IP Library Granted Patent US 10,775,699
Granted Patent B2
US 10,775,699 · App. 16/086,485 · Granted Sep 15, 2020

Negative photoresist composition for KRF laser, having high resolution and high aspect ratio

Inventors: Seung Hun Lee (Daegu, KR); Seung Hyun Lee (Daegu, KR); Su Jin Lee (Daegu, KR); Young Cheol Choi (Gumi-si, KR)
Assignee: YOUNG CHANG CHEMICAL CO., LTD
G03F7/038G03F7/004G03F7/0045G03F7/40
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,775,699
App. No.
16/086,485
Granted
Sep 15, 2020
Kind
B2
Abstract

Disclosed is a negative photoresist composition for a KrF laser, having high resolution and a high aspect ratio and, more particularly, a negative photoresist composition for a KrF laser, which includes a specific additive in order to improve the properties of a conventional negative photoresist, whereby the negative photoresist composition can prevent fine-pattern collapse even using a short-wavelength exposure light source, compared to conventional negative photoresists, and can also exhibit high resolution and a high aspect ratio and is thus suitable for use in semiconductor processing.

Claims (15)

1. A negative photoresist composition for a KrF laser, comprising:

(a) 5 to 60 wt % of a phenol polymer resin;

(b) 0.1 to 5 wt % of a novolac resin having a weight average molecular weight of 3,000 to 50,000 represented by Chemical Formula 1 below;

(c) 1 to 10 wt % of a crosslinking agent;

(d) 0.1 to 10 wt % of a photoacid generator;

(e) 0.01 to 5 wt % of an acid diffusion inhibitor; and

(f) a remainder of a solvent,

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:

wherein R 1 is a methyl group,

R2 is a hydroxyl group (—OH),

m is 1 to 9, and

n is 1 to 9.

2. 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, tetramethoxy methyl urea, tetramethoxy ethyl urea, and tetramethoxyethyl-2,4-diamino-1,3,5-triazine.

3. 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, diphenyliodonium perfluorooctane sulfonate, methoxydiphenyliodonium perfluorooctane sulfonate, di-t-butyldiphenyliodonium perfluorooctane sulfonate, N-hydroxysuccinimide perfluorooctane sulfonate, and norbornene dicarboxyimide perfluorooctane sulfonate.

4. 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 Sep 19, 2018
From: LEE, SEUNG HUN; LEE, SEUNG HYUN; LEE, SU JIN; CHOI, YOUNG CHEOL
To: YOUNG CHANG CHEMICAL CO., LTD
Reel/Frame 046913/0569 →
Priority Claims (1)
KR 10-2016-0033733 · Mar 22, 2016 · national
Continuity (1)
Related Publication 20190101827A1 · Apr 4, 2019