Classifications

• • 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
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
  • C23F3/00—Brightening metals by chemical means
• • 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
  • C09K3/1409—Abrasive particles per se
• • 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
  • C09K3/1463—Aqueous liquid suspensions
• • H—ELECTRICITY
  • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
  • H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
  • H10P52/00—Grinding, lapping or polishing of wafers, substrates or parts of devices
  • H10P52/40—Chemomechanical polishing [CMP]
  • H10P52/403—Chemomechanical polishing [CMP] of conductive or resistive materials

Definitions

• the mvention is directed to chemical mechanical polishing, CMP, of a semiconductor substrate having a copper metal circuit.
• a semiconductor substrate comprises, a semiconductor wafer and multiple layers of materials including, a layer of an insulating material, such as, silica, that is deposited and provided with troughs, and a metal conductor, such as, copper, that is deposited as a layer, and is in the troughs to form a copper circuit.
• the metal conductor is separated from the insulating material by a buffer material, such as, tantalum or tantalum nitride.
• CMP is performed as a process for removing excess copper. According to a process of CMP, a polishing pad is pressed against the substrate and is moved across the surface of the substrate while an aqueous polishing composition is interposed between the polishing pad and the surface of the substrate being polished.
• Abrasive particles in the polishing composition apply abrasion to increase the rate of removal by polishing.
• inorganic abrasive particles included; alumina, silica, ceria, germania, diamond, silicon carbide, titania, zirconia, boron nitride, boron carbide and mixtures thereof.
• the copper layer on the wafer is polished by performing CMP until the copper is cleared from the surface of the substrate.
• CMP desirably removes copper material from peaks or protrusions of the copper layer, which are those portions that are above the average surface height of the surface being polished. Copper material in valleys or recesses, including the copper circuit in the troughs, are below the average surface height. Removal of copper primarily from the peaks is desired, and is accomplished by removing the copper material from the peaks at a rate of removal that is faster than that of the copper material in valleys. However, the process of CMP has a tendency to remove copper in both the peaks and valleys. While polishing a copper circuit, i.e.
• dishing A need exists for an invention to significantly reduce, i.e., minimize, dishing.
• a polishing composition has organic polymer particles as abrasive particles.
• the copper layer on the wafer is polished by CMP using the polishing composition, according to the invention, to remove peaks of the copper layer. Copper is cleared from the surface of the substrate or wafer, with minimized, i.e., substantial reduction in, dishing of the copper circuit. Planarization herein refers to
• Planarized herein refers to a flat polished surface of the semiconductor substrate, and the copper in the troughs having minimized dishing, resulting from a process of CMP that has removed the copper layer.
• the organic polymer particles apply abrasion during CMP to remove "high spots" of the copper layer of semiconductor circuit and provide a planarized copper circuit.
• the polymer particles do not provide the same level of abrasion as inorganic particles but provide a substantially lower level of abrasion.
• Copper is a relatively soft metal and is easily eroded by polishing with the organic polymer particles.
• the organic polymer particles are selective in that only relatively soft copper is polished for clearing, i.e. removal and planarization, and not other layers of relatively hard material, such as, tantalum or tantalum nitride, of the buffer material.
• An embodiment of the polishing composition does not have inorganic abrasive particles.
• Another embodiment does have 0.01% up to 3% by weight of inorganic abrasive particles, for example, alumina and silica or mixtures thereof, to adjust an increase in the removal rate of copper during CMP.
• the polishing composition contains 0.1-5.0% by weight, based on the weight of the composition, of polymer particles having a number average molecular weight of at least 500,000 determined by GPC (gel permeation chromatography).
• One embodiment has a Tg (glass transition temperature) of at least 25°C.
• a further embodiment of the composition contains 0.25-1.0% by weight, based on the weight of the composition, of polymers have a number average molecular weight of 500,000 to 3,000,000 and a Tg of 25 to 130°C.
• An alternative of the further embodiment has a Tg of 25 to 90°C.
• the Tg of the polymer is measured using differential scanning calorimeter (DSC) from Texas Instruments (model 2010), and performing a known procedure, wherein, polymer samples are heated in nitrogen starting at ambient temperature and heating at 20°C per minute through the glass transition temperature recording mid point values.
• Embodiments of the polymer particles include those that have diameters in the range of 5 to 5,000, and those that have diameters in the range of 50 to 1500 nm.
• the polymer particles are formed by: a homogeneous polymer, a copolymer, a terpolymer, blends of two or more polymers, crosslinked homogeneous polymers,
• the polymer particles include particles of polymers, including, but not limited to, styrene, copolymers and terpolymers of styrene, acrylonitrile, methyl methacrylate, copolymers and terpolymers of methyl methacrylate and an alkyl acrylate wherein the alkyl group has 1-18 carbon atoms or an alkyl methacrylate where the alkyl group has 2- 18 carbon atoms and can contain small percentages of polymerized ethylenically unsaturated carboxylic acids, such as, methacrylic acid or acrylic acid or hydroxy alkyl acrylates or methacrylates or amino alkyl acrylates or methacrylates.
• the polymers can be crosslinked with monomers such as, divinyl benzene.
• One useful polymer is a polymer of styrene crosslinked with divinyl benzene, which can be in particle form of hollow spheres.
• the polymer particles include, and are not limited to, a graft copolymer, for example, a graft copolymer having a backbone of relatively high Tg polymer, like polymethyl methacrylate and side chains of a comparatively low Tg polymer of an alkyl acrylate, like butyl acrylate.
• the graft copolymer can have a backbone of a low Tg polymer, such as, 2 ethylhexyl acrylate and side chains of macromonomers containing a major amount of polymethyl methacrylate.
• Polymer particles of a core shell polymer can be used in which the shell is of a high Tg polymer, such as, polymethyl methacrylate and the core is a lower Tg polymer, such as, ethyl acrylate.
• Monomers that form the polymers of the particles are, for example, methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl methacrylate, pentyl methacrylate, hexyl methacrylate, octyl methacrylate, lauryl methacrylate, stearyl methacrylate, methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate, pentyl acrylate, hexyl acrylate, octyl acrylate, lauryl acrylate, stearyl acrylate, cyclohexyl acrylates and methacrylates, acrylonitrile, styrene, alpha methyl styrene, vinyl toluene, hydroxy alkyl acrylates and methacrylates such as hydroxy ethyl acrylate, hydroxy propyl acrylate, hydroxy butyl
• the polymers particles are formed by known techniques.
• An aqueous latex can be formed and added to form the polishing composition of this invention.
• solution polymerization techniques are used to form polymer particles, followed by having solvent removal.
• the polymer particles are dispersed in water and added directly to the polishing composition.
• An embodiment of the polishing composition contains about 0.05-2.0 % by weight, based on the weight of the composition, of carboxylic acid polymer particles comprising polymerized unsaturated carboxylic acid monomers and has a number average molecular weight of about 20,000 to 1,500,000. Blends of high and low number average molecular weight carboxylic acid polymers also can be used and are preferred for many polishing uses. These carboxylic acid polymers are in solution or are in the form of an aqueous dispersion. The number average molecular weight of the aforementioned polymers are determined by GPC (gel permeation cliromatography).
• high carboxylic acid containing copolymers and terpolymers can be used in which the carboxylic acid component comprises 5-75% by weight of the polymer.
• Typical of such polymer are polymers of (meth)acrylic acid and acrylamide or methacrylamide; polymers of (meth)acrylic acid and styrene and other vinyl aromatic monomers; polymers of alkyl (meth)acrylates (esters of acrylic or methacrylic acid) and a mono or dicarboxylic acid, such as, acrylic or methacrylic acid or itaconic acid; polymers of substituted vinyl aromatic monomers having substituents, such as, halogen, i.e., chlorine, fluorine, bromine, nitro, cyano, alkoxy, haloalkyl, carboxy, amino, amino alkyl and a unsaturated mono or dicarboxylic acid and an alkyl (meth)acrylate; polymers of monethylenically unsaturated monomers
• Further embodiments include, polymers that are biodegradeable, photodegradeable or degradable by other means.
• An example of such a composition that is biodegradeable is a polyacrylic acid polymer containing segments of poly(acrylate co methyl 2- cyanoacrylate).
• An oxidizer, or oxidizing agent, in the polishing composition converts metal on the surface of the substrate to an oxide to serve as a passivating layer that reduces further reaction of the metal with the polishing composition until removed by polishing.
• An embodiment of the polishing composition contains 1 to 15% by weight of an oxidizing agent.
• Typical oxidizing agents are hydrogen peroxide, iodates, such as, potassium iodate, nitrates, such as, cesium nitrate, barium nitrate, ammonium nitrate, mixtures of ammonium nitrate and cesium nitrate, carbonates, such as, ammonium carbonate, persulfates, such as, ammonium and sodium persulfate, and perchlorates.
• a further embodiment of the polishing composition contains about 5-10% by weight of an oxidizing agent.
• a further embodiment of the polishing composition contains about 9% by weight of hydrogen peroxide as the oxidizing agent.
• the polishing composition has about 50 to 5,000 ppm (parts per million) of an inhibitor, for example, BTA (benzotriazole), or TTA (tolyltriazole) or mixtures thereof.
• an inhibitor for example, BTA (benzotriazole), or TTA (tolyltriazole) or mixtures thereof.
• Other inhibitors include, and are not limited to: 1-hydroxybenzotriazole, N-(1H- benzorriazole-1-ylmethyl) formamide, 3,5-dimethylpyrazole, indazole, 4-bromopyrazole, 3-amino-5-phenylpyrazole, 3-amino-4-pyrazolecarbonitrile, 1-methylimidazole, h dolin QTS and the like.
• the polishing composition has up to 3.0% by weight, for example, 0.1-1.0% by weight, of a complexing agent, such as, malic acid, or, as disclosed in US 5,391,258, or a carboxylic acid having two or more carboxyl groups and having a hydroxyl group.
• complexing agents include, and are not limited to, straight chain monocarboxylic acids and their salts and dicarboxylic acids and their salts, such as, malic acid and malates, tartaric acid and tartarates, gluconic acid and gluconates, citric acid and citrates, malonic acid and malonates, formic acid and formates, lactic acid and lactates. Polyhydroxybenzoic acid, phthalic acid and salts thereof also can be used.
• Unsaturated carboxylic acid monomers include, and are not limited to, unsaturated monocarboxylic acids and unsaturated dicarboxylic acids.
• Typical unsaturated monocarboxylic acid monomers contain 3 to 6 carbon atoms and include acrylic acid, oligomeric acrylic acid, methacrylic acid, crotonic acid and vinyl acetic acid.
• unsaturated dicarboxylic acids contain 4 to 8 carbon atoms and include the anhydrides thereof and are, for example, maleic acid, maleic anhydride, fumaric acid, glutaric acid, itaconic acid, itaconic anhydride, and cyclohexene dicarboxylic acid. Water soluble salts of the aforementioned acids also can be used.
• An embodiment of the polishing composition is an aqueous composition that has a pH under 5.0.
• a further embodiment has a pH of 2.8 to 4.2.
• Yet a further embodiment has apH of2.8 to 3.8.
• EP 0 913 442 A2 discloses a polishing composition having a dishing reducing agent in the form of a polyacrylic acid to adhere to copper and minimize dishing during CMP.
• poly(meth)acrylic acid means polymers of acrylic acid or polymers of methacrylic acid. Particularly useful are poly(meth)acrylic acids having a number average molecular weight of about 20,000 to 150,000, preferably 25,000 to 75,000 and more preferably, 25,000 to 40,000. Blends of high and low number average molecular weight poly(meth)acrylic acids are particularly preferred.
• a low number average molecular weight poly(meth)acrylic acid having a number average molecular weight of 20,000 to 100,000 and preferably, 20,000 to 40,000 is used in combination with a high number average poly(meth)acrylic acid having a number average molecular weight of 200,000 to 1,500,00, preferably, 150,000 to 300,000.
• the weight ratio of the low number average molecular weight poly(meth) acrylic acid to the high number average molecular weight poly(meth)acrylic acid is 10:1 to 1:10, preferably 4:1 to 1:4, and more preferably 2:1 to 1:2.
• An embodiment comprises a polyacrylic acid having a number average molecular weight of about 30,000 and a polyacrylic acid having a number average molecular weight of about 250,000 in a 1:1 weight ratio.
• Embodiments of very low number average molecular weight poly(meth)acrylic acid polymers in the aforementioned blend include, for example, poly(meth)acrylic acid polymers having a number average molecular weight of 1,000 to 5,000.
• the polishing composition may further contain pH buffers, such as, amines, and may contain surfactants, deflocculants, viscosity modifiers, wetting agents, cleaning agents and the like.
• polishing pads can be used with the polishing composition to polish copper; a metals pad described in US 6,022,268, a polishing pad containing particles for polishing described in US 5,489,233, a polishing pad of polymer impregnated fiber
• polishing compositions were prepared:
• the polishing composition was prepared by blending the following constituents: 0.3 parts benzotriazole, 0.22 parts malic acid, 0.09 parts of polyacrylic acid having a number average molecular weight of 30,000, 0.9 parts of polyacrylic acid having a number average molecular weight of 250,000 and 9.0 parts hydrogen peroxide and sufficient deionized water to bring the total parts of polishing composition to 100.
• Polishing Composition 1 (1% "Sunspheres") - identical to the above control composition except that 1% by weight of "Sunspheres” polymer particles was blended with the control composition.
• "Sunspheres” have a diameter of 350 nm, are manufactured by Rohm and Haas Company and are hollow spheres composed of polystyrene crosslinked with divinyl benzene and have a Tg of 81°C.
• Polishing Composition 2 (1% "Rovace” 661) - identical to the above control composition except that 1.0% “Rovace” 661 was blended with the control composition.
• "Rovace” 661 have diameter of 300 nm, are manufactured by Rohm and Haas Company, and are polymer particles of polyvinyl acetate (PNA) having a number average molecular weight of approximately 1 million and have a Tg of 21°C.
• PNA polyvinyl acetate
• Polishing Composition 3 (1% "Ropaque” HP-1055) - identical to the above control composition except that 1 % "Ropaque HP-1055 was blended with the control composition.
• Ropaque HP-1055 are polymer particles having a diameter of 1000 nm, are manufactured by Rohm and Haas Company, are polymer particles of polystyrene that are crosslinked and have a Tg of 83 °C.
• Polishing Composition 4 (1% HG 74 P) - identical to the above control composition except that 1% HG 74 P was blended with the control composition.
• HG 74 P are polymer particles manufactured by Rohm and Haas Company, are polymer particles of polymethyl methacrylate having a number average molecular weight of approximately 1 million and have a Tg of 29°C.
• Conventional Polishing Composition 5 (1% “Klebosol”) - identical to the above control composition except that 1% “Klebosol was blended with the control composition.
• “Klebosol” is colloidal silica having a particle diameter of 12 nm, has inorganic abrasive characteristics and is manufactured by Clariant Corporation.
• Test Pad Metal 26 pad manufactured by Rodel Inc. Newark, Delaware (described in US Patent 6,022,268).
• polishing was continued except the down force was reduced to 3 psi ( 210.9 g/cm 2 ) until the endpoint trace on the polishing machine flattens (i.e., the slope of the curve is zero). At this point all removal of copper had stopped and no copper was present. The time was recorded for each of the above polishing steps.
• the dishing of the copper pattern lines of the wafer was measured on a Tencor PI profilometer.
• the 100 um lines in the center of the wafer were measured, the 100 um lines in the middle of the wafer were measured (i.e., halfway between the center and edge of the wafer) and the lOOum lines near the edge of the wafer were measured (i.e., about 1 inch from the edge of the wafer).
• Separate wafers as described above were polished under the same conditions with each of the above prepared Polishing Compositions 1-5. The results are shown below in Table 1 for each of the polishing compositions.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
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• General Chemical & Material Sciences (AREA)
• Mechanical Engineering (AREA)
• Metallurgy (AREA)
• Mechanical Treatment Of Semiconductor (AREA)
• Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)

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• 2002
  • 2002-01-23 US US10/055,535 patent/US20020173243A1/en not_active Abandoned
  • 2002-03-27 KR KR1020037012958A patent/KR100864617B1/ko not_active Expired - Fee Related
  • 2002-03-27 JP JP2002579953A patent/JP2004532521A/ja active Pending
  • 2002-03-27 WO PCT/US2002/009805 patent/WO2002081584A1/en not_active Ceased
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