JPS5925228A - Method for lift-off process - Google Patents
Method for lift-off processInfo
- Publication number
- JPS5925228A JPS5925228A JP13366682A JP13366682A JPS5925228A JP S5925228 A JPS5925228 A JP S5925228A JP 13366682 A JP13366682 A JP 13366682A JP 13366682 A JP13366682 A JP 13366682A JP S5925228 A JPS5925228 A JP S5925228A
- Authority
- JP
- Japan
- Prior art keywords
- film
- substrate
- resist
- lift
- ultraviolet
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title abstract description 18
- 239000000758 substrate Substances 0.000 claims abstract description 32
- 229910052751 metal Inorganic materials 0.000 claims abstract description 15
- 239000002184 metal Substances 0.000 claims abstract description 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000001301 oxygen Substances 0.000 claims abstract description 6
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 6
- 238000003672 processing method Methods 0.000 claims description 8
- 229910052753 mercury Inorganic materials 0.000 claims description 7
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 6
- 238000000151 deposition Methods 0.000 claims description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 3
- 239000010453 quartz Substances 0.000 claims 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract description 4
- 229910001882 dioxygen Inorganic materials 0.000 abstract description 4
- 239000007789 gas Substances 0.000 abstract description 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 abstract description 2
- 230000000694 effects Effects 0.000 abstract description 2
- 238000006552 photochemical reaction Methods 0.000 abstract description 2
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 230000002411 adverse Effects 0.000 abstract 1
- 230000006866 deterioration Effects 0.000 abstract 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000004140 cleaning Methods 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920002120 photoresistant polymer Polymers 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- 229910001020 Au alloy Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000011888 autopsy Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 238000001020 plasma etching Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004506 ultrasonic cleaning Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/302—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to change their surface-physical characteristics or shape, e.g. etching, polishing, cutting
- H01L21/306—Chemical or electrical treatment, e.g. electrolytic etching
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)
- Weting (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、リフトオフ加工法によるバタン形成技術に関
し、特に半導体集積回路装置、ジョセフノン集積回路装
置等の金属膜ないし絶縁膜から成るバタンを形成する場
合に適用して好適なリフトオフ加工方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a batten forming technique using a lift-off processing method, and is particularly suitable for application to forming battens made of a metal film or an insulating film for semiconductor integrated circuit devices, Josephnon integrated circuit devices, etc. This paper relates to a lift-off processing method.
捷ず、当該技術の現状について以下に概説する。The current state of this technology is outlined below.
リフトオフ加工法を用いたバタン形成方法において、基
板上に金属膜あるいは絶縁膜から成る所望のバタンを得
るKは、まず基板上にポジ型レジスト膜から成るリフト
オフ用スデン/ルを形成したのち、真空槽内で所望の金
属膜ないし絶縁膜を蒸着したのに引き続き、アセトン等
のレジストバタンンル拐の良溶媒中に浸111it L
で溶解し、同時に、レジストバタンノル上の不要な金属
膜ないし絶縁膜を機械的に除去することによって、所望
の金属膜ないし絶縁膜から成るバタンを得るものである
。In the batten forming method using the lift-off processing method, in order to obtain a desired batten made of a metal film or an insulating film on a substrate, first a lift-off pad made of a positive resist film is formed on the substrate, and then vacuum After depositing the desired metal film or insulating film in the tank, the film is immersed in a good solvent for removing the resist film, such as acetone.
At the same time, by mechanically removing unnecessary metal films or insulating films on the resist film, a desired film or insulating film is obtained.
」−記工程中、ポジ型し/スト膜から成るリフトオフ用
ステンンルを形成する工程において、ステンシルの形成
にシ1−1通當光露−)ICないし電子ヒーム露光に引
き続いて、ステンシルも構成するポジ型ホトレ/ストの
指定現像液にて現像することによってレジストバタンか
形成される。との場合、本来レジス)・膜が溶解・除去
されて基板表面が露出するステノ/ル開孔部、すなわち
、以後の工程において所望の金属膜ないし絶縁膜が被覆
すべき領域に、厚さ数λ〜数10人のレジスト残渣層の
存在か認められる。(例えは、既公開刊行物 1・、
11゜Kaplan and 13.に、 Bcrg
in ° ” 11.csicJuesfrom W
et1’roccssingof Po5itive
R,esists” 、 J 、 Elcctro
−cl+c+nic旧SOC,V(11,i27 、
No、 7 、 1980年2月号、l)、386〜I
)、396参照)このようなレジスト残渣層か存在する
基板上に蒸着膜を被覆した場合、当該蒸着膜の刺着性を
劣化させ、かつ寸だ下地金属膜と当該蒸着金属膜の電気
的接続を妨害する。- During the step of forming a lift-off stencil made of a positive type film, the stencil is formed using 1-1 light exposure -) Following the IC or electron beam exposure, the stencil is also formed. A resist baton is formed by developing with a specified positive photoresist developer. In this case, the resist film is dissolved and removed to expose the substrate surface, that is, the area where the desired metal film or insulating film is to be covered in the subsequent process is The presence of a resist residue layer of λ to several tens of layers is recognized. (For example, published publications 1.
11゜Kaplan and 13. To, Bcrg
in °” 11.csicJuesfrom W
et1'roccssingof Po5itive
R,esists”, J, Elcctro
-cl+c+nic old SOC, V (11, i27,
No. 7, February 1980, l), 386-I
), 396) When a deposited film is coated on a substrate on which such a resist residue layer exists, the adhesion of the deposited film deteriorates and the electrical connection between the underlying metal film and the deposited metal film is significantly reduced. interfere with
したかつて、上記したし/スト残渣層を除去する方法と
して、従来は蒸着膜を被覆する直前に、真空槽内を酸素
ガス雰囲気とし、I’CF電力を印加して、02カスプ
ラズマを発生させて、基板表面に刺着しているし/スト
残渣層をプラスマエノチングで除去する方法が一般に採
用されている。In the past, as a method for removing the above-mentioned ink/stamp residue layer, the conventional method was to create an oxygen gas atmosphere in the vacuum chamber and apply I'CF power to generate 02 gas plasma immediately before coating the vapor deposited film. Generally, a method is adopted in which the residual layer stuck to the substrate surface is removed by plasma etching.
コノような従来方法ては、酸素ノJスプラスマクリーニ
ング条件の制御を厳密に行なわねばならない。すなわち
、クリーニングが不十分な場合はし/ス(・残渣層の除
去か不完全であり、過剰な場合は、金属膜表面に不必要
な酸化物層を形成して、金属間の電気的接続に悪影響を
及はず。さらに、真空槽内で当該基板にRF電力を印加
するだめには、基板を取り伺けるホルダを真空槽の他の
部分と電気的に絶縁する必要があるだめ、装置構成上大
きな制約条件となる。丑だ、RF電力を印加することに
よって発生ずる02力スプシズマの密度を均一にするた
めにも、上記基板ホルダの構造と、真空槽の構造に制約
条件が太きい笠の欠点があるだめ、Oカスプラスマクリ
ーニンク法は管遍性に富む技術とは言い鮨、い。Conventional methods such as this require strict control of oxygen plasma cleaning conditions. In other words, if the cleaning is insufficient, the removal of the residual layer is incomplete, and if it is excessive, an unnecessary oxide layer will be formed on the surface of the metal film and the electrical connection between the metals will be damaged. In addition, in order to apply RF power to the substrate in the vacuum chamber, it is necessary to electrically insulate the holder from which the substrate can be accessed from other parts of the vacuum chamber. Unfortunately, in order to make the density of the 02 force spisma generated by applying RF power uniform, there are large constraints on the structure of the substrate holder and the structure of the vacuum chamber. Due to its shortcomings, the Ocasplus Mac Cleaning method is not a very versatile technique.
本発明の目的は、上述のような従来技術の欠点、すなわ
ち、し/ストステンシル形成後の開孔部基板表面に残存
するし/スト残渣層を、極めて簡単な処理で除去する新
規なリフトオフ加工方法を提供するととにある。The object of the present invention is to solve the above-mentioned drawbacks of the prior art, namely, to provide a novel lift-off process that removes the silica/stack residue layer remaining on the surface of the aperture substrate after the formation of the stencil with an extremely simple process. It is there to provide a method.
上記の目的の本発明のリフトオフ加工方法の特徴とする
ところは、清浄な大気中斗たけ酸素雰囲気中で点灯した
低圧石英水銀灯寸だは高圧水銀灯等の波長195 +1
111以内の紫外線を放射する紫外線光源下に、し/ス
ト膜がら成ろリフトオフ用ステン/ルか形成されている
基板表面を暴露したのち、真空槽内で前記の基板表面に
所望の金属膜ないし絶縁膜を蒸着することにある。The lift-off processing method of the present invention for the above purpose is characterized by a wavelength of 195 +1 compared to that of a low-pressure quartz-mercury lamp lit in a clean oxygen atmosphere and a high-pressure mercury lamp.
After exposing the surface of the substrate on which the lift-off stainless steel film is formed under an ultraviolet light source that emits ultraviolet light within 111 nm, a desired metal film or metal film is applied to the surface of the substrate in a vacuum chamber. The purpose is to deposit an insulating film.
このような本発明の方法によるときは、極めて容易に、
確実に基板表面に残存するし/スト残清層を除去して、
金属膜ないし絶縁膜を蒸着てきる効果をもたらすことが
できるものである。When using the method of the present invention, it is extremely easy to
Ensures that it remains on the substrate surface/removes the residual layer.
This can produce the effect of depositing a metal film or an insulating film.
本発明のリフトオフ加工方法における、紫外線光源下に
基板表面を暴露するために使用てきる紫外線照射装置の
一例の原理を示す側断面説明図を第1図に示す。FIG. 1 is a side cross-sectional view showing the principle of an example of an ultraviolet irradiation device that can be used to expose the substrate surface to an ultraviolet light source in the lift-off processing method of the present invention.
第1図において、符号1.1、・・・ は低圧水銀灯群
、2はウェーハ搬送ベルト、6は清浄空気捷だは酸素カ
ス導入孔、4は排気孔、5はウェーハである。In FIG. 1, numerals 1.1, . . . are a group of low-pressure mercury lamps, 2 is a wafer transport belt, 6 is a clean air vent or oxygen gas introduction hole, 4 is an exhaust hole, and 5 is a wafer.
ここで、低圧水銀灯群1.1、・・・・・は、外形がり
、J字型をした定格人力40Wのう/プ4絹から成り、
管」]質は短波長紫外線の吸収の少ない合成石英ガラス
である。管球の中心からウェー・・表面寸ての距離はお
およそ15 mmである。ウェー・・表向における紫外
線強度は波長184.9 nmの輝線が約50O/ハヘ
’/C1l+2.254.7111TIの輝線が約10
/lW/C1112てあり、そね、より長波長側の紫外
線の強さは、いずれも1μW以l・である。空気中−ま
たは酸素ガス雰囲気中において波長195 nm以内の
紫外線を照射すると、酸素ノjスの光化学反応により、
オゾンガスか発生する。この照射装置のウェーハ面伺近
におけるオシツノjス濃度を測定したところ50〜70
1)pmてあった。Here, the low-pressure mercury lamp group 1.1, .
The tube is made of synthetic quartz glass, which has low absorption of short-wavelength ultraviolet rays. The distance from the center of the tube to the surface of the tube is approximately 15 mm. The intensity of ultraviolet rays on the surface is approximately 50 O/hahe'/C1l+2.254.7111TI with a wavelength of 184.9 nm and approximately 10
/lW/C1112, and the intensity of ultraviolet rays on the longer wavelength side is 1 μW or less. When irradiated with ultraviolet rays with a wavelength of 195 nm or less in air or an oxygen gas atmosphere, a photochemical reaction of oxygen causes
Ozone gas is generated. When the concentration of osmotic acid near the wafer surface of this irradiation device was measured, it was 50 to 70.
1) It was pm.
以Fに、」−記の紫外線照射装置を使用したリフトオフ
加工方法の実施例について詳述する。Hereinafter, an embodiment of the lift-off processing method using the ultraviolet irradiation device described in "-" will be described in detail.
濃硫酸と過酸化水素水の混合液に約1o分間浸漬後、純
水洗浄および乾燥処理を施した、表面が薄いS + 0
2膜で被覆されているS1ウエーハに、ヘキザメチル/
/ラザン(111νIDS )を塗布したのに引き続き
、ボン型ホトレジスト
スl− ( Shiplcy社商品名)を回転塗布した
のち、70℃に加熱した対流式オーブン内て6o分間ブ
リヘーク処即を行なった。引き続き通常の光露光方式に
よって所望のパタンを転写し、その基板を温度20℃の
フロムベンセン液中に10分間浸漬・乾燥に続いて、純
水で1=1に箱釈したAZ現像液(液温20℃)中に6
分間浸漬して現像しだのち、純水にて洗浄・乾燥してレ
ジスト残渣層・/ルを形成し実施例試料とした。S + 0 with a thin surface, immersed in a mixture of concentrated sulfuric acid and hydrogen peroxide for about 10 minutes, then washed with pure water and dried.
Hexamethyl/
/ Lasan (111vIDS) was applied, followed by spin coating of Bonn type photoresist 1- (trade name of Shiplcy), followed by a brihake treatment for 60 minutes in a convection oven heated to 70°C. Subsequently, a desired pattern was transferred using a normal light exposure method, and the substrate was immersed in Frombensen solution at a temperature of 20°C for 10 minutes and dried. 6 during (temperature 20℃)
After being immersed for a minute and developed, it was washed with pure water and dried to form a resist residue layer, which was used as an example sample.
寸だ、比較試料として、轟該し/スト膜を塗布・プリベ
ーク処理した基板を、露光現像する代りに、メチルイソ
ブチルケトン(MI 13K )−iだはアセトン中に
浸漬、まだは硫酸と過酸化水素水の混合KI7.(11
2SO4/lI202)による洗浄て、し/スト膜を溶
解・除去した基板を用意した。As a comparative sample, instead of exposing and developing a substrate that had been coated and prebaked with a drying/stripping film, it was immersed in methyl isobutyl ketone (MI 13K)-i or acetone, or sulfuric acid and peroxide. Mixing hydrogen water KI7. (11
A substrate was prepared by washing with 2SO4/lI202) to dissolve and remove the desist film.
こののち、上記のそれぞれの試料の基板を前記の紫外線
照射装置を用いて、0,5〜5分間紫外線を照射し、レ
ジスト膜の膜厚とS【02基板表面の純水に対する接触
角を測定した。After that, the substrate of each of the above samples was irradiated with ultraviolet rays for 0.5 to 5 minutes using the above-mentioned ultraviolet irradiation device, and the thickness of the resist film and the contact angle of the surface of the S02 substrate with pure water were measured. did.
第2図は紫外線照射時間とAZ−1470し7スト膜の
膜厚の関係を示しだグラフて、初期膜厚1.47/珪〕
のレジスト膜か紫外線照射時間に応じて減少し、6分間
照射後には1.44μ田と300λの膜ベリか生じてい
ることがわかる。この結果から、紫外線照射によってレ
ジスト膜の成分が酸化され、C02と1120等に分解
・除去されているものと推定されろ。前述し、たよりな
厚さ数人〜数10Aのし7スト残渣層の除去には、1〜
2分程度の照射時間で十分目的か達ぜられることは明ら
かである。Figure 2 shows the relationship between ultraviolet irradiation time and film thickness of AZ-1470 7-stroke film.The graph shows the initial film thickness of 1.47/silicon.
It can be seen that the resist film size decreases depending on the UV irradiation time, and after 6 minutes of irradiation, film burrs of 1.44μ and 300λ have occurred. From this result, it can be inferred that the components of the resist film are oxidized by ultraviolet irradiation and decomposed and removed into CO2, 1120, and the like. As mentioned above, in order to remove a reliable layer of thickness from several to several tens of amps, it is necessary to
It is clear that an irradiation time of about 2 minutes is sufficient to achieve the objective.
第1表は、紫外線照射処理に、しってレジスト残清層か
完全に除去されたかいないかを知るだめ、処理前後の基
板表面の純水に対する接触角を測定した、実施例試享−
1と比較試料とについてのものである。硫酸と過酸化水
素水の混合液で洗浄処理して、有機物をはしめとする表
面汚染層イク除ツ、しだS Io 2基板表面の水に対
する接触角は、第1表に示すように、紫外線照射の有無
に係りなく 2°〜6°と親水性を示す。それに対して
、表面に有機物等の吸着汚染層か存在する場合は、一般
に大きな第 1 表
接触角を示し、親水性から疎水性に変化することが認め
られる。Table 1 shows an experimental example in which the contact angle of the substrate surface with pure water before and after the ultraviolet irradiation treatment was measured in order to know whether the resist residual layer was completely removed or not after the ultraviolet irradiation treatment.
1 and a comparative sample. After cleaning with a mixture of sulfuric acid and hydrogen peroxide to remove the surface contamination layer consisting of organic matter, the contact angle of the surface of the Shida S Io 2 substrate with water is as shown in Table 1. Shows hydrophilicity of 2° to 6° regardless of the presence or absence of irradiation. On the other hand, when there is a layer of adsorbed contaminants such as organic substances on the surface, the contact angle shown in Table 1 is generally large, and it is observed that the property changes from hydrophilic to hydrophobic.
第1表の実験結果から明らかなように、AZ−1470
レンストを塗布・プリベーキング後、1;1に希釈した
AZ現像液、またはM I 13 K、およびアセトン
中て約20分間超音波洗浄してし/スト膜を除去した8
102基板表面の接触角はいずれも20°〜60°と太
きいのに対して、上記各基板に紫外線照射処理を2分間
施すと、接触角は2°〜ろ0となり、疎水性から親水性
に変化している。従って、第1表の結果は、基板表面に
イで1着していたし/スト残 層が2分間の紫外線照射
処理によって除去できたことを示すものである。As is clear from the experimental results in Table 1, AZ-1470
After coating and pre-baking the Lenst, the Lenst film was removed by ultrasonic cleaning for about 20 minutes in AZ developer diluted to 1:1 or M I 13 K and acetone.
The contact angle of the 102 substrate surface is large, ranging from 20° to 60°, but when each of the above substrates is subjected to UV irradiation treatment for 2 minutes, the contact angle changes from 2° to 0, changing from hydrophobic to hydrophilic. is changing. Therefore, the results shown in Table 1 indicate that the residual layer of oxide/stain deposited on the surface of the substrate could be removed by UV irradiation treatment for 2 minutes.
捷だ、前記のレジストステン/ル基板上に膜厚的Q、
8 /Zlnの円)/LIT/Au合金膜、および、膜
厚的Q671+nのSiO膜を各々真空蒸着し、へ41
旧く液中で28kllZ・75W の超音波を印加して
、レヅストスデノンルを溶解すると同時にその」二〇不
・皮膜を除去して、リフトオフ処理によるバタン形成を
行なった。However, on the resist stain/ru substrate, the film thickness Q,
8/Zln circle)/LIT/Au alloy film and a SiO film with a film thickness of Q671+n were each vacuum-deposited to 41
Previously, ultrasonic waves of 28kllZ and 75W were applied in the liquid to dissolve the resin and at the same time remove the film, and form a batten by lift-off treatment.
この際、リフトオフ加工を行A:′)に必要以上の長時
間超&波を印加し、上記蒸着膜の基板からのはく離発生
の有無を目祝検剖した。この結果、紫外線照射処理を行
なわないものでば、1.’b / I IT /A、1
1膜では、20分、SiO膜では40分て膜のはく離の
発生力1忍められブこのに対し、紫外線照射を2分間行
なった試料では、各々約60分、約60分の処理におい
てもはく離の発生か認められず、両者に明らかな有意差
が認められた。At this time, ultraviolet waves were applied to row A:') for a longer time than necessary for the lift-off process, and a visual autopsy was performed to determine whether or not the above-mentioned vapor-deposited film had peeled off from the substrate. As a result, if the ultraviolet irradiation treatment is not performed, 1. 'b / I IT /A, 1
On the other hand, the sample exposed to ultraviolet rays for 2 minutes could withstand the force of peeling of the film for 20 minutes and 40 minutes for the SiO film. However, for the sample exposed to ultraviolet rays for 2 minutes, the force for peeling could be tolerated even after approximately 60 minutes and 60 minutes of treatment, respectively. No peeling was observed, and a clear significant difference was observed between the two.
以十に説明したように、本発明により、基板表面に存在
するレジスト残渣層の除去が簡単な装置で容易に実現て
きるようにな−〕だ結果、蒸着膜形成直前の(−)2カ
スプラスマクリーニンク処理の省略かり能となった結果
、蒸着装置の構造とリフトオフ上程の簡略化と蒸着装置
の低廉化がriJ能となり、この結果、とくにリフトオ
フ加工によるバタン形成技術を使用する7ヨセモ
造歩留りの向上と製造コストの低減化に大きく寄与しう
るものである。As explained above, according to the present invention, the resist residue layer existing on the substrate surface can be easily removed using a simple device. As a result of the omission of the plasma cleaning process, the structure of the vapor deposition equipment, the simplification of the lift-off process, and the reduction in the cost of the vapor deposition equipment have become the riJ performance. This can greatly contribute to improving yield and reducing manufacturing costs.
第1図は本発明のリフトオフ加工方法に使用てきる紫外
線照射装置の一例の原理を示す側断面説明図である。
第2図は八Z147[]レジストの紫外線照射時間に対
する残存膜厚を示すグラフである。
1・・・低圧水銀灯
2・・ウェーハ搬送ベルト
6 ・導入孔
4・・排気孔
5・・ウェーハ
特許出願人 日本電信電話公社
代理人弁理士 中利純之助
矛1図
′8P2図FIG. 1 is a side cross-sectional explanatory view showing the principle of an example of an ultraviolet irradiation device that can be used in the lift-off processing method of the present invention. FIG. 2 is a graph showing the remaining film thickness of the 8Z147[] resist with respect to the ultraviolet irradiation time. 1...Low-pressure mercury lamp 2...Wafer conveyor belt 6 -Introduction hole 4...Exhaust hole 5...Wafer patent applicant Nippon Telegraph and Telephone Corporation Representative Patent Attorney Junnosuke Nakatoshi 1 Figure '8P2 Figure
Claims (1)
銀灯まだは高圧水銀灯等の波長195 nm以内の紫外
線を放射する紫外線光源下に、レジスト膜から成るリフ
トオフ用ステンノルが形成されている基板表面を暴露し
たのち、真空槽内で前記の基板表面に所望の金属膜ない
し絶縁膜を蒸着することを特徴とするリフトオフ加工方
法。The substrate surface on which the lift-off stain made of the resist film is formed is exposed to an ultraviolet light source emitting ultraviolet light within a wavelength of 195 nm, such as a low-pressure quartz mercury lamp or a high-pressure mercury lamp, which is lit in clean air or an oxygen atmosphere. A lift-off processing method characterized by depositing a desired metal film or insulating film on the surface of the substrate in a vacuum chamber after the exposure.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13366682A JPS5925228A (en) | 1982-08-02 | 1982-08-02 | Method for lift-off process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13366682A JPS5925228A (en) | 1982-08-02 | 1982-08-02 | Method for lift-off process |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5925228A true JPS5925228A (en) | 1984-02-09 |
Family
ID=15110071
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13366682A Pending JPS5925228A (en) | 1982-08-02 | 1982-08-02 | Method for lift-off process |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5925228A (en) |
-
1982
- 1982-08-02 JP JP13366682A patent/JPS5925228A/en active Pending
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