Patent Application
20240111212
This non-provisional application claims priority under 35 U.S.C. § 119(a) on Patent Application No. 2022-139749 filed in Japan on Sep. 2, 2022, the entire contents of which are hereby incorporated by reference.
This invention relates to a resist composition and a pattern forming process.
To meet the demand for higher integration density and operating speed of LSIs, the effort to reduce the pattern rule is in rapid progress. As the use of 5G high-speed communications and artificial intelligence (AI) is widely spreading, high-performance devices are needed for their processing. As the advanced miniaturization technology, manufacturing of microelectronic devices at the 5-nm node by the lithography using EUV of wavelength 13.5 nm is implemented in a mass scale, and manufacturing of 3-nm node devices is started in a mass scale. Studies are made on the application of EUV lithography to 2-nm node devices of the next generation. For the fabrication of 1.4-nm node devices of the next-but-one generation, it is expected to apply the EUV lithography using a lens having a high NA for improving resolution.
As the pattern feature size is reduced, the edge roughness (LWR) of line patterns and the critical dimension uniformity (CDU) of hole or dot patterns are regarded significant. It is pointed out that these factors are affected by the segregation or agglomeration of a base polymer and acid generator and the diffusion of generated acid. There is a tendency that values of LWR and CDU increase as the resist film becomes thinner. A film thickness reduction to comply with the progress of size reduction causes a degradation of LWR or CDU, which poses a serious problem.
The EUV resist material must meet high sensitivity, high resolution and low LWR at the same time. As the acid diffusion distance is reduced, LWR or CDU is improved, but sensitivity becomes lower. For example, as the PEB temperature is lowered, the outcome is an improved LWR or CDU, but a lower sensitivity. As the amount of quencher added is increased, the outcome is an improved LWR or CDU, but a lower sensitivity. It is necessary to overcome the tradeoff relation between sensitivity and LWR.
For the purpose of suppressing acid diffusion, Patent Documents 1 and 2 propose resist compositions comprising an acid generator capable of generating a sulfonic acid bound to a polymer backbone upon light exposure. The polymer-bound acid generator is characterized by extremely short acid diffusion, which leads to an improvement in LWR.
Patent Documents 3 and 4 disclose resist compositions comprising a polymer-bound acid generator having a sulfonium cation bound to a polymer backbone. Since this polymer-bound acid generator generates a sulfonic acid which is not bound to the backbone, it entails a shortcoming of noticeable acid diffusion.
Patent Document 5 describes a resist composition comprising an onium salt having iodine in its anion. Since the iodine atom is strongly absorptive to EUV radiation, the efficiency of acid generation and contrast are improved. With the improvements in acid generation efficiency and contrast, a resist pattern having a high sensitivity, high resolution and minimized dimensional variation can be formed. This is followed by a series of iodine-containing acid generators as disclosed in Patent Documents 6 to 11. Furthermore, Patent Document 12 describes a resist composition comprising an acid generator having an iodine-containing anion and a sulfonium cation bound to a polymer backbone.
It is desired to develop a resist composition exhibiting a higher sensitivity than prior art resist compositions and capable of reducing the LWR of line patterns or improving the CDU of hole patterns.
An object of the invention is to provide a resist composition which achieves a high sensitivity, minimal LWR and improved CDU independent of whether it is of positive or negative tone, and a pattern forming process using the resist composition.
The inventors have found that a resist composition having a high sensitivity, improved LWR or CDU, high contrast, high resolution and wide process margin is obtained from a polymer comprising photo-decomposable repeat units derived from a sulfonium salt containing a polymerizable unsaturated bond and a sulfonium cation site and having a urethane, thiourethane or urea bond in a linker between the polymerizable unsaturated bond and the sulfonium cation site.
In one aspect, the invention provides a resist composition comprising a polymer comprising repeat units having the formula (a).
Herein RA is hydrogen or methyl,
In a preferred embodiment, M− is a strong acid anion selected from fluorosulfonic acid, fluoroimide acid and fluoromethide acid anions.
More preferably, the fluorosulfonic acid anion has the formula (a1-1), the fluoroimide acid anion has the formula (a1-2), and the fluoromethide acid anion has the formula (a1-3).
Herein Rfa is a C1-C40 hydrocarbyl group which may contain at least one moiety selected from ether bond, ester bond, sulfide bond, amide bond, urethane bond, carbonate bond, carbonyl, lactone ring, sultone ring, sulfonyl, sulfonic ester bond, cyano, nitro and halogen,
Preferably, Rfa is a C1-C40 hydrocarbyl group containing iodine.
In another preferred embodiment, M− is a weak acid anion selected from carboxylate, sulfonamide, fluorine-free methide acid, phenoxide, halide, nitrate and carbonate anions.
More preferably, the carboxylate anion has the formula (a2-1), the sulfonamide anion has the formula (a2-2), the fluorine-free methide acid anion has the formula (a2-3), and the phenoxide anion has the formula (a2-4).
Herein Rq1 is hydrogen, fluorine, or a C1-C24 hydrocarbyl group which may contain a heteroatom,
In a preferred embodiment, the polymer further comprises repeat units having the formula (b1) or (b2).
Herein RA is each independently hydrogen or methyl,
In one embodiment, the resist composition is a chemically amplified positive resist composition.
In another embodiment, the polymer is free of an acid labile group. The resist composition is a chemically amplified negative resist composition.
The resist composition may further comprise a quencher, an acid generator, an organic solvent, and/or a surfactant.
In another aspect, the invention provides a pattern forming process comprising the steps of applying the resist composition defined herein onto a substrate to form a resist film thereon, exposing the resist film to high-energy radiation, and developing the exposed resist film in a developer.
Typically, the high-energy radiation is ArF excimer laser of wavelength 193 nm, KrF excimer laser of wavelength 248 nm, EB, or EUV of wavelength 3 to 15 nm.
A resist film containing a polymer comprising photo-decomposable repeat units derived from a sulfonium salt containing a polymerizable unsaturated bond and a sulfonium cation site and having a urethane, thiourethane or urea bond in a linker between the polymerizable unsaturated bond and the sulfonium cation site is characterized in that the polymer has a higher glass transition temperature (Tg) due to the hydrogen bond in the urethane, thiourethane or urea bond and thus serves to control acid diffusion. This prevents a lowering of resolution due to blur by acid diffusion for thereby improving LWR or CDU. In the other embodiment wherein the anion moiety contains halogen, the resist composition has a higher acid generation efficiency and higher contrast due to more absorption of EUV radiation. A resist composition having a high sensitivity and improved LWR or CDU is thus constructed.
As used herein, the singular forms “a,” “an” and “the” include plural referents unless the context clearly dictates otherwise. The notation (Cn-Cm) means a group containing from n to m carbon atoms per group. As used herein, the terms “group” and “moiety” are interchangeable. In chemical formulae, Me stands for methyl, Ac for acetyl, and the broken line designates a valence bond.
The abbreviations and acronyms have the following meaning.
One embodiment of the invention is a resist composition comprising a polymer comprising photo-decomposable repeat units. Specifically, the resist composition contains a polymer comprising photo-decomposable repeat units derived from a sulfonium salt containing a polymerizable unsaturated bond and a sulfonium cation site and having a urethane, thiourethane or urea bond in a linker between the polymerizable unsaturated bond and the sulfonium cation site.
The photo-decomposable repeat unit is capable of generating an acid upon exposure to high-energy radiation. In the embodiment wherein the generated acid is a strong acid such as fluorosulfonic acid, fluoroimide acid or fluoromethide acid, the photo-decomposable repeat unit becomes an acid generator for inducing deprotection reaction for polarity switch. In the other embodiment wherein the generated acid is a weak acid such as carboxylic acid, sulfonamide, fluorine-free methide acid, phenol, halogen or carbonic acid, the sulfonium salt prior to decomposition functions as a quencher through an ion exchange with the strong acid.
Since the polymer comprising photo-decomposable repeat units has a cation moiety bound to the polymer backbone and a urethane, thiourethane or urea bond introduced therein, the hydrogen bonds in these groups serve to reduce acid diffusion. When the anion moiety has a halogen atom, the absorption of EUV radiation is increased, resulting in a high efficiency of acid generation. Since the acid generator is admixed at the monomer stage prior to polymerization, the acid generator is uniformed distributed in the polymer. This leads to improvements in LWR and CDU.
The acid generator comprising photo-decomposable repeat units exerts a LWR or CDU-improving effect, which may stand good either in positive and negative tone pattern formation by aqueous alkaline development or in negative tone pattern formation by organic solvent development.
The polymer comprising photo-decomposable repeat units used herein, designated Polymer A, hereinafter, is defined as comprising photo-decomposable repeat units derived from a sulfonium salt containing a polymerizable unsaturated bond and a sulfonium cation site and having a urethane, thiourethane or urea bond in a linker between the polymerizable unsaturated bond and the sulfonium cation site. The photo-decomposable repeat units are repeat units having the formula (a), also referred to as repeat units (a), hereinafter.
In formula (a), RA is hydrogen or methyl.
In formula (a), X1 is a C1-C10 hydrocarbylene group which may contain at least one moiety selected from ether bond, ester bond, carbonate bond, lactone ring, sultone ring, and halogen.
The C1-C10 hydrocarbylene group represented by X1 may be saturated or unsaturated and straight, branched or cyclic. Examples thereof include C1-C10 alkanediyl groups such as methanediyl, ethane-1,1-diyl, ethane-1,2-diyl, propane-1,3-diyl, butane-1,4-diyl, pentane-1,5-diyl, hexane-1,6-diyl, heptane-1,7-diyl, octane-1,8-diyl, nonane-1,9-diyl, decane-1,10-diyl; C3-C10 cyclic saturated hydrocarbylene groups such as cyclopentanediyl, methylcyclopentanediyl, dimethylcyclopentanediyl, trimethylcyclopentanediyl, tetramethylcyclopentanediyl, cyclohexanediyl, methylcyclohexanediyl, dimethylcyclohexanediyl, trimethylcyclohexanediyl, tetramethylcyclohexanediyl, norbomanediyl and adamantanediyl; C6-C10 arylene groups such as phenylene, methylphenylene, ethylphenylene, n-propylphenylene, isopropylphenylene, n-butylphenylene, isobutylphenylene, sec-butylphenylene, tert-butylphenylene, and naphthylene, and combinations thereof.
In formula (a), X2 is —O—, —S— or —N(H)—.
In formula (a), X3 is a C1-C14 hydrocarbylene group. The hydrocarbylene group may contain at least one moiety selected from ether bond, ester bond, sulfide bond, amide bond, and carbonate bond, and may be substituted with at least one moiety selected from halogen, cyano and nitro.
The C1-C14 hydrocarbylene group represented by X3 may be saturated or unsaturated and straight, branched or cyclic. Examples thereof include C1-C14 alkanediyl groups such as methanediyl, ethane-1,1-diyl, ethane-1,2-diyl, propane-1,3-diyl, butane-1,4-diyl, pentane-1,5-diyl, hexane-1,6-diyl, heptane-1,7-diyl, octane-1,8-diyl, nonane-1,9-diyl, decane-1,10-diyl, undecane-1,11-diyl, dodecane-1,12-diyl, tridecane-1,13-diyl, tetradecane-1,14-diyl; C3-C14 cyclic saturated hydrocarbylene groups such as cyclopentanediyl, methylcyclopentanediyl, dimethylcyclopentanediyl, trimethylcyclopentanediyl, tetramethylcyclopentanediyl, cyclohexanediyl, methylcyclohexanediyl, dimethylcyclohexanediyl, trimethylcyclohexanediyl, tetramethylcyclohexanediyl, norbomanediyl and adamantanediyl; C6-C14 arylene groups such as phenylene, methylphenylene, ethylphenylene, n-propylphenylene, isopropylphenylene, n-butylphenylene, isobutylphenylene, sec-butylphenylene, tert-butylphenylene, naphthylene, methylnaphthylene, ethylnaphthylene, n-propylnaphthylene, isopropylnaphthylene, n-butylnaphthylene, sec-butylnaphthylene, tert-butylnaphthylene, biphenyldiyl, methylbiphenyldiyl, and dimethylbiphenyldiyl; and combinations thereof.
In formula (a), R1 is hydrogen or methyl.
In formula (a), R2 and R3 are each independently halogen or a C1-C20 hydrocarbyl group which may contain a heteroatom. Also, R2 and R3, or R2 and X3 may bond together to form a ring with the sulfur atom to which they are attached.
Suitable halogen atoms represented by R2 and R3 include fluorine, chlorine, bromine and iodine.
The hydrocarbyl group represented by R2 and R3 may be saturated or unsaturated and straight, branched or cyclic. Examples thereof include C1-C20 alkyl groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, n-hexyl, n-octyl, n-nonyl, n-decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, heptadecyl, octadecyl, nonadecyl and icosyl; C3-C20 cyclic saturated hydrocarbyl groups such as cyclopropyl, cyclopentyl, cyclohexyl, cyclopropylmethyl, 4-methylcyclohexyl, cyclohexylmethyl, norbornyl, and adamantyl; C2-C20 alkenyl groups such as vinyl, propenyl, butenyl, and hexenyl; C3-C20 cyclic unsaturated aliphatic hydrocarbyl groups such as cyclohexenyl and norbornenyl; C2-C20 alkynyl groups such as ethynyl, propynyl and butynyl; C6-C20 aryl groups such as phenyl, methylphenyl, ethylphenyl, n-propylphenyl, isopropylphenyl, n-butylphenyl, isobutylphenyl, sec-butylphenyl, tert-butylphenyl, naphthyl, methylnaphthyl, ethylnaphthyl, n-propylnaphthyl, isopropylnaphthyl, n-butylnaphthyl, isobutylnaphthyl, sec-butylnaphthyl, and tert-butylnaphthyl; C7-C20 aralkyl groups such as benzyl and phenethyl; and combinations thereof. In the hydrocarbyl groups, some or all of the hydrogen atoms may be substituted by a moiety containing a heteroatom such as oxygen, sulfur, nitrogen or halogen, or some constituent —CH2— may be replaced by a moiety containing a heteroatom such as oxygen, sulfur or nitrogen, so that the group may contain a hydroxy moiety, fluorine, chlorine, bromine, iodine, cyano moiety, nitro moiety, carbonyl moiety, ether bond, ester bond, sulfonic ester bond, carbonate bond, lactone ring, sultone ring, carboxylic anhydride (—C(═O)—O—C(═O)—) or haloalkyl moiety.
Also, R2 and R3, or R2 and X3 may bond together to form a ring with the sulfur atom to which they are attached. Preferred examples of the ring are shown by the following structures.
Herein the broken line designates a point of attachment to X3 or R3.
Examples of the cation in the monomer from which repeat units (a) are derived are shown below, but not limited thereto. Herein, RA is as defined above.
In formula (a), M− is a non-nucleophilic counter ion. In one embodiment, the non-nucleophilic counter ion used herein is a strong acid anion selected from fluorosulfonic acid, fluoroimide acid and fluoromethide acid anions. In this embodiment, Polymer A functions as a photoacid generator, that is, polymer-bound photoacid generator.
Preferably, the fluorosulfonic acid anion has the formula (a1-1), the fluoroimide acid anion has the formula (a1-2), and the fluoromethide acid anion has the formula (a1-3).
In formula (a1-1), Rfa is a C1-C40 hydrocarbyl group which may contain at least one moiety selected from ether bond, ester bond, sulfide bond, amide bond, urethane bond, carbonate bond, carbonyl, lactone ring, sultone ring, sulfonyl, sulfonic ester bond, cyano, nitro and halogen.
In formula (a1-1), Rf1 to Rf4 are each independently hydrogen, fluorine or trifluoromethyl, at least one of Rf1 to Rf4 being fluorine or trifluoromethyl. Also, Rf1 and Rf2, taken together, may form a carbonyl group.
In formula (a1-2), Rfb1 and Rfb4 are each independently fluorine or a C1-C40 hydrocarbyl group which may contain a heteroatom. Rfb1 and Rfb2 may bond together to form a ring with the linkage: —CF2—SO2—N−—SO2—CF2— to which they are attached.
In formula (a1-3), Rfc1, Rfc2 and Rfc3 are each independently fluorine or a C1-C40 hydrocarbyl group which may contain a heteroatom. Rfc1 and Rfc2 may bond together to form a ring with the linkage: —CF2—SO2—C−—SO2—CF2— to which they are attached.
More preferably, the fluorosulfonic acid anion has the formula (a1-1-1) or (a1-1-2).
In formula (a1-1-1), RHF is hydrogen or trifluoromethyl, preferably trifluoromethyl.
In formulae (a1-1-1) and (a1-1-2), Rfa1 and Rfa2 are each independently a C1-C38 hydrocarbyl group which may contain a heteroatom. Suitable heteroatoms include oxygen, nitrogen, sulfur and halogen, with oxygen being preferred. Of the hydrocarbyl groups, those of 6 to 30 carbon atoms are preferred because a high resolution is available in fine pattern formation.
The hydrocarbyl group represented by Rfa1 and Rfa2 may be saturated or unsaturated and straight, branched or cyclic. Suitable hydrocarbyl groups include C1-C38 alkyl groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, pentyl, neopentyl, hexyl, heptyl, 2-ethylhexyl, nonyl, undecyl, tridecyl, pentadecyl, heptadecyl, icosyl; C3-C38 cyclic saturated hydrocarbyl groups such as cyclopentyl, cyclohexyl, 1-adamantyl, 2-adamantyl, 1-adamantylmethyl, norbornyl, norbornylmethyl, tricyclodecanyl, tetracyclododecanyl, tetracyclododecanylmethyl, dicyclohexylmethyl; C2-C38 unsaturated hydrocarbyl groups such as allyl and 3-cyclohexenyl: C6-C38 aryl groups such as phenyl, 1-naphthyl, 2-naphthyl; and C7-C38 aralkyl groups such as benzyl and diphenylmethyl.
In the hydrocarbyl group, some or all of the hydrogen atoms may be substituted by a moiety containing a heteroatom such as oxygen, sulfur, nitrogen or halogen, or some constituent —CH2— may be replaced by a moiety containing a heteroatom such as oxygen, sulfur or nitrogen, so that the group may contain a hydroxy, fluorine, chlorine, bromine, iodine, cyano, carbonyl, ether bond, ester bond, sulfonic ester bond, carbonate bond, lactone ring, sultone ring, carboxylic anhydride (—C(═O)—O—C(═O)—) or haloalkyl moiety. Examples of the heteroatom-containing hydrocarbyl group include tetrahydrofuryl, methoxymethyl, ethoxymethyl, methylthiomethyl, acetamidomethyl, trifluoroethyl, (2-methoxyethoxy)methyl, acetoxymethyl, 2-carboxy-1-cyclohexyl, 2-oxopropyl, 4-oxo-1-adamantyl, and 3-oxocyclohexyl.
With respect to the synthesis of the sulfonium salt having an anion of formula (a1-1-1), reference is made to JP-A 2007-145797, JP-A 2008-106045, JP-A 2009-007327, and JP-A 2009-258695. Also useful are the sulfonium salts described in JP-A 2010-215608, JP-A 2012-041320, JP-A 2012-106986, and JP-A 2012-153644.
Examples of the anion having formula (a1-1-1) are shown below, but not limited thereto.
With respect to the synthesis of a sulfonium salt containing the anion of formula (a1-1-2), reference is made to JP-A 2010-215608 and JP-A 2014-133723.
Examples of the anion having formula (a1-1-2) are shown below, but not limited thereto.
Of the fluorosulfonic acid anions having formula (a1-1), those wherein Rfa is a C1-C40 hydrocarbyl group containing iodine are preferred. Typical of the fluorosulfonic acid anion are fluorosulfonic acid anions containing an iodized aromatic ring, represented by the formula (a1-1-3).
In formula (a1-1-3), Rf1 to Rf4 are as defined above, p is an integer from 1 to 3, q is an integer from 1 to 5, r is an integer from 0 to 3, and q+r is from 1 to 5. Preferably q is an integer from 1 to 3, more preferably 2 or 3, and r is an integer from 0 to 2.
In formula (a1-1-3), L1 is a single bond, ether bond, ester bond, or a C1-C6 saturated hydrocarbylene group which may contain an ether bond or ester bond. The saturated hydrocarbylene group may be straight, branched or cyclic.
In formula (a1-1-3), in case of p=1, L2 is a single bond or C1-C20 divalent linking group. In case of p=2 or 3, L2 is a C1-C20 (p+1)-valent linking group which may contain an oxygen, sulfur or nitrogen atom.
In formula (a1-1-3), Rfa3 is a hydroxy, carboxy, fluorine, chlorine, bromine, amino, or a C1-C20 hydrocarbyl, C1-C20 hydrocarbyloxy, C2-C20 hydrocarbylcarbonyl, C2-C20 hydrocarbyloxycarbonyl, C2-C20 hydrocarbylcarbonyloxy or C1-C20 hydrocarbylsulfonyloxy group, which may contain fluorine, chlorine, bromine, hydroxy, amino or ether bond, or —N(Rfa3A)(Rfa3B), —N(Rfa3C(═O)—Rfa3D or —N(Rfa3C)—C(═O)—O—Rfa3D. Rfa3A and Rfa3B are each independently hydrogen or a C1-C6 saturated hydrocarbyl group. Rfa3C is hydrogen or a C1-C6 saturated hydrocarbyl group which may contain halogen, hydroxy, C1-C6 saturated hydrocarbyloxy, C2-C6 saturated hydrocarbylcarbonyl or C2-C6 saturated hydrocarbylcarbonyloxy moiety. Rfa3D is a C1-C16 aliphatic hydrocarbyl, C6-C12 aryl or C7-C15 aralkyl group, which may contain halogen, hydroxy, C1-C6 saturated hydrocarbyloxy, C2-C6 saturated hydrocarbylcarbonyl or C2-C6 saturated hydrocarbylcarbonyloxy moiety. The aliphatic hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. The hydrocarbyl, hydrocarbyloxy, hydrocarbylcarbonyl, hydrocarbyloxycarbonyl, hydrocarbylcarbonyloxy, and hydrocarbylsulfonyloxy groups may be straight, branched or cyclic. A plurality of Rfa3 may be the same or different when p and/or r is 2 or more. Of these, Rfa3 is preferably hydroxy, —N(Rfa3A)—C(═O)—Rfa3B, —N(Rfa3A)—C(═O)—O—Rfa3B, fluorine, chlorine, bromine, methyl or methoxy.
In the fluorosulfonate anion having formula (a1-1-3), the total number of carbon atoms included in the structure excluding —C(Rf1)(Rf2)—C(Rf3)(Rf4)—SO3
Examples of the anion having formula (a1-1-3) in the onium salt are shown below, but not limited thereto.
Also, the fluorosulfonate anion may be selected from the anions described in the following patent documents. JP-A 2011-085811, JP-A 2020-059708, JP-A 2021-020898, JP-A 2021-035935, JP-A 2021-070696, JP-A 2021-070695, JP-A 2021-070694, JP-A 2021-070693, JP-A 2021-070697, JP-A 2021-070698, JP-A 2021-075521, JP-A 2021-075522, JP-A 2021-075523, JP-A 2021-075524, JP-A 2021-070692, JP-A 2021-088549, JP-A 2021-107379, JP-A 2021-138684, JP-A 2021-147388, JP-A 2021-147389, JP-A 2021-147390, JP-A 2021-155427, JP-A 2021-155428, JP-A 2021-175724, JP-A 2021-169463, JP-A 2021-169471, JP-A 2021-071720, JP-A 2022-011870, JP-A 2016-047815, JP-A 2012-003249, JP-A 2022-001567, JP-A 2022-001568, JP-A 2022-008150, JP-A 2022-008151, JP-A 2022-028612, JP-A 2022-073968, JP-A 2019-026572, JP-A 2021-081708, JP-A 2020-181064, JP-A 2021-187843, JP-A 2021-187844, JP-A 2022-050325, JP-A 2022-077982, and JP-A 2022-075556.
Also, the non-nucleophilic counter ion M− may be a weak acid anion selected from carboxylate, sulfonamide, fluorine-free methide acid, phenoxide, halide, nitrate and carbonate anions. In this embodiment, Polymer A functions as a quencher, i.e., polymer-bound quencher.
Preferably, the carboxylate anion has the formula (a2-1), the sulfonamide anion has the formula (a2-2), the fluorine-free methide acid anion has the formula (a2-3), and the phenoxide anion has the formula (a2-4).
In formula (a2-1), Rq1 is hydrogen, fluorine, or a C1-C24 hydrocarbyl group which may contain a heteroatom. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. Examples thereof are as exemplified above for the hydrocarbyl groups Rfa1 and Rfa2 in formulae (a1-1-1) and (a1-1-2). In the hydrocarbyl group, some or all of the hydrogen atoms may be substituted by a moiety containing a heteroatom such as oxygen, sulfur, nitrogen or halogen, or some constituent —CH2— may be replaced by a moiety containing a heteroatom such as oxygen, sulfur or nitrogen, so that the group may contain a hydroxy moiety, fluorine, chlorine, bromine, iodine, cyano moiety, nitro moiety, mercapto moiety, carbonyl moiety, ether bond, ester bond, sulfonic ester bond, carbonate bond, lactone ring, sultone ring, carboxylic anhydride (—C(═O)—O—C(═O)—) or haloalkyl moiety.
In formula (a2-2), Rq2 is a C1-C20 hydrocarbyl group which may contain a heteroatom. Rq3 is hydrogen or a C1-C24 hydrocarbyl group which may contain a heteroatom. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. Examples thereof are as exemplified above for the hydrocarbyl groups Rfa1 and Rfa2 in formulae (a1-1-1) and (a1-1-2). In the hydrocarbyl group, some or all of the hydrogen atoms may be substituted by a moiety containing a heteroatom such as oxygen, sulfur, nitrogen or halogen, or some constituent —CH2— may be replaced by a moiety containing a heteroatom such as oxygen, sulfur or nitrogen, so that the group may contain a hydroxy moiety, fluorine, chlorine, bromine, iodine, cyano moiety, nitro moiety, mercapto moiety, carbonyl moiety, ether bond, ester bond, sulfonic ester bond, carbonate bond, lactone ring, sultone ring, carboxylic anhydride (—C(═O)—O—C(═O)—) or haloalkyl moiety.
In formula (a2-3), Rq4 to Rq6 are each independently a C1-C10 hydrocarbyl group which may contain a heteroatom. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. Examples thereof are as exemplified above for the hydrocarbyl groups Rfa1 and Rfa2 in formulae (a1-1-1) and (a1-1-2), but of 1 to 10 carbon atoms. In the hydrocarbyl group, some or all of the hydrogen atoms may be substituted by a moiety containing a heteroatom such as oxygen, sulfur, nitrogen or halogen, or some constituent —CH2— may be replaced by a moiety containing a heteroatom such as oxygen, sulfur or nitrogen, so that the group may contain a hydroxy moiety, fluorine, chlorine, bromine, iodine, cyano moiety, nitro moiety, mercapto moiety, carbonyl moiety, ether bond, ester bond, sulfonic ester bond, carbonate bond, lactone ring, sultone ring, carboxylic anhydride (—C(═O)—O—C(═O)—) or haloalkyl moiety.
In formula (a2-4), Rq7 is halogen, hydroxy, cyano, nitro, amino, a C2-C11 alkylcarbonylamino, C1-C10 alkylsulfonylamino, C1-C10 alkylsulfonyloxy, C1-C10 alkyl, phenyl, C1-C10 alkoxy, C1-C10 alkylthio, C2-C11 alkoxycarbonyl, C1-C10 acyl or C1-C10 acyloxy group, in which some or all of the carbon-bonded hydrogen atoms may be substituted by fluorine, and k is an integer of 0 to 5. A plurality of Rq7 may be the same or different when k is 2 or more.
Examples of the carboxylate anion are shown below, but not limited thereto.
Examples of the sulfonamide anion are shown below, but not limited thereto.
Examples of the fluorine-free methide acid anion are shown below, but not limited thereto.
Examples of the phenoxide anion are shown below, but not limited thereto.
The monomer from which repeat units (a) are derived can be synthesized by reacting a sulfonium salt having a hydroxy, amino or thiol group in its cation with a (meth)acrylate having an isocyanate group. A catalyst may be used in the reaction although the reaction takes place in a catalyst-free system. Suitable catalysts include organic tin compounds such as dibutyltin dilaurate, bismuth salts, and zinc carboxylates such as zinc 2-ethylhexanoate and zinc acetate, but are not limited thereto.
If impurities such as water, amine compounds, alcohol compounds, and carboxy-containing compounds are present in the system for reaction with a (meth)acrylate having an isocyanate group, reactions with the impurities can also take place and the purity of the desired compound becomes low. For this reason, it is necessary to fully remove impurities prior to the reaction.
It is also possible to use a (meth)acrylate having a blocked isocyanate group. The blocked isocyanate group is converted to an isocyanate group as a result of the blocking group being deprotected by heating or with the aid of the catalyst. Examples of the blocked isocyanate group include isocyanate groups substituted with an alcohol, phenol, thioalcohol, imine, ketimine, amine, lactam, pyrazole, oxime, or β-diketone.
Polymer A may also function as a base polymer. In the case of a chemically amplified positive tone resist composition, Polymer A comprises repeat units containing an acid labile group, preferably repeat units having the formula (b1) or repeat units having the formula (b2). These units are also referred to as repeat units (b1) and (b2), hereinafter.
In formulae (b1) and (b2), RA is each independently hydrogen or methyl. Y1 is a single bond, phenylene or naphthylene group, or C1-C12 linking group containing at least one moiety selected from ester bond, ether bond and lactone ring. Y2 is a single bond or ester bond. Y3 is a single bond, ether bond or ester bond. R11 and R12 are each independently an acid labile group. R13 is a C1-C4 saturated hydrocarbyl group, halogen, C2-C5 saturated hydrocarbylcarbonyl group, cyano group, or C2-C5 saturated hydrocarbyloxycarbonyl group. R14 is a single bond or a C1-C6 alkanediyl group which may contain an ether bond or ester bond. The subscript “a” is an integer of 0 to 4.
Examples of the monomer from which repeat units (b1) are derived are shown below, but not limited thereto. RA and R11 are as defined above.
Examples of the monomer from which repeat units (b2) are derived are shown below, but not limited thereto. RA and R12 are as defined above.
The acid labile groups represented by R11 and R12 in formulae (b1) and (b2) may be selected from a variety of such groups, for example, those groups described in JP-A 2013-080033 (U.S. Pat. No. 8,574,817) and JP-A 2013-083821 (U.S. Pat. No. 8,846,303).
Typical of the acid labile group are groups having the following formulae (AL-1) to (AL-3).
In formulae (AL-1) and (AL-2), RL1 and RL2 are each independently a C1-C40 hydrocarbyl group which may contain a heteroatom such as oxygen, sulfur, nitrogen or fluorine. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. Inter alia, C1-C40 saturated hydrocarbyl groups are preferred, and C1-C20 saturated hydrocarbyl groups are more preferred.
In formula (AL-1), b is an integer of 0 to 10, preferably 1 to 5.
In formula (AL-2), RL3 and RL4 are each independently hydrogen or a C1-C20 hydrocarbyl group which may contain a heteroatom such as oxygen, sulfur, nitrogen or fluorine. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. Inter alia, C1-C20 saturated hydrocarbyl groups are preferred. Any two of RL2, RL3 and RL4 may bond together to form a C3-C20 ring with the carbon atom or carbon and oxygen atoms to which they are attached. The ring preferably contains 4 to 16 carbon atoms and is typically alicyclic.
In formula (AL-3), RL5, RL6 and RL7 are each independently a C1-C20 hydrocarbyl group which may contain a heteroatom such as oxygen, sulfur, nitrogen or fluorine. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. Inter alia, C1-C20 saturated hydrocarbyl groups are preferred. Any two of RL5, RL6 and RL7 may bond together to form a C3-C20 ring with the carbon atom to which they are attached. The ring preferably contains 4 to 16 carbon atoms and is typically alicyclic.
Where Polymer A also functions as a base polymer, it may further comprise repeat units (c) having a phenolic hydroxy group as an adhesive group. Examples of the monomer from which repeat units (c) are derived are given below, but not limited thereto. Herein R is as defined above.
Where Polymer A also functions as a base polymer, it may further comprise repeat units (d) having another adhesive group selected from hydroxy group (other than the foregoing phenolic hydroxy), lactone ring, sultone ring, ether bond, ester bond, sulfonic ester bond, carbonyl group, sulfonyl group, cyano group, and carboxy group. Examples of the monomer from which repeat units (d) are derived are given below, but not limited thereto. Herein RA is as defined above.
Where Polymer A also functions as a base polymer, it may further comprise repeat units (e) derived from indene, benzofuran, benzothiophene, acenaphthylene, chromone, coumarin, norbornadiene, or derivatives thereof. Examples of the monomer from which repeat units (e) are derived are given below, but not limited thereto.
Where Polymer A also functions as a base polymer, it may further comprise repeat units (f) derived from indane, vinylpyridine, vinylcarbazole, or derivatives thereof.
Polymer A may further comprise repeat units (g) derived from an onium salt containing a polymerizable unsaturated bond, other than repeat units (a). Examples of repeat units (g) are described in JP-A 2017-008181, paragraph [0060].
The base polymer for formulating the positive resist composition comprises repeat units (a) and repeat units (b1) and/or (b2) having an acid labile group as essential components and additional repeat units (c), (d), (e), (f), and (g) as optional components. A fraction of units (a), (b1), (b2), (c), (d), (e), (f), and (g) is:
For the base polymer for formulating the negative resist composition, an acid labile group is not necessarily essential. The base polymer comprises essentially repeat units (a), and optionally repeat units (c), (d), (e), (f) and/or (g). A fraction of these units is:
It is noted that Polymer A may contain both repeat units wherein M− is a strong acid anion, referred to as repeat units (a1), and repeat units wherein M− is a weak acid anion, referred to as repeat units (a2), as repeat units (a). In the embodiment wherein Polymer A contains both repeat units (a1) and (a2), the ratio of repeat units (a1) to repeat units (a2), i.e., a1:a2 is preferably from 1:0.01 to 1:10, more preferably from 1:0.02 to 1:5, even more preferably from 1:0.05 to 1:4. It is noted that a=a1+a2. In the embodiment wherein Polymer A contains both repeat units (a1) and (a2), the resist composition may or may not contain an acid generator and quencher.
Polymer A may be synthesized by any desired methods, for example, by dissolving one or more monomers selected from the monomers corresponding to the foregoing repeat units in an organic solvent, adding a radical polymerization initiator thereto, and heating for polymerization. Examples of the organic solvent which can be used for polymerization include toluene, benzene, tetrahydrofuran (THF), diethyl ether, and dioxane. Examples of the polymerization initiator used herein include 2,2′-azobisisobutyronitrile (AIBN), 2,2′-azobis(2,4-dimethylvaleronitrile), dimethyl 2,2-azobis(2-methylpropionate), benzoyl peroxide, and lauroyl peroxide. Preferably, the reaction temperature is 50 to 80° C. and the reaction time is 2 to 100 hours, more preferably 5 to 20 hours.
Where a monomer having a hydroxy group is copolymerized, the hydroxy group may be replaced by an acetal group susceptible to deprotection with acid, typically ethoxyethoxy, prior to polymerization, and the polymerization be followed by deprotection with weak acid and water. Alternatively, the hydroxy group may be replaced by an acetyl, formyl, pivaloyl or similar group prior to polymerization, and the polymerization be followed by alkaline hydrolysis.
When hydroxystyrene or hydroxyvinylnaphthalene is copolymerized, an alternative method is possible. Specifically, acetoxystyrene or acetoxyvinylnaphthalene is used instead of hydroxystyrene or hydroxyvinylnaphthalene, and after polymerization, the acetoxy group is deprotected by alkaline hydrolysis, for thereby converting the polymer product to hydroxystyrene or hydroxyvinylnaphthalene. For alkaline hydrolysis, a base such as aqueous ammonia or triethylamine may be used. Preferably the reaction temperature is −20° C. to 100° C., more preferably 0° C. to 60° C., and the reaction time is 0.2 to 100 hours, more preferably 0.5 to 20 hours.
Polymer A should preferably have a weight average molecular weight (Mw) in the range of 1,000 to 500,000, and more preferably 2.000 to 30,000, as measured by GPC versus polystyrene standards using tetrahydrofuran (THF) solvent. A Mw in the range ensures that a resist film has satisfactory heat resistance.
If a polymer has a wide molecular weight distribution or dispersity (Mw/Mn), which indicates the presence of lower and higher molecular weight polymer fractions, there is a possibility that foreign matter is left on the pattern or the pattern profile is degraded. The influences of Mw and Mw/Mn become stronger as the pattern rule becomes finer. Therefore, Polymer A should preferably have a narrow dispersity (Mw/Mn) of 1.0 to 2.0, especially 1.0 to 1.5, in order to provide a resist composition suitable for micropatterning to a small feature size.
Polymer A may be a blend of two or more polymers which differ in compositional ratio, Mw or Mw/Mn.
The resist composition may contain an organic solvent. The organic solvent used herein is not particularly limited as long as the foregoing and other components are soluble therein. Examples of the organic solvent are described in JP-A 2008-111103, paragraphs [0144]-[0145] (U.S. Pat. No. 7,537,880). Exemplary solvents include ketones such as cyclohexanone, cyclopentanone, methyl-2-n-pentyl ketone and 2-heptanone; alcohols such as 3-methoxybutanol, 3-methyl-3-methoxybutanol, 1-methoxy-2-propanol, I-ethoxy-2-propanol, and diacetone alcohol (DAA); ethers such as propylene glycol monomethyl ether (PGME), ethylene glycol monomethyl ether, propylene glycol monoethyl ether, ethylene glycol monoethyl ether, propylene glycol dimethyl ether, and diethylene glycol dimethyl ether; esters such as propylene glycol monomethyl ether acetate (PGMEA), propylene glycol monoethyl ether acetate, ethyl lactate, ethyl pyruvate, butyl acetate, methyl 3-methoxypropionate, ethyl 3-ethoxypropionate, tert-butyl acetate, tert-butyl propionate, and propylene glycol mono-tert-butyl ether acetate; and lactones such as γ-butyrolactone.
The organic solvent is preferably added in an amount of 100 to 10,000 parts, and more preferably 200 to 8,000 parts by weight per 100 parts by weight of the base polymer. The organic solvent may be used alone or in admixture.
The resist composition may further contain a quencher. Inclusion of a quencher is preferred particularly when Polymer A contains an anion of strong acid as M−. As used herein, the quencher refers to a compound capable of trapping the acid, which is generated by the acid generator in the resist composition upon light exposure, to prevent the acid from diffusing to the unexposed region.
The quencher is typically selected from conventional basic compounds. Conventional basic compounds include primary, secondary, and tertiary aliphatic amines, mixed amines, aromatic amines, heterocyclic amines, nitrogen-containing compounds with carboxy group, nitrogen-containing compounds with sulfonyl group, nitrogen-containing compounds with hydroxy group, nitrogen-containing compounds with hydroxyphenyl group, alcoholic nitrogen-containing compounds, amide derivatives, imide derivatives, and carbamate derivatives. Also included are primary, secondary, and tertiary amine compounds, specifically amine compounds having a hydroxy group, ether bond, ester bond, lactone ring, cyano group, or sulfonic ester bond as described in JP-A 2008-111103, paragraphs [0146]-[0164], and compounds having a carbamate group as described in JP 3790649. Addition of a basic compound may be effective for further suppressing the diffusion rate of acid in the resist film or correcting the pattern profile.
Oniumn salts such as sulfonium salts, iodonium salts and ammonium salts of sulfonic acids which are not fluorinated at α-position may also be used as the quencher. While an α-fluorinated sulfonic acid, imide acid, and methide acid are necessary to deprotect the acid labile group of carboxylic acid ester, an α-non-fluorinated sulfonic acid or carboxylic acid is released by salt exchange with an α-non-fluorinated onium salt. An α-non-fluorinated sulfonic acid and a carboxylic acid function as a quencher because they do not induce deprotection reaction.
Also, onium salts of carboxylic acid having the formula (1) are useful quenchers.
R101—CO2−Mq+ (1)
In formula (1), R101 is a C1-C40 hydrocarbyl group which may contain a heteroatom. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. Examples thereof include C1-C40 alkyl groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, tert-pentyl, n-pentyl, n-hexyl, n-octyl, 2-ethylhexyl, n-nonyl, and n-decyl; C3-C40 cyclic saturated hydrocarbyl groups such as cyclopentyl, cyclohexyl, cyclopentylmethyl, cyclopentylethyl, cyclopentylbutyl, cyclohexylmethyl, cyclohexylethyl, cyclohexylbutyl, norbornyl, tricyclo[5.2.1.02,6]decanyl, adamantyl, and adamantylmethyl; C2-C40 alkenyl groups such as vinyl, allyl, propenyl, butenyl, and hexenyl; C3-C40 cyclic unsaturated aliphatic hydrocarbyl groups such as cyclohexenyl: C6-C40 aryl groups such as phenyl, naphthyl, alkylphenyl groups, e.g., 2-methylphenyl, 3-methylphenyl, 4-methylphenyl, 4-ethylphenyl, 4-tert-butylphenyl, 4-n-butylphenyl, di- or trialkylphenyl groups, e.g., 2,4-dimethylphenyl and 2,4,6-triisopropylphenyl, alkylnaphthyl groups, e.g., methylnaphthyl and ethylnaphthyl, dialkylnaphthyl groups, e.g., dimethylnaphthyl and diethylnaphthyl; and C7-C40 aralkyl groups such as benzyl, 1-phenylethyl and 2-phenylethyl.
In the hydrocarbyl group, some or all of the hydrogen atoms may be substituted by a moiety containing a heteroatom such as oxygen, sulfur, nitrogen or halogen, and some constituent —CH2— may be replaced by a moiety containing a heteroatom such as oxygen, sulfur or nitrogen, so that the group may contain a hydroxy moiety, fluorine, chlorine, bromine, iodine, cyano moiety, carbonyl moiety, ether bond, ester bond, sulfonic ester bond, carbonate bond, lactone ring, sultone ring, carboxylic anhydride (—C(═O)—O—C(═O)—), or haloalkyl moiety. Examples of the heteroatom-containing hydrocarbyl group include fluoroalkyl groups such as trifluoromethyl, trifluoroethyl, 2,2,2-trifluoro-1-methyl-1-hydroxyethyl, 2,2,2-trifluoro-1-(trifluoromethyl)-1-hydroxyethyl; fluoroaryl groups such as pentafluorophenyl and 4-trifluoromethylphenyl; heteroaryl groups such as thienyl and indolyl; 4-hydroxyphenyl, alkoxyphenyl groups such as 4-methoxyphenyl, 3-methoxyphenyl, 2-methoxyphenyl, 4-ethoxyphenyl, 4-tert-butoxyphenyl, and 3-tert-butoxyphenyl; alkoxynaphthyl groups such as methoxynaphthyl, ethoxynaphthyl, n-propoxynaphthyl and n-butoxynaphthyl; dialkoxynaphthyl groups such as dimethoxynaphthyl and diethoxynaphthyl; and aryloxoalkyl groups, typically 2-aryl-2-oxoethyl groups such as 2-phenyl-2-oxoethyl, 2-(1-naphthyl)-2-oxoethyl, and 2-(2-naphthyl)-2-oxoethyl.
In the onium salt of carboxylic acid, an anion having the formula (IA) is preferred.
Herein R102 and R103 are each independently hydrogen, fluorine, or trifluoromethyl. R104 is hydrogen, hydroxy, or a C1-C35 hydrocarbyl group which may contain a heteroatom. Examples of the hydrocarbyl group which may contain a heteroatom are as exemplified above for R101.
In formula (1), Mq+ is an onium cation. The preferred onium cations are sulfonium, iodonium and ammonium cations, with the sulfonium and iodonium cations being more preferred. Examples of the sulfonium cations are as will be exemplified later for the cation in the sulfonium salt having formula (2-1). Examples of the iodonium cations are as will be exemplified later for the cation in the iodonium salt having formula (2-2).
Also useful are quenchers of polymer type as described in U.S. Pat. No. 7,598,016 (JP-A 2008-239918). The polymeric quencher segregates at the resist film surface after coating and thus enhances the rectangularity of resist pattern. When a protective film is applied as is often the case in the immersion lithography, the polymeric quencher is also effective for preventing a film thickness loss of resist pattern or rounding of pattern top.
When the resist composition contains a quencher, the quencher is preferably added in an amount of 0.1 to 20 parts by weight, more preferably 1 to 10 parts by weight per 100 parts by weight of the base polymer. The quencher may be used alone or in admixture.
The resist composition may further contain an acid generator. Inclusion of an acid generator is preferred particularly when Polymer A contains an anion of weak acid as M−. The acid generator is typically a compound (PAG) capable of generating an acid upon exposure to actinic ray or radiation. Although the PAG used herein may be any compound capable of generating an acid upon exposure to high-energy radiation, those compounds capable of generating sulfonic acid, imide acid (imidic acid) or methide acid are preferred. Suitable PAGs include sulfonium salts, iodonium salts, sulfonyldiazomethane. N-sulfonyloxyimide, and oxime-O-sulfonate acid generators. Exemplary PAGs are described in JP-A 2008-111103, paragraphs [0122]-[0142] (U.S. Pat. No. 7,537,880).
Sulfonium salts having the formula (2-1) and iodonium salts having the formula (2-2) are also useful as the PAG.
In formulae (2-1) and (2-2), R201 to R205 are each independently halogen or a C1-C20 hydrocarbyl group which may contain a heteroatom. Suitable halogen atoms are as exemplified above. Examples of the C1-C20 hydrocarbyl group are as exemplified above for the hydrocarbyl groups R2 and R3 in formula (a). In the hydrocarbyl group, some or all of the hydrogen atoms may be substituted by a moiety containing a heteroatom such as oxygen, sulfur, nitrogen or halogen, and some constituent —CH2— may be replaced by a moiety containing a heteroatom such as oxygen, sulfur or nitrogen, so that the group may contain a hydroxy moiety, fluorine, chlorine, bromine, iodine, cyano moiety, nitro moiety, carbonyl moiety, ether bond, ester bond, sulfonic ester bond, carbonate bond, lactone ring, sultone ring, carboxylic anhydride (—C(═O)—O—C(═O)—), or haloalkyl moiety. Also, R201 and R202 may bond together to form a ring with the sulfur atom to which they are attached. Examples of the ring are as exemplified above for the ring that R2 and R3 in formula (a), taken together, form with the sulfur atom to which they are attached.
Examples of the cation in the sulfonium salt having formula (2-1) are shown below, but not limited thereto.
Examples of the cation in the iodonium salt having formula (2-2) are are shown below, but not limited thereto.
In formulae (2-1) and (2-2), Xa− is an anion of strong acid selected from fluorosulfonate anions, fluoroimide acid anions and fluoromethide acid anions. The fluorosulfonate anion preferably has formula (a1-1), the fluoroimide acid anion preferably has formula (a1-2), and the fluoromethide acid anion preferably has formula (a1-3).
When the resist composition contains the other acid generator, it is preferably used in an amount of 0.1 to 50 parts, more preferably 1 to 40 parts by weight per 100 parts by weight of the base polymer. The other acid generator may be used alone or in admixture.
In addition to the foregoing components, the resist composition may further contain a surfactant, dissolution inhibitor, crosslinker, water repellency improver, and acetylene alcohol. Each additional component may be used alone or in admixture of two or more.
Exemplary surfactants are described in JP-A 2008-111103, paragraphs [0165]-[0166]. Inclusion of a surfactant may improve or control the coating characteristics of the resist composition. The surfactant is preferably added in an amount of 0.0001 to 10 parts by weight per 100 parts by weight of the base polymer.
In the case of positive resist compositions, inclusion of a dissolution inhibitor may lead to an increased difference in dissolution rate between exposed and unexposed areas and a further improvement in resolution. The dissolution inhibitor which can be used herein is a compound having at least two phenolic hydroxy groups on the molecule, in which an average of from 0 to 100 mol % of all the hydrogen atoms on the phenolic hydroxy groups are replaced by acid labile groups or a compound having at least one carboxy group on the molecule, in which an average of 50 to 100 mol % of all the hydrogen atoms on the carboxy groups are replaced by acid labile groups, both the compounds having a molecular weight of 100 to 1,000, and preferably 150 to 800. Typical are bisphenol A, trisphenol, phenolphthalein, cresol novolac, naphthalenecarboxylic acid, adamantanecarboxylic acid, and cholic acid derivatives in which the hydrogen atom on the hydroxy or carboxy group is replaced by an acid labile group, as described in U.S. Pat. No. 7,771,914 (JP-A 2008-122932, paragraphs [0155]-[0178]).
In the positive resist composition, the dissolution inhibitor is preferably added in an amount of 0 to 50 parts, more preferably 5 to 40 parts by weight per 100 parts by weight of the base polymer.
In the case of negative resist compositions, a negative pattern may be formed by adding a crosslinker to reduce the dissolution rate of exposed area. Suitable crosslinkers which can be used herein include epoxy compounds, melamine compounds, guanamine compounds, glycoluril compounds and urea compounds having substituted thereon at least one group selected from among methylol, alkoxymethyl and acyloxymethyl groups, isocyanate compounds, azide compounds, and compounds having a double bond such as an alkenyloxy group. These compounds may be used as an additive or introduced into a polymer side chain as a pendant. Hydroxy-containing compounds may also be used as the crosslinker.
Suitable epoxy compounds include tris(2,3-epoxypropyl)isocyanurate, trimethylolmethane triglycidyl ether, trimethylolpropane triglycidyl ether, and triethylolethane triglycidyl ether. Examples of the melamine compound include hexamethylol melamine, hexamethoxymethyl melamine, hexamethylol melamine compounds having 1 to 6 methylol groups methoxymethylated and mixtures thereof, hexamethoxyethyl melamine, hexaacyloxymethyl melamine, hexamethylol melamine compounds having 1 to 6 methylol groups acyloxymethylated and mixtures thereof. Examples of the guanamine compound include tetramethylol guanamine, tetramethoxymethyl guanamine, tetramethylol guanamine compounds having 1 to 4 methylol groups methoxymethylated and mixtures thereof, tetramethoxyethyl guanamine, tetraacyloxyguanamine, tetramethylol guanamine compounds having 1 to 4 methylol groups acyloxymethylated and mixtures thereof. Examples of the glycoluril compound include tetramethylol glycoluril, tetramethoxyglycoluril, tetramethoxymethyl glycoluril, tetramethylol glycoluril compounds having 1 to 4 methylol groups methoxymethylated and mixtures thereof, tetramethylol glycoluril compounds having 1 to 4 methylol groups acyloxymethylated and mixtures thereof. Examples of the urea compound include tetramethylol urea, tetramethoxymethyl urea, tetramethylol urea compounds having 1 to 4 methylol groups methoxymethylated and mixtures thereof, and tetramethoxyethyl urea.
Suitable isocyanate compounds include tolylene diisocyanate, diphenylmethane diisocyanate, hexamethylene diisocyanate and cyclohexane diisocyanate. Suitable azide compounds include 1,1′-biphenyl-4,4′-bisazide, 4,4′-methylidenebisazide, and 4,4′-oxybisazide. Examples of the alkenyloxy-containing compound include ethylene glycol divinyl ether, triethylene glycol divinyl ether, 1,2-propanediol divinyl ether, 1,4-butanediol divinyl ether, tetramethylene glycol divinyl ether, neopentyl glycol divinyl ether, trimethylol propane trivinyl ether, hexanediol divinyl ether, 1,4-cyclohexanediol divinyl ether, pentaerythritol trivinyl ether, pentaerythritol tetravinyl ether, sorbitol tetravinyl ether, sorbitol pentavinyl ether, and trimethylol propane trivinyl ether.
In the negative resist composition, the crosslinker is preferably added in an amount of 0.1 to 50 parts, more preferably 1 to 40 parts by weight per 100 parts by weight of the base polymer.
To the resist composition, a water repellency improver may also be added for improving the water repellency on surface of a resist film. The water repellency improver may be used in the topcoatless immersion lithography. Suitable water repellency improvers include polymers having a fluoroalkyl group and polymers having a specific structure with a 1,1,1,3,3,3-hexafluoro-2-propanol residue and are described in JP-A 2007-297590 and JP-A 2008-111103, for example. The water repellency improver to be added to the resist composition should be soluble in alkaline developers and organic solvent developers. The water repellency improver of specific structure with a 1,1,1,3,3,3-hexafluoro-2-propanol residue is well soluble in the developer. A polymer comprising repeat units having an amino group or amine salt serves as the water repellency improver and is effective for preventing evaporation of acid during PEB, thus preventing any hole pattern opening failure after development. An appropriate amount of the water repellency improver is 0 to 20 parts, preferably 0.5 to 10 parts by weight per 100 parts by weight of the base polymer.
Also, an acetylene alcohol may be blended in the resist composition. Suitable acetylene alcohols are described in JP-A 2008-122932, paragraphs [0179]-[0182]. An appropriate amount of the acetylene alcohol blended is 0 to 5 parts by weight per 100 parts by weight of the base polymer.
The resist composition is used in the fabrication of various integrated circuits. Pattern formation using the resist composition may be performed by well-known lithography processes. The process generally involves the steps of applying the resist composition onto a substrate to form a resist film thereon, exposing the resist film to high-energy radiation, and developing the exposed resist film in a developer. If necessary, any additional steps may be added.
For example, the resist composition is first applied onto a substrate on which an integrated circuit is to be formed (e.g., Si, SiO2, SiN, SiON, TiN, WSi, BPSG, SOG, or organic antireflective coating) or a substrate on which a mask circuit is to be formed (e.g., Cr, CrO, CrON, MoSi2, or SiO2) by a suitable coating technique such as spin coating, roll coating, flow coating, dipping, spraying or doctor coating. The coating is prebaked on a hotplate at a temperature of 60 to 150° C. for 10 seconds to 30 minutes, preferably at 80 to 120° C. for 30 seconds to 20 minutes. The resulting resist film is generally 0.01 to 2 μm thick.
Then the resist film is exposed to high-energy radiation. Examples of the high-energy radiation include UV, deep-UV, EB, EUV of wavelength 3 to 15 nm, x-ray, soft x-ray, excimer laser light, γ-ray or synchrotron radiation. On use of UV, deep UV, EUV, x-ray, soft x-ray, excimer laser, γ-ray or synchrotron radiation, the resist film is exposed directly or through a mask having a desired pattern, preferably in a dose of about 1 to 200 mJ/cm2, more preferably about 10 to 100 mJ/cm2. On use of EB, a pattern may be written directly or through a mask having a desired pattern, preferably in a dose of about 0.1 to 100 μC/cm2, more preferably about 0.5 to 50 μC/cm2. The resist composition is suited for micropatterning using high-energy radiation such as KrF excimer laser, ArF excimer laser, EB, EUV, x-ray, soft x-ray, 7-ray or synchrotron radiation.
After the exposure, the resist film may be baked (PEB) on a hotplate or in an oven at 60 to 150° C. for 10 seconds to 30 minutes, preferably at 80 to 120° C. for 30 seconds to 20 minutes.
After the exposure or PEB, the resist film is developed with a developer in the form of an aqueous base solution for 3 seconds to 3 minutes, preferably 5 seconds to 2 minutes by conventional techniques such as dip, puddle and spray techniques. A typical developer is a 0.1 to 10 wt %, preferably 2 to 5 wt % aqueous solution of tetramethylammonium hydroxide (TMAH), tetraethylammonium hydroxide (TEAH), tetrapropylammonium hydroxide (TPAH), or tetrabutylammonium hydroxide (TBAH). In the case of positive resist, the resist film in the exposed area is dissolved in the developer whereas the resist film in the unexposed area is not dissolved. In this way, the desired positive pattern is formed on the substrate. Inversely in the case of negative resist, the exposed area of resist film is insolubilized and the unexposed area is dissolved in the developer.
In an alternative embodiment, a negative pattern may be formed via organic solvent development using a positive resist composition comprising a base polymer having an acid labile group. The developer used herein is preferably selected from among 2-octanone, 2-nonanone, 2-heptanone, 3-heptanone, 4-heptanone, 2-hexanone, 3-hexanone, diisobutyl ketone, methylcyclohexanone, acetophenone, methylacetophenone, propyl acetate, butyl acetate, isobutyl acetate, pentyl acetate, butenyl acetate, isopentyl acetate, propyl formate, butyl formate, isobutyl formate, pentyl formate, isopentyl formate, methyl valerate, methyl pentenoate, methyl crotonate, ethyl crotonate, methyl propionate, ethyl propionate, ethyl 3-ethoxypropionate, methyl lactate, ethyl lactate, propyl lactate, butyl lactate, isobutyl lactate, pentyl lactate, isopentyl lactate, methyl 2-hydroxyisobutyrate, ethyl 2-hydroxyisobutyrate, methyl benzoate, ethyl benzoate, phenyl acetate, benzyl acetate, methyl phenylacetate, benzyl formate, phenylethyl formate, methyl 3-phenylpropionate, benzyl propionate, ethyl phenylacetate, and 2-phenylethyl acetate, and mixtures thereof.
At the end of development, the resist film is rinsed. As the rinsing liquid, a solvent which is miscible with the developer and does not dissolve the resist film is preferred. Suitable solvents include alcohols of 3 to 10 carbon atoms, ether compounds of 8 to 12 carbon atoms, alkanes, alkenes, and alkynes of 6 to 12 carbon atoms, and aromatic solvents. Specifically, suitable alcohols of 3 to 10 carbon atoms include n-propyl alcohol, isopropyl alcohol, 1-butyl alcohol, 2-butyl alcohol, isobutyl alcohol, t-butyl alcohol, 1-pentanol, 2-pentanol, 3-pentanol, t-pentyl alcohol, neopentyl alcohol, 2-methyl-1-butanol, 3-methyl-1-butanol, 3-methyl-3-pentanol, cyclopentanol, 1-hexanol, 2-hexanol, 3-hexanol, 2,3-dimethyl-2-butanol, 3,3-dimethyl-1-butanol, 3,3-dimethyl-2-butanol, 2-ethyl-1-butanol, 2-methyl-1-pentanol, 2-methyl-2-pentanol, 2-methyl-3-pentanol, 3-methyl-1-pentanol, 3-methyl-2-pentanol, 3-methyl-3-pentanol, 4-methyl-1-pentanol, 4-methyl-2-pentanol, 4-methyl-3-pentanol, cyclohexanol, and 1-octanol. Suitable ether compounds of 8 to 12 carbon atoms include di-n-butyl ether, diisobutyl ether, di-s-butyl ether, di-n-pentyl ether, diisopentyl ether, di-s-pentyl ether, di-t-pentyl ether, and di-n-hexyl ether. Suitable alkanes of 6 to 12 carbon atoms include hexane, heptane, octane, nonane, decane, undecane, dodecane, methylcyclopentane, dimethylcyclopentane, cyclohexane, methylcyclohexane, dimethylcyclohexane, cycloheptane, cyclooctane, and cyclononane. Suitable alkenes of 6 to 12 carbon atoms include hexene, heptene, octene, cyclohexene, methylcyclohexene, dimethylcyclohexene, cycloheptene, and cyclooctene. Suitable alkynes of 6 to 12 carbon atoms include hexyne, heptyne, and octyne. Suitable aromatic solvents include toluene, xylene, ethylbenzene, isopropylbenzene, t-butylbenzene and mesitylene. The solvents may be used alone or in admixture.
Rinsing is effective for minimizing the risks of resist pattern collapse and defect formation. However, rinsing is not essential. If rinsing is omitted, the amount of solvent used may be reduced.
A hole or trench pattern after development may be shrunk by the thermal flow, RELACS® or DSA process. A hole pattern is shrunk by coating a shrink agent thereto, and baking such that the shrink agent may undergo crosslinking at the resist surface as a result of the acid catalyst diffusing from the resist layer during bake, and the shrink agent may attach to the sidewall of the hole pattern. The bake is preferably at a temperature of 70 to 180° C., more preferably 80 to 170° C., for a time of 10 to 300 seconds. The extra shrink agent is stripped and the hole pattern is shrunk.
Examples of the invention are given below by way of illustration and not by way of limitation. The abbreviation “pbw” is parts by weight.
In Synthesis Examples, Monomers PM-1 to PM-15, QM-1 to QM-22, cPM-1, cQM-1, AM-1 to AM-4 and FM-1 having the structure shown below were used.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 4.8 g of 4-hydroxystyrene, 11.5 g of Monomer PM-1, and 40 g of tetrahydrofuran (THF) solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of azobisisobutyronitrile (AIBN) was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of isopropyl alcohol (IPA) for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-1 in white solid form. Polymer P-1 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 4.8 g of 4-hydroxystyrene, 11.7 g of Monomer PM-2, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-2 in white solid form. Polymer P-2 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 11.1 g of Monomer AM-1, 4.8 g of 3-hydroxystyrene, 11.8 g of Monomer PM-3, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-3 in white solid form. Polymer P-3 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 11.1 g of Monomer AM-1, 4.8 g of 3-hydroxystyrene, 11.6 g of Monomer PM-4, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-4 in white solid form. Polymer P-4 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 4.6 g of 3-hydroxystyrene, 11.3 g of Monomer PM-5, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-5 in white solid form. Polymer P-5 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 7.9 g of Monomer AM-2, 3.6 g of Monomer AM-3, 4.6 g of 3-hydroxystyrene, 15.9 g of Monomer PM-6, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C. whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-6 in white solid form. Polymer P-6 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 7.9 g of Monomer AM-2, 3.6 g of Monomer AM-4, 4.8 g of 3-hydroxystyrene, 11.1 g of Monomer PM-7, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-7 in white solid form. Polymer P-7 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 3.6 g of 3-hydroxystyrene, 3.2 g of Monomer FM-1, 10.2 g of Monomer PM-8, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-8 in white solid form. Polymer P-8 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 4.3 g of 3-hydroxystyrene, 8.5 g of Monomer PM-9, 3.3 g of Monomer QM-5, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-9 in white solid form. Polymer P-9 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 3.1 g of 3-hydroxystyrene, 3.2 g of Monomer FM-1, 12.7 g of Monomer PM-10, 4.2 g of Monomer QM-11, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-10 in white solid form. Polymer P-10 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 2.8 g of Monomer QM-1, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-11 in white solid form. Polymer P-11 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 2.7 g of Monomer QM-2, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-12 in white solid form. Polymer P-12 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 2.8 g of Monomer QM-3, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-13 in white solid form. Polymer P-13 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 2.6 g of Monomer QM-4, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C. whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-14 in white solid form. Polymer P-14 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 3.9 g of Monomer QM-6, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C. whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-15 in white solid form. Polymer P-15 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 2.6 g of Monomer QM-7, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-16 in white solid form. Polymer P-16 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 2.5 g of Monomer QM-8, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-17 in white solid form. Polymer P-17 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 3.6 g of Monomer QM-9, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-18 in white solid form. Polymer P-18 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 2.7 g of Monomer QM-10, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C. whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-19 in white solid form. Polymer P-19 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 4.3 g of Monomer QM-12, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-20 in white solid form. Polymer P-20 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 2.2 g of Monomer QM-13, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-21 in white solid form. Polymer P-21 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 2.3 g of Monomer QM-14, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-22 in white solid form. Polymer P-22 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 11.1 g of Monomer AM-1, 4.8 g of 3-hydroxystyrene, 11.6 g of Monomer PM-11, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-23 in white solid form. Polymer P-23 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 11.1 g of Monomer AM-1, 4.8 g of 3-hydroxystyrene, 13.7 g of Monomer PM-12, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-24 in white solid form. Polymer P-24 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 11.1 g of Monomer AM-1, 4.8 g of 3-hydroxystyrene, 13.1 g of Monomer PM-13, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-25 in white solid form. Polymer P-25 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 2.0 g of Monomer QM-15, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-26 in white solid form. Polymer P-26 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 2.3 g of Monomer QM-16, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C. whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-27 in white solid form. Polymer P-27 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 2.6 g of Monomer QM-17, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-28 in white solid form. Polymer P-28 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn b GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 3.3 g of Monomer QM-18, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-29 in white solid form. Polymer P-29 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 5.5 g of 3-hydroxystyrene, 2.7 g of Monomer QM-19, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-30 in white solid form. Polymer P-30 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 4.3 g of 3-hydroxystyrene, 11.0 g of Monomer PM-14, 4.0 g of Monomer QM-18, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-31 in white solid form. Polymer P-31 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 4.3 g of 3-hydroxystyrene, 11.0 g of Monomer PM-14, 2.0 g of Monomer QM-20, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-32 in white solid form. Polymer P-32 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 4.3 g of 3-hydroxystyrene, 11.0 g of Monomer PM-14, 3.3 g of Monomer QM-21, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-33 in white solid form. Polymer P-33 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 4.3 g of 3-hydroxystyrene, 11.0 g of Monomer PM-14, 3.8 g of Monomer QM-22, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-34 in white solid form. Polymer P-34 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
A 2-L flask was charged with 8.4 g of 1-methyl-1-cyclopentyl methacrylate, 4.3 g of 4-hydroxystyrene, 11.7 g of Monomer PM-15, 3.8 g of Monomer QM-22, and 40 g of THF solvent. The reactor was cooled at −70° C. in nitrogen atmosphere, after which vacuum pumping and nitrogen blow were repeated three times. The reactor was warmed up to room temperature, whereupon 1.2 g of AIBN was added. The reactor was heated at 60° C., whereupon reaction ran for 15 hours. The reaction solution was poured into 1 L of IPA for precipitation. The precipitated white solid was collected by filtration and vacuum dried at 60° C., yielding Polymer P-35 in white solid form. Polymer P-35 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
Comparative Polymer cP-1 was obtained in white solid form by the same procedure as in Synthesis Example 1 except that Monomer PM-1 was replaced by Monomer cP1-1. Comparative Polymer cP-1 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
Comparative Polymer cP-2 was obtained in white solid form by the same procedure as in Synthesis Example 21 except that 3-hydroxystyrene was replaced by 4-hydroxystyrene and Monomer QM-13 was replaced by Monomer cQM-1. Comparative Polymer cP-2 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
Comparative Polymer cP-3 was obtained in white solid form by the same procedure as in Synthesis Example 1 except that Monomer PM-1 was omitted. Comparative Polymer cP-3 was analyzed for composition by 13C- and 1H-NMR and for Mw and Mw/Mn by GPC.
Resist compositions were prepared by dissolving various components in a solvent in accordance with the recipe shown in Tables 1 to 3, and filtering through a filter having a pore size of 0.2 μm. The solvent contained 30 ppm of surfactant PolyFox PF-636 (Omnova Solutions Inc.).
The components in Tables 1 to 3 are as identified below.
Acid generator: PAG-1
Each of the resist compositions in Tables 1 to 3 was spin coated on a silicon substrate having a 20-nm coating of silicon-containing spin-on hard mask SHB-A940 (Shin-Etsu Chemical Co., Ltd., Si content 43 wt %) and prebaked on a hotplate at 105° C. for 60 seconds to form a resist film of 50 nm thick. Using an EUV scanner NXE3400 (ASML, NA 0.33, a 0.9/0.6, quadrupole illumination), the resist film was exposed to EUV through a mask bearing a hole pattern at a pitch 46 nm and +20% bias (on-wafer size). The resist film was baked (PEB) on a hotplate at the temperature shown in Tables 1 to 3 for 60 seconds and developed in a 2.38 wt % TMAH aqueous solution for 30 seconds to form a hole pattern having a size of 23 nm.
The resist pattern was observed under CD-SEM (CG-6300, Hitachi High-Technologies Corp.). The exposure dose that provides a hole pattern having a size of 23 nm is reported as sensitivity. The size of 50 holes at that dose was measured, from which a 3-fold value (3σ) of the standard deviation (σ) was computed and reported as size variation or CDU.
The resist composition is shown in Tables 1 to 3 together with the sensitivity and CDU of EUV lithography.
It is demonstrated in Tables 1 to 3 that resist compositions comprising a polymer comprising repeat units having formula (a) offer a high sensitivity and improved CDU.
Japanese Patent Application No. 2022-139749 is incorporated herein by reference. Although some preferred embodiments have been described, many modifications and variations may be made thereto in light of the above teachings. It is therefore to be understood that the invention may be practiced otherwise than as specifically described without departing from the scope of the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2022-139749 | Sep 2022 | JP | national |
