CN109254507A - Photoresist release agent and photoresist stripping means - Google Patents

Photoresist release agent and photoresist stripping means Download PDF

Info

Publication number
CN109254507A
CN109254507A CN201811218943.6A CN201811218943A CN109254507A CN 109254507 A CN109254507 A CN 109254507A CN 201811218943 A CN201811218943 A CN 201811218943A CN 109254507 A CN109254507 A CN 109254507A
Authority
CN
China
Prior art keywords
photoresist
release agent
ether
glycol
agent according
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
Application number
CN201811218943.6A
Other languages
Chinese (zh)
Inventor
邓强
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.)
Suzhou Heng Kang New Material Co Ltd
Original Assignee
Suzhou Heng Kang New Material 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 Suzhou Heng Kang New Material Co Ltd filed Critical Suzhou Heng Kang New Material Co Ltd
Priority to CN201811218943.6A priority Critical patent/CN109254507A/en
Publication of CN109254507A publication Critical patent/CN109254507A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/26Processing photosensitive materials; Apparatus therefor
    • G03F7/42Stripping or agents therefor
    • G03F7/422Stripping or agents therefor using liquids only
    • G03F7/425Stripping or agents therefor using liquids only containing mineral alkaline compounds; containing organic basic compounds, e.g. quaternary ammonium compounds; containing heterocyclic basic compounds containing nitrogen

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Photosensitive Polymer And Photoresist Processing (AREA)
  • Exposure Of Semiconductors, Excluding Electron Or Ion Beam Exposure (AREA)

Abstract

Present invention discloses photoresist release agent, including following mass percent component, amine compound 10-25%, polar solvent 55-75%, anticorrosive 0.5-1.2%, water 10-20%.There is the present invention photoresist release agent of appropriate proportioning component to be conducive to its application in integrated circuit, semiconductor device or liquid crystal display.

Description

Photoresist release agent and photoresist stripping means
Technical field
The invention belongs to integrated circuit or semiconductor applied technical field more particularly to a kind of photoresist release agent and Photoresist stripping means.
Background technique
FPD is based on the various displaying principles such as LCD, LED, EL, VFD, FED, SED, PDP, has and fine lead has been arranged The electrode structure of line uses photoresist in its manufacturing process.For example, in a liquid crystal display, on being formed in substrate Al, Al alloy, painting photoresist on the insulating films such as conductive metals film, the SiO2 film such as Cu, Cu alloy, it is implemented to expose Light, development processing, resist pattern is formed, using the patterned resist as mask to above-mentioned conductive metal film, exhausted Velum etc. is etched, formed micro wire after, with remover remove should not resist layer, to manufacture liquid crystal display.
Photoresist is the essential substance in photolithography process, and photolithography process is general It is also applied to the semiconductor devices such as integrated circuit.After carrying out photolithographic process, photoresist at high temperature by Stripping solution removal, but there are problems that lower part metal film may be stripped solution corrosion too quickly in the process.
Photoresist should can be at low temperature in being removed in the short time, and it should have fabulous removing energy Power, so as to which photoresist residual substance is not present after rinsing in substrate.In addition, photoresist should have low-corrosiveness, To prevent metal film or the insulating film of photoresist lower layer to be damaged.Phase interaction occurs between the solvent of remover if constituted With, then the storage stability of remover will appear problem, and may due to the difference of order by merging when remover manufactures and Different property is shown, therefore, should have inertia and high-temperature stability between the mixed solvent of photoresist.Consider Environmental problem caused by safety or waste processing to staff, photoresist should also hypotoxicity.Work as photoresist When being removed in the high temperature process, if there is a large amount of volatilizations, then constituting composition ratio can change rapidly, to make remover Process stability and work reproducibility reduce.Therefore, photoresist should have low volatility.The remover institute of predetermined amount The substrate quantity that can be handled should be higher, and the component for forming remover should be easy to get, and component should be cheap, and discarded Remover should can be recycled by reprocessing, to should can ensure business efficiency.
Therefore, the photoresist release agent with appropriate proportioning component is conducive to it in integrated circuit, semiconductor device Or the application in liquid crystal display.
Summary of the invention
The purpose of the present invention is to solve above-mentioned technical problems, and provide a kind of photoresist release agent and photic anti- Agent stripping means is lost, to realize excellent photoresist removal and stripping performance.In order to achieve the above object, skill of the present invention Art scheme is as follows:
Photoresist release agent, including following mass percent component, amine compound 10-25%, polar solvent 55- 75%, anticorrosive 0.5-1.2%, water 10-20%.
Specifically, the amine compound includes at least one selected from chain amine compounds and cyclic amine compound.Tool Body, the chain amine compounds include (2- amino ethoxy) -1- ethyl alcohol (AEE), amino ethyl ethanolamine (AEEA), Dan Yi Hydramine, N- Methylethyl amine (N-MEA), 1- aminoisopropanol (AIP), methyl dimethoxy amine (MDEA), diethylenetriamines (DETA) one or more and in trien (TETA).
Specifically, the cyclic amine compound includes imidazole radicals -4- ethyl alcohol (IME), aminoethylpiperazine (AEP) and hydroxyl It is one or more in ethyl piperazidine (HEP).
Specifically, the polar solvent includes aprotic polar solvent and protic polar solvent.
Specifically, the aprotic polar solvent be dimethyl sulfoxide, N-METHYLFORMAMIDE, n-methyl-2-pyrrolidone, DMAC N,N' dimethyl acetamide, N,N-dimethylformamide, N, N- diethylformamide, N, N- methylimidazole, gamma-butyrolacton, It is one or more in sulfolane, tetrahydrofurfuryl alcohol.
Specifically, the protic polar solvent is ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, ethylene glycol first Ether, ethylene glycol ethyl ether, butyl glycol ether, diethylene glycol dimethyl ether, diethylene glycol ether, butyl, triethylene glycol methyl ether, Tri ethylene glycol ethyl ether, triethylene glycol butyl ether, dipropylene glycol methyl ether, diethylene glycol dimethyl ether, dipropylene glycol methyl ether and dipropyl two It is one or more in alcohol ether.
Specifically, the anticorrosive includes catechol, pyrogallol, gallic acid, phthalic acid, O-phthalic Acid anhydrides, wherein the ratio of each component is 1-2:0.2-0.5:0.3-0.7:0.4-0.5:1-2.
Photoresist stripping means, includes the following steps:
Photoresist is coated on conductive metal film or insulating film by S1, forms photoresist pattern;
S2 uses the photoresist of the pattern as conductive metal film described in mask etching or insulating film;
S3 removes photoresist using the photoresist release agent.
Compared with prior art, the beneficial effect master of photoresist release agent and photoresist stripping means of the present invention It is embodied in:
Photoresist can be at low temperature in removing in the short time, and has fabulous stripping ability, base after flushing Photoresist residual substance is not present on bottom;Photoresist release agent has low-corrosiveness, prevents photoresist lower layer Metal film or insulating film be damaged, constitute and do not interact between the solvent of remover, the storage stability of remover, There is inertia and high-temperature stability between the mixed solvent of photoresist;In view of safety or the waste processing of staff Caused by environmental problem, photoresist release agent hypotoxicity when photoresist is removed in the high temperature process Now a large amount of volatilizations, constituting composition ratio will not change rapidly, and the process of remover removing has stability;Photoresist removing Agent has low volatility, and the substrate quantity that the remover of predetermined amount can be handled is higher, and the component for forming remover is easy to get, Component is cheap, and discarded remover can be recycled by reprocessing, so as to ensure business efficiency.
Specific embodiment
Below by the technical scheme in the embodiment of the invention is clearly and completely described, it is clear that described implementation Example is only a part of the embodiment of the present invention, instead of all the embodiments.
Embodiment 1:
The present embodiment is photoresist release agent, including following mass percent component, amine compound 19%, polarity Solvent 66%, anticorrosive 0.9%, water 14.1%.
Amine compound includes at least one selected from chain amine compounds and cyclic amine compound.
Chain amine compounds include (2- amino ethoxy) -1- ethyl alcohol (AEE), amino ethyl ethanolamine (AEEA), Dan Yi Hydramine, N- Methylethyl amine (N-MEA), 1- aminoisopropanol (AIP), methyl dimethoxy amine (MDEA), diethylenetriamines (DETA) one or more and in trien (TETA).
Cyclic amine compound includes imidazole radicals -4- ethyl alcohol (IME), aminoethylpiperazine (AEP) and hydroxyethylpiperazin (HEP) one or more in.
Polar solvent includes aprotic polar solvent and protic polar solvent.
Aprotic polar solvent is dimethyl sulfoxide, N-METHYLFORMAMIDE, n-methyl-2-pyrrolidone, N, N- dimethyl Acetamide, N,N-dimethylformamide, N, N- diethylformamide, N, N- methylimidazole, gamma-butyrolacton, sulfolane, tetrahydro It is one or more in furfuryl alcohol.
Protic polar solvent is ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, ethylene glycol monomethyl ether, ethylene glycol ethyl ethers Ether, butyl glycol ether, diethylene glycol dimethyl ether, diethylene glycol ether, butyl, triethylene glycol methyl ether, triethylene glycol second One in ether, triethylene glycol butyl ether, dipropylene glycol methyl ether, diethylene glycol dimethyl ether, dipropylene glycol methyl ether and dipropylene glycol ethyl ether Kind is a variety of.
Anticorrosive includes catechol, pyrogallol, gallic acid, phthalic acid, phthalic anhydride, wherein respectively The ratio of component is 1.5:0.35:0.5:0.45:1.5.
Photoresist stripping means, includes the following steps:
Photoresist is coated on conductive metal film or insulating film by S1, forms photoresist pattern;
S2 uses the photoresist of the pattern as conductive metal film described in mask etching or insulating film;
S3 removes photoresist using photoresist release agent.
Embodiment 2:
Distinctive points relative to embodiment 1 are:
The present embodiment is photoresist release agent, including following mass percent component, amine compound 10%, polarity Solvent 75%, anticorrosive 0.5%, water 14.5%.
Anticorrosive includes catechol, pyrogallol, gallic acid, phthalic acid, phthalic anhydride, wherein respectively The ratio of component is 1:0.5:0.3:0.5:1.
Embodiment 3:
Distinctive points relative to embodiment 1 are:
The present embodiment is photoresist release agent, including following mass percent component, amine compound 25%, polarity Solvent 55%, anticorrosive 1.2%, water 18.8%.
Anticorrosive includes catechol, pyrogallol, gallic acid, phthalic acid, phthalic anhydride, wherein respectively The ratio of component is 2:0.2:0.7:0.4:2.
When using above-described embodiment, photoresist can be at low temperature in removing in the short time, and has fabulous Photoresist residual substance is not present in stripping ability in substrate after flushing;Photoresist release agent has low-corrosiveness, prevents Only the metal film or insulating film of photoresist lower layer are damaged, and constitute and do not interact between the solvent of remover, stripping Storage stability from agent has inertia and high-temperature stability between the mixed solvent of photoresist;In view of work people Environmental problem caused by the safety or waste of member is handled, photoresist release agent hypotoxicity, when photoresist is in high temperature mistake When being removed in journey, do not occur largely volatilizing, constituting composition ratio will not change rapidly, and the process of remover removing has steady It is qualitative;Photoresist release agent has low volatility, and the substrate quantity that the remover of predetermined amount can be handled is higher, composition stripping Component from agent is easy to get, and component is cheap, and discarded remover can be recycled by reprocessing, so as to ensure Business efficiency
Above-described is only some embodiments of the present invention.For those of ordinary skill in the art, not Under the premise of being detached from the invention design, various modifications and improvements can be made, these belong to protection model of the invention It encloses.

Claims (9)

1. photoresist release agent, it is characterised in that: including following mass percent component, amine compound 10-25%, pole Property solvent 55-75%, anticorrosive 0.5-1.2%, water 10-20%.
2. photoresist release agent according to claim 1, it is characterised in that: the amine compound includes being selected from chain At least one of shape amine compounds and cyclic amine compound.
3. photoresist release agent according to claim 2, it is characterised in that: the chain amine compounds include (2- Amino ethoxy) -1- ethyl alcohol (AEE), amino ethyl ethanolamine (AEEA), monoethanolamine, N- Methylethyl amine (N-MEA), 1- It is a kind of in aminoisopropanol (AIP), methyl dimethoxy amine (MDEA), diethylenetriamines (DETA) and trien (TETA) Or it is a variety of.
4. photoresist release agent according to claim 2, it is characterised in that: the cyclic amine compound includes imidazoles It is one or more in base -4- ethyl alcohol (IME), aminoethylpiperazine (AEP) and hydroxyethylpiperazin (HEP).
5. photoresist release agent according to claim 1, it is characterised in that: the polar solvent includes aprotic Polar solvent and protic polar solvent.
6. photoresist release agent according to claim 5, it is characterised in that: the aprotic polar solvent is two First sulfoxide, N-METHYLFORMAMIDE, n-methyl-2-pyrrolidone, DMAC N,N' dimethyl acetamide, N,N-dimethylformamide, N, N- Diethylformamide, N, it is N- methylimidazole, gamma-butyrolacton, sulfolane, one or more in tetrahydrofurfuryl alcohol.
7. photoresist release agent according to claim 5, it is characterised in that: the protic polar solvent is second two Alcohol, diethylene glycol, triethylene glycol, tetraethylene glycol, ethylene glycol monomethyl ether, ethylene glycol ethyl ether, butyl glycol ether, diethylene glycol dimethyl ether, Diethylene glycol ether, butyl, triethylene glycol methyl ether, tri ethylene glycol ethyl ether, triethylene glycol butyl ether, dipropylene glycol first It is one or more in ether, diethylene glycol dimethyl ether, dipropylene glycol methyl ether and dipropylene glycol ethyl ether.
8. photoresist release agent according to claim 1, it is characterised in that: the anticorrosive includes adjacent benzene two Phenol, pyrogallol, gallic acid, phthalic acid, phthalic anhydride, wherein the ratio of each component is 1-2:0.2-0.5: 0.3-0.7:0.4-0.5:1-2.
9. photoresist stripping means, which comprises the steps of:
Photoresist is coated on conductive metal film or insulating film by S1, forms photoresist pattern;
S2 uses the photoresist of the pattern as conductive metal film described in mask etching or insulating film;
S3 removes photoresist using photoresist release agent such as according to any one of claims 1 to 8.
CN201811218943.6A 2018-10-19 2018-10-19 Photoresist release agent and photoresist stripping means Pending CN109254507A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201811218943.6A CN109254507A (en) 2018-10-19 2018-10-19 Photoresist release agent and photoresist stripping means

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201811218943.6A CN109254507A (en) 2018-10-19 2018-10-19 Photoresist release agent and photoresist stripping means

Publications (1)

Publication Number Publication Date
CN109254507A true CN109254507A (en) 2019-01-22

Family

ID=65046226

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201811218943.6A Pending CN109254507A (en) 2018-10-19 2018-10-19 Photoresist release agent and photoresist stripping means

Country Status (1)

Country Link
CN (1) CN109254507A (en)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006178347A (en) * 2004-12-24 2006-07-06 Tosoh Corp Resist stripping agent
CN103631103A (en) * 2012-08-20 2014-03-12 株式会社东进世美肯 Photoresist stripping liquid composition
CN104903794A (en) * 2013-05-07 2015-09-09 株式会社Lg化学 Stripper composition for removing photoresist and method for stripping photoresist using same
CN106873319A (en) * 2015-12-14 2017-06-20 三星显示有限公司 Photoresist remover composition
CN107357142A (en) * 2017-07-03 2017-11-17 杭州格林达化学有限公司 A kind of water system photoresist stripper and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006178347A (en) * 2004-12-24 2006-07-06 Tosoh Corp Resist stripping agent
CN103631103A (en) * 2012-08-20 2014-03-12 株式会社东进世美肯 Photoresist stripping liquid composition
CN104903794A (en) * 2013-05-07 2015-09-09 株式会社Lg化学 Stripper composition for removing photoresist and method for stripping photoresist using same
CN106873319A (en) * 2015-12-14 2017-06-20 三星显示有限公司 Photoresist remover composition
CN107357142A (en) * 2017-07-03 2017-11-17 杭州格林达化学有限公司 A kind of water system photoresist stripper and preparation method thereof

Similar Documents

Publication Publication Date Title
JP6006711B2 (en) Photoresist stripping composition for LCD production containing primary alkanolamine
CN102216855B (en) A photoresist stripping composition for manufacturing LCD
KR100913048B1 (en) Stripper composition for photoresist
JP6277511B2 (en) Resist stripper
TWI494713B (en) Photoresist stripping solution
JP2005043873A (en) Photoresist stripping liquid composition and method for stripping photoresist by using the same
JP2018530774A (en) Photoresist stripping composition for LCD manufacturing
JP2014048667A (en) Stripper composition for thick negative photoresist
KR20140024625A (en) Composition for removing photoresist
WO2016151645A1 (en) Resist stripping liquid
KR101082515B1 (en) Stripper composition for photoresist and method for stripping photoresist
KR101051438B1 (en) Photoresist stripper composition and photoresist stripping method using the same
JP2012018982A (en) Resist stripping agent and stripping method using the same
KR20040098751A (en) Photoresist stripper composition
CN109254507A (en) Photoresist release agent and photoresist stripping means
CN112470079A (en) Cleaning method
JP2012242696A (en) Stripping liquid for photoresist
KR101821034B1 (en) A method of stripping photoresist
JP2019120926A (en) Stripping composition for removing dry film resist and method for stripping dry film resist using the same
KR20100125108A (en) Stripper composition for copper or copper alloy
KR100544888B1 (en) Photoresist stripper composition for copper tft
KR20170002933A (en) Stripper composition
KR20220124916A (en) Photo resist stripper composition
JP2013504782A (en) Resist removing composition for forming copper-based wiring
CN114008539A (en) Cleaning method

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20190122