Chemically amplified positive resist composition and resist pattern forming process
US-12164231-B2 · Dec 10, 2024 · US
US9529257B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9529257-B2 |
| Application number | US-201314420957-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 2, 2013 |
| Priority date | Oct 24, 2012 |
| Publication date | Dec 27, 2016 |
| Grant date | Dec 27, 2016 |
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Disclosed are a polymer represented by the Chemical Formula 1, a monomer represented by the Chemical Formula 2, and a solvent, wherein the monomer is included in the same or a higher amount than the polymer, and a method of forming patterns using the same.
Opening claim text (preview).
The invention claimed is: 1. A hardmask composition, comprising: a polymer including a repeating unit represented by the following Chemical Formula 1, a monomer represented by the following Chemical Formula 2, and a solvent, wherein the monomer is included in the same or a higher amount than the polymer: wherein, in the above Chemical Formulae 1 and 2, R 1 is a single bond or a substituted or unsubstituted C1 to C10 alkylene group, R 2 to R 6 are each independently hydrogen, a hydroxy group, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 cycloalkenyl group, a substituted or unsubstituted C7 to C20 arylalkyl group, a substituted or unsubstituted C1 to C20 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 heteroaryl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted C2 to C30 alkynyl group, a substituted or unsubstituted C1 to C20 aldehyde group, a substituted or unsubstituted C1 to C4 alkyl ether, a substituted or unsubstituted C7 to C20 arylalkylene ether, a substituted or unsubstituted C1 to C30 haloalkyl group, or a combination thereof, AR1 and AR2 are each independently a substituted or unsubstituted C6 to C20 aryl group, x+y=1, 0≦x≦1 and 0≦y≦1, and n is an integer ranging from 1 to 200. 2. The hardmask composition of claim 1 , wherein the polymer and the monomer are included in a weight ratio of about 1:9 to about 5:5. 3. The hardmask composition of claim 1 , wherein the AR1 and AR2 each independently include at least one selected from groups listed in the following Group 1: wherein, R 7 and R 8 are each independently hydrogen, a hydroxy group, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 cycloalkenyl group, a substituted or unsubstituted C7 to C20 arylalkyl group, a substituted or unsubstituted C1 to C20 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 heteroaryl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted C2 to C30 alkynyl group, a substituted or unsubstituted C1 to C20 aldehyde group, a substituted or unsubstituted C1 to C4 alkyl ether, a substituted or unsubstituted C7 to C20 arylalkylene ether, a substituted or unsubstituted C1 to C30 haloalkyl group, or a combination thereof. 4. The hardmask composition of claim 1 , wherein the polymer includes a repeating unit represented by the following Chemical Formula 1 a: wherein, in the above Chemical Formula 1 a, x+y=1, 0≦x≦1, and 0≦y≦1, and n is an integer ranging from 1 to 200. 5. The hardmask composition of claim 1 , wherein the monomer is represented by one of the following Chemical Formulae 2a to 2d: 6. The hardmask composition of claim 1 , wherein the polymer has a weight average molecular weight of 1,000 to 100,000 g/mol. 7. The hardmask composition of claim 1 , wherein the total amount of the polymer and the monomer is 1 to 50 parts by weight based on 100 parts by weight of the solvent. 8. The hardmask composition of claim 1 , further comprising at least one of a surfactant, an acid catalyst, or a cross-linking agent. 9. The hardmask composition of claim 8 , wherein the surfactant, acid catalyst, or cross-linking agent are included in an amount of 0.001 to 3 parts by weight based on 100 parts by weight of the hardmask composition. 10. A method of forming patterns, the method comprising: providing a material layer on a substrate, applying the hardmask composition of claim 1 on the material layer heat-treating the hardmask composition to form a hardmask layer, forming a silicon-containing thin film on the hardmask layer, forming a photoresist layer on the silicon-containing thin film, exposing and developing the photoresist layer to form a photoresist pattern, selectively removing the silicon-containing thin film and the hardmask layer using the photoresist pattern to expose a part of the material layer, and etching an exposed part of the material layer. 11. The method of claim 10 , wherein after forming the silicon-containing thin film, a bottom anti-reflective coating (BARC) is further formed on the silicon-containing thin film. 12. The method of claim 10 , wherein the hardmask composition is applied using a spin-on coating method. 13. The method of claim 10 , wherein the hardmask layer is heat-treated at 150 to 500° C. 14. The hardmask composition of claim 1 , wherein the monomer is included in the composition in an amount greater than an amount in which the polymer is included in the composition. 15. The hardmask composition of claim 1 , wherein AR1 and AR2 are different from one another.
Multiple processes, e.g. applying a further resist layer on an already in a previously step, processed pattern or textured surface · CPC title
Photosensitive materials (G03F7/12, G03F7/14 take precedence) · CPC title
Multilayer resist systems, e.g. planarising layers · CPC title
with organic non-macromolecular light-sensitive compounds not otherwise provided for, e.g. dissolution inhibitors · CPC title
Processing photosensitive materials; Apparatus therefor (G03F7/12 - G03F7/24 take precedence) · CPC title
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