Coating film-forming composition and method for manufacturing semiconductor device

Abstract

To provide a coating film formation composition which enables selective formation of a coating film on an insulation layer represented by a silicon oxide on a substrate having a wiring layer containing copper and the insulation layer without using a chemical substance limiting the use of a formic acid, and a method for manufacturing a semiconductor device using the same.SOLUTION: A coating film formation composition for selectively forming a coating film on an insulation layer on a substrate having a wiring layer containing copper and the insulation layer contains (a) a polymer including a structural unit represented by the following formula (1a) or (1b), and (b) a solvent containing 1-30 mass% of at least one organic solvent selected from the group consisting of propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, propylene glycol monomethyl ether, methyl 2-hydroxyisobutyrate, ethyl 3-ethoxypropionate and ethyl lactate, and 70-99 mass% of water.SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present invention relates to a coating film-forming composition and a method for manufacturing a semiconductor device. [Background technology]

[0002] In the field of semiconductor devices, where miniaturization is progressing, it has been proposed to form a resin layer to prevent the diffusion of metal components such as copper embedded as wiring material in the interlayer insulating layer of a semiconductor (Patent Document 1). However, it is required to prevent the resin layer from being formed on the wiring and to maintain electrical connection on the wiring surface. Non-Patent Document 1 describes that an organic film can be selectively formed on SiO2 using a composition containing polyethyleneimine and having its pH adjusted with formic acid. [Prior art documents] [Patent documents]

[0003] [Patent Document 1] International Publication No. 2010 / 137711 [Non-patent literature]

[0004] [Non-Patent Document 1] J. Phys. Chem. C 2015, 119, 22882-22888 Summary of the Invention [Problem to be solved by the invention]

[0005] The technique described in Non-Patent Document 1 requires the addition of formic acid as a pH adjuster to the composition. Since formic acid is designated as a deleterious substance under the Poisonous and Deleterious Substances Control Act in Japan, the use of materials containing formic acid is not suitable for industrialization.

[0006] The present invention has been made in view of the above circumstances, and aims to provide a coating film-forming composition that can selectively form a coating film on an insulating layer, which is on a substrate having a wiring layer containing copper and an insulating layer typified by silicon oxide or the like, without using a chemical substance whose use is restricted, such as formic acid, and a method for manufacturing a semiconductor device using the same. [Means for solving the problem]

[0007] As a result of extensive investigations to achieve the above object, the present inventors have found that the above problem can be solved by a composition containing a predetermined diallylamine polymer and a mixed solvent of a predetermined organic solvent and water, and have completed the present invention.

[0008] That is, the present invention provides the following coating film-forming composition and method for producing a semiconductor device. 1. (a) A polymer containing a structural unit represented by the following formula (1a) or (1b): (b) a solvent containing 1 to 30% by mass of at least one organic solvent selected from the group consisting of propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, propylene glycol monoethyl ether, methyl 2-hydroxyisobutyrate, ethyl 3-ethoxypropionate, and ethyl lactate, and 70 to 99% by mass of water; A coating film-forming composition for selectively forming a coating film on an insulating layer on a substrate having a copper-containing wiring layer and an insulating layer, the composition comprising: [ka] (wherein X is acetic acid, propionic acid, sulfamic acid, or a hydrogen halide; Y - is hydrogen sulfate, methyl sulfate, ethyl sulfate, or a halide ion, and R 1 is a hydrogen atom or a methyl group, and R 2 and R 3 are each independently a methyl group or an ethyl group. 2. The coating film-forming composition of 1, wherein the polymer further contains a structural unit represented by the following formula (2): [ka] 3. The coating film-forming composition of 2, wherein the molar ratio of the structural unit represented by formula (1a) or (1b) to the structural unit represented by formula (2) is 99 / 1 to 50 / 50. 4. The coating film forming composition of any one of 1 to 3, wherein the polymer has a weight average molecular weight of 300 to 1,000,000. 5. A coating film-forming composition according to any one of 1 to 4, wherein the content of component (a) in the composition is 0.1 to 20 mass %. 6. A method for manufacturing a semiconductor device, comprising the steps of: applying a coating film-forming composition according to any one of 1 to 5 to a surface of an insulating layer and a copper-containing wiring layer formed on a substrate; and baking the composition to form a coating film; and selectively removing the coating film on the wiring layer using water. 7. The method for manufacturing a semiconductor device according to claim 6, wherein the insulating layer is mainly composed of SiO2. 8. The method for producing a semiconductor device according to 6 or 7, wherein the insulating layer is mainly composed of porous silica and has silanol residues derived from the porous silica on its surface. [Effects of the Invention]

[0009] The coating film-forming composition of the present invention can be used industrially because it does not contain chemical substances whose use is restricted, such as formic acid. Furthermore, by using the coating film-forming composition of the present invention, a coating film can be selectively formed on an insulating layer by a simple method. DETAILED DESCRIPTION OF THE INVENTION

[0010] [Component (a)] The component (a) of the coating film-forming composition of the present invention is a diallylamine polymer, which contains a structural unit represented by the following formula (1a) or (1b). [ka]

[0011] In formula (1a), X is acetic acid, propionic acid, sulfamic acid, or a hydrogen halide. Examples of the hydrogen halide include hydrogen chloride, hydrogen bromide, and hydrogen iodide. X is preferably acetic acid or sulfamic acid.

[0012] In formula (1b), Y - is a hydrogen sulfate ion, a methyl sulfate ion, an ethyl sulfate ion, or a halide ion. Examples of the halide ion include a chloride ion, a bromide ion, and an iodide ion. Y - As the cation, ethyl sulfate ion is preferred.

[0013] In formula (1a), R 1 is a hydrogen atom or a methyl group. 2 and R 3 are each independently a methyl group or an ethyl group.

[0014] The polymer preferably further contains a structural unit represented by the following formula (2). [ka]

[0015] When the polymer is a copolymer containing a structural unit represented by formula (1a) or (1b) and a structural unit represented by formula (2), the copolymer may be an alternating copolymer in which the structural unit represented by formula (1a) or (1b) and the structural unit represented by formula (2) are bonded alternately, or a random copolymer in which these structural units are bonded randomly, with an alternating copolymer being particularly preferred.

[0016] The polymer may contain structural units other than the above-described structural units (hereinafter referred to as other structural units). Examples of other structural units include those derived from (meth)acrylamide, those derived from monoallylamine such as allylamine, N-methylallylamine, and N,N-dimethylallylamine, and those derived from acid addition salts of monoallylamine such as acetate, hydrochloride, hydrobromide, propionic acid, and sulfamic acid.

[0017] When the polymer of component (a) is the copolymer, the molar ratio of the structural units represented by formula (1a) or (1b) to the structural units represented by formula (2) is preferably in the range of about 99 / 1 to 50 / 50, more preferably in the range of about 90 / 10 to 50 / 50, and even more preferably 50 / 50 or thereabouts. When other structural units are contained, the content thereof is usually 10 mol % or less, preferably 5 mol % or less, of the total structural units.

[0018] The weight average molecular weight (Mw) of the polymer of component (a) is preferably 300 to 1,000,000, more preferably 500 to 500,000, even more preferably 800 to 100,000, and still more preferably 1,000 to 50,000. In the present invention, the Mw of the polymer of component (a) is a value measured by gel permeation chromatography (GPC) in terms of polyethylene glycol.

[0019] The polymer of component (a) can be synthesized by a conventionally known method, or a commercially available product can be used, such as PAA-D11-HCL, PAA-D41-HCL, PAA-D19-HCL, PAA-D19A, PAS-21CL, PAS-M-1L, PAS-M-1, PAS-22SA-40, PAS-M-1A, PAS-H-1L, PAS-H-5L, PAS-H-10L, PAS-24, PAS-92, PAS-92A, PAS-2401, PAS-2201CL, PAS-A-1, PAS-A-5, PAS-2141CL, PAS-J-81L, PAS-J-81, PAS-J-41, or PAS-880, all manufactured by Nittobo Medical Co., Ltd.

[0020] In the composition of the present invention, the content of component (a) is preferably from 0.1 to 20 mass %, more preferably from 1 to 5 mass %, from the viewpoint of film-forming properties.

[0021] [(b) Solvent] The solvent for component (b) contains 1 to 49% by mass of at least one organic solvent selected from the group consisting of propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, propylene glycol monoethyl ether, methyl 2-hydroxyisobutyrate, ethyl 3-ethoxypropionate, and ethyl lactate, and 51 to 99% by mass of water. If the content of the organic solvent is less than 1% by mass, the coatability may decrease, and if it exceeds 49% by mass, the solubility of the polymer for component (a) may decrease.

[0022] The organic solvent is preferably propylene glycol monomethyl ether or propylene glycol monomethyl ether acetate, and more preferably propylene glycol monomethyl ether.

[0023] In the (b) solvent, the content of the organic solvent is preferably 1 to 30% by mass, more preferably 5 to 25% by mass, and even more preferably 10 to 20% by mass, and the content of water is preferably 70 to 99% by mass, more preferably 75 to 95% by mass, and even more preferably 80 to 90% by mass.

[0024] [Other ingredients] The composition of the present invention may contain components other than the above-mentioned components (hereinafter referred to as "other components") within the scope of not impairing the effects of the present invention. Examples of other components include various additives such as surfactants. The surfactant is an additive for improving the coatability of the composition of the present invention to a substrate. Known surfactants such as nonionic surfactants and fluorine-based surfactants can be used as the surfactant.

[0025] [Method of manufacturing a semiconductor device] The method for manufacturing a semiconductor device of the present invention includes a step of applying the above-mentioned coating film-forming composition to the surfaces of an insulating layer and a copper-containing wiring layer (hereinafter referred to as a copper wiring layer) formed on a substrate on which the insulating layer and the copper wiring layer are formed, baking the composition to form a coating film, and a step of selectively removing the coating film on the copper wiring layer using water.

[0026] Examples of the insulating layer include those containing SiO2, and those containing low-k materials such as porous silica, SiOF, SiOC, hydrogenated silsesquioxane, and methylated silsesquioxane. Of these, the insulating layer is preferably one whose main component is SiO2, or one whose main component is porous silica and whose surface has silanol residues derived from the porous silica. In the present invention, the term "main component" refers to the component with the largest content.

[0027] The substrate on which the insulating layer and copper wiring layer are formed may be, for example, a substrate obtained by forming copper wiring by a method such as electroplating on a pattern formed in an insulating layer on a semiconductor substrate such as silicon, and then planarizing the pattern by chemical mechanical polishing (CMP).Furthermore, the substrate on which the insulating layer and copper wiring layer are formed may be a substrate on which, after CMP, an insulating layer or the like is further provided to form a multilayer structure and form trenches and vias.

[0028] The method for applying the coating film-forming composition may be a conventionally known method, such as spin coating, cast coating, blade coating, dip coating, roll coating, bar coating, die coating, inkjet printing, or the like.

[0029] The coating film-forming composition is applied to the surfaces of the insulating layer and the copper wiring layer on the substrate, and then baked to form a coating film. The baking temperature is preferably 50 to 300° C., more preferably 70 to 250° C. The baking time is preferably 10 seconds to 10 minutes, more preferably 30 seconds to 2 minutes.

[0030] The thickness of the resulting coating film is preferably 0.1 to 200 nm, more preferably 1 to 100 nm.

[0031] After forming the coating film, the coating film on the copper wiring layer is selectively removed using water. A method for removing the coating film includes applying water to the coating film to dissolve and remove the coating film on the copper wiring layer. Examples of the method for applying water include spin coating, cast coating, blade coating, dip coating, roll coating, bar coating, die coating, inkjet printing, and the like.

[0032] By using the method described above, an organic film can be selectively formed on the surface of an insulating layer. The organic film prevents the metal components of the wiring from diffusing into the insulating layer and also functions as a protective film for the insulating layer. [Example]

[0033] The present invention will be described in more detail below with reference to synthesis examples and examples, but the present invention is not limited to the following examples.

[0034] [Synthesis Example 1] 5.00 g of terephthalic acid diglycidyl ester (Denacol® EX711, manufactured by Nagase ChemteX Corporation), 3.15 g of 5-hydroxyisophthalic acid (manufactured by Tokyo Chemical Industry Co., Ltd.), and 0.20 g of benzyltriethylammonium chloride (manufactured by Tokyo Chemical Industry Co., Ltd.) were added to 35.60 g of propylene glycol monomethyl ether and dissolved. After purging the reaction vessel with nitrogen, the reaction was carried out at 135°C for 4 hours to obtain a polymer solution. The polymer had good solubility in propylene glycol monomethyl ether, and the solution did not become cloudy even when cooled to room temperature. GPC analysis (eluent: tetrahydrofuran, calibration curve: standard polystyrene) revealed that the Mw of the polymer in the resulting solution was 15,673 and the dispersity was 3.39. The polymer obtained in this synthesis example had a structural unit represented by the following formula (3) and a structural unit represented by the following formula (4). [ka]

[0035] [1] Preparation of coating film-forming composition [Example 1-1] Coating film-forming composition A was prepared by adding 11.2 g of ultrapure water and 3 g of propylene glycol monomethyl ether to 0.80 g of an aqueous solution containing 0.15 g of diallylamine acetate-sulfur dioxide copolymer (Nittobo Medical Co., Ltd., PAS-92A).

[0036] [Comparative Example 1-1] To 1.3 g of the polymer solution containing 0.24 g of polymer solids obtained in Synthesis Example 1, 12.8 g of polyethylene glycol monomethyl ether and 5.9 g of propylene glycol monomethyl ether acetate were added to prepare a coating film-forming composition B. The polymer contained in coating film-forming composition B of this comparative example does not fall under the category of polymers containing a structural unit represented by formula (1a) or (1b).

[0037] [Comparative Example 1-2] 14.2 g of ultrapure water was added to 0.80 g of an aqueous solution containing 0.15 g of diallylamine acetate-sulfur dioxide copolymer (PAS-92A, manufactured by Nittobo Medical Co., Ltd.) to prepare coating film-forming composition C. The solvent contained in coating film-forming composition C of this comparative example had an organic solvent content of less than 1% by mass (0% by mass).

[0038] [Comparative Example 1-3] A coating film-forming composition was prepared by adding 6.8 g of ultrapure water and 7.4 g of propylene glycol monomethyl ether to 0.80 g of an aqueous solution (PAS-92A, manufactured by Nittobo Medical Co., Ltd.) containing 0.15 g of diallylamine acetate-sulfur dioxide copolymer. However, the coating film-forming composition prepared in this comparative example suffered from polymer precipitation. The solvent contained in the coating film-forming composition of this comparative example had an organic solvent content of more than 49 mass%.

[0039] [2] Coating film formation evaluation A substrate (hereinafter referred to as SiO2 substrate) on which silicon oxide was vapor-deposited to a thickness of 300 nm was subjected to O2 ashing for 10 minutes using an etcher manufactured by Samco Corporation. The resulting SiO2 substrate was then cut into 3 cm squares and used to evaluate the coating properties of the insulating layer. In addition, the water contact angle of the SiO2 substrate was measured using a contact angle meter DM-701 (manufactured by Kyowa Interface Science Co., Ltd.), and this was used as the water contact angle before film formation.

[0040] A substrate on which copper had been vapor-deposited to a thickness of 100 nm (hereinafter referred to as Cu substrate) was immersed in a 0.5 mol / L sulfuric acid solution for 5 minutes, then washed with ultrapure water and dried. The resulting Cu substrate was then cut into 3 cm squares and used to evaluate the coating properties of the wiring layer. The water contact angle of the Cu substrate was measured using a contact angle meter DM-701 (manufactured by Kyowa Interface Science Co., Ltd.), and this was used as the water contact angle before film formation.

[0041] [Example 2-1] Coating film-forming composition A was applied to the SiO2 substrate and Cu substrate cut into 3 cm squares using a spin coater (manufactured by Brewer Science), and baked at 100°C for 60 seconds to form a coating film. Ultrapure water was then applied to the coating film using a spin coater (manufactured by Brewer Science), held for 60 seconds, and the coating films on the SiO2 substrate and Cu substrate were removed. The contact angle of water was then measured using a contact angle meter DM-701 (manufactured by Kyowa Interface Science Co., Ltd.). The results are shown in Table 1.

[0042] [Comparative Example 2-1] Coating film-forming composition B was applied to the SiO2 substrate and Cu substrate cut into 3 cm squares using a spin coater (manufactured by Brewer Science) and baked at 100°C for 60 seconds to form a coating film. Subsequently, propylene glycol monomethyl ether / propylene glycol monomethyl ether acetate = 7 / 3 (mass ratio) was applied to the coating film using a spin coater (manufactured by Brewer Science) and held for 60 seconds. The coating films on the SiO2 substrate and Cu substrate were then removed, and the water contact angle was measured using a contact angle meter DM-701 (manufactured by Kyowa Interface Science Co., Ltd.). The results are shown in Table 1.

[0043] [Table 1]

[0044] [Example 2-2] The water contact angle was measured in the same manner as in Example 2-1, except that the baking temperature was set to 200° C. The results are shown in Table 2.

[0045] [Comparative Example 2-2] The water contact angle was measured in the same manner as in Comparative Example 2-1, except that the baking temperature was set to 200° C. The results are shown in Table 2.

[0046] [Table 2]

[0047] [Comparative Example 2-3] An attempt was made to apply the coating film-forming composition C onto the SiO2 substrate and the Cu substrate by the above method, but it was not possible to apply it uniformly onto either substrate.

[0048] From Examples 2-1 and 2-2, when a coating film was formed on a SiO2 substrate using the coating film-forming composition A of the present invention, the contact angle changed before and after the coating film was formed, indicating that the coating film was not removed by water and remained on the SiO2 substrate. On the other hand, when a coating film was formed on a Cu substrate, the contact angle hardly changed before and after the coating film was formed, indicating that the coating film was removed by water.

[0049] Comparative Examples 2-1 and 2-2 show that when a coating film was formed on a Cu substrate using coating film-forming composition B, the contact angle changed before and after the formation, and therefore the coating film was not removed by propylene glycol monomethyl ether / propylene glycol monomethyl ether acetate = 7 / 3 (mass ratio) and remained on the Cu substrate. In other words, it was shown that the coating film obtained from coating film-forming composition B was not removed from the Cu substrate by propylene glycol monomethyl ether / propylene glycol monomethyl ether acetate = 7 / 3 (mass ratio).

[0050] The above results demonstrate that the use of the composition of the present invention makes it possible to selectively form a coating film on an insulating layer.

Claims

1. (a) a polymer containing a structural unit represented by the following formula (1a) or (1b), and (b) a solvent containing 1 to 30% by mass of at least one organic solvent selected from the group consisting of propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, propylene glycol monoethyl ether, methyl 2-hydroxyisobutyrate, ethyl 3-ethoxypropionate, and ethyl lactate, and 70 to 99% by mass of water; A coating film-forming composition for selectively forming a coating film on an insulating layer on a substrate having a copper-containing wiring layer and an insulating layer, the composition comprising: 【Chemistry 1】 (wherein X is acetic acid, propionic acid, sulfamic acid or hydrogen halide; Y - is a hydrogen sulfate ion, a methyl sulfate ion, an ethyl sulfate ion, or a halide ion, and R 1 is a hydrogen atom or a methyl group, and R 2 and R 3 are each independently a methyl group or an ethyl group.

2. 2. The coating film forming composition according to claim 1, wherein the weight average molecular weight of the polymer is 300 to 1,000,000.

3. 3. The coating film-forming composition according to claim 1, wherein the content of component (a) is 0.1 to 20% by mass in the composition.

4. 4. A method for manufacturing a semiconductor device, comprising: a step of applying the coating film-forming composition according to claim 1 to a surface of an insulating layer and a copper-containing wiring layer formed on a substrate, the insulating layer and the wiring layer, and baking the composition to form a coating film; and a step of selectively removing the coating film on the wiring layer using water.

5. The insulating layer is made of SiO 2 5. The method for manufacturing a semiconductor device according to claim 4, wherein the main component is

6. 6. The method for manufacturing a semiconductor device according to claim 4, wherein the insulating layer is mainly composed of porous silica and has silanol residues on the surface thereof derived from the porous silica.

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