IP Library Patent Application 11812702
Patent Application
App. No. 11/812,702

Chemically amplified resist material and pattern formation method using the same

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Quick Facts
Patent No.
US None
App. No.
11/812,702
Abstract

In the pattern formation method, a resist film is formed on a substrate by using a chemically amplified resist material including fumaric acid substituted by an acid labile group released by an acid; an alkali-soluble polymer soluble in an alkaline solution; and a photo-acid generator for generating an acid through irradiation with light. Subsequently, pattern exposure is carried out by selectively irradiating the resist film with exposing light, and a resist pattern is formed by developing the resist film after the pattern exposure.

Claims (60)

1 . A chemically amplified resist material comprising:

fumaric acid substituted by an acid labile group released by an acid;

an alkali-soluble polymer soluble in an alkaline solution; and

a photo-acid generator for generating an acid through irradiation with light.

2 . The chemically amplified resist material of claim 1 ,

wherein said acid labile group is a t-butyl group, a t-butyloxycarbonyl group, a methoxymethyl group, an adamantyloxymethyl group, an ethoxyethyl group or a 2-methyl-2-adamantyl group.

3 . The chemically amplified resist material of claim 1 ,

wherein said alkali-soluble polymer is polyacrylic acid, polymethacrylic acid, polynorbornene methyl carboxylic acid, polynorbornene carboxylic acid, polynorbornene methyl hexafluoroisopropyl alcohol, polynorbornene hexafluoroisopropyl alcohol or polyvinyl phenol.

4 . The chemically amplified resist material of claim 1 ,

wherein said photo-acid generator is triphenylsulfonium nonafluorobutane sulfonate, triphenylsulfonium trifluoromethane sulfonate or 1,3-diphenyl diazodisulfone.

5 . A chemically amplified resist material comprising:

fumaric acid substituted by a first acid labile group released by an acid;

a polymer in which an alkali-soluble polymer soluble in an alkaline solution is substituted by a second acid labile group; and

a photo-acid generator for generating an acid through irradiation with light.

6 . The chemically amplified resist material of claim 5 ,

wherein said first acid labile group is a t-butyl group, a t-butyloxycarbonyl group, a methoxymethyl group, an adamantyloxymethyl group, an ethoxyethyl group or a 2-methyl-2-adamantyl group.

7 . The chemically amplified resist material of claim 5 ,

wherein said second acid labile group is a t-butyl group, a t-butyloxycarbonyl group, a methoxymethyl group, an adamantyloxymethyl group, an ethoxyethyl group or a 2-methyl-2-adamantyl group.

8 . The chemically amplified resist material of claim 5 ,

wherein said alkali-soluble polymer is polyacrylic acid, polymethacrylic acid, polynorbornene methyl carboxylic acid, polynorbornene carboxylic acid, polynorbornene methyl hexafluoroisopropyl alcohol, polynorbornene hexafluoroisopropyl alcohol or polyvinyl phenol.

9 . The chemically amplified resist material of claim 5 ,

wherein said photo-acid generator is triphenylsulfonium nonafluorobutane sulfonate, triphenylsulfonium trifluoromethane sulfonate or 1,3-diphenyl diazodisulfone.

10 . A pattern formation method comprising the steps of:

forming, on a substrate, a resist film by using a chemically amplified resist material including fumaric acid substituted by a first acid labile group released by an acid, an alkali-soluble polymer soluble in an alkaline solution, and a photo-acid generator for generating an acid through irradiation with light;

performing pattern exposure by selectively irradiating said resist film with exposing light; and

forming a resist pattern by developing said resist film after the pattern exposure.

11 . The pattern formation method of claim 10 ,

wherein said alkali-soluble polymer is substituted by a second acid labile group released by an acid.

12 . The pattern formation method of claim 10 ,

wherein said first acid labile group is a t-butyl group, a t-butyloxycarbonyl group, a methoxymethyl group, an adamantyloxymethyl group, an ethoxyethyl group or a 2-methyl-2-adamantyl group.

13 . The pattern formation method of claim 10 ,

wherein said alkali-soluble polymer is polyacrylic acid, polymethacrylic acid, polynorbornene methyl carboxylic acid, polynorbornene carboxylic acid, polynorbornene methyl hexafluoroisopropyl alcohol, polynorbornene hexafluoroisopropyl alcohol or polyvinyl phenol.

14 . The pattern formation method of claim 10 ,

wherein said photo-acid generator is triphenylsulfonium nonafluorobutane sulfonate, triphenylsulfonium trifluoromethane sulfonate or 1,3-diphenyl diazodisulfone.

15 . The pattern formation method of claim 10 ,

wherein said exposing light is extreme ultraviolet (EUV) or electron beam (EB).

16 . The pattern formation method of claim 10 ,

wherein said exposing light is ArF excimer laser, KrF excimer laser, Xe 2 laser, F 2 laser, KrAr laser or Ar 2 laser.

17 . A pattern formation method comprising the steps of:

forming, on a substrate, a resist film by using a chemically amplified resist material including fumaric acid substituted by a first acid labile group released by an acid, an alkali-soluble polymer soluble in an alkaline solution, and a photo-acid generator for generating an acid through irradiation with light;

performing pattern exposure by selectively irradiating said resist film with exposing light with a liquid provided on said resist film; and

forming a resist pattern by developing said resist film after the pattern exposure.

18 . The pattern formation method of claim 17 ,

wherein said alkali-soluble polymer is substituted by a second acid labile group released by an acid.

19 . The pattern formation method of claim 18 ,

wherein said second acid labile group is a t-butyl group, a t-butyloxycarbonyl group, a methoxymethyl group, an adamantyloxymethyl group, an ethoxyethyl group or a 2-methyl-2-adamantyl group.

20 . The pattern formation method of claim 17 ,

wherein said first acid labile group is a t-butyl group, a t-butyloxycarbonyl group, a methoxymethyl group, an adamantyloxymethyl group, an ethoxyethyl group or a 2-methyl-2-adamantyl group.

21 . The pattern formation method of claim 17 ,

wherein said alkali-soluble polymer is polyacrylic acid, polymethacrylic acid, polynorbornene methyl carboxylic acid, polynorbornene carboxylic acid, polynorbornene methyl hexafluoroisopropyl alcohol, polynorbornene hexafluoroisopropyl alcohol or polyvinyl phenol.

22 . The pattern formation method of claim 17 ,

wherein said photo-acid generator is triphenylsulfonium nonafluorobutane sulfonate, triphenylsulfonium trifluoromethane sulfonate or 1,3-diphenyl diazodisulfone.

23 . The pattern formation method of claim 17 ,

wherein said liquid is water.

24 . The pattern formation method of claim 17 ,

wherein said liquid is an acidic solution.

25 . The pattern formation method of claim 24 ,

wherein said acidic solution is a cesium sulfate aqueous solution or a phosphoric acid aqueous solution.

26 . The pattern formation method of claim 17 ,

wherein said exposing light is ArF excimer laser, KrF excimer laser, Xe 2 laser, F 2 laser, KrAr laser or Ar 2 laser.

Assignments (2)
CHANGE OF NAME Recorded Nov 20, 2008
From: MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD.
To: PANASONIC CORPORATION
Reel/Frame 021897/0516 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 8, 2008
From: ENDO, MASAYUKI; SASAGO, MASARU
To: MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD.
Reel/Frame 020329/0972 →