IP Library Granted Patent US 10,162,261
Granted Patent B2
US 10,162,261 · App. 15/744,667 · Granted Dec 25, 2018

Negative photoresist composition for KrF laser for forming semiconductor patterns

Inventors: Seung Hun Lee (Daegu, KR); Seung Hyun Lee (Daegu, KR); Sang Woong Yoon (Seoul, KR); Su Jin Lee (Daegu, KR); Young Cheol Choi (Gumi-si Gyeongsangbuk-do, KR)
Assignee: YOUNG CHANG CHEMICAL CO., LTD
G03F7/0382G03F7/004G03F7/0045G03F7/033G03F7/038G03F7/0384
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Quick Facts
Patent No.
US 10,162,261
App. No.
15/744,667
Granted
Dec 25, 2018
Kind
B2
Abstract

Provided is a negative photoresist composition for a KrF laser for semiconductor pattern formation, which includes a predetermined compound in order to improve the properties of a conventional negative photoresist, thereby realizing high transparency, high resolution and an excellent profile, even in the presence of an exposure source having a short wavelength compared to the conventional negative photoresist, and is thus suitable for use in semiconductor processing.

Claims (8)

1. A negative photoresist composition for a KrF laser, comprising 5 to 60 wt % of a polymer resin, 0.1 to 4 wt % of a compound represented by Chemical Formula 3 below, 1 to 10 wt % of a crosslinking agent, 0.1 to 10 wt % of a photoacid generator, 0.01 to 5 wt % of an acid diffusion inhibitor and a remainder of a solvent:

in Chemical Formula 3, R is acryloyl.

2. The negative photoresist composition of claim 1 , wherein the compound represented by Chemical Formula 3 is obtained by subjecting 1,1,1-tri(4-hydroxyphenyl)ethane to a substitution reaction with acryloyl chloride.

3. The negative photoresist composition of claim 1 , wherein the polymer resin is at least one selected from the group consisting of a phenol polymer resin and a cresol polymer resin, each having a hydroxyl group.

4. The negative photoresist composition of claim 3 , wherein the phenol polymer resin is obtained from at least one monomer selected from the group consisting of 4-hydroxy-3-methyl benzoic acid, 4-hydroxy-2-methyl benzoic acid, 5-hydroxy-2-methyl benzoic acid, 3,5-di-tert-butyl-4-hydroxy benzoic acid, 4-hydroxy-3,5-dimethyl benzoic acid, 4-hydroxy isophthalic acid, 2,4,6-hydroxy toluene, 2,4,6-trihydroxy benzoic acid monohydrate and 2,4,6-trihydroxy benzaldehyde, and the cresol polymer resin is obtained from at least one monomer selected from the group consisting of o-cresol, p-cresol, m-cresol, epoxy o-cresol, epoxy p-cresol and epoxy m-cresol.

5. The negative photoresist composition of claim 1 , wherein the crosslinking agent includes at least one selected from the group consisting of tris(2,3-epoxypropyl)isocyanurate, trimethylolmethane triglycidyl ether, trimethylolpropane triglycidyl ether, hexamethylol melamine, trimethylolethane triglycidyl ether, hexamethoxymethyl melamine, hexamethoxyethyl melamine, tetramethylol 2,4-diamino-1,3,5-triazine, tetramethoxymethyl-2,4-diamino-1,3,5-triazine, tetramethylol glycoluril, tetramethoxymethyl glycoluril, tetramethoxyethyl glycoluril, tetramethylolurea, tetramethoxymethylurea, tetramethoxyethylurea and tetramethoxyethyl-2,4-diamino-1,3,5-triazine.

6. The negative photoresist composition of claim 1 , wherein the photoacid generator includes at least one selected from the group consisting of triphenylsulfonium triflate, triphenylsulfonium antimonate, diphenyliodonium triflate, diphenyliodonium antimonate, methoxydiphenyliodonium triflate, di-t-butyldiphenyliodonium triflate, norbornene dicarboxyimide triflate, triphenylsulfonium nonaflate, diphenyliodonium nonaflate, methoxydiphenyliodonium nonaflate, di-t-butyldiphenyliodonium nonaflate, N-hydroxysuccinimide nonaflate, norbornene dicarboxyimide nonaflate, triphenylsulfonium perfluorooctane sulfonate, diphenyl iodonium perfluorooctane sulfonate, methoxydiphenyl iodonium perfluorooctane sulfonate, di-t-butyldiphenyliodonium perfluorooctane sulfonate, N-hydroxysuccinimide perfluorooctane sulfonate and norbornene dicarboxyimide perfluorooctane sulfonate.

7. The negative photoresist composition of claim 1 , wherein the acid diffusion inhibitor includes at least one selected from the group consisting of dimethylamine, diethylamine, trimethylamine, triethylamine, tributylamine, dimethanolamine, diethanolamine, trimethanolamine, triethanolamine and tributanolamine.

Assignments (2)
CHANGE OF NAME Recorded Jul 14, 2023
From: YOUNG CHANG CHEMICAL CO., LTD
To: YCCHEM CO., LTD.
Reel/Frame 064276/0151 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2018
From: LEE, SEUNG HUN; LEE, SEUNG HYUN; YOON, SANG WOONG; LEE, SU JIN; CHOI, YOUNG CHEOL
To: YOUNG CHANG CHEMICAL CO., LTD
Reel/Frame 044613/0558 →
Priority Claims (1)
KR 10-2015-0103727 · Jul 22, 2015 · national
Continuity (1)
Related Publication 20180203351A1 · Jul 19, 2018