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Positive resist composition suitable for lift-off technique and pattern forming method

a technology of resist and lift-off technique, applied in the direction of photosensitive materials, instruments, photomechanical equipment, etc., can solve the problems of low processing precision, low reliability, and often complex steps of lift-off technique, and achieve the effect of improving the accuracy of the effect of forming and forming

Inactive Publication Date: 2001-08-30
SHIN ETSU CHEM CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The composition enables the formation of reliable conductor patterns with high precision and heat resistance through a simple process, independent of light source wavelength, while maintaining low costs and ensuring effective resist stripping without residues, thus enhancing processing reliability and precision.

Problems solved by technology

The above-mentioned process, however, suffers from low processing precision and a problem associated with etching procedure where difficult-to-etch metals such as gold and tantalum are used as the metallization.
However, where patterns are formed by the lift-off technique using conventional positive resist compositions, the resist stripping step does not effectively take place and can leave resist residues, arising a problem of reliability.
Therefore, the lift-off technique often employs a step requiring complex, cumbersome operations, for example, a dual layer resist process and an image reversal resist process.
If a novolak resin is synthesized to a lower average molecular weight, the resulting resist layer is improved in resolution, but becomes poor in heat resistance and film retention.
As the light source of an aligner shifts from g-line to i-line, light is not easily transmitted by a resist layer containing a conventionally used benzophenone photosensitive agent.
However, in order that a resist material for the lift-off technique having higher resolution as well as satisfactory dimensional control, heat resistance, and film retention be accomplished by combining such measures, many additional steps are necessary in the resist preparation process and undesirably cause a cost increase.
With a percent esterification of less than 2.5 mol %, film retention is poor and a resist composition cannot be configured to a pattern and ceases to be useful.
A novolak resin with a percent esterification of more than 27 mol % is less soluble in solvents such as ethyl cellosolve acetate, and a resist composition can not be prepared therefrom.
With a weight average molecular weight of less than 200, a resist film becomes extremely poor in heat resistance.
If the amount of the dissolution promoter is more than 60 parts, the effect of inhibiting dissolution of unexposed areas in an alkaline developer would become insufficient, permitting the pattern to be dissolved away.
Baking temperatures above 130.degree. C. would render resist stripping difficult.

Method used

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  • Positive resist composition suitable for lift-off technique and pattern forming method
  • Positive resist composition suitable for lift-off technique and pattern forming method
  • Positive resist composition suitable for lift-off technique and pattern forming method

Examples

Experimental program
Comparison scheme
Effect test

synthesis examples 1-5

Synthesis of Alkali-Soluble Resins

[0081] A three-necked flask equipped with a stirrer, condenser and thermometer was charged with 64.8 g (0.6 mol) of p-cresol, 162.3 g (1.50 mol) of m-cresol, 110.1 g (0.90 mol) of 3,5-xylenol, 133.8 g (1.65 mol) of an aqueous solution of 37 wt % formaldehyde, and 0.90 g (7.2.times.10.sup.-3 mol) of oxalic acid dihydrate as a polycondensation catalyst. The flask was immersed in an oil bath to maintain an internal temperature of 100.degree. C. and polycondensation reaction took place for one hour.

[0082] At the end of reaction, 1,500 ml of methyl isobutyl ketone (MIBK) was added to the reaction solution which was stirred for 30 minutes. The aqueous layer was separated off. The MIBK layer in which the product was extracted was washed 5 times with 900 ml of pure water, followed by separation and vacuum stripping by means of an evaporator at 4 mmHg and 150.degree. C. As a result, 245 g of a novolak resin A-1 was prepared.

[0083] Like novolak resin A-1, nov...

synthesis examples 6-15

Synthesis of 1,2-Naphthoquinonediazidosulfonyl-Introduced Novolak Resins

[0084] Under a light-shielded condition, a three-necked flask equipped with a stirrer, dropping funnel and thermometer was charged with 150 g (1.2 mol) of novolak resin A-1 (OH equivalent 124.4), 19.3 g (0.072 mol) of 1,2-naphthoquinone-2-diazido-5-sulfonyl chloride, and 760 g of 1,4-dioxane. At room temperature, 8.0 g (0.079 mol) of triethylamine was added dropwise to the solution. After the dropwise addition, stirring was continued for 10 hours. The reaction solution was poured into a large volume of a 0.12N hydrochloric acid solution whereupon the resin precipitated. The resin was prepared, dissolved in 600 g of ethyl acetate, and washed three times with 200 g of water. Separation and vacuum stripping at 40.degree. C. yielded 140 g of 1,2-naphthoquinone-2-diazido-5-sulfonyl-introduced novolak resin B-1.

[0085] As shown in Table 2, novolak resins B-2 through B-10 having a 1,2-naphthoquinone-2-diazido-4-sulfonyl...

synthesis example 16

Synthesis of 1,2-Quinonediazide Compound

[0086] Under a light-shielded condition, a three-necked flask equipped with a stirrer, dropping funnel and thermometer was charged with 10.0 g (43.4 mmol) of 2,3,4-trihydroxybenzophenone, 35.0 g (130 mmol) of 1,2-naphthoquinone-2-diazido-5-sulfonyl chloride, and 200 g of 1,4-dioxane. The flask was immersed in a water bath to control its temperature below 25.degree. C. To the flask, a solution of 10.50 g of 1,4-diazabicyclo[2.2.2]octane (DABCO) in 100 g of 1,4-dioxane as a catalyst was added dropwise through the dropping funnel. The precipitated DABCO hydrochloride salt was removed by filtration and with stirring, the filtrate was added dropwise to 1,800 g of 0.12N hydrochloric acid for re-precipitation. The solution was subject to filtration again. The precipitate was extracted with 300 ml of ethyl acetate, washed 5 times with 100 g of pure water and separated. Vacuum stripping by means of an evaporator below 40.degree. C. yielded 41.0 g of a ...

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Abstract

A positive resist composition contains (A) a novolak resin having a weight average molecular weight calculated as polystyrene of 2,000-20,000 wherein 2.5-27 mol % of the hydrogen atom of a hydroxyl group is replaced by a 1,2-naphthoquinonediazidosulfonyl group and (B) a low molecular aromatic compound having phenolic hydroxyl groups and 2-20 benzene rings wherein the ratio of the number of phenolic hydroxyl groups to the number of benzene rings is between 0.5 and 2.5. By forming a resist layer on a substrate from the positive resist composition and baking the resist layer at 90-130° C., followed by exposure and development, there is formed a resist pattern having an undercut of desired configuration. Owing to high resolution and improved dimensional control, heat resistance and film retention, the resist pattern lends itself to a lift-off technique.

Description

[0001] 1. Field of the Invention[0002] This invention relates to a positive resist composition which lends itself to a lift-off technique.[0003] 2. Prior Art[0004] In the prior art, dry and wet etching processes are commonly used in forming conductor patterns such as aluminum electrodes on semiconductor substrates. The process is illustrated in FIG. 3 as comprising metal layer sputtering and resist-patterning to form a resist pattern 3 on a metallization layer 2 on a substrate 1. The exposed area of the metallization layer 2, that is, those metallization portions which are not covered with the resist pattern 3 are etched away. By treating the structure with a stripping solution, the resist pattern 3 is stripped off to leave a conductor pattern 2 on the substrate 1.[0005] The above-mentioned process, however, suffers from low processing precision and a problem associated with etching procedure where difficult-to-etch metals such as gold and tantalum are used as the metallization. To ...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): G03F7/004G03F7/022G03F7/023G03F7/26G03F7/38G03F7/40H01L21/027H01L21/302H01L21/3065H01L21/3205
CPCG03F7/0226G03F7/0233
Inventor UEDA, TAKAFUMIKATO, HIDETOFUJII, TOSHIHIKOKOBAYASHI, MIKI
Owner SHIN ETSU CHEM CO LTD
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