WO2018124226A1 - Composition pour polissage, et procédé de polissage - Google Patents
Composition pour polissage, et procédé de polissage Download PDFInfo
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- WO2018124226A1 WO2018124226A1 PCT/JP2017/047077 JP2017047077W WO2018124226A1 WO 2018124226 A1 WO2018124226 A1 WO 2018124226A1 JP 2017047077 W JP2017047077 W JP 2017047077W WO 2018124226 A1 WO2018124226 A1 WO 2018124226A1
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- WIPO (PCT)
- Prior art keywords
- polishing
- polishing composition
- mass
- polyoxyalkylene
- ether
- Prior art date
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- 238000005498 polishing Methods 0.000 title claims abstract description 131
- 239000000203 mixture Substances 0.000 title claims abstract description 78
- 238000000034 method Methods 0.000 title claims description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 28
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 26
- 150000001875 compounds Chemical class 0.000 claims abstract description 26
- 239000003513 alkali Substances 0.000 claims abstract description 24
- 150000005215 alkyl ethers Chemical class 0.000 claims abstract description 22
- HOVAGTYPODGVJG-UVSYOFPXSA-N (3s,5r)-2-(hydroxymethyl)-6-methoxyoxane-3,4,5-triol Chemical compound COC1OC(CO)[C@@H](O)C(O)[C@H]1O HOVAGTYPODGVJG-UVSYOFPXSA-N 0.000 claims abstract description 14
- HOVAGTYPODGVJG-UHFFFAOYSA-N methyl beta-galactoside Natural products COC1OC(CO)C(O)C(O)C1O HOVAGTYPODGVJG-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 5
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 5
- -1 alkali metal salt Chemical class 0.000 claims description 25
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 12
- 229910052710 silicon Inorganic materials 0.000 claims description 12
- 239000010703 silicon Substances 0.000 claims description 12
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 8
- 239000006260 foam Substances 0.000 claims description 4
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 3
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 claims description 3
- 235000012431 wafers Nutrition 0.000 abstract description 29
- 229920000223 polyglycerol Polymers 0.000 abstract description 7
- 150000003839 salts Chemical class 0.000 abstract description 3
- 150000001340 alkali metals Chemical class 0.000 abstract 2
- 150000001342 alkaline earth metals Chemical class 0.000 abstract 2
- 150000004679 hydroxides Chemical class 0.000 abstract 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 30
- 230000000052 comparative effect Effects 0.000 description 25
- 230000007547 defect Effects 0.000 description 19
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 11
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 11
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 11
- 150000007514 bases Chemical class 0.000 description 10
- 229920001451 polypropylene glycol Polymers 0.000 description 10
- 235000011118 potassium hydroxide Nutrition 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 229920003169 water-soluble polymer Polymers 0.000 description 9
- 239000011362 coarse particle Substances 0.000 description 8
- 239000008119 colloidal silica Substances 0.000 description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
- 239000002245 particle Substances 0.000 description 7
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 235000011114 ammonium hydroxide Nutrition 0.000 description 6
- 239000004065 semiconductor Substances 0.000 description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 5
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000006061 abrasive grain Substances 0.000 description 4
- 239000002612 dispersion medium Substances 0.000 description 4
- 229910000027 potassium carbonate Inorganic materials 0.000 description 4
- 235000011181 potassium carbonates Nutrition 0.000 description 4
- 238000004220 aggregation Methods 0.000 description 3
- 230000002776 aggregation Effects 0.000 description 3
- 238000013329 compounding Methods 0.000 description 3
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 3
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 235000017550 sodium carbonate Nutrition 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 229930182478 glucoside Natural products 0.000 description 2
- 150000008131 glucosides Chemical class 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000007689 inspection Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 238000003486 chemical etching Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000004691 decahydrates Chemical class 0.000 description 1
- 239000000412 dendrimer Substances 0.000 description 1
- 229920000736 dendritic polymer Polymers 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000007518 final polishing process Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 239000011163 secondary particle Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24B—MACHINES, DEVICES, OR PROCESSES FOR GRINDING OR POLISHING; DRESSING OR CONDITIONING OF ABRADING SURFACES; FEEDING OF GRINDING, POLISHING, OR LAPPING AGENTS
- B24B37/00—Lapping machines or devices; Accessories
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09G—POLISHING COMPOSITIONS; SKI WAXES
- C09G1/00—Polishing compositions
- C09G1/02—Polishing compositions containing abrasives or grinding agents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/14—Anti-slip materials; Abrasives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/14—Anti-slip materials; Abrasives
- C09K3/1454—Abrasive powders, suspensions and pastes for polishing
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/302—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to change their surface-physical characteristics or shape, e.g. etching, polishing, cutting
- H01L21/304—Mechanical treatment, e.g. grinding, polishing, cutting
Definitions
- the present invention relates to a polishing composition and a polishing method.
- Polishing of a semiconductor wafer by CMP achieves high-precision smoothing and flattening by performing multi-stage polishing of three or four stages.
- the main purpose is to reduce haze (surface haze) and minute defects.
- the polishing composition used in the final polishing step of a semiconductor wafer generally contains a water-soluble polymer such as hydroxyethyl cellulose (HEC).
- HEC hydroxyethyl cellulose
- the water-soluble polymer has a role of making the surface of the semiconductor wafer hydrophilic, and suppresses damage to the semiconductor wafer due to adhesion of abrasive grains to the surface, excessive chemical etching, aggregation of abrasive grains, and the like. It is known that this can reduce haze and minute defects.
- HEC uses cellulose, which is a natural raw material, and may contain water-insoluble impurities derived from cellulose. Therefore, in the polishing composition containing HEC, a minute defect may occur due to the influence of this impurity.
- HEC having a molecular weight of about several hundred thousand to one million is often used.
- Japanese Patent Application Laid-Open No. 2015-109423 describes a silicon wafer polishing composition containing 0.01 to 0.5 mass% of silica particles, a nitrogen-containing basic compound, and a water-soluble polymer.
- the ratio of the number of oxygen atoms derived from hydroxyl groups to the number of oxygen atoms derived from polyoxyalkylene is 0.8 to 10.
- Japanese Patent No. 4021080 discloses 0.5 to 10% by weight of a chelating compound or a salt thereof, 0.05 to 10% by weight of a partially esterified product and / or partially etherified product of a polyhydric alcohol compound, water, A polishing liquid composition containing the above is described.
- An object of the present invention is to provide a polishing composition and a polishing method that can further reduce micro defects and haze of a polished wafer.
- the polishing composition according to one embodiment of the present invention includes silica particles, an inorganic alkali compound, polyglycerin, and a polychain polyoxyalkylene alkyl ether.
- the polychain alkyleneoxy ether is preferably at least one selected from polyoxyalkylene methyl glucoside and polyoxyalkylene polyglyceryl ether.
- the inorganic alkali compound is at least one selected from an alkali metal hydroxide, an alkali metal salt, an alkaline earth metal hydroxide, and an alkaline earth metal salt. It may be.
- a polishing method includes a step of finish polishing a silicon wafer using the above polishing composition and a foamed urethane pad having a hardness of 80 or less.
- fine defects and haze of a polished wafer can be further reduced.
- the present inventors conducted various studies in order to solve the above problems. As a result, the following knowledge was obtained.
- the number of coarse particles tends to increase.
- polyglycerin as a water-soluble polymer and containing a polychain polyoxyalkylene alkyl ether
- the coarse particles in the polishing composition The number can be reduced.
- the protection of the wafer is enhanced, and polishing that is softer and less damaging to the wafer can be performed.
- the final polishing of a silicon wafer is usually performed using a suede type polishing pad.
- fine defects can be further reduced by polishing using a urethane-type polishing pad.
- the polishing composition according to one embodiment of the present invention includes silica particles, an inorganic alkali compound, polyglycerin, and a polychain polyoxyalkylene alkyl ether.
- Silica particles are blended in the polishing composition as abrasive grains.
- silica particles those commonly used in this field can be used, and for example, colloidal silica, fumed silica and the like can be used.
- the content of the silica particles is not particularly limited, but is, for example, 0.15 to 20% by mass of the entire polishing composition.
- the lower limit of the content of silica particles is preferably 0.3% by mass, and more preferably 1.5% by mass.
- the upper limit of the content of silica particles is preferably 15% by mass, and more preferably 10% by mass.
- An inorganic alkali compound is chemically polished by etching the surface of the wafer.
- the inorganic alkali compounds include alkali metal hydroxides, alkali metal salts, alkaline earth metal hydroxides, alkaline earth metal salts, and the like.
- the inorganic alkali compound is potassium hydroxide, sodium hydroxide, potassium bicarbonate, potassium carbonate, sodium bicarbonate, sodium carbonate, potassium diphosphate, sodium tetraborate / decahydrate, etc.
- Sodium carbonate is particularly preferred.
- the inorganic alkali compounds described above may be used alone or in combination of two or more.
- the total content of the inorganic alkali compounds is not particularly limited, but is, for example, 0.0003 to 1.2% by mass of the entire polishing composition.
- the lower limit of the basic compound content is preferably 0.003% by mass.
- the upper limit of the content of the basic compound is preferably 0.6% by mass.
- the polishing composition according to the present embodiment contains polyglycerol as a water-soluble polymer.
- Polyglycerin forms a dispersion medium together with an inorganic alkali compound and is adsorbed on the surface of silica particles and the wafer surface.
- polishing with the silica particles becomes soft, and polishing scratches are suppressed.
- adhesion of polishing scratches and foreign matters is suppressed.
- the structure of polyglycerin is not particularly limited, and examples thereof include a linear type, a branched type, and a dendrimer type.
- the weight average molecular weight of polyglycerin is not particularly limited, but is, for example, 100 to 20000.
- the lower limit of the weight average molecular weight of the polyglycerol is preferably 300, more preferably 500.
- the upper limit of the weight average molecular weight of polyglycerol is preferably 10,000, and more preferably 5,000.
- the content of polyglycerin is not particularly limited, but is, for example, 0.15 to 3% by mass of the entire polishing composition.
- the lower limit of the polyglycerol content is preferably 0.2% by mass, and more preferably 0.3% by mass.
- the upper limit of the content of polyglycerin is preferably 2.5% by mass, and more preferably 2.0% by mass.
- the polishing composition according to the present embodiment contains a multi-chain polyoxyalkylene alkyl ether.
- polyoxyalkylene alkyl ethers of multi-chain type are alkylene oxide derivatives of methyl glucoside (polyoxyalkylene methyl glucoside), polyoxyalkylene glyceryl ether, polyoxyalkylene diglyceryl ether, polyoxyalkylene polyglyceryl ether, polyoxy Alkylene pentaerythritol ether, polyoxyalkylene trimethylolpropane, polyoxypropylene sorbite, and the like.
- examples thereof include glyceryl ether, polyoxyethylene polyglyceryl ether, polyoxypropylene polyglyceryl ether, polyoxyethylene polyoxypropylene pentaerythritol ether, polyoxyethylene polyoxypropylene trimethylolpropane, and polyoxypropylene sorbitol.
- polyoxyalkylene methyl glucoside or polyoxyalkylene polyglyceryl ether is preferable.
- the weight average molecular weight of the polyoxyalkylene methyl glucoside is not particularly limited, but is, for example, 100 to 10,000.
- the lower limit of the weight average molecular weight of the polyoxyalkylene glucoside is preferably 200, more preferably 500.
- the upper limit of the weight average molecular weight of the polyoxyalkylene glucoside is preferably 5000, more preferably 1000.
- the weight average molecular weight of the polyoxyalkylene polyglyceryl ether is not particularly limited, but is, for example, 100 to 10,000.
- the lower limit of the weight average molecular weight of the polyoxyalkylene polyglyceryl ether is preferably 200, more preferably 300.
- the upper limit of the weight average molecular weight of the polyoxyalkylene polyglyceryl ether is preferably 5000, and more preferably 3000.
- the content of the multi-chain polyoxyalkylene alkyl ether (when multiple types are included, the total amount thereof; the same shall apply hereinafter) is not particularly limited, but for example 0.003 to 0.3 mass of the entire polishing composition %.
- the lower limit of the content of the multi-chain polyoxyalkylene alkyl ether is preferably 0.005% by mass, and more preferably 0.015% by mass.
- the upper limit of the content of the multi-chain polyoxyalkylene alkyl ether is preferably 0.25% by mass, more preferably 0.15% by mass.
- the polishing composition according to the present embodiment may further contain a pH adjusting agent.
- the pH of the polishing composition according to this embodiment is preferably 8.0 to 12.0.
- polishing composition according to the present embodiment may optionally contain any compounding agent generally known in the field of polishing composition.
- the polishing composition according to this embodiment is prepared by appropriately mixing silica particles, an inorganic alkali compound, polyglycerin, a multi-chain polyoxyalkylene alkyl ether and other compounding materials and adding water.
- the polishing composition according to the present embodiment is produced by sequentially mixing silica particles, an inorganic alkali compound, polyglycerin, a multi-chain polyoxyalkylene alkyl ether, and other compounding materials in water.
- means for mixing these components means commonly used in the technical field of polishing compositions such as a homogenizer and ultrasonic waves are used.
- the polishing composition described above is used for polishing a silicon wafer after being diluted with water to an appropriate concentration.
- the polishing composition according to the present embodiment can be particularly suitably used for finish polishing of a silicon wafer.
- the polishing composition according to the present embodiment is suitable for polishing using a low-hardness urethane foam polishing pad.
- a polishing composition according to the present embodiment and a low-hardness urethane foam polishing pad By using the polishing composition according to the present embodiment and a low-hardness urethane foam polishing pad, a polymer coating film having an appropriate film thickness is formed, and a balance between wafer protection and defect removal is achieved. Can keep. By making the scraping amount suitable for the film thickness, a balanced polishing action can be exhibited with low damage. In addition, by reducing the concentration of the silica particles, aggregation during polishing is suppressed and low defects can be achieved.
- the hardness of the polishing pad is JIS-A standard hardness of 80 or less. When the hardness of the polishing pad exceeds 80, the contact area (contact area) between the wafer and the pad decreases, so that it becomes difficult to remove defects.
- the upper limit of the hardness of the polishing pad is preferably 78, more preferably 75.
- the lower limit of the hardness of the polishing pad is preferably 40, more preferably 50.
- Polishing compositions of Examples 1 to 4 and Comparative Examples 1 to 12 shown in Table 1 were prepared.
- particle diameter of “silica particles” represents the average secondary particle diameter of silica particles.
- KOH represents potassium hydroxide
- K 2 CO 3 represents potassium carbonate
- NH 4 OH represents an aqueous ammonia solution.
- PGL represents polyglycerin having a weight average molecular weight of 3000
- HEC represents hydroxyethyl cellulose having a weight average molecular weight of 800,000.
- polyoxyalkylene alkyl ether of the multi-chain type polyoxypropylene methyl glucoside having a weight average molecular weight of 775 was used. The balance of each polishing composition is water.
- the polishing composition of Example 1 contained 3% by mass of colloidal silica, 0.045% by mass of potassium hydroxide, 0.45% by mass of polyglycerol, and 0.045% by mass of polyoxypropylene methylglucoside.
- the polishing composition of Example 2 is based on the polishing composition of Example 1 and the content of polyoxypropylene methyl glucoside is 0.075% by mass.
- the polishing composition of Example 3 contains 1.5% by mass of colloidal silica, 0.045% by mass of potassium hydroxide, 0.75% by mass of polyglycerol, and 0.060% by mass of polyoxypropylene methylglucoside. did.
- the polishing composition of Example 4 is based on the polishing composition of Example 3 and contains potassium carbonate instead of potassium hydroxide.
- the polishing composition of Comparative Example 1 is based on the polishing composition of Example 1 with no polyoxypropylene methyl glucoside added.
- the polishing compositions of Comparative Examples 2 and 3 are based on the polishing composition of Comparative Example 1 and have a polyglycerin content of 0.30 mass% and 0.38 mass%, respectively.
- the polishing compositions of Comparative Examples 4 and 5 are based on the polishing composition of Comparative Example 1 and the potassium hydroxide contents are 0.090 mass% and 0.135 mass%, respectively.
- the polishing composition of Comparative Example 6 is obtained by changing the colloidal silica from a particle size of 65 nm to 70 nm based on the polishing composition of Comparative Example 1.
- the polishing composition of Comparative Example 7 is obtained by changing the basic compound from potassium hydroxide to potassium carbonate based on the polishing composition of Comparative Example 1.
- the polishing composition of Comparative Example 8 contained 10.5% by mass of colloidal silica, 0.390% by mass of aqueous ammonia, and 0.36% by mass of hydroxyethyl cellulose.
- the polishing composition of Comparative Example 9 contained 2% by mass of colloidal silica, 0.078% by mass of an aqueous ammonia solution, and 0.34% by mass of hydroxyethyl cellulose.
- the polishing composition of Comparative Example 10 contained 1% by mass of colloidal silica, 0.039% by mass of an aqueous ammonia solution, and 0.34% by mass of hydroxyethyl cellulose.
- the polishing composition of Comparative Example 11 contained 0.2% by mass of colloidal silica, 0.009% by mass of an aqueous ammonia solution, and 0.34% by mass of hydroxyethyl cellulose.
- the polishing composition of Comparative Example 12 was based on the polishing compositions of Examples 3 and 4, and contained an aqueous ammonia solution instead of an inorganic alkali compound (KOH, K 2 CO 3 ) as a basic compound. It is.
- a 12-inch silicon wafer was polished.
- the conductivity type of the silicon wafer was P type, and the resistivity was 0.1 ⁇ cm or more and less than 100 ⁇ cm.
- the polished surface was a ⁇ 100> surface.
- As the polishing apparatus an SPP800S single-side polishing apparatus manufactured by Okamoto Machine Tool Co., Ltd. was used.
- As the polishing pad a urethane foam type polishing pad having a hardness of 73 was used.
- the polishing composition was diluted 30 times and supplied at a supply rate of 0.6 L / min. Polishing was performed for 4 minutes with a platen rotating speed of 40 rpm, a carrier rotating speed of 39 rpm, and a polishing load of 100 gf / cm 2 .
- the minute defects were measured using a wafer surface inspection apparatus MAGICS M5640 (Lasertec).
- MAGICS M5640 Lasertec
- a wafer surface inspection device LS6600 manufactured by Hitachi Engineering Co., Ltd. was used. The results are shown in Table 1 above.
- Example 1 From the comparison between Example 1 and Comparative Example 1, it can be seen that the inclusion of a multi-chain polyoxyalkylene alkyl ether significantly reduces micro defects. Moreover, it turns out from a comparison with Example 3, 4 and the comparative example 12 that a micro defect reduces notably by using an inorganic alkali compound as a basic compound.
- Example 1 the number of coarse particles of the polishing composition (the number of particles having a particle diameter of 0.5 ⁇ m or more) was measured.
- the number of coarse particles AccuSize FX Nano Dual manufactured by Particle Sizing System was used. The results are shown in Table 2.
- the inclusion of multi-chain polyoxyalkylene alkyl ether reduced the number of coarse particles by about 30%.
- the decrease in the coarse particles is thought to be because the affinity between the particles and the dispersion medium is improved by the multi-chain polyoxyalkylene alkyl ether, and the particles are less likely to aggregate.
- Polishing compositions of Examples 1, 3 to 16, and Comparative Examples 1, 12, and 13 shown in Table 3 were prepared.
- the same formulation numbers were assigned the same examples and comparative examples (Examples 1, 3, and 4, Comparative Examples 1, 8, and 12).
- NaOH sodium hydroxide
- LiOH lithium hydroxide
- K 4 P 2 O 7 potassium diphosphate
- Na 2 CO 3 sodium carbonate
- a 12-inch silicon wafer was polished using the polishing compositions of Examples and Comparative Examples described in Table 3. Polishing was performed under the same conditions as in Polishing Example 1 except that a suede type polishing pad (Supreme (registered trademark) RN-H manufactured by Nitta Haas Co., Ltd.) was used as the polishing pad. And haze was measured. Further, the number of coarse particles was measured in the same manner as in Polishing Example 1. The results are shown in Table 4.
- the polishing of the silicon wafer is usually performed using a suede type polishing pad as in the polishing example 2.
- the polishing composition of Comparative Example 8 Polishing Example 1 (Table 1) polished with a suede type polishing pad and Polishing Example 2 (Table) polished with a foamed urethane type pad.
- the micro defects are reduced from 495 (Polishing Example 1) to 398 (Polishing Example 2). That is, in the conventional polishing composition, it is preferable to use a suede type polishing pad rather than a foamed urethane type pad.
- the polishing example 1 has fewer micro defects. That is, in the polishing composition according to the present embodiment, the number of minute defects can be further reduced by polishing using a foamed urethane pad.
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- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)
- Mechanical Treatment Of Semiconductor (AREA)
Abstract
Priority Applications (3)
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JP2018559608A JP7061968B2 (ja) | 2016-12-28 | 2017-12-27 | 研磨用組成物及び研磨方法 |
CN201780074856.5A CN110023449B (zh) | 2016-12-28 | 2017-12-27 | 研磨用组合物和研磨方法 |
KR1020197018210A KR102508181B1 (ko) | 2016-12-28 | 2017-12-27 | 연마용 조성물 및 연마 방법 |
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JP2016-255136 | 2016-12-28 | ||
JP2016255136 | 2016-12-28 |
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WO2018124226A1 true WO2018124226A1 (fr) | 2018-07-05 |
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PCT/JP2017/047077 WO2018124226A1 (fr) | 2016-12-28 | 2017-12-27 | Composition pour polissage, et procédé de polissage |
Country Status (5)
Country | Link |
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JP (1) | JP7061968B2 (fr) |
KR (1) | KR102508181B1 (fr) |
CN (1) | CN110023449B (fr) |
TW (1) | TWI753984B (fr) |
WO (1) | WO2018124226A1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2020107838A (ja) * | 2018-12-28 | 2020-07-09 | ニッタ・デュポン株式会社 | 半導体研磨用組成物 |
WO2021199723A1 (fr) * | 2020-03-31 | 2021-10-07 | 株式会社フジミインコーポレーテッド | Composition de polissage |
Citations (3)
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WO2013157442A1 (fr) * | 2012-04-18 | 2013-10-24 | 株式会社フジミインコーポレーテッド | Composition de polissage |
JP2014187268A (ja) * | 2013-03-25 | 2014-10-02 | Hitachi Chemical Co Ltd | Cmp研磨剤及び基板の研磨方法 |
JP2015109423A (ja) * | 2013-10-25 | 2015-06-11 | 花王株式会社 | シリコンウェーハ用研磨液組成物 |
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CN101153206A (zh) * | 2006-09-29 | 2008-04-02 | 安集微电子(上海)有限公司 | 用于抛光多晶硅的化学机械抛光液 |
SG185262A1 (en) * | 2007-09-28 | 2012-11-29 | Nitta Haas Inc | Polishing composition |
JP2009099819A (ja) * | 2007-10-18 | 2009-05-07 | Daicel Chem Ind Ltd | Cmp用研磨組成物及び該cmp用研磨組成物を使用したデバイスウェハの製造方法 |
EP2722872A4 (fr) * | 2011-06-14 | 2015-04-29 | Fujimi Inc | Composition de polissage |
JP6044629B2 (ja) * | 2012-02-21 | 2016-12-14 | 日立化成株式会社 | 研磨剤、研磨剤セット及び基体の研磨方法 |
JP2015088495A (ja) * | 2012-02-21 | 2015-05-07 | 日立化成株式会社 | 研磨剤、研磨剤セット及び基体の研磨方法 |
CN104321850B (zh) * | 2012-05-25 | 2016-11-23 | 日产化学工业株式会社 | 晶片用研磨液组合物 |
CN104582899B (zh) * | 2012-08-30 | 2018-11-09 | 日立化成株式会社 | 研磨剂、研磨剂套剂及基体的研磨方法 |
JP6343160B2 (ja) * | 2014-03-28 | 2018-06-13 | 株式会社フジミインコーポレーテッド | 研磨用組成物 |
WO2016031485A1 (fr) * | 2014-08-29 | 2016-03-03 | 株式会社フジミインコーポレーテッド | Composition de polissage et procédé permettant la production de composition de polissage |
JP6559936B2 (ja) * | 2014-09-05 | 2019-08-14 | 日本キャボット・マイクロエレクトロニクス株式会社 | スラリー組成物、リンス組成物、基板研磨方法およびリンス方法 |
JP6879202B2 (ja) * | 2015-03-10 | 2021-06-02 | 昭和電工マテリアルズ株式会社 | 研磨剤、研磨剤用貯蔵液及び研磨方法 |
CN105950115A (zh) * | 2016-05-13 | 2016-09-21 | 盐城工学院 | 一种适用于氧化镓衬底的环保研磨膏及其制备方法 |
-
2017
- 2017-12-27 CN CN201780074856.5A patent/CN110023449B/zh active Active
- 2017-12-27 KR KR1020197018210A patent/KR102508181B1/ko active IP Right Grant
- 2017-12-27 WO PCT/JP2017/047077 patent/WO2018124226A1/fr active Application Filing
- 2017-12-27 JP JP2018559608A patent/JP7061968B2/ja active Active
- 2017-12-28 TW TW106146204A patent/TWI753984B/zh active
Patent Citations (3)
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WO2013157442A1 (fr) * | 2012-04-18 | 2013-10-24 | 株式会社フジミインコーポレーテッド | Composition de polissage |
JP2014187268A (ja) * | 2013-03-25 | 2014-10-02 | Hitachi Chemical Co Ltd | Cmp研磨剤及び基板の研磨方法 |
JP2015109423A (ja) * | 2013-10-25 | 2015-06-11 | 花王株式会社 | シリコンウェーハ用研磨液組成物 |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2020107838A (ja) * | 2018-12-28 | 2020-07-09 | ニッタ・デュポン株式会社 | 半導体研磨用組成物 |
JP7158280B2 (ja) | 2018-12-28 | 2022-10-21 | ニッタ・デュポン株式会社 | 半導体研磨用組成物 |
WO2021199723A1 (fr) * | 2020-03-31 | 2021-10-07 | 株式会社フジミインコーポレーテッド | Composition de polissage |
Also Published As
Publication number | Publication date |
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CN110023449A (zh) | 2019-07-16 |
CN110023449B (zh) | 2021-08-17 |
TWI753984B (zh) | 2022-02-01 |
KR102508181B1 (ko) | 2023-03-09 |
JPWO2018124226A1 (ja) | 2019-10-31 |
KR20190098152A (ko) | 2019-08-21 |
JP7061968B2 (ja) | 2022-05-02 |
TW201831645A (zh) | 2018-09-01 |
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