することによる短絡は製品不良の直接的原因となる為、半導体製造プロセスで使用されるガスや洗浄水は夫々超高純度であることが要求されている。そのため真空チャンバー内壁、電極などの反応室構成材料、或はガス導入配管等についても、不純物ガスや微粒子を極力発生させることがない様な工夫を払うことが必要になっている。
【0003】
そこでガス放出性が少ない点及び一般的耐食性が優れている点などから、ステンレス鋼やアルミニウム合金が賞用されているが、この様な素材であっても、反応ガスやエッチングガスとして汎用されるハロゲン系ガス或はこれに由来するハロゲン系プラズマによる腐食は避け難く、例えばこれらの腐食環境に対して優れた耐食性を示すTiN,AlN,Al 等の皮膜を形成することが提案されている(実公昭61−13555、特開平1−312088、特公平5−53871)。またステンレス鋼について見ると、例えばオーステナイト系ステンレス鋼を電解研磨した後、酸化性ガス雰囲気中で加熱することによって非晶質酸化皮膜を形成し、表面からのガス放出量を抑制すること(特開昭64−87760)や、微粒子の発生源になったり不純物の吸着・放出サイトともなる非金属介在物の量を可及的に少なくすること(特開昭63−161145)などが知られている。
【0004】
しかしながら上記TiN,AlN,Al 等の皮膜は膜質によって耐ハロゲン系ガス腐食性に大きな差が現われ、特に、より腐食性の強い塩化水素ガスや弗化水素ガス、更にはハロゲン系プラズマに対して常に良好な耐食性を発揮させるということはできない様である。またステンレス鋼についての上記改質技術も上記の様な強い腐食環境の中では耐食効果が安定しない様である。そして腐食が始まると腐食生成物がガスの吸着・放出サイトとなってガス純度の維持が困難になるだけでなく、腐食生成物自身が微粒子となって、例えば装置の内面或は試料表面に付着して汚染する等、種々の不都合を招く。
【0005】
【発明が解決しようとする課題】
本発明はこの様な事情に着目してなされたものであって、常に安定して優れた耐ハロゲン系ガス腐食性及び耐ハロゲン系プラズマ腐食性を発揮することのできるコーティング膜並びに該コーティング膜を施した積層構造体の提供を目的とするものである。
【0006】
【課題を解決するための手段】
本発明のコーティング膜とは、Alの酸化物薄膜で構成され、該薄膜層がX線回折において半値幅5°以下のピークを有しないものであると共に、厚さが0.1〜20μmのものである。この様な特性を示すという事実は該Al酸化物が実質的に非晶質であることを意味する。本発明のコーティング膜の製造方法の一例としては、任意の基材上に、スパッタリング法で形成することが最適方法として説明される。
【0007】
【発明の実施の形態】
アルミニウム酸化物を金属材料等の保護皮膜として利用することは、既述の如く公知である(実公昭61−13555等)が、先に述べた様に膜質によって耐食性が左右されるという問題があったため、膜質と耐食性の関係について種々検討した。その結果耐ハロゲン系ガス腐食性及び耐ハロゲン系プラズマ腐食性を安定して有効に発揮させるためには、アルミニウム酸化物薄膜の膜質としては、X線回折において半値幅5°以下のピークを有しない(図1参照)、即ち実質的に非晶質であることが必要であることを見出した。これに対し全体が結晶質且つ多結晶体である様な膜、或は図2に示す如く結晶質の部分と非晶質の部分が混在する様な膜では、結晶質同士の粒界或は結晶質と非結晶質の界面部分がハロゲン系ガスやハロゲン系プラズマによって選択的に腐食され、クラックやピンホールを生じ、やがては保護すべき基板のダメージを招く。
【0008】
尚アルミニウム酸化物膜を単結晶体として形成したときは上記の様な選択的腐食は回避できるが、全体が非晶質であるものに比べると、耐弗素プラズマ性が総体的に劣る他、成膜時の残留膜応力が大きい為、使用前(コーティング直後)及び使用中にコーティング層の剥離や割れを生じ易い。従って全体を実質的に非晶質とすることがもっとも有利であることが確認された。
【0009】
非晶質アルミニウム酸化物膜の厚さが0.1μm未満であると、基板表面を完全に被覆することが困難で、被覆欠陥を内在して基板に部分的な腐食を招くので、0.1μm以上とする必要がある。好ましくは、0.5μm以上である。一方上限については、膜厚の増大に伴って耐食効果が向上する反面、膜にかかる絶対的な応力が増加してコーティング層の剥離や割れ招き易くなるので、安全性からは20μm以下とすることが望まれる。
【0010】
非晶質アルミニウム酸化物膜の形成方法としては、特に制限される訳ではないが、スパッタリング法または真空蒸着法が特に好ましく、この方法であれば、成膜条件を制御することにより、非晶質アルミニウム酸化物膜を均一に形成して良好な耐弗素プラズマ性を享受することができる。尚スパッタリング法としても特に制限されないが、代表的にはRF(高周波)マグネトロンスパッタリング法が、また真空蒸着法としては特にイオンアシスト真空蒸着法を採用することが望まれる。これに対しイオンプレーティング法や化学蒸着法等を採用すると結晶性アルミニウム酸化物膜が生成し易く、また組成ズレ等の問題を生じる恐れがあって好ましくない場合がある。
【0011】
本発明の非晶質アルミニウム酸化物膜によって被覆することが望まれる基材については一切制限しないが、代表的なものを示すと、Al,Mg,鋼などの各種金属材料の他、Si,Al,Ti等の酸化物,炭化物,窒化物,ほう化物などのセラミックス類、更にはプラスチックス類などが挙げられる。またその形状も板,棒,線,管など、目的・用途に応じて広範な適用が可能である。
【0012】
【実施例】
種々の基板材料上に気相成膜法によってアルミニウムの酸化物被覆層を形成した。また、比較のため無処理材も供試した。被覆材についてはX線回折法により結晶構造を調査した。これら材料の耐ハロゲン系ガス腐食性を評価するため、5%塩素−アルゴン混合ガス中、400℃、240分のガス腐食試験を行ない、試験後の外観により耐食性を評価した。また、485℃、RF出力300WでのNF プラズマ照射試験を延べ500分行ない、試験後の外観により耐プラズマ腐食性を評価した。評価結果を表1に示す。
【0013】
【表1】

Figure 0003634461
【0014】
表1より明らかな様に本発明の規定条件をすべて満たすNo.1〜8の実施例では、いずれの腐食試験でも優れた耐食性を示している。No.6については基板材料が低合金鋼であり、被覆膜厚が薄いため、またNo.8についてはイオンプレーティング法による成膜であるため、夫々若干耐食性は劣るものの、総合的には、十分な耐食性を有している。
【0015】
これに対して比較例No.9では、被覆層膜厚が少ないため、No.10〜13については結晶質が混在するため夫々耐食性は不十分であり、No.14、15の無処理材は特にプラズマ中での耐食性が極めて劣っている。
【0016】
【発明の効果】
本発明は以上の様に構成されたものであり、ハロゲン系ガス、ハロゲン系プラズマに対して優れた耐食性を示すコーティング膜構成及び当該膜の施された積層構造体が提供された。
【図面の簡単な説明】
【図1】本発明に係るアルミニウム酸化物膜のX線回折パターン。
【図2】結晶質混在のアルミニウム酸化物膜のX線回折パターン。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a coating film and a laminated structure exhibiting strong resistance to corrosive gas or plasma, and more specifically, halogen such as chlorine, bromine and fluorine or halogen-containing compound gas (hereinafter referred to as halogen-based gas). Furthermore, the present invention relates to a coating film exhibiting excellent corrosion resistance against a halogen-based plasma formed in the halogen-based gas atmosphere, and a laminated structure provided with the coating film.
[0002]
[Prior art]
In a semiconductor manufacturing apparatus, higher integration of elements has progressed, and the wiring interval has been required to have high precision in submicron units. On the other hand, in such an element, a short circuit due to adhesion of fine particles and bacteria directly causes a product failure, so that the gas and cleaning water used in the semiconductor manufacturing process are required to be ultrapure, respectively. . For this reason, it is necessary to devise measures to prevent generation of impurity gas and fine particles as much as possible for the inner wall of the vacuum chamber, the reaction chamber constituent materials such as electrodes, or the gas introduction pipe.
[0003]
Therefore, stainless steel and aluminum alloys have been awarded for their low outgassing properties and excellent general corrosion resistance, but even such materials are widely used as reactive gases and etching gases. Corrosion due to halogen-based gas or halogen-based plasma derived therefrom is unavoidable, and for example, it has been proposed to form a film such as TiN, AlN, Al 2 O 3 that exhibits excellent corrosion resistance against these corrosive environments. (Japanese Utility Model Publication No. 61-13555, Japanese Patent Application Laid-Open No. 1-312088, Japanese Patent Publication No. 5-53871). As for stainless steel, for example, after electropolishing austenitic stainless steel, it is heated in an oxidizing gas atmosphere to form an amorphous oxide film, thereby suppressing the amount of gas released from the surface (Japanese Patent Laid-Open No. 64-87760), and the amount of non-metallic inclusions that become a fine particle generation source and an impurity adsorption / desorption site as much as possible (Japanese Patent Laid-Open No. 63-161145) are known. .
[0004]
However, the coating films of TiN, AlN, Al 2 O 3 and the like have a large difference in halogen-based gas corrosion resistance depending on the film quality. In particular, the highly corrosive hydrogen chloride gas, hydrogen fluoride gas, and further halogen-based plasma. On the other hand, it seems that it cannot always exhibit good corrosion resistance. In addition, the above-described reforming technique for stainless steel does not seem to have a stable corrosion resistance effect in a strong corrosive environment as described above. When corrosion begins, the corrosion products become gas adsorption / release sites, making it difficult to maintain gas purity, and the corrosion products themselves become fine particles that adhere to, for example, the inner surface of the apparatus or the sample surface. This causes various inconveniences such as contamination.
[0005]
[Problems to be solved by the invention]
The present invention has been made paying attention to such a situation, and a coating film capable of constantly exhibiting excellent halogen-based gas corrosion resistance and halogen-based plasma corrosion resistance, and the coating film. The object is to provide a laminated structure.
[0006]
[Means for Solving the Problems]
The coating film of the present invention is composed of an Al oxide thin film, and the thin film layer has no peak with a half-value width of 5 ° or less in X-ray diffraction, and has a thickness of 0.1 to 20 μm. It is. The fact that it exhibits such characteristics means that the Al oxide is substantially amorphous. As an example of the manufacturing method of the coating film of this invention, forming on arbitrary base materials by sputtering method is demonstrated as an optimal method.
[0007]
DETAILED DESCRIPTION OF THE INVENTION
The use of aluminum oxide as a protective coating for metallic materials is known as described above (Jokho Sho 61-13555, etc.), but there is a problem that the corrosion resistance depends on the film quality as described above. Therefore, various studies were made on the relationship between film quality and corrosion resistance. As a result, in order to stably and effectively exhibit the halogen-based gas corrosion resistance and the halogen-based plasma corrosion resistance, the film quality of the aluminum oxide thin film does not have a peak with a half-value width of 5 ° or less in X-ray diffraction. It has been found that it is necessary to be substantially amorphous (see FIG. 1). On the other hand, in a film that is entirely crystalline and polycrystalline, or a film in which a crystalline part and an amorphous part are mixed as shown in FIG. The crystalline and non-crystalline interface portions are selectively corroded by the halogen-based gas or halogen-based plasma, causing cracks and pinholes, and eventually causing damage to the substrate to be protected.
[0008]
When the aluminum oxide film is formed as a single crystal, the selective corrosion as described above can be avoided. However, compared to the case where the whole is amorphous, the plasma resistance to fluorine is generally inferior, and the selective corrosion is not possible. Since the residual film stress at the time of filming is large, peeling or cracking of the coating layer tends to occur before use (immediately after coating) and during use. Therefore, it was confirmed that it is most advantageous to make the whole substantially amorphous.
[0009]
If the thickness of the amorphous aluminum oxide film is less than 0.1 μm, it is difficult to completely cover the substrate surface, and coating defects are inherently caused to cause partial corrosion on the substrate. It is necessary to do it above. Preferably, it is 0.5 μm or more. On the other hand, with respect to the upper limit, the corrosion resistance improves as the film thickness increases, but on the other hand, the absolute stress applied to the film increases and the coating layer is liable to be peeled off or cracked. Is desired.
[0010]
A method for forming the amorphous aluminum oxide film is not particularly limited, but a sputtering method or a vacuum deposition method is particularly preferable. By this method, the amorphous film can be formed by controlling the film formation conditions. An aluminum oxide film can be formed uniformly to enjoy good fluorine plasma resistance. The sputtering method is not particularly limited, but it is typically desirable to employ an RF (radio frequency) magnetron sputtering method, and particularly an ion-assisted vacuum deposition method as the vacuum deposition method. On the other hand, when an ion plating method, a chemical vapor deposition method, or the like is employed, a crystalline aluminum oxide film is likely to be formed, and there is a possibility that a problem such as a composition shift may occur.
[0011]
The substrate desired to be coated with the amorphous aluminum oxide film of the present invention is not limited at all, but representative examples include various metal materials such as Al, Mg, steel, Si, Al , Ti and other oxides, carbides, nitrides, borides and other ceramics, and plastics. Moreover, the shape can be widely applied according to the purpose and use, such as a plate, a bar, a wire, and a pipe.
[0012]
【Example】
Aluminum oxide coating layers were formed on various substrate materials by vapor deposition. For comparison, an untreated material was also used. About the coating | covering material, the crystal structure was investigated by the X ray diffraction method. In order to evaluate the halogen-based gas corrosion resistance of these materials, a gas corrosion test was conducted at 400 ° C. for 240 minutes in a 5% chlorine-argon mixed gas, and the corrosion resistance was evaluated by the appearance after the test. Further, an NF 3 plasma irradiation test at 485 ° C. and an RF output of 300 W was conducted for a total of 500 minutes, and the plasma corrosion resistance was evaluated by the appearance after the test. The evaluation results are shown in Table 1.
[0013]
[Table 1]
Figure 0003634461
[0014]
As is apparent from Table 1, No. 1 satisfying all the prescribed conditions of the present invention. In Examples 1 to 8, excellent corrosion resistance is exhibited in any corrosion test. No. For No. 6, since the substrate material is low alloy steel and the coating film thickness is thin, Since No. 8 is a film formed by an ion plating method, the corrosion resistance is slightly inferior, but overall, it has sufficient corrosion resistance.
[0015]
In contrast, Comparative Example No. In No. 9, the coating layer thickness is small, so Nos. 10 to 13 have insufficient corrosion resistance due to the presence of crystalline substances. The untreated materials 14 and 15 are particularly inferior in corrosion resistance in plasma.
[0016]
【The invention's effect】
The present invention is configured as described above, and a coating film configuration exhibiting excellent corrosion resistance against a halogen-based gas and a halogen-based plasma and a laminated structure provided with the film are provided.
[Brief description of the drawings]
FIG. 1 is an X-ray diffraction pattern of an aluminum oxide film according to the present invention.
FIG. 2 shows an X-ray diffraction pattern of a crystalline aluminum oxide film.

Claims (2)

Alの酸化物薄膜で構成され、該薄膜層がX線回折において半値幅5°以下のピークを有しないものであると共に、厚さが0.1〜20μmであることを特徴とする耐ハロゲン系ガス腐食性及び耐ハロゲン系プラズマ腐食性に優れたコーティング膜。Is composed of an oxide thin film of Al, resistant halogen der those thin film layer does not have a half-value width 5 ° following peaks in X-ray diffraction Rutotomoni, the thickness characterized in that it is a 0.1~20μm Coating film with excellent gas corrosion resistance and halogen-based plasma corrosion resistance. 請求項1に記載されたコーティング膜を基材上に形成したものであることを特徴とする積層構造体。Layered structure, characterized in that the coating described is obtained by forming on a substrate in claim 1.
JP25658395A 1995-10-03 1995-10-03 Coating film excellent in halogen-based gas corrosion resistance and halogen-based plasma corrosion resistance, and laminated structure provided with the coating film Expired - Lifetime JP3634461B2 (en)

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JP25658395A JP3634461B2 (en) 1995-10-03 1995-10-03 Coating film excellent in halogen-based gas corrosion resistance and halogen-based plasma corrosion resistance, and laminated structure provided with the coating film
PCT/JP1996/002887 WO2004076711A1 (en) 1995-10-03 1996-10-03 Coating film excellent in the resistance to corrosion with halogen-containing gases and plasmas, laminated structure coated therewith, and process for the production of both
US08/849,123 US6027792A (en) 1995-10-03 1996-10-03 Coating film excellent in resistance to halogen-containing gas corrosion and halogen-containing plasma corrosion, laminated structure coated with the same, and method for producing the same

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JP25658395A JP3634461B2 (en) 1995-10-03 1995-10-03 Coating film excellent in halogen-based gas corrosion resistance and halogen-based plasma corrosion resistance, and laminated structure provided with the coating film

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JP3634461B2 true JP3634461B2 (en) 2005-03-30

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