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JP2834129B2 - Low temperature dry etching method - Google Patents
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JP2834129B2 - Low temperature dry etching method - Google Patents

Low temperature dry etching method

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Publication number
JP2834129B2
JP2834129B2 JP63067385A JP6738588A JP2834129B2 JP 2834129 B2 JP2834129 B2 JP 2834129B2 JP 63067385 A JP63067385 A JP 63067385A JP 6738588 A JP6738588 A JP 6738588A JP 2834129 B2 JP2834129 B2 JP 2834129B2
Authority
JP
Japan
Prior art keywords
etching
gas
temperature
dry etching
silicon
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.)
Expired - Fee Related
Application number
JP63067385A
Other languages
Japanese (ja)
Other versions
JPH01241126A (en
Inventor
和典 辻本
新一 田地
定之 奥平
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.)
Hitachi Ltd
Original Assignee
Hitachi 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 Hitachi Ltd filed Critical Hitachi Ltd
Priority to JP63067385A priority Critical patent/JP2834129B2/en
Publication of JPH01241126A publication Critical patent/JPH01241126A/en
Application granted granted Critical
Publication of JP2834129B2 publication Critical patent/JP2834129B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は低温ドライエツチング方法に係り、特に、異
方性エツチングの達成できる試料温度範囲を、SF6のみ
用いる場合より高くでき、エツチング制御性を向上でき
る方法に関する。
Description: TECHNICAL FIELD The present invention relates to a low-temperature dry etching method, and in particular, a sample temperature range in which anisotropic etching can be achieved can be made higher than when only SF 6 is used, and etching controllability can be improved. And how it can be improved.

〔従来の技術〕[Conventional technology]

従来のシリコンエツチングでは、特開昭61−8926ある
いはジヤーナル・オブ・バニユーム・サイエンス・アン
ド・テクノロジー(Journal of Vacuum Science and Te
chnology)B5(2)Mar/Apr1987 P594に記載のように、
CF4,CBrF3等の堆積性ガスを主に用いている。これらの
ガスプラズマ中でエツチング側面に膜が形成され、サイ
ドエツチングが防止されることを利用して異方性エツチ
ングを行つていた。また、上記ガスの他に、さらに積極
的に膜を堆積させるための添加ガスを加える場合もあつ
た。
Conventional silicon etching is disclosed in Japanese Patent Application Laid-Open No. 61-8926 or Journal of Vacuum Science and Technology.
chnology) B5 (2) As described in Mar / Apr1987 P594,
Deposition gases such as CF 4 and CBrF 3 are mainly used. A film is formed on the side surface of the etching in these gas plasmas, and anisotropic etching is performed by utilizing the fact that side etching is prevented. In some cases, in addition to the above gases, an additive gas for more positively depositing a film is added.

〔発明が解決しようとする課題〕[Problems to be solved by the invention]

上記従来技術においては、エツチング側面に炭素系化
合物、酸化シリコン、アルミニウム系化合物等の膜が付
着することが明らかにされていた。これらの付着膜はド
ライエツチング後にも残存するので、膜除去のための後
処理が必要である等の問題があつた。また、付着膜の種
類、あるいは量によつては後処理によつても除去が困難
であることもあり、後工程において異物や汚染のもとに
なつていた。
In the above prior art, it has been clarified that a film of a carbon-based compound, silicon oxide, an aluminum-based compound, or the like adheres to the etching side surface. Since these adhered films remain after dry etching, there is a problem that post-treatment for removing the films is required. In addition, depending on the type or amount of the adhered film, it may be difficult to remove the film by post-processing, and this has caused foreign matter and contamination in the post-process.

同様のエツチング方法はSi以外のドライエツチングに
も広く用いられており、典型例としては、CCl4ガスによ
るアルミニウムのエツチング等がある。いずれの場合に
も、少なからず汚染等の問題が有り、好ましくはこの種
の膜形成されるガスを用いないことが良いが、従来技術
によるとこの種の非堆積性ガスによる異方性エツチング
は困難であつた。
The same etching method is widely used for dry etching other than Si, and a typical example is etching of aluminum with CCl 4 gas. In any case, there is a considerable problem of contamination and the like, and it is preferable not to use a gas for forming this kind of film. However, according to the prior art, anisotropic etching with this kind of non-depositing gas is difficult. It was difficult.

本発明の目的は、エツチング後にエツチング側面に付
着膜が残存しない方法で、異方性エツチングを達成する
ことにある。
An object of the present invention is to achieve anisotropic etching by a method in which an adhered film does not remain on an etching side surface after etching.

〔課題を解決するための手段〕[Means for solving the problem]

上記目的は、低温時にエツチング側面に付着し、室温
では揮発性になる物質を側壁保護膜として形成しながら
低温ドライエツチングすることによつて達成される。す
なわち、低温ドライエツチング時の温度における蒸気圧
が真空処理室内の圧力以下であり、室温における蒸気圧
が真空処理室内の圧力以上である物質を側壁保護膜とし
て用いる。具体例としては、SiCl4等を適用することが
できる。SiCl4は第2図の蒸気圧のグラフからわかるよ
うに、たとえば通常のエツチングガス圧力の範囲、0.1T
orrにおいて、約一100℃で吸着が始まる。したがつて、
試料温度を−100℃以下にすれば、この吸着層はエツチ
ング側面を被うサイドエツチング防止膜として働く。エ
ツチング後、試料を昇進する過程で、真空処理室内圧力
がたとえば0.2Torrであれば、約−100℃でSiCl4は蒸発
するので、汚染源となるようは膜な残らない。
The above object is achieved by performing low-temperature dry etching while forming a material which adheres to the etching side surface at low temperature and becomes volatile at room temperature as a side wall protective film. That is, a material whose vapor pressure at the time of low-temperature dry etching is lower than the pressure in the vacuum processing chamber and whose vapor pressure at room temperature is higher than the pressure in the vacuum processing chamber is used as the side wall protective film. As a specific example, SiCl 4 or the like can be applied. As can be seen from the vapor pressure graph of FIG. 2, for example, SiCl 4 is in a normal etching gas pressure range of 0.1 T
At orr, adsorption begins at about 1100 ° C. Therefore,
When the sample temperature is set to -100 ° C or lower, this adsorption layer functions as a side-etching prevention film covering the etching side surface. If the pressure in the vacuum processing chamber is, for example, 0.2 Torr during the process of elevating the sample after etching, SiCl 4 evaporates at about −100 ° C., so that no film remains as a contamination source.

〔作用〕[Action]

Siエツチングを例にとつて本発明の作用を詳しく説明
する。フツ素系ガスを用いてSiをエツチングする場合、
フツ素の活性粒子とSiが反応し、SiF4を形成して蒸発す
る。SiF4の蒸気圧は第2図のごとく、室温においては充
分高いので、室温では非常に早い速度でエツチングでき
る。反面、エツチング側面も反応しやすいのでサイドエ
ツチングを生ずる。試料を低温にするとSiF4の蒸気圧は
しだいに下がり、エツチング側面の反応が抑えられて異
方性エツチングが可能となるが、最適温度は−120〜−1
50℃と非常に低い。
The operation of the present invention will be described in detail by taking Si etching as an example. When etching Si using fluorine-based gas,
The active particles of fluorine react with Si to form SiF 4 and evaporate. Since the vapor pressure of SiF 4 is sufficiently high at room temperature as shown in FIG. 2, etching can be performed at a very high speed at room temperature. On the other hand, the side surface of the etching is also easily reacted, so that side etching occurs. When the sample is cooled to a low temperature, the vapor pressure of SiF 4 gradually decreases, and the reaction on the etching side is suppressed to enable anisotropic etching, but the optimum temperature is -120 to -1.
Very low at 50 ° C.

上記フツ素系ガスに塩素系ガスを混合すると、SiF4
他にSiCl4が生成される。SiCl4はSiF4よりも50〜80℃高
い温度で蒸発するので、上記エツチング条件において
は、SiCl4がSi表面に吸着し、第1図のようにサイドエ
ツチングを防止する保護膜として働く。したがつて、第
2図の斜線で示した条件に設定することによつて、異方
性エツチングが達成される。この最適温度範囲は、上記
フツ素系ガスのみを用いる場合より50〜80℃高いため、
試料温度の制御、および装置構造の点で信頼性が向上し
た。なお、上記のフツ素系ガスおよび塩素系ガスは汚染
防止の点からは非堆積性ガスでなければならないが、堆
積性ガスを用いても上記の作用は達成される。
When a chlorine-based gas is mixed with the above-mentioned fluorine-based gas, SiCl 4 is generated in addition to SiF 4 . Since SiCl 4 evaporates at a temperature higher by 50 to 80 ° C. than SiF 4 , under the above etching conditions, SiCl 4 is adsorbed on the Si surface and acts as a protective film for preventing side etching as shown in FIG. Accordingly, the anisotropic etching is achieved by setting the conditions shown by the oblique lines in FIG. This optimum temperature range is 50 to 80 ° C. higher than when only the above-mentioned fluorine-based gas is used,
The reliability was improved in the control of the sample temperature and the structure of the device. Note that the above-mentioned fluorine-based gas and chlorine-based gas must be non-sedimentary gases from the viewpoint of preventing pollution, but the above-mentioned effects can be achieved by using a sedimentary gas.

〔実施例〕〔Example〕

以下、本発明の実施例を説明する。 Hereinafter, embodiments of the present invention will be described.

[実施例] 真空処理室内に設けられた冷却試料台上にSiウエーハ
を設置し、液体窒素を用いて該ウエーハを−100℃に冷
却した。真空処理室内にSF6ガスCl2ガスを8:2の割合で
導入し、13.56MHZの高周波で放電した。ガス圧力を約0.
15Torr、ガス流量を約20cc/minとした。この時、Siウエ
ーハは約1μm/minの速度でエツチングされ、サイドエ
ツチングもほとんど検出されない(0.03μm)異方性エ
ツチングを達成できた。エツチング終了後、該Siウエー
ハを該処理室とは別の真空予備室に搬送し、そこでヒー
ターにより室温(約20℃)まで昇温した後大気中に搬出
した。その後、酸素プラズマによるレジストアツシング
工程を終た。アツシング後のSiウエーハを観察した結
果、後工程で障害となる異物や汚染は認められず、汚染
防止のための後処理は不要であることがわかつた。
[Example] An Si wafer was placed on a cooling sample stage provided in a vacuum processing chamber, and the wafer was cooled to -100 ° C using liquid nitrogen. A vacuum processing chamber with SF 6 gas Cl 2 gas 8: was introduced at a rate of 2, and discharging at a high frequency of 13.56MH Z. Gas pressure about 0.
The gas flow rate was 15 Torr and the gas flow rate was about 20 cc / min. At this time, the Si wafer was etched at a speed of about 1 μm / min, and anisotropic etching in which almost no side etching was detected (0.03 μm) was achieved. After the etching was completed, the Si wafer was transferred to a vacuum preparatory chamber separate from the processing chamber, where the temperature was raised to room temperature (about 20 ° C.) by a heater, and then transferred to the atmosphere. Thereafter, the resist assuring step using oxygen plasma was completed. As a result of observing the Si wafer after assuring, it was found that there was no foreign matter or contamination that would hinder the subsequent process, and that no post-treatment was required to prevent the contamination.

上記エツチング条件は変更可能であり、ガス圧力やガ
ス流量、入力パワー等の設定条件によつて、異方性エツ
チングの得られる試料温度範囲は、−50〜−120℃に変
わつた。
The above-mentioned etching conditions can be changed, and the sample temperature range in which anisotropic etching can be obtained is changed to -50 to -120 ° C depending on setting conditions such as gas pressure, gas flow rate, and input power.

上記の処理ガスは他の種類のものでも良く、フツ素系
ガスとしてはNF3,BF3,F2塩素系ガスとしてSiCl4,BCl3
用いてもほぼ同様の効果の得られることが認められた。
The above processing gas may be of another type, and it is recognized that almost the same effect can be obtained by using NF 3 , BF 3 , F 2 as a fluorine-based gas and SiCl 4 , BCl 3 as a chlorine-based gas. Was done.

〔発明の効果〕〔The invention's effect〕

本発明によれば、エツチング終了後、室温において蒸
発する物質を側壁保護膜として利用するので、汚染や異
物が問題とならない清浄なドライエツチングプロセスを
実現できる効果がある。しかも、エツチング速度が早
く、異方性のエツチングを容易に達成できる。
According to the present invention, a substance that evaporates at room temperature after etching is used as a side wall protective film, so that there is an effect that a clean dry etching process free from contamination and foreign matter can be realized. In addition, the etching speed is high, and anisotropic etching can be easily achieved.

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

第1図は本発明の効果を説明するための模式図、第2図
はSiCl4の蒸気圧と温度との関係を示すグラフである。 1……エツチングマスク、2……エツチング側面(たと
えばSi)、3……エツチング底面、4……反応生成物
(たとえばSiF4)、5……側面吸着物(たとえばSiC
l4)、6……イオン。
FIG. 1 is a schematic diagram for explaining the effect of the present invention, and FIG. 2 is a graph showing the relationship between the vapor pressure of SiCl 4 and the temperature. 1 Etching mask, 2 Etching side (for example, Si), 3 Etching bottom, 4 Reaction product (for example, SiF 4 ), 5.
l 4 ), 6 ... Ion.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭60−158627(JP,A) 特開 昭62−92324(JP,A) 特開 昭61−187238(JP,A) (58)調査した分野(Int.Cl.6,DB名) H01L 21/3065──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-60-158627 (JP, A) JP-A-62-292324 (JP, A) JP-A-61-187238 (JP, A) (58) Field (Int.Cl. 6 , DB name) H01L 21/3065

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】処理室内のシリコンを−120℃よりも高い
温度である第1の温度に冷却し、 フッ素系のエッチングガスと、塩素系の添加ガスとを前
記処理室内に導入し、 前記添加ガスと前記シリコンとを反応させ、前記シリコ
ンの側面に側壁保護膜を形成し、かつ前記エッチングガ
スにより前記シリコンをエッチングし、 前記第1の温度から室温に昇温させ、前記側壁保護膜を
揮発させて、前記シリコンをエッチング加工することを
特徴とするドライエッチング方法。
A first step of cooling silicon in the processing chamber to a first temperature higher than -120 ° C., introducing a fluorine-based etching gas and a chlorine-based additive gas into the processing chamber; Reacting a gas with the silicon to form a sidewall protection film on the side surface of the silicon, and etching the silicon with the etching gas; elevating the temperature from the first temperature to room temperature to volatilize the sidewall protection film; And dry etching the silicon.
【請求項2】前記第1の温度は−50℃以下であることを
特徴とする特許請求の範囲第1項記載のドライエッチン
グ方法。
2. The dry etching method according to claim 1, wherein said first temperature is -50 ° C. or lower.
JP63067385A 1988-03-23 1988-03-23 Low temperature dry etching method Expired - Fee Related JP2834129B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63067385A JP2834129B2 (en) 1988-03-23 1988-03-23 Low temperature dry etching method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63067385A JP2834129B2 (en) 1988-03-23 1988-03-23 Low temperature dry etching method

Publications (2)

Publication Number Publication Date
JPH01241126A JPH01241126A (en) 1989-09-26
JP2834129B2 true JP2834129B2 (en) 1998-12-09

Family

ID=13343481

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63067385A Expired - Fee Related JP2834129B2 (en) 1988-03-23 1988-03-23 Low temperature dry etching method

Country Status (1)

Country Link
JP (1) JP2834129B2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5356515A (en) * 1990-10-19 1994-10-18 Tokyo Electron Limited Dry etching method
TW204411B (en) * 1991-06-05 1993-04-21 Tokyo Electron Co Ltd
JP2884054B2 (en) * 1995-11-29 1999-04-19 工業技術院長 Fine processing method
WO2008007944A1 (en) * 2006-07-12 2008-01-17 Technische Universiteit Eindhoven Method and device for treating a substrate by means of a plasma
JP5499920B2 (en) * 2010-06-09 2014-05-21 住友電気工業株式会社 Manufacturing method of semiconductor optical device

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0626208B2 (en) * 1985-02-14 1994-04-06 株式会社東芝 Dry etching method
JPS6292324A (en) * 1985-10-18 1987-04-27 Toshiba Corp Dry etching method

Also Published As

Publication number Publication date
JPH01241126A (en) 1989-09-26

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