WO2004001502A1 - Developer-soluble metal alkoxide coatings for microelectronic applications - Google Patents
Developer-soluble metal alkoxide coatings for microelectronic applications Download PDFInfo
- Publication number
- WO2004001502A1 WO2004001502A1 PCT/US2003/019457 US0319457W WO2004001502A1 WO 2004001502 A1 WO2004001502 A1 WO 2004001502A1 US 0319457 W US0319457 W US 0319457W WO 2004001502 A1 WO2004001502 A1 WO 2004001502A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- composition
- group
- solvent system
- polymer
- substrate
- Prior art date
Links
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/26—Processing photosensitive materials; Apparatus therefor
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
- C08G79/10—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule a linkage containing aluminium
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L85/00—Compositions of macromolecular compounds obtained by reactions forming a linkage in the main chain of the macromolecule containing atoms other than silicon, sulfur, nitrogen, oxygen and carbon; Compositions of derivatives of such polymers
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/09—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers
- G03F7/091—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers characterised by antireflection means or light filtering or absorbing means, e.g. anti-halation, contrast enhancement
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/1053—Imaging affecting physical property or radiation sensitive material, or producing nonplanar or printing surface - process, composition, or product: radiation sensitive composition or product or process of making binder containing
- Y10S430/1055—Radiation sensitive composition or product or process of making
- Y10S430/106—Binder containing
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/1053—Imaging affecting physical property or radiation sensitive material, or producing nonplanar or printing surface - process, composition, or product: radiation sensitive composition or product or process of making binder containing
- Y10S430/1055—Radiation sensitive composition or product or process of making
- Y10S430/106—Binder containing
- Y10S430/11—Vinyl alcohol polymer or derivative
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/1053—Imaging affecting physical property or radiation sensitive material, or producing nonplanar or printing surface - process, composition, or product: radiation sensitive composition or product or process of making binder containing
- Y10S430/1055—Radiation sensitive composition or product or process of making
- Y10S430/106—Binder containing
- Y10S430/111—Polymer of unsaturated acid or ester
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/151—Matting or other surface reflectivity altering material
Definitions
- the present invention is concerned with new anti-reflective compositions for use in the manufacture of microelectronic devices. These compositions include polymeric metal alkoxides and are developable in aqueous photoresist developers.
- Integrated circuit manufacturers are consistently seeking to maximize substrate wafer sizes and minimize device feature dimensions in order to improve yield, reduce unit case, and increase on-chip computing power.
- Device feature sizes on silicon or other chips are now submicron in size with the advent of advanced deep ultraviolet (DUV) microlithographic processes.
- DUV deep ultraviolet
- wet developable anti-reflective coatings These types of coating can be removed along with the exposed areas of the photoresist material. That is, after the photoresist layer is exposed to light through a patterned mask, the exposed areas of the photoresist are wet developable and are subsequently removed with an aqueous developer to leave behind the desired trench and hole pattern. Wet developable anti-reflective coatings are removed during this developing step, thus eliminating the need for an additional removal step. Unfortunately, wet developable anti-reflective coatings have not seen widespread use due to the fact that they must also exhibit good spin bowl compatibility and superior optical properties to be useful as an anti-reflective coating. Thus, there is a need for anti-reflective coating compositions which are developable in conventional photoresist developers while simultaneously exhibiting good coating and optical properties.
- the present invention broadly comprises new microlithographic compositions that are useful in the manufacture of microelectronic devices.
- compositions comprise a polymer dispersed or dissolved in a solvent system.
- Preferred polymers include recurring units having the formula
- X is a light-attenuating moiety
- M is a metal
- each R is individually selected from the group consisting of hydrogen, alkyls (preferably C r C 8 ), aryls, alkoxys, and phenoxys.
- the most preferred R groups are -CH 3 and -OC 2 H 5 .
- the polymer preferably further comprises recurring units having the formula
- each R 1 is individually selected from the group consisting of hydrogen, alkyls (preferably Cj-Cg), aryls, alkoxys, and phenoxys, andM 1 is a metal.
- the most preferred R 1 groups are -CH 3 and -OC 2 H 5 .
- the most preferred metals are Ti, Zr, Si, and/or Al. It is also preferred that the light-attenuating moiety include a functional group for coordinating with the metal atom of the polymeric metal alkoxide. Such functional groups include carbonyl, alcohol, and phenol groups. Furthermore, the moiety (i.e., X) is preferably present in the polymer at a level of from about 5-50% by weight, and more preferably from about 10-25% by weight, based upon the total weight of the polymer taken as 100% by weight.
- Suitable light-attenuating moieties include those selected from the group consisting of moieties of trimethylol ethoxylate, 4- hydroxybenzaldehyde, and 2-cyano-3-(4-hydroxyphenyl)-acrylic acid ethyl ester. Also, in order to avoid photosensitivity in the composition, none of X, R, and R 1 should include any ethylenically unsaturated groups.
- the polymer is formed by reacting a polymeric metal alkoxide with an organic compound.
- the polymeric metal alkoxide includes recurring units having the formula
- each L is individually selected from the group consisting of diketo and alkoxide ligands.
- Preferred L groups have the formula
- each R is individually selected from the group consisting of hydrogen, alkyls (preferably C j -Cg), aryls, alkoxys, and phenoxys, with -CH 3 and -OC 2 H 5 being the most preferred R groups .
- a moiety of ethyl acetoacetate is the most preferred L group .
- the preferred metal atoms are the same as those discussed previously.
- the polymeric metal alkoxide having the structure of Formula I above can first be formed by reacting a polymeric metal alkoxide (e.g., poly(dibutyltitanate)) with a diketo or alkoxide ligand (e.g., ethyl acetoacetate).
- a starting monomer which already includes the diketo or alkoxide ligand as part of its structure can be formed into the desired polymer by hydrolyzing and then condensing the monomer.
- This type of starting monomer is titanium diisopropoxide bis(ethylacetoacetate) .
- the organic compound which is reacted with the polymeric metal alkoxide having the structure of Formula I above should comprise a functional group suitable for coordinating with the metal atom of the polymeric metal alkoxide.
- Suitable functional groups include alcohols, phenols, thioalcohols, thiophenols, and carbonyls.
- the most preferred organic compounds are trimethylol ethoxylate, 4-hydroxybenzaldehyde, and 2-cyano-3-(4-hydroxyphenyl)-acrylic acid ethyl ester.
- the anti-reflective compositions are formed by simply dispersing or dissolving the polymers in a suitable solvent system, preferably at ambient conditions and for a sufficient amount of time to form a substantially homogeneous dispersion.
- the polymer should be present in the composition at a level of 2-50% by weight, more preferably from about 5-30% by weight, and more preferably from about 7-15% by weight, based upon the total weight of solids in the composition taken as 100% by weight.
- the viscosity of this polymer is preferably from about 2,000- 5,000 cS, and more preferably from about 3,200-3,500 cS.
- Preferred solvent systems include a solvent selected from the group consisting of propylene glycol methyl ether acetate (PGMEA), propylene glycol methyl ether (PGME), propylene glycol ra-propyl ether (PnP), ethyl lactate, and mixtures thereof.
- the solvent system has a boiling point of from about 50-250°C, and more preferably from about 100-175°C.
- the solvent system should be utilized at a level of from about 70-95% by weight, and preferably from about 80-90% by weight, based upon the total weight of the solids in the composition taken as 100% by weight.
- any additional ingredients are also preferably dispersed in the solvent system along with the polymer.
- One such preferred additional ingredient is a second polymer or polymer binder such as those selected from the group consisting of epoxy novolac resins (e.g., Epon 164 ® , available from Araldite), acrylates (e.g., poly(glycidyl methacrylate)), polymerized aminoplasts (e.g., Cymel ® products available from Cytec Industries), glycourals (e.g., Powderlink ® products available from Cytec Industries), vinyl ethers, and mixtures thereof.
- the weight average molecular weight of this additional polymer is preferably from about 1 ,000-50,000 Daltons, and more preferably from about 5,000-25,000 Daltons.
- the composition should comprise from about 1-50% by weight of this additional polymer, and more preferably from about 5-25% by weight, based upon the total weight of the solids in the composition taken as 100% by weight. It will be appreciated that a number of other optional ingredients can be included in the composition as well. Typical optional ingredients include light attenuating compounds, surfactants, catalyst, crosslinkers, and adhesion promoters.
- the method of applying the fill or anti-reflective coating compositions to a substrate simply comprises applying a quantity of a composition hereof to the substrate surface by any known application method (including spin-coating).
- the substrate can be any conventional chip (e.g., silicon wafer), an ion implant layer, etc.
- the resulting layer should be heated to a temperature of from about 100-250°C to induce crosslinking. This will result in the evaporation of the solvent system as well as the volatilization of at least a portion of the organic constituents of the composition to yield a cured layer having alternating metal and oxygen atoms.
- the refractive index of this cured anti-reflective layer or coating will be at least about 1.4, preferably from about 1.5-2.0, and more preferably from about 1.6-1.7 at a wavelength of about 365 nm.
- the thickness of the cured layer on the surface of the substrate adjacent the edge of a contact or via hole should be at least about 60%, preferably at least about 75%, and more preferably at least about 85% of the thickness of the film on the substrate surface a distance away from the edge of the contact or via hole approximately equal to the diameter of the hole.
- a photoresist can be applied to the cured material, followed by exposing, developing, and etching of the photoresist. Following the methods of the invention will yield precursor structures for dual damascene and other microlithographic processes which have the foregoing desirable properties.
- the cured inventive compositions are wet developable. That is, the cured compositions can be removed with conventional aqueous developers such as tetramethyl ammonium hydroxide and KOH developers. Some of these developers are commercialized under the tradenames MF-319 (available from Shipley, Massachusetts), MF-320 (available from Shipley), andNMD3 (available from TOK, Japan) developers. At least about 95%, and preferably at least about 99% of the inventive coatings will be removed by a base developer such as tetramethyl ammonium hydroxide and KOH developers. This percent solubility in commercially- available developers is a significant advantage over the prior art as this shortens the manufacturing process and makes it less costly.
- aqueous developers such as tetramethyl ammonium hydroxide and KOH developers.
- the present composition is spin bowl compatible. This is determined by coating a four-inch sample wafer with the composition. After coating, the wafer is not baked, but is instead positioned upward in order to prevent film flow. The sample is allowed to dry for about
- the coated wafer is exposed to the particular test solvent (e.g., propylene glycol methyl ether acetate). This is accomplished by flooding the sample surface with the solvent for three minutes ( ⁇ five seconds) followed by spinning for 15 seconds at 1,500 rpm (20,000 rpm Ramp) and then for 30 seconds at 2500 rpm (20,000 rpm Ramp). The thickness of the sample is again measured at five locations, and the average final sample thickness is determined.
- the percent solubility is calculated as follows:
- % solubility * 100. (initial sample thickness)
- the inventive compositions yield a percent solubility of at least about 75%, and more preferably at least about 90%.
- Fig. lb is a schematic illustration similar to Fig. la but depicting a line feature having eroded sidewalls.
- the inventive composition is particularly advantageous because the above- described process avoids degradation and erosion of the contact or via hole and trench sidewalls and bottom wall. That is, with prior art compositions the sidewalls typically erode during the removal of the anti-reflective coating layers so that the sidewalls are no longer straight and upright. This often results in defects in the circuit.
- Fig. la depicts a portion of a starting circuit structure 10.
- Circuit structure 10 includes a substrate 12 and a line feature 14.
- Substrate 12 has an upper surface 16.
- Line feature 14 comprises an anti-reflective layer 18 and a photoresist layer 20.
- anti-reflective layer 18 has sidewalls 22a,b which are substantially vertical as preferred.
- Fig. lb depicts a portion of a second starting structure 24.
- Circuit structure 24 also includes a substrate 26 and a line feature 28.
- Substrate 26 has an upper surface 30 while line feature 28 comprises an anti-reflective layer 32 and a photoresist layer 34.
- Anti-reflective layer 32 has sidewalls 36a,b. Unlike the sidewalls 22a,b of circuit structure 10 in Fig. 1 a, the sidewalls 36a,b have suffered from degradation and erosion during further processing steps (e.g., during wet developing). This is highly undesirable as it can lead to defects.
- the present invention has the distinct advantage of minimizing or avoiding this degradation and erosion.
- angle “a” of a line feature formed according to the invention is from about 83-90° and preferably from about 87- 90°.
- angle “a” is the smallest angle formed by sidewall 36a and upper surface 30 or sidewall 36b and upper surface 30 (see Fig. lb).
- the percent erosion of a line feature formed according to the present invention is less than about 15%, more preferably less than about 10%, and even more preferably less than about 7%. As used herein, percent erosion is defined as:
- a formulation was prepared by dissolving 15.0 g of poly(dibutyltitanate) in 15.0 g of propylene glycol monomethyl ether (PGME). Next, a solution of 19.52 g of ethyl acetoacetate dissolved in 15.0 g of PGME was added to the reaction mixture followed by stirring for four hours. A solution of 0 trimethylolethoxylate was added to the mixture, and the mixture was stirred for one hour. The resulting formulation was then filtered through a 0.1 ⁇ m PTFE filter prior to use.
- PGME propylene glycol monomethyl ether
- composition was spin-coated onto a silicon wafer at 3000 rpm and subjected to a two-stage bake process at 130°C for 30 seconds followed by 168°C or 205°C for 60 seconds. Both examples exhibited solubility in base developer. 5
- EXAMPLE 2 In this example, a formulation was prepared by dissolving 5.0 g of poly(dibutyltitanate) in 20.0 g of PnP. Next, a solution of 6.5 g of ethyl acetoacetate dissolved in 18.5 g of PGME was added to the reaction mixture followed by stirring for 0 four hours. Cymel ® (an aminoplast crosslinking agent available from Cytec Industries) and 2-cyano-3-(4-hydroxyphenyl)-acrylic acid ethyl ester (CHAE) were added to the mixture, and the mixture was stirred for one hour. The formulation was diluted with 47.5 g of PnP and filtered through a 0.1 ⁇ m PTFE filter prior to use.
- Cymel ® an aminoplast crosslinking agent available from Cytec Industries
- CHOE 2-cyano-3-(4-hydroxyphenyl)-acrylic acid ethyl ester
- composition was spin-coated onto a silicon wafer at 3000 rpm and subjected to a two-stage bake process at 130°C for 30 seconds followed by baking at a temperature ranging from 168- 205°C for 60 seconds. All examples exhibited solubility in base developer.
- EXAMPLE 3 A mother liquor was prepared by dissolving 16.67 g of zirconium di-n- butoxide(bis-2,4-pentanedionate) (60% in butanol) in 99.59 g of PnP. Next, 0.41 g of water was added to the solution followed by stirring for 24 hours to yield the mother liquor.
- the anti-reflective coating formulation was prepared by mixing 11.67 g of the mother liquor with 0.25 g of CHAE followed by stirring for one hour. The formulation was then filtered through a 0.1 ⁇ m PTFE filter, and the composition was spin-coated onto a wafer at 3000 rpm and baked at 168°C for 60 seconds. The sample exhibited solubility in the base developer.
- EXAMPLE 4 Amother liquor was prepared by dissolving 10.00 g of titanium diisoproproxibe bis(ethylacetoacetate) and 1.23 g oftetraorthosihcate in 112.30 g of PnP. Next, 0.64 g of water was added to the solution followed by stirring for 24 hours to yield the mother liquor.
- the anti-reflective coating formulation was prepared by mixing 20.00 g of the mother liquor with 0.25 g of vanillin followed by stirring for four hours. The formulation was then filtered through a 0.1 ⁇ m PTFE filter, and the composition was spin-coated onto a wafer at 3000 rpm and baked at 168°C for 60 seconds. The sample exhibited solubility in the base developer.
- EXAMPLE 5 Determination of Properties 1. Optical Properties
- compositions prepared from the composition of Example 2 were tested for their spin bowl compatibility following the procedure described previously. Compositions were considered to be spin bowl compatible if they had a percent solubility of at least about 90%. The results of these tests are set forth in Table B.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Architecture (AREA)
- Structural Engineering (AREA)
- Engineering & Computer Science (AREA)
- Materials For Photolithography (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
- Silicon Polymers (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP03739224.8A EP1516226B1 (en) | 2002-06-25 | 2003-06-18 | Developer-soluble metal alkoxide coatings for microelectronic applications |
AU2003245596A AU2003245596A1 (en) | 2002-06-25 | 2003-06-18 | Developer-soluble metal alkoxide coatings for microelectronic applications |
KR1020047021093A KR101051617B1 (en) | 2002-06-25 | 2003-06-18 | Developer-soluble metal alkoxide coating composition for microelectronic device manufacturing |
JP2004516000A JP4550573B2 (en) | 2002-06-25 | 2003-06-18 | Developer-soluble alkoxide metal coatings for microelectronic applications |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/180,625 | 2002-06-25 | ||
US10/180,625 US6740469B2 (en) | 2002-06-25 | 2002-06-25 | Developer-soluble metal alkoxide coatings for microelectronic applications |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2004001502A1 true WO2004001502A1 (en) | 2003-12-31 |
Family
ID=29735075
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2003/019457 WO2004001502A1 (en) | 2002-06-25 | 2003-06-18 | Developer-soluble metal alkoxide coatings for microelectronic applications |
Country Status (8)
Country | Link |
---|---|
US (1) | US6740469B2 (en) |
EP (2) | EP2375288B1 (en) |
JP (2) | JP4550573B2 (en) |
KR (1) | KR101051617B1 (en) |
CN (1) | CN100435026C (en) |
AU (1) | AU2003245596A1 (en) |
TW (1) | TWI303014B (en) |
WO (1) | WO2004001502A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1546803A2 (en) * | 2002-06-25 | 2005-06-29 | Brewer Science, Inc. | Wet-developable anti-reflective compositions |
US8927201B2 (en) | 2011-03-30 | 2015-01-06 | Jsr Corporation | Multilayer resist process pattern-forming method and multilayer resist process inorganic film-forming composition |
US10090163B2 (en) | 2013-03-25 | 2018-10-02 | Jsr Corporation | Inorganic film-forming composition for multilayer resist processes, and pattern-forming method |
Families Citing this family (48)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7108958B2 (en) * | 2002-07-31 | 2006-09-19 | Brewer Science Inc. | Photosensitive bottom anti-reflective coatings |
US20040171743A1 (en) * | 2003-01-21 | 2004-09-02 | Terry Brewer, Ph.D. | Hybrid organic-inorganic polymer coatings with high refractive indices |
US7364832B2 (en) * | 2003-06-11 | 2008-04-29 | Brewer Science Inc. | Wet developable hard mask in conjunction with thin photoresist for micro photolithography |
US7364835B2 (en) * | 2003-10-15 | 2008-04-29 | Brewer Science Inc. | Developer-soluble materials and methods of using the same in via-first dual damascene applications |
US20070207406A1 (en) * | 2004-04-29 | 2007-09-06 | Guerrero Douglas J | Anti-reflective coatings using vinyl ether crosslinkers |
US20050255410A1 (en) * | 2004-04-29 | 2005-11-17 | Guerrero Douglas J | Anti-reflective coatings using vinyl ether crosslinkers |
WO2006040956A1 (en) * | 2004-10-14 | 2006-04-20 | Nissan Chemical Industries, Ltd. | Composition for forming bottom coating for lithography containing metal oxide |
US7914974B2 (en) | 2006-08-18 | 2011-03-29 | Brewer Science Inc. | Anti-reflective imaging layer for multiple patterning process |
US8168372B2 (en) * | 2006-09-25 | 2012-05-01 | Brewer Science Inc. | Method of creating photolithographic structures with developer-trimmed hard mask |
KR101647158B1 (en) * | 2008-01-29 | 2016-08-09 | 브레우어 사이언스 인코포레이션 | On-track process for patterning hardmask by multiple dark field exposures |
US20090325106A1 (en) * | 2008-06-27 | 2009-12-31 | Conley Willard E | Method for Implant Imaging with Spin-on Hard Masks |
US9640396B2 (en) | 2009-01-07 | 2017-05-02 | Brewer Science Inc. | Spin-on spacer materials for double- and triple-patterning lithography |
CN102356526B (en) * | 2009-03-19 | 2013-08-28 | 昭和电工株式会社 | Composition for discharge-gap filling and electro-static discharge protector |
JP4734480B2 (en) * | 2009-07-15 | 2011-07-27 | 日本発條株式会社 | Back protection sheet for solar cell and method for producing the same |
JP5825177B2 (en) * | 2011-03-30 | 2015-12-02 | Jsr株式会社 | Inorganic film forming composition for multilayer resist process and pattern forming method |
US8568958B2 (en) * | 2011-06-21 | 2013-10-29 | Az Electronic Materials Usa Corp. | Underlayer composition and process thereof |
JP5650086B2 (en) | 2011-06-28 | 2015-01-07 | 信越化学工業株式会社 | Resist underlayer film forming composition and pattern forming method |
US8647809B2 (en) * | 2011-07-07 | 2014-02-11 | Brewer Science Inc. | Metal-oxide films from small molecules for lithographic applications |
JP5889568B2 (en) | 2011-08-11 | 2016-03-22 | メルク、パテント、ゲゼルシャフト、ミット、ベシュレンクテル、ハフツングMerck Patent GmbH | Composition for forming tungsten oxide film and method for producing tungsten oxide film using the same |
KR102061919B1 (en) | 2011-11-21 | 2020-01-02 | 브레우어 사이언스 인코포레이션 | Assist layers for euv lithography |
JP5882776B2 (en) | 2012-02-14 | 2016-03-09 | 信越化学工業株式会社 | Resist underlayer film forming composition and pattern forming method |
JP5739360B2 (en) | 2012-02-14 | 2015-06-24 | 信越化学工業株式会社 | Silicon-containing resist underlayer film forming composition and pattern forming method |
US9070548B2 (en) | 2012-03-06 | 2015-06-30 | Rohm And Haas Electronic Materials Llc | Metal hardmask compositions |
US8795774B2 (en) | 2012-09-23 | 2014-08-05 | Rohm And Haas Electronic Materials Llc | Hardmask |
US9315636B2 (en) | 2012-12-07 | 2016-04-19 | Az Electronic Materials (Luxembourg) S.A.R.L. | Stable metal compounds, their compositions and methods |
JP5756134B2 (en) | 2013-01-08 | 2015-07-29 | 信越化学工業株式会社 | Metal oxide-containing film forming composition and pattern forming method |
US9171720B2 (en) | 2013-01-19 | 2015-10-27 | Rohm And Haas Electronic Materials Llc | Hardmask surface treatment |
US9136123B2 (en) | 2013-01-19 | 2015-09-15 | Rohm And Haas Electronic Materials Llc | Hardmask surface treatment |
JP5830044B2 (en) | 2013-02-15 | 2015-12-09 | 信越化学工業株式会社 | Resist underlayer film forming composition and pattern forming method |
US8759220B1 (en) | 2013-02-28 | 2014-06-24 | Shin-Etsu Chemical Co., Ltd. | Patterning process |
JP6189758B2 (en) | 2013-03-15 | 2017-08-30 | 信越化学工業株式会社 | Titanium-containing resist underlayer film forming composition and pattern forming method |
JP5830048B2 (en) | 2013-03-15 | 2015-12-09 | 信越化学工業株式会社 | Titanium-containing resist underlayer film forming composition and pattern forming method |
US9201305B2 (en) | 2013-06-28 | 2015-12-01 | Az Electronic Materials (Luxembourg) S.A.R.L. | Spin-on compositions of soluble metal oxide carboxylates and methods of their use |
US9296922B2 (en) | 2013-08-30 | 2016-03-29 | Az Electronic Materials (Luxembourg) S.A.R.L. | Stable metal compounds as hardmasks and filling materials, their compositions and methods of use |
US9296879B2 (en) | 2013-09-03 | 2016-03-29 | Rohm And Haas Electronic Materials Llc | Hardmask |
WO2015037398A1 (en) * | 2013-09-11 | 2015-03-19 | Jsr株式会社 | Composition for forming inorganic film for multilayer resist process, and pattern formation method |
US9409793B2 (en) | 2014-01-14 | 2016-08-09 | Az Electronic Materials (Luxembourg) S.A.R.L. | Spin coatable metallic hard mask compositions and processes thereof |
JP6399083B2 (en) | 2014-03-12 | 2018-10-03 | Jsr株式会社 | Composition for multilayer resist process and pattern forming method using the composition for multilayer resist process |
JP6141902B2 (en) * | 2014-07-04 | 2017-06-07 | 富士フイルム株式会社 | Curable composition, method for producing cured film, cured film, touch panel, and display device |
CN105223775B (en) * | 2014-07-04 | 2020-03-13 | 富士胶片株式会社 | Curable composition, method for producing cured film, touch panel, and display device |
US9515272B2 (en) | 2014-11-12 | 2016-12-06 | Rohm And Haas Electronic Materials Llc | Display device manufacture using a sacrificial layer interposed between a carrier and a display device substrate |
US9499698B2 (en) | 2015-02-11 | 2016-11-22 | Az Electronic Materials (Luxembourg)S.A.R.L. | Metal hardmask composition and processes for forming fine patterns on semiconductor substrates |
JP6439520B2 (en) * | 2015-03-16 | 2018-12-19 | Jsr株式会社 | Composition for manufacturing semiconductor device and method for manufacturing processed substrate |
US9442377B1 (en) | 2015-06-15 | 2016-09-13 | Rohm And Haas Electronic Materials Llc | Wet-strippable silicon-containing antireflectant |
CN111051570B (en) | 2017-09-06 | 2022-05-10 | 默克专利股份有限公司 | Spin-on inorganic oxide containing compositions and fill materials having improved thermal stability useful as hard masks |
JP7024744B2 (en) * | 2018-02-22 | 2022-02-24 | 信越化学工業株式会社 | Resist material and pattern formation method using it |
US20220197142A1 (en) * | 2020-12-17 | 2022-06-23 | Rohm And Haas Electronic Materials Llc | Photoresist underlayer compositions and patterning methods |
JPWO2022138541A1 (en) * | 2020-12-25 | 2022-06-30 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3949463A (en) * | 1973-02-13 | 1976-04-13 | Communications Satellite Corporation (Comsat) | Method of applying an anti-reflective coating to a solar cell |
JPH10149531A (en) * | 1996-11-15 | 1998-06-02 | Sony Corp | Magnetic recording medium and its production |
US6380611B1 (en) * | 1998-09-03 | 2002-04-30 | Micron Technology, Inc. | Treatment for film surface to reduce photo footing |
Family Cites Families (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5936955B2 (en) * | 1977-09-12 | 1984-09-06 | 住友化学工業株式会社 | Titanium oxide film formation method |
US4244799A (en) | 1978-09-11 | 1981-01-13 | Bell Telephone Laboratories, Incorporated | Fabrication of integrated circuits utilizing thick high-resolution patterns |
US4369090A (en) * | 1980-11-06 | 1983-01-18 | Texas Instruments Incorporated | Process for etching sloped vias in polyimide insulators |
JPH0612452B2 (en) * | 1982-09-30 | 1994-02-16 | ブリュ−ワ−・サイエンス・インコ−ポレイテッド | Method of manufacturing integrated circuit device |
US4910122A (en) * | 1982-09-30 | 1990-03-20 | Brewer Science, Inc. | Anti-reflective coating |
JPS60262150A (en) | 1984-06-11 | 1985-12-25 | Nippon Telegr & Teleph Corp <Ntt> | Intermediate layer for 3-layer resist material and method for using it |
US4683024A (en) | 1985-02-04 | 1987-07-28 | American Telephone And Telegraph Company, At&T Bell Laboratories | Device fabrication method using spin-on glass resins |
US4732841A (en) | 1986-03-24 | 1988-03-22 | Fairchild Semiconductor Corporation | Tri-level resist process for fine resolution photolithography |
JPS63165435A (en) * | 1986-12-27 | 1988-07-08 | Nippon Steel Corp | Production of organometallic polymer composition |
US4891303A (en) | 1988-05-26 | 1990-01-02 | Texas Instruments Incorporated | Trilayer microlithographic process using a silicon-based resist as the middle layer |
US5126231A (en) | 1990-02-26 | 1992-06-30 | Applied Materials, Inc. | Process for multi-layer photoresist etching with minimal feature undercut and unchanging photoresist load during etch |
JP3041972B2 (en) | 1991-01-10 | 2000-05-15 | 富士通株式会社 | Method for manufacturing semiconductor device |
US5370969A (en) | 1992-07-28 | 1994-12-06 | Sharp Kabushiki Kaisha | Trilayer lithographic process |
JPH07183194A (en) | 1993-12-24 | 1995-07-21 | Sony Corp | Multilayer resist pattern formation method |
KR100206597B1 (en) | 1995-12-29 | 1999-07-01 | 김영환 | Fine-patterning method of semiconductor device |
KR100223329B1 (en) | 1995-12-29 | 1999-10-15 | 김영환 | Method for manufacturing fine pattern of semiconductor device |
US5652317A (en) * | 1996-08-16 | 1997-07-29 | Hoechst Celanese Corporation | Antireflective coatings for photoresist compositions |
JP3680469B2 (en) * | 1997-01-24 | 2005-08-10 | Jsr株式会社 | Curable composition |
JPH11258813A (en) * | 1998-03-13 | 1999-09-24 | Jsr Corp | Composition for forming antireflection film and antireflection film |
US6156665A (en) | 1998-04-13 | 2000-12-05 | Lucent Technologies Inc. | Trilayer lift-off process for semiconductor device metallization |
JP3673399B2 (en) * | 1998-06-03 | 2005-07-20 | クラリアント インターナショナル リミテッド | Anti-reflection coating composition |
JP2000010293A (en) | 1998-06-17 | 2000-01-14 | Jsr Corp | Composition for forming antireflection film and antireflection film |
US6136511A (en) | 1999-01-20 | 2000-10-24 | Micron Technology, Inc. | Method of patterning substrates using multilayer resist processing |
US6303270B1 (en) * | 1999-03-01 | 2001-10-16 | The Curators Of The University Of Missouri | Highly plasma etch-resistant photoresist composition containing a photosensitive polymeric titania precursor |
AU5600200A (en) * | 1999-06-10 | 2001-01-02 | Allied-Signal Inc. | Spin-on-glass anti-reflective coatings for photolithography |
US6632535B1 (en) * | 2000-06-08 | 2003-10-14 | Q2100, Inc. | Method of forming antireflective coatings |
JP4868639B2 (en) * | 2000-06-12 | 2012-02-01 | 株式会社Adeka | Raw material for chemical vapor deposition and method for producing thin film using the same |
JP2003238573A (en) * | 2002-02-18 | 2003-08-27 | Toray Ind Inc | Composition containing organometallic compound, display member and display |
-
2002
- 2002-06-25 US US10/180,625 patent/US6740469B2/en not_active Expired - Lifetime
-
2003
- 2003-06-06 TW TW092115340A patent/TWI303014B/en not_active IP Right Cessation
- 2003-06-18 CN CNB038151987A patent/CN100435026C/en not_active Expired - Lifetime
- 2003-06-18 EP EP11004386.6A patent/EP2375288B1/en not_active Expired - Lifetime
- 2003-06-18 KR KR1020047021093A patent/KR101051617B1/en active IP Right Grant
- 2003-06-18 JP JP2004516000A patent/JP4550573B2/en not_active Expired - Lifetime
- 2003-06-18 EP EP03739224.8A patent/EP1516226B1/en not_active Expired - Lifetime
- 2003-06-18 WO PCT/US2003/019457 patent/WO2004001502A1/en active Application Filing
- 2003-06-18 AU AU2003245596A patent/AU2003245596A1/en not_active Abandoned
-
2010
- 2010-05-06 JP JP2010106668A patent/JP5023183B2/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3949463A (en) * | 1973-02-13 | 1976-04-13 | Communications Satellite Corporation (Comsat) | Method of applying an anti-reflective coating to a solar cell |
JPH10149531A (en) * | 1996-11-15 | 1998-06-02 | Sony Corp | Magnetic recording medium and its production |
US6380611B1 (en) * | 1998-09-03 | 2002-04-30 | Micron Technology, Inc. | Treatment for film surface to reduce photo footing |
Non-Patent Citations (1)
Title |
---|
See also references of EP1516226A4 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1546803A2 (en) * | 2002-06-25 | 2005-06-29 | Brewer Science, Inc. | Wet-developable anti-reflective compositions |
EP1546803A4 (en) * | 2002-06-25 | 2009-03-11 | Brewer Science Inc | Wet-developable anti-reflective compositions |
US8927201B2 (en) | 2011-03-30 | 2015-01-06 | Jsr Corporation | Multilayer resist process pattern-forming method and multilayer resist process inorganic film-forming composition |
US10090163B2 (en) | 2013-03-25 | 2018-10-02 | Jsr Corporation | Inorganic film-forming composition for multilayer resist processes, and pattern-forming method |
Also Published As
Publication number | Publication date |
---|---|
JP2010224554A (en) | 2010-10-07 |
US6740469B2 (en) | 2004-05-25 |
CN1666146A (en) | 2005-09-07 |
TWI303014B (en) | 2008-11-11 |
AU2003245596A1 (en) | 2004-01-06 |
EP1516226A1 (en) | 2005-03-23 |
JP2005537502A (en) | 2005-12-08 |
KR20050024385A (en) | 2005-03-10 |
JP5023183B2 (en) | 2012-09-12 |
JP4550573B2 (en) | 2010-09-22 |
TW200401166A (en) | 2004-01-16 |
EP2375288B1 (en) | 2014-10-22 |
EP1516226A4 (en) | 2010-02-17 |
EP2375288A3 (en) | 2012-09-05 |
EP1516226B1 (en) | 2016-03-16 |
KR101051617B1 (en) | 2011-07-26 |
CN100435026C (en) | 2008-11-19 |
US20030235786A1 (en) | 2003-12-25 |
EP2375288A2 (en) | 2011-10-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6740469B2 (en) | Developer-soluble metal alkoxide coatings for microelectronic applications | |
EP1546803B1 (en) | Wet-developable anti-reflective compositions | |
EP1743219B1 (en) | Method of forming a microelectronique structure having an anti-reflective coating using vinyl ether crosslinkers | |
US7507783B2 (en) | Thermally curable middle layer comprising polyhedral oligomeric silsesouioxanes for 193-nm trilayer resist process | |
EP1392508B1 (en) | Anti-reflective coating composition with improved spin bowl compatibility | |
US7364832B2 (en) | Wet developable hard mask in conjunction with thin photoresist for micro photolithography | |
TW201247734A (en) | Antireflective coating composition and process thereof | |
EP1554322B1 (en) | Anti-reflective coatings and dual damascene fill compositions comprising styrene-allyl alcohol copolymers | |
US6576408B2 (en) | Thermosetting anti-reflective coatings comprising aryl urethanes of hydroxypropyl cellulose | |
US20040242759A1 (en) | Bottom anti-reflective coating compositions comprising silicon containing polymers to improve adhesion towards photoresists |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL TJ TM TN TR TT TZ UA UG UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2003739224 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2004516000 Country of ref document: JP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1020047021093 Country of ref document: KR |
|
WWE | Wipo information: entry into national phase |
Ref document number: 20038151987 Country of ref document: CN |
|
WWP | Wipo information: published in national office |
Ref document number: 1020047021093 Country of ref document: KR |
|
WWP | Wipo information: published in national office |
Ref document number: 2003739224 Country of ref document: EP |