JPS6056231B2 - plasma etching method - Google Patents
plasma etching methodInfo
- Publication number
- JPS6056231B2 JPS6056231B2 JP12420779A JP12420779A JPS6056231B2 JP S6056231 B2 JPS6056231 B2 JP S6056231B2 JP 12420779 A JP12420779 A JP 12420779A JP 12420779 A JP12420779 A JP 12420779A JP S6056231 B2 JPS6056231 B2 JP S6056231B2
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- Prior art keywords
- etching
- gas
- ccl4
- ratio
- film
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Description
【発明の詳細な説明】
本発明は改良されたプラズマエッチング方法に関する
。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improved plasma etching method.
最近、互いに対向して設けられた電極に高周波(RF
)電力を印加して前記電極間に反応性ガスからガスプラ
ズマを形成し、前記電極上でエッチングを行なうプラズ
マエッチング方法が酸化シリコン(SiO2)の他シリ
コをン(Si)やアルミニウム(Al)膜をもエッチン
グ出来ることからICやLSIの分野で注目されている
。Recently, radio frequency (RF)
) A plasma etching method in which a gas plasma is formed from a reactive gas between the electrodes by applying electric power, and etching is performed on the electrodes. It is attracting attention in the IC and LSI fields because it can also etch.
ところでICやトIではAl膜が電極や配線として広
く使われているが、SiやSiO。By the way, Al films are widely used as electrodes and wiring in ICs and ICs, but Si and SiO.
に対してAl膜を選択エッチングすることはその導入に
あたつて重要な問題となる。例えばおよそ素子形成の済
んだ基板全面にAlを堆積し、適当なパターンをエッチ
ングマスクとして前記Al膜から電極や配線を形成する
。しかしAl膜は段差部での実効的厚みが(基板面に垂
直に測つて)大きくなるので、この部位でのエッチング
が完了する前に平坦部のN膜エッチングは完了してしま
う。従つてエツ・チング選択性が悪いとフィールド酸化
膜表面がエッチングされたり、コンタクトホール内でA
l膜パターンからはずれた基板表面がエッチングされP
n接合が損傷を受けてリーク電流の原因となつたりする
。即ち基板表面の逆導電型領域に設けら・れたコンタク
トホールは、高密度化を図るために開口が1〜2μ四角
になると最早マスク合わせの点でAlパターンをコンタ
クトホール全体を覆うように設けるのは困難で、一部が
コンタクトホールに接触する状態でも許容するようにな
る。ノ 従来Nエッチング時の導入ガスとしては毒性も
少く取り扱い易いCCI。(四塩化炭素)が広く試みら
れて来たが、エッチング速度が遅く、またAl/SiO
2特にAl/Siエッチング選択比が悪く未だ実用化に
は至つていない。本発明は上記事情に鑑みて為されたも
ので、互いに対向して設けられた電極に高周波電力を印
加して前記電極間にガスプラズマを形成し、前記電極上
でエッチングを行なうにあたり、CCl4ガスにCl2
ガスを加えたCl2/CCl4+Cl2圧力比が0.8
以下であるガスを用いて前記ガスプラズマを形成し、0
.1T0rr以下の高真空下でアルミニウム膜をエッチ
ングすることを特徴とするプラズマエッチング方法を提
供するものである。Selective etching of the Al film is an important issue in its introduction. For example, Al is deposited over the entire surface of the substrate on which elements have been formed, and electrodes and wiring are formed from the Al film using an appropriate pattern as an etching mask. However, since the effective thickness of the Al film becomes larger at the step portion (measured perpendicular to the substrate surface), the N film etching at the flat portion is completed before the etching at this portion is completed. Therefore, if the etching selectivity is poor, the surface of the field oxide film may be etched, or A may be etched in the contact hole.
The substrate surface that deviates from the l film pattern is etched.
The n-junction may be damaged and cause leakage current. In other words, in order to increase the density of contact holes formed in opposite conductivity type regions on the substrate surface, when the openings are 1 to 2μ square, it is no longer necessary to form an Al pattern to cover the entire contact hole for mask alignment. It is difficult to do so, and it is now possible to allow a part of the contact hole to come into contact with the contact hole. CCI is less toxic and easier to handle as a gas introduced during conventional N etching. (carbon tetrachloride) has been widely tried, but the etching rate is slow and Al/SiO
2 In particular, the Al/Si etching selectivity is poor, and it has not yet been put to practical use. The present invention has been made in view of the above-mentioned circumstances, and includes applying high-frequency power to electrodes provided facing each other to form gas plasma between the electrodes, and performing etching on the electrodes using CCl4 gas. to Cl2
Cl2/CCl4+Cl2 pressure ratio with gas added is 0.8
The gas plasma is formed using a gas that is 0
.. The present invention provides a plasma etching method characterized by etching an aluminum film under a high vacuum of 1T0rr or less.
以下、本発明の実施例を図面を参照して詳述する。Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings.
第1図は本実施例で用いたプラズマエッチング装置の概
略を示す装置断面図である。FIG. 1 is a sectional view schematically showing the plasma etching apparatus used in this example.
ステンレス製の真空容器1にはガス導入口2,3が設け
られ、夫々CCl4ガスとCl2ガスが導入される。両
電極4,5は平行平板状を為し、夫々絶縁物(ここでは
テフロン)6,6″によつて容器から絶縁されている。
電極4には真空シール7を通して13.56MHzのR
F電源8が整合器9を経て接続され、電極5は接地の状
態にしてあり、このようにして電極4,5には200W
(7)RF電力が印加される。A vacuum container 1 made of stainless steel is provided with gas inlets 2 and 3, through which CCl4 gas and Cl2 gas are introduced, respectively. Both electrodes 4 and 5 have a parallel plate shape and are insulated from the container by insulators (Teflon in this case) 6 and 6'', respectively.
Electrode 4 is connected to R of 13.56MHz through vacuum seal 7.
The F power source 8 is connected via a matching box 9, and the electrode 5 is grounded. In this way, 200W is applied to the electrodes 4 and 5.
(7) RF power is applied.
また両電極4,5は水冷バイブ10,1『により冷却さ
れ、ガスは拡散ポンプやルーツポンプ、ロータリーポン
プなどの排気手段11で容器1が0.01T0rr以下
に達した後に導入され、コンダクタンスバルブ12,1
2″によつて真空容器1内の真空度即ちエッチング圧力
が調整される。尚コンダクタンスバルブ12,12″間
には液体窒素トラップ13が設けられている。このよう
にしてグロー放電により電極4,5間にガスプラズマが
形成され、減圧下で電極4上の試料14がエッチングさ
れる。Both electrodes 4 and 5 are cooled by water-cooled vibrators 10 and 1'', and gas is introduced after the container 1 reaches 0.01T0rr or less by an exhaust means 11 such as a diffusion pump, Roots pump, or rotary pump, and a conductance valve 12 ,1
2'' adjusts the degree of vacuum in the vacuum container 1, that is, the etching pressure.A liquid nitrogen trap 13 is provided between the conductance valves 12 and 12''. In this way, gas plasma is formed between the electrodes 4 and 5 by glow discharge, and the sample 14 on the electrode 4 is etched under reduced pressure.
第2図は先述装置でAl膜、Si膜、SiO,膜をエッ
チングした時の塩素ガス混合比即ちCl2/CCl4:
,+Cl2圧力比を変化させてエッチング速度及びエッ
チング選択比との関係を示した特性図である。Figure 2 shows the chlorine gas mixture ratio, Cl2/CCl4:
, +Cl2 pressure ratio is changed to show the relationship between etching rate and etching selectivity.
ここでは真空容器1内の真空度即ちエッチング圧力を0
.1T0rrと一定にした。曲線A,b,cはエッチン
グ終了後にエッチング深さとエッチング時4間とから算
出した夫々Al,Si,SiO2のエッチング速度、曲
線D,eはその結果を用いて得た夫々A1/Si,Al
/SiO2のエッチング選択比を示す。Cl2ガスの混
合比を増加させてゆくと、Al,Si,SlO2のエッ
チング速度は夫々Cl2/CCl4+Cl2比が0.7
5を最大とするような特性を示すが、なかでもNの変化
割合が大きい。そして曲線D,eに示すようにA1/S
i,Al/SlO,のエッチング選択比は共にCl2/
CCl4+Cl2比が0.8以下では、Cl2/CCl
4+Cl2比が零即ちCCl4ガス単独でエッチングす
るよりも選択性及びAl膜のエッチング速度が向上して
いる。Here, the degree of vacuum in the vacuum container 1, that is, the etching pressure is set to 0.
.. It was kept constant at 1T0rr. Curves A, b, and c are the etching rates of Al, Si, and SiO2 calculated from the etching depth and etching time of 4 hours after the completion of etching, and curves D and e are the etching rates of A1/Si and Al, respectively, calculated using the results.
/SiO2 etching selectivity. As the mixing ratio of Cl2 gas increases, the etching rate of Al, Si, and SlO2 decreases to 0.7 when the Cl2/CCl4+Cl2 ratio is 0.7, respectively.
5 is the maximum, but the rate of change in N is particularly large. And as shown in curves D and e, A1/S
The etching selectivity of i, Al/SIO, is both Cl2/
When the CCl4+Cl2 ratio is below 0.8, Cl2/CCl
4+Cl2 ratio is zero, that is, the selectivity and etching rate of the Al film are improved compared to etching with CCl4 gas alone.
第3図はエッチング圧力を0.04T0rrと一定にし
て第2図と説明したと同様にAl,Si,SiO2膜を
エッチングした時のCl2/CCl,+Cl2圧力比を
変化させてエッチング速度及びエッチング選択比との関
係を第2図で説明したと同様に求めた特性図である。Figure 3 shows the etching rate and etching selection by changing the Cl2/CCl, +Cl2 pressure ratio when etching Al, Si, and SiO2 films in the same way as explained in Figure 2 with the etching pressure kept constant at 0.04T0rr. FIG. 2 is a characteristic diagram showing the relationship with the ratio obtained in the same manner as explained in FIG. 2.
曲線a″,b″,c″は夫々Al,Si,SiO2のエ
ッ門チング速度、曲線d゛,e″は夫々A1/Si,A
l/SiO2のエッチング選択比を示す。Cl2ガスの
混合比を増加させてゆくと、先述Cl2/CCl4+C
l2比が0.8以下では、CCl4ガス単独でエッチン
グするよりもA1膜のエッチング速度及びAl/Si,
Al/SiO2のエッチング選択性が向上した。Curves a″, b″, and c″ are the etching rates of Al, Si, and SiO2, respectively, and curves d″ and e″ are the etching rates of Al, Si, and A1/Si, respectively.
The etching selectivity ratio of l/SiO2 is shown. As the mixing ratio of Cl2 gas increases, the aforementioned Cl2/CCl4+C
When the l2 ratio is 0.8 or less, the etching rate of the A1 film and Al/Si,
The etching selectivity of Al/SiO2 was improved.
A1膜は0.9では全んどエッチングされなくなつた。
第4図はN膜、Si膜、SiO2膜をエッチングした時
のエッチング圧力とエッチング速度及びエッチング選択
比の関係を示す特性図である。The A1 film was no longer etched at all at 0.9.
FIG. 4 is a characteristic diagram showing the relationship between etching pressure, etching rate, and etching selectivity when etching N film, Si film, and SiO2 film.
エッチング圧力はCCl4ガスを0.025T0rr.
.C12ガスを0.015T0rrの圧力で導入しなが
ら先述コンダクタンスバルブを用いて0.04,0.0
5,0.07,0.085,0.1,0.11,0.1
2の各圧力に設定した。ここではCl2/CCl4+C
l2比は0.015/0.4である。曲線A,b,cは
夫々Al,Sj,SiO2のエッチング速度、曲線D,
eは夫々A1/Si,Al/SiO2のエッチング選択
比を示す。図に示すようにエッチング圧力を増加させて
ゆくに伴ないA1/Si,Al/SiO2エッチング選
択比も上昇し、0.1T0rrで夫々5,100に達し
た。The etching pressure was 0.025T0rr.CCl4 gas.
.. While introducing C12 gas at a pressure of 0.015T0rr, using the conductance valve described above,
5,0.07,0.085,0.1,0.11,0.1
2 pressures were set. Here Cl2/CCl4+C
The l2 ratio is 0.015/0.4. Curves A, b, and c are the etching rates of Al, Sj, and SiO2, respectively, and curves D,
e represents the etching selectivity of A1/Si and Al/SiO2, respectively. As shown in the figure, as the etching pressure was increased, the etching selectivity ratios of A1/Si and Al/SiO2 also increased, reaching 5,100 at 0.1 T0rr.
尚、0.15T0rrではA1は全んどエッチングされ
なくなつた。この他さらに種々条件を変えて実験を行な
つたが何れにおいてもエッチング選択比、Al膜エッチ
ング速度から総合的に判断して、CCl4ガス単独でエ
ッチングするより優れていると判断されるCl2/CC
l4+Cl2比を、この比が0.8以下の範囲に認める
ことが出来た。Incidentally, at 0.15T0rr, A1 was no longer etched at all. In addition, experiments were conducted under various conditions, and in all cases, Cl2/CC was judged to be superior to etching with CCl4 gas alone, judging comprehensively from the etching selectivity and Al film etching speed.
The l4+Cl2 ratio was found to be within a range of 0.8 or less.
例えば高周波電力を種々変えたが同様であつた。For example, the results were the same even though the high frequency power was varied.
第5図aは高周波電力100W(0.12W/Clt)
、200W(0.24W/Cfi)、300W(0.3
6W/C7lf)でのCl2/CCl4+Cl。Figure 5 a shows high frequency power of 100W (0.12W/Clt)
, 200W (0.24W/Cfi), 300W (0.3
Cl2/CCl4+Cl at 6W/C7lf).
圧力比と陰極降下電圧■Dcとの関係を示す。陰極とは
RF電源が接続される電極を指す。即ち陰極には高周波
の正の半周期でプラズマ中の電子が流入し、次の負の半
周期でプラズマ中の正イオンが流入するが、正イオンよ
り電子の易動度の方が大きいので両者の差がなくなるよ
うに陰極の電位は低下して自己補正される。この電位の
低下は陰極降下電圧・■DC(VdC=ψ)と呼はれ第
4図bに説明図を示す。(V,:最大値、V2最小値)
。第5図aで曲線F,g,hは夫々100W,200W
,300Wの場合を示し、夫々CI2添加量に対しほぼ
不変であつた。The relationship between pressure ratio and cathode drop voltage ■Dc is shown. Cathode refers to the electrode to which the RF power source is connected. In other words, electrons in the plasma flow into the cathode during the positive half cycle of the high frequency, and positive ions in the plasma flow into the cathode during the next negative half cycle, but since the mobility of the electrons is greater than that of the positive ions, both The potential of the cathode is lowered and self-corrected so that the difference disappears. This decrease in potential is called cathode drop voltage/■DC (VdC=ψ), and an explanatory diagram is shown in FIG. 4b. (V,: maximum value, V2 minimum value)
. In Figure 5 a, curves F, g, and h are 100W and 200W, respectively.
, 300W, and remained almost unchanged with respect to the amount of CI2 added.
ところで、第2図、第3図の結果で示されるに膜のエッ
チング速度の変化は次のように推察される。By the way, the change in the etching rate of the film shown in the results shown in FIGS. 2 and 3 is inferred as follows.
即ちCl2/CCl4+Cl2比を増すに伴ないCCI
4が多い間には過剰なCがAI膜表面をカバーし、Al
膜のエッチング速度は低く、Cl2添加によつてこのC
はCl2によりCCl4となり除去されCl2/CCl
4+Cl2比0.75でN膜エッチングは最良となるが
、その後は大気中で形成されたN表面部のAl2O3薄
層のCCl3+による環元がCCl4ガスが少ないため
行なわれ難くなりエッチング速度が急激に減少したもの
と考えられる。尚、Cl2添加による効果はCl2/C
Cl4+Cl。That is, as the Cl2/CCl4+Cl2 ratio increases, the CCI
While there is a lot of 4, excessive C covers the AI film surface and Al
The etching rate of the film is low, and by adding Cl2, this C
becomes CCl4 with Cl2 and is removed, Cl2/CCl
N film etching is best at a 4+Cl2 ratio of 0.75, but after that, the etching rate rapidly increases as the ring element by CCl3+ of the thin Al2O3 layer on the N surface formed in the atmosphere becomes difficult to perform due to the lack of CCl4 gas. It is thought that this has decreased. In addition, the effect of Cl2 addition is Cl2/C
Cl4+Cl.
比が0.1特に0.2から明瞭に現われ始める。なかで
も0.4〜0.諾に0.6〜0.8の範囲が顕著であつ
た。又、A1膜のエッチング速度やA]/Si,AI/
SlO2選択比の急変部を除くにはCl2/CCl4+
Cl2比は0.7以下特に0.6以下が好ましい。さら
にエッチング圧力は、0.01特に0.0肝0rr′を
下限、0.06T0rrを上限とする範囲で選択性効果
は顕著に表われた。The ratio begins to appear clearly from 0.1, especially from 0.2. Among them, 0.4 to 0. The range of 0.6 to 0.8 was particularly significant. In addition, the etching rate of the A1 film and A]/Si, AI/
To remove sudden changes in SlO2 selection ratio, Cl2/CCl4+
The Cl2 ratio is preferably 0.7 or less, particularly 0.6 or less. Furthermore, the selectivity effect was remarkable when the etching pressure ranged from a lower limit of 0.01, especially 0.0rr', to an upper limit of 0.06T0rr.
又、N膜上に被着するエッチングマスクとして用いるパ
ターンのA1膜エッチング時の損傷や、マスク下のアン
ダーカットを考慮する場合には少なくとも100(0.
12W/d)〜300W(イ).36W/c#i)程度
の高周波電力、陰極降下電圧にして−20〜−220V
にする必要があつた。In addition, when considering damage during etching of the A1 film of a pattern used as an etching mask deposited on the N film and undercuts under the mask, at least 100 (0.
12W/d) ~ 300W (a). High frequency power of about 36W/c#i), cathode drop voltage -20 to -220V
It was necessary to do so.
これらについて詳しく説明する。第6図は、エッチング
圧力を変化させた時の各d電力に対するVdcの変化を
示している。ここではCCl4ガス0.025T0rr
′、Cl2ガス0.015T0rrで流しながら前記圧
力調節をした。曲線aはd電力100W(0.12W/
Clt)、bは200W(0.24W/d)、cは30
0W(4).36W/C7lf)の場合を示し、d電力
が大きい程Vdcは大きく、またエッチング圧力が低い
程Vdcが大きい。第7図aに示すようにSiO2で被
覆されたウェハ31上に1μm厚のアルミニウム32を
堆積し、ポジ型レジストマスク33を形成して0.1T
0rr,200Wでエッチングを行なつたが図に示すよ
うに大きなアンダーカット34が生じ、また下地SiO
2上に重合物35が堆積した。These will be explained in detail. FIG. 6 shows the change in Vdc for each d power when the etching pressure is changed. Here, CCl4 gas 0.025T0rr
', the pressure was adjusted as described above while flowing Cl2 gas at 0.015T0rr. Curve a is d power 100W (0.12W/
Clt), b is 200W (0.24W/d), c is 30
0W(4). 36W/C7lf), the larger the d power, the larger Vdc, and the lower the etching pressure, the larger Vdc. As shown in FIG. 7a, aluminum 32 with a thickness of 1 μm is deposited on a wafer 31 coated with SiO2, a positive resist mask 33 is formed, and 0.1T
Etching was performed at 0rr and 200W, but as shown in the figure, a large undercut 34 occurred, and the underlying SiO
Polymer 35 was deposited on 2.
又、0.04T0rr−(CCl4O.O25TOrr
,Cl。O.Ol5TOrT′)の圧力下で100W,
200W,300Wの各Rf電力で同様にしてエッチン
グを行なつたが100Wはアンダーカットが生じた。第
8図にはエッチング圧力とアンダーカット量(横方向エ
ッチング食い込み量)との関係(実線)を示す。Also, 0.04T0rr-(CCl4O.O25TOrr
, Cl. O. 100W under the pressure of
Etching was carried out in the same manner with Rf powers of 200 W and 300 W, but undercutting occurred with 100 W. FIG. 8 shows the relationship (solid line) between etching pressure and undercut amount (lateral etching depth).
CCl4O.O25TOrr′,Cl2O.Ol5TO
rrで流しながら圧力調節し、Rf電力は200Wとし
た。その結果0.1T0rrではN膜厚以上の著しく大
きなアンダーカットが生じた。このようにアンダーカッ
トは■Dcと密接に関係し、少なくともVdcは−20
Vより低い状態でエッチングを行なうことが著しく大き
なアンダーカットを避ける上で必要であつた。CCl4O. O25TOrr', Cl2O. Ol5TO
The pressure was adjusted while flowing with rr, and the Rf power was 200W. As a result, at 0.1T0rr, a significantly large undercut larger than the N film thickness occurred. In this way, undercut is closely related to ■Dc, and at least Vdc is -20
Etching below V was necessary to avoid significant undercuts.
■Dcが0Vに近くなると試料に垂直に入射するCCl
3+等のイオン種によるエッチングが減少し、中性種に
よるエッチングが増す結果エッチングに方向性が得られ
なくなるものと推察される。0.04T0rr(CCl
4O.O25TOrr,Cl2O.Ol5TOrr)の
圧力下、Rf電力200Wの条件ではレジストマスクは
殆んどエッチングされず、またアンダーカットも殆んど
認められなかつた。■When Dc approaches 0V, CCl enters the sample perpendicularly.
It is presumed that etching by ion species such as 3+ is reduced and etching by neutral species is increased, making it impossible to obtain directionality in etching. 0.04T0rr(CCl
4O. O25TOrr, Cl2O. Under the conditions of Rf power of 200 W and under a pressure of 200 W (Ol5 TOrr), the resist mask was hardly etched, and almost no undercut was observed.
この様子を第9図aに示す。This situation is shown in FIG. 9a.
即ちエッチングされたA1膜の側壁に堆積物51が観ら
られた。こ・の堆積物はEPMA(ElectrOnP
rObeMicrO.Arlalysis)測定からに
を主体とする物質であることが判明した。Alエッチン
グ時にエッチングに伴ないその側壁に堆積物が附着して
ゆき、この堆積物によりにのアンダーカットを防いでい
るものと考えられる。第9図aの状態のレジストは酸素
プラズマによつて灰化されるが、第9図bのように堆積
物は灰化されないで残る。ところがaの状態のウェハー
をレジスト剥離液(東京応化製J−100)等の中でレ
ジスト剥離条件(11CfC,5分)を用いるとcのよ
うにレジストばかりでなく堆積物51も同時にエッチン
グされて、微細加工されたアンダーカットのないA1膜
のパターンが現われた。このようにした1μ厚で1μm
幅のラインアンドスペースのパターンが達成された。第
10図はCl2添加量即ちCl2/CCl4+Cl2圧
力比に対するアンダーカット量の変化(実線)を示し、
エッチング圧力0.04T0rr,.rf電力200W
の条件である。Cl2/CCl4+Cl2圧力比が0.
3〜0.35では殆んどアンダーカットは認められなか
つた。That is, deposits 51 were observed on the sidewalls of the etched A1 film. This deposit is made of EPMA (ElectrOnP
rObeMicrO. (Arlalysis) measurements revealed that it was a substance mainly composed of crab. It is believed that during Al etching, deposits are attached to the sidewalls of the Al, and this deposit prevents undercuts. The resist in the state shown in FIG. 9a is ashed by oxygen plasma, but the deposits remain un-ashed as shown in FIG. 9b. However, when the wafer in the state of a is used in a resist stripping solution (J-100 manufactured by Tokyo Ohka Co., Ltd.) under resist stripping conditions (11CfC, 5 minutes), not only the resist but also the deposit 51 is etched at the same time as shown in c. , a microfabricated pattern of A1 film without undercuts appeared. The 1μ thickness made like this is 1μm.
A pattern of wide lines and spaces was achieved. Figure 10 shows the change in undercut amount (solid line) with respect to the Cl2 addition amount, that is, the Cl2/CCl4 + Cl2 pressure ratio,
Etching pressure 0.04T0rr,. rf power 200W
This is the condition. Cl2/CCl4+Cl2 pressure ratio is 0.
3 to 0.35, almost no undercut was observed.
これは先述側壁堆積物による効果である。前記比からは
ずれるに従い効果は薄れてゆくが、Cl2/CCl4+
CI2比が0.6以下であればCCl4単独即ちCl2
/CCl4+Cl2比零よりアンダーカットは少なかつ
た。This is the effect of the sidewall deposits mentioned above. The effect weakens as the ratio deviates from the above, but Cl2/CCl4+
If the CI2 ratio is 0.6 or less, CCl4 alone, that is, Cl2
/CCl4+Cl2 ratio was less than that of zero.
特にCl2/CCl4+Cl2圧力比が0.2〜0.4
5であればアンダーカットは実質的に零となる。Especially when the Cl2/CCl4+Cl2 pressure ratio is 0.2 to 0.4
If it is 5, the undercut will be substantially zero.
本発明はさらにレジストマスクの変形防止に有効である
。The present invention is also effective in preventing deformation of resist masks.
200W,C12/CCl,+Cl2比が0.3〜0.
35ではエッチング後のレジストは原形のままの状態で
あるが、第10図(Rf電力200W,0.04T0r
r)に示すよう(破線)にCl。200W, C12/CCl, +Cl2 ratio of 0.3 to 0.
In Fig. 35, the resist after etching remains in its original form, but in Fig. 10 (Rf power 200W, 0.04T0r
Cl as shown in r) (dashed line).
/CCl4+Cl。圧力比によつてはにエッチング後の
レジストには大きな膨潤が生じ(膨潤量は横方向への拡
がりとして現わ−した)例えばCl2/CCl4+Cl
2比0.7では第7図bに示すように大きな膨潤を示す
と共に下地SiO2上に重合物を生じる。このようにC
l2/CCl,+Cl2比が0.61).下であればC
Cl,単独の場合よりもレジストの変形は小さ.い。/CCl4+Cl. Depending on the pressure ratio, large swelling occurred in the resist after etching (the amount of swelling appeared as a spread in the lateral direction).For example, Cl2/CCl4+Cl
When the 2 ratio is 0.7, as shown in FIG. 7b, large swelling is exhibited and a polymer is formed on the base SiO2. In this way C
l2/CCl, +Cl2 ratio is 0.61). C if below
The deformation of the resist is smaller than when using Cl alone. stomach.
第8図破線もレジスト膨潤量を示す。The broken line in FIG. 8 also indicates the amount of resist swelling.
尚、Vdcが−220■、特に−330Vより低い状態
になるとエッチング種の大きな運動エネルギーによつて
レジストマスクは損傷を受ける。It should be noted that when Vdc is lower than -220V, particularly -330V, the resist mask is damaged by the large kinetic energy of the etching species.
又、アル・ミニウム膜のエッチング速度、A1/Si,
Al/SiO2エッチング選択性を考慮すれば上記Cl
2/CCl4+Cl2比は0.2〜0.6が良い。又、
Vdcは−20V以下からさらに−50V以下になると
アンダーカット、レジスト膨潤を防ぐのにさらに有効で
ある。尚、以上の結果は数%の銅やシリコンを含むアル
ミニウム膜でも同様であり本発明はこれらをも含むもの
である。特に下地露出後のアンダーカットは純Nより数
%Siが入つたアルミニウム膜の方が進行が遅かつた。
尚、CCl4へのCl.添加は上記効果に止まらず、7
CCI,中のCや重合物であるC2Cl等の汚染原因と
なる物質をCCl4に再び環元し、エッチングの再現性
を良くし、排気系のオイルやポンプの劣化を防ぐという
付加的効果もあることが判明した。In addition, the etching rate of the aluminum film, A1/Si,
Considering Al/SiO2 etching selectivity, the above Cl
The 2/CCl4+Cl2 ratio is preferably 0.2 to 0.6. or,
When Vdc is lowered from -20V or lower to -50V or lower, it is more effective in preventing undercuts and resist swelling. Incidentally, the above results are similar even for aluminum films containing several percent of copper or silicon, and the present invention also includes these. In particular, the undercut after exposing the base progressed more slowly in the aluminum film containing several percent Si than in the case of pure N.
In addition, Cl. to CCl4. The addition does not stop at the above effects, but also has 7
It has the additional effect of recirculating substances that cause contamination, such as C in CCI and the polymer C2Cl, into CCl4, improving etching reproducibility, and preventing deterioration of exhaust system oil and pumps. It has been found.
本発明はシリコンや酸化シリコン層上のアルミニウム膜
をエッチングするのに好適である。又、シリコンは多結
晶、単結晶シリコン共に同様な効果を示す。The present invention is suitable for etching an aluminum film on a silicon or silicon oxide layer. Furthermore, both polycrystalline and single-crystalline silicon exhibit similar effects.
第1図はプラズマエッチング装置の概略的な断゛面図、
第2図はエッチング圧力0.1T0rrにおけるCl2
混合比に対するエッチング速度及びエッチング選択比の
特性図、第3図はエッチング圧力0.04T0rrにお
けるCl。Figure 1 is a schematic cross-sectional view of a plasma etching device.
Figure 2 shows Cl2 at an etching pressure of 0.1T0rr.
A characteristic diagram of etching rate and etching selectivity with respect to mixing ratio, FIG. 3 shows Cl at an etching pressure of 0.04T0rr.
Claims (1)
して前記電極間にガスプラズマを形成し、前記電極上で
エッチングを行なうにあたり、CCl_4ガスにCl_
2ガスを加えたCl_2/CCl_4+Cl_2圧力比
が0.8以下であるガスを用いて前記ガスプラズマを形
成し、0.1Torr以下の高真空下でアルミニウム膜
をエッチングすることを特徴とするプラズマエッチング
方法。 2 Cl_2/CCl_4+Cl_2圧力比が0.6以
下であるとともに陰極降下電圧が−20ボルト以下であ
ることを特徴とする特許請求の範囲第1項に記載したプ
ラズマエッチング方法。[Claims] 1. When high-frequency power is applied to electrodes provided facing each other to form gas plasma between the electrodes and etching is performed on the electrodes, Cl_4 gas is added to CCl_4 gas.
A plasma etching method characterized in that the gas plasma is formed using a gas having a pressure ratio of Cl_2/CCl_4+Cl_2 of 0.8 or less, and the aluminum film is etched under a high vacuum of 0.1 Torr or less. . 2. The plasma etching method according to claim 1, wherein the Cl_2/CCl_4+Cl_2 pressure ratio is 0.6 or less and the cathode drop voltage is -20 volts or less.
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12420779A JPS6056231B2 (en) | 1979-09-28 | 1979-09-28 | plasma etching method |
| DE3030814A DE3030814C2 (en) | 1979-08-17 | 1980-08-14 | Process for plasma etching a workpiece |
| US06/177,910 US4341593A (en) | 1979-08-17 | 1980-08-14 | Plasma etching method for aluminum-based films |
| FR8018069A FR2463976A1 (en) | 1979-08-17 | 1980-08-18 | PLASMA ETCHING PROCESS FOR ALUMINUM FILMS |
| GB8026885A GB2059879B (en) | 1979-08-17 | 1980-08-18 | Plasma etching method for aluminumbased films |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12420779A JPS6056231B2 (en) | 1979-09-28 | 1979-09-28 | plasma etching method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5647568A JPS5647568A (en) | 1981-04-30 |
| JPS6056231B2 true JPS6056231B2 (en) | 1985-12-09 |
Family
ID=14879634
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12420779A Expired JPS6056231B2 (en) | 1979-08-17 | 1979-09-28 | plasma etching method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6056231B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61123141A (en) * | 1984-11-20 | 1986-06-11 | Fujitsu Ltd | Etching method |
-
1979
- 1979-09-28 JP JP12420779A patent/JPS6056231B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5647568A (en) | 1981-04-30 |
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