JPS58110038A - Pattern formation - Google Patents

Pattern formation

Info

Publication number
JPS58110038A
JPS58110038A JP56208797A JP20879781A JPS58110038A JP S58110038 A JPS58110038 A JP S58110038A JP 56208797 A JP56208797 A JP 56208797A JP 20879781 A JP20879781 A JP 20879781A JP S58110038 A JPS58110038 A JP S58110038A
Authority
JP
Japan
Prior art keywords
resist
etching
film
etched
mask
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
JP56208797A
Other languages
Japanese (ja)
Other versions
JPH0542810B2 (en
Inventor
Shinji Matsui
真二 松井
Nobuhiro Endo
遠藤 伸裕
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.)
NEC Corp
Original Assignee
NEC Corp
Nippon Electric 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 NEC Corp, Nippon Electric Co Ltd filed Critical NEC Corp
Priority to JP56208797A priority Critical patent/JPS58110038A/en
Publication of JPS58110038A publication Critical patent/JPS58110038A/en
Publication of JPH0542810B2 publication Critical patent/JPH0542810B2/ja
Granted legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02107Forming insulating materials on a substrate
    • H01L21/02109Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
    • H01L21/02112Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer
    • H01L21/02118Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer carbon based polymeric organic or inorganic material, e.g. polyimides, poly cyclobutene or PVC

Landscapes

  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Manufacturing & Machinery (AREA)
  • Computer Hardware Design (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Power Engineering (AREA)
  • Electron Beam Exposure (AREA)
  • Formation Of Insulating Films (AREA)
  • Exposure Of Semiconductors, Excluding Electron Or Ion Beam Exposure (AREA)
  • Drying Of Semiconductors (AREA)

Abstract

PURPOSE:To contrive the reduction of pattern formation processes by a method wherein SiOx obtained by heating at 100 deg.C or over the applied film of a mixture including organosilanol in an organic solvent is used as an intermediate layer in the structure of a resist-intermediate layer-ground organic high molecular coating on an Si substrate. CONSTITUTION:A positive-type resist film is superposed on an oxide film on an Si substrate, and a CH3Si(OH)3 alcohol solution is rotationally applied, and the solution is easily changed into SiOx (1<x<=2) except alcohol at 100 deg.C or over. This film is etched by CF4 plasma and becomes a mask by O2 plasma. Then, a fine pattern can be transferred by a conventional lithography technique without the hindrance of weak resistance against proximity effect or dry etching. The formation of the intermediate layer is easily completed by only spin application and heat treatment within a short period. The film thickness of the SiOx can arbitrarily set by the viscosity of solution and rotating speed, and the same heat treatment atmosphere as that for a normal lithography process is acceptable. This composition reduces pattern formation processes and improves production efficiency and yield.

Description

【発明の詳細な説明】 この発明はリング2フイにおけるレジストパターンを被
エツチング蹟、板に転写するためのパターン形成方法に
関するものでめる。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a pattern forming method for transferring a resist pattern on a ring 2 fin to a plate to be etched.

従来、基板にPir望するパターンを#成する一合、党
の照射によって起る化学EFJな反1らで、ある的剤に
対する溶解性が著しく変化す仝感シむ性8゛億尚子材料
、所謂レジストを塗叡し、・での恢珈冗パターンの描画
されたカラスマスクと九字的+叡とを用いてjI元、現
像プロセスを施゛じ、レジストパターンを形成するとい
う151r請リソグフフイを行った儀、基板W科tウェ
ット又扛ドライ法でエッチングしていた。最近超L8ル
ベルの一密度化集槓回路の#!造に伴い、パターンの倣
−化が要求され1μm又はそれ以下の寸法を十分制御し
てパターン形成することが必要となってきており、この
ためリングラフィ手段として光学面方法から電子ビーム
の@捩描画方法への移行が提案されてきている。そこで
、この電子ビームリングラフィにおいても電子ビームに
感応する、例えばPMMA(ポリメチルメタクリレート
)やP GMA (ポリグリシギルメタクリレート)が
用いられ、同様々現像プロセスを経て、パターン形成さ
れていた。しかるにこれらの電子ビーム用レジストを用
いて実際に集積回路等で使われるパターンを形成する場
合に、近接効果とドライエツチングに対する耐性とが大
きな問題となっていた。すなわち電子ビームが熱射され
ると、主に基板表面で先生した2次電子がレジスト中で
紋乱されるため、近接したパターンの大小によって入射
された鎖酸のレジスト感kが式化するという近−幼米と
lF?#′i、れる塊象が生じ、この効果がパターンの
淑梢化と共に顕著となり制m性や解像度に支障をきたし
ていた。また尚解藏注OPbaMムやPGMAのような
電子ビーム用Vシストはスパッタエツチング等のドライ
エツチング手段によって基板への転写【行う場合、レジ
ストのエツチング速度が速く、エツチングマスクとして
十分に耐え難い欠点があり、レジスートパターンを基板
材料に積置よく転写できない間組力・めった。
Conventionally, when forming a desired pattern on a substrate, materials with 80 million yen sensitivity, whose solubility to a certain target agent changes markedly due to chemical EFJ reactions caused by irradiation, are used. A 151R printing process was performed in which a so-called resist was applied, and a resist pattern was formed by applying a development process using a crow mask with a red pattern drawn in . However, the substrate was etched using a wet or dry method. Recently, # of the ultra-L8 Lebel single-density concentrator circuit! As phosphorography advances, pattern copying is required, and it has become necessary to form patterns with sufficient control over dimensions of 1 μm or smaller. For this reason, phosphorography methods have changed from optical surface methods to electron beam @twisting. A transition to a drawing method has been proposed. Therefore, in this electron beam phosphorography, materials sensitive to electron beams, such as PMMA (polymethyl methacrylate) and PGMA (polyglycygyl methacrylate), are used, and patterns are formed through a similar development process. However, when using these electron beam resists to form patterns that are actually used in integrated circuits, the proximity effect and resistance to dry etching have become major problems. In other words, when an electron beam is thermally irradiated, the secondary electrons emitted mainly on the substrate surface are disturbed in the resist, so the resist sensitivity k of the incident chain acid is expressed by the size of the nearby pattern. Kin-Youmai and IF? #'i, a lumpy phenomenon occurs, and this effect becomes noticeable as the pattern becomes thinner, causing problems in controllability and resolution. In addition, V-sist for electron beams such as OPBAM and PGMA is transferred to the substrate by dry etching means such as sputter etching, but the etching speed of the resist is high and it has the drawback that it cannot withstand sufficiently as an etching mask. However, the resist pattern may not be properly transferred to the substrate material due to assembly force or failure.

これらの問題点を軽減するために3#w#4がベル研究
所のJ、M、Moran等によってジャーナルオフ/(
キ^−ムサンエンスアンドテクノロジー16巻1620
 X (J 、 Vacum 5cience and
 ’i’echno−10g7 16.1920(19
79))に提案されている。こoamm造はレジストを
マスクとして中間層をエツチング除去し、続いて中間層
をマスクとして下地有機高分子塗映を選択的にエツチン
グすることによって得られる。匠米の該:3r*m造で
は中間層にシリコン歇化−9輩化−、シリコン課等のよ
うに酸素ガスを使用するドライエツチングにお込て蝕刻
され醋い無機吻實初糾が遇はれでおりこれらの中間層形
成力&としてt龜で#1層する必要からプラズマCVD
法や真空蒸着法やスパッタ法轡が用いられていた。し〃
為し、これらの中間層形成に関するPjr一工程が艮い
ために、生産能率や歩貿シの低下を未たす欠点があった
In order to alleviate these problems, 3#w#4 was published by J, M, Moran and others at Bell Laboratories in a journal off/(
Kim^-Musience and Technology Volume 16 1620
X (J, Vacuum 5science and
'i'echno-10g7 16.1920 (19
79)). The Oamm structure is obtained by etching and removing the intermediate layer using a resist as a mask, and then selectively etching the underlying organic polymer coating using the intermediate layer as a mask. Takumai's classification: In 3R*M production, the middle layer is made of silicon, and as in the silicon section, the first hardening of the inorganic material that is etched in dry etching using oxygen gas is encountered. Due to swelling, it is necessary to form a #1 layer in order to form an intermediate layer using plasma CVD.
method, vacuum evaporation method, and sputter method were used. death〃
However, since the Pjr process related to the formation of these intermediate layers is complicated, there is a drawback that production efficiency and trade volume are lowered.

本曲は、上記3鳩嬉造におけ1中間層に有機M媒中に少
くともオルガノシラノール(一般式kLn b i (
(Jlリ  、n=1〜3)kn有する混合物を塗 −
Q 布し100℃以上で加熱して得られるシリコン酸化l1
lI!!倉用いて所季工程を大幅に減少させるεとがで
きるパターン形成方法を提供するものである。
This song contains at least organosilanol (general formula kLn b i (
(Jlli, n=1-3) Apply a mixture with kn -
Q Silicon oxide l1 obtained by applying cloth and heating at 100℃ or higher
lI! ! The purpose of the present invention is to provide a pattern forming method that can be used in a warehouse and that can significantly reduce the number of seasonal steps.

本発明によれば披エツチング材上に有機高分子塗−を形
成し、該壱憬^分子塗良上に有機溶媒中に少くともオル
ガノシラノールを含有する混合物を塗醜し、こγLt−
100℃以上の温良で加熱してシリコン改化−金形槙し
、次いで該シリコン酸化真上にレジスト礁を設けるか、
あるいは被エツチング材上に有ai!尚分子皇−を形成
し、該M磯高分子塗編上に有機溶媒中に少くともオルガ
ノシラノールを1有する混合物を盆−し、該血−上にレ
ジス) 1mt−wiけ、これを100℃以上の温度で
加熱して前記混合物の塗膜をシリコン改化膜となした後
、リソグラフィ技術を用いて前記レジスト限に6【望の
パターンを形成し、該パターンか形成された前記レジス
ト嚢をマスクとして前記シリコン藏化挾をドライエツチ
ングした後、エツチングされずに残った該シリコン酸化
映をマスクとして前記有慎^分子m@を少くとも#/、
累ガスを宮む反応ガスを用いてドライエラチンブレ、そ
の披エツチングされずに!lI!った前記シリコン膜ま
たはエツチングされずに残りfc前記竹機扁分子汰−を
マスクとして前記被エツチング材tエツチングすること
を特徴とするパターン形成方法を得る。
According to the present invention, an organic polymer coating is formed on the etching material, and a mixture containing at least organosilanol in an organic solvent is coated on the polymer coating.
Either by heating at a temperature of 100° C. or higher to modify the silicon and molding it, and then providing a resist reef directly above the silicon oxidation, or
Or there is a problem on the material to be etched! A mixture containing at least 1 organosilanol in an organic solvent was placed on the Miso polymer coated layer, 1 mt-width (1 mt. After heating the mixture at a temperature above to form a silicone modified film, a lithography technique is used to form a desired pattern on the resist area, and the resist bag formed with the pattern is After dry-etching the silicon oxide film as a mask, the silicon oxide film remaining unetched is used as a mask to dry-etch the silicon oxide film at least #/,
Dry erasure using a reactive gas that absorbs the accumulated gas, without being exposed! lI! There is obtained a pattern forming method characterized in that the material to be etched is etched using the etched silicon film or the remaining unetched silicon film as a mask.

以下本発明の効果を一笑地νui用いIHしく述ヘル0
本発明の一央抛丙はオルガノシラノールの一植C鵬”i
 C0ki)s 【アルコール中に台上させた混合物を
用いたものである。これはレジストのように所定の粘!
を含有するようにアルコールcc俗舛させた塗布atス
ピン飯布でウェハ上に均−VC塗布し100℃以上の熱
処理によってアルコールケ除去した結果bi(Jx @
 (1(x≦2)が優られるものである、従って該31
1#構造の形成に要する工程はスピン迩布と熱処理だけ
であり極めて短時間に容易に形成でさる。このδ1(j
x−の廁厚は上記塗1献の枯匿、スピンme時のウェハ
の回転速gjte制(財)することによって任意に設定
することができる。
Below, I will explain the effects of the present invention in detail using νui.
The present invention is based on organosilanol.
C0ki)s [Uses a mixture placed on a bench in alcohol. This has a certain viscosity like a resist!
As a result of uniformly coating VC on the wafer with a spin cloth and removing the alcohol by heat treatment at 100°C or higher, the result was bi(Jx @
(1 (x≦2) is superior, so the 31
The steps required to form the 1# structure are only spin-spinning and heat treatment, and can be easily formed in an extremely short time. This δ1(j
The thickness of x- can be arbitrarily set by controlling the ablation of the coating described above and the rotational speed gjte of the wafer during spin me.

また上記熱処理時の雰囲気は濾水、酸素、窒気等通常の
リングラフイエ根で用いられる尽囲気を用いることρ為
できる。
Further, the atmosphere during the above heat treatment can be an exhaust atmosphere such as filtered water, oxygen, nitrogen, etc., which is normally used for lingulae roots.

本案mvsにおいては仮エツチング−がシリコン酸化−
である、第1凶は本貝地列を祝−するための図で、上部
3mm造の形成及びエツチングにおける主要工程での#
l1ifを朧を退りて俣式的に示した図である。段差の
めるシリコン&板1OIKC■D散化良102倉約l刷
n■−厚で堆積させ、丙えはシラフレー社が線速するホ
ン形レジストでめるAZ−1350J(−品名) 10
3 kill 1.5nmの平均−厚で通称の一転血布
法によっ1仮躾し、150℃以上の温[−″C熱処堀す
る。続いてスピン遊布法によって”aS i (0ki
)s tアルコールに嬉解シた塗布線1厚さ100OA
たけ?A布し104.さらにその上KPGMA1111
05をjlll[L、前焼きする。その後電子ビームで
直接描画し現像す5(b)図)。
In this MVS, temporary etching is silicon oxidation.
The first figure is a diagram to celebrate the main shell formation, and shows the ## in the main process of forming and etching the upper 3mm structure.
It is a diagram showing l1if in a less hazy manner. Silicone & plate to fill the step 1OIKC■D Diffusion quality 102 degrees Celsius Printing n■-Thickness is deposited, and the second one is made by Silafray Co., Ltd. with line speed Hong type resist AZ-1350J (-Product name) 10
3. The average thickness of 1.5 nm is temporarily tempered by the so-called ichikin blood cloth method, and then heat-treated at a temperature of 150°C or higher [-"C. Then, by the spin spread method, "aS i (0ki
) s 1 coated line coated with alcohol, thickness 100OA
Take? A cloth 104. Furthermore, KPGMA1111
05 jllll [L, pre-bake. After that, it is directly written with an electron beam and developed (Fig. 5(b)).

現像1[m! して%溶剤t1m去Li’GMAII1
105をマスクとして% ”’4 k反応ガスとして反
応性スパッタエツチング法によシ該中1一層104を除
去する((G)図)。続いて該中11a盾104をマス
クとして酸素ガスを反応ガスとした反応性スパッタエツ
チングを行うと、基板に対して垂直に近い断面をもつ九
ムz−tisoJs<のパターンが形成される((d)
図)、第2図に酸素ガスを用いた反応スパッタエツチン
グにおける上記AZ−1350Jl1mと上記8ム(J
x@のエツチング選択肢を示した。エツチング条件は酸
素ガス圧80mTorr、fitsoδccm。
Development 1 [m! % solvent t1m removedLi'GMAII1
The middle layer 104 is removed by a reactive sputter etching method using 105 as a mask and %''4k reactive gas (Figure (G)).Subsequently, using the middle 11a shield 104 as a mask, oxygen gas is removed as a reactive gas. When reactive sputter etching is performed with
Figure 2 shows the above AZ-1350Jl1m and the above 8mm (J
The etching options for x@ are shown. The etching conditions were an oxygen gas pressure of 80 mTorr and a fitso δccm.

パワーα0^号−である。選択比は約50で十分実用に
耐え得るものである。この選択比は健米中間層としてI
@かられていたシリコン酸化膜、シリコン窒化II、シ
リコン−と同等である。
The power is α0^. The selection ratio is about 50, which is sufficient for practical use. This selection ratio is I as a healthy middle class.
It is equivalent to the silicon oxide film, silicon nitride II, and silicon-, which were made from @.

続いて該中間層104又は*AZ−13501k103
をマスクとして、 CF4 +”tを反応カスとした反
応性スパッタエツチングによってCVI)酸化m102
をエツチングすると(a)図におけるP GMA 績1
05のパターン寸法と同1[の寸法を有する酸化−10
2のパターンが形成される((C)図)。その転写精度
は従来列と同等であった。また転写寸法として0.3μ
mが得られた。
Subsequently, the intermediate layer 104 or *AZ-13501k103
CVI) oxidized m102 by reactive sputter etching using CF4+”t as a mask and reactive scum.
By etching, (a) P GMA result 1 in figure
Oxidation-10 with the same pattern dimensions as 05 and 1[
2 patterns are formed (Figure (C)). The transfer accuracy was equivalent to that of the conventional column. Also, the transfer size is 0.3μ
m was obtained.

ここでは有機尚分子暎材料としてAZ−135OJ−を
用いたが、特に元や電子ビームによって感応するレジス
トとは限らず、塗布できるポリイミドる。
Here, AZ-135OJ- was used as the organic molecular weight material, but it is not limited to resists that are particularly sensitive to electron beams or polyimides that can be coated.

この実fl丙では、中間l曽としてCf% b i (
”’ )sをアルコールを主成分とする俗解したwag
を用いた。これは100℃以上の熱処理によって容易に
8i()x(1<X≦2)に変換されるのでCF番プラ
ズマに対してエツチングされるが、T万O17′″ラズ
マでは十分マスク注ft有する。本実施列では有機島分
子−を塗布した後、熱処理したが3層を連続的にスピン
塗布した後、最故に熱処理して本兄明と同じ効果を有す
る3層構造を形成することも可能である。また、中Id
1層としてはCH,8i((JH)nに限らずオルガノ
シラノールであればよい。
In this actual fl C, Cf% b i (
``') s is a slang term for wag whose main ingredient is alcohol.
was used. This is easily converted into 8i()x (1<X≦2) by heat treatment at 100° C. or higher, so it is etched in the CF plasma, but with a T0,000, 17″ plasma, it has a sufficient masking effect. In this example, the organic island molecules were coated and then heat treated, but it is also possible to form a three-layer structure with the same effect as the present invention by sequentially spin-coating three layers and then heat-treating them. There is. Also, middle Id
The first layer is not limited to CH, 8i((JH)n, but may be any organosilanol.

また本案−ガではレジスト−としてネガ屋のPGMAI
Iを用いたが、他の極類のレジストでも。
In addition, as a resist for this project, PGMAI of the negative store was used.
I was used, but other polar class resists were also used.

さらにポジ鑞のレジストを用いても本祐明の効果は変わ
らない。
Furthermore, even if a positive resist is used, the effect of Moto Yumei remains the same.

また1本SA施列では中間層、有礪尚分子塗−1被エツ
チング面をそれぞれ反応ガスの異なる反応性スパッタエ
ツチング法を朗いたが、反応ガスを切)換えるだけで同
一真空チャンバー内でエツチングすることが可能である
。さらに何磯^分子塗膜のエツチングには反応性スパッ
タエツチング法の他に円tttimプラズマエッナング
法やイオンミリング法が使用でき、それらの方法ヲ用い
ても、上紀実施岡と同じ効果が得られる。
In addition, in the case of one-line SA processing, the intermediate layer and the surface to be etched with a rich molecule coating-1 were etched using a reactive sputter etching method using different reactive gases, but etching can be performed in the same vacuum chamber by simply switching the reactive gas. It is possible to do so. Furthermore, in addition to the reactive sputter etching method, circular tttim plasma etching method and ion milling method can be used for etching molecular coatings, and even if these methods are used, the same effect as that of Jouki Jitsugoka can be obtained. can get.

を九被エツチング材とじて本実施列ではシリコン酸化−
を用いたが他にも金網、8i、シリザイド、 8i、N
4.Ax、u、 、(iaAs等の1n−v族化合物。
In this example, silicon oxidation was performed with nine etching materials.
We used wire mesh, 8i, silizide, 8i, N
4. Ax, u, (1n-v group compounds such as iaAs).

II−VI族化合物等も本兄明によれはiJ舵である。According to the present inventor, II-VI group compounds are also iJ rudders.

以上l!明したように本発明によるパターン形成方法で
は工程がきわめて容易で短時間であ)かつエツチングに
ついても少くとも従来列と同等の効果が得られており倣
祷なパターンを有する集積回路の製造工程に尋人するこ
とができる。
That’s all! As explained above, the pattern forming method according to the present invention is extremely easy and takes a short time), and the etching effect is at least equivalent to that of the conventional method. Can be interrogated.

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

1111図(a)(b)(C)(d)(e)各図は本発
明の一実施内を6L明するための図で、詳細な説明中で
述べた3層II造の形成及びエツチングにおける主要工
程でO該3層祷造の断面を顔を追って示した模式争縞2
図は本発明で中間層として用^た5i(Jx暎と有ll
1IIII分子膜として用いたAZ−”1350J1m
との@素を反応カスとして用いたスパッタエラf7”K
Thけるエツチング速度を示したものである。 図中の壷号は以下のものを示している。 101・・・シリコン&板、102・・・被エツチング
―。 1os−ht−1350Jh、104−m布fblfc
 ! D 形成ッチング速度。 (d/) Ce) 第2図 工・ンモンゲe存r句 c勺っ
1111 Figures (a), (b), (C), (d), and (e) are diagrams for explaining one implementation of the present invention, and show the formation and etching of the three-layer II structure described in the detailed description. Schematic diagram 2 showing the cross section of the three-layer construction in the main process.
The figure shows the 5i (Jx and
AZ-”1350J1m used as 1III molecular membrane
Sputtering error f7”K using @ element as reaction residue
This figure shows the etching speed. The bottle numbers in the figure indicate the following. 101...Silicon & board, 102...To be etched. 1os-ht-1350Jh, 104-m cloth fblfc
! D formation etching rate. (d/) Ce) 2nd drawing/nmonge e existr phrase c 勺

Claims (1)

【特許請求の範囲】[Claims] 被エツチング材上に有機−分子血−を形成し、該有機両
分子li!−上に有m溶媒中に少くともオルガノシラノ
ールを含有する混合物t−塗映しこれt100℃以上の
m度で加熱してシリコン鈑化imt−形成し、次いで販
シリコン販化−上にレジスト餉を設けるかあるいは被エ
ツチング材上に有機^分子*映を形成し、#&有機尚分
子塗映上に有愼溶媒中に少くともオルガノシラノールt
−)有する混合物tllllllシ、該厘決上にレジス
ト−を設け、これt100℃以上の一度でD0熱して前
記混合物の翅楓をシリコン教化−となした後、リングラ
フィ婢術を出いてm記しジスト映に所望のパターンを形
成し該パターンが形成された前記レジスト−をマスクと
し″C前d己シリコン1k11SllIt”ドライエツ
チングした故、エツチング避ntに残った該シリコン鹸
化v4をマスクとして前記有−簡分子違膜を少くとも酸
素ガスを含む反応ガスを槓いてドライエツチングし、そ
の故エツチングされずに残った目σ6己シリコン酸化−
またはエツチングされずに残った1Ak2有機高分子塗
論をマスクとして@mlm二値チング材をエツチングす
ることt−特畝と・rるパターン形成方法。
An organic molecular blood is formed on the material to be etched, and both organic molecules li! - A mixture containing at least organosilanol in a solvent is coated on top and heated at 100°C or more to form a silicon plate, and then a resist plate is applied on the silicon plate. or by forming an organic molecule coating on the material to be etched, and adding at least an organosilanol t in a solvent on the #&organic molecule coating.
-) A resist is placed on the mixture, and the resist is heated to a temperature of 100°C or higher to convert the mixture into silicone. A desired pattern was formed on the resist image, and the resist with the pattern formed thereon was used as a mask for dry etching.The saponified silicon V4 remaining in the etching area was then used as a mask for dry etching. The simple molecular film is dry-etched using a reactive gas containing at least oxygen gas, and therefore the remaining unetched portions are oxidized to silicon.
Alternatively, etching the @mlm binary etching material using the 1Ak2 organic polymer coating that remained unetched as a mask is a method of forming a pattern with special ridges.
JP56208797A 1981-12-23 1981-12-23 Pattern formation Granted JPS58110038A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56208797A JPS58110038A (en) 1981-12-23 1981-12-23 Pattern formation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56208797A JPS58110038A (en) 1981-12-23 1981-12-23 Pattern formation

Publications (2)

Publication Number Publication Date
JPS58110038A true JPS58110038A (en) 1983-06-30
JPH0542810B2 JPH0542810B2 (en) 1993-06-29

Family

ID=16562271

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56208797A Granted JPS58110038A (en) 1981-12-23 1981-12-23 Pattern formation

Country Status (1)

Country Link
JP (1) JPS58110038A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6125141A (en) * 1984-07-16 1986-02-04 Tokyo Denshi Kagaku Kabushiki Mask forming material
JPS62291119A (en) * 1986-06-11 1987-12-17 Toray Ind Inc Manufacture of semiconductor element
JPS6316623A (en) * 1986-07-08 1988-01-23 Fujitsu Ltd Manufacture of semiconductor device
JPS63140539A (en) * 1986-12-02 1988-06-13 Nec Corp Manufacture of semiconductor device

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4244799A (en) * 1978-09-11 1981-01-13 Bell Telephone Laboratories, Incorporated Fabrication of integrated circuits utilizing thick high-resolution patterns
JPS5649540A (en) * 1979-06-21 1981-05-06 Fujitsu Ltd Semiconductor device
JPS5858734A (en) * 1981-05-07 1983-04-07 ハネウエル・インコ−ポレ−テツド Method of generating positive electronic resist video with high sensitivity

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4244799A (en) * 1978-09-11 1981-01-13 Bell Telephone Laboratories, Incorporated Fabrication of integrated circuits utilizing thick high-resolution patterns
JPS5649540A (en) * 1979-06-21 1981-05-06 Fujitsu Ltd Semiconductor device
JPS5858734A (en) * 1981-05-07 1983-04-07 ハネウエル・インコ−ポレ−テツド Method of generating positive electronic resist video with high sensitivity

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6125141A (en) * 1984-07-16 1986-02-04 Tokyo Denshi Kagaku Kabushiki Mask forming material
JPS62291119A (en) * 1986-06-11 1987-12-17 Toray Ind Inc Manufacture of semiconductor element
JPS6316623A (en) * 1986-07-08 1988-01-23 Fujitsu Ltd Manufacture of semiconductor device
JPS63140539A (en) * 1986-12-02 1988-06-13 Nec Corp Manufacture of semiconductor device

Also Published As

Publication number Publication date
JPH0542810B2 (en) 1993-06-29

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