JPH0342824A - Reaction gas for etching - Google Patents

Reaction gas for etching

Info

Publication number
JPH0342824A
JPH0342824A JP17770989A JP17770989A JPH0342824A JP H0342824 A JPH0342824 A JP H0342824A JP 17770989 A JP17770989 A JP 17770989A JP 17770989 A JP17770989 A JP 17770989A JP H0342824 A JPH0342824 A JP H0342824A
Authority
JP
Japan
Prior art keywords
etching
gas
reaction gas
chamber
chcl2f
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
Application number
JP17770989A
Other languages
Japanese (ja)
Other versions
JPH088240B2 (en
Inventor
Isamu Hijikata
土方 勇
Akira Uehara
植原 晃
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tokyo Ohka Kogyo Co Ltd
Original Assignee
Tokyo Ohka Kogyo Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Tokyo Ohka Kogyo Co Ltd filed Critical Tokyo Ohka Kogyo Co Ltd
Priority to JP1177709A priority Critical patent/JPH088240B2/en
Publication of JPH0342824A publication Critical patent/JPH0342824A/en
Publication of JPH088240B2 publication Critical patent/JPH088240B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To enable a title item to be superb in etching rate and cleanness and deviation of selection ratio after etching and then to be miniaturized by using a mixed gas of at least one kind selected from CHCl2CF3, CH3CCl2F, CH2FCF3, and CHCl2F as a reaction gas. CONSTITUTION:A wafer 4 is set onto a table 5 within a chamber 3 and then a reaction gas, namely a mixed gas with at least one kind selected from SF6, CHCl2CF3, CH3CCl2F, CH2FCF3, and CHCl2F is introduced into a chamber 3 from a reaction gas supply source 9. At this time, blending ratio of the latter group of gas is set to 5-95vol.%.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は半導体ウェハー等の試料表面のエツチングに用
いる反応ガスに関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a reactive gas used for etching the surface of a sample such as a semiconductor wafer.

(従来の技術) LSIチップの製造工程の1つに、半導体ウェハー表面
にマスクを形成し、このマスクに覆われてない部分を反
応ガスによってエツチングする方法が従来から採用され
ている。
(Prior Art) As one of the manufacturing processes for LSI chips, a method has conventionally been adopted in which a mask is formed on the surface of a semiconductor wafer and the portions not covered by the mask are etched using a reactive gas.

具体的には特公昭50−9545号公報或いは特公昭5
3−34462号公報等にも開示されるように、マイク
ロ波によるプラズマ空間に試料をセットするとともに反
応ガスを導入し、更は該プラズマ空間に磁場を作用させ
ることで効率よくエツチングを行うようにした技術が知
られている。
Specifically, Special Publication No. 50-9545 or Special Publication No. 5
As disclosed in Publication No. 3-34462, etching can be carried out efficiently by setting a sample in a microwave plasma space, introducing a reaction gas, and applying a magnetic field to the plasma space. The technology is known.

そして、上記のプラズマ空間に導入される反応ガスとし
てCJZ2やCF4. SF6などのフロンガスやこれ
らの混合ガス等が使用されているが、加工精度エツチン
グレート、均−性及び選択比等の点でSF6+C2CJ
2 sFs (フレオン113) 、C2C互。F4が
盛んに使用されている。
CJZ2, CF4. Freon gases such as SF6 and mixtures of these gases are used, but SF6+C2CJ is preferred in terms of processing accuracy, etching rate, uniformity, and selectivity.
2 sFs (Freon 113), C2C mutual. F4 is widely used.

(発明が解決しようとする課題) 最近ではLSIチップの更なる高密度化が要求され、こ
のため従来の反応ガスよりもその特性において優れたも
のが不可欠となり、またフレオン113やC2Cj2 
、F4はオゾン層破壊の要因とも考えられているため、
製造禁止となり使用できなくなる可能性が大である。
(Problems to be Solved by the Invention) Recently, there has been a demand for higher density LSI chips, and for this reason, it has become essential to have a reaction gas that has better properties than conventional reactant gases, and Freon 113 and C2Cj2
, F4 is also considered to be a factor in ozone layer depletion, so
There is a high possibility that production will be prohibited and it will no longer be possible to use it.

(課題を解決するための手段) 上記課題を解決すべく本発明は、エツチング用反応ガス
をSF6と CHCfl 2CF5.CI(3CCj2
2F、CH2FCh及びCHCl2Fの中から選ばれた
少なくとも1種との混合ガスとし、しかも後者の群のガ
スの配合割合を5〜95vO196とした。
(Means for Solving the Problems) In order to solve the above problems, the present invention uses etching reaction gases of SF6 and CHCfl2CF5. CI(3CCj2
The gas was mixed with at least one selected from 2F, CH2FCh and CHCl2F, and the ratio of the latter group of gases was 5 to 95vO196.

(作用) CICjZ 2cFs、CHsCCIt 2F、CH2
FCF3及びC)ICj22Fの中から選ばれた少なく
とも1種とSF6との混合ガスを反応ガスとして用いる
ことで、エツチングレート、選択比、基板上の汚染など
の点において従来のC2cJ2sFsよりも好結果が得
られる。
(Action) CICjZ 2cFs, CHsCCIt 2F, CH2
By using a mixed gas of SF6 and at least one selected from FCF3 and C) ICj22F as a reactive gas, better results than conventional C2cJ2sFs can be obtained in terms of etching rate, selectivity, and contamination on the substrate. can get.

(実施例) 以下に本発明の実施例を添付図面に基づいて説明する。(Example) Embodiments of the present invention will be described below based on the accompanying drawings.

第1図は本発明に係る反応ガスを用いてエツチングを行
う装置の一例を示すものであり、エツチング装置はアー
スされた装置本体1の開口2上に合成石英からなるチャ
ンバー3を固定し、このチャンバー3内に試料としての
ウェハー4を七ッ卜するテーブル5を設け、このテーブ
ル5を13.55MHzの高周波電源6に接続している
。また、チャンバー3内をバルブ7を介して真空ポンプ
8につなげ、チャンバー3内を高真空状態にし得るよう
にするとともに、チャンバー3内には反応ガス供給源9
から本発明に係る反応ガス、即ちSF。
FIG. 1 shows an example of an apparatus for performing etching using a reactive gas according to the present invention. A table 5 on which a wafer 4 as a sample is placed is provided in the chamber 3, and the table 5 is connected to a high frequency power source 6 of 13.55 MHz. Further, the inside of the chamber 3 is connected to a vacuum pump 8 via a valve 7 so that the inside of the chamber 3 can be brought into a high vacuum state, and a reaction gas supply source 9 is provided inside the chamber 3.
to the reactive gas according to the present invention, namely SF.

と C)IcI 2cFs、(:LC(:422F、C
H2FCF3及び CHI2Fの中から選ばれた少なく
とも1種との混合ガスを導入するようにしている。
and C) IcI 2cFs, (:LC(:422F,C
A mixed gas with at least one selected from H2FCF3 and CHI2F is introduced.

また、チャンバー3は導波管10にて囲まれ、2.45
6)Izのマイクロ波発振器11からのマイクロ波(よ
ってチャンバー3内を放電空間つまりプラズマ発生空間
とし、更に導波管10の外側にはマイクロ波電界に直交
する方向の磁場を発生させるコイル12を配置している
Further, the chamber 3 is surrounded by a waveguide 10, and the chamber 3 is surrounded by a waveguide 10,
6) Microwaves from the microwave oscillator 11 of Iz (therefore, the inside of the chamber 3 is used as a discharge space, that is, a plasma generation space, and a coil 12 that generates a magnetic field in a direction perpendicular to the microwave electric field is installed outside the waveguide 10). It is placed.

以上の如き構成のエツチング装置を用いた具体的な実施
例を以下に述べる。
A specific example using the etching apparatus configured as described above will be described below.

哀凰璽ユ SF、とC)IC,e2Chの混合比を1:1どした混
合ガスの流量を36 secmとし、マイクロ波出力を
200W、高周波出力を100W、真空度を6 mTo
rrの条件下でポリシリコンをエツチングしたところ、
エツチング速度は5000人/minで表面に付着物の
ない異方性エツチングが得られた。
The flow rate of the mixed gas with a 1:1 mixing ratio of Aiou Seal SF, C) IC, and e2Ch was 36 sec, the microwave output was 200 W, the high frequency output was 100 W, and the degree of vacuum was 6 mTo.
When polysilicon was etched under rr conditions,
The etching speed was 5000 people/min, and anisotropic etching with no deposits on the surface was obtained.

また、ポリシリコンに代えてシリコン酸化膜をエツチン
グしたときのエツチング速度は第2図に示すとおりで、
第2図にはSF6と CHi 2C:F、の配合割合が
及ぼすエツチング速度の関係、及びポシリシリコン酸化
膜との選択エツチング比についても併せて示した。
Furthermore, the etching speed when etching a silicon oxide film instead of polysilicon is as shown in Figure 2.
FIG. 2 also shows the relationship between the etching rate and the mixing ratio of SF6 and CHi 2C:F, and the selective etching ratio with respect to the polysilicon oxide film.

これらの結果から本発明はエツチング速度、選択エツチ
ング比に優れ、基板にパーティクル等の付着物がなく、
実用性に富んだエツチングガスであることが確認できた
These results show that the present invention has excellent etching speed and selective etching ratio, and has no deposits such as particles on the substrate.
It was confirmed that this is a highly practical etching gas.

X徴里ユ 実施例1におけるCHCJZ2CF、に代えて、(:H
3CCJ2 zF、C)I2FCh、CHI、l12F
を使用しても同様な結果が得られた。
In place of CHCJZ2CF in Example 1, (:H
3CCJ2 zF, C) I2FCh, CHI, l12F
Similar results were obtained using .

犬亘里旦 SF、を10 sccmで、 C)ICj22Fを20
 sccmQ割合で流しながら、マイクロ波出力200
W、高周波出力100W、真空度8 mTorrの条件
下でポリシリコンをエツチングしたところ、エツチング
速度が2600人/ll1in  、均一性が3%であ
り、異方性に優れたエツチングが得られた。
Inuwaritan SF, 10 sccm, C) ICj22F, 20
Microwave output 200 while flowing at sccmQ rate
When polysilicon was etched under the conditions of W, high-frequency output of 100 W, and vacuum level of 8 mTorr, the etching rate was 2,600 people/11in, the uniformity was 3%, and etching with excellent anisotropy was obtained.

実施例4 実施例3におけるC1(J 2F 20 secmの代
りにCHCJ12F 10 sccm、 CHCJZ 
2CF3をt o sccmを用いた以外は同様の条件
でポリシリコンのエツチングを行ったが、は・とんとエ
ツチング結果に差異はなかった。
Example 4 C1 in Example 3 (CHCJ12F 10 sccm instead of J 2F 20 sec, CHCJZ
Polysilicon was etched under the same conditions except that 2CF3 was used at sccm, but there was no difference in the etching results.

塩旦男 実施例3におけるC)lcj22Fの代りにC2CJ2
3hを用いたところ、エツチング後にポリシリコン表面
にパーティクルの付着がみられた。
C2CJ2 instead of C) lcj22F in Shiotanman Example 3
When 3 hours were used, particles were observed to adhere to the polysilicon surface after etching.

以上総合的に判断すれば、SF8と CHCJ12Ch
Judging from the above, SF8 and CHCJ12Ch
.

CHsCCu 2F、C)12FCF3及びCHCu 
、Fの中から選ばれた少なくとも1種との混合ガスは従
来の混合ガスよりも優れ、且つ後者の群から選ばれたガ
スの配合割合は5〜95vo目とするのが好ましい。
CHsCCu 2F, C) 12FCF3 and CHCu
, F is superior to conventional mixed gases, and the blending ratio of the gas selected from the latter group is preferably 5 to 95 vo.

(発明の効果) 以上に説明した如く本発明に係るエツチング用反応ガス
は、従来の反応ガスに比べ、エツチングレート、エツチ
ング後の清浄性及び選択比のいずれにおいても優れ、更
なる微細化の要求に十分に応えることができ、処理室の
汚れも少なく、クリーンな処理が可能で安全上でも有利
である。
(Effects of the Invention) As explained above, the reaction gas for etching according to the present invention is superior to conventional reaction gases in terms of etching rate, cleanliness after etching, and selectivity, and is suitable for further refinement. It is advantageous in terms of safety because it can sufficiently respond to the needs of customers, has less dirt in the processing chamber, enables clean processing, and is also advantageous in terms of safety.

【図面の簡単な説明】[Brief explanation of drawings]

第1図はエツチング装置の概略図、第2図は本発明に係
る反応ガスを用いたときのガスの混合割合とエツチング
速度と、選択エツチング比との関係を示すグラフである
。 尚、図面中3はチャンバー 4はウェハー 8は真空ポ
ンプ、9は反応ガス供給源、11はマイクロ波発振器、
12はコイルである。 特 許 出 願 人  東京応化工業株式会社代 理 
人 弁理士   下  1)容−即問   弁理士  
 大  橋 邦 度量    弁理士    小  山
      省第2図
FIG. 1 is a schematic diagram of an etching apparatus, and FIG. 2 is a graph showing the relationship between gas mixing ratio, etching rate, and selective etching ratio when using the reactive gas according to the present invention. In the drawing, 3 is a chamber, 4 is a wafer, 8 is a vacuum pump, 9 is a reactant gas supply source, 11 is a microwave oscillator,
12 is a coil. Patent applicant: Tokyo Ohka Kogyo Co., Ltd. Agent
Person Patent Attorney Part 2 1) Yong-Immediate Question Patent Attorney
Kuni Ohashi Patent Attorney Koyama Ministry Figure 2

Claims (1)

【特許請求の範囲】[Claims]  試料をセットしたチャンバー内に導入されるエッチン
グ用反応ガスにおいて、この反応ガスはSF_6とCH
Cl_2CF_3CH_3CCl_2F,CH_2FC
F_3及びCHCl_2Fの中から選ばれた少なくとも
1種との混合ガスであり、後者の群のガスの配合割合は
5〜95vol%であることを特徴とするエッチング用
反応ガス。
In the etching reaction gas introduced into the chamber where the sample is set, this reaction gas contains SF_6 and CH
Cl_2CF_3CH_3CCl_2F, CH_2FC
A reactive gas for etching, characterized in that it is a mixed gas with at least one selected from F_3 and CHCl_2F, and the proportion of the latter group of gases is 5 to 95 vol%.
JP1177709A 1989-07-10 1989-07-10 Reactive gas for etching Expired - Lifetime JPH088240B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1177709A JPH088240B2 (en) 1989-07-10 1989-07-10 Reactive gas for etching

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1177709A JPH088240B2 (en) 1989-07-10 1989-07-10 Reactive gas for etching

Publications (2)

Publication Number Publication Date
JPH0342824A true JPH0342824A (en) 1991-02-25
JPH088240B2 JPH088240B2 (en) 1996-01-29

Family

ID=16035737

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1177709A Expired - Lifetime JPH088240B2 (en) 1989-07-10 1989-07-10 Reactive gas for etching

Country Status (1)

Country Link
JP (1) JPH088240B2 (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60115232A (en) * 1983-11-28 1985-06-21 Hitachi Ltd Dry etching gas
JPS61131456A (en) * 1984-11-30 1986-06-19 Canon Inc Dry etching gas for silicon compound

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60115232A (en) * 1983-11-28 1985-06-21 Hitachi Ltd Dry etching gas
JPS61131456A (en) * 1984-11-30 1986-06-19 Canon Inc Dry etching gas for silicon compound

Also Published As

Publication number Publication date
JPH088240B2 (en) 1996-01-29

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