Method of producing layer structure, and method of forming patterns

Patent metadata

Field	Value
Publication number	US-10663863-B2
Application number	US-201615264654-A
Country	US
Kind code	B2
Filing date	Sep 14, 2016
Priority date	Oct 23, 2015
Publication date	May 26, 2020
Grant date	May 26, 2020

Abstract

A method of producing a layer structure and a method of forming a pattern, the method of producing a layer structure including coating a first composition on a substrate that has a pattern thereon; curing the coated first composition to form a first organic layer; applying a liquid material to the first organic layer to remove a part of the first organic layer; and coating a second composition on remaining parts of the first organic layer; and curing the coated second composition on the remaining parts of the first organic layer to form a second organic layer: wherein the first composition and the second composition each independently include a solvent, and a polymer including a structural unit represented by Chemical Formula 1,

* A 1 -B 1 *.  [Chemical Formula 1]

First claim

What is claimed is:

1. A method of producing a layer structure, the method comprising:
coating a first composition on a substrate that has a pattern thereon;
curing the coated first composition to form a first organic layer;
applying a liquid material to the first organic layer to remove a part of the first organic layer; and
coating a second composition on remaining parts of the first organic layer such that the coating of the second composition is performed in the same manner as the coating of the first composition; and
curing the coated second composition on the remaining parts of the first organic layer to form a second organic layer:
wherein the first composition and the second composition each independently include:
a solvent, and
a polymer including a structural unit represented by Chemical Formula 1,
* A 1 -B 1 *  [Chemical Formula 1]

wherein, in Chemical Formula 1,
A 1 is a divalent cyclic group including at least one of a substituted or unsubstituted benzene ring,
B 1 is a divalent organic group, and
* is a linking point, and
wherein the liquid material includes γ-butyrolactone, δ-valerolactone, ethyllactate, ethyl-3-ethoxypropionate, propylene glycolmonomethyl ether acetate, β-hydroxy β-methylbutyrate, methanol, ethanol, 2-butanol, ethylene glycol, propylene glycol, glycerol, 1,6-hexanediol, cyclo hexanediol, sorbitol, xylitol, 2-methyl-2,4-pentanediol, 1,3-butanediol, 1,4-butanediol, ethylene glycol monomethyl ether, diethylene glycol, dipropylene glycol, propylene glycol monomethyl ether, diethylene glycol monomethyl ether, triethylene glycol, poly(ethylene glycol), propylene glycol monomethyl ether, dipropylene glycol monomethyl ether, tripropylene glycol monomethyl ether, diethylene glycol monobutyl ether, propylene glycol monomethyl ether acetate, ethylethoxy propionate, propylene glycol monomethyl ether propionate, ethylene glycol diacetate, ethyl lactate, butyl lactate, methyl 2-hydroxyisobutyrate, n-butyl acetate, formamide, monomethylformamide, dimethyl formamide, acetamide, monomethylacetamide, dimethyl acetamide, monoethylacetamide, diethylacetamide, N-methylpyrrolidone, methoxy methyl propionate, methoxy ethyl propionate, methoxy propyl propionate, methoxy butyl propionate, ethoxy methyl propionate, ethoxy ethylpropionate, ethoxy propyl propionate, ethoxy butyl propionate, dimethyl sulfone, dimethyl sulfoxide, sulfolane, acetone, acetyl acetone, methylethyl ketone, methyl isobutyl ketone, or a combination thereof.

2. The method as claimed in claim 1 , wherein the remaining parts of the first organic layer remain inside gaps of the pattern.

3. The method as claimed in claim 1 , wherein the liquid material is applied in an amount of about 0.1 cc to about 100 cc.

4. The method as claimed in claim 1 , wherein the first organic layer and the second organic layer are a hardmask layer.

5. The method as claimed in claim 4 , wherein the second organic layer is directly on the remaining parts of the first organic layer.

6. The method as claimed in claim 1 , wherein, in Chemical Formula 1, A 1 is a divalent cyclic group including at least two rings in its structure.

7. The method as claimed in claim 1 , wherein, in Chemical Formula 1, A 1 is a substituted or unsubstituted divalent cyclic group of one of the following compounds:

wherein, in the above compounds,
M is a substituted or unsubstituted C1 to C5 alkylene group, —O—, —S—, —SO 2 —, or carbonyl, and
R 0 and R 1 are each independently hydrogen, a hydroxy group, a methoxy group, an ethoxy group, a halogen atom, a halogen-containing group, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a combination thereof.

8. The method as claimed in claim 1 , wherein, in Chemical Formula 1, A 1 is a group that is substituted with a hydroxy group, a thionyl group, a thiol group, a cyano group, an amino group, a C1 to C10 alkyl group, a C6 to C30 aryl group, a C1 to C30 alkoxy group, or a combination thereof.

9. The method as claimed in claim 1 , wherein the polymer further includes a structural unit represented by Chemical Formula 2:
* A 2 -B 1 *  [Chemical Formula 2]

wherein, in Chemical Formula 2,
A 2 is a divalent cyclic group including at least one of a substituted or unsubstituted benzene ring, and
B 1 and * are defined the same as those of Chemical Formula 1, and
wherein the structural unit represented by Chemical Formula 2 is different from the structural unit represented by Chemical Formula 1.

10. The method as claimed in claim 1 , wherein, in Chemical Formula 1, B 1 is represented by Chemical Formula 3:

wherein, in Chemical Formula 3,
a and b are each independently an integer of 0 to 2, and
L is a substituted or unsubstituted divalent cyclic group of one of the following compounds,

wherein, in the above compounds, M is a substituted or unsubstituted C1 to C5 alkylene group, —O—, —S—, —SO 2 —, or carbonyl.

11. The method as claimed in claim 1 , wherein the polymer has a weight average molecular weight of about 500 to about 200,000.

12. The method as claimed in claim 1 , wherein the curing after applying the second composition is performed at a temperature that is higher than a temperature at which the curing after applying the first composition is performed.

13. The method as claimed in claim 1 , wherein the first composition and the second composition each independently include a surfactant, a plasticizer, a cross-linking agent, a thermal acid generator, a photoacid generator, or a combination thereof.

14. The method as claimed in claim 13 , wherein:
at least one of the first composition or the second composition includes the cross-linking agent, and
the cross-linking agent includes methoxymethylated glycoluril, butoxymethylated glycoluril, methoxymethylated melamine, butoxymethylated melamine, methoxymethylated benzoguanamine, butoxymethylated benzoguanamine, methoxymethylated urea, butoxymethylated urea, methoxymethylated thiourea, butoxymethylated thiourea, methoxymethylatedbenzene, butoxymethylated benzene, methoxymethylated phenol, butoxymethylated phenol, or a combination thereof.

15. The method as claimed in claim 1 , wherein the solvent of the first composition and the solvent of second composition each independently include propylene glycol, propylene glycol diacetate, methoxy propanediol, diethylene glycol, diethylene glycol butylether, tri(ethylene glycol)monomethylether, propylene glycol monomethylether, propylene glycol monomethylether acetate, cyclohexanone, ethyllactate, gamma-butyrolactone, N,N-dimethyl formamide, N,N-dimethyl acetamide, methylpyrrolidone, methylpyrr

Assignees

• Samsung Sdi Co Ltd

Inventors

• Jeong Seulgi
• Kim Minsoo
• Kim Sunghwan
• SONG Hyunji
• KANG Sunhae
• Kim Youngmin
• Kim Yoona
• Kim Jinhyung
• Nam Younhee
• Baek Jaeyeol
• Yoon Byeri
• Lee Chungheon
• Hong Seunghee
• Hwang Sunmin

Classifications

• G03F7/11 Primary

  having cover layers or intermediate layers, e.g. subbing layers {(G03F7/091 - G03F7/093, B41N3/03 take precedence)} · CPC title

• G03F7/09 Primary

  characterised by structural details, e.g. supports, auxiliary layers (supports for printing plates in general B41N) · CPC title

• G03F7/091

  characterised by antireflection means or light filtering or absorbing means, e.g. anti-halation, contrast enhancement · CPC title

• G03F7/004

  Photosensitive materials (G03F7/12, G03F7/14 take precedence) · CPC title