Patent Grant
11835860
This non-provisional application claims priority under 35 U.S.C. § 119(a) on Patent Application No. 2020-123046 filed in Japan on Jul. 17, 2020, 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. In particular, the enlargement of the logic memory market to comply with the wide-spread use of smart phones drives forward the miniaturization technology. As the advanced miniaturization technology, manufacturing of microelectronic devices at the 10-nm node by double patterning of the ArF immersion lithography has been implemented in a mass scale. Manufacturing of 7-nm node devices as the next generation by the double patterning technology is approaching to the verge of high-volume application. The candidate for 5-nm node devices as the next generation but one is EUV lithography.
The EUV lithography has the problem that defects in a mask blank consisting of total 80 layers of Mo and Si are transferred, and the problem that a high strength pellicle which causes only a little lowering of light intensity and is devoid of the risk of failure during exposure is not available, allowing particles to deposit from the exposure tool onto a mask. It is urgently required to reduce defects. Since the EUV lithography enables to form patterns to a feature size of less than half of the size achieved by the standard ArF immersion lithography, the probability of defect occurrence is increased. A higher level of defect control is thus necessary.
In conjunction with resist materials for the ArF immersion lithography, Patent Document 1 proposes a fluorinated polymer additive which segregates on the surface of a resist film to improve water repellency. This additive containing a 1,1,1,3,3,3-hexafluoro-2-propanol (HFA) group is effective for improving the solubility in alkaline developer at the resist film surface and reducing bridge defects on the resist surface.
Patent Documents 2 and 3 disclose that a polymer comprising repeat units having a HFA group and robust repeat units having an aromatic group is added for reducing outgassing from the resist film during EUV exposure. The modification of resist film surface can lead to a possibility of reducing pattern defects or suppressing outgassing.
Patent Documents 4 and 5 disclose resist compositions comprising iodized base polymers. Iodine atoms have remarkably high absorption of EUV and thus achieve a sensitizing effect, from which an increase of sensitivity is expectable. Regrettably, iodine atoms have a low solubility in alkaline developer. Then a base polymer having iodine introduced therein has a low dissolution rate in alkaline developer, which indicates a lowering of sensitivity and causes residues to be left in space regions of resist patterns.
In conjunction with resist compositions comprising a fluorine-containing polymer which segregates on the surface of a resist film to improve water repellency, Patent Documents 6 and 7 propose to introduce an amino group or ammonium salt into the fluorine-containing polymer. This is effective for suppressing acid diffusion on the resist film surface and improving the rectangularity of a resist pattern as developed. Since EUV absorption is not so high, the sensitizing effect is limitative.
For the acid-catalyzed chemically amplified resist, it is desired to develop a resist composition capable of minimizing nano-bridging and collapse of line patterns, eliminating any residues in the space region, and improving a sensitivity.
An object of the invention is to provide a resist composition which exhibits a high sensitivity and is unsusceptible to nano-bridging, pattern collapse or residue formation, independent of whether it is of positive tone or negative tone; and a pattern forming process using the same.
The inventor has found that when a polymer comprising repeat units having an ammonium salt structure of an iodine or bromine-substituted phenol compound and repeat units of at least one type selected from repeat units having a trifluoromethylalcohol group which may be substituted with an acid labile group and repeat units having a fluorinated hydrocarbyl group (referred to as “ammonium salt and fluorine-containing polymer” or “additive polymer”, hereinafter) is added to a base polymer, there is obtained a resist composition which is effective for preventing nano-bridging and pattern collapse, providing a wide process margin, forming a line pattern with improved LWR or a hole pattern with improved CDU, and leaving no residues in the space region.
In one aspect, the invention provides a resist composition comprising an ammonium salt and fluorine-containing polymer comprising repeat units AU having an ammonium salt structure of an iodine or bromine-substituted phenol compound and repeat units of at least one type selected from repeat units FU-1 having a trifluoromethylalcohol group which may be substituted with an acid labile group and repeat units FU-2 having a fluorinated hydrocarbyl group, and a base polymer.
Preferably, the repeat unit AU has the formula (AU), the repeat unit FU-1 has the formula (FU-1), and the repeat unit FU-2 has the formula (FU-2).
Herein m1 is an integer of 1 to 5, m2 is an integer of 0 to 3, n1 is 1 or 2, n2 is a positive number in the range: 0<n2/n1<; 1, n3 is 1 or 2. RA is each independently hydrogen or methyl. Xbi is iodine or bromine. X1A is a single bond, phenylene group, ester bond or amide bond. X1B is a single bond or a C1-C20 (n1+1)-valent hydrocarbon group which may contain an ether bond, carbonyl moiety, ester bond, amide bond, sultone ring, lactam ring, carbonate bond, halogen, hydroxy moiety or carboxy moiety. X2A is a single bond, phenylene, —O—, —C(═O)—O— or —C(═O)—NH—. X2B is a C1-C12 (n3+1)-valent saturated hydrocarbon group or (n3+1)-valent aromatic hydrocarbon group, which may contain fluorine, hydroxy moiety, ester bond or ether bond. X3 is a single bond, phenylene, —O—, —C(═O)—O—X31—X32— or —C(═O)—NH—X31—X32—, wherein X31 is a single bond or C1-C4 alkanediyl group, and X32 is a single bond, ester bond, ether bond or sulfonamide bond. R1, R2 and R3 are each independently hydrogen, a C1-C12 alkyl group, C2-C12 alkenyl group, C6-C12 aryl group or C7-C12 aralkyl group, a pair of R1 and R2 or R1 and X1B may bond together to form a ring with the nitrogen atom to which they are attached, the ring may contain oxygen, sulfur, nitrogen or a double bond. R4 is a hydroxy group, optionally fluorinated or chlorinated C1-C6 saturated hydrocarbyl group, optionally fluorinated or chlorinated C1-C6 saturated hydrocarbyloxy group, formyl group, optionally fluorinated or chlorinated C2-C7 saturated hydrocarbylcarbonyl group, optionally fluorinated or chlorinated C2-C7 saturated hydrocarbylcarbonyloxy group, optionally fluorinated or chlorinated C2-C7 saturated hydrocarbyloxycarbonyl group, optionally fluorinated or chlorinated C1-C4 saturated hydrocarbylsulfonyloxy group, C6-C10 aryl group, fluorine, chlorine, amino, nitro, cyano, —N(R4A)—C(═O)—R4B, or —N(RA)—C(═O)—O—R4B, wherein R4A is hydrogen or a C1-C6 saturated hydrocarbyl group, and R4B is a C1-C6 saturated hydrocarbyl group or C2-C8 unsaturated aliphatic hydrocarbyl group. R5 is a single bond, ester bond, or a C1-C12 saturated hydrocarbylene group in which some or all of the hydrogen atoms may be substituted by fluorine and some carbon may be replaced by an ester bond or ether bond. R6 is hydrogen, fluorine, methyl, trifluoromethyl or difluoromethyl, a pair of R5 and R6 may bond together to form a ring with the carbon atom to which they are attached, the ring may contain an ether bond, fluorine or trifluoromethyl. R7 is hydrogen or an acid labile group. R8 is a C1-C20 hydrocarbyl group which is substituted with at least one fluorine, and in which some carbon may be replaced by an ester bond or ether bond.
In a preferred embodiment, 0.001 to 20 parts by weight of the ammonium salt and fluorine-containing polymer is present per 100 parts by weight of the base polymer.
The resist composition may further comprise an acid generator capable of generating a sulfonic acid, imide acid or methide acid, an organic solvent, and/or a surfactant.
In one preferred embodiment, the base polymer comprises repeat units having the formula (a1) or repeat units having the formula (a2).
Herein RA is each independently hydrogen or methyl, R11 and R12 each are an acid labile group, R13 is fluorine, trifluoromethyl, a C1-C5 saturated hydrocarbyl group or C1-C5 saturated hydrocarbyloxy group, Y1 is a single bond, phenylene group, naphthylene group, or C1-C12 divalent linking group containing at least one moiety selected from ester bond and lactone ring, Y2 is a single bond or ester bond, and a is an integer of 0 to 4.
In one embodiment, the resist composition is a chemically amplified positive resist composition.
In another embodiment, the base polymer is free of an acid labile group. Typically, the resist composition is a chemically amplified negative resist composition.
In one preferred embodiment, the base polymer comprises repeat units of at least one type selected from repeat units having the formulae (f1) to (f3).
Herein RA is each independently hydrogen or methyl. Z1 is a single bond, a C1-C6 aliphatic hydrocarbylene group, phenylene group, naphthylene group, or C7-C18 group to obtained by combining the foregoing, or —O—Z11—, —C(═O)—O—Z11— or —C(═O)—NH—Z11—, wherein Z11 is a C1-C6 aliphatic hydrocarbylene group, phenylene group, naphthylene group, or C7-C18 group obtained by combining the foregoing, which may contain a carbonyl moiety, ester bond, ether bond or hydroxy moiety. Z2 is a single bond or ester bond. Z3 is a single bond, —Z31—C(═O)—O—, —Z31—O— or —Z31—O—C(═O)—, wherein Z3 is a is C1-C12 hydrocarbylene group, phenylene group, or C7-C18 group obtained by combining the foregoing, which may contain a carbonyl moiety, ester bond, ether bond, iodine or bromine.
Z4 is a methylene, 2,2,2-trifluoro-1,1-ethanediyl or carbonyl group. Z5 is a single bond, methylene, ethylene, phenylene, fluorinated phenylene, trifluoromethyl-substituted phenylene group, —O—Z51—, —C(═O)—O—Z51—, or —C(═O)—NH—Z51—, wherein Z51 is a C1-C6 aliphatic hydrocarbylene group, phenylene group, fluorinated phenylene group, or trifluoromethyl-substituted phenylene group, which may contain a carbonyl moiety, ester bond, ether bond or hydroxy moiety. R21 to R22 are each independently halogen or a C1-C20 hydrocarbyl group which may contain a heteroatom, a pair of R23 and R24 or R26 and R27 may bond together to form a ring with the sulfur atom to which they are attached. M− is a non-nucleophilic counter ion.
In another aspect, the invention provides a process for forming a pattern comprising the steps of applying the resist composition defined above 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 radiation of wavelength 193 un, KrF excimer laser radiation of wavelength 248 nm, EB, or EUV of wavelength 3 to 15 nm.
The ammonium salt and fluorine-containing polymer (or additive polymer) is a quencher of polymer type which is fully soluble in an alkaline developer. When a resist composition comprising the additive polymer and a base polymer is applied to form a resist film, the additive polymer segregates on the film surface because fluorine-containing units are incorporated therein. The additive polymer is effective for increasing the absorption of exposure light on the resist film surface due to iodine or bromine atoms whereby a sensitizing effect is exerted. The additive polymer is also effective for controlling acid diffusion in proximity to the resist film surface and preventing evaporation of acid from the resist film surface whereby the resist pattern as developed is enhanced in rectangularity and the LWR of line patterns or CDU of hole patterns on top-down observation is improved. Further, the solubility of the resist film surface in alkaline developer is increased whereby bridge defects or pattern collapse after pattern formation is minimized.
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 term “iodized” or “brominated” compound means an iodine or bromine-substituted compound. Also, the terms “group” and “moiety” are interchangeable.
The abbreviations and acronyms have the following meaning.
EB: electron beam
EUV: extreme ultraviolet
Mw: weight average molecular weight
Mn: number average molecular weight
Mw/Mn: molecular weight distribution or dispersity
GPC: gel permeation chromatography
PEB: post-exposure bake
PAG: photoacid generator
LWR: line width roughness
CDU: critical dimension uniformity
Resist Composition
One embodiment of the invention is a resist composition comprising an ammonium salt and fluorine-containing polymer and a base polymer.
Ammonium Salt and Fluorine-Containing Polymer
The ammonium salt and fluorine-containing polymer is defined as comprising repeat units AU having an ammonium salt structure of an iodine or bromine-substituted phenol compound and repeat units of at least one type selected from repeat units FU-1 having a trifluoromethylalcohol group which may be substituted with an acid labile group and repeat units FU-2 having a fluorinated hydrocarbyl group.
The repeat unit AU is preferably a unit having the ammonium salt structure as a pendant and more preferably has the following formula (AU).
In formula (AU), m1 is an integer of 1 to 5, m2 is an integer of 0 to 3, n1 is 1 or 2, and n2 is a positive number in the range: 0<n2/n1≤1.
RA is each independently hydrogen or methyl.
Xbi is iodine or bromine.
X1A is a single bond, phenylene group, ester bond or amide bond. X1B is a single bond or a C1-C20 (n1+1)-valent hydrocarbon group which may contain an ether bond, carbonyl moiety, ester bond, amide bond, sultone ring, lactam ring, carbonate bond, halogen, hydroxy moiety or carboxy moiety.
The C1-C20 (n1+1)-valent hydrocarbon group represented by X1B is a group obtained by removing (n1+1) number of hydrogen atoms from a C1-C20 aliphatic hydrocarbon or C6-C20 aromatic hydrocarbon and may be straight, branched or cyclic. Examples thereof include groups obtained by removing (n1+1) number of hydrogen atoms from C1-C20 saturated hydrocarbons such as methane, ethane, propane, butane, pentane, hexane, heptane, octane, nonane, decane, undecane, dodecane, cyclopropane, cyclobutane, cyclopentane, cyclohexane, methylcyclopentane, ethylcyclopentane, methylcyclohexane, ethylcyclohexane, 1-propylcyclohexane, isopropylcyclohexane, norbomane, adamantane, methylnorbomane, ethylnorbornane, methyladamantane, ethyladamantane, and tetrahydrodicyclopentadiene; groups obtained by removing (n1+1) number of hydrogen atoms from aromatic hydrocarbons such as benzene, toluene, xylene, ethylbenzene, 1-propylbenzene, isopropylbenzene, and naphthalene; and combinations thereof.
In formula (AU), R1, R2 and R3 are each independently hydrogen, a C1-C12 alkyl group, C2-C12 alkenyl group, C6-C12 aryl group or C7-C12 aralkyl group. A pair of R1 and R2, or R1 and X1B may bond together to form a ring with the nitrogen atom to which they are attached, the ring may contain oxygen, sulfur, nitrogen or a double bond. The ring is preferably of 3 to 12 carbon atoms.
Of the groups represented by R1, R2 and R3, the C1-C12 alkyl group may be straight, branched or cyclic, and examples thereof include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl, and n-dodecyl. Examples of the C2-C12 alkenyl group include vinyl, 1-propenyl, 2-propenyl, butenyl, and hexenyl. Examples of the C6-C12 aryl group include phenyl, tolyl, xylyl, 1-naphthyl, and 2-naphthyl. Typical of the C7-C12 aralkyl group is benzyl.
In formula (AU), R4 is a hydroxy group, optionally fluorinated or chlorinated C1-C6 saturated hydrocarbyl group, optionally fluorinated or chlorinated C1-C6 saturated hydrocarbyloxy group, formyl group, optionally fluorinated or chlorinated C2-C7 saturated hydrocarbylcarbonyl group, optionally fluorinated or chlorinated C2-C7 saturated hydrocarbylcarbonyloxy group, optionally fluorinated or chlorinated C2-C7 saturated hydrocarbyloxycarbonyl group, optionally fluorinated or chlorinated C1-C4 saturated hydrocarbylsulfonyloxy group, C6-C10 aryl group, fluorine, chlorine, amino group, nitro group, cyano group, —N(R4A)—C(═O)—R4B, or —N(R4A)—C(═O)—O—R4B. R4A is hydrogen or a C1-C6 saturated hydrocarbyl group. R4B is a C1-C6 saturated hydrocarbyl group or C2-C8 unsaturated aliphatic hydrocarbyl group.
The C1-C6 saturated hydrocarbyl group represented by R4, R4A and R4B may be straight, branched or cyclic and examples thereof include C1-C6 alkyl groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, and n-hexyl, and C3-C6 cycloalkyl groups such as cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. Examples of the saturated hydrocarbyl moiety in the C1-C6 saturated hydrocarbyloxy group, C2-C7 saturated hydrocarbylcarbonyl group, C2-C7 saturated hydrocarbylcarbonyloxy group, and C2-C7 saturated hydrocarbyloxycarbonyl group, represented by R4, are as exemplified above for the saturated hydrocarbyl group. Examples of the saturated hydrocarbyl moiety in the C1-C4 saturated hydrocarbylsulfonyloxy group are as exemplified above for the saturated hydrocarbyl group, but of 1 to 4 carbon atoms. Examples of the C6-C10 aryl group represented by R4 include phenyl and naphthyl.
The C2-C8 unsaturated aliphatic hydrocarbyl group represented by R4B may be straight, branched or cyclic and examples thereof include C2-C8 alkenyl groups such as vinyl, 1-propenyl, 2-propenyl, butenyl and hexenyl, and C3-C8 cyclic unsaturated aliphatic hydrocarbyl groups such as cyclohexenyl.
Examples of the cation in the monomer from which repeat units AU are derived are shown below, but not limited thereto. Herein RA is as defined above.
Examples of the anion in the monomer from which repeat units AU are derived are shown below, but not limited thereto.
The monomer from which repeat units AU are derived is a polymerizable ammonium salt type monomer. This ammonium salt type monomer may be obtained via neutralization reaction of a monomer which is an amine compound of the structure that one hydrogen atom bonded to the nitrogen atom in the cation of the repeat unit AU is removed with an iodine or bromine-substituted phenol compound.
The repeat unit AU is formed via polymerization reaction of the ammonium salt type monomer. The repeat unit AU may also be formed by performing polymerization reaction of the monomer in the form of the amine compound, adding the iodine or bromine-substituted phenol compound to the resulting reaction solution or a solution to containing the purified polymer, and performing neutralization reaction. Although the neutralization reaction is ideally performed under the conditions that the amino group on the amine compound and the phenol compound are in a stoichiometric ratio (molar ratio) of 1:1, it is acceptable that the phenol compound is in excess or short relative to the amino group.
The repeat units FU-1 and FU-2 preferably have the following formulae (FU-1) and (FU-2), respectively.
In formula (FU-1), n3 is 1 or 2.
In formulae (FU-1) and (FU-2), RA is each independently hydrogen or methyl.
In formula (FU-1), X2A is a single bond, phenylene, —O—, —C(═O)—O— or —C(═O)—NH—. X2B is a C1-C12 (n3+1)-valent saturated hydrocarbon group or (n3+1)-valent aromatic hydrocarbon group, which may contain fluorine, hydroxy moiety, ester bond or ether bond.
The C1-C12 (n3+1)-valent saturated hydrocarbon group represented by X2B may be straight, branched or cyclic and examples thereof include groups obtained by removing (n3+1) number of hydrogen atoms from saturated hydrocarbons such as methane, ethane, propane, butane, pentane, hexane, heptane, octane, nonane, decane, undecane, dodecane, cyclopropane, cyclobutane, cyclopentane, cyclohexane, methylcyclopentane, ethylcyclopentane, methylcyclohexane, ethylcyclohexane, 1-propylcyclohexane, isopropylcyclohexane, norbornane, adamantane, methylnorbornane, ethylnorbornane, methyladamantane, ethyladamantane, and tetrahydrodicyclopentadiene. Examples of the (n3+1)-valent aromatic hydrocarbon group represented by X2B include groups obtained by to removing (n3+1) number of hydrogen atoms from aromatic hydrocarbons such as benzene, toluene, xylene, ethylbenzene, 1-propylbenzene, isopropylbenzene, and naphthalene.
In formula (FU-2), X3 is a single bond, phenylene, —O—, —C(═O)—O—X31—X32— or —C(═O)—NH—X31—X32—. X31 is a single bond or C1-C4 alkanediyl group. X32 is a single bond, ester bond, ether bond or sulfonamide bond. Examples of the C1-C4 alkanediyl group include methanediyl, ethane-1,1-diyl, ethane-1,2-diyl, propane-1,1-diyl, propane-1,2-diyl, propane-1,3-diyl, propane-2,2-diyl, butane-1,1-diyl, butane-1,2-diyl, butane-1,3-diyl, butane-2,3-diyl, butane-1,4-diyl, and 1,1-dimethylethane-1,2-diyl.
In formula (FU-1), R5 is a single bond, ester bond, or a C1-C12 saturated hydrocarbylene group. In the saturated hydrocarbylene group, some or all of the hydrogen atoms may be substituted by fluorine. In the saturated hydrocarbylene group, some carbon may be replaced by an ester bond or ether bond. The saturated hydrocarbylene group may be straight, branched or cyclic.
In formula (FU-1), R6 is hydrogen, fluorine, methyl, trifluoromethyl or difluoromethyl. A pair of R5 and R6 may bond together to form a ring with the carbon atom to which they are attached, and the ring may contain an ether bond, fluorine or trifluoromethyl.
In formula (FU-1), R7 is hydrogen or an acid labile group, examples of which will be described later.
In formula (FU-2), R8 is a C1-C20 hydrocarbyl group which is substituted with at least one fluorine, and in which some carbon may be replaced by an ester bond or ether bond. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic, and examples thereof are as will be exemplified later for groups R101 to R105 in formulae (1-1) and (1-2). Of these, C1-C20 saturated hydrocarbyl groups and C6-C20 aryl groups are preferred.
Examples of the monomer from which repeat units (FU-1) are derived are shown below, but not limited thereto. Herein RA and R7 are as defined above.
Examples of the monomer from which repeat units (FU-2) are derived are shown below, but not limited thereto. Herein RA is as defined above.
After a resist film is formed, the ammonium salt and fluorine-containing polymer is likely to segregate on the surface of the resist film because repeat units of at least one type selected from repeat units FU-1 and FU-2 are incorporated therein.
Besides the repeat units AU, FU-1 and FU-2, the ammonium salt and fluorine-containing polymer may further comprise repeat units having an acid generator function. Typical of these repeat units are units having formulae (f1) to (f3) as will be described later.
The fraction of repeat units AU, FU-1 and FU-2 is preferably 0<AU<1.0, 0≤(FU-1)<1.0, 0≤(FU-2)<1.0, and 0<(FU-1)+(FU-2)<1.0; more preferably 0.001≤AU≤0.7, 0≤(FU-1)≤0.95, 0≤(FU-2)≥0.95, and 0.1≤(FU-1)+(FU-2)≤0.99; even more preferably 0.01<AU≤0.5, 0≤(FU-1)≤0.8, 0≤(FU-2)≤0.8, and 0.2≤(FU-1)+(FU-2)≤0.98. Although the ammonium salt and fluorine-containing polymer may further comprise other repeat units as long as the benefits of the invention are not compromised, it is preferred that the polymer do not include other units (i.e., AU+(FU-1)+(FU-2)=1).
The ammonium salt and fluorine-containing polymer preferably has a weight average molecular weight (Mw) of 1,000 to 1,000,000, more preferably 2,000 to 100,000. Also, the polymer preferably has a molecular weight distribution (Mw/Mn) of 1.0 to 3.0. Notably, Mw and Mn are as measured by gel permeation chromatography (GPC) using tetrahydrofuran (THF) solvent versus polystyrene standards.
The ammonium salt and fluorine-containing polymer segregates on the surface of a resist film whereby the solubility of the resist film surface in an alkaline developer is improved for thereby preventing bridging defects and collapse of patterns.
In the resist composition, the ammonium salt and fluorine-containing polymer is preferably present in an amount of 0.001 to 20 parts by weight, more preferably 0.01 to parts by weight per 100 parts by weight of the base polymer, as viewed from sensitivity and acid diffusion controlling effect.
Base Polymer
Where the resist composition is of positive tone, the base polymer comprises repeat units containing an acid labile group, preferably repeat units having the formula (a1) or repeat units having the formula (a2). These units are simply referred to as repeat units (a1) and (a2).
In formulae (a1) and (a2), RA is each independently hydrogen or methyl. R11 and R12 are each independently an acid labile group. R11 and R12 may be the same or different when the base polymer contains both repeat units (a1) and (a2). R13 is fluorine, trifluoromethyl, to a C1-C5 saturated hydrocarbyl group or C1-C5 saturated hydrocarbyloxy group. Y is a single bond, phenylene or naphthylene group, or C1-C12 divalent linking group containing an ester bond and/or lactone ring. Y2 is a single bond or ester bond. The subscript “a” is an integer of 0 to 4.
Examples of the monomer from which the repeat units (a1) are derived are shown below, but not limited thereto. RA and R11 are as defined above.
Examples of the monomer from which the repeat units (a2) are derived are shown below, but not limited thereto. RA and R12 are as defined above.
The acid labile groups represented by R7 in formula (FU-1), R11 in formula (a1), and R12 in formula (a2) 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 of 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 being preferably of 4 to 16 carbon atoms and especially 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 being preferably of 4 to 16 carbon atoms and especially alicyclic.
The base polymer may further comprise repeat units (b) having a phenolic hydroxy group as an adhesive group. Examples of suitable monomers from which repeat units (b) are derived are given below, but not limited thereto. Herein RA is as defined above.
Further, repeat units (c) having another adhesive group selected from hydroxy (other than the foregoing phenolic hydroxy), lactone ring, sultone ring, ether bond, ester bond, sulfonate bond, carbonyl, sulfonyl, cyano, and carboxy groups may also be incorporated in the base polymer. Examples of suitable monomers from which repeat units (c) are derived are given below, but not limited thereto. Herein RA is as defined above.
In another preferred embodiment, the base polymer may further comprise repeat units (d) selected from units of indene, benzofuran, benzothiophene, acenaphthylene, chromone, coumarin, and norbornadiene, or derivatives thereof. Suitable monomers are exemplified below.
The base polymer may further comprise repeat units (e) derived from styrene, vinylnaphthalene, vinylanthracene, vinylpyrene, methyleneindene, vinylpyridine, and vinylcarbazole.
The base polymer may further comprise repeat units (f) derived from an onium salt having a polymerizable unsaturated bond. Preferred repeat units (f) include repeat units having formula (f1), repeat units having formula (f2) and repeat units having formula (f3). These units are simply referred to as repeat units (f1), (f2) and (f3), which may be used alone or in combination of two or more types.
In formulae (f1) to (f3), RA is each independently hydrogen or methyl. Z1 is a single bond, a C1-C6 aliphatic hydrocarbylene group, phenylene group, naphthylene group, or C7-C18 group obtained by combining the foregoing, or —O—Z11—, —C(═O)—O—Z11— or —C(═O)—NH—Z11—. Z11 is a C1-C6 aliphatic hydrocarbylene group, phenylene group, naphthylene group, or C7-C18 group obtained by combining the foregoing, which may contain a carbonyl moiety, ester bond, ether bond or hydroxy moiety. Z2 is a single bond or ester bond. Z3 is a single bond, —Z31—C(═O)—O—, —Z31—O— or —Z31—O—C(═O)—. Z31 is a C1-C12 hydrocarbylene group, phenylene group or C7-C18 group obtained by combining the foregoing, which may contain a carbonyl moiety, ester bond, ether bond, iodine or bromine. Z4 is a methylene, 2,2,2-trifluoro-1,1-ethanediyl or carbonyl group. Z5 is a single bond, methylene, ethylene, phenylene, fluorinated phenylene, trifluoromethyl-substituted phenylene group, —O—Z51—, —C(═O)—O—Z51—, or —C(═O)—NH—Z51—. Z51 is a C1-C6 aliphatic hydrocarbylene group, phenylene group, fluorinated phenylene group, or trifluoromethyl-substituted phenylene group, which may contain a carbonyl moiety, ester bond, ether bond or hydroxy moiety.
In formulae (f1) to (f3), R21 to R28 are each independently halogen or a C1-C20 hydrocarbyl group which may contain a heteroatom. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. Examples thereof are as will be exemplified later for the groups R101 to R105 in formulae (1-1) and (1-2). A pair of R23 and R24 or R26 and R27 may bond together to form a ring with the sulfur atom to which they are attached. Examples of the ring are as will be exemplified later for the ring that R101 and R102 in formula (1-1), taken together, form with the sulfur atom to which they are attached.
In formula (f1), M− is a non-nucleophilic counter ion. Examples of the non-nucleophilic counter ion include halide ions such as chloride and bromide ions; fluoroalkylsulfonate ions such as triflate, 1,1,1-trifluoroethanesulfonate, and nonafluorobutanesulfonate; arylsulfonate ions such as tosylate, benzenesulfonate, 4-fluorobenzenesulfonate, and 1,2,3,4,5-pentafluorobenzenesulfonate; alkylsulfonate ions such as mesylate and butanesulfonate; imide ions such as bis(trifluoromethylsulfonyl)imide, bis(perfluoroethylsulfonyl)imide and bis(perfluorobutylsulfonyl)imide; methide ions such as tris(trifluoromethylsulfonyl)methide and tris(perfluoroethylsulfonyl)methide.
Also included are sulfonate ions having fluorine substituted at α-position as represented by the formula (f1-1) and sulfonate ions having fluorine substituted at α-position and trifluoromethyl substituted at β-position as represented by the formula (f1-2).
In formula (f1-1), R31 is hydrogen or a C1-C20 hydrocarbyl group which may contain an ether bond, ester bond, carbonyl moiety, lactone ring, or fluorine atom. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. Examples thereof are as will be exemplified for the hydrocarbyl group R11′ in formula (1A′).
In formula (f1-2), R32 is hydrogen or a C1-C30 hydrocarbyl or C2-C30 hydrocarbylcarbonyl group, which may contain an ether bond, ester bond, carbonyl moiety or lactone ring. The hydrocarbyl group and the hydrocarbyl moiety in the hydrocarbylcarbonyl group may be saturated or unsaturated and straight, branched or cyclic. Examples thereof are as will be exemplified for the hydrocarbyl group R111 in formula (1A′).
Examples of the cation in the monomer from which repeat unit (f1) is derived are shown below, but not limited thereto. RA is as defined above.
Examples of the cation in the monomer from which repeat unit (f2) or (f3) is derived are as will be exemplified for the cation in the sulfonium salt having formula (1-1).
Examples of the anion in the monomer from which repeat unit (f2) is derived are shown below, but not limited thereto. RA is as defined above.
Examples of the anion in the monomer from which repeat unit (f3) is derived are shown below, but not limited thereto. RA is as defined above.
The attachment of an acid generator to the polymer main chain is effective in restraining acid diffusion, thereby preventing a reduction of resolution due to blur by acid diffusion. Also LWR or CDU is improved since the acid generator is uniformly distributed. Where a base polymer containing repeat units (f), i.e., polymer-bound acid generator is used, the addition of an acid generator of addition type may be omitted.
The base polymer for formulating the positive resist composition comprises repeat units (a1) or (a2) having an acid labile group as essential component and additional repeat units (b), (c), (d), (e), and (f) as optional components. A fraction of units (a1), (a2), (b), (c), (d), (e), and (f) is: preferably 0≤a1<1.0, 0≤a2<1.0, 0<a1+a2<1.0, 0≤b≤0.9, 0≤c≤0.9, 0≤d≤0.8, 0≤e≤0.8, and 0≤f≤0.5; more preferably 0≤a1≤0.9, 0≤a2≤0.9, 0.1≤a1+a2≤0.9, 0≤b≤0.8, 0≤c≤0.8, 0≤d≤0.7, 0≤e≤0.7, and 0≤f≤0.4; and even more preferably 0≤a1≤0.8, 0≤a2≤0.8, 0.1≤a1+a2≤0.8, 0≤b≤0.75, 0≤c≤0.75, 0≤d≤0.6, 0≤e≤0.6, and 0≤f≤0.3. Notably, f=f1+f2+f3, meaning that unit (f) is at least one of units (f1) to (f3), and a1+a2+b+c+d+e+f=1.0.
For the base polymer for formulating the negative resist composition, an acid labile group is not necessarily essential. The base polymer comprises repeat units (b), and optionally repeat units (c), (d), (e), and/or (f). A fraction of these units is: preferably 0<b≤1.0, 0≤c≤0.9, 0≤d≤0.8, 0≤e≤0.8, and 0≤f≤0.5; more preferably 0.2≤b≤1.0, 0≤c≤0.8, 0≤d≤0.7, 0≤e≤0.7, and 0≤f≤0.4; and even more preferably 0.3≤b≤1.0, 0≤c≤0.75, 0≤d≤0.6, 0≤e≤0.6, and 0≤f≤0.3. Notably, f=f1+f2+f3, meaning that unit (f) is at least one of units (f1) to (f3), and b+c+d+e+f=1.0.
The base polymer 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 polymerization 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.
The base polymer should preferably have a 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 THF solvent. A Mw in the range ensures that the resist film has heat resistance and solubility in alkaline developer.
If a base polymer has a wide 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, the base polymer 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.
The base polymer may be a blend of two or more polymers which differ in compositional ratio, Mw or Mw/Mn.
Acid Generator
The resist composition may comprise an acid generator capable of generating a strong acid (referred to as acid generator of addition type, hereinafter). As used herein, the term “strong acid” refers to a compound having a sufficient acidity to induce deprotection reaction of an acid labile group on the base polymer in the case of a chemically amplified positive resist composition, or a compound having a sufficient acidity to induce acid-catalyzed polarity switch reaction or crosslinking reaction in the case of a chemically amplified negative resist composition. The inclusion of such an acid generator ensures that the inventive resist composition functions as a chemically amplified positive or negative resist composition.
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).
As the PAG used herein, sulfonium salts having the formula (1-1) and iodonium salts having the formula (1-2) are also preferred.
In formulae (1-1) and (1-2), R101 to R105 are each independently halogen or a C1-C20 hydrocarbyl group which may contain a heteroatom. Suitable halogen atoms include fluorine, chlorine, bromine and iodine. The C1-C20 hydrocarbyl group 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 saturated cyclic 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; C2-C20 alkynyl groups such as ethynyl, propynyl and butynyl; C3-C20 unsaturated alicyclic hydrocarbyl groups such as cyclohexenyl and norbornenyl; 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 foregoing 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 carbon may be replaced by a moiety containing a heteroatom such as oxygen, sulfur or nitrogen, so that the group may contain a hydroxy moiety, cyano moiety, nitro moiety, carbonyl moiety, ether bond, ester bond, sulfonic ester bond, carbonate bond, lactone ring, sultone ring, carboxylic anhydride or haloalkyl moiety.
Also, R101 and R102 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 structure.
Herein the broken line designates a point of attachment to R103.
Examples of the cation in the sulfonium salt having formula (1-1) are shown below, but not limited thereto.
Examples of the cation in the iodonium salt having formula (1-2) are shown below, but not limited thereto.
In formulae (1-1) and (1-2), Xa− is an anion selected from the following formulae (1A) to (1D).
In formula (1A), Rfa is fluorine or a C1-C40 hydrocarbyl group which may contain a heteroatom. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic, and examples thereof are as will be exemplified for the hydrocarbyl group R111 in formula (1A′).
Of the anions of formula (1A), a structure having the following formula (1A′) is preferred.
In formula (1A′), RHF is hydrogen or trifluoromethyl, preferably trifluoromethyl.
R111 is 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 may be saturated or unsaturated and straight, branched or cyclic. Suitable hydrocarbyl groups include C1-C38 alkyl groups such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, neopentyl, hexyl, heptyl, 2-ethylhexyl, nonyl, undecyl, tridecyl, pentadecyl, heptadecyl, icosanyl; C3-C38 cyclic saturated hydrocarbyl groups such as to cyclopentyl, cyclohexyl, 1-adamantyl, 2-adamantyl, 1-adamantylmethyl, norbornyl, norbornylmethyl, tricyclodecanyl, tetracyclododecanyl, tetracyclododecanylmethyl, dicyclohexylmethyl; C2-C38 unsaturated aliphatic hydrocarbyl groups such as allyl and 3-cyclohexenyl; C6-C38 aryl groups such as phenyl, 1-naphthyl, 2-naphthyl; C7-C38 aralkyl groups such as benzyl and diphenylmethyl; and combinations thereof.
In these 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 carbon may be replaced by a moiety containing a heteroatom such as oxygen, sulfur or nitrogen, so that the group may contain a hydroxy, cyano, carbonyl, ether bond, ester bond, sulfonic acid ester bond, carbonate bond, lactone ring, sultone ring, carboxylic anhydride 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 (1A′), 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 (1A) are as exemplified for the anion having formula (1A) in JP-A 2018-197853 (US 20180335696).
In formula (1B), Rfb1 and Rfb2 are each independently fluorine or a C1-C40 hydrocarbyl group which may contain a heteroatom. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. Suitable hydrocarbyl groups are as exemplified above for R111 in formula (1A′). Preferably Rfb1 and Rfb2 each are fluorine or a straight C1-C4 fluorinated alkyl group. A pair of Rfb1 and Rfb2 may bond together to form a ring with the linkage (—CF2—SO2—N−—SO2—CF2—) to which they are attached, and the ring-forming pair is preferably a fluorinated ethylene or fluorinated propylene group.
In formula (1C), Rfc1, Rfc2 and Rfc3 are each independently fluorine or a C1-C40 hydrocarbyl group which may contain a heteroatom. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. Suitable hydrocarbyl groups are as exemplified above for R111 in formula (1A′). Preferably Rfc1, Rfc2 and Rfc3 each are fluorine or a straight C1-C4 fluorinated alkyl group. A pair of Rfc1 and Rfc2 may bond to together to form a ring with the linkage (—CF2—SO2—C−—SO2—CF2—) to which they are attached, and the ring-forming pair is preferably a fluorinated ethylene or fluorinated propylene group.
In formula (1D), Rfd is a C1-C40 hydrocarbyl group which may contain a heteroatom. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. Suitable hydrocarbyl groups are as exemplified above for R111.
With respect to the synthesis of the sulfonium salt having an anion of formula (1D), reference is made to JP-A 2010-215608 and JP-A 2014-133723.
Examples of the anion having formula (1D) are as exemplified for the anion having formula (1D) in JP-A 2018-197853 (US 20180335696).
The compound having the anion of formula (1D) has a sufficient acid strength to cleave acid labile groups in the base polymer because it is free of fluorine at α-position of sulfo group, but has two trifluoromethyl groups at β-position. Thus the compound is a useful PAG.
Also compounds having the formula (2) are useful as the PAG.
In formula (2), R201 and R202 are each independently halogen or a C1-C30 hydrocarbyl group which may contain a heteroatom. R203 is a C1-C30 hydrocarbylene group which may contain a heteroatom. Any two of R201, R202 and R203 may bond together to form a ring with the sulfur atom to which they are attached. Exemplary rings are the same as described above for the ring that R101 and R102 in formula (1-1), taken together, form with the sulfur atom to which they are attached.
The hydrocarbyl groups R201 and R202 may be saturated or unsaturated and straight, branched or cyclic. Examples thereof include C1-C30 alkyl groups such as methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, n-pentyl, tert-pentyl, n-hexyl, n-octyl, 2-ethylhexyl, n-nonyl, and n-decyl; C3-C30 cyclic saturated hydrocarbyl groups such as cyclopentyl, cyclohexyl, cyclopentylmethyl, cyclopentylethyl, cyclopentylbutyl, cyclohexylmethyl, cyclohexylethyl, cyclohexylbutyl, norbornyl, oxanorbornyl, tricyclo[5.2.1.02,6]decanyl, and adamantyl; C6-C30 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, tert-butylnaphthyl, and anthracenyl; and combinations thereof. In these 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 carbon may be replaced by a moiety containing a heteroatom such as oxygen, sulfur or nitrogen, so that the group may contain a hydroxy, cyano, carbonyl, ether bond, ester bond, sulfonic acid ester bond, carbonate bond, lactone ring, sultone ring, carboxylic anhydride or haloalkyl moiety.
The hydrocarbylene group R203 may be saturated or unsaturated and straight, branched or cyclic. Examples thereof include C1-C30 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, pentadecane-1,15-diyl, hexadecane-1,16-diyl, and heptadecane-1,17-diyl; C3-C30 cyclic saturated hydrocarbylene groups such as cyclopentanediyl, cyclohexanediyl, norbomanediyl and adamantanediyl; C6-C30 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, isobutylnaphthylene, sec-butylnaphthylene, and tert-butylnaphthylene; and combinations thereof. In these 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 carbon may be replaced by a moiety containing a heteroatom such as oxygen, sulfur or nitrogen, so that the group may contain a hydroxy, cyano, carbonyl, ether bond, ester bond, sulfonic acid ester bond, carbonate bond, lactone ring, sultone ring, carboxylic anhydride or haloalkyl moiety. Of the heteroatoms, oxygen is preferred.
In formula (2), LA is a single bond, ether bond or a C1-C20 hydrocarbylene group which may contain a heteroatom. The hydrocarbylene group may be saturated or unsaturated and straight, branched or cyclic. Examples thereof are as exemplified above for R203.
In formula (2), XA, XB, XC and XD are each independently hydrogen, fluorine or trifluoromethyl, with the proviso that at least one of XA, XB, XC and XD is fluorine or trifluoromethyl.
In formula (2), k is an integer of 0 to 3.
Of the PAGs having formula (2), those having formula (2′) are preferred.
In formula (2′), LA is as defined above. RHF is hydrogen or trifluoromethyl, preferably trifluoromethyl. R301, R302 and R303 are each independently hydrogen or a C1-C20 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 R111 in formula (1A′). The subscripts x and y are each independently an integer of 0 to 5, and z is an integer of 0 to 4.
Examples of the PAG having formula (2) are as exemplified for the PAG having formula (2) in JP-A 2017-026980.
Of the foregoing PAGs, those having an anion of formula (1A′) or (1D) are especially preferred because of reduced acid diffusion and high solubility in the solvent. Also those having formula (2′) are especially preferred because of extremely reduced acid diffusion.
Also, a sulfonium or iodonium salt having an anion containing an iodized or brominated aromatic ring may be used as the PAG. Suitable are sulfonium and iodonium salts having the formulae (3-1) and (3-2).
In formulae (3-1) and (3-2), p is an integer of 1 to 3, q is an integer of 1 to 5, and r is an integer of 0 to 3, meeting 1≤q+r≤5. Preferably, q is 1, 2 or 3, more preferably 2 or 3, and r is 0, 1 or 2.
In formulae (3-1) and (3-2), XB1 is iodine or bromine, and may be the same or different when p and/or q is 2 or more.
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.
L2 is a single bond or a C1-C20 divalent linking group when p is 1, and a C1-C20 tri- or tetravalent linking group which may contain oxygen, sulfur or nitrogen when p is 2 or 3.
R401 is a hydroxy group, carboxy group, fluorine, chlorine, bromine, amino group, or a C1-C20 saturated hydrocarbyl, C1-C20 saturated hydrocarbyloxy, C2-C20 saturated hydrocarbylcarbonyl, C2-C20 saturated hydrocarbyloxycarbonyl, C2-C20 saturated hydrocarbylcarbonyloxy or C1-C20 saturated hydrocarbylsulfonyloxy group, which may contain fluorine, chlorine, bromine, hydroxy, amino or ether bond, or —N(R401A)(R401B), —N(R401C)—C(═O)—R401D or —N(R401C)—C(═O)—O—R401D. R401A and R401B are each independently hydrogen or a C1-C6 saturated hydrocarbyl group. R401C 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. R401D is a C1-C16 aliphatic hydrocarbyl group, C6-C14 aryl group 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 saturated hydrocarbyl, saturated hydrocarbyloxy, saturated hydrocarbyloxycarbonyl, saturated hydrocarbylcarbonyl, and saturated hydrocarbylcarbonyloxy groups may be straight, branched or cyclic. Groups R401 may be the same or different when p and/or r is 2 or more. Of these, R401 is preferably hydroxy, —N(R401C)—C(═O)—R401D, —N(R401C)—C(═O)—O—R401D, fluorine, chlorine, bromine, methyl or methoxy.
In formulae (3-1) and (3-2), Rf1 to Rf4 are each independently hydrogen, fluorine or trifluoromethyl, at least one of Rf1 to Rf4 being fluorine or trifluoromethyl. Rf1 and Rf2, taken together, may form a carbonyl group. Preferably, both Rf3 and Rf4 are fluorine.
R402 to R406 are each independently halogen or a C1-C20 hydrocarbyl group which may contain a heteroatom. The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. Examples thereof include those exemplified above for the hydrocarbyl groups R101 to R105 in formulae (1-1) and (1-2). In these groups, some or all of the hydrogen atoms may be substituted by hydroxy, carboxy, halogen, cyano, nitro, mercapto, sultone, sulfone, or sulfonium salt-containing moieties, and some carbon may be replaced by an ether bond, ester bond, carbonyl moiety, amide bond, carbonate bond or sulfonic acid ester bond. R402 and R403 may bond together to form a ring with the sulfur atom to which they are attached. Exemplary rings are the same as described above for the ring that R101 and R102 in formula (1-1), taken together, form with the sulfur atom to which they are attached.
Examples of the cation in the sulfonium salt having formula (3-1) include those exemplified above as the cation in the sulfonium salt having formula (1-1). Examples of the cation in the iodonium salt having formula (3-2) include those exemplified above as the cation in the iodonium salt having formula (1-2).
Examples of the anion in the onium salts having formulae (3-1) and (3-2) are shown below, but not limited thereto. Herein XBI is as defined above.
When used, the acid generator of addition type is preferably added in an amount of 0.1 to 50 parts, and more preferably to 40 parts by weight per 100 parts by weight of the base polymer. The resist composition functions as a chemically amplified resist composition when the base polymer includes repeat units (f) and/or the acid generator of addition type is contained.
Organic Solvent
An organic solvent may be added to the resist composition. 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, 1-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, which may be used alone or in admixture.
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.
Other Components
With the foregoing components, other components such as a quencher other than the ammonium salt and fluorine-containing polymer (referred to as other quencher, hereinafter), surfactant, dissolution inhibitor, and crosslinker may be blended in any desired combination to formulate a positive or negative resist composition. This positive or negative resist composition has a very high sensitivity in that the dissolution rate in developer of the base polymer in exposed areas is accelerated by catalytic reaction. In addition, the resist film has a high dissolution contrast, resolution, exposure latitude, and process adaptability, and provides a good pattern profile after exposure, and minimal proximity bias because of to restrained acid diffusion. By virtue of these advantages, the composition is fully useful in commercial application and suited as a pattern-forming material for the fabrication of VLSIs.
The other 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 acid 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.
Amine compounds having an iodized aromatic group as described in JP-A 2020-027297 are also useful quenchers. These compounds exert a sensitizing effect due to remarkable absorption of EUV and an acid diffusion controlling effect due to a high molecular weight.
Onium salts such as sulfonium salts, iodonium salts and ammonium salts of sulfonic acids which are not fluorinated at α-position as described in U.S. Pat. No. 8,795,942 (JP-A 2008-158339) and similar onium salts of carboxylic acid may also be used as the other 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 and a carboxylic acid are 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.
Examples of the quencher include a compound (onium salt of α-non-fluorinated sulfonic acid) having the formula (4) and a compound (onium salt of carboxylic acid) having the formula (5).
In formula (4), R501 is hydrogen or a C1-C40 hydrocarbyl group which may contain a heteroatom, exclusive of the hydrocarbyl group in which the hydrogen bonded to the carbon atom at α-position of the sulfo group is substituted by fluorine or fluoroalkyl moiety.
The hydrocarbyl group may be saturated or unsaturated and straight, branched or cyclic. Examples thereof include alkyl groups such as methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, tert-pentyl, n-pentyl, n-hexyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl; 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; alkenyl groups such as vinyl, allyl, propenyl, butenyl and hexenyl; cyclic unsaturated aliphatic hydrocarbyl groups such as cyclohexenyl; aryl groups such as phenyl, naphthyl, alkylphenyl groups (e.g., 2-methylphenyl, 3-methylphenyl, 4-methylphenyl, 4-ethylphenyl, 4-tert-butylphenyl, 4-n-butylphenyl), dialkylphenyl 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); heteroaryl groups such as thienyl; and aralkyl groups such as benzyl, 1-phenylethyl and 2-phenylethyl.
In these groups, some hydrogen may be substituted by a moiety containing a heteroatom such as oxygen, sulfur, nitrogen or halogen, and some carbon may be replaced by a moiety containing a heteroatom such as oxygen, sulfur or nitrogen, so that the group may contain a hydroxy moiety, cyano moiety, carbonyl moiety, ether bond, ester bond, sulfonic acid ester bond, carbonate bond, lactone ring, sultone ring, carboxylic anhydride, or haloalkyl moiety. Suitable heteroatom-containing hydrocarbyl groups include 4-hydroxyphenyl, alkoxyphenyl groups such as 4-methoxyphenyl, 3-methoxyphenyl, 2-methoxyphenyl, 4-ethoxyphenyl, 4-tert-butoxyphenyl, 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 formula (5), R502 is a C1-C40 hydrocarbyl group which may contain a heteroatom. Examples of the hydrocarbyl group R502 are as exemplified above for the hydrocarbyl group R501. Also included are fluorinated alkyl groups such as trifluoromethyl, trifluoroethyl, 2,2,2-trifluoro-1-methyl-1-hydroxyethyl, 2,2,2-trifluoro-1-(trifluoromethyl)-1-hydroxyethyl, and fluorinated aryl groups such as pentafluorophenyl and 4-trifluoromethylphenyl.
In formulae (4) and (5), Mq+ is an onium cation. The onium cation is preferably selected from sulfonium, iodonium and ammonium cations, more preferably sulfonium and iodonium cations. Exemplary sulfonium cations are as exemplified above for the cation in the sulfonium salt having formula (1-1). Exemplary iodonium cations are as exemplified above for the cation in the iodonium salt having formula (1-2).
A sulfonium salt of iodized benzene ring-containing carboxylic acid having the formula (6) is also useful as the other quencher.
In formula (6), x′ is an integer of 1 to 5, y′ is an integer of 0 to 3, and z′ is an integer of 1 to 3.
In formula (6), R601 is hydroxy, fluorine, chlorine, bromine, amino, nitro, cyano, or a C1-C6 saturated hydrocarbyl, C1-C6 saturated hydrocarbyloxy, C2-C6 saturated hydrocarbylcarbonyloxy or C1-C4 saturated hydrocarbylsulfonyloxy group, in which some or all hydrogen may be substituted by halogen, or —N(R601A)—C(═O)—R601B, or —N(R601A)—C(═O)—O—R601B. R601A is hydrogen or a C1-C6 saturated hydrocarbyl group. R601B is a C1-C6 saturated hydrocarbyl or C2-C8 unsaturated aliphatic hydrocarbyl group.
In formula (6), L11 is a single bond, or a C1-C20 (z′+1)-valent linking group which may contain at least one moiety selected from ether bond, carbonyl moiety, ester bond, amide bond, sultone ring, lactam ring, carbonate bond, halogen, hydroxy moiety, and carboxy moiety. The saturated hydrocarbyl, saturated hydrocarbyloxy, saturated hydrocarbylcarbonyloxy, and saturated hydrocarbylsulfonyloxy groups may be straight, branched or cyclic. Groups R60 may be the same or different when y′ and/or z′ is 2 or 3.
In formula (6), R602, R603 and R604 are each independently halogen, or a C1-C20 to 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 R101 to R105 in formulae (1-1) and (1-2). In these groups, some or all hydrogen may be substituted by hydroxy, carboxy, halogen, oxo, cyano, nitro, sultone, sulfone, or sulfonium salt-containing moiety, or some carbon is may be replaced by an ether bond, ester bond, carbonyl moiety, amide bond, carbonate bond or sulfonic acid ester bond. Also R602 and R603 may bond together to form a ring with the sulfur atom to which they are attached.
Examples of the compound having formula (6) include those described in U.S. Pat. No. 10,295,904 (JP-A 2017-219836). These compounds exert a sensitizing effect due to remarkable absorption and an acid diffusion controlling effect.
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 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 used, the other quencher is preferably added in an amount of 0 to 5 parts, more preferably 0 to 4 parts by weight per 100 parts by weight of the base polymer. The other quencher may be used alone or in admixture.
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. When used, the surfactant is preferably added in an amount of 0.0001 to parts by weight per 100 parts by weight of the base polymer. The surfactant may be used alone or in admixture.
When the resist composition is of positive tone, the 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]).
When the resist composition is of positive tone and contains a dissolution inhibitor, the dissolution inhibitor is preferably added in an amount of 0 to 50 parts, more preferably to 40 parts by weight per 100 parts by weight of the base polymer. The dissolution inhibitor may be used alone or in admixture.
When the resist composition is of negative tone, a negative pattern may be formed by adding a crosslinker to reduce the dissolution rate of a resist film in exposed area. Suitable crosslinkers 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.
Examples of the epoxy compound 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 guanamme compounds having 1 to 4 methylol groups methoxymethylated and mixtures thereof, tetramethoxyethyl guanamine, tetraacyloxyguanamme, 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 to 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 group-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.
When the resist composition is of negative tone and contains a crosslinker, 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. The crosslinker may be used alone or in admixture.
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 acetylene alcohols may be used alone or in admixture.
Pattern Forming Process
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.
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 hot plate 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.
The resist film is then exposed to a desired pattern of high-energy radiation such as UV, deep-UV, EB, EUV of wavelength 3-15 nm, x-ray, soft x-ray, excimer laser light, γ-ray or synchrotron radiation. When UV, deep-UV, EUV, x-ray, soft x-ray, excimer laser light, γ-ray or synchrotron radiation is used as the high-energy radiation, the resist film is exposed thereto directly or through a mask having a desired pattern in a dose of preferably about 1 to 200 mJ/cm2, more preferably about 10 to 100 mJ/cm2. When EB is used as the high-energy radiation, the resist film is exposed thereto directly or through a mask having a desired pattern in a dose of preferably about 0.1 to 100 μC/cm2, more preferably about 0.5 to 50 μC/cm2. It is appreciated that the inventive resist composition is suited in micropatterning using KrF excimer laser, ArF excimer laser, EB, EUV, x-ray, soft x-ray, γ-ray or synchrotron radiation, especially in micropatterning using EB or EUV.
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 in 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 (TMAMH), 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 shrink.
Examples of the invention are given below by way of illustration and not by way of limitation. The abbreviation “pbw” is parts by weight.
Monomer M-1 was prepared by mixing 2-(dimethylamino)ethyl methacrylate with 2,4,6-triiodophenol in a molar ratio of 1:1. Similarly, Monomers M-2 to M-14 and cM-1 were prepared by mixing a nitrogen-containing monomer with an iodine or bromine-substituted phenol compound or unsubstituted phenol (for comparison).
Fluorine-containing monomers FM-1 to FM-11 and PAG monomer PM-1 used in the synthesis of polymers have the structure shown below.
Synthesis of Polymer AP-1
A 2-L flask was charged with 6.3 g of M-1, 26.5 g of FM-1, and 60 g of tetrahydrofuran (THF) solvent. The reactor was cooled at −70° C. in a 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) as polymerization initiator was added. The reactor was heated at 60° C. and held at the temperature for 15 hours for reaction. The reaction solution was poured into 1 L of isopropyl alcohol (IPA) for precipitation. The resulting white solid was collected by to filtration and dried in vacuum at 60° C., obtaining Polymer AP-1. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-2
A 2-L flask was charged with 6.3 g of M-1, 20.8 g of FM-1, 6.6 g of 3,3,4,4,5,5,6,6,6-nonafluorohexyl methacrylate, and 60 g of THE solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for 15 hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-2. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-3
A 2-L flask was charged with 7.0 g of M-2, 20.8 g of FM-1, 6.0 g of 1H,1H,5H-octafluoropentyl methacrylate, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for to 15 hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-3. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-4
A 2-L flask was charged with 5.7 g of M-3, 34.0 g of FM-2, 6.0 g of 1H,1H,5H-octafluoropentyl methacrylate, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-4. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-5
A 2-L flask was charged with 8.9 g of M-4, 24.0 g of FM-3, 7.1 g of 1,1,1,3,3,3-hexafluoroisopropyl methacrylate, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-5. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-6
A 2-L flask was charged with 3.9 g of M-5, 18.0 g of FM-4, 7.1 g of 1,1,1,3,3,3-hexafluoroisopropyl methacrylate, and 60 g of THE solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-6. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-7
A 2-L flask was charged with 6.5 g of M-6, 26.5 g of FM-5, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for 15 hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-7. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-8
A 2-L flask was charged with 6.0 g of M-7, 43.0 g of FM-6, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for 15 hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-8. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-9
A 2-L flask was charged with 4.6 g of M-8, 15.7 g of FM-7, 9.0 g of 1H,1H,5H-octafluoropentyl methacrylate, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-9. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-10
A 2-L flask was charged with 4.7 g of M-9, 19.7 g of FM-8, 9.0 g of 1H,1H,5H-octafluoropentyl methacrylate, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-10. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-11
A 2-L flask was charged with 5.1 g of M-10, 20.7 g of FM-8, 9.0 g of 1H,1H,5H-octafluoropentyl methacrylate, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for to 15 hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-11. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-12
A 2-L flask was charged with 6.4 g of M-11, 19.7 g of FM-8, 9.0 g of 1H,1H,5H-octafluoropentyl methacrylate, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-12. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-13
A 2-L flask was charged with 7.5 g of M-12, 19.7 g of FM-8, 9.0 g of 1H,1H,5H-octafluoropentyl methacrylate, and 60 g of THE solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-13. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-14
A 2-L flask was charged with 6.5 g of M-13, 19.7 g of FM-8, 9.0 g of 1H,1H,5H-octafluoropentyl methacrylate, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for 15 hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-14. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-15
A 2-L flask was charged with 5.2 g of M-14, 19.7 g of FM-8, 9.0 g of 1H,1H,5H-octafluoropentyl methacrylate, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-15. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-16
A 2-L flask was charged with 6.5 g of M-13, 11.9 g of FM-9, 9.8 g of FM-8, 9.0 g of 1H,1H,5H-octafluoropentyl methacrylate, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-16. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-17
A 2-L flask was charged with 6.5 g of M-13, 11.7 g of FM-10, 9.8 g of FM-8, 9.0 g of 1H,1H,5H-octafluoropentyl methacrylate, and 60 g of THE solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-17. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-18
A 2-L flask was charged with 6.4 g of M-11, 19.7 g of FM-8, 13.3 g of FM-11, and 60 g of THE solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for 15 hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-18. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Polymer AP-19
A 2-L flask was charged with 6.4 g of M-11, 26.2 g of FM-8, 7.4 g of PM-1, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for 15 hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Polymer AP-19. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Comparative Polymer cP-1
A 2-L flask was charged with 40.0 g of FM-2, 6.0 g of 1H,1H,5H-octafluoropentyl methacrylate, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for 15 hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Comparative Polymer cP-1. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Comparative Polymer cP-2
A 2-L flask was charged with 1.6 g of 2-(dimethylamino)ethyl methacrylate, 35.0 g of FM-2, 6.0 g of 1H,1H,5H-octafluoropentyl methacrylate, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for 15 hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Comparative Polymer cP-2. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
Synthesis of Comparative Polymer cP-3
A 2-L flask was charged with 2.5 g of cM-1, 35.0 g of FM-2, 6.0 g of 1H,1H,5H-octafluoropentyl methacrylate, and 60 g of THF solvent. The reactor was cooled at −70° C. in a 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. and held at the temperature for hours for reaction. The reaction solution was poured into 1 L of IPA for precipitation. The resulting white solid was collected by filtration and dried in vacuum at 60° C., obtaining Comparative Polymer cP-3. The polymer was analyzed for composition by 13C- and 1H-NMR spectroscopy and for Mw and Mw/Mn by GPC.
It is noted that the foregoing inventive and comparative polymers are shown under the column of “additive polymer” in Tables 1 and 2.
Synthesis of Base Polymers BP-1 and BP-2
Base polymers (BP-1 and BP-2) were prepared by combining suitable monomers, effecting copolymerization reaction thereof in THE solvent, pouring the reaction solution into methanol for precipitation, repeatedly washing the solid precipitate with hexane, isolation, and drying. The resulting polymers were analyzed for composition by 1H-NMR spectroscopy, and for Mw and Mw/Mn by GPC versus polystyrene standards using THF solvent.
(1) Preparation of Resist Compositions
Resist compositions were prepared by dissolving the selected components in a solvent in accordance with the recipe shown in Tables 1 and 2, and filtering through a filter having a pore size of 0.2 μm. The solvent contained 100 ppm of surfactant PolyFox PF-636 (Omnova Solutions Inc.). The resist compositions of Examples 1 to 23 and Comparative Examples 1 to 4 were of positive tone while the resist compositions of Example 24 and Comparative Example 5 were of negative tone. The components in Tables 1 and 2 are as identified below.
Organic Solvents:
PGMEA (propylene glycol monomethyl ether acetate)
DAA (diacetone alcohol)
Acid generators: PAG-1 to PAG-4 of the following structural formulae
Quenchers: Q-1 to Q-4 of the following structural formulae
(2) EUV Lithography Test
Each of the resist compositions in Tables 1 and 2 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., silicon content 43 wt %) and prebaked on a hotplate at 100° C. for 60 seconds to form a resist film of 40 nm thick. Using an EUV scanner NXE3300 (ASML, NA 0.33, a 0.9, 900 dipole illumination), the resist film was exposed to EUV through a mask bearing a 18-nm 1:1 line-and-space (LS) pattern in the case of positive resist film or a mask bearing a 22-nm 1:1 LS pattern in the case of negative resist film. The resist film was baked (PEB) on a hotplate at the temperature shown in Tables 1 and 2 to for 60 seconds and developed in a 2.38 wt % TMAH aqueous solution for 30 seconds to form a LS pattern having a size of 18 nm in Examples 1 to 23 and Comparative Examples 1 to 4 or a LS pattern having a size of 22 nm in Example 24 and Comparative Example 5.
The resist pattern was observed under CD-SEM (CG-5000, Hitachi High-Technologies Corp.). The exposure dose that provides a LS pattern at 1:1 is reported as sensitivity. The LWR of the pattern at that dose was measured. Reported as a window is the size of the thickest line in the under-exposed region where no stringy bridges are formed between lines minus the size of the thinnest line in the over-exposed region where no lines collapse.
The resist composition is shown in Tables 1 and 2 together with the sensitivity, window and LWR of EUV lithography.
It is evident from Tables 1 and 2 that resist compositions having an ammonium salt and fluorine-containing polymer added thereto offer a high sensitivity, reduced LWR and broad window.
Japanese Patent Application No. 2020-123046 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 |
|---|---|---|---|
| 2020-123046 | Jul 2020 | JP | national |
| Number | Name | Date | Kind |
|---|---|---|---|
| 7598016 | Kobayashi | Oct 2009 | B2 |
| 9152050 | Hatakeyama | Oct 2015 | B2 |
| 9250523 | Tatakeyama et al. | Feb 2016 | B2 |
| 10495968 | Aqad et al. | Dec 2019 | B2 |
| 20090011365 | Kobayashi et al. | Jan 2009 | A1 |
| 20100136486 | Harada | Jun 2010 | A1 |
| Number | Date | Country |
|---|---|---|
| 2007-297590 | Nov 2007 | JP |
| 2008-239918 | Oct 2008 | JP |
| 2009-31767 | Feb 2009 | JP |
| 2013083957 | May 2013 | JP |
| 2014-67012 | Apr 2014 | JP |
| 2014-67014 | Apr 2014 | JP |
| 2015-161823 | Sep 2015 | JP |
| 2019-1997 | Jan 2019 | JP |
| 2015129355 | Sep 2015 | WO |
| Entry |
|---|
| Translated Description of Ando (JP-2013083957-A) (Year: 2013). |
| Translated Claims of Ando (JP-2013083957-A) (Year: 2013). |
| Translated Caims of Ando (Year: 2013). |
| Translated Claims of Ando (Year: 2013). |
| Translated Description of Ando (Year: 2013). |
| Number | Date | Country | |
|---|---|---|---|
| 20220026804 A1 | Jan 2022 | US |
