TWI730913B - Resistor Stripping Liquid - Google Patents

Abstract

Provided is a resist stripping solution that can inhibit undercutting of copper or molybdenum when stripping hard-baked resists on a copper/molybdenum laminated film. This resist stripping solution includes: 0.5 to 5 mass% of the secondary cyclic amine relative to the total amount of the peeling liquid; 5 to 10 mass% of the basic amino acid relative to the aforementioned secondary cyclic amine; 10 to 30 relative to the aforementioned basic amino acid Mass% protective agent; 10-50 mass% sugar alcohol relative to the aforementioned secondary cyclic amine; organic polar solvent; and water.

Description

Resistor Stripping Liquid

The present invention relates to a resist stripping solution used to strip the photoresist used in the photolithography process.

At present, transmission formats that can provide high-quality playback such as 4K and 8K have been proposed, and playback tests have also been launched. A TV with a large screen is also provided accordingly. LCD TVs are the mainstream of current TVs, and transistors corresponding to pixels are formed on a transparent substrate (glass) used as a large screen. The above-mentioned formation step uses photolithography technology.

Due to the increase in screen size, it is necessary to reduce the resistance of the conductive portion formed on the transparent substrate. For this reason, copper is used as a conductive part. Copper has high conductivity. However, the adhesion to the transparent substrate is low. Therefore, molybdenum is used as an undercoat layer between the transparent substrate and the copper.

Molybdenum is generally a metal that is not easily corroded, but it is known that when molybdenum and copper form a two-layer structure, molybdenum is significantly corroded.

Patent Document 1 discloses a peeling solution. After etching two layers of a two-layer structure in which a copper layer is provided on a molybdenum layer, the peeling solution for peeling off the resist layer contains two or more nitrogens and does not have two levels. Or tertiary alkanolamine, and amino acid with thiol group and amide structure, so it can inhibit the corrosion of molybdenum and peel off the resist.

Furthermore, the feature of Patent Document 1 also includes that since a copper corrosion protection agent such as benzotriazole is used, precipitation is generated on the copper surface, so this corrosion protection agent is not used.

In addition, compared with the transparent substrate used at the time of filing Patent Document 1, the transparent substrate currently used is larger. Therefore, in the case of forming components on a large screen by photolithography technology, strict production management will be implemented, and failure of any component will not be allowed. Therefore, it is required that the coated photoresist film peeling problem that is directly related to the etching error should not occur. As a result, the temperature of the photoresist baking treatment (also referred to as calcination treatment) before exposure tends to increase. [Prior Art Literature] [Patent Literature]

[Patent Document 1] International Patent Publication No. 2010/0738887

It is known that amino acids can strongly corrode copper. That is, the peeling liquid system of Patent Document 1 uses amines that corrode copper and amino acids that strongly corrode copper to a low degree, and does not use a copper protective agent. However, the peeling liquid of Patent Document 1 suppresses the corrosion of copper and also the corrosion of molybdenum of the undercoat layer.

It is considered that the reason is as follows. When the stripping liquid is used, oxygen is reduced on the surface of the copper. Therefore, electrons are supplied from the surface of the copper to the side of the stripping liquid. Here, if amines that are hard to corrode copper are used, electrons are supplied from molybdenum instead of copper. Therefore, the molybdenum is corroded.

On the other hand, here, by using an amino acid that corrodes copper at the same time, electrons are also released from copper, thereby suppressing the corrosion of molybdenum. That is, it is a method in which the resist is peeled off by alkanolamine, which is difficult to corrode copper, and the electrons generated on the copper surface for reduction are supplied not only from molybdenum but also from copper itself.

In other words, the method of protecting the molybdenum layer by deliberately etching a little copper layer is also a method of trying to use the balance between the alkanolamine and the amino acid to protect the two layers.

However, compared to the time when Patent Document 1 was filed, the calcination temperature of the current resist in the manufacturing process becomes higher (hard baking), and the resist itself cannot be peeled off by the alkanolamine. Therefore, there is a need for an alkaline substance that is more suitable for decomposing the resist after hard baking than alkanolamine.

Furthermore, the conductive part near the pixel has a relatively thin pattern, and the conductive part from each pixel is integrated in the part around the screen, so it has a pattern with a large width.

As described above, when a strong base is used in a state where a pattern with a large width and a pattern with a small width are mixed, it is difficult to adjust the balance between the amine and the amino acid. That is, in this method, molybdenum is corroded when there are few amino acids (more amines), and copper is corroded when there are many amino acids (less amines). However, since there are both a pattern with a large width and a pattern with a small width, the range in which the balance between the amino acid and the amine can be achieved becomes very narrow, and it is impossible to provide a peeling liquid that is substantially balanced.

The present invention is conceived in view of the above-mentioned problems. The present invention provides that molybdenum and copper can be suppressed both in the part of the pattern with a large width and the part of the pattern with a small width while sufficiently peeling off the photoresist after hard baking. The corrosion inhibitor stripping liquid.

Therefore, in the present invention, under the premise of using cyclic amines and amino acids, a copper protective agent is used. In addition, an excessive amount of amino acid is added to the amine to inhibit the corrosion of molybdenum, and the degree of corrosion of copper is adjusted with a protective agent.

More specifically, the resist stripping liquid according to the present invention includes: 0.5 to 5 mass% of the secondary cyclic amine relative to the total amount of the stripping liquid; 5 to 10 mass% of the basic amine relative to the aforementioned secondary cyclic amine Base acid; 10 to 30% by mass of protective agent relative to the aforementioned basic amino acid; 10 to 50% by mass of sugar alcohol relative to the aforementioned secondary cyclic amine; organic polar solvent; and water; wherein the aforementioned secondary ring At least one of amine-based imidazole and piperidine.

According to the resist stripping solution of the present invention, an excessive amount of a basic amino acid that strongly corrodes copper is mixed in a secondary cyclic amine that is hard to corrode copper and is strongly alkaline. In this way, copper will be corroded, but the degree of corrosion of copper can be adjusted according to the amount of protective agent. That is, instead of achieving a balance between two corrosive agents, the protective agent is used to inhibit the effect of one of the corrosive agents. Therefore, even when there are patterns with a large width and a pattern with a small width, the corrosion of molybdenum and the corrosion of copper can be suppressed within the practical application range.

Furthermore, since sugar alcohol is mixed, it is also possible to suppress corrosion between molybdenum and copper.

Moreover, since the composition of the peeling liquid does not contain inorganic acids or inorganic bases, it does not corrode the conductive parts of aluminum.

Hereinafter, embodiments of the resist stripping liquid according to the present invention will be described and explained. In addition, the following description describes an embodiment and an example of the present invention, and the present invention is not limited to the following description. The following description can be modified without departing from the spirit of the present invention. Furthermore, in the following description, "~" is sometimes used to indicate a range, which means from "above (equal to and greater than this value) to less than (equal to and less than this value)".

The resist stripping liquid according to the present invention includes a secondary cyclic amine, a basic amino acid, an organic polar solvent, a protective agent, water, and a sugar alcohol.

Furthermore, the target object of the present invention is a conductive part in which copper is laminated on molybdenum. In particular, a conductive portion with a width of approximately 5 to 15 μm and a conductive portion with a width of 300 to 500 μm are mixed. Moreover, there are conductive parts made of aluminum.

The thickness of molybdenum is about 30-50nm, and the thickness of copper is 400-800nm. The aluminum part has a thickness of 200 to 400 nm. With regard to these thicknesses, it is necessary to be within a range in which problems of undercut of molybdenum, corrosion of copper, and corrosion of aluminum do not occur in practical applications.

Furthermore, the resist is a positive photoresist, which includes a novolak resin and Diazonaphthoquinone (Diazonaphthoquinone). In addition, a photoresist that has been calcined at a temperature of 150°C or higher is targeted. The photoresist is usually heat-treated at a temperature of about 100°C. Therefore, heat treatment at 150°C or higher is called high temperature treatment (hard bake).

For secondary cyclic amines, imidazole (CAS number: 288-32-4) and piperidine (CAS number: 110-89-4) are suitable for use. Imidazole and piperidine can peel off the photoresist after hard baking. Relative to the total amount of the peeling liquid, the content of the secondary cyclic amine is preferably 0.5 to 5 mass%, and more preferably 0.7 to 2.0 mass%.

As the amino acid, a basic amino acid can be used. It can strongly dissolve copper. It is particularly preferable to use arginine and lysine acid. Although histidine is classified as a basic amino acid, it is less effective for molybdenum corrosion resistance when used in the resist stripping liquid according to the present invention.

The content of the amino acid relative to the cyclic amine is 5-10% by mass, preferably 6-8% by mass. When converted into the total amount of the peeling liquid, it is equivalent to 0.025 to 0.5% by mass.

The protective agent is a substance that inhibits the corrosion of copper by amino acids. Specifically, it can be benzotriazole, 5-methyl-1H-benzotriazole, 2-mercaptobenzimidazole, 2-mercaptobenzothiazole, 2-mercapto-5-methylbenzimidazole, 1 -[N,N-bis(2-ethylhexyl)aminomethyl]-1H-benzotriazole, 2,2 ' -[[((methyl-1H-benzotriazol-1-yl) Methyl]imino]diethanol. Therefore, at least one substance can be selected from the group consisting of these compounds as the metal surface protective agent.

The amount of the protective agent can be adjusted to 10 to 30% by mass relative to the basic amino acid. It is equivalent to 0.0025 to 0.15% by mass of the entire peeling liquid. If the amount of the protective agent is too large with respect to the basic amino acid, the corrosion of copper is excessively suppressed, and the corrosion of molybdenum increases. However, by setting its content within the above range, regardless of whether the width of the conductive portion is large or small, the molybdenum content can be appropriately obtained. The balance between corrosion and copper corrosion.

Sugar alcohol can prevent corrosion of the boundary between molybdenum and copper (called "undercutting of copper"). It is suitable to use glycerol or sorbitol as the sugar alcohol. Relative to the cyclic amine, the content of sugar alcohol is preferably 10-50% by mass. This corresponds to 0.05 to 2.5% by mass relative to the total amount of the peeling solution.

The organic polar solvent is preferably an aprotic organic solvent. Protic organic solvents tend to corrode the molybdenum of the undercoat layer. Specifically, the organic polar solvent can be diethylformamide, N-methylformamide, dimethylformamide, N-methyl-2-pyrrolidone, tetrahydrofuran, dimethyl sulfide, etc. Be applicable.

The amount of water is suitably 10-30% by mass of the total amount of the peeling liquid. Furthermore, the organic polar solvent may be the residue of the aforementioned cyclic amine, water, protective agent, and sugar alcohol.

[Example]

Hereinafter, examples of the resist stripping liquid according to the present invention will be described. The sample peeling liquids of the Examples and Comparative Examples having the composition shown below were prepared, and the resist peeling test was performed on the test piece for resist peeling.

<Test piece for resist peeling>

Molybdenum (Mo) with a thickness of 30 nm was deposited on the glass substrate, and copper (Cu) with a thickness of 500 nm was laminated thereon. Then, a layer of SiN with a thickness of 300 nm was deposited on it. This is called a silicon laminate.

A contact hole with a diameter of 1 μm was formed at a predetermined position of the SiN layer on the silicon build-up layer sheet. Then, molybdenum (Mo) with a thickness of 30 nm was further laminated, and copper (Cu) with a thickness of 500 nm was laminated thereon.

Next, a positive photoresist is coated on the uppermost copper layer, and fired (baked) at a predetermined temperature. In addition, high-temperature baking is usually carried out at 150°C for about 2 minutes, but in order to confirm the peeling force of the resist stripping solution, baking was carried out at 170°C for 5 minutes. As a result, the resist film has undergone a strong calcination treatment. After baking, the gate line pattern is exposed and developed, and then etched The upper copper layer and molybdenum layer are carved to obtain a copper test piece for resist peeling.

That is, in the copper test piece for resist peeling, the molybdenum layer and the copper layer in which the gate line pattern was etched were provided, and the resist film after a calcination process was deposited on it. Furthermore, this resist film also covers the contact hole portion.

Furthermore, aluminum (Al) was deposited with a thickness of 500 nm on the silicon build-up sheet, and the gate line pattern was etched on the aluminum layer in the same manner as the copper test piece for resist stripping. The calcination treatment of the resist layer was similarly performed at 170°C for 5 minutes. As described above, an aluminum test piece for resist peeling was obtained.

<evaluation>

As an evaluation of the ability to peel the resist (hereinafter referred to as "peel force"), each test piece was treated with various peeling solutions heated to 40°C for 40 seconds, and the remaining state of the resist was confirmed using an optical microscope. Then, the case where the resist is obviously remaining on the surface is evaluated as "×" (means unqualified or failed), and if the resist is peeled off without problems, it is evaluated as "○" (means pass Or the meaning of success).

In addition, to evaluate the ability to inhibit corrosion of the metal surface (hereinafter referred to as "metal damage"), the test piece was immersed in a sample stripping solution at 40°C for 4 minutes, and then the test piece was observed using SEM (Scanning Electron Microscope) The corrosion state of the metal film. In the above observation, the etched part was observed with a magnified surface view angle and a cross-sectional view angle.

In the magnified view of the surface, the corrosion state of the surface of the copper layer and the aluminum layer was confirmed. In particular, check the state of the copper on the surface of the gate line and the edge of the contact hole. Furthermore, in the cross-sectional view, the roughness, the inclination angle, and the copper undercut of the inclined surface of the etched metal layer were confirmed.

Then, in each perspective, the state judged as unqualified manufacturing is evaluated as "x" (meaning unqualified or failed), and the state judged as qualified as manufacturing is evaluated as "○" (representing qualified or successful the meaning of).

<Sample Stripping Solution>

The composition of various sample stripping solutions is described below. The following abbreviations are sometimes used to indicate the following various compounds. Imidazole: IZ (CAS number: 288-32-4), piperidine: PIP (CAS number: 110-89-4), diethylmethamide: DEF (CAS number: 617-84-5), N- Methyl formamide: NMF (CAS number: 123-39-7), diethylene glycol monobutyl ether: BDG (CAS number: 112-34-5), 2,2'-[[[(methyl-1H -Benzotriazol-1-yl)methyl]imino]diethanol: MBET (CAS number: 88477-37-6), N-methyl-2-pyrrolidone: NMP (CAS number: 872-50- 4) Piperazine: PIZ (CAS number: 110-85-0), N-methylethanolamine: MMA (CAS number: 109-83-1). 5-Methylbenzotriazole: 5M-BTA (CAS Number: 136-85-6), Arginine: Arg (CAS Number: 74-79-3), Lysine: Lys (CAS Number: 70- 54-2), Histidine: His (CAS Number: 71-00-1), Glycerol: Glycerol (CAS Number: 56-81-5), Sorbitol: Stol (CAS Number: 50-70-4) .

(Example 1)

The sample peeling liquid of Example 1 was prepared using the following composition.

1.0g of IZ as a cyclic amine compound, 0.07g of Arg as an amino acid (7% by mass relative to the cyclic amine compound), 0.01g of MBET as a protective agent (14.3% by mass relative to the amino acid), 0.30g Glycerol as a sugar alcohol (30% by mass relative to the cyclic amine compound), 71.62 g of NMP as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Example 1.

(Example 2)

The sample peeling liquid of Example 2 was prepared using the following composition.

4.0g of IZ as a cyclic amine compound, 0.32g of Arg as an amino acid (8% by mass relative to the cyclic amine compound), 0.09g of MBET as a protective agent (28.1% by mass relative to the amino acid), 1.60g Glycerol as a sugar alcohol (40% by mass relative to the cyclic amine compound), 66.99 g of DEF as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Example 2.

(Example 3)

The sample peeling liquid of Example 3 was prepared using the following composition.

1.0g of PIP as a cyclic amine compound, 0.07g of Arg as an amino acid (7% by mass relative to the cyclic amine compound), 0.01g of MBET as a protective agent (14.3% by mass relative to the amino acid), 0.30g Glycerol as a sugar alcohol (30% by mass with respect to the cyclic amine compound), 71.62 g of DEF as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Example 3.

(Example 4)

The sample peeling liquid of Example 4 was prepared using the following composition.

4.0 g of PIP as a cyclic amine compound, 0.32 g of Arg as an amino acid (8% by mass relative to the cyclic amine compound), 0.09 g of 5M-BTA as a protective agent (28.1% by mass relative to the amino acid), 1.60 g of Glycerol as a sugar alcohol (40% by mass relative to the cyclic amine compound), 66.99 g of NMF as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Example 4.

(Example 5)

The sample peeling liquid of Example 5 was prepared using the following composition.

3.0 g of PIP as a cyclic amine compound, 0.21 g of Arg as an amino acid (7% by mass relative to the cyclic amine compound), 0.03 g of MBET as a protective agent (14.3% by mass relative to the amino acid), 0.90 g Stol as a sugar alcohol (30% by mass relative to the cyclic amine compound), 68.86 g of DEF as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Example 5.

(Example 6)

The sample peeling liquid of Example 6 was prepared using the following composition.

1.0g of PIP as a cyclic amine compound, 0.07g of Lys as an amino acid (7% by mass relative to the cyclic amine compound), 0.01g of MBET as a protective agent (14.3% by mass relative to the amino acid), 0.10g Glycerol as a sugar alcohol (10% by mass relative to the cyclic amine compound), 71.82 g of NMP as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Example 6.

(Comparative example 1)

The sample peeling liquid of Comparative Example 1 was prepared using the following composition.

1.0g of IZ as a cyclic amine compound, 0.03g of Arg as an amino acid (3% by mass relative to the cyclic amine compound), 0.006g of MBET as a protective agent (20% by mass relative to an amino acid), 0.30g Glycerol as a sugar alcohol (30% by mass relative to the cyclic amine compound), 71.664 g of NMP as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Comparative Example 1.

(Comparative example 2)

The sample peeling liquid of Comparative Example 2 was prepared using the following composition.

4.0 g of IZ as a cyclic amine compound, 0.60 g of Arg as an amino acid (15% by mass relative to the cyclic amine compound), 0.18 g of MBET as a protective agent (30% by mass relative to the amino acid), 1.60 g Glycerol as a sugar alcohol (40% by mass relative to the cyclic amine compound), 66.62 g of DEF as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Comparative Example 2.

(Comparative example 3)

The sample peeling liquid of Comparative Example 3 was prepared using the following composition.

1.0g of PIP as a cyclic amine compound, 0.07g of Arg as an amino acid (7% by mass relative to the cyclic amine compound), 0.003g of MBET as a protective agent (4.3% by mass relative to the amino acid), 0.30g Glycerol as a sugar alcohol (30% by mass relative to the cyclic amine compound), 71.627 g of DEF as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Comparative Example 3.

(Comparative Example 4)

The sample peeling liquid of Comparative Example 4 was prepared using the following composition.

4.0 g of PIP as a cyclic amine compound, 0.32 g of Arg as an amino acid (8% by mass relative to the cyclic amine compound), 0.10 g of 5M-BTA as a protective agent (31% by mass relative to the amino acid), 1.60 g of Glycerol as a sugar alcohol (40% by mass relative to the cyclic amine compound), 66.98 g of NMF as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Comparative Example 4.

(Comparative Example 5)

The sample peeling liquid of Comparative Example 5 was prepared using the following composition.

1.0g of PIZ as a cyclic amine compound, 0.07g of Arg as an amino acid (7% by mass relative to the cyclic amine compound), 0.01g of MBET as a protective agent (14.3% by mass relative to the amino acid), 0.30g Glycerol as a sugar alcohol (30% by mass relative to the cyclic amine compound), 71.62 g of DEF as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Comparative Example 5.

(Comparative Example 6)

The sample peeling liquid of Comparative Example 6 was prepared using the following composition.

1.0g MMA as a cyclic amine compound, 0.07g Lys as an amino acid (7% by mass relative to the cyclic amine compound), 0.01g MBET as a protective agent (14.3% by mass relative to the amino acid), 0.10g Glycerol as a sugar alcohol (10% by mass relative to the cyclic amine compound), 71.82 g of NMP as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Comparative Example 6.

(Comparative Example 7)

The sample peeling liquid of Comparative Example 7 was prepared using the following composition.

3.0g IZ as a cyclic amine compound, 0.21g Lys as an amino acid (7% by mass relative to the cyclic amine compound), 0.03g MBET as a protective agent (14.3% by mass relative to the amino acid), 0.00g Glycerol as a sugar alcohol (without sugar alcohol), 69.76 g of NMP as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Comparative Example 7.

(Comparative Example 8)

The sample peeling liquid of Comparative Example 8 was prepared using the following composition.

1.0g of PIP as a cyclic amine compound, 0.07g of Arg as an amino acid (7% by mass relative to the cyclic amine compound), 0.01g of MBET as a protective agent (14.3% by mass relative to the amino acid), 0.30g Glycerol as a sugar alcohol (30% by mass relative to the cyclic amine compound), 71.62 g of BDG as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Comparative Example 8.

(Comparative Example 9)

The sample peeling liquid of Comparative Example 9 was prepared using the following composition.

1.0g of PIP as a cyclic amine compound, 0.07g of His as an amino acid (7% by mass relative to the cyclic amine compound), 0.01g of MBET as a protective agent (14.3% by mass relative to the amino acid), 0.30g Glycerol as a sugar alcohol (30% by mass relative to the cyclic amine compound), 71.62 g of DEF as a polar solvent, 27.0 g of water, and the above components were mixed as a sample of Comparative Example 9.

Prepare the above-mentioned sample stripping solution and conduct a stripping test. The composition of the sample peeling liquid of the Example and the results of the peeling test are shown in Table 1, and the composition of the sample peeling liquid of the Comparative Example and the results of the peeling test are shown in Tables 2 and 3.

[Table 1]

[Table 2]

[table 3]

Refer to Table 1, which are Examples 1 to 6 of the composition of the present invention. The resist film that has been heat-treated at 170°C for 5 minutes can be peeled off at 40°C for 40 seconds. Therefore, the peeling force was evaluated as "〇". Furthermore, when observed by SEM, the copper film in the gate line and the contact hole was also in a good state, so the metal damage was also evaluated as "o". Furthermore, the undercut due to corrosion of molybdenum and the undercut of copper between molybdenum and copper were also evaluated as "o". In addition, the peeling force of the aluminum layer was also evaluated as "〇". In addition, regarding aluminum, no problem occurred in the Examples and Comparative Examples.

On the other hand, Comparative Example 1 and Comparative Example 2 are cases where there are too few amino acids (Comparative Example 1) and cases where there are too many amino acids (Comparative Example 2). When the amino acid is too low, undercutting of molybdenum occurs. This is because the copper film cannot be corroded properly. On the other hand, when there are too many amino acids, the surface of copper will be corroded.

In addition, Comparative Example 3 and Comparative Example 4 are the case where the protective agent is too little (Comparative Example 3) and the case where it is too much (Comparative Example 4). When the protective agent is too small, the corrosion of the copper film by the amino acid cannot be prevented. On the other hand, when the protective agent is too much, the copper surface will not be corroded, but corrosion of molybdenum (undercut) will occur.

In Comparative Example 5, the amine is piperazine. Although piperazine is a cyclic amine, it cannot peel off the hard-baked resist film. In Comparative Example 6, N-methylethanolamine (alkanolamine) was substituted for the amine. However, in this case, the hard-baked resist film could not be peeled off.

Comparative Example 7 is a case where no sugar alcohol is added. In this case, corrosion occurred between molybdenum and copper, and undercutting of copper occurred (indicated by "Cu U.C." in the table).

Comparative Example 8 is a case where diethylene glycol monobutyl ether, which is a protic organic solvent, is used as a polar solvent. When the organic polar solvent is protonated, undercutting of molybdenum easily occurs.

Comparative Example 9 is a case where histidine is used as the amino acid. Although histidine is a basic amino acid, undercutting of molybdenum occurs. In the composition of the stripping liquid according to the present invention, it can be considered that histidine is less corrosive to copper than lysine and arginine.

As described above, when a wiring composed of molybdenum, copper, and aluminum is formed by photolithography, the resist stripping solution according to the present invention can suppress surface roughness and undercuts caused by corrosion of molybdenum and copper. [Industrial Profitability]

The present invention can be applied to the resist peeling step in the manufacturing process of a large-area display device.

no.

no.

Claims (4)

A resist stripping liquid, comprising: 0.5 to 5 mass% of secondary cyclic amine relative to the total amount of the stripping liquid; 5 to 10 mass% of basic amino acid relative to the aforementioned secondary cyclic amine; relative to the aforementioned alkali The amino acid is 10-30% by mass of the protective agent; the sugar alcohol is 10-50% by mass relative to the aforementioned secondary cyclic amine; the organic polar solvent; and water; wherein the aforementioned secondary cyclic amine is imidazole and piperidine At least one of. The resist stripping liquid according to claim 1, wherein the basic amino acid includes at least one of arginine and lysine. The resist stripping solution according to claim 1, wherein the aforementioned protective agent is selected from the group consisting of benzotriazole, 5-methyl-1H-benzotriazole, 2-mercaptobenzimidazole, 2-mercaptobenzothiazole, 2-Mercapto-5-methylbenzimidazole, 1-[N,N-bis(2-ethylhexyl)aminomethyl]-1H-benzotriazole, 2,2'-[[(methyl -1H-benzotriazol-1-yl)methyl]imino]diethanol. The resist stripping liquid according to claim 1, wherein the sugar alcohol is at least one of glycerin and sorbitol.