Patent Application
20130164694
The present invention relates to a rinse solution for lithography. Specifically, this invention relates to a rinse solution suitable for development of a photosensitive resin composition used in a lithographic process for manufacturing semiconductor devices, color filters, flat panel displays (FPDs) such as liquid crystal displays, and the like. The present invention also relates to a pattern formation method employing the above rinse solution.
Hitherto, photolithography has been adopted for microfabrication or for formation of fine elements in extensive fields including the manufacture of semiconductor integrated circuits such as LSIs, the preparation of FPD screens, and the production of circuit boards for color filters, thermal heads and the like. In the photolithography, a positive- or negative-working photosensitive resin composition is employed for resist pattern formation. Widely used examples of the positive-working photoresist include a photosensitive resin composition comprising an alkali-soluble resin and a photosensitive substance of quinonediazide compound.
Meanwhile, according as the integration degree of LSIs has needed to be increased more and more recently, it has been required to increase fineness of resist patterns. In order to meet this requirement, it is becoming practical for a lithographic process to use radiation of shorter wavelength such as deep UV light emitted from a KrF excimer laser (248 nm), an ArF excimer laser (193 nm), an Extreme Ultra-violet (EUV; 13 nm), X-ray or an electron beam or the like. For coping with finer fabrication, the photoresist used in microfabrication must be a photosensitive resin composition capable of giving a pattern of high resolution. Further, it is also desired that the photosensitive resin composition be improved not only in resolution but also in sensitivity and in accuracy on shape and dimension of the pattern. In view of that, a “chemically amplified photosensitive resin composition” is proposed as a radiation-sensitive resin composition having sensitivity to the radiation of short wavelength and giving a pattern of high resolution. The chemically amplified photosensitive resin composition comprises a compound that generates an acid when exposed to radiation, and hence when the radiation is applied, the compound generates an acid and the acid serves as a catalyst in image-formation to improve sensitivity. Because of its high sensitivity, the chemically amplified photosensitive resin composition is becoming widely used in place of conventional photosensitive resin compositions.
However, in accordance with increasing the fineness in pattern fabrication as described above, problems such as pattern collapse and pattern roughness are liable to get worse. To cope with those problems, various methods have been researched. For example, it is studied to change or improve components of the resist compositions.
When a resist pattern is washed with pure water after development, the surface tension of pure water may apply negative pressure on the pattern. This is thought to be a cause of the pattern collapse. Based on this thought, it is proposed to wash the pattern not with pure water but with a rinse solution containing a particular component (see, Patent documents 1 to 4). Those patent documents propose rinse solutions for lithography, and the proposed solutions contain particular nonionic surfactants.
[Patent document 1] Japanese Patent Laid-Open No. 2004-184648
[Patent document 4] Japanese Patent Laid-Open No. 2008-146099
However, although the solutions described in the above documents somewhat reduce the pattern collapse, they are still desired to be improved. Further, taking into consideration that miniaturization often induces melting of patterns, there is much room for improvement in the above solutions. Accordingly, it is desired to provide such a rinse solution for lithography or a resist substrate treatment method as can solve both the pattern collapse and the melting at the same time.
The present invention resides in a rinse solution for lithography, which comprises water and at least one nitrogen-containing compound selected from the group consisting of the compounds represented by the following formulas (1) to (3):
in which R1, R2, R3 are independently a hydrogen atom or a saturated or unsaturated hydrocarbon chain of 1 to 10 carbon atoms, provided that
a hydrogen atom connecting to the carbon atom constituting said hydrocarbon chain may be substituted with —OH, —F, ═O or —NH2,
said hydrocarbon chain may contain therein —(CO)—, —(COO)—, —(CONH)—, —O—, —NH— or —N═,
two of R1, R2, R3 may combine with each other to form a ring,
one terminal of the R1, R2, R3 may connect to a polymer main chain of 20000 or less carbon atoms, and
at least one of R1, R2, R3 comprises two or more carbon atoms;
in which R4, R5, R6, R7 are independently a hydrogen atom or a saturated or unsaturated hydrocarbon chain of 1 to 10 carbon atoms, provided that
a hydrogen atom connecting to the carbon atom constituting said hydrocarbon chain may be substituted with —OH, —F, ═O or —NH2,
said hydrocarbon chain may contain therein —(CO)—, —(COO)—, (CONH)—, —O—, —NH— or —N═,
two of the R4, R5, R6, R7 may combine with each other to form a ring,
all R4, R5, R6, R7 are not hydrogen atoms at the same time, and
L is a hydrocarbon chain of 1 to 10 carbon atoms; and
in which R8, R9, R10, R11 are independently a hydrogen atom or a saturated or unsaturated hydrocarbon chain of 1 to 10 carbon atoms, provided that
a hydrogen atom connecting to the carbon atom constituting said hydrocarbon chain may be substituted with —OH, —F, ═O or —NH2,
said hydrocarbon chain may contain therein —(CO)—, —O—, —(COO)—, —(CONH)—, —NH— or —N═,
two of R8, R9, R10, R11 may combine with each other to form a ring,
all R8, R9, R10, R11 are not hydrogen atoms at the same time,
L′ is a hydrocarbon chain of 1 to 10 carbon atoms, and
m is the number of 1 to 1000 for indicating the repeating degree.
The present invention also resides in a pattern formation method comprising the steps of:
(1) coating a substrate with a photosensitive resin composition to form a photosensitive resin composition layer,
(2) subjecting said photosensitive resin composition layer to exposure,
(3) developing the photosensitive resin composition layer with a developing solution, and
(4) treating the substrate with the above rinse solution for lithography.
The rinse solution of the present invention for lithography enables to prevent a fine resist pattern, particularly, a miniaturized pattern of ArF resist or of deep UV resist, from collapsing and melting at the same time, and thereby it becomes possible to form a more precise and accurate pattern.
Embodiments of the present invention are described below in detail.
The rinse solution for lithography according to the present invention comprises water and a particular nitrogen-containing compound having an organic group. The nitrogen-containing compound used in the present invention is represented by one of the following formulas (1) to (3):
in which R1, R2, R3 are independently a hydrogen atom or a saturated or unsaturated hydrocarbon chain of 1 to 10 carbon atoms, provided that
a hydrogen atom connecting to the carbon atom constituting said hydrocarbon chain may be substituted with —OH, —F, ═O or —NH2,
said hydrocarbon chain may contain therein —(CO)—, —(COO)—, —(CONH)—, —O—, —NH— or —N═,
two of R1, R2, R3 may combine with each other to form a ring,
one terminal of the R1, R2, R3 may connect to a polymer main chain of 20000 or less carbon atoms, and
at least one of R1, R2, R3 comprises two or more carbon atoms;
in which R4, R5, R6, R7 are independently a hydrogen atom or a saturated or unsaturated hydrocarbon chain of 1 to 10, preferably 1 to 4 carbon atoms, provided that
a hydrogen atom connecting to the carbon atom constituting said hydrocarbon chain may be substituted with —OH, —F, ═O or —NH2,
said hydrocarbon chain may contain therein —(CO)—, —(COO)—, —(CONH)—, —O—, —NH— or —N═,
two of R4, R5, R6, R7 may combine with each other to form a ring,
all R4, R5, R6, R7 are not hydrogen atoms at the same time, and three or more of the R2s are preferably hydrocarbon chains and all the R2s are most preferably hydrocarbon chains, and
L is a hydrocarbon chain of 1 to 10 carbon atom, preferably 1 to 6, further preferably 1 to 4 carbon atoms; and
in which R8, R9, R10, R11 are independently a hydrogen atom or a saturated or unsaturated hydrocarbon chain of 1 to 10 carbon atoms, provided that
a hydrogen atom connecting to the carbon atom constituting said hydrocarbon chain may be substituted with —OH, —F, ═O or —NH2,
said hydrocarbon chain may contain therein —(CO)—, —(COO)—, —(CONH)—, —O—, —NH— or —N═,
two of R8, R9, R10, R11 may combine with each other to form a ring,
all R8, R9, R10, R11 are not hydrogen atoms at the same time,
L′ is a hydrocarbon chain of 1 to 10, preferably 1 to 5 carbon atoms, and
m is the number of 1 to 1000, preferably 1 to 50 for indicating the repeating degree.
In each of the formulas (1) to (3), any two of R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11 in a molecule may combine with each other to form a ring, such as, piperazine ring, piperidine ring, pyridine ring, pyrazoline ring, pyrazolidine ring, pyrroline ring or morpholine ring.
Further, in the formula (1), one terminal of R1, R2, R3 may connect to a polymer main chain. In that case, the nitrogen-containing compound of the formula (1) is regarded as a side chain connecting to the polymer main chain. There is no particular restriction on the polymer main chain, which may be a polymer obtained by normal polymerization such as addition polymerization of vinyl groups, condensation polymerization of acid amide bonds, or dehydration condensation polymerization of acidic groups. If being too long, the polymer main chain may have such high hydrophobicity and such poor water solubility that solid substances may remain on the resultant pattern. Accordingly, the polymer main chain contains 20000 or less carbon atoms, preferably 10000 or less carbon atoms, most preferably 1000 or less carbon atoms.
In each formula, all R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11 are not hydrogen atoms at the same time. This means that at least one of R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11 is the above hydrocarbon chain. All of them are preferably hydrocarbon chains.
Among the nitrogen-containing compounds represented by the formulas (1) to (3), those of the formula (2) are preferred because the effect of the present invention remarkably emerges with them. Because of easy availability and outstanding effect of the invention, tetraalkylenediamines are particularly preferred. Accordingly, the nitrogen-containing compound is preferably selected from the group consisting of:
Besides the above, the nitrogen-containing compound may be also preferably represented by one of the following formulas (a1) to (a8):
in which each R′ is independently a hydrogen atom or a saturated or unsaturated hydrocarbon chain of 1 to 10 carbon atoms, provided that a hydrogen atom connecting to the carbon atom constituting said hydrocarbon chain may be substituted with —OH, —F, ═O or —NH2. Preferred examples of the R′ include methyl, ethyl, methoxy, ethoxy, and trifluoromethyl.
In the above formulas, x is the number of substituents connecting to the ring; and n is 1 or 2. This means that each of the rings in (a5) to (a7) consists of five- or six members. The number x ranges from 0 to the maximum determined by the ring size and other substituents.
Further, the nitrogen-containing compound may be still also preferably represented by one of the following formulas (b1) to (b4):
in which R′, x and n are the same as described above; p is 0 to 2; and q is 1 to 10000, preferably 1 to 1000.
The nitrogen-containing compounds of (b1) to (b4) are polymers including the nitrogen-containing compounds represented by the above formula (1) as the side chains.
The nitrogen-containing compounds may be used in combination of two or more.
The rinse solution for lithography according to the present invention comprises water as a solvent, as well as the above nitrogen-containing compound. The water is preferably subjected to distillation, ion-exchange treatment, filtration or various adsorption treatments, so as to remove organic impurities, metal ions and the like. Accordingly, pure water is particularly preferred.
The lithographic rinse solution of the present invention may further contain a surfactant. The surfactant improves wettability of the resist surface to the rinse solution, and also it controls the surface tension to prevent the pattern from collapsing and peeling off. Accordingly, the rinse solution preferably comprises a surfactant.
The surfactant may be a nonionic, cationic, anionic or amphoteric one. However, preferred is a nonionic surfactant, and particularly preferred is a nonionic surfactant containing an alkyleneoxy group because such surfactant works in cooperation with the above nitrogen-containing compound to enhance the effect of the present invention. Preferred examples thereof include a nonionic surfactant represented by the following formula (S1) or (S2):
in which EO and PO represent —(CH2)2—O— and —CH2—CH(CH3)—O—, respectively, provided that the units of each of EO and PO may combine with each other either randomly or to form a block; L1 is a 1 to 30 carbon atom-hydrocarbon chain which may contain an unsaturated bond. The hydrocarbon chain L1 is preferably represented by the following formula:
in which each Rb is independently a saturated or unsaturated, straight-chain or branched-chain hydrocarbon chain of 3 to 10 carbon atoms, provided that a hydrogen atom connecting to the carbon atom constituting said hydrocarbon chain may be substituted with —OH. The Ra is a saturated or unsaturated hydrocarbon chain of 5 to 30 carbon atoms. Each of r1 to r3 and s1 to s3 is an integer of 20 or less for indicating the repeating degree of EO or PO, and each of r1+s1 and r2+s2 is independently an integer of 0 to 20 provided that r1+s1+r2+s2 is an integer of 1 or more. Each of r1+s1 and r2+s2 is preferably an integer of 2 to 10, and r3+s3 is an integer of 1 to 20, preferably 2 to 10.
Since strongly preventing the pattern from melting, the above surfactant preferably has high hydrophobicity. Accordingly, L1 or Ra preferably contains many carbon atoms and the group EO or PO is preferably less repeated because the groups L1 and Ra are hydrophobic and the groups EO and PO are relatively hydrophilic.
Two or more surfactants can be used in combination, if necessary.
The rinse solution for lithography according to the present invention may further contain various additives, if necessary. Examples of the additives include acids, bases, and organic solvents.
The acids or bases may be incorporated for controlling the pH value of the solution or for improving the solubility of each component. Any acid or base can be selected to use unless it impairs the effect of the present invention. They are, for example, carboxylic acids, amines or ammonium salts. They include fatty acids, aromatic carboxylic acids, primary amines, secondary amines, tertiary amines and ammonium compounds, each of which may be substituted with any substituent. Concrete examples of them include formic acid, acetic acid, propionic acid, benzoic acid, phthalic acid, salicylic acid, lactic acid, malic acid, citric acid, oxalic acid, malonic acid, succinic acid, fumaric acid, maleic acid, aconitic acid, glutaric acid, adipic acid, monoethanolamine, diethanolamine, triethanolamine, triisopropanolamine and tetramethylammonium.
In addition to water, an organic solvent can be used as a co-solvent. The organic solvent may have functions of controlling the surface tension of the rinse solution and of improving the wettability thereof to the resist surface. The solvent used for this purpose is selected from water-soluble organic solvents. Examples of the organic solvent include: alcohols such as methanol, ethanol iso-propanol and t-butanol; glycols, such as ethylene glycol or diethyleneglycol; ketones such as acetone and methyl ethyl ketone; and esters such as methyl acetate, ethyl acetate and ethyl lactate; dimethyl formamide, dimethyl sulfoxide, methyl cellosolve, cellosolve, butyl cellosolve, cellosolve acetate, alkyl cellosolve acetate, propylene glycol alkyl ether, propylene glycol alkyl ether acetate, butyl carbitol, carbitol acetate, and tetrahydrofuran.
However, the above organic solvent may dissolve or denature the resist of the pattern, and accordingly it must be incorporated in a small amount, if used. The amount thereof is normally 15 weight parts or less but preferably not less than 0.1 wt % based on the total weight of said rinse solution. For the purpose of keeping the resist from being dissolved or denatured, it is preferred not to use the organic solvent at all.
In addition the lithographic rinse solution may comprise a preservative, bactericidal and/or fungicidal agent. These agents are employed in order to avoid the growth of bacteria or fungi in an aging rinse solution. Examples include alcohols, such as phenoxyethanol, or isothiazolones, and the like. Notably useful are the preservatives, fungicides and bactericides marketed under the tradename BestCide provided by Nippon Soda Co. Typically, these agents do not have any effect on the performance of the lithographic rinse solution and are added in amount of not more than 1 wt %, preferably less than 0.1 wt % but preferably not less than 0.001 wt %.
The lithographic rinse solution of the present invention comprises water as a solvent and other components dissolved therein. The content of each component is freely determined according to the use of the rinse solution, the kind of the resist to be treated and the solubility of each component. If containing the nitrogen-containing compound in a large amount, the rinse solution generally shows large effect on improving the pattern collapse. On the other hand, however, if containing the nitrogen-containing compound in a small amount, the rinse solution tends to show large effect on improving the melting. In practice, therefore, the content is properly determined in view of the balance between them. For example, the content of the nitrogen-containing compound is not less than 0.005%, but not more than 5%, based on the total weight of the solution. Especially, in the case where the rinse solution contains no surfactant, the content of the nitrogen-containing compound is preferably not less than 0.01%, more preferably not less than 0.05%, and preferably not more than 5%, more preferably not more than 2%, based on the total weight of the solution. If the solution contains a surfactant, the nitrogen-containing compound is incorporated in an amount of preferably not less than 0.005%, more preferably not less than 0.01%, and preferably not more than 1%, more preferably not more than 0.5%, based on the total weight of the solution. Further, the content of the surfactant is generally not less than 0.01%, preferably not less than 0.03%, more preferably not less than 0.1%, and generally not more than 10%, preferably not more than 1%, more preferably not more than 0.5%, based on the total weight of the solution. In either case, water, the nitrogen-containing compound and the surfactant are main components and hence the rinse solution contains other components in an amount of preferably 1% or less, more preferably 0.5% or less, based on the total weight of the solution.
The pattern formation method according to the present invention is described below in detail. In the pattern formation method of the present invention, there is no particular restriction on the lithographic process. Accordingly, the lithographic process can be carried out in any known manner of forming a resist pattern from a conventional positive- or negative-working photosensitive resin composition. The following describes a typical pattern formation method employing the lithographic rinse solution of the present invention.
First, a photosensitive resin composition is coated on a surface, which may be pretreated, if necessary, of a substrate, such as a silicon substrate or a glass substrate, according to a known coating method such as spin-coating method, to form a photosensitive resin composition layer. Prior to the coating of the photosensitive resin composition, an antireflection film can be beforehand formed under or above the resist by coating. The antireflection film can improve the section shape and the exposure margin.
Any known photosensitive resin composition can be used in the pattern formation method of the present invention. Representative examples of the compositions usable in the present invention include: a composition comprising a quininediazide type photosensitive substance and an alkali-soluble resin, a chemically amplified photosensitive resin composition (which are positive-working compositions); a composition comprising a photosensitive functional group-containing polymer such as polyvinyl cinnamate, a composition comprising an azide compound such as an aromatic azide compound or a bisazide compound with a cyclized rubber, a composition comprising a diazo resin, a photo-polymerizable composition comprising an addition-polymerizable unsaturated compound, and a chemically amplified negative-working photosensitive resin composition (which are negative-working compositions).
Examples of the quinonediazide type photo-sensitive substance used in the positive-working composition comprising a quinonediazide type photosensitive substance and an alkali-soluble resin include: 1,2-benzoquinonediazide-4-sufonic acid, 1,2-naphthoquinonediazide-4-sufonic acid, 1,2-naphthoquinonediazide-5-sufonic acid, and sufonic esters or amides thereof. Examples of the alkali-soluble resin include: novolak resin, polyvinyl phenol, polyvinyl alcohol, and copolymers of acrylic acid or methacrylic acid. The novolak resin is preferably prepared from one or more phenols such as phenol, o-cresol, m-cresol, p-cresol and xylenol in combination with one or more aldehydes such as formaldehyde and paraformaldehyde.
Either positive- or negative-working chemically amplified photosensitive resin composition can be used in the pattern formation method of the present invention. The chemically amplified resist generates an acid when exposed to radiation, and the acid serves as a catalyst to promote chemical reaction by which solubility to the developing solution is changed within the areas irradiated with the radiation to form a pattern. For example, the chemically amplified photosensitive resin composition comprises an acid-generating compound, which generates an acid when exposed to radiation, and an acid-sensitive functional group-containing resin, which decomposes in the presence of acid to form an alkali-soluble group such as phenolic hydroxyl or carboxyl group. The composition may comprise an alkali-soluble resin, a crosslinking agent and an acid-generating compound.
The photosensitive resin composition layer formed on the substrate is prebaked, for example, on a hot plate to remove solvent contained in the composition, to form a photoresist film of normally 0.5 to 2.5 μm thickness. The prebaking temperature depends on the solvent and the photosensitive resin composition, but is normally 20 to 200° C., preferably 50 to 150° C.
The photoresist film is then subjected to exposure through a mask, if necessary, by means of known exposure apparatus such as a high-pressure mercury lamp, a metal halide lamp, an ultra-high pressure mercury lamp, a KrF excimer laser, an ArF excimer laser, a soft X-ray irradiation system, and an electron beam lithography system.
After the exposure, baking treatment may be carried out, if necessary, and then development such as paddle development is carried out to form a resist pattern. The resist is normally developed with an alkaline developing solution. Examples of the alkaline developing solution include an aqueous solution of sodium hydroxide or tetramethylammonium hydroxide (TMAH). After the development, the resist pattern is rinsed (washed) with the rinse solution. The thus-formed resist pattern is employed as a resist for etching, plating, ion diffusion or dyeing, and then, if necessary, peeled away.
According to the pattern formation method of the present invention, even a pattern of high fineness and of high aspect ratio can be effectively prevented from collapsing and melting. Here, the term “aspect ratio” means the ratio of height to width in the resist pattern. Accordingly, the method of the present invention is preferably combined with a lithographic process capable of giving a fine resist pattern, such as, a lithographic process comprising exposure at a wavelength of 250 nm or shorter by use of a light source of a KrF excimer laser, an ArF excimer laser, an X-ray irradiation system or an electron beam lithography system. Further, the lithographic process preferably produces a resist pattern having a pattern dimension in which a line width of the line-and-space pattern or a hole diameter of the contact hole pattern is not more than 300 nm, preferably not more than 50 nm.
In the pattern formation method according to the present invention, the resist pattern after developed is treated with the aforementioned rinse solution for lithography. There is no particular restriction on how long the resist substrate is in contact with the rinse solution for lithography, namely, on the treating time. However, the treating time is generally not less than 1 second so as to obtain the effect of the present invention. There is also no particular restriction on how the resist is brought into contact with the rinse solution. For example, the resist substrate may be immersed in the rinse solution, or otherwise the rinse solution may be dropped or sprayed onto the resist substrate while the substrate is being spun.
Further, the pattern formation method of the present invention may comprise washing procedure with pure water after the development. The developed resist pattern may be washed with pure water before and/or after treated with the rinse solution for lithography according to the present invention. The washing with pure water before the treatment with the rinse solution is for the purpose of washing out the developing solution remaining on the resist pattern, and that after the treatment is for the purpose of washing out the rinse solution. The washing with pure water can be carried out in any manner. For example, the resist substrate may be immersed in pure water, or otherwise pure water may be dropped or sprayed onto the resist substrate while the substrate is being spun. The washing with pure water can be performed either or both of before and after the treatment. The washing after the development is preferred because it removes residues of the resist and the developing solution remaining on the substrate and thereby enhances the effect of the invention. On the other hand, the washing after the treatment can remove the rinse solution. Particularly in the case where the resist pattern is treated with the rinse solution of more than 1% concentration, the washing with pure water after the treatment sometimes enables the present invention to show the best effect because it enhances the effect on improvement in preventing the melting.
It is not completely clear at present why the prevention of melting is improved by treating the developed resist with the rinse solution for lithography according to the present invention. However, it is presumed to be as follows.
On the resist substrate after developed, many deprotected carboxylic acid groups are thought to remain. When brought into contact with an aqueous solution such as a common rinse solution, the carboxylic acid groups are ionized and hence the resist becomes water-soluble to cause the melting. However, if the resist is treated with the rinse solution of the present invention, the carboxylic acid groups react and combine with the nitrogen-containing compound. Since the formed structure is similar to an organic salt, the combined carboxylic acid groups are hard to be ionized and accordingly the resultant resist has a relatively low solubility to aqueous solutions. As a result, the rinse solution of the present invention improves the prevention of melting. In the above mechanism, the nitrogen-containing compound combines with the carboxylic acid group at the hydrophobic moiety, namely, at the hydrocarbon chain. Accordingly, the longer hydrocarbon chain the compound has, the more strongly the present invention tends to improve the prevention of melting.
In the case where the nitrogen-containing compound has two or more basic groups in a molecule, plural carboxylic acid groups on the resist substrate are crosslinked to improve the prevention of melting. Accordingly, the more basic groups the compound has in a molecule, the more the resist is hardened.
On the other hand, if having a low molecular weight, the nitrogen-containing compound in the rinse solution soaks from the resist surface into the inside when the resist pattern is treated with the rinse solution. Since the compound soaking into the resist can combine with the carboxylic acid groups inside of the resist, the prevention of melting is also enhanced.
The present invention is further explained by use of the following examples, but they by no means restrict embodiments of the present invention.
A silicon substrate was coated with a bottom anti-reflection layer-forming composition of KrF exposure type (KrF-17B [trademark], manufactured by AZ Electronic Materials (Japan) K.K.), to form an anti-reflection layer of 80 nm thickness. After that, an ArF resist composition (DX6270 [trademark], manufactured by AZ Electronic Materials (Japan) K.K.) was spread thereon to form a layer of 620 nm thickness, and then subjected to baking at 130° C. for 90 seconds to prepare a substrate having a resist layer. The obtained substrate was subjected to exposure by means of a KrF exposure apparatus (FPA-EX5 [trademark], manufactured by Canon Inc.), and thereafter developed to produce a developed resist substrate having line patterns. In the exposure step, the exposure conditions were so varied that the line width might be changed to form plural patterns of different aspect ratios.
The formed patterns were observed to estimate the maximum aspect ratio that did not cause pattern collapse. As a result of Comparative Example A101, the aspect ratio was 3.0 that did not cause pattern collapse.
Successively, melting behavior of the formed patterns was also evaluated. The substrate was placed in a furnace and heated at 130° C. for 70 seconds, and then the patterns were observed and found to be slightly melted.
In addition to the procedure of Comparative Example A101, a rinse treatment was performed by use of a rinse solution after the development. The substrate was then evaluated. Specifically, after the developed resist pattern was washed with pure water, the rinse treatment was carried out by dipping the resist pattern into the rinse solution for 8 to 10 seconds. The rinse solution contained each nitrogen-containing compound shown in Table 1. The results were as set forth in Table 1.
In Table 1, the pattern collapse was evaluated and classified into the following grades:
A: the pattern collapse was caused in an aspect ratio of more than 4.0, and hence was remarkably improved;
B: the pattern collapse was caused in an aspect ratio of 3.4 to 4.0, and hence was slightly improved; and
C: the pattern collapse was caused in an aspect ratio of less than 3.4, and hence was hardly or not at all improved.
Further in Table 1, the melting was also evaluated and classified into the following grades:
A: the melting was not at all caused;
B: the melting was slightly caused but negligible from the practical viewpoint; and
C: the melting was so seriously caused that the pattern was impossible to use practically.
The procedure of Comparative Example A101 was repeated except for using a rinse solution containing trimethylamine or N,N,N′,N′-tetramethylethylenediamine as the nitrogen-containing compound, to evaluate the patterns. The concentration of the nitrogen-containing compound was varied as shown in Table 2. The results were as set forth in Table 2.
In Table 2, the grades of the melting are the same as those in Table 1.
The procedure of Comparative Example A101 was repeated except for using a rinse solution containing a nitrogen-containing compound and/or a nonionic surfactant, to evaluate the patterns. As the nitrogen-containing compound, N,N,N′,N′-tetramethylethylenediamine was used. The nonionic surfactant was a compound represented by the following formula (S-1), (S-2) or (S-3). The results were as set forth in Table 3.
In the above formulas, Rb1 is methyl and Rb2 is isbutyl and r11, s11, r21 and s21 are integers satisfying the conditions of r11+r21=5, s11+s21=2, respectively; Ra2 is C18H37 and r12 is an integer satisfying the condition of r12=15; and Ra3 is C18H37 and r13 and s13 are integers satisfying the conditions of r13=10 and s13=5, respectively.
A silicon substrate was coated with a bottom anti-reflection layer-forming composition of ArF exposure type (ArF1C5D [trademark], manufactured by AZ Electronic Materials (Japan) K.K.), to form an anti-reflection layer of 37 nm thickness. After that, an ArF resist composition (AX2110P [trademark], manufactured by AZ Electronic Materials (Japan) K.K.) was spread thereon to form a layer of 90 nm thickness, and then subjected to baking at 110° C. for 60 seconds to prepare a substrate having a resist layer. The obtained substrate was subjected to exposure by means of an ArF exposure apparatus (NSR-S306C [trademark], manufactured by Nikon Corporation), and thereafter developed to produce a developed resist substrate having line patterns. In the exposure step, the exposure conditions were so varied that the line width might be changed to form plural patterns of different aspect ratios (Comparative Example B101). With respect to the pattern collapse and the melting, the sample of Comparative Example B101 was evaluated in the same manner as in Comparative Example A101.
Further, the procedure of Comparative Example B101 was repeated except for using a rinse solution containing a nitrogen-containing compound and/or a nonionic surfactant, to evaluate the patterns. As the nonionic surfactant, the nonionic surfactant (S-1) was used. The nitrogen-containing compound used in each Example was shown in Table 4. The results were as set forth in Table 4.
The following example shows that the addition of a bactericidal agent improves the shelf life of the lithographic rinse solution.
Two liter of the formulation of Example B217 was divided in two equal parts (C101 and C102). To formulation C102 was added 0.2 g of a 5% aqueous solution of Bestcide 600C, (a commercial bactericide manufactured by Nisso Chemical). Each of these two solutions was divided in nine parts, and left in open beakers for 12 hours. Subsequently, the beakers were tightly closed and stored for a certain period at a certain temperature as detailed in table 5. After that the solutions examined for bacteria using a proprietary incubation protocol from Nomura Microscience. The bacteria counts revealed that the material including the bactericide (C102) did have a significantly longer shelf life than the solution having no bactericide (C101).
One liter of the rinse solution was prepared by the same preparation as B218 except for changing the concentration of N,N,N′,N′-tetrabutyl ethylenediamene to 1.0%. The solution was then divided into two equal parts (D101 and D102), and 10 ml isopropanol was added to D102, while 10 ml water was added to D101. Both solutions were mixed well, placed into closed glass bottles and left alone at RT for seven days. Visual inspection of the bottles indicated that in both cases clear solutions were obtained.
However, when each of the two rinse solutions was hand dispensed on a resist coated, but unexposed 8 inch wafer, prepared as outlined in comparative example A101, visual inspection of the wafer surface revealed that the wetting was improved when a solution of D102 was coated on the resist.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2010-181305 | Aug 2010 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2011/068109 | 8/9/2011 | WO | 00 | 1/28/2013 |
