JPH02297931A - Vapor-phase etching method - Google Patents
Vapor-phase etching methodInfo
- Publication number
- JPH02297931A JPH02297931A JP28254489A JP28254489A JPH02297931A JP H02297931 A JPH02297931 A JP H02297931A JP 28254489 A JP28254489 A JP 28254489A JP 28254489 A JP28254489 A JP 28254489A JP H02297931 A JPH02297931 A JP H02297931A
- Authority
- JP
- Japan
- Prior art keywords
- substrate
- gas
- etching
- reactive gas
- electrode
- 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
- 238000005530 etching Methods 0.000 title claims abstract description 42
- 238000000034 method Methods 0.000 title claims description 15
- 239000012808 vapor phase Substances 0.000 title claims description 5
- 239000000758 substrate Substances 0.000 claims description 37
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 239000007789 gas Substances 0.000 abstract description 39
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 abstract description 16
- 230000005684 electric field Effects 0.000 abstract description 11
- 229910052786 argon Inorganic materials 0.000 abstract description 8
- 238000007599 discharging Methods 0.000 abstract 1
- 230000001105 regulatory effect Effects 0.000 abstract 1
- 239000004065 semiconductor Substances 0.000 description 10
- 238000001020 plasma etching Methods 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- GVGCUCJTUSOZKP-UHFFFAOYSA-N nitrogen trifluoride Chemical compound FN(F)F GVGCUCJTUSOZKP-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 229910002601 GaN Inorganic materials 0.000 description 1
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 238000001994 activation Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910021417 amorphous silicon Inorganic materials 0.000 description 1
- 238000004380 ashing Methods 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 230000005281 excited state Effects 0.000 description 1
- 230000005669 field effect Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910052743 krypton Inorganic materials 0.000 description 1
- DNNSSWSSYDEUBZ-UHFFFAOYSA-N krypton atom Chemical compound [Kr] DNNSSWSSYDEUBZ-UHFFFAOYSA-N 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052754 neon Inorganic materials 0.000 description 1
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 1
- 150000002829 nitrogen Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- 229910021332 silicide Inorganic materials 0.000 description 1
- -1 silicide metals Chemical class 0.000 description 1
- 150000003376 silicon Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Landscapes
- ing And Chemical Polishing (AREA)
- Drying Of Semiconductors (AREA)
Abstract
Description
【発明の詳細な説明】
r発明の利用分野1
本発明は、ターボ分子ボシプを用いて不要反応性気体を
排気させつつ電子サイクロトロン共鳴を用い、エツチン
グ用反応性気体を活性化または分解せしめ、さらにエツ
チングされるべき基板表面に垂直方向に高周波または直
流電界を同時に加えることにより、基板または基板上の
被エツチング材料に異方性エツチングを行わしめる気相
エツチング方法に関する。Detailed Description of the Invention Field of Application of the Invention 1 The present invention utilizes electron cyclotron resonance to activate or decompose a reactive gas for etching while exhausting unnecessary reactive gas using a turbo molecular boss. The present invention relates to a vapor phase etching method in which a substrate or a material to be etched on a substrate is anisotropically etched by simultaneously applying a high frequency or direct current electric field perpendicularly to the surface of the substrate to be etched.
「従来技術1
気相エツチング反応によるエツチング(気相化学的除去
方法)技術として、高周波または直流電界により反応性
気体を活性にさせるプラズマエツチング法(グロー放電
エツチング法)が知られている。"Prior Art 1" As an etching technique (vapor phase chemical removal method) using a gas phase etching reaction, a plasma etching method (glow discharge etching method) in which a reactive gas is activated by a high frequency or a direct current electric field is known.
しかし、かかるグロー放電を用いる異方性エツチング法
においては、被膜の異方性が超LSIの進歩に比べて十
分でな(、さらにその異方性エツチングの精度をさらに
向上することが求められていた。However, in the anisotropic etching method using such glow discharge, the anisotropy of the film is insufficient compared to the progress of VLSI (furthermore, there is a need to further improve the accuracy of the anisotropic etching). Ta.
他方、電子サイクロトロン共鳴を用いたエツチング法が
知られている。しかしかかる方法は被膜全体のエツチン
グを行うことを可とするが、選択的な異方性エツチング
には不充分であった。なぜなら、共鳴により反応性気体
が基板表面に平行に移動するため、凹部での形成がほと
んど不可能であり、加えて共鳴させる時、例えば共鳴原
子としてアルゴンを用い、周波数を2.45GIIzと
すると、875ガウスの強磁場を必要とする。このため
磁場作用の空心コイルが大きくなりがちで、励起気体を
大面積に広げることができない。結果として、サブミク
ロン(1μ以下例えば0.2μ)の巾または径を有し、
深さが2〜4μを有する穴状のエツチングはまったく不
可能であった。On the other hand, an etching method using electron cyclotron resonance is known. However, although such a method allows etching of the entire film, it is insufficient for selective anisotropic etching. This is because the reactive gas moves parallel to the substrate surface due to resonance, so it is almost impossible to form it in a recess.In addition, when creating resonance, for example, if argon is used as the resonant atom and the frequency is set to 2.45 GIIz, Requires a strong magnetic field of 875 Gauss. For this reason, the air-core coil that acts on the magnetic field tends to be large, making it impossible to spread the excited gas over a large area. As a result, it has a width or diameter of submicron (less than 1μ, e.g. 0.2μ),
Hole-like etching with a depth of 2 to 4 microns was not possible at all.
r問題を解決すべき手段」
本発・明はこれらの問題を解決するため、反応性気体の
活性化はサイクロトロン共鳴を用いて行う。Means to Solve the r Problem" In order to solve these problems, the present invention uses cyclotron resonance to activate the reactive gas.
このため、電子または活性化気体によりエツチング用反
応性気体の活性化、分解または反応がきわめて効率よく
行うことができる。この活性状態の気体をグロー放電が
行われている雰囲気に導き、共鳴エネルギの共鳴がな(
なった後も活性状態を持続し、かつこの電界を基板に垂
直とすることによりその方向性を与え、基板または基板
上の被エツチング材料を異方性エツチングさせんとする
もので、基板上部にサブミクロンレベルでも十分深い凹
部を有し得るようにしたものである。Therefore, activation, decomposition, or reaction of the reactive gas for etching can be carried out extremely efficiently using electrons or activated gas. This active gas is introduced into the atmosphere where the glow discharge is occurring, and the resonance energy is released (
The purpose is to maintain the active state even after the etching has occurred, and to give directionality to the electric field by making it perpendicular to the substrate, thereby anisotropically etching the substrate or the material to be etched on the substrate. It is possible to have a sufficiently deep recess even at a submicron level.
1作用」
するとこのプラズマグロー放電の技術により、活性状態
の気体は広い空間に広げられ、このため広い面積にわた
って基板または基板上の被エツチング材料を多量に高精
度の異方性エツチングを場所的なバラツキもなく均一に
行うことが可能となる。1 effect.'' This plasma glow discharge technology spreads the active gas over a wide space, allowing a large amount of highly accurate anisotropic etching to be performed locally over a wide area of the substrate or the material to be etched on the substrate. It becomes possible to perform the process uniformly without any variation.
本発明においてはグロー放電用電源としては直流電源を
用いた。しかし高周波グロー放電であっても励起した反
応性気体の励起状態を持続し、同時に作られるセルフバ
イアスにより異方性エツチングを行うことができる。In the present invention, a DC power source was used as the glow discharge power source. However, even with high-frequency glow discharge, the excited state of the excited reactive gas can be maintained, and anisotropic etching can be performed by the self-bias created at the same time.
さらにサイクロトロン共鳴は不活性気体または非生成物
気体(分解または反応をしてもそれ自体は気体しか生じ
ない気体)を用いる。不活性気体としてはアルゴンが代
表的なものである。しかしヘリューム、ネオン、クリプ
トンを用いてもよい。Furthermore, cyclotron resonance uses an inert gas or a non-product gas (a gas that itself produces only a gas when decomposed or reacted). Argon is a typical inert gas. However, helium, neon, or krypton may also be used.
エツチング用非生成物反応性気体としては、CF、。The non-product reactive gas for etching is CF.
CFJz、CFH+、CFJ、CCl4.弗化窒素(N
F3.N2F6)、弗化水素(HF) 、弗素(h)、
塩化水素01CI)、塩素(ch)またはこれらにキャ
リアガスまたは酸素を混合した気体が代表的なものであ
る。CFJz, CFH+, CFJ, CCl4. Nitrogen fluoride (N
F3. N2F6), hydrogen fluoride (HF), fluorine (h),
Typical examples include hydrogen chloride (01CI), chlorine (ch), or a mixture of these with a carrier gas or oxygen.
これらの非生成物エツチング気体をサイクロトロン共鳴
をさせて活性化せしめ、この共鳴領域より外部の反応空
間で生成物気体と混合し、励起エネルギを生成物気体に
移す。するとエツチング用気体にきわめて大きい電磁エ
ネルギを受けるため、はぼ100χ活性化または分解さ
せることができ、かつ異方性エツチングをするための電
界により加速されて基板上に所定の角度一般には基板に
垂直に衝突しエツチング反応をする。さらに室′a〜3
00℃の温度で基板を加熱することにより、この基板ま
たは基板上の被エツチング材料を異方性エツチングさせ
ることができる。These non-product etching gases are activated by cyclotron resonance, mixed with the product gas in a reaction space outside the resonance region, and excitation energy is transferred to the product gas. As the etching gas receives an extremely large electromagnetic energy, the etching gas can be activated or decomposed by approximately 100 χ, and is accelerated by the electric field for anisotropic etching and etched onto the substrate at a predetermined angle, generally perpendicular to the substrate. collides with and causes an etching reaction. Furthermore, rooms 'a~3
By heating the substrate at a temperature of 0.000C, the substrate or the material to be etched on the substrate can be anisotropically etched.
以下に実施例に従い本発明を示す。The present invention will be illustrated below with reference to Examples.
実施例1
第1図は本発明のサイクロトロン共鳴型プラズマエッチ
ング装置の概要を示す。Example 1 FIG. 1 shows an outline of a cyclotron resonance type plasma etching apparatus of the present invention.
図面において、ステンレス容器(1°)は蓋(1”)を
有し反応空間(1)を構成させている。この容器(1゛
)は、上部に基板(10)を基板ホルダ(10’)に設
け、その裏側の蓋(1”)側にはハロゲンランプヒータ
(7)を設け、基板の装着の時はI(1”)を上方向に
開けて行う。石英窓(19)を通して赤外線を基板に照
射し加熱している。さらにこの基板の裏側に一つの網状
電極(20°)と容器(1°)の下部には他の一方の網
状電極(20)とを有せしめ、ここに高周波または直流
電源(6)より13.56MHzまたは直流の電界を加
える。基板(10)はこの電界に垂直に第1図では位置
させている。In the drawing, a stainless steel container (1°) has a lid (1") and constitutes a reaction space (1). This container (1°) has a substrate (10) on the top and a substrate holder (10'). A halogen lamp heater (7) is installed on the back side of the lid (1"), and when mounting the board, open I (1") upwards. Infrared rays are emitted through the quartz window (19). The substrate is irradiated and heated.Furthermore, one mesh electrode (20°) is provided on the back side of this substrate, and the other mesh electrode (20) is provided at the bottom of the container (1°). Alternatively, a 13.56 MHz or DC electric field is applied from a DC power source (6).The substrate (10) is positioned perpendicular to this electric field in FIG.
また非生成物気体をドーピング系(13)より(18)
を経て石英管(29)で作られた共鳴空間(2)に供給
する。この共鳴空間はその外側に空心コイル(5)。In addition, the non-product gas is extracted from the doping system (13) (18)
It is then supplied to the resonant space (2) made of a quartz tube (29). This resonant space has an air-core coil (5) outside it.
(5゛)を配し磁場を加える。同時にマイクロ波発振器
(3)によりアナライザー(′4)を経て例えば2.4
5GHzのマイクロ波が共鳴空間(2)に供給される。(5゛) and apply a magnetic field. At the same time, for example, 2.4
5 GHz microwave is supplied to the resonant space (2).
この空間では共鳴を起こすべく非生成物気体をアルゴン
とするとその質量、周波数により決められた磁場(例え
ば875ガウス)が空心コイルにより加えられる。In this space, when the non-product gas is argon, a magnetic field (for example, 875 Gauss) determined by its mass and frequency is applied by an air-core coil in order to cause resonance.
このため、アルゴンガスが励起して磁場によりビンチン
グすると同時に共鳴し、十分励起した後に反応空間(1
)へ電子および励起したアルゴンガスとして放出(21
)される。この空間の出口にはエツチング用気体がドー
ピング系(13°)の系(16)を経て複数のリング状
ノズル(17)により放出(22)される。その結果、
エツチング用気体(22)は非生成物気体(21)によ
り励起され、活性化する。加えて一対の電極(20)
、 (20’ )により生じた電界が同時にこれら反応
性気体に加えられる。For this reason, the argon gas is excited and resonates at the same time as it is binned by the magnetic field, and after being sufficiently excited, the reaction space (1
) is released as electrons and excited argon gas (21
) to be done. At the outlet of this space, etching gas is discharged (22) through a doping system (13°) system (16) by a plurality of ring-shaped nozzles (17). the result,
The etching gas (22) is excited and activated by the non-product gas (21). In addition, a pair of electrodes (20)
, (20') is simultaneously applied to these reactive gases.
その結果、この電界にそって活性化した気体は飛翔し、
基板を選択的にエツチングさせることができる。As a result, the activated gas flies along this electric field,
The substrate can be selectively etched.
また反応性気体を十分反応室で広げ、かつサイクロトロ
ンをさせるため、反応空間(1)、共鳴空間(2)の圧
力を1〜10−4torr例えば0.03〜0.001
torrとした。この圧力は排気系(11)のコントロ
ールバルブ(14)によりターボポンプを併用して真空
ポンプ(9)の排気量を調整して行った。In addition, in order to sufficiently spread the reactive gas in the reaction chamber and to activate the cyclotron, the pressure in the reaction space (1) and resonance space (2) is set to 1 to 10-4 torr, for example 0.03 to 0.001.
It was set to torr. This pressure was achieved by adjusting the displacement of the vacuum pump (9) using a turbo pump together with the control valve (14) of the exhaust system (11).
実験例1
この実験例は実施例1を用い、シリコン半導体を弗化窒
嶽にてエツチングさせたものである。Experimental Example 1 In this experimental example, Example 1 was used, and a silicon semiconductor was etched using fluorinated nitrogen.
即ち反応空間の圧力0.003Lorr 、非生成物気
体として(18)よりアルゴンを50cc/分で供給し
た。That is, the pressure in the reaction space was 0.003 Lorr, and argon was supplied as a non-product gas from (18) at a rate of 50 cc/min.
加えて、NF3を(16)より20cc/分で供給した
。電界は自己バイアスが加わった13.56MHzの高
周波電界を加えた。マイクロ波は2.45GIIzの周
波数を有し、30〜500−の出力例えば200−で調
整した。磁場(5) 、 (5°)の共鳴強度は875
ガウスとした。In addition, NF3 was supplied from (16) at 20 cc/min. A high frequency electric field of 13.56 MHz to which a self-bias was added was applied as an electric field. The microwave had a frequency of 2.45 GIIz and was adjusted with a power of 30-500-, for example 200-. The resonance intensity of the magnetic field (5), (5°) is 875
Gaussian.
基板(lO)はシリコン半導体とし、その上面には選択
的にフォトレジストがコーティングされているものを用
いた。この非単結晶半導体例えばアモルファスシリコン
半導体を除去し、不要気体を排気系(11)より放出し
な。するとエツチング速度15人/秒を得ることができ
た。この速度はプラズマエツチングのみで得られる5人
/秒に比べ3倍の速さである。またこのシリコン基板上
に0.3μの巾のレジストによるパターンを切っておく
と、0゜3μ巾深さ4μの異方性エツチングを得ること
ができた。The substrate (lO) was a silicon semiconductor whose upper surface was selectively coated with photoresist. This non-single crystal semiconductor, such as an amorphous silicon semiconductor, is removed and unnecessary gases are discharged from the exhaust system (11). As a result, it was possible to obtain an etching speed of 15 people/second. This speed is three times faster than the 5 per second obtained with plasma etching alone. Furthermore, by cutting a resist pattern with a width of 0.3μ on this silicon substrate, it was possible to obtain anisotropic etching with a width of 0°3μ and a depth of 4μ.
さらにこれを異方性エツチングの後反応性気体を除去し
、かわりに酸素を導入し、このエツチング後二の表面に
残っているレジストをアッシングして除去することは有
効である。Furthermore, it is effective to remove the reactive gas after anisotropic etching, introduce oxygen instead, and remove the resist remaining on the second surface by ashing after this etching.
r効果1
本発明は、以上の説明より明らかなごとく、大面積の基
板または基板上の被エツチング材料を異方性エツチング
をするにあたり、被エツチング面の損傷をきわめて少な
くして成就させることができた。加えて、サイクロトロ
ン共鳴を用いているため、大きいエツチング速度を得る
ことができる。r Effect 1 As is clear from the above description, the present invention can perform anisotropic etching of a large area substrate or a material to be etched on a substrate with extremely little damage to the surface to be etched. Ta. In addition, since cyclotron resonance is used, a high etching rate can be obtained.
本発明のエツチング方法は半導体装置である光電変換装
置、発光素子、旧S、FET(電界効果半導体装置)、
SL素子(スーパーラティス素子)、Il叶T素子およ
び超LSIに十分応用し得る。さらに、その他生導体レ
ーザまたは光集積回路に対しても本発明は有効である。The etching method of the present invention is applied to semiconductor devices such as photoelectric conversion devices, light emitting devices, old S, FET (field effect semiconductor devices),
It can be fully applied to SL elements (super lattice elements), IlO T elements, and very large scale integrated circuits. Furthermore, the present invention is also effective for other live conductor lasers or optical integrated circuits.
本発明のサイクロトロン共鳴を用いたエツチング方法に
おいて、同時に光エネルギを加え光エッチングを併用さ
せることは有効である。特に光源として低圧水銀灯では
なくエキシマレーザ(波長100〜400nm) 、ア
ルゴンレーザ、窒素レーザ等を用い共鳴波長を選択する
ことは有効である。In the etching method using cyclotron resonance of the present invention, it is effective to simultaneously apply optical energy and perform optical etching. In particular, it is effective to use an excimer laser (wavelength: 100 to 400 nm), argon laser, nitrogen laser, etc. as a light source instead of a low-pressure mercury lamp, and select a resonant wavelength.
本発明において、エツチングされるべき基板としてはシ
リコン半導体、ガラス基板、ステンレス基板が主たるも
のである。しかし、加えて■−■化合物例えばGaAs
、GaAlAs、 InP、GaN等、またアルミニュ
ーム、珪化物金属も用い得る。In the present invention, the substrates to be etched are mainly silicon semiconductors, glass substrates, and stainless steel substrates. However, in addition ■-■ compounds such as GaAs
, GaAlAs, InP, GaN, aluminum, and silicide metals may also be used.
又本発明のエツチング方法は単結晶半導体のみではなく
非単結晶半導体、例えばアモルファス半導体を5t(7
)みならず5iGei−x (0<X<1)、5iOz
−x(0<X<2)、5ixC+−x (0<X<1)
、5kJ4−x (0<X<4) に対しても有効であ
る。Furthermore, the etching method of the present invention etches not only single crystal semiconductors but also non-single crystal semiconductors, such as amorphous semiconductors.
) as well as 5iGei-x (0<X<1), 5iOz
-x (0<X<2), 5ixC+-x (0<X<1)
, 5kJ4-x (0<X<4).
さらに第1図において、基板を下側または垂直構造とし
、サイクロトロンおよび電界を上方向より下方向または
横方向に放出してもよい。Further, in FIG. 1, the substrate may be in a lower or vertical structure, and the cyclotron and electric field may be emitted downward or laterally from the upper direction.
第1図は本発明のサイクロトロン共鳴型プラズマエツチ
ング装置を示す。FIG. 1 shows a cyclotron resonance type plasma etching apparatus of the present invention.
Claims (1)
エッチング用反応性気体を導入するとともに、前記容器
内の圧力を1〜10^−^4torrに保持するため、
ターボ分子ポンプを用いた真空排気系により排気量を調
整しつつ、不要反応性気体を排気することにより、基板
の裏面に配設された一方の電極と、該電極とは離れて設
けられた他方の電極との間にバイアスを加えつつ高周波
または直流エネルギを加えることにより前記反応性気体
をプラズマグロー放電させることにより前記基板または
基板上の被エッチング材料にサブミクロン(1μm以下
)の巾または径を有する異方性エッチングを行うことを
特徴とする気相エッチング方法。 2、空心コイルの内部にはマイクロ波を供給することに
よりサイクロトロン共鳴を生ぜしめる共鳴空間を構成せ
しめ、この共鳴空間と連結された反応空間を有する容器
内にハロゲン元素を発生するエッチング用反応性気体を
導入するとともに、前記容器内の圧力を1〜10^−^
4torrに保持するため、ターボ分子ポンプを用いた
真空排気系により排気量を調整しつつ不要反応性気体を
排気することにより、基板の裏面に配設させた一方の電
極と、該電極とは離れて設けられた他方の電極との間に
バイアスを加えつつ高周波または直流エネルギを加える
ことにより前記反応性気体をプラズマグロー放電させる
ことにより前記基板または基板上の被エッチング材料を
サブミクロン(1μm以下)の巾または径の異方性エッ
チングを行うことを特徴とする気相エッチング方法。[Claims] 1. In order to introduce a reactive gas for etching that generates a halogen element into a container having a reaction space, and to maintain the pressure inside the container at 1 to 10^-^4 torr,
By evacuating unnecessary reactive gas while adjusting the exhaust volume using a vacuum evacuation system using a turbo molecular pump, one electrode disposed on the back surface of the substrate and the other disposed apart from the electrode are separated. A submicron (1 μm or less) width or diameter is formed on the substrate or the material to be etched on the substrate by causing a plasma glow discharge of the reactive gas by applying high frequency or direct current energy while applying a bias between the substrate and the electrode. A vapor phase etching method characterized by performing anisotropic etching. 2. A resonant space that generates cyclotron resonance is formed inside the air-core coil by supplying microwaves, and a reactive gas for etching that generates a halogen element is contained in a container that has a reaction space connected to this resonant space. was introduced, and the pressure inside the container was increased to 1 to 10^-^.
In order to maintain the pressure at 4 torr, one electrode disposed on the back side of the substrate is separated from the other electrode by adjusting the exhaust volume and exhausting unnecessary reactive gas using a vacuum exhaust system using a turbo molecular pump. The substrate or the material to be etched on the substrate is etched into submicron (1 μm or less) by causing plasma glow discharge in the reactive gas by applying high frequency or direct current energy while applying a bias between the substrate and the other electrode provided on the substrate. A vapor phase etching method characterized by performing anisotropic etching with a width or diameter of .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1282544A JP2564664B2 (en) | 1989-10-30 | 1989-10-30 | Vapor phase etching method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1282544A JP2564664B2 (en) | 1989-10-30 | 1989-10-30 | Vapor phase etching method |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP22808185A Division JPS6289882A (en) | 1985-10-14 | 1985-10-14 | Vapor phase etching method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02297931A true JPH02297931A (en) | 1990-12-10 |
| JP2564664B2 JP2564664B2 (en) | 1996-12-18 |
Family
ID=17653853
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1282544A Expired - Fee Related JP2564664B2 (en) | 1989-10-30 | 1989-10-30 | Vapor phase etching method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2564664B2 (en) |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5779621A (en) * | 1980-11-05 | 1982-05-18 | Mitsubishi Electric Corp | Plasma processing device |
| JPS5813627A (en) * | 1981-06-16 | 1983-01-26 | モンサント・カンパニ− | Acid halide functional substance and acyl lactam functional substance |
| JPS60198394A (en) * | 1984-03-21 | 1985-10-07 | Anelva Corp | Gas discharging device in vacuum disposer |
| JPS617245U (en) * | 1984-06-15 | 1986-01-17 | 株式会社日立製作所 | Oil intrusion prevention device for oil-supplied vacuum pump direct-coupled generators |
| JPS6289882A (en) * | 1985-10-14 | 1987-04-24 | Semiconductor Energy Lab Co Ltd | Vapor phase etching method |
-
1989
- 1989-10-30 JP JP1282544A patent/JP2564664B2/en not_active Expired - Fee Related
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5779621A (en) * | 1980-11-05 | 1982-05-18 | Mitsubishi Electric Corp | Plasma processing device |
| JPS5813627A (en) * | 1981-06-16 | 1983-01-26 | モンサント・カンパニ− | Acid halide functional substance and acyl lactam functional substance |
| JPS60198394A (en) * | 1984-03-21 | 1985-10-07 | Anelva Corp | Gas discharging device in vacuum disposer |
| JPS617245U (en) * | 1984-06-15 | 1986-01-17 | 株式会社日立製作所 | Oil intrusion prevention device for oil-supplied vacuum pump direct-coupled generators |
| JPS6289882A (en) * | 1985-10-14 | 1987-04-24 | Semiconductor Energy Lab Co Ltd | Vapor phase etching method |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2564664B2 (en) | 1996-12-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4689112A (en) | Method and apparatus for dry processing of substrates | |
| US4190488A (en) | Etching method using noble gas halides | |
| Samukawa et al. | Time‐modulated electron cyclotron resonance plasma discharge for controlling generation of reactive species | |
| US4699689A (en) | Method and apparatus for dry processing of substrates | |
| EP0379301B1 (en) | Method of stripping organic material | |
| EP0714119B1 (en) | Pattern forming process and process for preparing semiconductor device utilizing said pattern forming process | |
| US4687544A (en) | Method and apparatus for dry processing of substrates | |
| JP4907827B2 (en) | Method for improving polysilicon etch uniformity and reducing etch rate variation | |
| JPH02503614A (en) | Etching method using gas plasma | |
| US5246529A (en) | Plasma processing method | |
| US5304514A (en) | Dry etching method | |
| JPS6289882A (en) | Vapor phase etching method | |
| US6838387B1 (en) | Fast etching system and process | |
| EP0203560A1 (en) | Plasma trench etch | |
| JPH02297931A (en) | Vapor-phase etching method | |
| EP0546493B1 (en) | Photochemical dry etching method | |
| JPH02224229A (en) | Vapor phase etching | |
| JP2700297B2 (en) | Processing method | |
| JP2564663B2 (en) | Vapor phase etching equipment | |
| JPH02225681A (en) | Method for vapor-phase etching | |
| JP2532353B2 (en) | Vapor phase etching method and apparatus | |
| JPH05251399A (en) | Etching method for silicon nitriding film based on leaflet type etcher | |
| JP2535517B2 (en) | Processing method | |
| JPS62237729A (en) | Dry etching method for silicon oxide | |
| JP2966036B2 (en) | Method of forming etching pattern |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |