Resist composition and method of forming resist pattern
US-2019384174-A1 · Dec 19, 2019 · US
US12275693B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12275693-B2 |
| Application number | US-202016858160-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 24, 2020 |
| Priority date | May 24, 2019 |
| Publication date | Apr 15, 2025 |
| Grant date | Apr 15, 2025 |
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An onium salt of formula (1) and a chemically amplified resist composition comprising the same as a PAG are provided. When processed by lithography, the resist composition exhibits a high sensitivity, minimal LWR and improved CDU independent of whether it is of positive or negative tone.
Opening claim text (preview).
The invention claimed is: 1. An onium salt having the formula (1): wherein R 1 is a C 1 -C 20 di- to tetravalent hydrocarbon group, R 2 is a single bond or a C 1 -C 20 divalent hydrocarbon group, R 3 is fluorine, a C 1 -C 10 alkoxy group, nitro group, or C 1 -C 10 monovalent hydrocarbon group, R f1 and R f2 each are fluorine, R f3 is trifluoromethyl, and R f4 is hydrogen, L1 is —CO—O—, m is 1, n is 1, k is 1, 2 or 3, p is an integer of 1 to 3, q is an integer of 0 to 3, r is 0 or 1, M + is a sulfonium cation having the formula (1A) or iodonium cation having the formula (1B): wherein R 11 to R 15 are each independently a C 1 -C 20 monovalent hydrocarbon group which may contain a heteroatom, any two of R 11 , R 12 and R 13 may bond together to form a ring with the sulfur atom to which they are attached, and wherein the sulfonate anion in the onium salt is selected from the group consisting of the following formulae: wherein A 1 is trifluoromethyl, and Me is methyl. 2. A photoacid generator comprising the onium salt of claim 1 . 3. A chemically amplified resist composition comprising the photoacid generator of claim 2 . 4. The resist composition of claim 3 , further comprising a base polymer comprising recurring units adapted for polarity switch under the action of acid, of at least one type selected from recurring units having the formulae (A1) and (A2), and recurring units of at least one type selected from recurring units having the formulae (B) to (E): wherein R A is hydrogen, fluorine, methyl or trifluoromethyl, R 21 is each independently hydrogen or a C 1 -C 6 alkyl group which may contain an ether bond or carbonyl moiety, L 11 is a single bond, carbonyloxy or amide group, L 12 is a single bond or a C 1 -C 7 alkanediyl group which may contain an ether bond or carbonyl moiety, a is an integer satisfying a≤5+2c−b, b is an integer of 1 to 5, c is an integer of 0 to 2, X A is an acid labile group, Y 1 to Y 4 are each independently a single bond, methylene, ethylene, phenylene, fluorinated phenylene, naphthylene, —O—Y 5 —, —C(═O)—O—Y 5 — or —C(—O)—NH—Y 5 —, Y 5 is a C 1 -C 6 alkanediyl, C 2 -C 6 alkenediyl, phenylene, or naphthylene group, which may contain a carbonyl moiety, ester bond, ether bond or hydroxyl moiety, Z 1 is a C 1 -C 20 fluoroalcohol-containing substituent group, Z 2 is a C 1 -C 20 phenolic hydroxyl-containing substituent group, Z 3 is a C 1 -C 20 carboxy-containing substituent group, and Z 4 is a substituent group containing a lactone skeleton, sultone skeleton, carbonate skeleton, cyclic ether skeleton, acid anhydride skeleton, alcoholic hydroxyl moiety, alkoxycarbonyl moiety, sulfonamide moiety or carbamoyl moiety. 5. The resist composition of claim 4 wherein the base polymer further comprises recurring units of at least one type selected from recurring units having the formulae (F1) to (F4): wherein R A is hydrogen, fluorine, methyl or trifluoromethyl, L 21 is a single bond, phenylene, —O—L 21A —, —C(═O)—O—L 21A —, or —C(═O)—NH—L 21A —, L 21A is a C 1 -C 20 alkanediyl, C 2 -C 20 alkenediyl or phenylene group, which may contain a heteroatom, L 22 and L 23 are each independently a single bond or a C 1 -C 20 divalent hydrocarbon group which may contain a heteroatom, L 24 is a single bond, methylene, ethylene, phenylene, fluorinated phenylene, —O—L 24A —, —C(═O)—O—L 24A — or —C(═O)—NH—L 24A —, L 24A is an optionally substituted phenylene group, R 31 to R 41 are each independently a C 1 -C 20 monovalent hydrocarbon group which may contain a heteroatom, any two of L 21 , R 31 and R 32 may bond together to form a ring with the sulfur atom to which they are attached, any two of R 33 , R 34 and R 35 , any two of R 36 , R 37 and R 38 , or any two of R 39 , R 40 and R 41 may bond together to form a ring with the sulfur atom to which they are attached, X C − is a non-nucleophilic counter ion, A 1 is hydrogen or trifluoromethyl, n 1 is 0 or 1, n 1 is 0 when L 22 is a single bond, n 2 is 0 or 1, n 2 is 0 when L 23 is a single bond. 6. A process for forming a pattern comprising the steps of applying the resist composition of claim 5 onto a substrate to form a resist film thereon, exposing a selected region of the resist film to high-energy radiation, and developing the exposed resist film in a developer. 7. The pattern forming process of claim 6 wherein the developing step uses an alkaline aqueous solution as the developer, thereby forming a positive pattern in which an exposed region of the resist film is dissolved away and an unexposed region of the resist film is not dissolved. 8. The pattern forming process of claim 6 wherein the developing step uses an organic solvent as the developer, thereby forming a negative pattern in which an unexposed region of the resist film is dissolved away and an exposed region of the resist film is not dissolved.
the macromolecular compound being present in a chemically amplified negative photoresist composition · CPC title
with organic non-macromolecular light-sensitive compounds not otherwise provided for, e.g. dissolution inhibitors · CPC title
the macromolecular compound being present in a chemically amplified positive photoresist composition · CPC title
Aqueous alkaline compositions · CPC title
Inorganic compounds; Onium compounds; Organic compounds having hetero atoms other than oxygen, nitrogen or sulfur · CPC title
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