Method for forming a resist under layer film and patterning process
US-9230827-B2 · Jan 5, 2016 · US
US9568825B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9568825-B2 |
| Application number | US-201514748911-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 24, 2015 |
| Priority date | Jul 15, 2014 |
| Publication date | Feb 14, 2017 |
| Grant date | Feb 14, 2017 |
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A hardmask composition includes a polymer including a moiety represented by the following Chemical Formula 1 and a solvent. In the Chemical Formula 1, A, B, R 1 and R 2 are the same as defined in the detailed description.
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What is claimed is: 1. A hardmask composition, comprising: a polymer represented by the following Chemical Formula 2: wherein, in Chemical Formula 2, A 1 , A 2 , B 1 and B 2 are independently a substituted or unsubstituted aromatic ring group, R 1a , R 2a , R 1b , R 2b , R 1c , R 2c , R 1d and R 2d are independently fluorine, a hydroxy group, a substituted or unsubstituted aromatic ring group, or a combination thereof, and m and n are integers of 0≦m≦200 and 0≦n≦200, provided that the sum of the m and n is at least 1; and a solvent. 2. The hardmask composition as claimed in claim 1 , wherein the A 1 , A 2 , B 1 and B 2 are independently a substituted or unsubstituted C6 to C50 arylene group. 3. The hardmask composition as claimed in claim 1 , wherein the A 1 , A 2 , B 1 and B 2 are independently one of the groups listed in the Group 1 and Group 2: wherein in the Group 1, R 3 and R 4 are independently hydrogen, a hydroxy group, a methoxy group, an ethoxy group, a halogen, a substituted or unsubstituted C3 to C30 cycloalkenyl group, a substituted or unsubstituted C1 to C20 alkylamine 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 C4 alkyl ether group, a substituted or unsubstituted C7 to C20 arylalkylene ether group, a substituted or unsubstituted C1 to C30 haloalkyl group, or a combination thereof, wherein in the Group 2, X 1 and X 2 are independently one of groups listed in the following Group 1, and R 5 and R 6 are independently hydrogen, a hydroxy group, a methoxy group, an ethoxy group, a halogen, a substituted or unsubstituted C3 to C30 cycloalkenyl group, a substituted or unsubstituted C1 to C20 alkylamine 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 C4 alkyl ether group, a substituted or unsubstituted C7 to C20 arylalkylene ether group, a substituted or unsubstituted C1 to C30 haloalkyl group, or a combination thereof. 4. The hardmask composition as claimed in claim 1 , wherein at least one of R 1a , R 2a , R 1b , R 2b , R 1c , R 2c , R 1d and R 2d is the substituted or unsubstituted aromatic ring group, the substituted or unsubstituted aromatic ring group being a substituted or unsubstituted naphthalene group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted pyrene group, a substituted or unsubstituted binaphthalene group, a substituted or unsubstituted anthracene group, a substituted or unsubstituted fluorene group, or a combination thereof. 5. The hardmask composition as claimed in claim 1 , wherein the polymer has a weight average molecular weight of about 1,000 to about 200,000. 6. The hardmask composition as claimed in claim 1 , wherein the polymer is included in an amount of about 0.1 wt % to about 30 wt % based on the total weight of the organic layer composition. 7. A method of forming patterns, the method comprising: providing a material layer on a substrate; applying the hardmask composition as claimed in claim 1 on the material layer; heat-treating the hardmask composition to form a hardmask layer; forming a silicon-containing thin layer on the hardmask layer; forming a photoresist layer on the silicon-containing thin layer; exposing and developing the photoresist layer to form a photoresist pattern; selectively removing the silicon-containing thin layer 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. 8. The method as claimed in claim 7 , wherein the hardmask composition is applied using a spin-on coating method. 9. The method as claimed in claim 7 , wherein the hardmask layer is formed by heat-treating at about 100° C. to about 500° C. 10. The method as claimed in claim 7 , further comprising forming a bottom antireflective coating (BARC) before forming the photoresist layer. 11. The method as claimed in claim 7 , wherein the silicon-containing thin layer includes silicon oxynitride (SiON).
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the material containing Si, O and at least one of H, N, C, F or other non-metal elements, e.g. SiOC, SiOC:H or SiONC · CPC title
Formation of intermediate materials · CPC title
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