Resist overlayer film forming composition and method for producing semiconductor device including the same

US9977331B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9977331-B2
Application numberUS-201515119209-A
CountryUS
Kind codeB2
Filing dateFeb 13, 2015
Priority dateFeb 26, 2014
Publication dateMay 22, 2018
Grant dateMay 22, 2018

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

A resist overlayer film forming composition for use in a lithography process in semiconductor device production does not intermix with a resist, blocks undesirable exposure light particularly in EUV exposure, for example, UV and DUV and selectively transmits EUV alone, and can be developed with a developer after exposure. A resist overlayer film forming composition includes: a polymer (P) including unit structures of Formula (1) and Formula (2) and having a weight average molecular weight, measured by gel permeation chromatography, of 500 to 2,000; and a C 8-16 ether compound as a solvent

First claim

Opening claim text (preview).

The invention claimed is: 1. A resist overlayer film forming composition comprising: a polymer (P) including unit structures of Formula (1) and Formula (2) and having a weight average molecular weight, measured by gel permeation chromatography, of 500 to 2,000; and a C 8-16 ether compound as a solvent: [in Formula (1) or Formula (2), R 1 and R 2 are the same or different and are each a hydrogen atom or a C 1-10 alkyl group; Q 1 and Q 2 are the same or different and are each a single bond, an ester bond (—C(═O)—O— or —O—C(═O)—), or an amide bond (—NH—CO— or —CO—NH—); X 2 is a single bond, a C 1-6 alkylene group, or a C 6-14 arylene group; R 1a is a C 1-10 alkyl group; n1 is an integer of 1 to 3; and m1 is an integer of 0 to 2]. 2. The composition according to claim 1 , wherein the polymer (P) further includes a unit structure of Formula (3): [in Formula (3), R 3 is a hydrogen atom or a C 1-10 alkyl group; Q 3 is a single bond, an ester bond (—C(═O)—O— or —O—C(═O)—), or an amide bond (—NH—CO— or —CO—NH—); X 3 is a single bond, a C 1-6 alkylene group, or a C 6-14 arylene group; and R 3a s are the same or different and are each a hydrogen atom, a C 1-10 alkyl group, or a C 1-4 acyl group]. 3. The composition according to claim 1 , wherein the polymer (P) further includes a unit structure of Formula (4): [in Formula (4), R 4 is a hydrogen atom or a C 1-10 alkyl group; Q 4 is a single bond, an ester bond (—C(═O)—O— or —O—C(═O)—), or an amide bond (—NH—CO— or —CO—NH—); and R 4a is (i) a C 1-10 alkyl group in which some or all of hydrogen atoms are optionally substituted with fluorine atoms, or (ii) a C 6-14 aryl group in which some or all of hydrogen atoms of the C 6-14 aryl group are optionally substituted with a C 1-10 alkyl group in which some or all of hydrogen atoms of the C 1-10 alkyl group are optionally substituted with fluorine atoms]. 4. The composition according to claim 2 , wherein the polymer (P) further includes a unit structure of Formula (4): [in Formula (4), R 4 is a hydrogen atom or a C 1-10 alkyl group; Q 4 is a single bond, an ester bond (—C(═O)—O— or —O—C(═O)—), or an amide bond (—NH—CO— or —CO—NH—); and R 4a is (i) a C 1-10 alkyl group in which some or all of hydrogen atoms are optionally substituted with fluorine atoms, or (ii) a C 6-14 aryl group in which some or all of hydrogen atoms of the C 6-14 aryl group are optionally substituted with a C 1-10 alkyl group in which some or all of hydrogen atoms of the C 1-10 alkyl group are optionally substituted with fluorine atoms]. 5. The composition according to claim 3 , wherein the R 4a is a monovalent group of Formula (5): [in Formula (5), W 1 and W 2 are the same or different and are each a hydrogen atom, a fluorine atom, a trifluoromethyl group, a difluoromethyl group, or a monofluoromethyl group; three w 3 s are each independently a hydrogen atom, a fluorine atom, or a combination of the hydrogen atom and the fluorine atom; at least one of W 1 , W 2 , and w 3 is a trifluoromethyl group, a difluoromethyl group, a monofluoromethyl group, or a fluorine atom; m2 is an integer of 0 to 9; and the maximum number of carbon atoms included in Formula (5) is 10]. 6. The composition according to claim 1 , wherein the ether compound is dibutyl ether, diisoamyl ether, diisobutyl ether, or a combination of dibutyl ether, diisoamyl ether, and diisobutyl ether. 7. The composition according to claim 1 , wherein the ether compound has a proportion, in the solvent, of not less than 87% by mass and not more than 100% by mass. 8. The composition according to claim 1 , further comprising a separate acid compound or a separate acid generator compound, to adjust an acidity of the composition. 9. The composition according to claim 8 , wherein the acid compound is a sulfonic acid compound or a sulfonic acid ester compound. 10. The composition according to claim 8 , wherein the acid compound is an onium salt acid generator, a halogen-containing compound acid generator, or a sulfonic acid acid generator. 11. The composition according to claim 1 , further comprising a basic compound. 12. A method for producing a semiconductor device, the method comprising: forming a resist film on a substrate; applying the resist overlayer film forming composition as claimed in claim 1 on the resist film and baking the composition to form a resist overlayer film; exposing the semiconductor substrate covered with the resist overlayer film and the resist film to an exposure light; and developing a pattern on the substrate after exposure by removing the resist overlayer film and the resist film. 13. The method according to claim 12 , wherein the exposure is performed with EUV light (wavelength of 13.5 nm). 14. A method for forming a resist pattern for use in production of a semiconductor device, the method comprising applying the resist overlayer film forming composition as claimed in claim 1 on a resist film formed on a semiconductor substrate and baking the composition to form a resist overlayer film. 15. A method for producing the resist overlayer film forming composition as claimed in claim 1 , the method comprising mixing the polymer (P) and a C 8-16 ether compound as a solvent.

Assignees

Inventors

Classifications

  • of masks comprising organic materials · CPC title

  • Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof · CPC title

  • Liquid compositions therefor, e.g. developers · CPC title

  • G03F7/11Primary

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

  • Monomers containing a branched unsaturated aliphatic radical or a ring substituted by an alkyl radical · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9977331B2 cover?
A resist overlayer film forming composition for use in a lithography process in semiconductor device production does not intermix with a resist, blocks undesirable exposure light particularly in EUV exposure, for example, UV and DUV and selectively transmits EUV alone, and can be developed with a developer after exposure. A resist overlayer film forming composition includes: a polymer (P) inclu…
Who is the assignee on this patent?
Nissan Chemical Ind Ltd
What technology area does this patent fall under?
Primary CPC classification G03F7/11. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue May 22 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).