JPH0521336B2 - - Google Patents

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Publication number
JPH0521336B2
JPH0521336B2 JP60189600A JP18960085A JPH0521336B2 JP H0521336 B2 JPH0521336 B2 JP H0521336B2 JP 60189600 A JP60189600 A JP 60189600A JP 18960085 A JP18960085 A JP 18960085A JP H0521336 B2 JPH0521336 B2 JP H0521336B2
Authority
JP
Japan
Prior art keywords
wafer
substrate
temperature
photosensitive resin
chamber
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP60189600A
Other languages
Japanese (ja)
Other versions
JPS6251225A (en
Inventor
Kenji Shibata
Yasuhiro Mochizuki
Hiroyuki Shichida
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.)
Hitachi Ltd
Mitsubishi Power Ltd
Original Assignee
Babcock Hitachi KK
Hitachi 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 Babcock Hitachi KK, Hitachi Ltd filed Critical Babcock Hitachi KK
Priority to JP18960085A priority Critical patent/JPS6251225A/en
Publication of JPS6251225A publication Critical patent/JPS6251225A/en
Publication of JPH0521336B2 publication Critical patent/JPH0521336B2/ja
Granted legal-status Critical Current

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  • Drying Of Semiconductors (AREA)
  • Exposure Of Semiconductors, Excluding Electron Or Ion Beam Exposure (AREA)

Description

【発明の詳細な説明】 〔発明の利用分野〕 本発明は光化学反応方法に係り、特に基板上に
存在する有機物層を迅速に気化、分解させ、これ
を除去する方法に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Application of the Invention] The present invention relates to a photochemical reaction method, and particularly to a method for rapidly vaporizing and decomposing an organic layer present on a substrate and removing it.

〔発明の背景〕[Background of the invention]

ウエハ上に存在する感光性樹脂を除去する方法
として種々の方法が実施されているが、自動化が
容易、メンテナンスが簡単、ウエハの損傷が少い
といつた有利点から、UVオゾン法が注目されて
いる。以下第3図を用いてUVオゾン法の1例を
示す。チヤンバ1内にはウエハ3を置くためのサ
セプタ2、サセプタ2を介してウエハ3を加熱す
るための抵抗式ヒータ7があり、チヤンバ1内に
ガス供給ノズル4から酸素ガスを供給した状態
で、ウエハ3上に低圧水銀灯5により紫外光
(UV)を照射できるようになつている。低圧水
銀灯5は波長185nm及び254nmの強度の強いも
のを用いる。この装置でサセプタ2上に感光性樹
脂を塗布したウエハ3を置き、紫外線を照射する
と、所定時間経過後にはウエハ3上の感光性樹脂
層が気化、分解して除却される。この原理は感光
性樹脂層中の分子結合(例えばC−C、C−H結
合)が紫外線のエネルギにより分解する反応と、
酸素に紫外線を照射することにより生成したオゾ
ンや酸素ラジカルが、これら接合を解かれた炭素
原子や水素原子等と反応し、二酸化炭素や水等を
生じる気化反応とによつて生じると考えられてい
る。
Various methods have been used to remove the photosensitive resin present on wafers, but the UV ozone method is attracting attention because of its advantages such as easy automation, easy maintenance, and less damage to the wafer. There is. An example of the UV ozone method is shown below using Figure 3. Inside the chamber 1, there is a susceptor 2 for placing the wafer 3, and a resistance heater 7 for heating the wafer 3 via the susceptor 2.With oxygen gas being supplied into the chamber 1 from the gas supply nozzle 4, Ultraviolet light (UV) can be irradiated onto the wafer 3 by a low-pressure mercury lamp 5. The low-pressure mercury lamp 5 used has strong wavelengths of 185 nm and 254 nm. With this device, a wafer 3 coated with a photosensitive resin is placed on a susceptor 2 and irradiated with ultraviolet rays, and after a predetermined period of time, the photosensitive resin layer on the wafer 3 is vaporized, decomposed, and removed. This principle is based on a reaction in which molecular bonds (e.g. C-C, C-H bonds) in the photosensitive resin layer are decomposed by the energy of ultraviolet rays.
It is thought that ozone and oxygen radicals generated by irradiating oxygen with ultraviolet rays react with these unbonded carbon atoms, hydrogen atoms, etc., resulting in a vaporization reaction that produces carbon dioxide, water, etc. There is.

第4図は感光性樹脂の気化分解速度Rに及ぼす
ウエハ温度Twの影響を実験により求めたもので
ある。RはTwにより強く影響を受け、Twを高
くすればRは飛躍的に大きくなる。しかしTwを
300℃とした時は、ウエハ上の感光性樹脂の大部
分は第4図に示すような高速で気化分解したが、
局部的に非常に分解し難い成分が残り、この成分
を全て分解しようとすればTwが150℃のときよ
りも却つて長時間を要することが判つた。
FIG. 4 shows the influence of the wafer temperature Tw on the vaporization decomposition rate R of the photosensitive resin, which was determined through experiments. R is strongly influenced by Tw, and as Tw is increased, R increases dramatically. But Tw
At 300℃, most of the photosensitive resin on the wafer was vaporized and decomposed at a high rate as shown in Figure 4.
It was found that some components that are extremely difficult to decompose locally remained, and that it would take much longer to decompose all of these components than when Tw was 150°C.

第5図はこのようにして厚さ1μmの感光性樹
脂層の残膜厚さの最大値tが、紫外光の照射時間
Tに伴つて減少する経過を、ウエハ温度Twが
150と300℃との時で比較したものである。Twが
300℃のときは、当初は高い気化分解速度のため
膜厚さtは急速に減少するが、難分解性成分の気
化分解に多くの時間がかかり、結局Twが150℃
のときよりも長時間を要することがわかる。
Figure 5 shows how the maximum residual film thickness t of a 1 μm thick photosensitive resin layer decreases as the ultraviolet light irradiation time T increases as the wafer temperature Tw increases.
This is a comparison between 150 and 300℃. Tw is
At 300℃, the film thickness t decreases rapidly due to the initially high rate of vaporization, but it takes a long time to vaporize and decompose the refractory components, and eventually Tw reaches 150℃.
It can be seen that it takes a longer time than when

ウエハ温度Twを300℃にした時に難分解性成
分が生じた理由は明らかではないが、ウエハ上の
局所的な温度分布によつて感光性樹脂の熱膨張量
に差が生じ、感光性樹脂のたい積現象が生じるた
めではないかと考えられる。なお難分解性成分が
生じる温度は、感光性樹脂の種類により異なる。
The reason why persistent components were generated when the wafer temperature Tw was set to 300℃ is not clear, but the local temperature distribution on the wafer causes a difference in the amount of thermal expansion of the photosensitive resin. This is thought to be due to the accumulation phenomenon. Note that the temperature at which the hardly decomposable component is generated differs depending on the type of photosensitive resin.

このように従来技術では、ウエハ温度が高い時
に感光性樹脂の気化分解速度が大きいという効果
を活用しきれず、これよりも低い温度で長時間を
要する運用をせざるを得なかつた。
As described above, in the conventional technology, the effect that the rate of vaporization and decomposition of the photosensitive resin is high when the wafer temperature is high cannot be fully utilized, and the operation has to be performed at a lower temperature for a long time.

なお、関連する技術としては、 UV Resist−Stripping for High−Speed and
Damage−Free Process/Exten and Abstracts
of the 15th Cont.on Solid State Devices and
Materials Tokyo 1983.Kiyoshi Ozawa etal./
Fujitsu Lab. Ltd.に記載がある。
In addition, related technologies include UV Resist−Stripping for High−Speed and
Damage−Free Process/Exten and Abstracts
of the 15th Cont.on Solid State Devices and
Materials Tokyo 1983.Kiyoshi Ozawa etal./
Described in Fujitsu Lab. Ltd.

〔発明の目的〕[Purpose of the invention]

本発明の目的は、このような従来技術の欠点を
なくし、高速で有機物層を気化分解できる方法を
提供するにある。
An object of the present invention is to eliminate such drawbacks of the prior art and to provide a method capable of vaporizing and decomposing an organic layer at high speed.

〔発明の概要〕[Summary of the invention]

本発明は、チヤンバ内に配置されたサセプタ上
に表面に有機物層の存在する基板を載置する工程
と、チヤンバ内に酸素を導入し、基板に紫外線を
照射しながら、基板の温度を150℃から基板上の
有機物層が分解除去されるまで除除に増加させる
工程とを具備することにより、該有機物層の除去
に要する時間を短縮するようにしたものである。
The present invention involves the steps of placing a substrate with an organic layer on its surface on a susceptor placed in a chamber, introducing oxygen into the chamber, and increasing the temperature of the substrate to 150°C while irradiating the substrate with ultraviolet rays. The time required to remove the organic layer on the substrate is reduced by gradually increasing the amount of organic layer on the substrate until it is decomposed and removed.

〔発明の実施例〕[Embodiments of the invention]

第1図に本発明になる方法を実施するのに好適
な、感光性樹脂除去装置の1例を示す。チヤンバ
11にはウエハ13を設置するためのサセプタ1
2があり、チヤンバ11内にガス供給ノズル14
からO2ガスを供給した状態で、ウエハ13上に
光源15より光を照射する。光源15には低圧水
銀灯を用いるが、紫外線の波長の光を放射する他
の光源を用いてもよい。ウエハは抵抗式ヒータ1
7によつて加熱する。抵抗式ヒータ17の出力
は、ウエハ温度調節装置19によつて調節され
る。このような装置で予め抵抗式ヒータ17によ
り150℃に加熱されたサセプタ12上にウエハ1
3を置き、酸素雰囲気中で紫外線を照射する。ウ
エハ13が紫外線の照射を受け始めたことを示す
信号は、図示されない発信器によりウエハ温度調
節装置19に入力され、予め組込まれたシーケン
スに基づいて抵抗式ヒータ17の出力が徐々に増
加する。シーケンスには、これに先立つて行われ
た実験にもとづいて、感光性樹脂層の厚さが
200nm程度となる頃に、ウエハ温度Twが300℃
となるように設定しておく。
FIG. 1 shows an example of a photosensitive resin removal apparatus suitable for carrying out the method of the present invention. The chamber 11 has a susceptor 1 for installing the wafer 13.
2, and a gas supply nozzle 14 inside the chamber 11.
Light is irradiated onto the wafer 13 from the light source 15 while O 2 gas is supplied from the wafer 13 . Although a low-pressure mercury lamp is used as the light source 15, other light sources that emit light at ultraviolet wavelengths may also be used. Wafer is resistance type heater 1
Heat at 7. The output of the resistive heater 17 is adjusted by a wafer temperature adjustment device 19. With such a device, the wafer 1 is placed on the susceptor 12 which has been heated to 150°C by the resistance heater 17.
3 and irradiated with ultraviolet rays in an oxygen atmosphere. A signal indicating that the wafer 13 has begun to be irradiated with ultraviolet light is input to the wafer temperature control device 19 by a transmitter (not shown), and the output of the resistive heater 17 is gradually increased based on a preset sequence. The sequence includes the thickness of the photosensitive resin layer based on previous experiments.
By the time the wafer becomes about 200nm, the wafer temperature Tw has reached 300℃.
Set it so that

第2図の実線はこのようにして実験した結果の
1例であり、抵抗式ヒータ出力の増加パターン、
ウエハ温度Twの150℃からの上昇パターン及び
ウエハ上の感光性樹脂層厚さtの移り変わりを、
ウエハ面への紫外線照射時間に対して示す。図中
には比較のためTwを150℃一定に保つたときの
データを破線で示した。第2図から明らかなよう
に、基板の温度を150℃から基板上の有機物層が
分解除去されるまで除除に増加させれば、感光性
樹脂層の除去に要する時間は従来法(Tw=150
℃)のときの約1/3に短縮することができ、本法
による効果を確認した。
The solid line in Figure 2 is an example of the results of this experiment, and shows the pattern of increase in resistance heater output,
The increase pattern of the wafer temperature Tw from 150℃ and the change in the photosensitive resin layer thickness t on the wafer are shown below.
It is shown in relation to the UV irradiation time on the wafer surface. In the figure, for comparison, the data when Tw was kept constant at 150°C is shown by a broken line. As is clear from Figure 2, if the temperature of the substrate is gradually increased from 150°C until the organic layer on the substrate is decomposed and removed, the time required to remove the photosensitive resin layer is reduced by the conventional method (Tw = 150
It was possible to shorten the time to about 1/3 of that at 30°F (°C), confirming the effectiveness of this method.

第6図は本発明の応用例で、有機物からなる保
護膜(ワツクス等)の基体からの除去に用いた例
である。チヤンバ21には保護膜の付着した基体
23があり、ガス供給ノズル24から酸素を供給
した状態で、基体23に紫外線を照射することが
できる。基体23の加熱には複数個のランプ式ヒ
ータ27を用いており、ランプ式ヒータの点滅
は、基体温度調節装置29に予め組込まれてある
シーケンスに従つて調節される。
FIG. 6 shows an application example of the present invention, in which a protective film (such as wax) made of an organic substance is removed from a substrate. The chamber 21 has a base body 23 to which a protective film is attached, and the base body 23 can be irradiated with ultraviolet light while oxygen is supplied from the gas supply nozzle 24 . A plurality of lamp-type heaters 27 are used to heat the base 23, and the blinking of the lamp-type heaters is adjusted according to a sequence pre-installed in the base temperature control device 29.

第7図の実線はこのようにして保護膜を気化分
解し、基体からの除込に用いたシーケンスの例で
あり、保護膜の残膜厚さt、基体の表面温度Ts、
及びランプ式ヒータの点灯数の移り変わりと、基
体面への紫外線照射時間に対して示している。基
体がチヤンバ21内に入つた当初全ランプ式ヒー
タ27が点灯して急速に基体表面を加熱する。表
面が一定の温度に達したらランプ式ヒータ27の
一部を一旦消灯し、この後保護膜厚さtの減少に
伴つてランプ式ヒータの点灯数を逐次増加する。
このシーケンスにより基体23の表面温度はステ
ツプ状に変化するが、本発明による効果は同様に
発揮される。第7図中には基体温度を一定とした
場合の処理例を破線で示したが、これに対して本
実施例の処理時間は約1/4であつた。本実施例の
特有の効果としては、基体が平板でない形状のも
のにも適用できること、基体表面温度をランプ式
ヒータの点滅により調節したことにより温度調節
のシーケンスが簡略化できること、及び有機物性
保護膜の気化分解にも適用できることである。
The solid line in FIG. 7 is an example of a sequence used to vaporize and decompose the protective film and remove it from the substrate.
It also shows changes in the number of lamp-type heaters turned on and the duration of ultraviolet irradiation on the substrate surface. When the substrate enters the chamber 21, all the lamp type heaters 27 are turned on to rapidly heat the surface of the substrate. When the surface reaches a certain temperature, a part of the lamp heater 27 is temporarily turned off, and thereafter, as the protective film thickness t decreases, the number of lamp heaters turned on is sequentially increased.
Although the surface temperature of the substrate 23 changes in steps due to this sequence, the effects of the present invention are similarly exhibited. In FIG. 7, a processing example in which the substrate temperature is kept constant is shown by a broken line, and in contrast, the processing time of this example was about 1/4. The unique effects of this example are that it can be applied to substrates that are not flat, that the temperature adjustment sequence can be simplified by adjusting the substrate surface temperature by blinking a lamp heater, and that it has an organic protective film. This can also be applied to the vaporization and decomposition of

〔発明の効果〕〔Effect of the invention〕

本発明を実施することにより、有機物層の除去
に要する時間を、従来法の1/3〜1/4に短縮するこ
とができる。
By implementing the present invention, the time required to remove the organic layer can be shortened to 1/3 to 1/4 of the conventional method.

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

第1図は本発明の一実施例の断面図、第2図は
第1図に示す装置を用いて行つた実験結果で本発
明の実施例と効果を示す線図、第3図は従来の装
置を示す断面図、第4図は感光性樹脂の気化分解
速度とウエハ温度の関係線図、第5図はウエハ温
度が異なる場合の感光性樹脂層厚さの経時変化の
違いを示す線図、第6図は本発明の応用例の装置
の断面図、第7図は第6図に示す装置を用いて行
つた実験結果を示す線図である。 1……チヤンバ、2……サセプタ、3……ウエ
ハ、4……ガス供給ノズル、5……低圧水銀灯、
6……ガス排出ノズル、11……チヤンバ、12
……サセプタ、13……ウエハ、14……ガス供
給ノズル、15……光源、16……ガス排出ノズ
ル、17……抵抗式ヒータ、21……チヤンバ、
23……基体、24……ガス供給ノズル、25…
…低圧水銀灯、26……ガス排出ノズル、29…
…基体温度調節装置。
Fig. 1 is a cross-sectional view of an embodiment of the present invention, Fig. 2 is a diagram showing the embodiment and effects of the present invention based on the experimental results conducted using the apparatus shown in Fig. 1, and Fig. 3 is a diagram of the conventional A cross-sectional view showing the device, Fig. 4 is a diagram showing the relationship between the vaporization decomposition rate of photosensitive resin and wafer temperature, and Fig. 5 is a diagram showing the difference in the change in photosensitive resin layer thickness over time when the wafer temperature is different. , FIG. 6 is a sectional view of an apparatus according to an applied example of the present invention, and FIG. 7 is a diagram showing the results of an experiment conducted using the apparatus shown in FIG. 6. 1... Chamber, 2... Susceptor, 3... Wafer, 4... Gas supply nozzle, 5... Low pressure mercury lamp,
6... Gas discharge nozzle, 11... Chamber, 12
... Susceptor, 13 ... Wafer, 14 ... Gas supply nozzle, 15 ... Light source, 16 ... Gas discharge nozzle, 17 ... Resistance type heater, 21 ... Chamber,
23...Base body, 24...Gas supply nozzle, 25...
...Low pressure mercury lamp, 26...Gas discharge nozzle, 29...
...Substrate temperature control device.

Claims (1)

【特許請求の範囲】 1 チヤンバ内に配置されたサセプタ上に表面に
有機物層の存在する基板を載置する工程と、 チヤンバ内に酸素を導入し、基板に紫外線を照
射しながら、基板の温度を150℃から基板上の有
機物層が分解除去されるまで徐除に増加させる工
程とを具備することを特徴とする光化学反応方
法。
[Claims] 1. A step of placing a substrate having an organic layer on its surface on a susceptor placed in a chamber, and introducing oxygen into the chamber and controlling the temperature of the substrate while irradiating the substrate with ultraviolet rays. A photochemical reaction method comprising the step of gradually increasing the temperature from 150°C until the organic layer on the substrate is decomposed and removed.
JP18960085A 1985-08-30 1985-08-30 Photochemical reaction method Granted JPS6251225A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18960085A JPS6251225A (en) 1985-08-30 1985-08-30 Photochemical reaction method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18960085A JPS6251225A (en) 1985-08-30 1985-08-30 Photochemical reaction method

Publications (2)

Publication Number Publication Date
JPS6251225A JPS6251225A (en) 1987-03-05
JPH0521336B2 true JPH0521336B2 (en) 1993-03-24

Family

ID=16244023

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18960085A Granted JPS6251225A (en) 1985-08-30 1985-08-30 Photochemical reaction method

Country Status (1)

Country Link
JP (1) JPS6251225A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63276225A (en) * 1987-05-08 1988-11-14 Tokyo Electron Ltd Ashing system
CN106896194A (en) * 2017-04-17 2017-06-27 武汉华星光电技术有限公司 A kind of device and method for monitoring ozone content in coating developing apparatus lamp box
JP7232886B2 (en) * 2017-11-13 2023-03-03 東京エレクトロン株式会社 SUBSTRATE PROCESSING APPARATUS, SUBSTRATE PROCESSING METHOD, AND STORAGE MEDIUM

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6049630A (en) * 1983-08-29 1985-03-18 Fujitsu Ltd Manufacture of semiconductor device

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6049630A (en) * 1983-08-29 1985-03-18 Fujitsu Ltd Manufacture of semiconductor device

Also Published As

Publication number Publication date
JPS6251225A (en) 1987-03-05

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