Hardmask compositions, hardmask layers, and patterning methods

Abstract

To provide a hardmask composition effectively applicable to a hardmask layer.SOLUTION: The hardmask composition comprises a compound represented by the chemical formula 1 in the figure, and a solvent, where the definition in the chemical formula 1 is as described in the specification.SELECTED DRAWING: None

Description

[Technical field]

[0001] The present invention relates to a hardmask composition, a hardmask layer including a cured product of the hardmask composition, and a pattern forming method using the hardmask composition. [Background technology]

[0002] Recently, the semiconductor industry has been evolving from patterns of hundreds of nanometers to ultrafine technology with patterns of several to tens of nanometers. Effective lithographic techniques are essential to realize such ultrafine technology.

[0003] A typical lithographic technique includes forming a material layer on a semiconductor substrate, coating a photoresist layer thereon, exposing and developing the photoresist pattern to form a photoresist pattern, and then etching the material layer using the photoresist pattern as a mask.

[0004] In recent years, as the size of a pattern to be formed decreases, it may be difficult to form a fine pattern having a good profile using only the above-mentioned typical lithographic techniques. Therefore, a technology for forming a fine pattern by forming an auxiliary layer, called a hard mask layer, between a material layer to be etched and a photoresist layer is being developed. [Prior art documents] [Patent documents]

[0005] [Patent Document 1] Korean Patent Publication No. 10-2023-0137101 Summary of the Invention [Problem to be solved by the invention]

[0006] It is an object of the present invention to provide a hardmask composition that can be effectively applied to a hardmask layer.

[0007] Another object of the present invention is to provide a hard mask layer comprising a cured product of the above hard mask composition.

[0008] It is still another object of the present invention to provide a pattern forming method using the above hard mask composition. [Means for solving the problem]

[0009] A hard mask composition according to an embodiment of the present invention includes a compound represented by the following Formula 1 and a solvent.

[0010] [ka]

[0011] In the above chemical formula 1, R 1 and R 3 each independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 30 carbon atoms, or a combination thereof, R 2 and R 4 are each independently a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 30 carbon atoms, a substituted or unsubstituted monovalent saturated or unsaturated alicyclic hydrocarbon group having 3 to 30 carbon atoms, or a combination thereof.

[0012] R in the above Chemical Formula 1 1 and R 3 each independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 20 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 20 carbon atoms, or a combination thereof; R 2 and R 4may each independently be a substituted or unsubstituted aromatic hydrocarbon group having 6 to 24 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 24 carbon atoms, a substituted or unsubstituted monovalent unsaturated alicyclic hydrocarbon group having 3 to 24 carbon atoms, or a combination thereof.

[0013] R in the above Chemical Formula 1 1 and R 3 each independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, R 2 and R 4 may each independently be a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 30 carbon atoms, or a combination thereof.

[0014] R in the above Chemical Formula 1 1 and R 3 each independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 20 carbon atoms, R 2 and R 4 may each independently be a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms.

[0015] R in the above Chemical Formula 1 1 and R 3 are each independently any one of substituted or unsubstituted moieties selected from Group 1 and Group 2 below, R 2 and R 4 may each independently be any one of substituted or unsubstituted moieties selected from Group 1 to Group 3 below.

[0016] [ka]

[0017] [ka]

[0018] [ka]

[0019] In Group 2 above, Z 1 and Z 2 are each independently -O-, -S-, or -NR a - (where R a is a hydrogen atom, a deuterium atom, or a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms), or a combination thereof.

[0020] R in the above Chemical Formula 1 1 ~R 4 may each independently be any one of substituted or unsubstituted moieties selected from Group 1-1 below.

[0021] [ka]

[0022] The compound represented by the above formula 1 preferably has a symmetric structure.

[0023] The compound represented by the above chemical formula 1 is preferably at least one selected from the group consisting of compounds represented by the following chemical formulas 1-1 to 1-5.

[0024] [ka]

[0025] [ka]

[0026] In the above Chemical Formula 1-1 to the above Chemical Formula 1-5, R a and R beach independently represents a hydroxy group, a substituted or unsubstituted alkoxy group having 1 to 4 carbon atoms, a halogen atom, an amino group, a thiol group, or a combination thereof, and each of m and n independently represents an integer of 0 to 9.

[0027] The molecular weight of the above compound is preferably 300 g / mol to 5,000 g / mol.

[0028] The compound is preferably contained in an amount of 0.1% by mass to 30% by mass based on the total mass of the hard mask composition.

[0029] The solvent is preferably propylene glycol, propylene glycol diacetate, methoxypropanediol, diethylene glycol, diethylene glycol butyl ether, tri(ethylene glycol) monomethyl ether, propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, cyclohexanone, ethyl lactate, γ-butyrolactone, N,N-dimethylformamide, N,N-dimethylacetamide, methylpyrrolidone, methylpyrrolidinone, acetylacetone, or ethyl 3-ethoxypropionate.

[0030] According to another embodiment of the present invention, there is provided a hardmask layer comprising a cured product of the hardmask composition described above.

[0031] According to yet another embodiment of the present invention, there is provided a patterning method including the steps of: providing a material layer on a substrate; applying the above-described hard mask composition on the material layer; heat-treating the hard mask composition to form a hard mask layer; forming a photoresist layer on the hard mask layer; exposing and developing the photoresist layer to form a photoresist pattern; selectively removing the hard mask layer using the photoresist pattern to expose a portion of the material layer; and etching the exposed portion of the material layer.

[0032] The step of forming the hard mask layer preferably includes a step of performing a heat treatment at a temperature of 100°C to 1,000°C. Effect of the Invention

[0033] According to the present invention, a hardmask composition can be provided that can be effectively applied to a hardmask layer. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0034] DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will now be described in detail with reference to exemplary embodiments thereof, so that those skilled in the art will be able to easily practice the present invention. However, the present invention may be embodied in many different forms and is not limited to the embodiments set forth herein.

[0035] Unless otherwise defined in this specification, "substituted" means that a hydrogen atom in a compound is replaced with a halogen atom (F, Br, Cl, or I), a hydroxy group, an alkoxy group, a nitro group, a cyano group, an amino group, an azido group, an amidino group, a hydrazino group, a hydrazono group, a carbonyl group, a carbamoyl group, a thiol group, an ester group, a carboxy group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a vinyl group, an alkyl group having 1 to 20 carbon atoms, an alkenyl group having 2 to 20 carbon atoms, an alkyl ... It means that the alkyl group is substituted with a substituent selected from an alkynyl group having from 20 carbon atoms, an aryl group having from 6 to 30 carbon atoms, an arylalkyl group having from 7 to 30 carbon atoms, an arylaryl group having from 9 to 30 carbon atoms, an alkoxy group having from 1 to 30 carbon atoms, a heteroalkyl group having from 1 to 20 carbon atoms, a heteroarylalkyl group having from 3 to 20 carbon atoms, a cycloalkyl group having from 3 to 30 carbon atoms, a cycloalkenyl group having from 3 to 15 carbon atoms, a cycloalkynyl group having from 6 to 15 carbon atoms, a heterocycloalkyl group having from 3 to 30 carbon atoms, and combinations thereof.

[0036] Further, the above-mentioned substituted halogen atoms (F, Br, Cl, or I), hydroxyl groups, nitro groups, cyano groups, amino groups, azido groups, amidino groups, hydrazino groups, hydrazono groups, carbonyl groups, carbamoyl groups, thiol groups, ester groups, carboxy groups or salts thereof, sulfonic acid groups or salts thereof, phosphoric acid groups or salts thereof, vinyl groups, alkyl groups having 1 to 20 carbon atoms, alkenyl groups having 2 to 20 carbon atoms, alkynyl groups having 2 to 20 carbon atoms, carbon Two adjacent substituents in an aryl group having 6 to 30 carbon atoms, an arylalkyl group having 7 to 30 carbon atoms, an arylaryl group having 9 to 30 carbon atoms, an alkoxy group having 1 to 30 carbon atoms, a heteroalkyl group having 1 to 20 carbon atoms, a heteroarylalkyl group having 3 to 20 carbon atoms, a cycloalkyl group having 3 to 30 carbon atoms, a cycloalkenyl group having 3 to 15 carbon atoms, a cycloalkynyl group having 6 to 15 carbon atoms, or a heterocyclic group having 2 to 30 carbon atoms can be bonded to form a ring.

[0037] Unless otherwise defined in this specification, "aromatic hydrocarbon" refers to a group having one or more hydrocarbon aromatic moieties, and includes not only non-fused aromatic hydrocarbon rings and fused aromatic hydrocarbon rings, but also forms in which hydrocarbon aromatic moieties are linked by single bonds, forms in which hydrocarbon aromatic moieties are directly or indirectly fused to non-aromatic fused rings, or combinations thereof.

[0038] More specifically, the substituted or unsubstituted aromatic hydrocarbon ring may be, but is not limited to, a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthracenyl group, a substituted or unsubstituted phenanthryl group, a substituted or unsubstituted naphthacenyl group, a substituted or unsubstituted pyrenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted quaterphenyl group, a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted triphenylenyl group, a substituted or unsubstituted perylenyl group, a substituted or unsubstituted indenyl group, a combination thereof, or a condensed form of a combination thereof.

[0039] Unless otherwise defined herein, "hetero" means containing one or more heteroatoms selected from the group consisting of N, O, S, Se, and P.

[0040] Unless otherwise defined herein, an "aromatic heterocycle" refers to an aromatic hydrocarbon ring containing one or more heteroatoms selected from N, O, S, Se and P in place of carbon (C). Two or more aromatic heterocycles may be directly linked through a sigma bond, and two or more aromatic heterocycles may be fused to each other. When an aromatic heterocycle is a fused ring, the entire fused ring or each ring may contain 1 to 3 heteroatoms.

[0041] As used herein, the term "polymer" includes both oligomers and polymers.

[0042] Unless otherwise specified in this specification, the "weight average molecular weight" is measured by dissolving a powder sample in tetrahydrofuran (THF) and then using a 1200 series gel permeation chromatography (GPC) manufactured by Agilent Technologies (using a Shodex LF-804 column and Shodex polystyrene as a standard sample).

[0043] In the semiconductor industry, there is a constant demand to reduce the size of chips, and to meet this demand, the line width of the resist patterned by lithography technology must be several tens of nanometers. Therefore, the height that can withstand the line width of the resist pattern is limited, and the resist may not have sufficient resistance in the etching step. To compensate for this, an auxiliary layer called a hardmask layer is used between the material layer to be etched and the photoresist layer. This hardmask layer serves as an intermediate film that transfers the fine pattern of the photoresist to the material layer through selective etching, and therefore the hardmask layer is required to have etching resistance so that it can withstand the etching process required for pattern transfer.

[0044] Existing hard mask layers are formed by chemical or physical vapor deposition, which requires large equipment and high process costs, resulting in poor economic efficiency. Recently, a technology for forming a hard mask layer by spin coating has been developed. The spin coating method is easier to process than conventional methods, and the gap fill and planarization characteristics of the hard mask layer formed by the spin coating method may be superior, but the etching resistance required for the hard mask layer tends to be somewhat lower. Therefore, a hard mask composition that can be applied to the spin coating method is required, and the hard mask layer formed by the spin coating method is required to have the same etching resistance as the hard mask layer formed by the chemical or physical vapor deposition method.

[0045] Therefore, in order to improve the etching resistance of the hard mask layer, research has been actively conducted to maximize the carbon content of the hard mask composition. However, as the carbon content of the compound contained in the hard mask composition increases, the solubility in the solvent tends to decrease. Therefore, it is required to maximize the carbon content of the compound contained in the hard mask composition to improve the etching resistance of the hard mask layer formed therefrom, without decreasing the solubility of the compound in the solvent.

[0046] The hard mask composition according to the embodiment of the present invention can increase the carbon content by including a compound having a large number of aromatic hydrocarbon rings or aromatic heterocycles in one molecule. Therefore, the hard mask layer obtained from the composition can have improved etching resistance. In addition, the compound can improve the solubility of the compound having a large number of aromatic hydrocarbon rings or aromatic heterocycles in a solvent by including a specific functional group in the aromatic hydrocarbon ring or aromatic heterocycle.

[0047] Specifically, the hard mask composition according to an embodiment of the present invention includes a compound represented by the following Formula 1, and a solvent.

[0048] [ka]

[0049] In the above chemical formula 1, R 1 and R 3 each independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 30 carbon atoms, or a combination thereof, R 2 and R 4 are each independently a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 30 carbon atoms, a substituted or unsubstituted monovalent saturated or unsaturated alicyclic hydrocarbon group having 3 to 30 carbon atoms, or a combination thereof.

[0050] The compound represented by Chemical Formula 1 included in the hard mask composition according to an embodiment of the present invention can increase the carbon content in the compound by including a structure in which two carbon-carbon triple bonds are connected to a carbon-carbon double bond.In addition, the compound can increase the carbon content in the compound by independently connecting an aromatic hydrocarbon group, an aromatic heterocyclic group, or a saturated or unsaturated alicyclic hydrocarbon group to the double bond and the triple bond, respectively.

[0051] In addition, when a composition including the compound is heat-treated, additional carbon rings may be formed due to electron transfer within the compound, and thus the carbon content in a hard mask layer manufactured from the composition may be maximized, and the hard mask layer may exhibit excellent etching resistance.

[0052] R in the above Chemical Formula 1 1 and R 3 are each independently a substituted or unsubstituted aromatic hydrocarbon group having 6 to 20 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 20 carbon atoms, or a combination thereof, for example, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, for example, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 20 carbon atoms, but are not limited to these.

[0053] R in the above Chemical Formula 1 1 and R 3 When R is a substituted aromatic hydrocarbon or heteroaromatic ring group, the substitution may be, for example, a hydroxy group, a substituted or unsubstituted alkoxy group having 1 to 4 carbon atoms, a halogen atom, an amino group, a thiol group, or a combination thereof, and examples thereof include, but are not limited to, a hydroxy group, a methoxy group, or an ethoxy group. 1 and R 3 When is substituted with a substituent as described above, the solubility of the compound in a solvent can be further improved.

[0054] In one embodiment, R in Formula 1 above 1 and R 3can each independently be any one of substituted or unsubstituted moieties selected from Group 1 and Group 2 below, but are not limited to these.

[0055] [ka]

[0056] [ka]

[0057] In Group 2 above, Z 1 and Z 2 are each independently -O-, -S-, or -NR a - (where R a is a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms, or a combination thereof.

[0058] R in the above Chemical Formula 1 2 and R 4 are each independently a substituted or unsubstituted aromatic hydrocarbon group having 6 to 24 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 24 carbon atoms, a substituted or unsubstituted monovalent unsaturated alicyclic hydrocarbon group having 3 to 24 carbon atoms, or a combination thereof, for example, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 30 carbon atoms, or a combination thereof, for example, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, but is not limited to these.

[0059] In one embodiment, R 2 and R 4 may each independently be any one of substituted or unsubstituted moieties selected from Group 1 above, Group 2, and Group 3 below, but are not limited thereto.

[0060] [ka]

[0061] As an example, R 1 ~R 4 may each independently be any one of substituted or unsubstituted moieties selected from Group 1-1 below, but is not limited thereto.

[0062] [ka]

[0063] R in the above Chemical Formula 1 1 ~R 4 may be different or the same, for example, R 1 ~R 4 Two of the are identical, or R 1 ~R 4 may all be the same. 1 ~R 4 R of 1 and R 3 are identical to each other and R 2 and R 4 may be the same, in which case the compound represented by the above formula 1 may have a symmetric structure. 1 ~R 4 R of 1 and R 3 are different from each other or R 2 and R 4 may be different from each other, in which case the compound represented by Chemical Formula 1 may have an asymmetric structure.

[0064] As an example, the compound represented by the above Chemical Formula 1 is preferably at least one selected from the group consisting of compounds represented by the following Chemical Formulas 1-1 to 1-5.

[0065] [ka]

[0066] [ka]

[0067] In the above Chemical Formula 1-1 to Chemical Formula 1-5, R a and R b may each independently be a hydroxy group, a substituted or unsubstituted alkoxy group having 1 to 4 carbon atoms, a halogen atom, an amino group, a thiol group, or a combination thereof, and m and n are each independently an integer from 0 to 9.

[0068] The compound may have a molecular weight of 300 g / mol to 5,000 g / mol. For example, it may have a molecular weight of 300 g / mol to 4,500 g / mol, for example, 300 g / mol to 4,000 g / mol, for example, 400 g / mol to 4,500 g / mol, for example, 400 g / mol to 4,000 g / mol, for example, 500 g / mol to 5,000 g / mol, for example, 500 g / mol to 4,500 g / mol, for example, 500 g / mol to 4,000 g / mol, for example, 500 g / mol to 3,500 g / mol, but is not limited thereto. By having a molecular weight in the above range, the carbon content and solubility in a solvent of the hard mask composition containing the compound may be adjusted and optimized.

[0069] The compound may be included in an amount of 0.1% by mass to 30% by mass based on the total mass of the hard mask composition. For example, it may be 0.2% by mass to 30% by mass, for example, 0.5% by mass to 30% by mass, for example, 1% by mass to 30% by mass, for example, 1% by mass to 25% by mass, for example, 1% by mass to 20% by mass, but is not limited thereto. By including the compound in the above content range, the thickness, surface roughness, and flatness of the hard mask can be easily adjusted.

[0070] The above compounds can be synthesized by appropriately referring to conventionally known synthesis methods. More specifically, those skilled in the art can easily synthesize the compounds by referring to the synthesis methods described in the Examples.

[0071] The hard mask composition according to one embodiment of the present invention may include a solvent. Specific examples of the solvent include, but are not limited to, at least one selected from the group consisting of propylene glycol, propylene glycol diacetate, methoxypropanediol, diethylene glycol, diethylene glycol butyl ether, tri(ethylene glycol) monomethyl ether, propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, cyclohexanone, ethyl lactate, γ-butyrolactone, N,N-dimethylformamide, N,N-dimethylacetamide, methylpyrrolidone, methylpyrrolidinone, acetylacetone, and ethyl 3-ethoxypropionate. The solvent is not particularly limited as long as it has sufficient solubility and / or dispersibility for the compound.

[0072] The hard mask composition of the present invention may further include additives such as a surfactant, a crosslinking agent, a thermal acid generator, a plasticizer, and the like.

[0073] Examples of the surfactant that can be used include, but are not limited to, fluoroalkyl compounds, alkylbenzenesulfonates, alkylpyridinium salts, polyethylene glycols, and quaternary ammonium salts.

[0074] The type of crosslinking agent may be, for example, a melamine-based agent, a substituted urea-based agent, or a polymer-based agent thereof. The crosslinking agent is preferably a crosslinking agent having at least two crosslink-forming substituents, and for example, compounds such as methoxymethylated glycoluril, butoxymethylated glycoluril, methoxymethylated melamine, butoxymethylated melamine, methoxymethylated benzoguanamine, butoxymethylated benzoguanamine, methoxymethylated urea, butoxymethylated urea, methoxymethylated thiourea, or butoxymethylated thiourea may be used.

[0075] In addition, a crosslinking agent having high heat resistance can be used as the crosslinking agent. As the crosslinking agent having high heat resistance, a compound containing a crosslinking-forming substituent having an aromatic hydrocarbon ring (e.g., a benzene ring or a naphthalene ring) in the molecule can be used.

[0076] Examples of the thermal acid generator that can be used include, but are not limited to, acidic compounds such as p-toluenesulfonic acid, trifluoromethanesulfonic acid, pyridinium p-toluenesulfonate, salicylic acid, sulfosalicylic acid, citric acid, benzoic acid, hydroxybenzoic acid, and naphthalenecarboxylic acid, and / or 2,4,4,6-tetrabromocyclohexadienone, benzoin tosylate, 2-nitrobenzyl tosylate, and other organic sulfonic acid alkyl esters.

[0077] According to another embodiment of the present invention, there is provided a hardmask layer comprising a cured product of the hardmask composition described above.

[0078] A method for forming a pattern using the above-described hard mask composition will now be described.

[0079] A patterning method according to one embodiment of the present invention includes the steps of providing a material layer on a substrate, applying a hard mask composition comprising the above-mentioned compound and a solvent onto the material layer, heat-treating the hard mask composition to form a hard mask layer, forming a photoresist layer on the hard mask layer, exposing and developing the photoresist layer to form a photoresist pattern, selectively removing the hard mask layer using the photoresist pattern to expose portions of the material layer, and etching the exposed portions of the material layer.

[0080] The substrate may be, for example, a silicon wafer, a glass substrate, or a polymer substrate. The material layer is the material to be ultimately patterned, and may be, for example, a metal layer such as aluminum, copper, etc., a semiconductor layer such as silicon, or an insulating layer such as silicon oxide, silicon nitride, etc. The material layer may be formed, for example, by chemical vapor deposition.

[0081] The hard mask composition may be prepared in the form of a solution and applied by spin coating, as described above. In this case, the thickness of the hard mask composition is not particularly limited, but may be, for example, 50 to 200,000 Å.

[0082] The step of heat treating the hard mask composition may be performed for 10 seconds to 1 hour at a temperature of, for example, 100° C. to 1,000° C. In one embodiment, the step of heat treating the hard mask composition may include a plurality of heat treatment steps, for example, a first heat treatment step and a second heat treatment step.

[0083] In one embodiment, the step of heat treating the hard mask composition may include a heat treatment step performed at a temperature of, for example, 100° C. to 1000° C. for 10 seconds to 1 hour. For example, the heat treatment step may be performed in an air atmosphere or a nitrogen atmosphere, or in an atmosphere having an oxygen concentration of 1% by weight or less.

[0084] In an embodiment, the step of heat treating the hard mask composition includes a first heat treatment step performed at a temperature of, for example, 100° C. to 1,000° C., for example, 100° C. to 800° C., for example, 100° C. to 500° C., for example, 150° C. to 400° C., for 30 seconds to 1 hour, for example, 30 seconds to 30 minutes, for example, 30 seconds to 10 minutes, for example, 30 seconds to 5 minutes.

[0085] Also, it may include a second heat treatment step which is successively performed for 30 seconds to 1 hour, for example, 30 seconds to 30 minutes, for example, 30 seconds to 10 minutes, for example, 30 seconds to 5 minutes, under temperature conditions of, for example, 100° C. to 1,000° C., for example, 300° C. to 1,000° C., for example, 500° C. to 1,000° C., for example, 500° C. to 600° C. As an example, the first heat treatment step and the second heat treatment step may be performed in an air atmosphere or a nitrogen atmosphere, or may be performed in an atmosphere with an oxygen concentration of 1% by mass or less.

[0086] At least one of the steps of heat treating the hard mask composition is performed at a high temperature of 200° C. or higher, whereby the hard mask composition can exhibit high etching resistance that can withstand etching gases and chemical solutions to which the hard mask composition is exposed in subsequent steps, including an etching step.

[0087] In one embodiment, the step of forming the hard mask layer may include a UV-visible light curing step and / or a near infrared light curing step.

[0088] In one embodiment, the step of forming the hard mask layer may include at least one of a first heat treatment step, a second heat treatment step, a UV-visible light curing step, and a NIR curing step, or may include two or more of these steps consecutively.

[0089] In one embodiment, the method may further include forming a silicon-containing thin film layer on the hard mask layer. The silicon-containing thin film layer may be formed of a material such as, for example, SiCN, SiOC, SiON, SiOCN, SiC, SiO, and / or SiN.

[0090] In one embodiment, before the step of forming the photoresist layer, a bottom anti-reflective coating (BARC) may be further formed on the silicon-containing thin film layer or the hard mask layer.

[0091] In one embodiment, the step of exposing the photoresist layer can be performed using, for example, ArF, KrF, or EUV, etc. After the exposure, a heat treatment process can be performed at 100° C. to 700° C.

[0092] In one embodiment, the step of etching the exposed portions of the material layer may be performed by dry etching using an etching gas, which may be, for example, N2 / O2, CHF3, CF4, Cl2, BCl3, and mixtures thereof.

[0093] The etched material layer may be formed in a variety of patterns, which may be metal patterns, semiconductor patterns, insulating patterns, etc., and may be applied as a variety of patterns within a semiconductor integrated circuit device, for example. EXAMPLES

[0094] The above-mentioned embodiments of the present invention will be described in more detail with reference to the following examples. However, the following examples are merely for illustrative purposes and are not intended to limit the scope of the present invention.

[0095] [Synthesis of compounds] (Synthesis Example 1) In a 100mL round-bottom flask equipped with a stirrer and a cooling tube, 1.5mol (2.33g) of diethylzinc, 3mol (3.79g) of 1-phenylacetylene, and 12g of toluene were added under a nitrogen atmosphere, and then the mixture was stirred at 120°C for 5 hours. After cooling the system to 0°C, 0.5mol (1.45g) of 1-pyrenecarboxaldehyde was gradually added over 20 minutes, and the mixture was stirred at room temperature for 12 hours. After confirming the completion of the reaction by thin layer chromatography (TLC), 10mL of saturated aqueous ammonium chloride solution was added to the intermediate product, which was extracted with ethyl acetate, and the organic layer was dried using sodium sulfate. The product was then purified by column chromatography to obtain compound A represented by the following chemical formula A.

[0096] [ka]

[0097] In a 100mL round bottom flask equipped with a stirrer, 2mol (2.13g) of titanium tetrachloride, 3mol (1.7g) of triethylamine, and 89g of dichloromethane were added and stirred at 0℃ under a nitrogen atmosphere. Then, 2mol (5.13g) of the above compound A was added and stirred at room temperature for 10 hours. After the reaction was completed, 25g of a saturated aqueous ammonium chloride solution was added and stirred for 10 minutes. After separating the organic layer, the aqueous layer was extracted using dichloromethane. The mixed organic layer was washed using a saturated aqueous sodium chloride solution, the solvent was removed using sodium sulfate, and the residue was subjected to silica gel column chromatography using hexane as an eluent to obtain compound 1 represented by the following chemical formula A-1.

[0098] [ka]

[0099] (Synthesis Example 2) Compound B represented by the following chemical formula B was obtained by synthesizing in the same manner as in Synthesis Example 1 above, except that 1.55 g of 6-hydroxypyrene-2-carbaldehyde was used instead of 1-pyrenecarboxaldehyde.

[0100] [ka]

[0101] Compound 2 represented by the following chemical formula B-1 was obtained by synthesizing in the same manner as in Synthesis Example 1 above, except that compound B obtained above was used instead of compound A.

[0102] [ka]

[0103] (Synthesis Example 3) Compound C represented by the following chemical formula C was obtained by synthesizing in the same manner as in Synthesis Example 1 above, except that 2.07 g of coronenecarboxaldehyde was used instead of 1-pyrenecarboxaldehyde.

[0104] [ka]

[0105] Compound 3 represented by the following chemical formula C-1 was obtained by synthesizing in the same manner as in Synthesis Example 1 above, except that compound C obtained above was used instead of compound A.

[0106] [ka]

[0107] (Synthesis Example 4) Compound D represented by the following chemical formula D was obtained by synthesizing in the same manner as in Synthesis Example 1 above, except that 8.54 g of 1-ethynylpyrene was used instead of 1-phenylacetylene and 1.08 g of 6-hydroxy-2-naphthaldehyde was used instead of 1-pyrenecarboxaldehyde.

[0108] [ka]

[0109] Compound 4 represented by the following chemical formula D-1 was obtained by synthesizing in the same manner as in Synthesis Example 1 above, except that compound D obtained above was used instead of compound A.

[0110] [ka]

[0111] (Synthesis Example 5) Compound E represented by the following chemical formula E was obtained by synthesizing in the same manner as in Synthesis Example 1 above, except that 8.54 g of 1-ethynylpyrene was used instead of 1-phenylacetylene, and 1.55 g of 6-hydroxy-2-pyrenecarboxaldehyde was used instead of 1-pyrenecarboxaldehyde.

[0112] [ka]

[0113] Compound 5 represented by the following chemical formula E-1 was obtained by synthesizing in the same manner as in Synthesis Example 1 above, except that compound E obtained above was used instead of compound A.

[0114] [ka]

[0115] (Comparative Synthesis Example 1) A 100mL round-bottom flask equipped with a stirrer and a condenser was placed in an ice bath, and 0.011mol (2.44g) of 1-methoxypyrene, 0.022mol (5.56g) of pyrene-1-carbonyl chloride, and 32.00g of 1,2-dichloromethane were added to the flask and stirred. Under a nitrogen atmosphere, 2.87g of aluminum chloride was added in three portions at 10-minute intervals. After removing from the ice bath and leaving at room temperature for 10 hours, the reaction was terminated (Mw=689Da). The flask was again moved to the ice bath, and a small amount of tetrahydrofuran (THF) and distilled water (DIW) was added dropwise to the reaction solution and stirred to remove HCl gas. The reaction solution was transferred to a separatory funnel, and the catalyst was removed using ethyl acetate and distilled water, and the organic layer was separated and dried under reduced pressure to remove the solvent. The compound dissolved in 40g of tetrahydrofuran was gradually dropped into 400mL of normal hexane to precipitate, and then purified and dried with a filter to obtain 6.02g of the compound in powder form. The obtained powder was dried in a 40°C vacuum oven to completely remove the solvent. The above powder, 0.027mol (11.45g) of 1-dodecanethiol, 0.036mol (4.231g) of potassium hydroxide, and 34.11g of 1-methyl-2-pyrrolidine were added to a 250mL round-bottom flask and stirred. After heating to 90°C, the reaction was terminated after 8 hours (Mw=675Da). After cooling to 50°C, 20g of normal hexane was added, stirred for 30 minutes, and left to stand for 3 hours. After removing the supernatant, the reaction liquid was transferred to a separatory funnel, and the catalyst was removed using 1,2-dichloromethane, distilled water, and a 5% by weight aqueous HCl solution. When the pH reached 6, the organic layer was separated and dried under reduced pressure to remove the solvent. The compound dissolved in 40g of tetrahydrofuran was gradually dropped into 400mL of normal hexane to precipitate, and then purified and dried using a filter to obtain 4.89g of the compound in powder form. The obtained powder was placed in a 100mL round-bottom flask together with 19.56g of tetrahydrofuran and stirred in an ice bath. In a separate PP bottle, 0.056mol (2.19g) of sodium borohydride (NaBH4) was dissolved in 19.56g of distilled water (DIW) and then added in three portions. The flask was transferred to an oil bath, stabilized for 10 minutes, and heated to 50°C.The reaction was terminated after 4 hours (Mw=679Da). After cooling, the mixture was transferred to a separatory funnel in the same manner as in the previous step, and the catalyst was removed using 1,2-dichloromethane, distilled water, and a 5% by weight aqueous HCl solution. The compound dissolved in 40 g of tetrahydrofuran was gradually dropped into 400 mL of normal hexane to cause precipitation, which was then purified with a filter and dried to obtain comparative compound 1 represented by the following chemical formula F.

[0116] [ka]

[0117] (Comparative Synthesis Example 2) Comparative compound 2 represented by the following chemical formula G was obtained by synthesizing in the same manner as in Comparative Synthesis Example 1, except that 1,4-benzenedicarbonyl dichloride and pyrene were used instead of 1-methoxypyrene and pyrene-1-carbonyl chloride.

[0118] [ka]

[0119] [Preparation of hard mask composition] Example 1 3.5 g of the compound 1 represented by the chemical formula A-1 obtained in Synthesis Example 1 was dissolved in 10 g of a solvent in which propylene glycol methyl ether acetate and cyclohexanone were mixed in a volume ratio of 7:3, and then filtered through a syringe filter to prepare a hard mask composition.

[0120] Example 2 A hard mask composition was prepared in the same manner as in Example 1, except that the compound 2 represented by the formula B-1 was used instead of the compound represented by the formula A-1.

[0121] Example 3 A hard mask composition was prepared in the same manner as in Example 1, except that the compound 3 represented by the formula C-1 was used instead of the compound represented by the formula A-1.

[0122] Example 4 A hard mask composition was prepared in the same manner as in Example 1, except that the compound 4 represented by the formula D-1 was used instead of the compound represented by the formula A-1.

[0123] Example 5 A hard mask composition was prepared in the same manner as in Example 1, except that the compound 5 represented by the formula E-1 was used instead of the compound represented by the formula A-1.

[0124] Comparative Example 1 A hard mask composition was prepared in the same manner as in Example 1, except that Comparative Compound 1 represented by Formula F was used instead of the compound represented by Formula A-1.

[0125] Comparative Example 2 A hard mask composition was prepared in the same manner as in Example 1, except that Comparative Compound 2 represented by Formula G was used instead of the compound represented by Formula A-1.

[0126] (Evaluation 1: Evaluation of etching resistance) The compositions according to the examples and the comparative examples were each coated on a silicon wafer by spin coating, and baked at 200°C for 60 seconds to form a hard mask layer with a thickness of 1,500 Å. On each of the formed hard mask layers, an ArF photoresist was coated, baked at 110°C for 60 seconds, and then exposed using an exposure device (XT:1450G, NA0.93) manufactured by ASML. Then, each was developed with a 2.38% by mass aqueous solution of TMAH (tetramethylammonium hydroxide) to obtain a 60 nm line and space pattern. The photoresist pattern was further cured at 110°C for 60 seconds, and the photoresist pattern and the hard mask layer were dry etched for 20 seconds using a CHF3 / CF4 mixed gas, and the cross section was observed with a FE-SEM to measure the etching rate, and the etching resistance against halogen plasma was evaluated. The evaluation criteria for etching resistance were as follows, and the evaluation results are shown in Table 1 below: <Evaluation criteria for etching resistance> ◎: Etching speed less than 10 Å / sec ○: Etching speed 10 Å / sec or more and less than 11 Å / sec △: Etching speed 11 Å / sec or more and less than 12 Å / sec ×: Etching speed 12 Å / sec or more.

[0127] [Table 1]

[0128] Referring to Table 1 above, it was confirmed that the hard mask layers formed from the hard mask compositions according to Examples 1 to 5 had an etching rate of less than 10 Å / sec, which is lower than the etching rates of the hard mask layers formed from the hard mask compositions according to Comparative Examples 1 and 2, which were 10 Å / sec or more. In other words, it was confirmed that the etching resistance of the hard mask layers formed from the hard mask compositions according to Examples 1 to 5 was superior to that of the Comparative Examples.

[0129] Although the preferred embodiments of the present invention have been described in detail above, the scope of the present invention is not limited thereto, and various modifications and improvements made by those skilled in the art using the basic concept of the invention defined in the claims below also fall within the scope of the present invention.

Claims

1. A hard mask composition comprising a compound represented by the following Chemical Formula 1 and a solvent: 【Chemistry 1】 In the above Chemical Formula 1, R １ and R ３ each independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 30 carbon atoms, or a combination thereof; R ２ and R ４ are each independently a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 30 carbon atoms, a substituted or unsubstituted monovalent saturated or unsaturated alicyclic hydrocarbon group having 3 to 30 carbon atoms, or a combination thereof.

2. R in Formula 1 １ and R ３ each independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 20 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 20 carbon atoms, or a combination thereof; R in Formula 1 ２ and R ４ each independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 24 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 24 carbon atoms, a substituted or unsubstituted monovalent unsaturated alicyclic hydrocarbon group having 3 to 24 carbon atoms, or a combination thereof.

3. R in Formula 1 １ and R ３ each independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, R in Formula 1 ２ and R ４ wherein each independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 30 carbon atoms, or a combination thereof.

4. R in Formula 1 １ and R ３ each independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 20 carbon atoms, R in Formula 1 ２ and R ４ and each independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms.

5. R in Formula 1 １ and R ３ are each independently any one of substituted or unsubstituted moieties selected from Group 1 and Group 2 below, R in Formula 1 ２ and R ４ The hard mask composition of claim 1 , wherein each of the groups is independently any one of substituted or unsubstituted moieties selected from Groups 1 to 3 below: 【Chemistry 2】 【Chemistry 3】 【Chemistry 4】 In Group 2, Z １ and Z ２ are each independently -O-, -S-, or -NR ａ - (where R ａ is a hydrogen atom, a deuterium atom, or a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms, or a combination thereof.

6. R in Formula 1 １ ~R ４ The hard mask composition of claim 1 , wherein each of the groups is independently any one of substituted or unsubstituted moieties selected from Group 1-1 below: 【Chemistry 5】

7. The hard mask composition of claim 1 , wherein the compound represented by Formula 1 has a symmetric structure.

8. The hard mask composition according to claim 1, wherein the compound represented by Chemical Formula 1 is at least one selected from the group consisting of compounds represented by the following Chemical Formulas 1-1 to 1-5: 【Chemistry 6】 【Chemistry 7】 In the above Chemical Formula 1-1 to Chemical Formula 1-5, R ａ and R ｂ each independently represents a hydroxy group, a substituted or unsubstituted alkoxy group having 1 to 4 carbon atoms, a halogen atom, an amino group, a thiol group, or a combination thereof; m and n are each independently an integer from 0 to 9.

9. 2. The hard mask composition of claim 1, wherein the compound has a molecular weight of 300 g / mol to 5,000 g / mol.

10. The hard mask composition of claim 1 , wherein the compound is contained in an amount of 0.1% by mass to 30% by mass based on the total mass of the hard mask composition.

11. 2. The hard mask composition of claim 1, wherein the solvent is at least one selected from the group consisting of propylene glycol, propylene glycol diacetate, methoxypropanediol, diethylene glycol, diethylene glycol butyl ether, tri(ethylene glycol) monomethyl ether, propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, cyclohexanone, ethyl lactate, γ-butyrolactone, N,N-dimethylformamide, N,N-dimethylacetamide, methylpyrrolidone, methylpyrrolidinone, acetylacetone, and ethyl 3-ethoxypropionate.

12. A hardmask layer comprising a cured product of the hardmask composition according to any one of claims 1 to 11.

13. providing a layer of material over a substrate; applying a hard mask composition according to any one of claims 1 to 11 onto the material layer; heat-treating the hard mask composition to form a hard mask layer; forming a photoresist layer over the hard mask layer; exposing and developing the photoresist layer to form a photoresist pattern; selectively removing the hard mask layer utilizing the photoresist pattern to expose portions of the material layer; and etching exposed portions of the layer of material; A pattern forming method comprising:

14. The method of claim 13, wherein the step of forming the hard mask layer comprises a step of performing a heat treatment at a temperature of 100° C. to 1,000° C.

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