JPH0262542A - Pellicle for excimer laser lithography - Google Patents
Pellicle for excimer laser lithographyInfo
- Publication number
- JPH0262542A JPH0262542A JP63214294A JP21429488A JPH0262542A JP H0262542 A JPH0262542 A JP H0262542A JP 63214294 A JP63214294 A JP 63214294A JP 21429488 A JP21429488 A JP 21429488A JP H0262542 A JPH0262542 A JP H0262542A
- Authority
- JP
- Japan
- Prior art keywords
- pellicle
- excimer laser
- film
- sio2
- substrate
- 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.)
- Pending
Links
- 238000001459 lithography Methods 0.000 title claims abstract description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 27
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 6
- 239000000758 substrate Substances 0.000 abstract description 13
- 238000002834 transmittance Methods 0.000 abstract description 12
- 229910052681 coesite Inorganic materials 0.000 abstract description 9
- 229910052906 cristobalite Inorganic materials 0.000 abstract description 9
- 239000000377 silicon dioxide Substances 0.000 abstract description 9
- 235000012239 silicon dioxide Nutrition 0.000 abstract description 9
- 229910052682 stishovite Inorganic materials 0.000 abstract description 9
- 229910052905 tridymite Inorganic materials 0.000 abstract description 9
- 239000000428 dust Substances 0.000 abstract description 4
- 239000013078 crystal Substances 0.000 abstract description 3
- 238000001312 dry etching Methods 0.000 abstract description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 abstract description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 abstract description 2
- 229910017604 nitric acid Inorganic materials 0.000 abstract description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 abstract 2
- 230000005540 biological transmission Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 238000009832 plasma treatment Methods 0.000 abstract 1
- 235000010288 sodium nitrite Nutrition 0.000 abstract 1
- 239000010408 film Substances 0.000 description 17
- 229910052710 silicon Inorganic materials 0.000 description 9
- 239000010703 silicon Substances 0.000 description 9
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 8
- 239000010409 thin film Substances 0.000 description 7
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 239000004065 semiconductor Substances 0.000 description 4
- 150000003376 silicon Chemical class 0.000 description 4
- 239000007789 gas Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000020 Nitrocellulose Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 210000003127 knee Anatomy 0.000 description 2
- 238000001755 magnetron sputter deposition Methods 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 2
- 101710179738 6,7-dimethyl-8-ribityllumazine synthase 1 Proteins 0.000 description 1
- 101710186608 Lipoyl synthase 1 Proteins 0.000 description 1
- 101710137584 Lipoyl synthase 1, chloroplastic Proteins 0.000 description 1
- 101710090391 Lipoyl synthase 1, mitochondrial Proteins 0.000 description 1
- 208000003251 Pruritus Diseases 0.000 description 1
- OBNDGIHQAIXEAO-UHFFFAOYSA-N [O].[Si] Chemical compound [O].[Si] OBNDGIHQAIXEAO-UHFFFAOYSA-N 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はエキシマレーザ−リソグラフィー用ペリクル、
特にはLSI、超LSIなどの半導体装置を製造すると
きに使用されるエキシマレーザ−光を用いる露光方式に
おける、このエキシマレーザ−リソグラフィー用のゴミ
よけ用ペリクルに関するものである。Detailed Description of the Invention (Industrial Application Field) The present invention relates to a pellicle for excimer laser lithography,
In particular, the present invention relates to a dust-preventing pellicle for excimer laser lithography in an exposure method using excimer laser light used when manufacturing semiconductor devices such as LSI and VLSI.
(従来の技術)
従来LS 1.超LSIの半導体装置の製造においては
、半導体ウェーハに光を照射してパターニングを作成す
るのであるが、この場合に用いられている露光原板にゴ
ミが付着していると、このゴミが光を吸収したり、ある
いは光を曲げてしまうために転写したパターニングが変
形したり、エツジががさついたものとなり、さらには白
地が黒く汚れたりして、寸法1品質ならびに外観が損な
われるという不利がある。(Conventional technology) Conventional LS 1. In the manufacturing of VLSI semiconductor devices, semiconductor wafers are irradiated with light to create patterns, but if there is dust attached to the exposure plate used in this case, this dust will absorb the light. Otherwise, the transferred patterning may be deformed due to the bending of the light, the edges may become rough, and the white background may become black and smeared, resulting in a disadvantage that the dimension quality and appearance are impaired.
そのため、この種の作業は通常クリーンルームで行なわ
れるのであるが、このクリーンルーム内でも露光原板を
常に清浄に保つことは難しいので。For this reason, this type of work is usually carried out in a clean room, but even within this clean room it is difficult to keep the exposed original plate clean at all times.
これには露光原板の表面にゴミよけのために露光用の光
をよく通過するニトロセルロースや酢酸セルロースなど
の薄膜をペリクルとして貼着するという方法が採られて
いるが、この種のペリクルは150〜300nmのよう
な短波長域では大きな吸収端がでてくるために半導体装
置の露光に波長が175〜300止であるエキシマレー
ザ−リソグラフィーを用いる場合には使用できないとい
う不利があり、このエキシマレーザ−リソグラフィー用
のペリクルの出現が求められている。This method involves attaching a thin film such as nitrocellulose or cellulose acetate, which allows the exposure light to pass easily, as a pellicle to the surface of the exposure plate to prevent dust. Because a large absorption edge appears in a short wavelength region such as 150 to 300 nm, there is a disadvantage that it cannot be used when using excimer laser lithography with a wavelength of 175 to 300 nm for exposure of semiconductor devices. There is a need for the advent of pellicles for laser lithography.
(発明の構成)
本発明は従来例における不利を解決したエキシマレーザ
−リソグラフィー用のペリクルに関するものであり、こ
れはエキシマレーザ−光(波長175〜300nm)を
用いる露光方式において酸化けい素膜をゴミよけ用ペリ
クルとして用いることを特徴とするものである。(Structure of the Invention) The present invention relates to a pellicle for excimer laser lithography that solves the disadvantages of the conventional example. It is characterized by being used as a shielding pellicle.
すなわち、本発明者らはエキシマレーザ−リソグラフィ
ー用のペリクルを開発すべく種々検討した結果、従来公
知のニトロセルロース、酢酸セルロースに代えて酸化け
い素膜をペリクルとして使用したところ、このものはエ
キシマレーザ−光をよく通過させるため、150〜30
0nmの短波長域でも大きな吸収端を生ずることがない
のでエキシマレーザ−リソグラフィー用のペリクルとし
て有用とされるということを見出し、このペリクルとし
ての酸化けい素薄膜の形状、構造、その製造方法などに
ついての研究を進めて本発明を完成させた。That is, as a result of various studies aimed at developing a pellicle for excimer laser lithography, the present inventors used a silicon oxide film as a pellicle in place of the conventionally known nitrocellulose and cellulose acetate. - 150-30 to allow light to pass through well
We discovered that it is useful as a pellicle for excimer laser lithography because it does not produce a large absorption edge even in the short wavelength range of 0 nm, and we have learned about the shape, structure, and manufacturing method of the silicon oxide thin film used as this pellicle. The present invention was completed by conducting research on the following.
本発明で用いられるペルクルとしての酸化けい素は薄膜
状のものとすればよいが、これはその厚さが0.5μm
よりうずいとメンブレン化したときの膜強度が不足し、
10μ騰より厚くなると光の透過率が低下するので0.
5〜10μ■の範囲のものとする必要があるが、この好
ましい範囲は1〜5μ騰とされる。The silicon oxide as the percle used in the present invention may be in the form of a thin film, which has a thickness of 0.5 μm.
It becomes more itchy and the membrane strength is insufficient when it is formed into a membrane.
If it becomes thicker than 10μ, the light transmittance will decrease, so 0.
It is necessary to have a thickness in the range of 5 to 10 .mu.m, and the preferred range is 1 to 5 .mu.m.
また、この酸化けい素薄膜は公知のプラズマCVD法で
または高周波マグネトロンスパッタ法などで作ることが
できるので、したがってこれは例えばシリコン単結晶な
どの基板上にSiH4ガスとN20ガスを流し、これを
プラズマCVD法で処理してSi結晶の両面に酸化けい
素(S iOW膜を形成させたのち、裏面のSiO□の
一部をCF4102などでドライエツチングし、ついで
HNO,、HF、NaN0.(7)混合液ニ浸漬シテS
i基板を選択エツチングすれば1表面のSiO2の自立
膜を容易にがっ安定して得ることができる。In addition, this silicon oxide thin film can be made by the well-known plasma CVD method or high frequency magnetron sputtering method, so it is possible to make this by flowing SiH4 gas and N20 gas onto a substrate such as silicon single crystal, and then plasma After forming a silicon oxide (SiOW) film on both sides of the Si crystal by CVD, a part of the SiO□ on the back side is dry etched with CF4102, etc., and then HNO, HF, NaN0.(7) Mixed liquid dipped shite S
By selectively etching the i-substrate, a self-supporting film of SiO2 on one surface can be easily and stably obtained.
このようにして得られた酸化けい素薄膜は紫外線透過率
が高く、波長が175〜3.0On+*であるエキシマ
レーザ−光もよく通過させるので、エキシマレーザ−リ
ソグラフィー用のペリクルとして特に有用とされる。The silicon oxide thin film obtained in this way has high ultraviolet transmittance and easily passes excimer laser light with a wavelength of 175 to 3.0 On+*, so it is considered to be particularly useful as a pellicle for excimer laser lithography. Ru.
つぎに本発明の実施例をあげる。Next, examples of the present invention will be given.
実施例1
厚さが400timの4インチのシリコン基板のく10
0>面に、S i H420C,C,、N、0 2,0
ooc、c、を流し、プラズマCVDにがけて厚さ2μ
−のSin、膜を形成させた。Example 1 4-inch silicon substrate 10 with a thickness of 400tim
0> side, S i H420C,C,,N,0 2,0
ooc, c, and subjected to plasma CVD to a thickness of 2μ
-, a film was formed.
ついてこのシリコン基板のフラットネス(BOW)をS
i O,@形成の前後でm定り、SiO,lliの残
留応力を測定したところ、これは3.3 X 109ダ
イン/dの引張応力であった。The flatness (BOW) of this silicon substrate is S
The residual stress of SiO,lli was measured before and after the i O,@ formation, and it was found to be a tensile stress of 3.3 x 109 dynes/d.
また、このシリコン基板については上記と同じ方法でそ
の裏面にも厚さ2」のSin、膜を形成させたのち、c
F、10aでドライエツチングして裏面のSiO□膜
中心部に50mm角の開口部を設け、これを95a+Q
のHNO3(65%)、5mQのHF (40%)と1
gのNaN0.の混合液に浸してシリコン基板を選択エ
ツチングしたところ。Furthermore, after forming a 2" thick Sin film on the back surface of this silicon substrate using the same method as above,
F, dry etching with 10a to create a 50 mm square opening in the center of the SiO□ film on the back side, and then dry etching with 95a+Q
of HNO3 (65%), 5 mQ of HF (40%) and 1
g of NaN0. A silicon substrate was selectively etched by immersing it in a mixed solution.
50m口の厚さ2t1MのS i O,膜の自立膜が得
られた。A self-supporting SiO film with a diameter of 50 m and a thickness of 2t1M was obtained.
つぎのこのものの紫外線透過率をしらべたところ、第1
図に示したとおりの結果が得られ、これに高さ5+m、
肉厚2■、60mφのアルミニウムを第2図に示したよ
うに接着して補強してペリクルを作成したところ、この
ものはKrFエキシマレーザ−光(249mn)で92
%の透過率を示した。When I investigated the ultraviolet transmittance of the following items, I found that
The results shown in the figure are obtained, and the height is 5+m,
A pellicle was made by gluing and reinforcing aluminum with a wall thickness of 2 mm and a diameter of 60 m as shown in Figure 2. This pellicle was 92 mm thick with KrF excimer laser light (249 mm).
% transmittance.
実施例2
実施例1におけるSiHいN、OガスをS i H42
0C,C,,0,20C,C,としたほかは実施例1と
同様に処理したところ、シリコン基板の表面に厚さ0.
511MのSiO2膜が形成された。Example 2 The SiH N, O gas in Example 1 was replaced with SiH42
0C,C,,0,20C,C was treated in the same manner as in Example 1, except that the surface of the silicon substrate had a thickness of 0.
A 511M SiO2 film was formed.
ついで、このシリコン基板の裏面に上記と同様の方法で
厚さ0.5pのSiO□膜を形成させ、以下実施例1と
同様に処理して厚さ0.51のS i O,膜の自立膜
を作り、このものの紫外線透過率を測定したところ、第
1図に併記したとおりの結果が得られ、これから実施例
1と同様の方法で作成したペリクルはArFエキシマレ
ーザ−光193+an)で74%の透過率を示した。Next, a SiO□ film with a thickness of 0.5p was formed on the back surface of this silicon substrate in the same manner as described above, and then treated in the same manner as in Example 1 to form a SiO□ film with a thickness of 0.51p and the film to be self-supporting. When a film was made and the ultraviolet transmittance of this material was measured, the results shown in Fig. 1 were obtained, and a pellicle made from this in the same manner as in Example 1 was 74% irradiated with ArF excimer laser light (193 + an). It showed a transmittance of .
実施例3
実施例1で使用したシリコン基板上に、S i 、 H
,2QCoC,,0,50C,C,のガスを流し、ニー
に13.56MHzの高周波を印加し、高周波マグネト
ロンスパッター法でこシに厚さ5μmのS i O2膜
を形成させたところ、このSin、膜の残留反応は引張
応力で1.lX10’ダイン/dであった。Example 3 On the silicon substrate used in Example 1, S i , H
,2QCoC,,0,50C,C, was flowed, a high frequency of 13.56 MHz was applied to the knee, and a 5 μm thick SiO2 film was formed on the knee using high frequency magnetron sputtering. , the residual reaction of the film is 1. due to tensile stress. It was 1×10′ dynes/d.
ついで、このシリコンの裏面に上記と同様の方法で厚さ
5pのSiO□膜を形成させ、以下実施例1と同様に処
理して厚さ5−のSiO□膜の自立膜を作り、この紫外
線透過率を測定したところ。Next, a SiO□ film with a thickness of 5p is formed on the back surface of this silicon in the same manner as described above, and the following treatment is performed in the same manner as in Example 1 to form a self-supporting film of a SiO□ film with a thickness of 5−1. The transmittance was measured.
第1図に併記したとおりの結果が得られ、これから実施
例1と同様の方法で作成したペリクルはArFエキシマ
レーザ−光(193nm)で48%の透過率を示した。The results shown in FIG. 1 were obtained, and a pellicle prepared using the same method as in Example 1 exhibited a transmittance of 48% with ArF excimer laser light (193 nm).
第1図は本発明のペリクルとしての酸化けい製薄膜の紫
外線透過率を示すグラフ、第2図は本発明の酸素けい製
薄膜ペリクルの構造を示す縦断面図、第3図は従来公知
のニトロセルロースペリクルの光線透過率を示すグラフ
である。
7゜
一−◆追長(nm)
第1図
第2図
Al1管
第3図FIG. 1 is a graph showing the ultraviolet transmittance of a silicon oxide thin film as a pellicle of the present invention, FIG. 2 is a longitudinal cross-sectional view showing the structure of the oxygen silicon thin film pellicle of the present invention, and FIG. It is a graph showing the light transmittance of a cellulose pellicle. 7゜1-◆Additional length (nm) Fig. 1 Fig. 2 Al1 tube Fig. 3
Claims (1)
化けい素膜をゴミよけ用ペリクルとして用いてなること
を特徴とするエキシマレーザーリソグラフィー用ペリク
ル。 2、酸化けい素膜が厚さ0.5〜10μmのものである
請求項1に記載のエキシマレーザーリソグラフィー用ペ
リクル。 3、エキシマレーザー光が波長175〜300nmのも
のである請求項1に記載のエキシマレーザーリソグラフ
ィー用ペリクル。[Scope of Claims] 1. A pellicle for excimer laser lithography, characterized in that a silicon oxide film is used as a dust-proof pellicle in an exposure method using excimer laser light. 2. The pellicle for excimer laser lithography according to claim 1, wherein the silicon oxide film has a thickness of 0.5 to 10 μm. 3. The pellicle for excimer laser lithography according to claim 1, wherein the excimer laser light has a wavelength of 175 to 300 nm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63214294A JPH0262542A (en) | 1988-08-29 | 1988-08-29 | Pellicle for excimer laser lithography |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63214294A JPH0262542A (en) | 1988-08-29 | 1988-08-29 | Pellicle for excimer laser lithography |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0262542A true JPH0262542A (en) | 1990-03-02 |
Family
ID=16653345
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63214294A Pending JPH0262542A (en) | 1988-08-29 | 1988-08-29 | Pellicle for excimer laser lithography |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0262542A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6368683B1 (en) | 1999-04-02 | 2002-04-09 | Shin-Etsu Chemical Co., Ltd. | Pellicle for photolithography |
JP2009116284A (en) * | 2007-10-18 | 2009-05-28 | Shin Etsu Chem Co Ltd | Pellicle and method for manufacturing pellicle |
JP2009271262A (en) * | 2008-05-02 | 2009-11-19 | Shin Etsu Chem Co Ltd | Pellicle and method of producing pellicle |
JP2009282298A (en) * | 2008-05-22 | 2009-12-03 | Shin-Etsu Chemical Co Ltd | Pellicle and method for manufacturing pellicle |
JP2018531426A (en) * | 2015-10-22 | 2018-10-25 | エーエスエムエル ネザーランズ ビー.ブイ. | Method for manufacturing a pellicle for a lithographic apparatus, pellicle for a lithographic apparatus, lithographic apparatus, device manufacturing method, apparatus for processing a pellicle, and method for processing a pellicle |
US10488751B2 (en) * | 2014-09-19 | 2019-11-26 | Mitsui Chemicals, Inc. | Pellicle, production method thereof, exposure method |
US10585348B2 (en) | 2014-09-19 | 2020-03-10 | Mitsui Chemicals, Inc. | Pellicle, pellicle production method and exposure method using pellicle |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6235359A (en) * | 1985-08-09 | 1987-02-16 | Daicel Chem Ind Ltd | Production of coated thin film |
JPS63262651A (en) * | 1987-04-21 | 1988-10-28 | Seiko Epson Corp | Photomask protective film |
-
1988
- 1988-08-29 JP JP63214294A patent/JPH0262542A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6235359A (en) * | 1985-08-09 | 1987-02-16 | Daicel Chem Ind Ltd | Production of coated thin film |
JPS63262651A (en) * | 1987-04-21 | 1988-10-28 | Seiko Epson Corp | Photomask protective film |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6368683B1 (en) | 1999-04-02 | 2002-04-09 | Shin-Etsu Chemical Co., Ltd. | Pellicle for photolithography |
JP2009116284A (en) * | 2007-10-18 | 2009-05-28 | Shin Etsu Chem Co Ltd | Pellicle and method for manufacturing pellicle |
JP2009271262A (en) * | 2008-05-02 | 2009-11-19 | Shin Etsu Chem Co Ltd | Pellicle and method of producing pellicle |
JP2009282298A (en) * | 2008-05-22 | 2009-12-03 | Shin-Etsu Chemical Co Ltd | Pellicle and method for manufacturing pellicle |
US10488751B2 (en) * | 2014-09-19 | 2019-11-26 | Mitsui Chemicals, Inc. | Pellicle, production method thereof, exposure method |
US10585348B2 (en) | 2014-09-19 | 2020-03-10 | Mitsui Chemicals, Inc. | Pellicle, pellicle production method and exposure method using pellicle |
JP2018531426A (en) * | 2015-10-22 | 2018-10-25 | エーエスエムエル ネザーランズ ビー.ブイ. | Method for manufacturing a pellicle for a lithographic apparatus, pellicle for a lithographic apparatus, lithographic apparatus, device manufacturing method, apparatus for processing a pellicle, and method for processing a pellicle |
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