WO2002045144A1 - Composition d'agent de gravure humide - Google Patents

Composition d'agent de gravure humide Download PDF

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Publication number
WO2002045144A1
WO2002045144A1 PCT/JP2001/010161 JP0110161W WO0245144A1 WO 2002045144 A1 WO2002045144 A1 WO 2002045144A1 JP 0110161 W JP0110161 W JP 0110161W WO 0245144 A1 WO0245144 A1 WO 0245144A1
Authority
WO
WIPO (PCT)
Prior art keywords
etching
ether sulfate
aqueous solution
wet
oxalic acid
Prior art date
Application number
PCT/JP2001/010161
Other languages
English (en)
French (fr)
Japanese (ja)
Inventor
Satoshi Namba
Taketo Maruyama
Hisaki Abe
Tetsuo Aoyama
Original Assignee
Mitsubishi Gas Chemical Company, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mitsubishi Gas Chemical Company, Inc. filed Critical Mitsubishi Gas Chemical Company, Inc.
Priority to JP2002547213A priority Critical patent/JP4122971B2/ja
Publication of WO2002045144A1 publication Critical patent/WO2002045144A1/ja

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K13/00Etching, surface-brightening or pickling compositions
    • C09K13/04Etching, surface-brightening or pickling compositions containing an inorganic acid
    • C09K13/06Etching, surface-brightening or pickling compositions containing an inorganic acid with organic material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L31/00Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
    • H01L31/18Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof
    • H01L31/1884Manufacture of transparent electrodes, e.g. TCO, ITO
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/04Manufacture 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
    • H01L21/18Manufacture 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
    • H01L21/30Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
    • H01L21/31Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
    • H01L21/3205Deposition of non-insulating-, e.g. conductive- or resistive-, layers on insulating layers; After-treatment of these layers
    • H01L21/321After treatment
    • H01L21/3213Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer
    • H01L21/32133Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only
    • H01L21/32134Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only by liquid etching only
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy

Definitions

  • the present invention relates to an etchant composition used for wet etching of a transparent conductive film such as ITO (indium tin oxide) used as a pixel electrode in a liquid crystal display or the like.
  • a transparent conductive film such as ITO (indium tin oxide) used as a pixel electrode in a liquid crystal display or the like.
  • Transparent conductive films such as ITO films have been widely used in the field of electronic devices such as antistatic films, heat reflective films, photoelectric conversion elements, and transparent electrodes for various flat panel displays.
  • LCDs liquid crystal displays
  • a transparent conductive film such as an ITO film is used as a display electrode of a pixel and is formed by etching using photolithography.
  • polycrystalline ITO has been used, but as the size of the substrate increases, it becomes more difficult to achieve uniform polycrystalline ITO. ing.
  • a photoresist is coated on a transparent conductive film, and after exposure and development, the photoresist remaining after etching is etched using an etching agent using the photoresist as a mask. It is formed by peeling.
  • Aqueous / hydrochloric acid aqueous solution, iodic acid aqueous solution, phosphoric acid aqueous solution, hydrochloric acid / nitric acid aqueous solution (aqua regia) have been used.
  • the wet etching agent such as ITO causes corrosion to A1 and the like during patterning, and selective etching proceeds from the grain boundaries, so that it is difficult to perform patterning with high processing accuracy.
  • the present invention provides a transparent conductive film characterized by being an aqueous solution containing oxalic acid, polyoxyethylene alkyl ether sulfate and z or polyoxyethylene alkyl ether sulfate. (4) It relates to an etchant composition.
  • FIG. 1 shows that an insulating film, SiN, is formed on a glass substrate, amorphous ITO is formed, a resist is applied on the amorphous ITO, and the substrate is developed.
  • FIG. 2 is a cross-sectional view.
  • FIG. 2 is a state diagram after the substrate of FIG. 1 has been etched with the etching agent described in Comparative Example 1 and the resist has been stripped with a basic resist stripping solution.
  • BEST MODE FOR CARRYING OUT THE INVENTION The concentration of oxalic acid used in the present invention ranges from 0.01% to 10% by weight. When the concentration is 0.01% by weight or less, the etching rate is low. When the concentration is 10% by weight or more, the etching rate does not improve. Not a good idea.
  • polyoxyethylene alkyl ether sulfate used in the present invention is represented by the general formula [I]:
  • R represents an alkyl group having 6 to 22 carbon atoms
  • n represents an integer of 1 to 50 °
  • M represents an ammonia, an organic amine, a quaternary ammonium or an alkali metal.
  • Emar 20C Kao
  • Hytenol 325D Hytenol 325D (Daiichi Kogyo Pharmaceutical)
  • Alscope AP-30 Alscope LE-240 (Toho Chemical)
  • Sannole 605N Lion And the like are preferably used.
  • concentration of the above polyoxyethylene alkyl ether sulfate or polyoxyethylene alkyl phenyl ether sulfate is less than 0.0001% by weight, a residue at the time of etching is generated. This is not preferable because the etching rate of the transparent conductive film decreases.
  • the use concentration of the present invention is from normal temperature to 90 ° C., and the use time is about 1 to 30 minutes. Further, the present invention is suitably used for wet etching such as IZO (indium monooxide, oxide) in addition to amorphous ITO.
  • IZO indium monooxide, oxide
  • FIG. 1 shows that an insulating film, SiN (2), is formed on a glass substrate (1), an amorphous ITO (3) is formed, and a resist is applied on the amorphous ITO.
  • FIG. 4 is a cross-sectional view of the substrate after application and development. Using the substrate shown in FIG.
  • Example 1 The substrate used in Example 1 was etched at 40 ° C. for 2 minutes using an etching agent which is an aqueous solution containing 3.4% by weight of oxalic acid, washed with water, and dried. After the resist was stripped off with a basic resist stripping solution, it was washed with water. As a result of SEM observation, the amorphous ITO had been etched, but as shown in FIG. 2, many residues (5) were observed. .
  • an etching agent which is an aqueous solution containing 3.4% by weight of oxalic acid
  • Oxalic acid 3.4 weight 0 /. , 0.1 weight 0/0 of polyoxyethylene alkylphenyl ether sulfate (trade name: Hitenol N-12, manufactured by Dai-ichi Kogyo Seiyaku Co.) using an etching agent is an aqueous solution containing, used in Example 1
  • the substrate thus obtained was subjected to etching at 40 ° C. for 2 minutes, washed with water, further stripped of the resist with a basic resist stripper, washed with water, and dried.
  • the amorphous ITO was etched well and the remaining No residue was observed at all.
  • etchant is an aqueous solution containing
  • the substrate used in Example 1 was subjected to etching at 40 ° C. for 2 minutes, washed with water, and then, after the resist was stripped with a basic resist stripping solution, washed with water and dried.
  • the amorphous ITO was etched well and no residue was observed.
  • Example 1 Oxalate 1.0 wt 0/0, 0.1 weight 0/0 of polyoxyethylene alkylphenyl ether sulfate (trade name: Hitenol N-12, manufactured by Dai-ichi Kogyo Seiyaku Co.) which is an aqueous solution containing etching
  • the substrate used in Example 1 was etched at 40 ° C. for 2 minutes, washed with water, and further, the resist was peeled off with a basic resist stripper, washed with water, and dried.
  • the amorphous ITO was favorably etched, and no residue was observed.

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Computer Hardware Design (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Power Engineering (AREA)
  • Electromagnetism (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Weting (AREA)
  • Photosensitive Polymer And Photoresist Processing (AREA)
PCT/JP2001/010161 2000-11-29 2001-11-21 Composition d'agent de gravure humide WO2002045144A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2002547213A JP4122971B2 (ja) 2000-11-29 2001-11-21 ウエットエッチング剤組成物

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2000362351 2000-11-29
JP2000-362351 2000-11-29

Publications (1)

Publication Number Publication Date
WO2002045144A1 true WO2002045144A1 (fr) 2002-06-06

Family

ID=18833645

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2001/010161 WO2002045144A1 (fr) 2000-11-29 2001-11-21 Composition d'agent de gravure humide

Country Status (5)

Country Link
JP (1) JP4122971B2 (ko)
KR (1) KR100761602B1 (ko)
CN (1) CN1214449C (ko)
TW (1) TW529098B (ko)
WO (1) WO2002045144A1 (ko)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1300829C (zh) * 2003-09-29 2007-02-14 中芯国际集成电路制造(上海)有限公司 静电蚀刻方法及其装置
CN101792907A (zh) * 2010-04-01 2010-08-04 江阴市江化微电子材料有限公司 一种铝钼蚀刻液
CN102241985A (zh) * 2011-04-29 2011-11-16 西安东旺精细化学有限公司 透明导电膜湿法蚀刻液组合物
CN103472968A (zh) * 2013-09-26 2013-12-25 无锡宇宁光电科技有限公司 一种单层膜实现多点触控的电容屏工艺
CN105659365B (zh) * 2013-10-30 2020-07-31 三菱瓦斯化学株式会社 实质上由锌、锡和氧组成的氧化物的蚀刻液和蚀刻方法
KR102148851B1 (ko) * 2014-01-07 2020-08-27 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 아연과 주석을 포함하는 산화물의 에칭액 및 에칭방법
CN104388090B (zh) * 2014-10-21 2017-05-17 深圳新宙邦科技股份有限公司 一种草酸系ito蚀刻液及其制备方法和应用

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000008184A (ja) * 1998-06-24 2000-01-11 Toppan Printing Co Ltd 多層導電膜のエッチング方法
JP2000021809A (ja) * 1998-07-03 2000-01-21 Matsushita Electron Corp パターン形成方法
US6265309B1 (en) * 1998-05-14 2001-07-24 Mitsubishi Gas Chemicals Co., Inc. Cleaning agent for use in producing semiconductor devices and process for producing semiconductor devices using the same

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6265309B1 (en) * 1998-05-14 2001-07-24 Mitsubishi Gas Chemicals Co., Inc. Cleaning agent for use in producing semiconductor devices and process for producing semiconductor devices using the same
JP2000008184A (ja) * 1998-06-24 2000-01-11 Toppan Printing Co Ltd 多層導電膜のエッチング方法
JP2000021809A (ja) * 1998-07-03 2000-01-21 Matsushita Electron Corp パターン形成方法

Also Published As

Publication number Publication date
CN1397090A (zh) 2003-02-12
KR100761602B1 (ko) 2007-10-04
CN1214449C (zh) 2005-08-10
JPWO2002045144A1 (ja) 2004-04-08
TW529098B (en) 2003-04-21
JP4122971B2 (ja) 2008-07-23
KR20020086896A (ko) 2002-11-20

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