Patent Application
20110183264
The present invention relates to a resist processing method and a use of a positive type resist composition, and in particular, relates to a resist processing method used in the formation of a micro resist pattern through a double patterning method or a double imaging method and the use of the positive type resist composition.
In recent years, there is an increasing demand for miniaturization of micro-processing for semiconductors using lithographic techniques. A double patterning method (for example, Patent Document 1) and a double imaging method (for example, Non-Patent Document 1) have been proposed as processes that realize a line width in a resist pattern of 32 nm or less. A double patterning method as used herein represents a method which uses double the spacing of the target resist pattern to execute normal exposure, developing and etching steps thereby executing a first transcription and then, in the resulting spaces, executes again the same exposure, developing and etching steps thereby executing a second transcription, and obtain the target micro resist pattern. A double imaging method is a method which uses double the spacing of the target resist pattern to execute normal exposure, developing steps, and processes the resist pattern using a chemical solution termed a freezing agent, thereafter, executes again the same exposure and developing with the spaces thereby obtaining the target micro resist pattern.
Patent Document 1: JP-2007-311508-A
Non-Patent Document 1: Proceedings of SPIE. Vol. 6520, 65202F (2007)
The present invention has the object of providing a method of resist processing and a use of a positive type resist composition that enable a double patterning method or a double imaging method.
The present inventions are as follows.
<1>
A resist processing method comprising the steps of:
(1) forming a first resist film by applying a first resist composition comprising:
a resin (A) including a structural unit represented by the formula (XX), and having an acid-labile group, being insoluble or poorly soluble in alkali aqueous solution, and being rendered soluble in alkali aqueous solution through the action of an acid, and
a photo acid generator (B)
onto a substrate and drying;
(2) prebaking the first resist film;
(3) exposing the first resist film;
(4) post-exposure baking of the first resist film;
(5) developing with a first alkali developer to obtain a first resist pattern;
(6) hard-baking the first resist pattern,
(7) obtaining a second resist film by applying a second resist composition onto the first resist pattern, and then drying;
(8) pre-baking the second resist film;
(9) exposing the second resist film;
(10) post-exposure baking the second resist film; and
(11) developing with a second alkali developer to obtain a second resist pattern.
wherein, Ra1 represents a hydrogen atom, a halogen atom or a C1 to C3 saturated hydrocarbon group which may be substituted with a halogen atom;
Ra2 represents a single bond or a divalent organic group;
Ra3 represents a hydrogen atom, a C1 to C12 saturated hydrocarbon group which may be substituted with a hydroxy group, or a group —Ra3′—O—Ra3′—, wherein, Ra3′ represents a C1 to C10 saturated hydrocarbon group which may be substituted with a hydroxy group; and
Ra4 represent a C1 to C12 saturated hydrocarbon group.
<2>
The resist processing method according to <1>, wherein the first resist composition further contains a cross-linking agent (C).
<3>
The resist processing method according to <1> or <2>, wherein the cross-linking agent (C) is at least one selected from the group consisting of a urea cross-linking agent, an alkylene urea cross-linking agent and a glycoluril cross-linking agent.
<4>
The resist processing method according to any one of <1> to <3>, wherein the content of the cross-linking agent (C) is 0.5 to 30 parts by weight relative to 100 parts by weight of the resin.
<5>
The resist processing method according to any one of <1> to <4>, wherein the acid-labile group of the resin (A) is a group having an alkyl ester group or lactone ring, in which a carbon atom that bonds to an oxygen atom of —COO— is a quaternary carbon atom, or a group having a carboxylate.
<6>
The resist processing method according to any one of <1> to <5>, wherein the photo acid generator (B) is a compound represented by the formula (I).
wherein, Ra1 and Ra2 independently represent a C1 to C30 linear or branched chain, or cyclic hydrocarbon group, a five- to nine-membered heterocyclic group containing oxygen atom, or a group —Ra1′—O—Ra2′—, wherein, Ra1′ and Ra2′ independently represent a C1 to C29 linear or branched chain, or cyclic hydrocarbon group, a five- to nine-membered heterocyclic group containing oxygen atom, the Ra1, Ra2, Ra1′ and Ra2′ may be substituted with at least one selected from the group consisting of an oxo group, a C1 to C6 alkyl group, a C1 to C6 alkoxy group, a C1 to C4 perfluoroalkyl group, a C1 to C6 hydroxyalkyl group, a hydroxy group and a cyano group;
A+ represents an organic counter ion;
Y1 and Y2 independently represent a fluorine atom or a C1 to C6 perfluoroalkyl group;
g represents 0 or an integer of 1.
<7>
The resist processing method according to any one of <1> to <5>, wherein the photo acid generator (B) is a compound represented by the formula (III).
wherein Y1 and Y2 independently represent a fluorine atom or a C1 to C6 perfluoroalkyl group;
X represents —OH or —Y—OH, wherein, Y represents a C1 to C6 linear or branched chain alkylene group;
n represents an integer of 1 to 9;
A+ represents an organic counter ion.
<8>
The resist processing method according to any one of <1> to <7>, wherein the photo acid generator (B) is a compound containing one or more cations selected from the group consisting of the formulae (IIa), (IIb), (IIc), (IId) and (IV).
wherein P1 to P5 and P10 to P21 independently represent a hydrogen atom, a hydroxy group, a C1 to C12 alkyl group or a C1 to C12 alkoxy group;
P6 and P7 independently represent a C1 to C12 alkyl group or a C3 to C12 cycloalkyl group, or P6 and P7 are bonded to form a C3 to C12 divalent hydrocarbon group;
P8 represents a hydrogen atom;
P9 represents a C1 to C12 alkyl group, a C3 to C12 cycloalkyl group or an optionally substituted aromatic group, or P8 and P9 are bonded to form a C3 to C12 divalent hydrocarbon group;
D represents a sulfur atom or an oxygen atom;
m represents 0 or 1; and
r represents an integer of 1 to 3.
<9>
The resist processing method according to any one of <1> to <8>, which further contains a thermal acid generator (D).
<10>
A use of a positive type resist composition comprising
a resin (A) including a structural unit represented by the formula (XX), and having an acid-labile group, being insoluble or poorly soluble in alkali aqueous solution, and being rendered soluble in alkali aqueous solution through the action of an acid, and a photo acid generator (B).
wherein, Ra1 represents a hydrogen atom, a halogen atom or a C1 to C3 saturated hydrocarbon group which may be substituted with a halogen atom;
Ra2 represents a single bond or a divalent organic group;
Ra3 represents a hydrogen atom, a C1 to C12 saturated hydrocarbon group which may be substituted with a hydroxy group, or a group —Ra3′—O—Ra3′—, wherein, Ra3′ represents a C1 to C10 saturated hydrocarbon group which may be substituted with a hydroxy group); and
Ra4 represent a C1 to C12 saturated hydrocarbon group, for forming a pattern through a double patterning method or a double imaging method.
According to the method of resist processing of the present invention, double patterning method and a double imaging method are enabled, that is a first-layer resist pattern can be formed in a desire shape more accurately with reliability, as well as the shape of the first-layer resist pattern is maintained without deforming even through the processing of second and subsequent layers, as a result, an extremely fine pattern can be formed.
The resin (A) in the resist composition of the present invention includes a structural unite represented by the formula (XX) described above, has an acid-labile group, and prior to exposure, is insoluble or poorly soluble in an alkali aqueous solution, the resin can be dissolved in an alkali aqueous solution as a result of cleaving through the catalytic action on the acid-labile groups in the resin by acid produced from a photo acid generator (B) during exposure. Meanwhile, in unexposed portions of the resin, alkali insolubility characteristics are retained. The resist composition enables formation of a positive type resist pattern by subsequent development using an alkali aqueous solution. Here, “insoluble or poorly soluble in alkali aqueous solution” means a solubility wherein about 100 mL or more of alkali aqueous solution generally used as a developer is required, in order to generally dissolve 1 g or 1 mL of the resist composition, although this can vary, depending on the kinds of the alkali aqueous solutions, concentration thereof, and the like. “Soluble” means solubility wherein less than 100 mL of the alkali aqueous solution is enough to dissolve 1 g or 1 mL of the resist composition.
As described above, the acid-labile group in the resin (A) used in the present invention means a group which undergoes cleavage or tends to undergo cleavage by an acid produced from the photo acid generator (B) described below.
In the formula (XX), examples of the halogen atom include fluorine atom, bromine atom, chlorine atom or iodine atom.
Examples of the saturated hydrocarbon group may be either a chain or a cyclic hydrocarbon, among these, the chain saturated hydrocarbon, in particular, an alkyl group is preferable. Examples of the alkyl group include methyl group, ethyl group, n-propyl group, iso-propyl group, n-butyl group, sec-butyl group, tert-butyl group, pentyl group, hexyl group, octyl group and 2-ethylhexyl group. Examples of the cyclic hydrocarbon group include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclodecyl, cyclohexenyl, bicyclobutyl, bicyclohexyl, 8,9,10-trinorbonyl.
Examples of the divalent organic group include an alkylene having 1 to 6 carbon atoms. The —CH2— in the alkylene group may be replaced by —O— or —CO—. Examples of the alkylene group include a group represented by (Y-1) to (Y-31).
Examples of the structural unit represented by the formula (XX) include the followings. In the following formula, h is 2 or 3, and k is 2 to 12.
The resin (A) also has the acid-labile group.
Examples thereof include;
a group having an alkyl ester group in which a carbon atom that bonds to the oxygen atom of —COO— is a quaternary carbon atom;
a group having a lactone ring in which a carbon atom that bonds to the oxygen atom of —COO— is a quaternary carbon atom;
a group having a carboxylate such as acetal type ester and alicyclic ester.
Among these, preferred is a group giving a carboxyl group by the action of the acid which is produced from the photo acid generator (B) described below. Here a quaternary carbon atom means a carbon atom which bonds to substituents other than a hydrogen atom and does not bond to hydrogen atom. In particular, the carbon atom of the carbon atom that bonds to an oxygen atom of —COO— is preferably a quaternary carbon atom bonding to three carbon atoms as the acid-labile group.
When a group having carboxylate, which is one of the acid-labile group, is exemplified as “R ester of —COOR”, examples include an alkyl ester in which a carbon atom that bonds to the oxygen atom of —COO— is a quaternary carbon atom such as a tert-butyl ester group, typically “—COO—C(CH3)3”;
an acetal type ester group or lactone ring-containing group, such as methoxymethyl ester, ethoxymethyl ester, 1-ethoxyethyl ester, 1-isobutoxyethyl ester, 1-isopropoxyethyl ester, 1-ethoxypropyl ester, 1-(2-methoxyethoxy)ethyl ester, 1-(2-acetoxyethoxy)ethyl ester, 1-[2-(1-adamantyloxy)ethoxy]ethyl ester, 1-[2-(1-adamantanecarbonyloxy)ethoxy]ethyl ester, tetrahydro-2-furyl ester and tetrahydro-2-pyranyl ester group;
an alicyclic ester group in which a carbon atom bonding to the oxygen atom of —COO— is quaternary carbon atom, such as an isobornyl ester, 1-alkykycloalkyl ester, 2-alkyl-2-adamantyl ester and 1-(1-adamantyl)-1-alkylalkyl ester group.
Examples of such group having an carboxylate include a group having (meth)acrylate, a group having norbornene carboxylate, a group having tricyclodecene carboxylate, and a group having tetracyclodecene caroxylate.
The resin (A) can be produced by addition polymerization of a monomer having an acid-labile group and an olefinic double bonds.
Monomers having a bulky group such as an alicyclic structure, in particular, a bridged structure as an acid-labile group (e.g. a 2-alkyl-2-adamantyl group and 1-(1-adamantyl)-1-alkylalkyl group) are preferable as the monomer used, since resolution of the obtained resist has a tendency to be excellent. Examples of such monomer having the bulky group include a 2-alkyl-2-adamantyl (meth)acrylate, a 1-(1-adamantyl)-1-alkylalkyl (meth)acrylate, a 2-alkyl-2-adamantyl 5-norbornene-2-carboxylate, a 1-(1-adamantyl)-1-alkylalkyl 5-norbornene-2-carboxylate.
Particularly, the 2-alkyl-2-adamantyl (meth)acrylate as the monomer is preferably used because a resist composition having excellent resolution tends to be obtained.
Examples of the 2-alkyl-2-adamantyl (meth)acrylate include 2-methyl-2-adamantyl acrylate, 2-methyl-2-adamantyl methacrylate, 2-ethyl-2-adamantyl acrylate, 2-ethyl-2-adamantyl methacrylate, 2-isopropyl-2-adamantyl acrylate, 2-isopropyl-2-adamantyl methacrylate and 2-n-butyl-2-adamantyl acrylate, for example.
Among these, 2-ethyl-2-adamantyl (meth)acrylate or 2-isopropyl-2-adamantyl (meth)acrylate is preferably used because a resist composition having excellent sensitivity and heat resistance tends to be obtained.
The 2-alkyl-2-adamantyl (meth)acrylate can be usually produced by reacting a 2-alkyl-2-adamantanol or a metal salt thereof with an acrylic halide or a methacrylic halide.
The resin (A) also may include structural units having high-polarity substituents. Example of such structural units includes a structural unit derived from 2-norbornene to which one or more hydroxy groups are bonded; a structural unit derived from (meth)acrylonitrile; a structural unit derived from a (meth)acrylic esters such as 1-adamantyl ester or an alkyl ester in which a carbon atom which bonds to an oxygen atom of —COO— is a secondary carbon atom or a tertiary carbon atom to which one or more hydroxy groups are bonded; a structural unit derived from a (meth)acrylic esters such as 1-adamantyl ester to which one or more carbonyl groups are bonded; a structural unit derived from a styrene monomer such as p- or m-hydroxystyrene; a structural unit derived from (meth)acryloyloxy-γ-butyrolactone in which the lactone ring may be substituted with an alkyl group. A 1-adamantyl ester, in which the carbon atom which bonds to an oxygen atom of —COO— is quaternary atoms, is an acid-stable group.
Specific examples of the monomer having the high-polarity substituent include 3-hydroxy-1-adamantyl (meth)acrylate; 3,5-dihydroxy-1-adamantyl (meth)acrylate; α-(meth)acryloyloxy-γ-butyrolactone; β-(meth)acryloyloxy-γ-butyrolactone; a monomer represented by the formula (a) below, a monomer represented by the formula (b), and hydroxystyrene.
wherein R1 and R2 independently represent a hydrogen atom or a methyl group;
R3 and R4 independently represent a hydrogen atom, a methyl group or a trifluoromethyl or a halogen atom;
p and q represent an integer of 1 to 3, when p is 2 or 3, the plurality of R3 may be the different from one another or one when q is 2 or 3, the plurality of R4 may be different from one another.
Among these, the resist obtained from a resin having any of the structural unit derived from 3-hydroxy-1-adamantyl (meth)acrylate, the structural unit derived from 3,5-dihydroxy-1-adamantyl (meth)acrylate, the structural unit derived from α-(meth)acryloyloxy-γ-butyrolactone, the structural unit derived from 13-(meth)acryloyloxy-γ-butyrolactone, the structural unit represented by the formula (a), and the structural unit represented by the formula (b) is preferable because improvement of the adhesiveness of resist to a substrate and of the resolution of resist tends to be obtained.
The resin (A) may further include the following structural units. Example thereof include a structural unit derived from a monomer having a free carboxylic acid group such as acrylic acid or methacrylic acid, a structural unit derived from an aliphatic unsaturated dicarboxylic anhydride such as maleic anhydride and itaconic anhydride, and a structural unit derived from 2-norbornene, a structural unit derived from (meth)acrylic esters such as an 1-adamantyl ester or alkyl ester in which a carbon atom which bonds to an oxygen atom of —COO— is a secondary carbon atom or a tertiary carbon atom. A 1-adamantyl ester, in which the carbon atom which bonds to an oxygen atom of —COO— is quaternary atoms, is an acid-stable group.
Monomers such as 3-hydroxy-1-adamantyl (meth)acrylate and 3,5-dihydroxy-1-adamantyl (meth)acrylate are commercially available, and they can also be produced, for example, by reacting a corresponding hydroxyadamantane with (meth)acrylic acid or its acid halide.
A monomer such as (meth)acryloyloxy-γ-butyrolactone can be produced by reacting α- or β-bromo-γ-butyrolactone in which the lactone ring may be substituted with a alkyl group with acrylic acid or methacrylic acid, or reacting α- or β-hydroxy-γ-butyrolactone in which the lactone ring may be substituted with a alkyl group with an acrylic halide or a methacrylic halide.
Monomers to give structural units represented by the formula (a) and the formula (b) include a (meth)acrylate of an alicyclic lactone having the hydroxy group described below, and mixtures thereof. These esters can be produced, for example, by reacting a corresponding alicyclic lactone having the hydroxy group with (meth)acrylic acid (see, for example, JP 2000-26446 A).
Examples of the (meth)acryloyloxy-γ-butyrolactone include α-acryloyloxy-γ-butyrolactone, α-methacryloyloxy-γ-butyrolactone, α-acryloyloxy-β,β-dimethyl-γ-butyrolactone, α-methacryloyloxy-β,β-dimethyl-γ-butyrolactone, α-cryloyloxy-α-methyl-γ-butyrolactone, α-methacryloyloxy-α-methyl-γ-butyrolactone, β-acryloyloxy-γ-butyrolactone, β-methacryloyloxy-γ-butyrolactone and β-methacryloyloxy-α-methyl-γ-butyrolactone.
In the case of KrF excimer laser exposure, sufficient transmittance can be obtained even the structural unit derived from a styrene monomer such as p- or m-hydroxystrene is used as the structural unit of the resin. Such copolymerized resin can be obtained by radical-polymerizing with corresponding (meth)acrylic ester monomer, acetoxystyrene and styrene, and then de-acetylating with an acid.
The resin having a structural unit derived from 2-norbornene results in a sturdy structure because the main chain directly has an alicyclic backbone and allow dry etching resistance. The structural unit derived from 2-norbornene can be introduced into the main chain, for example, by radical polymerization with the combined use of an aliphatic unsaturated dicarboxylic anhydride such as maleic anhydride or itaconic anhydride in addition to the corresponding 2-norbornene. Accordingly, the structural unit formed upon the opening of the double bond in the norbornene structure can be represented by the formula (c), whereas structural unit formed upon the opening of the double bond of maleic anhydride and itaconic anhydride can be represented by the formulas (d) and (e), respectively.
wherein R5 and/or R6 independently represent a hydrogen atom, a C1 to C3 alkyl group, a carboxyl group, a cyano group, or —COOU wherein U is an alcohol residue, or R5 and R6 can be bonded together to form a carboxylic anhydride residue represented by —C(═O)OC(═O)—.
When R5 and/or R6 is —COOU group, it is an ester formed from carboxyl group. Examples of the alcohol residue corresponding to U include an optionally substituted C1 to C8 alkyl group, and 2-oxooxolan-3- or -4-yl group. The alkyl group may be substituted with a hydroxy group or an alicyclic hydrocarbon group.
Examples of the alkyl group include methyl group, ethyl group, n-propyl group, iso-propyl group, n-butyl group, sec-butyl group, tert-butyl group, pentyl group, hexyl group, octyl group and 2-ethylhexyl group.
Examples of a hydroxy group-bound alkyl group, i.e., a hydroxyalkyl group include hydroxymethyl group and 2-hydroxyethyl group.
Examples of the alicyclic hydrocarbon group include the group having about 3 to 30 carbon atoms, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclodecyl, cyclohexenyl, bicyclobutyl, bicyclohexyl, bicyclooctyl and 2-norbonyl.
In the present specification, any group exemplified is applicable to any of the chemical formulae having a similar group with optionally selecting the number of carbon atoms, unless otherwise specified. When a group enables linear and branched chain, and cyclic structures, all structures may be included and may simultaneously present in one group, unless otherwise specified (the same applies hereafter).
The followings can be specific examples of the norbornene structures represented by the formula (c), which are monomers giving an acid-stable structure.
When the U of the —COOU of R5 and/or R6 in the formula (c) is an acid-labile group, such as an aliphatic ester in which a carbon atom bonded to the oxygen atom of —COO— is quaternary carbon atom, the group will be a structure unit having an acid-labile group, despite having a norbornene structure.
Examples of the monomer having a norbornene structure and an acid-labile group include t-butyl 5-norbornene-2-carboxylate, 1-cyclohexyl-1-methylethyl 5-norbornene-2-carboxylate, 1-methylcyclohexyl-5-norbornene-2-carboxylate, 2-methyl-2-adamantyl 5-norbornene-2-carboxylate, 2-ethyl-2-adamantyl 5-norbornene-2-carboxylate, 1-(4-methylcyclohexyl)-1-methylethyl 5-norbornene-2-carboxylate, 1-(4-hydroxycyclohexyl)-1-methylethyl 5-norbornene-2-carboxylate, 1-methyl-1-(4-oxocyclohexyl)ethyl 5-norbornene-2-carboxylate and 1-(1-adamantyl)-1-methylethyl 5-norbornene-2-carboxylate.
In the resin (A) of the resist composition used in the present invention, usually, the content of the structural unit(s) of the formula (XX) in the whole resin is preferably adjusted in the range of 1 to 10 mol % though the content varies depending on the kind of radiation for patterning exposure, the kind of an acid-labile group, and the like.
When the structural unit derived from 2-alkyl-2-adamantyl (meth)acrylate or 1-(1-adamantyl)-1-alkylalkyl (meth)acrylate in particular is included as the structural unit derived from the monomer with the acid-labile group, adjusting the content to 15 mol % or more with respect to the total structural units constituting the resin is advantageous in terms of the dry etching resistance of the resulting resist because the resin will have an alicyclic group and will be a sturdy structure.
When an alicyclic compound and an aliphatic unsaturated dicarboxylic anhydride having an olefinic double bond in its molecule are used as the monomer, they are preferably used in excess amounts from the viewpoint of a tendency that the addition polymerization does not easily proceed.
Further, the monomers that are used may be a combination of monomers that have the same olefinic double bond moieties but different acid-labile groups, combinations of monomers with the same acid-labile groups and different olefinic double bond moieties, and combinations of monomers with different combinations of acid-labile groups and olefinic double bond moieties.
There is no particular limitation on the photo acid generator (B) that is used in the present invention as long as an acid is produced by exposure, and any known substance in this field may be used.
For example, compounds represented by formula (I) may be used as the photo acid generator (B).
wherein, Ra1 and Ra2 independently represent a Ci to C30 linear or branched chain, or cyclic hydrocarbon group, a five- to nine-membered heterocyclic group containing oxygen atom, or a group —Ra1′—O—Ra2′—, wherein, Ra1′ and Ra2′ independently represent a C1 to C29 linear or branched chain, or cyclic hydrocarbon group, a five- to nine-membered heterocyclic group containing oxygen atom, the Ra1, Ra2, Ra1′ and Ra2′ may be substituted with at least one selected from the group consisting of an oxo group, a C1 to C6 alkyl group, a C1 to C6 alkoxy group, a C1 to C4 perfluoroalkyl group, a C1 to C6 hydroxyalkyl group, a hydroxy group or a cyano group;
A+ represents an organic counter ion;
Y1 and Y2 independently represent a fluorine atom or a C1 to C6 perfluoroalkyl group;
g represents 0 or an integer of 1.
Here, the hydrocarbon may be the same as the alkyl group described above and may be a group introduced at least one double bond or triple bond into any site on the alkyl group. Among these, an alkyl group is preferred.
A C3 to C30 cyclic hydrocarbon group may or may not be an aromatic group. The hydrocarbon group includes a monocyclic or a bicyclic hydrocarbon group, an aryl group or an aralkyl group. More specifically, in addition to the alicyclic hydrocarbon group described above such as a C4 to C8 cycloalkyl and norbornyl, other examples include phenyl, indenyl, naphthyl, adamantyl, norbornenyl, tolyl and benzyl.
Examples of the alkoxyl group include methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, sec-butoxy, tert-butoxy, pentoxy, hexoxy, octyloxy and 2-ethylhexyloxy groups.
Examples of the perfluoroalkyl group include perfluoromethyl, perfluoroethyl, perfluoropropyl and perfluorobutyl.
The photo acid generator (B) may be a compound represented by the following formula (V) or the formula (VI).
wherein a ring E represents an C3 to C30 cyclic hydrocarbon group, the ring E may be substituted with at least one selected from the group consisting of a C1 to C6 alkyl group, a C1 to C6 alkoxy group, a C1 to C4 perfluoroalkyl group, a C1 to C6 hydroxyalkyl group, a hydroxy group and a cyano group;
Z′ represents a single bond or a C1 to C4 alkylene group;
A+, Y1 and Y2 have the same meaning as defined above.
Examples of an alkylene group include the following groups represented by (Y-1) to (Y-12).
The photo acid generator (B) may be a compound represented by the following formula (III).
wherein Y1 and Y2 independently represent a fluorine atom or a C1 to C6 perfluoroalkyl group;
X represents —OH or —Y—OH, wherein, Y represents C1 to C6 linear or branched chain alkylene group;
n represents an integer of 1 to 9;
A+ has the same meaning as defined above.
Y1 or Y2 is preferably a fluorine atom.
n is preferably an integer of 1 to 2.
Examples of the Y include, for example, the following groups represented by (Y-1) to (Y-12). Among these, (Y-1) and (Y-2) are preferable due to their ease of production.
Examples of the anion in the compound represented by the formula (I), (III), (V) or (VI) include the following compounds.
The photo acid generator may be a compound represented by the following formula (VII).
A+—O3S—Rb (VII)
wherein Rb represents a C1 to C6 linear or branched chain alkyl group or a perfluoroalkyl group;
A+ has the same meaning as defined above.
Rb is preferably a C1 to C6 perfluoroalkyl group.
Specific examples of the anion of the formula (VII) include an ion such as trifluoromethanesulfonate, pentafluoroethanesulfonate, heptafluoropropansulfonate and perfluorobutanesulfonate.
Examples of the organic counter ion of A+ in the compounds represented by the formula (I), (III), (V) to (VII) include a cation represented by the formula (VIII).
wherein Pa to Pc independently represent a C1 to C30 linear or branched chain alkyl group or a C3 to C30 cyclic hydrocarbon group; when Pa to Pc are alkyl groups, the groups may be included one or more selected from the group consisting of a hydroxy group, a C1 to C12 alkoxy group, a C3 to C12 cyclic hydrocarbon group, an ether group, an ester group, a carbonyl group, a cyano group, an amino group, an amino group substituted with a C1 to C4 alkyl group and an amide group as a substituent, when Pa to Pc are cyclic hydrocarbon groups, the groups may be include one or more selected from the group consisting of a hydroxy group, a C1 to C12 alkyl group, a C1 to C12 alkoxy group, an ether group, an ester group, a carbonyl group, a cyano group, an amino group, an amino group substituted with a C1 to C4 alkyl group and an amide group as a substituent.
In particular, the following cations represented by the formula (IIa), the formula (IIb), the formula (IIc) and the formula (IId) are exemplified.
wherein P1 to P3 independently represent a hydrogen atom, a hydroxy group, a C1 to C12 alkyl group, a C1 to C12 alkoxy group, an ether group, an ester group, a carbonyl group, a cyano group, an amino group optionally substituted with a C1 to C4 alkyl group and an amide group,
The alkyl group and the alkoxy group include the same examples as the above.
Among cations represented by the formula (IIa), a cation represented by the formula (IIe) is preferable due to its ease of production.
wherein P22 to P24 independently represent a hydrogen atom or a C1 to C4 alkyl group. The alkyl group may be a linear or branched chain.
Further, the organic counter ion of A+ may be a cation represented by the formula (IIb) containing iodine cation.
wherein P4 and P5 independently represent a hydrogen atom, a hydroxy group, a C1 to C12 alkyl group or a C1 to C12 alkoxy group.
Furthermore, the organic counter ion of A+ may be a cation represented by the formula (IIc).
wherein P6 and P7 independently represent a C1 to C12 alkyl group or a C3 to C12 cycloalkyl group. The alkyl group may be a linear or branched chain.
Examples of the cycloalkyl group include cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, cycloheptyl group and cyclodecyl group.
Also, P6 and P7 may be bonded together to form a C3 to C12 divalent hydrocarbon group. A carbon atom containing in the divalent hydrocarbon group can be replaced by a carbonyl group, an oxygen atom or a sulfur atom.
The divalent hydrocarbon group may be any of a saturated, unsaturated, chained or cyclic hydrocarbon. Among these, chained saturated hydrocarbon groups, and in particular, alkylene groups are preferred. Example of the alkylene group includes, for example, trimethylene, tetramethylene, pentamethylene and hexamethylene.
P8 represents a hydrogen atom, P9 represents a C1 to C12 alkyl group, a C3 to C12 cycloalkyl group or an optionally substituted aromatic group, or P8 and P9 may be bonded together to form a C3 to C12 divalent hydrocarbon group.
The alkyl group, the cycloalkyl group and the divalent hydrocarbon group include the same examples as the above.
The aromatic group preferably has 6 to 20 carbon atoms, and for example, is preferably an aryl group or an aralkyl group, and more specifically, includes phenyl, tolyl, xylyl, biphenyl, naphthyl, benzyl, phenethyl and anthracenyl groups. Among these, phenyl group and benzyl group are preferred. A group which may be substituted in the aromatic group include a hydroxy group, a C1 to C6 alkyl group and a C1 to C6 hydroxyalkyl group.
Also, examples of the organic counter ion of A+ may be a cation represented by the formula (IId).
wherein P10 to P21 independently represent a hydrogen atom, a hydroxy group, a C1 to C12 alkyl group or a C1 to C12 alkoxy group.
The alkyl group and the alkoxy group include the same examples as the above.
D represents a sulfur atom or an oxygen atom.
m represents 0 or 1.
Specific examples of the cation A+ of the formula (IIa) include cations represented by the following formulae.
Specific examples of the cation A+ of the formula (IIb) include cations represented by the following formulae.
Specific examples of the cation A+ of the formula (IIc) include cations represented by the following formulae.
Specific examples of the cation A+ of the formula (IId) include cations represented by the following formulae.
Examples of the cation A+ of the compound represented by the formula (I), (III), (V) to (VII) may be a cation represented by the formula (IV).
wherein r represents an integer of 1 to 3.
In the formula (IV), r is preferably 1 to 2, and most preferably 2.
There is no particular limitation on the position of bond for a hydroxy group, but it is preferably at 4-position due to their ease of availability and low cost.
Specific examples of the cation of the formula (IV) include cation represented by the following formulae.
In particular, compounds represented by the formulae (IXa) to (IXe) are preferred as the compound represented by the formula (I) or (III) of the present invention since they form a photo acid generator giving a chemically-amplified resist having an excellent pattern shape and resolution.
wherein, P6 to P9 and P22 to P24, Y1, Y2 have the same meaning as defined above, and P25 to P27 independently represent a hydrogen atom or a C1 to C4 alkyl group.
Among these, the compounds below are suitably used due to their ease of production.
The compounds of the formulae (I), (III), (V) to (VII) can be produced, for example, using a method disclosed in JP-2006-257078-A or an according method.
In particular, the manufacturing method of the compound represented by the formula (V) or the formula (VI) includes a method by reacting a salt represented by the formula (1) or the formula (2) with an onium salt represented by the formula (3) being stirred in an inert solvent such as acetonitrile, water or methanol at a temperature in the range of about 0° C. to 150° C., and preferably 0° C. to 100° C.
wherein Z′ and E have the same meaning as defined above, and
M represents Li, Na, K or Ag.
A+Z− (3)
wherein A+ has the same meaning as defined above, and
Z represents F, Cl, Br, I, BF4, AsF6, SbF6, PF6 or ClO4.
The onium salt of the formula (3) is generally used in an amount of about 0.5 to 2 mols with respect to 1 mol of the salt represented by the formula (1) or the formula (2). The compound represented by the formula (V) or the formula (VI) may be purified by recrystallization or washing with water.
The salt represented by the formula (1) or the formula (2) that is used to produce the compound represented by the formula (V) or the formula (VI) can be produced, for example, by first esterification-reacting between an alcohol represented by the formula (4) or the formula (5) with a carboxylic acid represented by the formula (6).
wherein E and Z′ have the same meaning as defined above.
M+-O3SCF2COOH (6)
wherein M has the same meaning as defined above.
As another method, the salt represented by the formula (1) or the formula (2) can be also produced, for example, by first esterification-reacting between an alcohol represented by the formula (4) or the formula (5) with a carboxylic acid represented by the formula (7), and then hydrolyzing with MOH wherein M has the same meaning as defined above.
FO2SCF2COOH (7)
The esterification reaction may usually be carried out by stirring in an aprotic solvent such as dichloroethane, toluene, ethyl benzene, monochlorobenzene and acetonitrile at a temperature in the range of about 20° C. to 200° C., and preferably about 50° C. to 150° C. An organic acid such as p-toluenesulfonic acid and/or an inorganic acid such as sulfuric acid is usually added as an acid catalyst during the esterification reaction.
The esterification reaction is also preferably carried out along with dehydration using a Dean-Stark device, etc., because the reaction time tends to be shorter.
The carboxylic acid represented by the formula (6) in the esterification reaction is generally used in an amount of about 0.2 to 3 mol, and preferably about 0.5 to 2 mol, with respect to 1 mol of the alcohol represented by the formula (4) or the formula (5). The amount of the acid catalyst in the esterification reaction may be a catalytic amount or an amount corresponding to the solvent, and is usually about 0.001 to 5 mol.
There are also methods for obtaining salts represented by the formula (VI) or the formula (2) by reducing the salt represented by the formula (V) or the formula (1).
The reducing reaction can be brought about using a reducing agent, including borohydrides such as sodium borohydride, zinc borohydride, lithium tri-sec-butyl borohydride and borane; aluminum hydrides such as lithium tri-t-butoxyaluminum hydride and diisobutylaluminum hydride; organosilicon hydrides such as Et3SiH and Ph2SiH2; or organotin hydrides such as Bu2SnH, in a solvent such as water, alcohol, acetonitrile, N,N-dimethyl formamide, diglyme, tetrahydrofuran, diethyl ether, dichloromethane, 1,2-dimethoxyethane, or benzene. The reaction may be brought about while stirred at a temperature in the range from about −80° C. to 100° C., and preferably about −10° C. to 60° C.
Photo acid generators shown in (B1) and (B2) below may be used as the photo acid generator (B).
(B1) is not particularly limited as long as a hydroxy group is present in the cation and an acid is produced by exposure. Such cations include those represented by formula (IV) above.
The anion in (B1) is not particularly limited and for example known anions as an onium salt type acid generator may be suitably used.
For example, an anion represented by the formula (X-1), formula (X-2), (X-3) or (X-4).
wherein R7 is a linear or branched chain, or cyclic alkyl group or a fluoroalkyl group;
Xa represents a C2 to C6 alkylene group in which at least one hydrogen atom is substituted by a fluorine atom;
Ya and Za independently represent a C1 to C10 alkyl group in which at least one hydrogen atom is substituted by a fluorine atom;
R10 is a substituted or non-substituted linear or branched chain, or cyclic C1 to C20 alkyl group, or a substituted or non-substituted C6 to C14 aryl group can be used.
The linear or branched chain alkyl group preferably has 1 to 10 carbon atoms, more preferably 1 to 8 carbon atoms, and most preferably 1 to 4 carbon atoms.
R7, as the cyclic alkyl group, preferably has 4 to 15 carbon atoms, more preferably 4 to 12 carbon atoms, and still more preferably 4 to 10, 5 to 10, and 6 to 10 carbon atoms.
The fluoroalkyl group preferably has 1 to 10 carbon atoms, more preferably 1 to 8 carbon atoms, and most preferably 1 to 4 carbon atoms.
The rate of fluorination of the fluoroalkyl group (the proportion of the number of fluorine atoms substituted by fluorination relative to the total number of hydrogen atoms in the alkyl group prior to fluorination, same hereafter) is preferably 10 to 100%, and more preferably 50 to 100% and, in particular, all hydrogen atoms substituted by fluorine atoms is preferred since the strength of the acid is increased.
R7 is more preferably a linear chain or cyclic alkyl group, or a fluorinated alkyl group.
In the formula (X-2), Xa represents a linear or branched chain alkylene group in which at least one hydrogen atom is substituted by a fluorine atom. The number of carbon atoms in the alkylene group is preferably 2 to 6, more preferably 3 to 5 carbon atoms, and most preferably 3 carbon atoms.
In the formula (X-3), Ya, Za independently represent a linear or branched chain alkyl group in which at least one hydrogen atom is substituted by a fluorine atom. The number of carbon atoms in the alkyl group is preferably 1 to 10, more preferably 1 to 7 carbon atoms, and most preferably 1 to 3 carbon atoms.
The number of carbon atoms in the alkylene group Xa or the number of carbon atoms in the alkyl group Ya, Za is preferably as small as possible within the above scope of the carbon atoms due reasons such as a preferred effect on the solubility in the resist solvent and the like.
The strength of the acid is increased as the number of hydrogen atoms substituted by fluorine atoms increases in the alkylene group Xa or the alkyl group Ya, Za, and is preferred due to an improvement in transparency to high-energy light of 200 nm or less or an electron beam. The fluorination rate of the alkylene group or the alkyl group is preferably 70 to 100%, more preferably 90 to 100% and most preferably is a perfluoroalkylene group or a perfluoroalkyl group in which all hydrogen atoms are substituted by fluorine atoms.
Examples of the aryl group include phenyl, tolyl, xylyl, cumenyl, mesityl, naphthyl, biphenyl, anthryl and phenanthryl.
Examples of the substituent which may be substituted alkyl or aryl group include, for example, one or more substituent selected from a group consisting of a hydroxy group, a C1 to C12 alkyl group, a C1 to C12 alkoxy group, an ether group, an ester group, a carbonyl group, a cyano group, an amino group, an amino group substituted with a C1 to C4 alkyl group and an amide group.
The anion of (B1) may be combine with the anion represented by A+ in formula (I) or the like.
(B1) is preferably has an anion represented by the formula (X-1) described above, and in particular, one in which R7 is a fluorinated alkyl group is preferred.
For example, specific examples of the formula (B1) include the photo acid generator represented by the following formulae.
There is no particular limitation on (B2) as long as the cation does not include a hydroxy group, and any compound proposed as an acid generator for a chemically-amplified resist may be used.
Examples of such acid generator includes a variety of acid generators, an onium salt type acid generator such as an iodonium salt and a sulfonium salt; an oxime sulfonate type acid generator; a diazomethane type acid generator such as bisalkyl or bisaryl sulfonyl diazomethane or poly (bis-sulfonyl) diazomethane; a nitrobenzyl sulfonate acid generator, an iminosulfonate acid generator and a disulfone acid generator.
An onium salt acid generator for example may preferably be an acid generator as represented by the formula (XI).
wherein R51 represents a linear or branched chain, or cyclic alkyl group or a linear or branched chain, or cyclic fluoroalkyl group;
R52 represents a hydrogen atom, a hydroxy group, a halogen atom, a linear or branched chain alkyl group, a linear or branched chain halogenated alkyl group, or a linear or branched chain alkoxy group;
R53 represents an optionally substituted aryl group;
t represents an integer of 1 to 3.
In the formula (XI), R51 can have the same carbon atom number and fluorination rate as the substituent R7 described above.
R51 is most preferably a linear chain alkyl group or a fluoroalkyl group.
A fluorine atom is preferred as the halogen atom.
In R52, the alkyl group is preferably a group in which it is linear or branched chain and preferably has 1 to 5 carbon atoms, and in particular 1 to 4, and more preferably 1 to 3.
In R52, the halogenated alkyl group is a group in which a part or all of the hydrogen atoms in the alkyl group are substituted by halogen atoms. The alkyl group and the substituting halogen atoms are the same examples as the above. In the halogenated alkyl group, 50 to 100% of all of the hydrogen atoms are preferably substituted by halogen atoms, and substitution of all atoms is more preferred.
In R52, the alkoxy group is a group in which it is linear or branched chain and preferably has 1 to 5 carbon atoms, and in particular 1 to 4, and more preferably 1 to 3.
Among these, R52 is preferably a hydrogen atom.
From the point of view of absorption of exposure light such as an ArF excimer laser, R53 is preferably a phenyl group.
Examples of the substituent in the aryl group include a hydroxy group, a lower alkyl group (linear or branched chain, for example, with 1 to 6 carbon atoms, more preferably 1 to 4 carbon atoms, and in particular a methyl group is preferred), a lower alkoxy group.
The aryl group of R53 more preferably does not include a substituent.
t is an integer of 1 to 3, 2 or 3 are preferred and in particular, 3 is desirable.
Specific examples of the acid generator represented by the formula (XI) include the following compounds.
Acid generators represented by the formula (XII) and (XIII) may be used as the onium salt acid generator.
wherein R21 to R23 and R25 to R26 independently represent an aryl group or an alkyl group;
R24 represents a linear or branched chain, or cyclic alkyl group or fluorinated alkyl group;
at least one of R21 to R23 is an aryl group, at least one of R25 to R26 is an aryl group.
Two or more of R21 to R23 are preferably aryl groups, and it is most preferred that all of R21 to R23 are aryl groups.
The aryl group of R21 to R23 is, for example, a C6 to C20 aryl group. A part or all of the hydrogen atoms in the aryl group may be substituted with an alkyl group, an alkoxy group or a halogen atom. The aryl group is preferably a C6 to C10 aryl group in view of cost-effective synthesis. Specific examples include a phenyl group and naphtyl group.
The alkyl group which may substitute for the hydrogen atom in the aryl group is preferably a C1 to C5 alkyl group, and most preferably methyl group, ethyl group, propyl group, n-butyl group and tert-butyl group.
The alkoxy group which may substitute for the hydrogen atom in the aryl group is preferably a C1 to C5 alkoxy group, and most preferably methoxy group or ethoxy group.
The halogen atom which may substitute for the hydrogen atom in the aryl group is preferably a fluorine atom.
The alkyl group in R21 to R23 is, for example, a C1 to C10 linear or branched chain, or cyclic alkyl group. From the point of view of excellent resolution characteristics, C1 to C5 is preferred. Specific examples include methyl group, ethyl group, n-propyl group, iso-propyl group, n-butyl group, isobutyl group, n-pentyl group, cylopentyl group, hexyl group, cyclohexyl group, nonyl group and decanyl group. The methyl group is preferably in view of excellent resolution and cost-effective synthesis.
Among these, R21 to R23 are most preferably a phenyl group or a naphtyl group, respectively.
R24 includes the same groups as mentioned in the above R7.
It is preferred that all of R25 to R26 are aryl groups.
Among these, it is most preferred that all of R25 to R26 are phenyl groups.
Example of the onium salt type acid generator represented by the formula (XII) and the formula (XIII) include;
There onium salts in which an anion is replaced by methansulfonate, n-propanesulfonate, n-butanesulfonate, n-octanesulfonate can be also used.
In the formula (XII) or (XIII), an onium salt type acid generator in which anion is replaced by an anion represented by the formulae (X-1) to (X-3) can be also used.
The following compounds may be also used.
An oxime sulfonate type acid generator is a compound having at least one group represented by the formula (XIV) and is characterized by producing an acid as a result of irradiation with radiation. This type of oxime sulfonate type acid generator, which is often used as a composition for a chemically-amplified resist, may optionally be also used.
Wherein, R31 and R32 independently represent an organic group.
The organic groups of R31, R32 are groups which contain carbon atoms, and may include atoms other than carbon atoms (for example, one or more atom such as a hydrogen atom, an oxygen atom, a nitrogen atom, a sulfur atom, a halogen atom).
The organic group R31 is preferably a linear or branched chain, or cyclic alkyl or aryl group. The alkyl and aryl groups may include a substituent. There is no particular limitation on the substituent, and for example, it may be a fluorine atom, a C1 to C6 linear or branched chain, or cyclic alkyl group.
The alkyl group preferably includes 1 to 20 carbon atoms, more preferably 1 to 10 carbon atoms, still more preferably 1 to 8 carbon atoms, yet more preferably 1 to 6 carbon atoms, and most preferably 1 to 4 carbon atoms. It is particularly preferred that the alkyl group is a partially or completely halogenated alkyl group (hereafter, this may be referred to as a halogenated alkyl group). A partially halogenated alkyl group means an alkyl group in which a part of the hydrogen atoms are substituted by halogen atoms, and a completely halogenated alkyl group means an alkyl group in which all the hydrogen atoms are substituted by halogen atoms. The halogen atom includes a fluorine atom, a chlorine atom, a bromine atom, and an iodide atom, and a fluorine atom is particularly preferred. In other words, the halogenated alkyl group is preferably a fluorinated alkyl group.
The aryl group preferably includes 4 to 20 carbon atoms, more preferably 4 to 10 carbon atoms, and most preferably 6 to 10 carbon atoms. It is particularly preferred that the aryl group is a partially or completely halogenated aryl group.
It is particularly preferred that the R31 is a non-substituted C1 to C4 alkyl group or a C1 to C4 fluorinated alkyl group.
The organic group of R32 is preferably a linear and branched chain, or cyclic alkyl group, aryl group or cyano group. The alkyl or aryl group of R32 is the same as the alkyl or aryl group of R31.
It is particularly preferred that the R32 is a cyano group, a non-substituted C1 to C8 alkyl or a C1 to C8 fluorinated alkyl group.
The oxime sulfonate type acid generator is more preferably a compound represented by the formula (XVII) or (XVIII).
wherein (XVII), R33 represents a cyano group, a non-substituted alkyl group or a halogenated alkyl group. R34 represents an aryl group. R35 represents a non-substituted alkyl group or a halogenated alkyl group.
In the formula (XVIII), R36 represents a cyano group, a non-substituted alkyl group or a halogenated alkyl group. R37 represents a divalent or trivalent aromatic hydrocarbon group. R38 represents a non-substituted alkyl group or a halogenated alkyl group. w is 2 or 3, and preferably is 2.
In the formula (XVII), the non-substituted alkyl group or the halogenated alkyl group of R33 preferably has 1 to 10 carbon atoms, more preferably 1 to 8 carbon atoms and most preferably 1 to 6 carbon atoms.
R33 is preferably a halogenated alkyl group, and more preferably a fluorinated alkyl group.
In the fluorinated alkyl group of R33, it is preferred that 50% or more of the hydrogen atoms in the alkyl groups are fluorinated, more preferably 70% or more, and further preferably 90% or more. It is most preferred that it is a completely fluorinated alkyl group in which 100% of the hydrogen atoms are substituted. This is in order to increase the strength of the resulting acid.
The aryl group of R34 includes a group in which one hydrogen atom is removed from an aromatic hydrocarbon ring such as phenyl group, biphenyl group, fluorenyl group, naphthyl group, anthracenyl group, phenanthrenyl group, and a heteroaryl group in which a part of the carbon atoms forming the ring of such groups is replaced by a hetero atom such as an oxygen atom, a sulfur atom, or a nitrogen atom. Among these, a fluorenyl group is preferred.
The aryl group of R34 may include substituent such as a C1 to C10 alkyl group, a halogenated alkyl group or an alkoxy group. The alkyl group or the halogenated alkyl group in the substituent preferably has 1 to 8 carbon atoms, and more preferably 1 to 4 carbon atoms. The halogenated alkyl group is preferably a fluorinated alkyl group.
The non-substituted alkyl group or the halogenated alkyl group in R35 is exemplified by the same examples as described in above R33.
In the formula (XVIII), the non-substituted alkyl group or the halogenated alkyl group in R36 is the same examples as described in above R33.
The divalent or trivalent aromatic hydrocarbon group in R37 includes a group in which a further one or two hydrogen atoms are removed from the aryl group in above R34.
The non-substituted alkyl group or the halogenated alkyl group in R38 is the same as described in above R.
The oxime sulfonate type acid generator includes a compound discussed in paragraph [0122] of JP2007-286161-A, the oxime sulfonate type acid generators disclosed in [Chem.18] to [Chem.19] in paragraphs [0012] to [0014] of JPH09-208554-A, and the oxime sulfonate type acid generators disclosed in Examples 1 to 40 on pages 65 to 85 of WO2004/074242A2.
The following examples are preferred.
Types of bisalkyl or bisaryl sulfonyl diazomethane among the diazomethane acid generators include bis(isopropylsulfonyl) diazomethane, bis(p-toluene sulfonyl) diazomethane, bis(1,1-dimethylethyl sulfonyl) diazomethane, bis(cyclohexyl sulfonyl) diazomethane and bis(2,4-dimethylphenyl sulfonyl) diazomethane.
The diazomethane type acid generators disclosed in JPH11-035551-A, JPH11-035552-A, and JPH11-035573-A may also be suitably used.
Types of poly (bis-sulfonyl) diazomethane include, for example, 1,3-bis (phenylsulfonyl diazomethylsulfonyl) propane, 1,4-bis(phenylsulfonyl diazomethylsulfonyl) butane, 1,6-bis(phenylsulfonyl diazomethylsulfonyl) hexane, 1,10-bis(phenylsulfonyl diazomethylsulfonyl) decane, 1,2-bis(cyclohexylsulfonyl diazomethylsulfonyl)ethane, 1,3-bis(cyclohexylsulfonyl diazomethylsulfonyl) propane, 1,6-bis(cyclohexylsulfonyl diazomethylsulfonyl) hexane, 1,10-bis(cyclohexylsulfonyl diazomethylsulfonyl) decane, as disclosed in JPH11-322707-A.
Among these, an onium salt having an anion formed from a fluorinated alkyl sulfonic acid ion is preferably used as a component of (B2).
In the present invention, the photo acid generator may be used singly or in a mixture of two or more agents.
The resist composition used in the present invention with reference to total solid content preferably contains about 70 to 99.9 wt % of the resin (A), about 0.1 to 30 wt %, preferably about 0.1 to 20 wt %, and more preferably about 1 to 10 wt % of the photo acid generator. This range enables sufficient execution of pattern forming in addition to obtaining homogenous solution and excellent storage stability.
The resist composition used in the present invention may include a cross-linking agent (C).
There is no particular limitation on the cross-linking agent (C) and the agent may be suitably selected from cross-linking agents used in this field.
Examples include a compound produced by reacting formaldehyde, or formaldehyde and a lower alcohol with a compound containing an amino group such as acetoguanamine, benzoguanamine, urea, ethylene urea, propylene urea, and glycoluril, and replacing hydrogen atoms in the amino group by a hydroxymethyl group or a lower alkoxy methyl group; or an aliphatic hydrocarbon having two ore more ethylene oxide structural moiety. A compound using urea is hereinafter termed a urea cross-linking agent, a compound using an alkylene urea such as ethylene urea and propylene urea is hereinafter termed an alkylene urea cross-linking agent, and a compound using glycoluril is hereinafter termed a glycoluril cross-linking agent. Among these, urea cross-linking agents, alkylene urea cross-linking agents and glycoluril cross-linking agents are preferred, and glycoluril cross-linking agents are more preferred.
A urea cross-linking agent includes a compound in which urea is reacted with formaldehyde, and the hydrogen atoms in the amino group are replaced by a hydroxymethyl group, or a compound in which urea, formaldehyde and a lower alcohol are reacted, and the hydrogen atoms in the amino group are replaced by a lower alkoxy methyl group. Specific examples include bis(methoxymethyl)urea, bis(ethoxymethyl)urea, bis(propoxymethyl)urea, and bis(butoxymethyl)urea. Among these, bis(methoxymethyl)urea is preferred.
The alkylene urea cross-linking group includes a compounds represented by the formula (XIX).
wherein R8 and R9 independently represent a hydroxy group or a lower alkoxy group, R8′ and R9′ independently represent a hydrogen atom, a hydroxy group or a lower alkoxy group, and v is 0 or an integer of 1 to 2.
When R8′ and R9′ are a lower alkoxy group, the alkoxy group preferably has 1 to 4 carbon atoms and may be linear or branched chain. R8′ and R9′ may be the same, or may be different from each other. It is more preferred that R8′ and R9′ are the same.
When R8 and R9 are a lower alkoxy group, the alkoxy group preferably has 1 to 4 carbon atoms and may be linear of branched chain. R8 and R9 may be the same, or may be different from each other. It is more preferred that R8 and R9 are the same.
v is 0 or an integer of 1 to 2, and is preferably 0 or 1.
It is particularly preferred that the alkylene urea cross-linking agent is a compound in which v is 0 (an ethylene urea cross-linking agent) and/or a compound in which v is 1 (a propylene urea cross-linking agent).
A compound represented by the formula (XIII) above can be obtained by condensation-reacting alkylene urea with formalin, or by reacting the resulting product with a lower alcohol.
Specific examples of the alkylene urea cross-linking agent include ethylene urea cross-linking agents such as mono- and/or di-hydroxymethylated ethylene urea, mono- and/or di-methoxymethylated ethylene urea, mono- and/or di-ethoxymethylated ethylene urea, mono- and/or di-propoxymethylated ethylene urea, and mono- and/or di-butoxymethylated ethylene urea; and propylene urea cross-linking agents such as mono- and/or di-hydroxymethylated propylene urea, mono- and/or di-methoxymethylated propylene urea, mono- and/or di-ethoxymethylated propylene urea, mono- and/or di-propoxymethylated propylene urea, and mono- and/or di-butoxymethylated propylene urea; 1,3-di(methoxymethyl)-4,5-dihydroxy-2-imidazolidinone and 1,3-di(methoxymethyl)-4,5-dimethoxy-2-imidazolidinone.
Examples of the glycoluril cross-linking agent include a glycoluril derivative in which the N-position is substituted with either or both a hydroxyalkyl group and/or a C1 to C4 alkoxyalkyl group. The glycoluril derivative can be obtained by subjecting a glycoluril and formalin to a condensation reaction, or by further reacting the product of this reaction with a lower alcohol.
Specific examples of the glycoluril cross-linking agent include mono-, di-, tri- or tetra-hydroxymethylated glycoluril, mono-, di-, tri- and/or tetra-methoxymethylated glycoluril, mono-, di-, tri- and/or tetra-ethoxymethylated glycoluril, mono-, di-, tri- and/or tetra-propoxymethylated glycoluril, and mono-, di-, tri- and/or tetra-butoxymethylated glycoluril.
The cross-linking agent (C) may be used singly or in a combination of two or more agents.
The content of the cross-linking agent (C) is preferably 0.5 to 30 parts by weight relative to 100 parts by weight of the resin (A) component, and more preferably 0.5 to 10 parts by weight, and still more preferably 1 to 5 parts by weight. Within this range, the formation of cross-linking is sufficiently promoted and obtains a superior resist pattern, as well as storage stability of the resist coating liquid is superior and deterioration over time of its sensitivity can be suppressed.
The resist compound used in the present invention preferably contains a thermal acid generator (D). A thermal acid generator as used herein refers a compound which is stable at a temperature which is lower than a hard bake temperature (as described hereafter) for a resist which uses the thermal acid generator, but decomposes at greater than or equal to the hard bake temperature and thereby produces acids. In contrast, the photo acid generator is stable at a pre-bake temperature (as described hereafter) or a post-exposure bake temperature (as described hereafter) and produces acids as a result of exposure. This distinction can be obtained fluidly depending on the aspect in which the present invention is used. That is to say, it can function as both a thermal acid generator and a photo acid generator depending on the applied processing temperature, or may only function as a photo acid generator, in the same resist. Although it does not function as a thermal acid generator in a certain resist, it may function as a thermal acid generator in another resist.
The thermal acid generator includes, for example, various known thermal acid generators such as benzoin tosylate, nitrobenzyl tosylate (in particular, 4-nitrobenzyl tosylate), and other alkylesters of organic sulfonic acids.
The content of the thermal acid generator (D) preferably be 0.5 to 30 parts by weight relative to 100 parts by weight of the resin (A), more preferably 0.5 to 15 parts by weight, and most preferably 1 to 10 parts by weight.
The resist composition of the present invention may include a basic compound, preferably a nitrogen-containing basic compound, in particular, an amine or an ammonium salt is preferable. The basic compound can be added as a quencher to improve performance from being compromised by the inactivation of the acid while the material is standing after exposure. When the basic compound is used, the content thereof is preferably 0.01 to 1 weight % with reference to total solid content of the resist composition.
The examples of such basic compounds include those represented by the following formulae.
wherein R11 and R12 independently represent a hydrogen atom, an alkyl group, a cycloalkyl group or an aryl group, the alkyl group preferably has about 1 to 6 carbon atoms, the cycloalkyl group preferably has about 5 to 10 carbon atoms, the aryl group preferably has about 6 to 10 carbon atoms;
R13, R14 and R15 independently represent a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group or an alkoxy group, the alkyl group, the cycloalkyl group, and the aryl group are the same as described in R11 and R12, the alkoxy group preferably has 1 to 6 carbon atoms.
R16 represents an alkyl group or a cycloalkyl group, the alkyl group and the cycloalkyl group are the same as described in R11 and R12.
R17, R18, R19 and R20 independently represent an alkyl group, a cycloalkyl group or an aryl group, the alkyl group, the cycloalkyl group and the aryl group are the same as described in R11, R12 and R17.
Further, at least one hydrogen atom in the alkyl group, the cycloalkyl group and the alkoxy group may be independently replaced by a hydroxy group, an amino group or a C1 to C6 alkoxy group. At least one hydrogen atom in the amino group may be replaced by a C1 to C4 alkyl group.
W represents an alkylene group, a carbonyl group, an imino group, a sulfide group or a disulfide group. The alkylene group preferably has about 2 to 6 carbon atoms.
In R11 to R20, if the group may be linear or branched chain, either one is included.
Examples of such compounds include a compound disclosed in JP-2006-257078-A.
Furthermore, hindered amine compounds with a piperidine skeleton such as those disclosed in JP-H11-52575-A can be used as a quencher.
The resist composition used in the present invention may also include various additives known in this field such as sensitizers, dissolution inhibitors, other resins, surfactants, stabilizers and dyes, as needed.
The resist composition used in the present invention is normally used as a resist liquid composition in a state in which each component is dissolved in a solvent. This type of resist composition is used at least as a first resist composition. In this manner, it is possible to use a so-called double imaging method. In the double imaging method, a fine resist pattern can be obtained that has half the pattern pitch by twice repeating the process of resist coating, exposure and development. This type of process may be repeated a plurality of three or more times (N times). In this manner, a finer resist pattern having a pattern pitch of 1/N can be obtained. The present invention can be suitably applied to this type of double, triple imaging method and multi-imaging method.
The above resist composition may be used as a second resist composition. In this case, there is no necessity for the composition to always be the same as the first resist composition.
In the resist processing method of the present invention, firstly the resist liquid composition described above (hereafter may be referred to as the first resist composition) is applied onto a substrate and dried thereby obtaining a first resist film. There is no particular limitation on the thickness of the first resist film as used herein, and the thickness may be suitably set with reference to a direction of film thickness to substantially equal to or less than a level sufficiently enabling exposure and developing during following steps, and for example, may be of the level of several tenths of micrometers to several millimeters.
There is no particular limitation on the substrate and for example various materials such as a semiconductor substrate such as a silicon wafer, a plastic, metal or ceramic substrate, a substrate having an insulating film or conducting layer thereon can be used.
There is no particular limitation on the method of coating the composition and a method used in normal industrial processing such as spin coating may be used.
Any substance can be used as a solvent used to obtain the resist liquid composition as long as the substance dissolves each component, has a suitable drying speed and obtains a flat uniform coating after evaporation of the solvent. Normally-used general solvents in this area may be applied.
Examples thereof include glycol ether esters such as ethylcellosolve acetate, methylcellosolve acetate and propylene glycol monomethyl ether acetate; glycol ethers such as propylene glycol monomethyl ether; esters such as ethyl lactate, butyl acetate, amyl acetate and ethyl pyruvate; ketones such as acetone, methyl isobutyl ketone, 2-heptanone and cyclohexanone; and cyclic esters such as γ-butyrolactone. These solvents can be used alone or in combination of two or more.
The drying process includes natural drying, draft drying, and reduced pressure drying. The specific heating temperature may be about 10 to 120° C., and more preferably about 25 to 80° C. The heating period is about 10 seconds to 60 minutes and preferably about 30 seconds to 30 minutes.
Next, the resulting first resist film is pre-baked. The pre-baking is conducted for example in a temperature range of about 80 to 140° C. and in the range of about 30 seconds to 10 minutes.
Then an exposure process for patterning is carried out. The exposure process is preferably carried out using any exposure device that is conventionally used in this field, such as a scanning exposure type, i.e. a scanning stepper type projection exposure device (exposure device). Various types of exposure light source can be used, for example, irradiation with ultraviolet lasers such as KrF excimer laser (wavelength: 248 nm), ArF excimer laser (wavelength: 193 nm), F2 laser (wavelength: 157 nm), or irradiation with harmonic laser light of far-ultraviolet wavelength or vacuum ultraviolet wavelength which is converted from a solid-state laser source (YAG or semiconductor laser or the like).
Thereafter, the resulted first resist film is post-exposure baked. This heating process can promote a protection deblocking reaction. The heating process, for example, is executed in a temperature range of about 70 to 140° C. and for a range of about 30 seconds to 10 minutes.
Then, a first resist pattern is obtained by developing with a first alkali developer. The alkali developer includes various types of aqueous alkali solutions used in this field, and normally an aqueous solution such as tetramethylammonium hydroxide (2-hydroxyethyl) trimethylammonium hydroxide (common name: choline) is used.
Thereafter, the obtained first resist pattern is hard-baked. This heating process promotes cross-linking reactions. The heating process herein, for example, is executed in a relatively high temperature range of about 120 to 250° C. and for a range of about 30 seconds to 10 minutes.
Furthermore, a second resist composition is coated on the first resist pattern formed using the resist composition above and then dried to thereby form a second resist film. This is pre-baked, and subjected to exposure processing for patterning. An arbitrary heating process, and a usual post-exposure bake are performed. Thereafter, a second resist pattern can be formed by developing with a second alkali developer.
The conditions for coating, drying, pre-baking, exposure and post-exposure baking with respect to the second resist composition are the same as those conditions described with reference to the first resist composition.
There is no particular limitation on the second resist composition, and either a negative or a positive resist composition may be used and any known composition used in this field may be used. Any of the resist compositions described above may be used and, in that case, it is not necessary for the second resist composition to always be the same as the first resist composition.
In the present invention, even with a double imaging method including at least two exposures and developing processes and multiple heating processes, a first resist film which retains an original shape and does not cause deformation of the pattern is used and, therefore, it is possible to create an extremely fine pattern.
The present invention will be described more specifically by way of examples. All percentages and parts expressing the content or amounts used in the Examples are based on weight, unless otherwise specified. The weight average molecular weight is a value determined by gel permeation chromatography, the conditions thereof describes below.
Column: TSK gel Multipore HXLM×3+guardcolumn (manufactured by Toso Co. ltd.)
Eluant: tetrahydrofran
Flow rate: 1.0 mL/min
Detecting device: R1 detector
Column temperature: 40° C.
Injection amount: 100 μL
Standard material for calculating molecular weight: standard polysthylene (manufactured by Toso Co. ltd.)
The monomers used in synthesis of resin are follows.
Example of Resin Synthesis 1: Synthesis of Resin 1
Into a four-neck flask provided with a thermometer, a reflux condenser and a stirrer, 25.1 parts of 1,4-dioxane was charged and elevated temperature to 77° C.
A solution was prepared by dissolving 17.4 parts of monomer A, 2.8 parts of monomer B, 8.0 parts of monomer C, 0.5 parts of monomer H, 13.3 parts of monomer D, 0.3 parts of 2,2′-azobisisobutyronitrile, 1.5 parts of 2,2′ azobis (2,4-dimethylvaleronitrile) in 37.7 parts of 1,4-dioxane.
This solution was added dropwise over 2 hours into the above described four-neck flask.
Thereafter, the reaction solution was kept the heat for 5 hours while maintaining a temperature of 77° C., and diluted with 46 parts of 1,4-dioxane. A resin solution was poured into a mixed solvent of 435 parts of methanol and 109 parts of to obtain a precipitate.
Then, the precipitate was washed 3 times with methanol and dried to obtain resin powder. Yield: 82%, Mw: 12500 and Mw/Mn: 2.25.
Example of Resin Synthesis 2: Synthesis of Resin 2
A resin powder was obtained by synthesizing in the same manner as the Example of Resin Synthesis 1 with the exception that 1.2 parts of monomer H and 12.3 parts of monomer D were used. Yield: 82%, Mw: 13000 and Mw/Mn: 2.33.
Example of Resin Synthesis 3: Synthesis of Resin 3
Into a four-neck flask provided with a thermometer, a reflux condenser and a stirrer, 25.1 parts of 1,4-dioxane was charged and elevated temperature to 72° C.
A solution was prepared by dissolving 30.9 parts of monomer A, 5.4 parts of monomer B, 16.6 parts of monomer C, 1.0 parts of monomer E, 27.2 parts of monomer D, 0.5 parts of 2,2′-azobisisobutyronitrile, 2.3 parts of 2,2′ azobis (2,4-dimethylvaleronitrile) in 37.7 parts of 1,4-dioxane.
A resin powder was obtained by synthesizing in the same manner as the Example of Resin Synthesis 1. Yield: 87%, Mw: 14700 and Mw/Mn: 2.50.
Example of Resin Synthesis 4: Synthesis of Resin 2
The resin powder was obtained by synthesizing in the same manner as the Example of Resin Synthesis 1 with the exception that 2.5 parts of monomer E and 25.2 parts of monomer D were used. Yield: 87%, Mw: 13500 and Mw/Mn: 2.34.
Example of Resin Synthesis 5: Synthesis of Resin 5
Into a four-neck flask provided with a thermometer and a reflux condenser, 27.78 parts of 1,4-dioxane was charged and bubbling with a nitrogen gas for 30 minutes was performed. After elevating temperature to 73° C. under a nitrogen seal, a solution being a mixture of 15.00 parts of monomer F, 5.61 parts of monomer B, 2.89 parts of monomer C, 12.02 parts of monomer G, 10.77 parts of monomer D, 0.34 parts of azobisisobutyronitrile, 1.52 parts of azobis-2,4-dimethylvaleronitrile and 63.85 parts of 1,4-dioxane was added dropwise over 2 hours while maintaining a temperature of 73° C. After completion of dropwise addition, a temperature of 73° C. was kept the heat for 5 hours. After cooling, the reaction solution was diluted with 50.92 parts of 1,4-dioxane. The diluted mass was poured into a mixed solvent of 481 parts of methanol and 120 parts of ion-exchanged water while stirring, and a precipitate resin was collected by filtrating. The filtrated material was placed into a liquid being 301 parts of methanol and filtration was performed after stirring. The operation of placing the resulting filtrated material in the same liquid, stirring and filtrating was repeated twice. Thereafter reduced pressure drying was performed to obtain 37.0 parts of resin having structure units below. Yield: 80%, Mw: 7900, Mw/Mn: 1.96.
Example of Resin Synthesis 6: Synthesis of Resin 6
Into a four-neck flask provided with a thermometer, a reflux condenser and a stirrer, 42.7 parts of 1,4-dioxane was charged and elevated temperature to 68° C.
A solution was prepared by dissolving 14.9 parts of monomer A, 4.6 parts of monomer B, 26.8 parts of monomer C, 19.9 parts of monomer D, 0.4 parts of 2,2′-azobisisobutyronitrile, 20. parts of 2,2′ azobis (2,4-dimethylvaleronitrile) in 44.4 parts of 1,4-dioxane.
This solution was added dropwise over 2 hours into the above described four-neck flask.
Thereafter, the reaction solution was kept the heat for 5 hours while maintaining a temperature of 68° C. and, was diluted with 83 parts of 1,4-dioxane. A resin solution was poured into a mixed solvent of 739 parts of methanol and 185 parts of water to obtain a precipitate.
Then, the precipitate was washed 3 times with methanol and dried to obtain resin powder. Yield: 82%, Mw: 15400 and Mw/Mn: 1.71.
Example of Resin Synthesis 7: Synthesis of Resin 7
Into a four-neck flask provided with a thermometer, a reflux condenser and a stirrer, 16.2 parts of 1,4-dioxane was charged and elevated temperature to 65° C.
A solution was prepared by dissolving 7.8 parts of monomer A, 1.8 parts of monomer B, 5.5 parts of monomer C, 8.6 parts of monomer D, 0.3 parts of monomer H, 3.1 parts of monomer I, 0.2 parts of 2,2′-azobisisobutyronitrile, 0.8 parts of 2,2′ azobis (2,4-dimethylvaleronitrile) in 44.4 parts of 1,4-dioxane.
This solution was added dropwise over 2 hours into the above described four-neck flask.
Thereafter, the reaction solution was kept the heat for 5 hours while maintaining a temperature of 65° C., and was diluted with 30 parts of 1,4-dioxane. A resin solution was poured into a mixed solvent of 282 parts of methanol and 70 parts of water to obtain a precipitate.
Then, the precipitate was washed 3 times with methanol and dried to obtain resin powder. Yield: 82%, Mw: 17300 and Mw/Mn: 2.15.
Each of resist compositions was prepared by mixing and dissolving each of the components below, and then filtering through a fluororesin filter having 0.2 μm pore diameter.
The components used in Table 1 were shown below.
<Photo Acid Generator>
The photo acid generator was synthesized according to the method described in JP 2007-224008 A.
<Cross-Linking Agent>
<Quencher>
Quencher 1: 2,6-diisopropylaniline
Quencher 2: trimethoxyethoxyethylamine (TMEA)
<Solvent>
PMGE Solvent 1:
PMGE Solvent 2:
PMGE Solvent 3:
A composition for an organic antireflective film, “ARC-29A-8”, manufactured by Brewer Co. Ltd., was applied onto silicon wafers and baked for 60 seconds at 205° C. to form a 78 nm thick organic antireflective film. The resist liquid in which the resist composition shown in Example 1 in Table 1 was dissolved in the PMGE solvent 1 described above was spin-coated thereon as the first resist composition so that the thickness of the resulted film became 0.08 μm after drying.
After applying the resist liquid, 60 seconds of pre-baking at 90° C. was performed on a direct hot plate.
The whole surface of the obtained resist film on each wafer was exposed at the exposure amount of 3.0 mJ/cm2 by using an ArF excimer stepper (“FPA5000-AS3” manufactured by Canon: NA=0.75, ⅔ Annular). Subsequently, each of the wafers was pattern-exposed at the exposure amount of 43 mJ/cm2 by using an ArF excimer stepper (“FPA5000-AS3” manufactured by Canon: NA=0.75, ⅔ Annular) and a mask having 1:1 line and space patterns having a line width of 100 nm.
After the exposure, post-exposure baking was performed on a hotplate at 100° C. for 60 seconds.
Further, puddle development with 2.38 wt % tetramethylammonium hydroxide aqueous solution was performed for 60 seconds to form a desired pattern.
Thereafter, hard-baking was performed for 60 seconds at 150° C., and then for 60 seconds at 170° C.
When the resulted first line and space pattern was observed using a scanning electron microscope, it was confirmed that a good and precise pattern was formed.
Then, as a second resist liquid, a resist liquid in which the resist composition of Reference Example in Table 1 was dissolved in the above PMGE solvent 2 was applied on the obtained first line and space pattern so that the thickness of the resulted film became 0.08 μm after drying.
After applying the second resist liquid, pre-baking was performed for 60 seconds at 85° C. on a direct hot plate.
A second line and space pattern was exposed at the exposure amount of 33 mJ/cm2 by using an ArF excimer stepper (“FPA5000-AS3” manufactured by Canon: NA=0.75, ⅔ Annular) onto thus obtained a second resist film so as to be in a direction perpendicular to the first line and space pattern by rotating the pattern by 90°.
After the exposure, post-exposure baking was performed on a hotplate at 85° C. for 60 seconds.
Further, puddle development with 2.38 wt % tetramethylammonium hydroxide aqueous solution was performed for 60 seconds to form a lattice-shaped pattern.
When the resulted first and second line and space patterns were observed using a scanning electron microscope, it was confirmed that the second line and space pattern was formed with a good shape on the first line and space pattern, the shape of the first line and space pattern was retained, and overall a good pattern was formed. Further, the shape of the cross-section thereof was also good.
The composition for an organic antireflective film, “ARC-29A-8”, by Brewer Co. Ltd., was applied onto silicon wafers and baked for 60 seconds at 205° C. to form a 78 nm thick organic antireflective film.
Resist liquids in which the resist compositions of Examples 2, 4 to 6 described in Table 1 were dissolved in the above PMGE solvent 1 was then applied thereon by spin coating so that the thickness of the resulting film became 0.09 μm after drying.
After applying the resist liquid, 60 seconds of pre-baking at 105° C. was performed on a direct hot plate.
The whole surface of the obtained resist film was exposed at the exposure amount of 3.0 mJ/cm2 by using an ArF excimer stepper (“FPA5000-AS3” manufactured by Canon: NA=0.75, ⅔ Annular). Subsequently, each of the wafers was pattern-exposed at the exposure amount described in Table 2 by using an ArF excimer stepper (“FPA5000-AS3” manufactured by Canon: NA=0.75, ⅔ Annular) and a mask having 1:1.5 line and space patterns having a line width of 150 nm.
After the exposure, post-exposure baking was performed on a hotplate at 105° C. for 60 seconds.
Further, puddle development with 2.38 wt % tetramethylammonium hydroxide aqueous solution was performed for 60 seconds to form a desired pattern.
Thereafter, hard-baking was performed for 60 seconds at 155° C., and then for 60 seconds at 180° C.
When the resulted first line and space pattern was observed using a scanning electron microscope, it was confirmed that a good and precise 1:3 line and space pattern with line width of 94 nm was formed.
Then, as a second resist liquid, a resist liquid in which the resist composition of Reference Example in Table 1 was dissolved in the above PMGE solvent 2 was applied on the obtained first line and space pattern so that the thickness of the resulted film became 0.07 μm after drying.
After applying the second resist liquid, pre-baking was performed for 60 seconds at 85° C. on a direct hot plate.
Onto thus obtained a second resist film, a second line and space pattern was exposed at the exposure amount of 38 mJ/cm2 by using an ArF excimer stepper (“FPA5000-AS3” manufactured by Canon: NA=0.75, ⅔ Annular) and a mask having 1:1.5 line and space patterns having a line width of 150 nm.
After the exposure, post-exposure baking was performed on a hotplate at 85° C. for 60 seconds.
Further, puddle development with 2.38 wt % tetramethylammonium hydroxide aqueous solution was performed for 60 seconds to form a fine line and space pattern with overall half pitch, in which the second line and space pattern was formed intermediately between the first line and space pattern.
When the resulting first and second line and space patterns are observed using a scanning electron microscope, it was confirmed that the second line and space pattern between the first line and space pattern was formed with a preferred shape between the first line and space pattern, in addition that the shape of the first line and space pattern was maintained, and overall a superior pattern was formed. The profile shape was also superior.
A composition for an organic antireflective film, “ARC-29A-8”, manufactured by Brewer Co. Ltd., was applied onto silicon wafers and baked for 60 seconds at 205° C. to form a 78 nm thick organic antireflective film. The resist liquid in which the resist composition shown in Example 3 of Table 1 was dissolved in the PMGE solvent 1 described above was spin-coated thereon as the first resist composition so that the thickness of the resulted film became 0.09 μm after drying.
Thereafter, 60 seconds of pre-baking at 105° C. was performed on a direct hot plate.
The whole surface of the obtained resist film on each wafer was exposed at the exposure amount of 3.0 mJ/cm2 by using an ArF excimer stepper (“FPA5000-AS3” manufactured by Canon: NA=0.75, ⅔ Annular).
After exposure, post-exposure baking was performed on a hotplate at 105° C. for 60 seconds.
Further, puddle development with 2.38 wt % tetramethylammonium hydroxide aqueous solution was performed for 60 seconds to form a desired pattern.
Then, hard-baking was performed for 60 seconds at 155° C., and then for 60 seconds at 180° C.
(Evaluation of Resistance to the Solvent Evaluation of Example 3)
The wafer after hard-baking was treated using 3.75 cc of a mixture solution with 3:7 of propylene glycol monomethyl ether:propylene glycol monomethyl ether acetate while rotating wafer with revolution speed of 1000 rpm. The result was shown in Table 3.
A composition for an organic antireflective film, “ARC-29A-8”, by Brewer Co. Ltd., was applied onto silicon wafers and baked for 60 seconds at 205° C. to form a 78 nm thick organic antireflective film.
Resist liquids in which the resist compositions of Example 7 described in Table 1 was dissolved in the PMGE solvent 3 described above was spin-coated thereon as the first resist composition so that the thickness of the resulted film became 0.09 μm after drying.
After application of the resist liquid, 60 seconds of pre-baking at 120° C. was performed on a direct hot plate.
A pattern was then exposed onto thus obtained resist film at the exposure amount of 26 mJ/cm2 by using an ArF excimer stepper (“FPA5000-AS3” manufactured by Canon: NA=0.75, ⅔ Annular) and a mask having 1:1.5 line and space patterns having a line width of 150 nm.
After exposure, post-exposure baking was performed on a hotplate at 120° C. for 60 seconds.
Further, puddle development with 2.38 wt % tetramethylammonium hydroxide aqueous solution was performed for 60 seconds to form a desired pattern.
Then, hard-baking was performed for 20 seconds at 205° C.
When the resulting first line and space pattern was observed using a scanning electron microscope, it was confirmed that a 1:3 line and space precise pattern with 94 nm line width was formed.
Then a resist liquid in which the resist composition of Reference Example described in Table 1 was dissolved in the PMGE solvent 2 was applied on the obtained first line and space pattern so that the thickness of the resulted film became 0.07 μm after drying.
After application of the second resist liquid, 60 seconds of pre-baking at 85° C. was performed on a direct hot plate.
A pattern was then exposed onto thus obtained a second resist film at the exposure amount of 38 mJ/cm2 by using an ArF excimer stepper (“FPA5000-AS3” manufactured by Canon: NA=0.75, ⅔ Annular) and a mask having 1:1.5 line and space patterns having a line width of 150 nm.
After exposure, post-exposure baking was performed on a hotplate at 85° C. for 60 seconds.
Further, puddle development with 2.38 wt % tetramethylammonium hydroxide aqueous solution was performed for 60 seconds.
Finally, a line and space patterns in which the second line pattern was formed between the first line patterns and has a half pitch as a whole was formed.
When the resulted first and second line and space patterns were observed using a scanning electron microscope, it was confirmed that the second line and space pattern was formed with a good shape between the first line and space pattern, the shape of the first line and space pattern was retained, and overall a good pattern was formed. Further, the shape of the cross-section thereof was also good.
According to the resist processing method of the present invention, an extremely fine and highly accurate resist pattern can be formed which is obtained using the resist composition for forming a first resist pattern in a multi-patterning method or a multi-imaging method such as a double patterning method, double imaging method.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2008-234207 | Sep 2008 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2009/065628 | 9/8/2009 | WO | 00 | 4/4/2011 |
