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JPS6210305B2 - - Google Patents
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JPS6210305B2 - - Google Patents

Info

Publication number
JPS6210305B2
JPS6210305B2 JP22865382A JP22865382A JPS6210305B2 JP S6210305 B2 JPS6210305 B2 JP S6210305B2 JP 22865382 A JP22865382 A JP 22865382A JP 22865382 A JP22865382 A JP 22865382A JP S6210305 B2 JPS6210305 B2 JP S6210305B2
Authority
JP
Japan
Prior art keywords
etching
electrode
sample
reaction gas
chamber
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
Application number
JP22865382A
Other languages
Japanese (ja)
Other versions
JPS59123770A (en
Inventor
Eiichi Hoshino
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.)
Fujitsu Ltd
Original Assignee
Fujitsu 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 Fujitsu Ltd filed Critical Fujitsu Ltd
Priority to JP22865382A priority Critical patent/JPS59123770A/en
Publication of JPS59123770A publication Critical patent/JPS59123770A/en
Publication of JPS6210305B2 publication Critical patent/JPS6210305B2/ja
Granted legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J37/00Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
    • H01J37/32Gas-filled discharge tubes
    • H01J37/32431Constructional details of the reactor
    • H01J37/3244Gas supply means

Landscapes

  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Plasma & Fusion (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • ing And Chemical Polishing (AREA)

Description

【発明の詳細な説明】 (1) 発明の技術分野 本発明はエツチング方法、詳しくはドライエツ
チングにおいてエツチングを均一性をもたせて実
施する方法に関する。
DETAILED DESCRIPTION OF THE INVENTION (1) Technical Field of the Invention The present invention relates to an etching method, and more particularly to a method for performing dry etching with uniformity.

(2) 技術の背景 例えばウエハの露光に用いるマスクは、ガラス
基板全面上にクロム(Cr)膜を、次いで全面に
レジスト膜を塗布形成し、このレジスト膜をパタ
ーニングして得られるパターンをマスクにして
Cr膜をエツチングしてクロムのパターンを形成
することによつて作られる。
(2) Background of the technology For example, a mask used for exposing a wafer is made by coating a chromium (Cr) film on the entire surface of a glass substrate, then coating the entire surface with a resist film, and then patterning this resist film to use the resulting pattern as a mask. hand
It is made by etching a Cr film to form a chromium pattern.

上記したエツチング(リアクテイブイオンエツ
チング)は第1図に示されるカソードカツプリン
グ方式のドライエツチング装置内で、プラズマ化
された反応ガスを用いて行うもので、同図におい
て、1はエツチング室(チエンバ)、2は円板状
の平行平板型の対向電極(アノード)、3は電極
(カソード)、4は試料例えばマスク、5は絶縁
体、6は高周波電源、7はエツチングのための反
応ガスをチエンバ1内に供給するリング状に配置
された反応ガス導入管、8は反応ガス排気口を示
す。マスク全面上には前記したCr膜が形成され
ており、それをレジストパターンをマスクにして
リアクテイブイオンエツチングでパターニングす
るのである。クロムのエツチングにおいては、例
えば反応ガスとして四塩化炭素ガス(CCl4)を
120SCCM、酸素ガス(O2)を70SCCMの導入量で
供給する。
The above-mentioned etching (reactive ion etching) is carried out using a plasma reactive gas in a cathode coupling type dry etching apparatus shown in FIG. ), 2 is a disk-shaped parallel plate counter electrode (anode), 3 is an electrode (cathode), 4 is a sample such as a mask, 5 is an insulator, 6 is a high frequency power source, and 7 is a reactive gas for etching. A reaction gas introduction pipe arranged in a ring shape is supplied into the chamber 1, and reference numeral 8 indicates a reaction gas exhaust port. The aforementioned Cr film is formed on the entire surface of the mask, and is patterned by reactive ion etching using the resist pattern as a mask. In etching chromium, for example, carbon tetrachloride gas (CCl 4 ) is used as the reaction gas.
120SCCM, and oxygen gas (O 2 ) is supplied at an introduction rate of 70SCCM.

(3) 従来技術と問題点 上記したエツチングは、リアクテイブイオンエ
ツチングに耐性をもつたチエンバを用いてなされ
るのであるが、第1に、ガス導入管7がチエンバ
1内で異常放電が発生する原因となつている問題
がある。かかる異常放電は、例えばレジストパタ
ーンをマスクにしてクロムをエツチングするとき
の選択比すなわち(クロムのエツチング速度)/
(レジストのエツチング速度)に悪影響を及ぼ
し、レジスト膜を厚く形成する必要が生じ、レジ
スト膜を厚くすると、レジスト膜の描画精度が低
下し、クロム膜のパターンが乱れる結果となる。
(3) Prior Art and Problems The above-mentioned etching is carried out using a chamber resistant to reactive ion etching. There is a problem causing it. Such abnormal discharge is caused by, for example, the selectivity ratio when etching chromium using a resist pattern as a mask, that is, (chromium etching speed)/
This adversely affects (the etching speed of the resist), and it becomes necessary to form a thick resist film, and when the resist film is made thicker, the writing accuracy of the resist film decreases, resulting in a disordered pattern of the chromium film.

次に、前記したエツチングにおいては、エツチ
ングの均一性(uniformity)が要求される。エツ
チング速度が試料の各場所毎に異なるものであれ
ば、レジスト膜の損失に差異が生じ、レジストパ
ターンが細るとクロムのパターンが細くなり、最
後に形成されるクロムパターンが乱れて均一でな
くなる。
Next, in the etching described above, etching uniformity is required. If the etching rate is different for each location on the sample, there will be differences in the loss of the resist film, and as the resist pattern becomes thinner, the chromium pattern will become thinner, and the chromium pattern that is finally formed will be disordered and not uniform.

エツチングに用いる反応ガス、例えばクロムの
エツチングの際に用いる(CCl4+O2)ガスは、チ
エンバ1内を流れている間にプラズマ化される。
このプラズマ化にはそれぞれの場合に応じて所定
の時間を要するので、チエンバ1内での反応ガス
の滞留時間の長短がエツチングの均一性に重大な
影響をもつ。従来の装置において、反応ガスの滞
留時間は排気口8の近くにおいては短く、反対側
においては長く、これを試料から見ると、その上
方の反応ガスの滞留時間が均一でないことにな
る。そこで、反応ガスの空間移動速度
(spacevelocity)を遅くし、試料上での反応ガス
の滞留時間を均一に長くしたいのであるが、従来
の装置ではそれの実現は容易ではなかつた。
A reactive gas used for etching, for example (CCl 4 +O 2 ) gas used for etching chromium, is turned into plasma while flowing inside the chamber 1 .
Since this plasma formation requires a certain amount of time depending on each case, the length of residence time of the reaction gas in the chamber 1 has a significant influence on the uniformity of etching. In the conventional apparatus, the residence time of the reaction gas is short near the exhaust port 8 and long on the opposite side, and when viewed from the sample, this means that the residence time of the reaction gas above the exhaust port 8 is not uniform. Therefore, it is desired to slow down the space velocity of the reaction gas and uniformly lengthen the residence time of the reaction gas on the sample, but this has not been easy to achieve with conventional equipment.

(4) 発明の目的 本発明は上記従来の問題点に鑑み、リアクテイ
ブイオンエツチングに耐性をもつたエツチングチ
エンバを用いるドライエツチングにおいて、反応
ガスの試料上の滞留時間を均一性に長くし、それ
によつて均一性をもつたリアクテイブイオンエツ
チングを行いうるエツチング方法を提供すること
を目的とする。
(4) Purpose of the Invention In view of the above-mentioned conventional problems, the present invention provides a method for uniformly increasing the residence time of a reactive gas on a sample in dry etching using an etching chamber resistant to reactive ion etching. It is an object of the present invention to provide an etching method capable of performing reactive ion etching with uniformity.

(5) 発明の構成 そしてこの目的は本発明によれば、チエンバ内
に対向して設けられた1対の電極のうち一方の電
極上にエツチングされる試料を載置し、かつ該一
方の電極とほぼ同一平面の位置で前記電極を囲ん
で配置された反応ガス導入管から他方の電極の方
向に反応ガスを噴出させ、該反応ガスを活性化し
てリアクテイブイオンエツチングを行うことを特
徴とするエツチング方法を提供することによつて
達成される。
(5) Structure of the Invention According to the present invention, a sample to be etched is placed on one of a pair of electrodes provided in a chamber facing each other, and A reactive ion etching is performed by ejecting a reactive gas in the direction of the other electrode from a reactive gas inlet tube arranged around the electrode at a position substantially in the same plane as the other electrode, and activating the reactive gas. This is accomplished by providing an etching method.

(6) 発明の実施例 以下本発明実施例を図面によつて詳述する。(6) Examples of the invention Embodiments of the present invention will be described in detail below with reference to the drawings.

本発明者は前記した問題を検討した結果、チエ
ンバ内に配置された試料の上に反応ガスを可能な
かぎり長く滞留させるために、排気口8による反
応ガスの排気の影響を少なくする方法を考えつい
た。かかる方法を実施するための装置は第2図に
概略断面図に示され、同図において第1図に示し
た部分と同じ部分は同一符号を付して示す。
As a result of studying the above-mentioned problems, the present inventor came up with a method for reducing the effect of exhausting the reaction gas through the exhaust port 8 in order to make the reaction gas stay above the sample placed in the chamber for as long as possible. Ta. An apparatus for carrying out such a method is shown in a schematic cross-sectional view in FIG. 2, in which parts that are the same as those shown in FIG. 1 are designated with the same reference numerals.

第2図に示す装置においては、ガス導入管7
を、従来の装置における場合よりも排気口8から
遠ざけて、マスク4が配置される側の電極3とほ
ぼ同一平面の位置に、電極3を囲む如くに配置す
る。そのために、反応ガス導入管7は、絶縁体5
を囲んで設けられたフランジ9の内に埋め込む。
しかも、反応ガス導入管は、マスク4の配置され
たチエンバの部分の平面図である第3図に示され
る如く、電極3を載置した絶縁体5を囲む如くに
配置した、反応ガスは、第2図に見て上方に噴出
する構成とする。
In the device shown in FIG.
are arranged so as to surround the electrode 3, at a position substantially flush with the electrode 3 on the side where the mask 4 is arranged, and further away from the exhaust port 8 than in the conventional device. For this purpose, the reaction gas introduction pipe 7 has an insulator 5
It is embedded in a flange 9 provided surrounding the flange 9.
Moreover, as shown in FIG. 3, which is a plan view of the part of the chamber where the mask 4 is placed, the reaction gas introduction tube is arranged so as to surround the insulator 5 on which the electrode 3 is placed. As shown in Fig. 2, the structure is such that it ejects upward.

反応ガスを上記の如き配置の導入管から噴出さ
せると、反応ガスのマスク上の滞留時間が長くな
り、活性プラズマが発生し易くなり、しかもプラ
ズマ化した反応ガスは排気口8による排気によつ
てほとんど影響されないから、マスク4上を均一
の空間移動速度で動き、エツチングはマスク4の
全面にわたつて均一に行われる。
When the reactive gas is ejected from the inlet pipe arranged as described above, the residence time of the reactive gas on the mask becomes longer and active plasma is more likely to be generated. Since it is almost unaffected, it moves on the mask 4 at a uniform spatial velocity, and etching is performed uniformly over the entire surface of the mask 4.

(7) 発明の効果 以上詳細に説明したように、本発明の方法によ
ると、反応ガスの滞留時間が長くなり、活性化プ
ラズマが試料上全体にわたつて発生し易くなり、
かつ、反応ガスはチエンバの排気口から最も遠い
ところで噴出されるため、前記したプラズマ化し
たガスは試料上を均一に流れ、ドライエツチング
が試料全面にわたつて均一に行われるので、例え
ばパターンがすべての場所で均一に形成され、製
造される半導体装置の信頼性向上に効果大であ
る。
(7) Effects of the invention As explained in detail above, according to the method of the present invention, the residence time of the reaction gas becomes longer, and activated plasma is more likely to be generated over the entire surface of the sample.
In addition, since the reaction gas is ejected at the farthest point from the exhaust port of the chamber, the above-mentioned plasma gas flows uniformly over the sample, and dry etching is performed uniformly over the entire surface of the sample. This is highly effective in improving the reliability of manufactured semiconductor devices.

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

第1図は従来のリアクテイブイオンエツチング
のチエンバの概略断面図、第2図は本発明の方法
を実施するチエンバの概略断面図、第3図は第2
図の装置の試料の載置された部分の平面図であ
る。 1……チエンバ、2……対向電極(アノー
ド)、3……電極(カソード)、4……マスク、5
……絶縁体、6……高周波電源、7……反応ガス
導入管、8……反応ガス排気口、9……フラン
ジ。
FIG. 1 is a schematic sectional view of a conventional reactive ion etching chamber, FIG. 2 is a schematic sectional view of a chamber implementing the method of the present invention, and FIG.
FIG. 3 is a plan view of a portion of the illustrated apparatus on which a sample is placed; 1... Chamber, 2... Counter electrode (anode), 3... Electrode (cathode), 4... Mask, 5
... Insulator, 6 ... High frequency power supply, 7 ... Reaction gas introduction pipe, 8 ... Reaction gas exhaust port, 9 ... Flange.

Claims (1)

【特許請求の範囲】[Claims] 1 チエンバ内に対向して設けられた1対の電極
のうち一方の電極上にエツチングされる試料を載
置し、かつ該一方の電極とほぼ同一平面の位置で
前記電極を囲んで配置された反応ガス導入管から
他方の電極の方向に反応ガスを噴出させ、該反応
ガスを活性化してリアクテイブイオンエツチング
を行うことを特徴とするエツチング方法。
1. A sample to be etched is placed on one of a pair of electrodes provided facing each other in the chamber, and the sample is placed surrounding the electrode at a position substantially on the same plane as the one electrode. An etching method characterized in that reactive ion etching is performed by ejecting a reactive gas from a reactive gas introduction tube in the direction of the other electrode and activating the reactive gas.
JP22865382A 1982-12-28 1982-12-28 Etching method Granted JPS59123770A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22865382A JPS59123770A (en) 1982-12-28 1982-12-28 Etching method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22865382A JPS59123770A (en) 1982-12-28 1982-12-28 Etching method

Publications (2)

Publication Number Publication Date
JPS59123770A JPS59123770A (en) 1984-07-17
JPS6210305B2 true JPS6210305B2 (en) 1987-03-05

Family

ID=16879703

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22865382A Granted JPS59123770A (en) 1982-12-28 1982-12-28 Etching method

Country Status (1)

Country Link
JP (1) JPS59123770A (en)

Also Published As

Publication number Publication date
JPS59123770A (en) 1984-07-17

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