JPH02255593A - Graphite susceptor for plasma cvd - Google Patents
Graphite susceptor for plasma cvdInfo
- Publication number
- JPH02255593A JPH02255593A JP7577789A JP7577789A JPH02255593A JP H02255593 A JPH02255593 A JP H02255593A JP 7577789 A JP7577789 A JP 7577789A JP 7577789 A JP7577789 A JP 7577789A JP H02255593 A JPH02255593 A JP H02255593A
- Authority
- JP
- Japan
- Prior art keywords
- susceptor
- film
- main body
- plasma cvd
- roughness
- 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
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 17
- 229910002804 graphite Inorganic materials 0.000 title claims abstract description 15
- 239000010439 graphite Substances 0.000 title claims abstract description 15
- 229910021397 glassy carbon Inorganic materials 0.000 claims abstract description 18
- 230000003746 surface roughness Effects 0.000 claims abstract description 12
- 238000005268 plasma chemical vapour deposition Methods 0.000 claims description 14
- 239000007833 carbon precursor Substances 0.000 abstract description 5
- 239000012298 atmosphere Substances 0.000 abstract description 4
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 229920000620 organic polymer Polymers 0.000 abstract description 2
- 235000012431 wafers Nutrition 0.000 description 16
- 229910052581 Si3N4 Inorganic materials 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 6
- 229910052814 silicon oxide Inorganic materials 0.000 description 5
- 238000000576 coating method Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 239000003082 abrasive agent Substances 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000003754 machining Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000012771 pancakes Nutrition 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Landscapes
- Crystals, And After-Treatments Of Crystals (AREA)
- Chemical Vapour Deposition (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、プラズマCVDで使用する黒鉛サセプターに
関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a graphite susceptor used in plasma CVD.
(従来の技術)
従来、プラズマCVD用サセプターとしては、単に黒鉛
を機械加工したもの、加工後に純化処理をおこなって表
面加工精度な〜(Ra2〜5μm、 ’Bxax 15
〜3 Q py@ )としたもの、ガラス状炭素で表面
を被覆し鏡面状に仕上げたものが知られている(例えば
特開昭64−47019号公報)。(Prior art) Conventionally, susceptors for plasma CVD have been made by simply machining graphite, or by performing purification treatment after machining to achieve surface processing accuracy of ~ (Ra2~5μm, 'Bxax 15
~3Qpy@) and those whose surfaces are coated with glassy carbon to give a mirror finish are known (for example, JP-A-64-47019).
(発明が解決しようとする課題)
しかしながら、このような黒鉛サセプターに於いては、
プラズマCVDによりウエノ・上にシリコン酸化膜やシ
リコン窒化膜を成膜するさいに1その膜内にサセプター
から発生したダストが取シ込まれ、異物を含まない優れ
た膜を安定してつくシに<<、シかも、サセプターの表
面通常加工では、表面がちらいために、外部加熱により
サセプターに与えられた熱がウエノ1に均一に伝わらな
いのでウェハ内あるいはウェハ間において均一な膜の形
成が困難である、等の欠点があった。(Problem to be solved by the invention) However, in such a graphite susceptor,
When a silicon oxide film or silicon nitride film is formed on Ueno by plasma CVD, the dust generated from the susceptor is incorporated into the film, making it possible to stably form an excellent film that does not contain foreign matter. <<However, in normal processing of the surface of the susceptor, the heat applied to the susceptor by external heating is not uniformly transmitted to the wafer 1 due to the scattering of the surface, making it difficult to form a uniform film within the wafer or between wafers. There were drawbacks such as.
へた、ガラス状炭素被覆サセプターにおいては、シリコ
ン酸化膜やシリコン窒化膜を成膜するさいに、サセプタ
ー上に堆積するシリコン酸化膜やシリコン窒化膜がサセ
プター表面が鏡面のために剥がれやすくそれが形成膜中
に取り込まれる等の欠点があった。However, when forming a silicon oxide film or silicon nitride film on a glassy carbon-coated susceptor, the silicon oxide film or silicon nitride film deposited on the susceptor tends to peel off because the susceptor surface is mirror-finished. It had drawbacks such as being incorporated into the membrane.
本発明は、以上の欠点を解決することを目的とするもの
である。The present invention aims to solve the above-mentioned drawbacks.
(課題を解決するための手段)
即ち、本発明は、ウェハ接触面の表面粗さをそれ以外の
他面よりも小さくし、しかも表面全体をガラス“状炭素
で被覆してなることを特徴とするプラズマCVD用黒鉛
サセプターである。(Means for Solving the Problems) That is, the present invention is characterized in that the surface roughness of the wafer contact surface is made smaller than that of other surfaces, and the entire surface is coated with glassy carbon. This is a graphite susceptor for plasma CVD.
以下、さらに詳しく本発明を説明すると、本発明の好ま
しい態様は、ウェハ接触面の表面粗さをRa 1am以
下、Rmax 10μm以下、好ましくはRa O,5
μm以下、Rxnax 7μm以下にし、それ以外の他
面の表面粗さをRa 2〜5 Jim、Rxnax 1
5〜40μmにし、しかもサセプター全面を膜厚2〜5
μmのガラス状炭素で被覆してなるプラズマCVD用黒
鉛サセプターである。Hereinafter, the present invention will be described in more detail. In a preferred embodiment of the present invention, the surface roughness of the wafer contact surface is Ra 1am or less, Rmax 10μm or less, preferably Ra O,5
μm or less, Rxnax 7 μm or less, and the surface roughness of the other surface is Ra 2-5 Jim, Rxnax 1
5 to 40 μm, and the entire surface of the susceptor has a film thickness of 2 to 5 μm.
This is a graphite susceptor for plasma CVD coated with μm glassy carbon.
ウェハ接触面の表面粗さを上記のようにすることにより
、外部ヒータからサセプターに与えられた熱が均一にウ
ェハに伝わシ形成膜の均一性が向上する。また、ウェハ
に接触しない他面の表面粗さを上記のようにしかつサセ
プター全面な膜厚2〜5μmのガラス状炭素で被覆する
ことによシ、サセプター表面が鏡面とならないため、サ
セプター表面に堆積されるシリコン酸化膜やシリコン窒
化膜の剥離が生じない。しかも、表面がガラス状炭素で
被覆されているために黒鉛ダストの発生がなく、異物を
含まない優れた膜を安定してつくれるようになる。ガラ
ス状炭素を5μmこえて被覆するとサセプター表面が鏡
面化してしまい剥離が生じゃすくなシ、ウェハ上に成膜
されるシリコン酸化膜やシリコン窒化膜に剥離した物質
が取り込まれやすくなるので好ましくはない。By setting the surface roughness of the wafer contact surface as described above, the heat applied to the susceptor from the external heater is uniformly transmitted to the wafer, thereby improving the uniformity of the formed film. In addition, by adjusting the surface roughness of the other side that does not contact the wafer as described above and coating the entire surface of the susceptor with glassy carbon with a thickness of 2 to 5 μm, the susceptor surface does not become a mirror surface, so that deposits can be deposited on the susceptor surface. No peeling of the silicon oxide film or silicon nitride film occurs. In addition, since the surface is coated with glassy carbon, graphite dust is not generated, making it possible to stably produce an excellent film that does not contain foreign substances. If glassy carbon is coated with a thickness exceeding 5 μm, the surface of the susceptor becomes mirror-like, making it difficult to peel off, and it is not preferable because the peeled off material is likely to be incorporated into the silicon oxide film or silicon nitride film formed on the wafer. .
以下、本発明の具体的な製造方法の例を示す。Examples of specific manufacturing methods of the present invention will be shown below.
まず第1図に例示したようなプラズマCVD用サセプタ
ーを従来法に従い表面精度〜
で機械加工する。サセプターは、この形状に限定される
ことなく、例えば、パンケーキ状、毎葉式形状であって
もよい。このとき表面粗さはRa 2〜5μm、 Rm
ax 15〜3 Q p@となるので、次いで、サセプ
ター基材のウェハ接触面のみをサンドペーパー 工業用
バットなどの研磨材を用いて、表面層する。あるいは、
サセプター全面をサンドペーパー 工業用バットなどの
研磨材を用いて表面粗さRa 1 μm以下、 Rma
x 1Qμm以下、好ましくはRa Q、5 μm以下
、 Rmax 7 fim以下に研磨した後、ウェハ接
触面のみをがムテープ、ざ一ル紙等でマスクしサンドブ
ラスト等で他の表面なRa 2μm以上、 Rmax
15μm以上にあらしてもよい。First, a susceptor for plasma CVD as illustrated in FIG. 1 is machined according to a conventional method to a surface accuracy of .about. The shape of the susceptor is not limited to this, and may be, for example, a pancake shape or a leaflet shape. At this time, the surface roughness is Ra 2 to 5 μm, Rm
Since ax 15-3 Q p@, only the wafer contacting surface of the susceptor base material is then surface-layered using an abrasive material such as sandpaper or an industrial bat. or,
Sand the entire surface of the susceptor using an abrasive material such as an industrial bat to achieve a surface roughness Ra of 1 μm or less, Rma
After polishing to x 1 Q μm or less, preferably Ra Q, 5 μm or less, and Rmax 7 fim or less, only the wafer contact surface is masked with tape, paper, etc., and other surfaces are sandblasted, etc. to Ra of 2 μm or more, Rmax
The thickness may be 15 μm or more.
以上のようにして得られたサセプター基材の表面を、特
公昭52−39684号公報に記載の方法を用いて、膜
厚2〜5μmのガラス状炭素で被覆する。以下、その被
覆方法について簡単に説明すると、ガラス状炭素の原料
であるポリ塩化ビニール等の有機物ポリマーを不活性化
雰囲気下。The surface of the susceptor substrate obtained as described above is coated with glassy carbon having a thickness of 2 to 5 μm using the method described in Japanese Patent Publication No. 52-39684. The coating method will be briefly explained below. An organic polymer such as polyvinyl chloride, which is the raw material for glassy carbon, is coated in an inert atmosphere.
350〜450℃で熱分解しピッチ状の炭素前駆体を得
る。この炭素前駆体をトリクレンなどの有機溶剤に溶解
し、それをサセプター基材表面に塗布した後、真空中も
しくは不活性化雰囲気下、1000℃以上で焼成する。Pyrolysis is performed at 350 to 450°C to obtain a pitch-like carbon precursor. This carbon precursor is dissolved in an organic solvent such as trichlene, applied to the surface of the susceptor substrate, and then fired at 1000° C. or higher in vacuum or in an inert atmosphere.
この塗布−焼成工程を繰シ返し行ない、゛サセプター基
材表面をガラス状炭素で被覆する。高純度が要求される
用途にたいしては、必要に応じて、例えば1600℃以
上で塩素、フッ素等のハロデフガスな導入することで高
純度のサセプターを得ることができる。This coating-firing step is repeated to coat the surface of the susceptor substrate with glassy carbon. For applications requiring high purity, a high purity susceptor can be obtained by introducing a halodef gas such as chlorine or fluorine at a temperature of 1600° C. or higher, if necessary.
(実施例)
以下、実施例と比較例をあげてさらに具体的に本発明を
説明する。(Example) Hereinafter, the present invention will be explained in more detail by giving Examples and Comparative Examples.
実施例1
第1図に示すプラズマCVD用サセプター(800x1
50x4)を機械加工(表面精度Ra3.2μ@ 、
Rmax 22μWL)シウエハ接触面を工業用バット
(住友スリーエム■社製スコッチシライト 7448)
で鏡面に仕上げた( Ra015μm ’Rmax 6
.5 Am )。このサセプターの表面にポリ塩化ビニ
ールを窒素雰囲気中390℃で熱分解しタール状の炭素
前駆体ぎツチを得、トリクレンにこの炭素前駆体を濃度
15重量%で溶解し、その溶液をサセプター基材の表面
に塗布し、真空雰囲気下、1200℃で焼成した。この
塗布−焼成工程を4回縁シ返し行ない、膜厚6.5μm
でガラス状炭素を基サセプター表面に被覆した。Example 1 Plasma CVD susceptor (800x1
50x4) was machined (surface accuracy Ra3.2μ@,
Rmax 22μWL) The contact surface of the wafer was covered with an industrial bat (Sumitomo 3M Scotch Silite 7448).
(Ra015μm 'Rmax 6
.. 5 Am). On the surface of this susceptor, polyvinyl chloride was thermally decomposed at 390°C in a nitrogen atmosphere to obtain a tar-like carbon precursor. This carbon precursor was dissolved in trichlene at a concentration of 15% by weight, and the solution was used as a susceptor substrate. and baked at 1200°C in a vacuum atmosphere. This coating-baking process was repeated four times, resulting in a film thickness of 6.5 μm.
Glassy carbon was coated on the surface of the base susceptor.
その結果、ガラス状炭素被覆後の表面粗さは、ウェハ接
触面がRa[]、3μ7FL、 Rmax 6.0μr
rL1それ以外の他面がRa 3.0 μm 、 R
max 21μmのゾラズWCVD用黒鉛サセプターが
得られた。As a result, the surface roughness after coating with glassy carbon was as follows: Ra[] on the wafer contact surface, 3μ7FL, Rmax 6.0μr
The other surface other than rL1 is Ra 3.0 μm, R
A graphite susceptor for Zolaz WCVD with a maximum diameter of 21 μm was obtained.
比較例1
表面をガラス状炭素で被覆しないこと以外は、実施例1
と同様にしてプラズマCVD用黒鉛サセプターを製造し
た。Comparative Example 1 Example 1 except that the surface was not coated with glassy carbon.
A graphite susceptor for plasma CVD was manufactured in the same manner.
比較例2
サセプター基材のウエノ・接触面の鏡面仕上げ及びガラ
ス状炭素被覆を施さない以外は実施例1と同様にしてプ
ラズマCVD用黒鉛サセプターを製造した。Comparative Example 2 A graphite susceptor for plasma CVD was manufactured in the same manner as in Example 1, except that the Ueno contact surface of the susceptor base material was not mirror-finished and the glassy carbon coating was not applied.
比較例6
ウェハ接触面とそれ以外の他面との表面粗さを変えるこ
となく、サセプター基材の全面をスコッチプライト74
48で鏡面に仕上げた後、ガラス状炭素な膜厚3.5μ
mで被覆したこと以外は実施例1と同様処してプラズマ
CVD用黒鉛サセプターを得た。Comparative Example 6 The entire surface of the susceptor base material was coated with Scotch Prite 74 without changing the surface roughness of the wafer contact surface and other surfaces.
After mirror finishing with 48, glassy carbon film thickness 3.5μ
A graphite susceptor for plasma CVD was obtained in the same manner as in Example 1 except that it was coated with m.
上記4例のサセプターを評価するため、拡散炉型プラズ
マCVD装置を用い、4インチS1ウエハを5枚ずつセ
ットしてペルジャー内に入れ、外部加熱によりそれを3
00℃に加熱しサセプター間に高周波13.56 MH
zをかけ81)1.とNH5を原料ガスとしてペルジャ
ー内に導入し真空度1torrで高周波プラズマを立て
、S1ウエノ蔦上にシリコン窒化膜を1.2μ雷形成し
たときの膜厚のバラツキ及び異物量を顕微鏡で調べた。In order to evaluate the above four examples of susceptors, using a diffusion furnace type plasma CVD system, five 4-inch S1 wafers were set in a Pelger, and heated three times by external heating.
Heated to 00℃ and applied high frequency 13.56 MH between the susceptors.
Multiply by z81)1. and NH5 were introduced into a Pelger as raw material gases, high-frequency plasma was generated at a vacuum degree of 1 torr, and a silicon nitride film of 1.2 μm was formed on the S1 vines. The variation in film thickness and the amount of foreign matter were examined using a microscope.
その結果を第1表に示す。The results are shown in Table 1.
(発明の効果)
本発明のプラズマCVD用黒鉛サセプターを用いると生
成膜の電気比抵抗及び均一性が向上する。(Effects of the Invention) When the graphite susceptor for plasma CVD of the present invention is used, the electrical resistivity and uniformity of the produced film are improved.
これKよシ成膜の歩留りが向上し生産コストの低下等を
図ることができる。This improves the yield of K film formation and reduces production costs.
第1図は、本発明のプラズマCVD用黒鉛サセプターの
1例を示す概略正面図である。
1・・・サセプター本体、2・・・ウェハ接触面、3.
、。
それ以外の他面、4・・・ビン
特許出願人 電気化学工業株式会社FIG. 1 is a schematic front view showing an example of a graphite susceptor for plasma CVD according to the present invention. 1... Susceptor main body, 2... Wafer contact surface, 3.
,. Other than that, 4...bin patent applicant Denki Kagaku Kogyo Co., Ltd.
Claims (1)
さくし、しかも表面全体をガラス状炭素で被覆してなる
ことを特徴とするプラズマCVD用黒鉛サセプター。1. A graphite susceptor for plasma CVD, characterized in that the surface roughness of the wafer contact surface is smaller than that of other surfaces, and the entire surface is coated with glassy carbon.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1075777A JPH0647516B2 (en) | 1989-03-28 | 1989-03-28 | Graphite susceptor for plasma CVD |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1075777A JPH0647516B2 (en) | 1989-03-28 | 1989-03-28 | Graphite susceptor for plasma CVD |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02255593A true JPH02255593A (en) | 1990-10-16 |
| JPH0647516B2 JPH0647516B2 (en) | 1994-06-22 |
Family
ID=13585985
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1075777A Expired - Lifetime JPH0647516B2 (en) | 1989-03-28 | 1989-03-28 | Graphite susceptor for plasma CVD |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0647516B2 (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0814174A1 (en) * | 1996-06-20 | 1997-12-29 | Qqc, Inc. | Glassy carbon coatings having water repellant and corrosion-erosion-, and wear-resistant characteristics |
| JP2002043397A (en) * | 2000-07-26 | 2002-02-08 | Hitachi Chem Co Ltd | Susceptor |
| US20080006207A1 (en) * | 2006-07-07 | 2008-01-10 | Tokyo Electron Limited | Heat-transfer structure and substrate processing apparatus |
| JP2012221987A (en) * | 2011-04-04 | 2012-11-12 | Shimadzu Corp | Substrate cart, thin film formation apparatus, and thin film formation apparatus for manufacturing solar cells |
| JP2013251367A (en) * | 2012-05-31 | 2013-12-12 | Shimadzu Corp | Plasma cvd deposition apparatus |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5595700A (en) * | 1979-01-11 | 1980-07-21 | Nec Corp | Vapor phase growing jig |
| JPS6317294A (en) * | 1986-07-08 | 1988-01-25 | Denki Kagaku Kogyo Kk | Glassy carbon coated susceptor and production thereof |
| JPS6447019A (en) * | 1987-08-18 | 1989-02-21 | Denki Kagaku Kogyo Kk | Glassy carbon coated susceptor |
-
1989
- 1989-03-28 JP JP1075777A patent/JPH0647516B2/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5595700A (en) * | 1979-01-11 | 1980-07-21 | Nec Corp | Vapor phase growing jig |
| JPS6317294A (en) * | 1986-07-08 | 1988-01-25 | Denki Kagaku Kogyo Kk | Glassy carbon coated susceptor and production thereof |
| JPS6447019A (en) * | 1987-08-18 | 1989-02-21 | Denki Kagaku Kogyo Kk | Glassy carbon coated susceptor |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0814174A1 (en) * | 1996-06-20 | 1997-12-29 | Qqc, Inc. | Glassy carbon coatings having water repellant and corrosion-erosion-, and wear-resistant characteristics |
| JP2002043397A (en) * | 2000-07-26 | 2002-02-08 | Hitachi Chem Co Ltd | Susceptor |
| US20080006207A1 (en) * | 2006-07-07 | 2008-01-10 | Tokyo Electron Limited | Heat-transfer structure and substrate processing apparatus |
| US8524005B2 (en) * | 2006-07-07 | 2013-09-03 | Tokyo Electron Limited | Heat-transfer structure and substrate processing apparatus |
| JP2012221987A (en) * | 2011-04-04 | 2012-11-12 | Shimadzu Corp | Substrate cart, thin film formation apparatus, and thin film formation apparatus for manufacturing solar cells |
| JP2013251367A (en) * | 2012-05-31 | 2013-12-12 | Shimadzu Corp | Plasma cvd deposition apparatus |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0647516B2 (en) | 1994-06-22 |
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