JP4528164B2 - Etching solution composition - Google Patents

Etching solution composition Download PDF

Info

Publication number
JP4528164B2
JP4528164B2 JP2005069252A JP2005069252A JP4528164B2 JP 4528164 B2 JP4528164 B2 JP 4528164B2 JP 2005069252 A JP2005069252 A JP 2005069252A JP 2005069252 A JP2005069252 A JP 2005069252A JP 4528164 B2 JP4528164 B2 JP 4528164B2
Authority
JP
Japan
Prior art keywords
acid
etching
mol
composition
phosphoric acid
Prior art date
Legal status (The legal status 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 status listed.)
Active
Application number
JP2005069252A
Other languages
Japanese (ja)
Other versions
JP2006253473A (en
Inventor
健次 黒岩
勝 加藤
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kanto Chemical Co Inc
Original Assignee
Kanto Chemical Co 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 Kanto Chemical Co Inc filed Critical Kanto Chemical Co Inc
Priority to JP2005069252A priority Critical patent/JP4528164B2/en
Priority to TW095105030A priority patent/TWI402330B/en
Priority to KR1020060022371A priority patent/KR101299254B1/en
Priority to CNB2006100547447A priority patent/CN100543188C/en
Publication of JP2006253473A publication Critical patent/JP2006253473A/en
Application granted granted Critical
Publication of JP4528164B2 publication Critical patent/JP4528164B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

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
    • 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
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23FNON-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
    • C23F1/00Etching metallic material by chemical means
    • C23F1/10Etching compositions
    • C23F1/14Aqueous compositions
    • C23F1/16Acidic compositions
    • C23F1/30Acidic compositions for etching other metallic material
    • 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 at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer
    • H01L21/18Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic System 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
    • H01L21/302Treatment 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
    • H01L21/306Chemical or electrical treatment, e.g. electrolytic etching
    • H01L21/30604Chemical etching
    • 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 at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer
    • H01L21/18Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic System 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
    • H01L21/3105After-treatment
    • H01L21/311Etching the insulating layers by chemical or physical means
    • H01L21/31105Etching inorganic layers
    • H01L21/31111Etching inorganic layers by chemical means
    • C11D2111/22

Description

本発明は、半導体装置およびフラットパネルディスプレイ装置等の各種電子装置の製造工程において、金属薄膜および金属酸化物薄膜をエッチングする際に用いるエッチング液組成物に関する。   The present invention relates to an etching solution composition used for etching a metal thin film and a metal oxide thin film in a manufacturing process of various electronic devices such as a semiconductor device and a flat panel display device.

電子装置の製造において、各種の金属薄膜や金属酸化物薄膜が用いられるが、従来から半導体装置の配線材料として、また、液晶ディスプレイ装置の反射板または反射電極材料として、アルミニウムおよびアルミニウム合金が用いられてきた。
近年、液晶ディスプレイ装置の反射板または反射電極材料として銀または銀を主成分とする合金が、また、透明電極材料として酸化インジウム錫(ITO)および酸化インジウム亜鉛(IZO)が使用されている。これらの配線、反射板、反射電極あるいは透明電極等を形成する際に使用する金属薄膜および金属酸化物薄膜のエッチング液組成物としては、アルミニウムおよびアルミニウム合金の金属薄膜の場合、従来からりん酸、硝酸、酢酸、水からなるエッチング液組成物(以下「混酸」と称する)が知られている。
Various metal thin films and metal oxide thin films are used in the manufacture of electronic devices. Conventionally, aluminum and aluminum alloys have been used as wiring materials for semiconductor devices and as reflectors or reflective electrode materials for liquid crystal display devices. I came.
In recent years, silver or an alloy containing silver as a main component is used as a reflective plate or a reflective electrode material of a liquid crystal display device, and indium tin oxide (ITO) and indium zinc oxide (IZO) are used as a transparent electrode material. As an etching solution composition of a metal thin film and a metal oxide thin film used when forming these wiring, reflector, reflective electrode or transparent electrode, in the case of a metal thin film of aluminum and aluminum alloy, phosphoric acid, An etchant composition (hereinafter referred to as “mixed acid”) comprising nitric acid, acetic acid and water is known.

一方、銀を主成分とする金属薄膜の場合、アルミニウムおよびアルミニウム合金のエッチング液として用いられている混酸をそのまま用いると、エッチングレートが高くなり、エッチングの制御性が悪くなる場合があるため、混酸の組成成分比を銀系金属薄膜用に最適化したもの(特許文献1)およびITOあるいはIZOと銀あるいはアルミニウム等の金属薄膜との積層膜の場合、混酸の組成成分比を該積層膜の一括エッチング用に最適化したもの(特許文献2)が本発明の出願人により特許出願されている。
また、銀系金属薄膜用として、混酸にエチレングリコールまたはグリセリンを添加してエッチングレートを最適化したものが開示されている(特許文献3)。
On the other hand, in the case of a metal thin film containing silver as a main component, if the mixed acid used as an etching solution for aluminum and aluminum alloy is used as it is, the etching rate may be increased and the controllability of etching may be deteriorated. In the case where the composition component ratio is optimized for a silver-based metal thin film (Patent Document 1) and the laminated film of ITO or IZO and a metal thin film such as silver or aluminum, the composition ratio of the mixed acid is collectively determined for the laminated film. An application optimized for etching (Patent Document 2) has been filed by the applicant of the present invention.
In addition, for silver-based metal thin films, an etching rate optimized by adding ethylene glycol or glycerin to a mixed acid is disclosed (Patent Document 3).

このように、混酸は金属薄膜および金属酸化物薄膜のエッチング液として報告ないし使用されている。混酸中の硝酸は主として被エッチング材料を酸化する働きを有し、酢酸は被エッチング材料への濡れ性を向上させるとともに、エッチングレートをコントロールする役割を担うものであり、混酸の組成成分比率によりエッチング促進剤として、また、減速剤としても作用する。このため、混酸は、その組成成分比率を最適化することにより、制御性の良いエッチングレートで、エッチングを進行させることができる優れたエッチング液である。
しかし、混酸中の酢酸が高い揮発性を有するため、エッチング処理中に液組成が変化してしまい、安定したエッチング性能が保てなくなるという問題の主要因ともなっており、また、その刺激臭により作業環境を悪化させるという問題も有している。
混酸と類似のエッチング液組成物としてフッ酸、硝酸、酢酸および水からなるものが報告されているが(特許文献4)、酢酸を含むことによる臭気の問題を同様に有するものであり、さらにエッチングレートをコントロールするために、過酸化水素水を添加する必要があり、操作が煩雑となる問題がある。
Thus, the mixed acid has been reported or used as an etching solution for metal thin films and metal oxide thin films. Nitric acid in the mixed acid mainly functions to oxidize the material to be etched, and acetic acid improves the wettability to the material to be etched and plays a role in controlling the etching rate. Etching depends on the composition ratio of the mixed acid. Acts as an accelerator and as a moderator. For this reason, the mixed acid is an excellent etching solution that can advance the etching at an etching rate with good controllability by optimizing the composition component ratio.
However, the acetic acid in the mixed acid has high volatility, so the liquid composition changes during the etching process, which is the main cause of the problem that the stable etching performance cannot be maintained. It also has the problem of deteriorating the environment.
A composition composed of hydrofluoric acid, nitric acid, acetic acid and water has been reported as an etching solution composition similar to the mixed acid (Patent Document 4), but also has the problem of odor due to containing acetic acid, and further etched. In order to control the rate, it is necessary to add a hydrogen peroxide solution, and there is a problem that the operation becomes complicated.

酢酸の臭気という問題を解決するために、混酸の組成成分から酢酸を除いた、即ち、りん酸および硝酸からなるエッチング液組成物も報告されているが、エッチングレートの保持等のために、エッチング液組成物に硝酸を適宜供給する(特許文献5)、エッチング液組成物中に過酸化水素または硝酸を適宜供給する(特許文献6)等の工程を要し、いずれも操作が煩雑であって実用性がない。また、りん酸および硝酸のみからなるエッチング液組成物は、濡れ性が低いため、エッチング残渣が生じる、サイドエッチングが進行するなどの問題があり、精細なパターンの処理には不向きである。
さらに、混酸の組成成分である酢酸の代わりにクエン酸を用いたエッチング液組成物が開示されているが(特許文献7)、クエン酸には濡れ性向上効果がないため、精細なパターンエッジ形状は得られない、エッチング残渣を生じるなどの問題を有している。また、同文献は、NOxの発生を抑制するために尿素を添加するエッチング液組成物について開示するが、尿素はエッチング液組成物に対する溶解度が比較的低く、また、添加によりエッチングレートを大幅に抑制するという問題を有している。
このように、酢酸の臭気の問題がなく、エッチング性能に優れ、また取り扱いが容易で実用的に優れたエッチング液組成物は今まで知られていない。
In order to solve the problem of acetic acid odor, an etching solution composition in which acetic acid is removed from the mixed acid composition component, ie, phosphoric acid and nitric acid has been reported. Nitric acid is appropriately supplied to the liquid composition (Patent Document 5), hydrogen peroxide or nitric acid is appropriately supplied to the etching liquid composition (Patent Document 6), and the operation is complicated. There is no practicality. In addition, an etchant composition composed only of phosphoric acid and nitric acid has low wettability, and thus has problems such as etching residues and side etching, and is not suitable for processing fine patterns.
Furthermore, although an etching solution composition using citric acid instead of acetic acid, which is a composition component of mixed acid, is disclosed (Patent Document 7), since citric acid has no effect of improving wettability, a fine pattern edge shape is disclosed. Cannot be obtained, and etching residue is generated. The same document discloses an etchant composition in which urea is added to suppress the generation of NOx, but urea has a relatively low solubility in the etchant composition, and the addition significantly suppresses the etching rate. Have the problem of
Thus, an etching solution composition that does not have a problem of odor of acetic acid, has excellent etching performance, is easy to handle and is practically excellent has not been known so far.

特開2004−176115号公報JP 2004-176115 A 特開2004−1567070号公報JP 2004-1567070 A 特開2002−231706号公報Japanese Patent Laid-Open No. 2002-231706 特開平5−102122号公報Japanese Patent Laid-Open No. 5-102122 特開2002−129361号公報JP 2002-129361 A 特公昭49−45035号公報Japanese Patent Publication No.49-45035 特開平10−130870号公報JP-A-10-130870

すなわち本発明の課題は、半導体装置およびフラットパネルディスプレイ装置等の各種電子装置の製造工程において、金属薄膜をエッチングする際に用いることができるエッチング液組成物であって、臭気の問題がなく、かつ、安定したエッチング性能を維持できる、エッチング液組成物を提供することにある。   That is, an object of the present invention is an etching solution composition that can be used when etching a metal thin film in a manufacturing process of various electronic devices such as a semiconductor device and a flat panel display device, and has no odor problem. An object of the present invention is to provide an etching solution composition capable of maintaining stable etching performance.

上記課題を解決するため鋭意検討する中で、りん酸および硝酸に対する安定性および混和性等を有し、かつ臭気の問題がなく、さらにりん酸および硝酸に配合した時、混酸と少なくとも同等のエッチング性能を付与できる有機酸を使用するエッチング液組成物、即ち、酢酸以外の有機酸と、りん酸および硝酸を配合してなるエッチング液組成物が本課題を解決する手段となり得ることに着目した。   In an intensive study to solve the above problems, there is no problem of odor with stability and miscibility with phosphoric acid and nitric acid, and when mixed with phosphoric acid and nitric acid, etching at least equivalent to mixed acid It was noted that an etching solution composition using an organic acid capable of imparting performance, that is, an etching solution composition comprising an organic acid other than acetic acid, phosphoric acid and nitric acid can be a means for solving this problem.

それら有機酸の中でメトキシ酢酸は、りん酸および硝酸に任意の割合で混合でき、また、刺激臭がなく、常温で液体であるため、エッチング槽の液面付近および配管内で析出することなく、被エッチング物表面に対する濡れ性を高めることができ、かつ酢酸に匹敵するエッチングレート制御効果があることが確認され、りん酸、硝酸、メトキシ酢酸および水を配合してなる組成物が本課題を解決できるエッチング液組成物であることを見出すに至り、さらに研究を進めた結果、本発明を完成するに至った。   Among these organic acids, methoxyacetic acid can be mixed with phosphoric acid and nitric acid in any ratio, and since it has no irritating odor and is liquid at room temperature, it does not deposit near the liquid level in the etching tank or in the piping. It has been confirmed that the wettability to the surface of the object to be etched can be improved and that the etching rate control effect is comparable to that of acetic acid, and a composition comprising phosphoric acid, nitric acid, methoxyacetic acid and water has this problem. As a result of finding the etching solution composition that can be solved, and further research, the present invention has been completed.

すなわち、本発明は、金属薄膜をエッチングするエッチング液組成物であって、りん酸、硝酸、メトキシ酢酸および水を含有する、前記エッチング液組成物に関する。
また、本発明は、アミン化合物がさらに配合された、前記エッチング液組成物に関する。
さらに、本発明は、アミン化合物が、グリシン、アスパラギン酸、イミノ二酢酸から選択される1種または2種以上である、前記エッチング液組成物に関する。
また、本発明は、金属薄膜が銀または銀合金薄膜である、前記エッチング液組成物に関する。
さらに、本発明は、りん酸4〜9mol/L、硝酸0.1〜2mol/L、メトキシ酢酸2〜7mol/L、および水を含有する、前記エッチング液組成物に関する。
また、本発明は、りん酸4〜9mol/L、硝酸0.1〜2mol/L、メトキシ酢酸2〜7mol/L、およびアミン化合物の1種または2種以上を、合計して0.05〜1mol/L、および水を配合してなる、前記エッチング液組成物に関する。
That is, the present invention relates to an etching solution composition for etching a metal thin film, which contains phosphoric acid, nitric acid, methoxyacetic acid and water.
The present invention also relates to the above-mentioned etching solution composition, which further contains an amine compound.
Furthermore, this invention relates to the said etching liquid composition whose amine compound is 1 type (s) or 2 or more types selected from glycine, aspartic acid, and iminodiacetic acid.
Moreover, this invention relates to the said etching liquid composition whose metal thin film is a silver or silver alloy thin film.
Furthermore, this invention relates to the said etching liquid composition containing phosphoric acid 4-9 mol / L, nitric acid 0.1-2 mol / L, methoxyacetic acid 2-7 mol / L, and water.
In addition, the present invention provides a total of 0.05 to 0.05 mol of phosphoric acid 4 to 9 mol / L, nitric acid 0.1 to 2 mol / L, methoxyacetic acid 2 to 7 mol / L, and one or more amine compounds. It is related with the said etching liquid composition formed by mix | blending 1 mol / L and water.

本発明のエッチング液組成物は、従来のエッチング液である混酸における組成成分の酢酸をメトキシ酢酸に代えた新規エッチング液組成物であり、刺激臭がなく、しかも、常温で液体であるメトキシ酢酸は、酢酸と同様に濡れ性を高める作用を有するため、該組成物はパターンエッジ形状等にも優れ、混酸と同等のエッチング性能を有する。また、従来の酢酸系では、酢酸揮発による成分変動のために安定した性能を維持できない傾向があるのに対し、本発明では、これに代えてメトキシ酢酸を用いているため、そのような問題がなく、液寿命が長い。
さらに、該組成物にグリシン等のアミン化合物を添加すると、エッチング処理後に密閉保管した際、あるいは短時間に多量のエッチング処理を行った際に、液が青く変色したり、発泡が生じたりするのを防止することができ、またエッチングレートの増大を抑制することができるため、その使用性は一層向上する。これは、系内に蓄積する過剰なNOx(とくにNO2 )と反応するアミン化合物が、NOx抑制効果を有することによるものと考えられる。
The etching solution composition of the present invention is a novel etching solution composition in which acetic acid as a composition component in a mixed acid that is a conventional etching solution is replaced with methoxyacetic acid, has no irritating odor, and is liquid at room temperature. Since it has the effect of increasing wettability like acetic acid, the composition is excellent in pattern edge shape and the like and has etching performance equivalent to that of mixed acid. In addition, in the conventional acetic acid system, there is a tendency that stable performance cannot be maintained due to component fluctuation due to volatilization of acetic acid, whereas in the present invention, methoxyacetic acid is used instead of this, so such a problem is caused. Long life of liquid.
Furthermore, when an amine compound such as glycine is added to the composition, the solution may turn blue or foam when stored in a sealed state after the etching process or when a large amount of etching process is performed in a short time. Can be prevented, and an increase in the etching rate can be suppressed, so that the usability is further improved. This is presumably because the amine compound that reacts with excess NOx (particularly NO 2 ) accumulated in the system has a NOx suppressing effect.

以下に本発明の実施の形態について詳述する。
本発明のエッチング液組成物は、りん酸、硝酸、メトキシ酢酸および水を含有することを特徴とするものである。
Hereinafter, embodiments of the present invention will be described in detail.
The etching solution composition of the present invention contains phosphoric acid, nitric acid, methoxyacetic acid and water.

本発明のエッチング液組成物において、りん酸および硝酸の配合量はサイドエッチングが少なく、精度良くエッチング加工することができる範囲、とくにエッチングレート、エッチング残渣およびエッチングムラの発生などの観点から適宜決定する。エッチングレートが高い場合には、エッチング活性は良好であるが、エッチング反応時に多量の気泡が発生し、エッチングムラの原因になることがある。従って、エッチングする金属薄膜が銀または銀合金薄膜の場合、りん酸の配合量は好ましくは4〜9mol/L、より好ましくは5〜8mol/Lであり、硝酸の配合量は好ましくは0.1〜2mol/L、より好ましくは0.3〜1.5mol/Lである。一方、メトキシ酢酸の配合量は、エッチングレートを一定の範囲に保持することができ、エッチング残渣やパターンエッジ形状の凹凸等の問題も発生しない範囲とすることが好ましい。これらの観点からメトキシ酢酸の配合量は好ましくは2〜7mol/L、より好ましくは3〜6mol/Lである。   In the etching solution composition of the present invention, the blending amount of phosphoric acid and nitric acid is appropriately determined from the viewpoint of less side etching and accurate etching processing, particularly from the viewpoint of etching rate, etching residue, and etching unevenness. . When the etching rate is high, the etching activity is good, but a large amount of bubbles are generated during the etching reaction, which may cause etching unevenness. Therefore, when the metal thin film to be etched is a silver or silver alloy thin film, the amount of phosphoric acid is preferably 4 to 9 mol / L, more preferably 5 to 8 mol / L, and the amount of nitric acid is preferably 0.1. ˜2 mol / L, more preferably 0.3 to 1.5 mol / L. On the other hand, the amount of methoxyacetic acid is preferably in a range where the etching rate can be maintained within a certain range and problems such as etching residue and pattern edge shape unevenness do not occur. From these viewpoints, the amount of methoxyacetic acid is preferably 2 to 7 mol / L, more preferably 3 to 6 mol / L.

本発明のエッチング液組成物にはNOx抑制剤を適宜添加することができる。添加するNOx抑制剤は、NOx抑制効果を有するものであれば特に限定されないが、アミン系化合物が好ましく、典型的には尿素、グリシン、アスパラギン酸およびイミノ二酢酸などが挙げられる。特に、りん酸、硝酸、メトキシ酢酸、および水を含む混酸への溶解性の高さや、エッチング阻害性の低さから、グリシン、アスパラギン酸およびイミノ二酢酸が好ましい。配合するアミン化合物は1種でも、また2種以上を組み合わせ配合してもよい。アミン化合物の組合せは、りん酸、硝酸、メトキシ酢酸および水に対する溶解性やエッチング阻害性等を考慮して適宜選択する。
アミン化合物の添加に際しては、NOx抑制効果およびエッチングレートを考慮してその添加量を調整する。また、りん酸、硝酸、メトキシ酢酸および水の配合比によって、エッチング液組成物へのアミン化合物の溶解性が変動するので、この点も考慮の上添加量を調整することが好ましい。なお、銀エッチング量が多い場合には、アミン化合物を多く添加することが好ましい。
1種類のアミン化合物を使用する場合は、銀のエッチング量が4g/Lのとき、グリシンは0.2mol/L以上、アスパラギン酸は0.1mol/L以上、イミノ二酢酸は0.05mol/L以上の濃度でNOx抑制効果が認められる。また、これらのアミン化合物の上限は好ましくは1mol/L以下、より好ましくは0.5mol/L以下である。2種類以上のアミン化合物を使用する場合には、銀のエッチング量が4g/Lの場合には、好ましくは0.05〜1mol/L、より好ましくは0.1〜0.5mol/Lである。
A NOx inhibitor can be appropriately added to the etching solution composition of the present invention. The NOx inhibitor to be added is not particularly limited as long as it has a NOx suppressing effect, but is preferably an amine compound, and typically includes urea, glycine, aspartic acid, iminodiacetic acid, and the like. In particular, glycine, aspartic acid, and iminodiacetic acid are preferred because of their high solubility in mixed acids including phosphoric acid, nitric acid, methoxyacetic acid, and water, and low etching inhibition. The amine compound to mix | blend may be 1 type, and may mix | blend 2 or more types in combination. The combination of amine compounds is appropriately selected in consideration of solubility in phosphoric acid, nitric acid, methoxyacetic acid and water, etching inhibition properties, and the like.
When adding the amine compound, the addition amount is adjusted in consideration of the NOx suppressing effect and the etching rate. Further, since the solubility of the amine compound in the etching solution composition varies depending on the mixing ratio of phosphoric acid, nitric acid, methoxyacetic acid and water, it is preferable to adjust the addition amount in consideration of this point. In addition, when there is much silver etching amount, it is preferable to add many amine compounds.
When one kind of amine compound is used, when the etching amount of silver is 4 g / L, glycine is 0.2 mol / L or more, aspartic acid is 0.1 mol / L or more, and iminodiacetic acid is 0.05 mol / L. The NOx suppression effect is recognized at the above concentrations. Moreover, the upper limit of these amine compounds is preferably 1 mol / L or less, more preferably 0.5 mol / L or less. When two or more types of amine compounds are used, when the etching amount of silver is 4 g / L, it is preferably 0.05 to 1 mol / L, more preferably 0.1 to 0.5 mol / L. .

本発明のエッチング液組成物でエッチングを行う温度については、低温ではエッチングレートが低く、エッチング所用時間が長くなりすぎることがあり、一方高温ではエッチングレートが高く、エッチングの制御性が悪くなることなどを考慮し、その温度は、好ましくは20〜40℃である。   As for the temperature at which etching is performed with the etching solution composition of the present invention, the etching rate is low at low temperatures and the etching time may be too long, while the etching rate is high at high temperatures, resulting in poor etching controllability, etc. , The temperature is preferably 20-40 ° C.

さらに、被エッチング薄膜表面に対する濡れ性を改善するため、界面活性剤を含んでもよい。界面活性剤としてはノニオン系が望ましい。   Furthermore, in order to improve the wettability with respect to the surface of the thin film to be etched, a surfactant may be included. As the surfactant, a nonionic system is desirable.

また、本発明のエッチング液組成物は、りん酸、硝酸、メトキシ酢酸、水の配合量を適宜選択することにより、アルミニウム、銀、銅、モリブデン、ニッケル等の金属およびそれぞれの金属を主成分とする合金並びにITO、IZO等の金属酸化物よりなる薄膜のエッチング液として使用することができる。ここで、銀を主成分とする合金とは、典型的には銀(Ag)−パラジウム(Pd)、Ag−Pd−銅(Cu)、またはAg−ネオジウム(Nd)−Cuである。
また、本発明のエッチング液組成物は、アミン化合物の種類および配合量を適宜選択して配合することにより、NOxの過剰な発生を抑制することができる。
In addition, the etching solution composition of the present invention is mainly composed of metals such as aluminum, silver, copper, molybdenum, nickel, and the respective metals by appropriately selecting the blending amounts of phosphoric acid, nitric acid, methoxyacetic acid, and water. It can be used as an etching solution for a thin film made of an alloy and a metal oxide such as ITO or IZO. Here, the alloy containing silver as a main component is typically silver (Ag) -palladium (Pd), Ag-Pd-copper (Cu), or Ag-neodymium (Nd) -Cu.
Moreover, the etching liquid composition of this invention can suppress the excessive generation | occurrence | production of NOx by selecting and mixing suitably the kind and compounding quantity of an amine compound.

以下に、実施例と比較例を挙げて本発明をさらに詳細に説明するが、これらは本発明を何ら限定するものではない。なお、以下に記載したエッチングレートは、同一液で複数回エッチング操作を行い、安定したエッチングレートに至った時の数値を採用した。   Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples, but these do not limit the present invention in any way. In addition, the etching rate described below employ | adopted the numerical value when etching operation was performed in multiple times with the same liquid and it reached the stable etching rate.

[評価試験1] メトキシ酢酸の効果
酢酸代替物としてのメトキシ酢酸の効果を確認するために、りん酸6.0mol/L、硝酸1.0mol/Lおよび水からなる組成と、ここに酢酸またはメトキシ酢酸を5.0mol/L添加した組成で、りん酸/硝酸系への溶解性、エッチングレート(被エッチング材料:純銀箔(2cm角、厚さ50μm)、液温:30℃、安定なエッチングレートに至った後1分間、無攪拌)等を比較した結果を表1に示す。
これにより、メトキシ酢酸は酢酸と同様のエッチングレート制御効果と、りん酸/硝酸系への良好な溶解性を有するとともに、刺激臭がない等の長所があることを確認した。
[Evaluation Test 1] Effect of methoxyacetic acid In order to confirm the effect of methoxyacetic acid as a substitute for acetic acid, a composition comprising phosphoric acid 6.0 mol / L, nitric acid 1.0 mol / L and water, and acetic acid or methoxy Composition with acetic acid added at 5.0 mol / L, solubility in phosphoric acid / nitric acid system, etching rate (material to be etched: pure silver foil (2 cm square, thickness 50 μm), liquid temperature: 30 ° C., stable etching rate Table 1 shows the results of comparison of 1 minute, no stirring, etc.
As a result, it was confirmed that methoxyacetic acid has the same etching rate control effect as acetic acid, good solubility in phosphoric acid / nitric acid system, and no irritating odor.

Figure 0004528164
Figure 0004528164

[評価試験2] エッチング液組成物の液寿命
りん酸6.0mol/L、硝酸0.6mol/L、酢酸7.0mol/Lおよび水からなる組成(比較例3)と、りん酸6.0mol/L、硝酸0.9mol/L、メトキシ酢酸5.0mol/Lおよび水からなる組成(実施例2)を用いて、液温30℃、弱撹拌条件にて24時間開放放置し、8時間ごとに各組成の成分をキャピラリー電気泳動法にて分析した結果を、表3および図1、2に示す。
りん酸/硝酸/酢酸系では、酢酸は揮発により大幅に減少し、りん酸および硝酸は大幅に濃縮される。りん酸/硝酸/酢酸系は、大幅な成分変動により初期性能を維持できず、長期使用が不可能なことは明白である。
これに対し、りん酸/硝酸/メトキシ酢酸系では、若干の濃縮傾向はあるものの、前記りん酸/硝酸/酢酸系に比べれば変動は軽微である。各成分が若干濃縮されているのは、主に水分揮発に起因するもので、水を補給すれば回復可能である。このように、りん酸/硝酸/メトキシ酢酸系は、従来のりん酸/硝酸/酢酸系に比べて、開放放置時の成分変動が少なく、長期使用に適した組成であることを確認した。

Figure 0004528164
Figure 0004528164
[Evaluation Test 2] Liquid Life of Etching Solution Composition A composition comprising phosphoric acid 6.0 mol / L, nitric acid 0.6 mol / L, acetic acid 7.0 mol / L and water (Comparative Example 3), and phosphoric acid 6.0 mol / L, 0.9 mol / L of nitric acid, 5.0 mol / L of methoxyacetic acid and water (Example 2) and left open at a liquid temperature of 30 ° C. under weak stirring conditions for 24 hours, every 8 hours Table 3 and FIGS. 1 and 2 show the results of analyzing the components of each composition by capillary electrophoresis.
In the phosphoric acid / nitric acid / acetic acid system, acetic acid is greatly reduced by volatilization, and phosphoric acid and nitric acid are greatly concentrated. It is obvious that the phosphoric acid / nitric acid / acetic acid system cannot maintain the initial performance due to a large component variation and cannot be used for a long time.
On the other hand, in the phosphoric acid / nitric acid / methoxyacetic acid system, although there is a slight concentration tendency, the fluctuation is slight compared with the phosphoric acid / nitric acid / acetic acid system. The reason why each component is slightly concentrated is mainly due to moisture volatilization and can be recovered by replenishing water. As described above, it was confirmed that the phosphoric acid / nitric acid / methoxyacetic acid system had a smaller component fluctuation when left open than the conventional phosphoric acid / nitric acid / acetic acid system, and was suitable for long-term use.
Figure 0004528164
Figure 0004528164

[評価試験3] エッチング液組成物の加工性能
りん酸7.0mol/L、硝酸0.5mol/Lおよび水からなる組成(比較例4)と、ここに酢酸またはメトキシ酢酸を5.0mol/L添加した組成(比較例5、および実施例3)にて、液温30℃、安定なエッチングレートに至った後1分間、無攪拌条件で純銀箔(2cm角、厚さ50μm)のエッチングレートを測定した。また、膜厚200nmの銀合金(Ag−Pd−Cu)膜上に、レジストパターンを形成したガラス基板を準備し、前記3種のエッチング液組成物を用いて、液温30℃、安定なエッチングレートに至った後のジャストエッチング時間、無撹拌条件でエッチング処理を行った。これらの結果を表5に示す。
この結果、りん酸/硝酸系での純銀箔のエッチングレートは240nm/min.であった。銀合金基板のエッチング状態は、サイドエッチングが4.0μmと大きいうえ、パターンエッジ形状も粗く、不良であった。これに対して、りん酸/硝酸/酢酸系、りん酸/硝酸/メトキシ酢酸系では、純銀箔のエッチングレートはそれぞれ850nm/min.、700nm/min.であり、銀合金基板のエッチング状態はサイドエッチングも少なく、パターンエッジ形状も滑らかな、良好なエッチング状態を得た。
このように、りん酸/硝酸系に、酢酸またはメトキシ酢酸を添加したエッチング液組成物では、無添加系に比べて、エッチングレートおよび銀合金基板のエッチング状態が向上すること、並びにメトキシ酢酸が酢酸と同等以上の添加効果を示すことを確認した。

Figure 0004528164
Figure 0004528164
[Evaluation Test 3] Processing Performance of Etching Solution Composition Composition (Comparative Example 4) composed of 7.0 mol / L phosphoric acid, 0.5 mol / L nitric acid and water, and 5.0 mol / L acetic acid or methoxyacetic acid. With the added composition (Comparative Example 5 and Example 3), the etching rate of pure silver foil (2 cm square, thickness 50 μm) was set for 1 minute after reaching a stable etching rate at a liquid temperature of 30 ° C. under a non-stirring condition. It was measured. In addition, a glass substrate having a resist pattern formed on a silver alloy (Ag—Pd—Cu) film having a thickness of 200 nm is prepared, and a stable etching is performed at a liquid temperature of 30 ° C. using the above three kinds of etching liquid compositions. Etching was carried out under the conditions of just etching and no stirring after reaching the rate. These results are shown in Table 5.
As a result, the etching rate of pure silver foil in the phosphoric acid / nitric acid system was 240 nm / min. Met. The etching state of the silver alloy substrate was poor because side etching was as large as 4.0 μm and the pattern edge shape was rough. On the other hand, in the phosphoric acid / nitric acid / acetic acid system and phosphoric acid / nitric acid / methoxyacetic acid system, the etching rate of pure silver foil was 850 nm / min. 700 nm / min. As a result, the etching state of the silver alloy substrate was small and the side etching was small, and the pattern edge shape was smooth and a good etching state was obtained.
Thus, in the etching solution composition in which acetic acid or methoxyacetic acid is added to the phosphoric acid / nitric acid system, the etching rate and the etching state of the silver alloy substrate are improved as compared with the non-added system, and methoxyacetic acid is acetic acid. It was confirmed that the effect of addition was equal to or greater than.
Figure 0004528164
Figure 0004528164

[評価試験4] アミン化合物添加による効果
りん酸6.0mol/L、硝酸1.0mol/L、メトキシ酢酸5.0mol/Lおよび水からなる基本組成に、各アミン化合物を各種配合量で添加し、銀を4g/L溶解した後に密封保管した際の液安定性を評価した。この結果を表6に示す。
1週間の密封保管後のエッチング液組成物の安定性は、グリシンを0.2mol/L、アスパラギン酸を0.1mol/L、イミノ二酢酸を0.05mol/L添加することで良好となる。
[Evaluation Test 4] Effect of adding amine compound Each amine compound was added in various amounts to a basic composition composed of 6.0 mol / L phosphoric acid, 1.0 mol / L nitric acid, 5.0 mol / L methoxyacetic acid and water. The liquid stability when silver was dissolved in 4 g / L and stored hermetically was evaluated. The results are shown in Table 6.
The stability of the etching solution composition after sealed storage for 1 week is improved by adding 0.2 mol / L of glycine, 0.1 mol / L of aspartic acid, and 0.05 mol / L of iminodiacetic acid.

Figure 0004528164
Figure 0004528164

[評価試験5] アミン化合物がエッチングレートに与える影響
りん酸6.0mol/L、硝酸1.0mol/L、メトキシ酢酸5.0mol/Lおよび水からなる基本組成に、各アミン化合物を0.5mol/L添加した組成のエッチングレートについて、評価試験1と同一条件で評価した結果を表7に示す。
[Evaluation Test 5] Effect of Amine Compound on Etching Rate 0.5 mol of each amine compound was added to a basic composition consisting of 6.0 mol / L phosphoric acid, 1.0 mol / L nitric acid, 5.0 mol / L methoxyacetic acid and water. Table 7 shows the results of evaluating the etching rate of the composition added with / L under the same conditions as in Evaluation Test 1.

グリシン、アスパラギン酸、またはイミノ二酢酸を添加した実施例10〜12は、エッチングレートの大幅な低下がなく、実施例1と同等の好適なエッチングレートが得られた。   In Examples 10 to 12 to which glycine, aspartic acid, or iminodiacetic acid was added, there was no significant decrease in the etching rate, and a suitable etching rate equivalent to that in Example 1 was obtained.

Figure 0004528164
Figure 0004528164

[評価試験6] 硝酸の濃度範囲
りん酸6.0mol/L、メトキシ酢酸5.0mol/L、グリシン0.2mol/Lに固定し、りん酸配合量を変更した組成におけるエッチングレートについて、評価試験1と同一条件で評価した結果を表8に示す。りん酸/硝酸/メトキシ酢酸/グリシン系のエッチングレートは、硝酸配合量によっても自由に調節が可能である。
[Evaluation Test 6] Concentration range of nitric acid Evaluation test for etching rate in a composition in which phosphoric acid was fixed at 6.0 mol / L, methoxyacetic acid 5.0 mol / L, glycine 0.2 mol / L, and the amount of phosphoric acid was changed Table 8 shows the results of evaluation under the same conditions as 1. The etching rate of phosphoric acid / nitric acid / methoxyacetic acid / glycine system can be freely adjusted by the nitric acid content.

Figure 0004528164
Figure 0004528164

[評価試験7] りん酸の濃度範囲
硝酸1.0mol/L、メトキシ酢酸5.0mol/L、グリシン0.2mol/Lに固定し、りん酸配合量を変更した組成におけるエッチングレートについて、評価試験1と同一条件で評価した結果を表9に示す。りん酸/硝酸/メトキシ酢酸/グリシン系のエッチングレートは、りん酸配合量により自由に調節が可能である。
[Evaluation Test 7] Phosphoric Acid Concentration Range Evaluation Test for Etching Rate in Composition with Fixed Nitric Acid 1.0mol / L, Methoxyacetic Acid 5.0mol / L, and Glycine 0.2mol / L Table 9 shows the results of evaluation under the same conditions as in Table 1. The etching rate of phosphoric acid / nitric acid / methoxyacetic acid / glycine system can be freely adjusted by the amount of phosphoric acid.

Figure 0004528164
Figure 0004528164

[評価試験8] メトキシ酢酸の濃度範囲
りん酸6.0mol/L、硝酸1.0mol/L、グリシン0.2mol/Lに固定し、メトキシ酢酸配合量を変更した組成におけるエッチングレートについて、評価試験1と同一条件で評価した結果を表10に示す。りん酸/硝酸/メトキシ酢酸/グリシン系のエッチングレートは、メトキシ酢酸配合量によってもある程度調節できるが、その効果はりん酸または硝酸に比べると穏やかである。
[Evaluation Test 8] Concentration range of methoxyacetic acid Evaluation test for etching rate in a composition in which phosphoric acid was fixed at 6.0 mol / L, nitric acid 1.0 mol / L, glycine 0.2 mol / L, and the methoxyacetic acid compounding amount was changed. Table 10 shows the results of evaluation under the same conditions as in Table 1 . The etching rate of the phosphoric acid / nitric acid / methoxyacetic acid / glycine system can be adjusted to some extent by the amount of methoxyacetic acid, but the effect is milder than that of phosphoric acid or nitric acid.

Figure 0004528164
Figure 0004528164

[評価試験9] 銀、銀合金のエッチング
りん酸6.0mol/L、硝酸1.0mol/L、メトキシ酢酸5.0mol/L、グリシン0.2mol/L、および水からなる、実施例6のエッチング液組成物にて、液温30℃、安定なエッチングレートに至った後1分間、無攪拌条件で純銀箔(2cm角、厚さ50μm)のエッチングレートを測定したところ、エッチングレートは760nm/min.であった。
膜厚200nmの銀合金(Ag−Pd−Cu)膜上に、レジストパターンを形成したガラス基板を準備し、実施例6のエッチング液組成物を用いて、液温30℃、安定なエッチングレートに至った後のジャストエッチング時間、無撹拌条件でエッチング処理を行った。
[Evaluation Test 9] Etching of Silver and Silver Alloy of Example 6 consisting of 6.0 mol / L phosphoric acid, 1.0 mol / L nitric acid, 5.0 mol / L methoxyacetic acid, 0.2 mol / L glycine, and water The etching rate of the pure silver foil (2 cm square, thickness 50 μm) was measured under the condition of no stirring for 1 minute after reaching a stable etching rate at a liquid temperature of 30 ° C. with the etching solution composition. min. Met.
A glass substrate on which a resist pattern is formed on a silver alloy (Ag—Pd—Cu) film having a thickness of 200 nm is prepared. Using the etching solution composition of Example 6, the liquid temperature is 30 ° C. and the etching rate is stable. Etching was performed under the conditions of just etching after the arrival and no stirring.

ジャストエッチング時間は光学顕微鏡にて、残渣がないことを確認して判定した。この結果、サイドエッチングが少なく、パターンエッジ形状も滑らかで、エッチング残渣もない、良好なエッチング状態を得た。   The just etching time was determined by confirming no residue with an optical microscope. As a result, a good etching state was obtained in which there was little side etching, the pattern edge shape was smooth, and there was no etching residue.

上記エッチング液組成物は、エッチング処理中および使用後の保管中にNOxが発生することはなく、液安定性は良好であり、繰り返し使用可能であり、保存安定性が優れていた。   The etching solution composition did not generate NOx during the etching process and during storage after use, had good solution stability, could be used repeatedly, and had excellent storage stability.

[評価試験10] 銀、銀合金のエッチング
りん酸6.0mol/L、硝酸1.0mol/L、メトキシ酢酸5.0mol/L、アスパラギン酸0.2mol/L、および水からなる、実施例6のエッチング液組成物を用いたこと以外は、評価試験9と同じ条件でエッチング試験を行った。
[Evaluation Test 10] Etching of silver and silver alloy Example 6 consisting of phosphoric acid 6.0 mol / L, nitric acid 1.0 mol / L, methoxyacetic acid 5.0 mol / L, aspartic acid 0.2 mol / L, and water The etching test was conducted under the same conditions as in the evaluation test 9 except that the etching solution composition was used.

この結果、純銀箔でのエッチングレートは820nm/min.であった。銀合金/ガラス基板ではサイドエッチングが少なく、パターンエッジ形状も滑らかで、エッチング残渣もない、良好なエッチング状態を得た。   As a result, the etching rate with pure silver foil was 820 nm / min. Met. The silver alloy / glass substrate obtained a good etching state with little side etching, a smooth pattern edge shape, and no etching residue.

上記エッチング液組成物は、エッチング処理中および使用後の保管中にNOxが発生することはなく、液安定性は良好であり、繰り返し使用可能であり、保存安定性が優れていた。   The etching solution composition did not generate NOx during the etching process and during storage after use, had good solution stability, could be used repeatedly, and had excellent storage stability.

[評価試験11] 銀、銀合金のエッチング
りん酸6.0mol/L、硝酸1.0mol/L、メトキシ酢酸5.0mol/L、イミノ二酢酸0.2mol/L、および水からなる、実施例9のエッチング液組成物を用いたこと以外は、評価試験9と同じ条件でエッチング試験を行った。
[Evaluation Test 11] Etching of silver and silver alloy Examples comprising phosphoric acid 6.0 mol / L, nitric acid 1.0 mol / L, methoxyacetic acid 5.0 mol / L, iminodiacetic acid 0.2 mol / L, and water The etching test was performed under the same conditions as in the evaluation test 9 except that the etching solution composition of 9 was used.

この結果、純銀箔でのエッチングレートは670nm/min.であった。銀合金/ガラス基板ではサイドエッチングが少なく、パターンエッジ形状も滑らかで、エッチング残渣もない、良好なエッチング状態を得た。   As a result, the etching rate with pure silver foil was 670 nm / min. Met. The silver alloy / glass substrate obtained a good etching state with little side etching, a smooth pattern edge shape, and no etching residue.

上記エッチング液組成物は、エッチング処理中および使用後の保管中にNOxが発生することはなく、液安定性は良好であり、繰り返し使用可能であり、保存安定性が優れていた。   The etching solution composition did not generate NOx during the etching process and during storage after use, had good solution stability, could be used repeatedly, and had excellent storage stability.

上記銀、銀合金のエッチング評価試験より、りん酸、硝酸、メトキシ酢酸および水を配合してなるエッチング液組成物に、グリシン、アスパラギン酸、イミノニ酢酸から選択される1種または2種以上からなるアミノ化合物をさらに配合するエッチング液組成物は銀および銀合金に対して、良好なエッチング性能と液安定性を有することが確認された。   From the above-mentioned etching evaluation test of silver and silver alloys, the etching solution composition comprising phosphoric acid, nitric acid, methoxyacetic acid and water is composed of one or more selected from glycine, aspartic acid and iminoacetic acid. It was confirmed that the etching solution composition further blended with the amino compound has good etching performance and solution stability with respect to silver and silver alloys.

本発明によるエッチング液組成物は、半導体装置ならびにフラットパネルディスプレイ装置等の電子装置の製造工程において、配線、電極ならびに反射板等を形成する際の各種金属薄膜および金属酸化物薄膜のエッチング液として使用することが可能である。   The etching solution composition according to the present invention is used as an etching solution for various metal thin films and metal oxide thin films when forming wirings, electrodes, reflectors, etc. in the manufacturing process of electronic devices such as semiconductor devices and flat panel display devices. Is possible.

比較例3のエッチング液組成物の成分変動を示した図である。It is the figure which showed the component fluctuation | variation of the etching liquid composition of the comparative example 3. 実施例2のエッチング液組成物の成分変動を示した図である。FIG. 5 is a diagram showing component fluctuations in the etching solution composition of Example 2.

Claims (5)

銀または銀合金薄膜をエッチングするエッチング液組成物であって、りん酸、硝酸、メトキシ酢酸および水からなる、前記エッチング液組成物。 The silver or silver alloy thin film to a etchant composition for etching, phosphoric acid, nitric acid, consisting of methoxy acetic acid and water, the etchant composition. 銀または銀合金薄膜をエッチングするエッチング液組成物であって、りん酸、硝酸、メトキシ酢酸、水およびアミン化合物からなる、前記エッチング液組成物。An etching solution composition for etching a silver or silver alloy thin film, the etching solution composition comprising phosphoric acid, nitric acid, methoxyacetic acid, water, and an amine compound. アミン化合物が、グリシン、アスパラギン酸、イミノ二酢酸から選択される1種または2種以上である、請求項2に記載のエッチング液組成物。   The etching liquid composition according to claim 2, wherein the amine compound is one or more selected from glycine, aspartic acid, and iminodiacetic acid. りん酸4〜9mol/L、硝酸0.1〜2mol/L、メトキシ酢酸2〜7mol/L、および水を含有する、請求項1〜のいずれかに記載のエッチング液組成物。 The etching liquid composition in any one of Claims 1-3 containing phosphoric acid 4-9 mol / L, nitric acid 0.1-2 mol / L, methoxyacetic acid 2-7 mol / L, and water. りん酸4〜9mol/L、硝酸0.1〜2mol/L、メトキシ酢酸2〜7mol/L、およびアミン化合物の1種または2種以上を、合計して0.05〜1mol/L、および水を配合してなる、請求項2〜に記載のエッチング液組成物。
A total of 0.05 to 1 mol / L of phosphoric acid 4 to 9 mol / L, nitric acid 0.1 to 2 mol / L, methoxyacetic acid 2 to 7 mol / L, and one or more amine compounds, and water by blending the etchant composition according to claim 2-3.
JP2005069252A 2005-03-11 2005-03-11 Etching solution composition Active JP4528164B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2005069252A JP4528164B2 (en) 2005-03-11 2005-03-11 Etching solution composition
TW095105030A TWI402330B (en) 2005-03-11 2006-02-15 Etching liquid composition
KR1020060022371A KR101299254B1 (en) 2005-03-11 2006-03-09 Etching liquid composition
CNB2006100547447A CN100543188C (en) 2005-03-11 2006-03-10 Etchant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2005069252A JP4528164B2 (en) 2005-03-11 2005-03-11 Etching solution composition

Publications (2)

Publication Number Publication Date
JP2006253473A JP2006253473A (en) 2006-09-21
JP4528164B2 true JP4528164B2 (en) 2010-08-18

Family

ID=37093620

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2005069252A Active JP4528164B2 (en) 2005-03-11 2005-03-11 Etching solution composition

Country Status (4)

Country Link
JP (1) JP4528164B2 (en)
KR (1) KR101299254B1 (en)
CN (1) CN100543188C (en)
TW (1) TWI402330B (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5158339B2 (en) * 2007-12-11 2013-03-06 東ソー株式会社 Etching composition and etching method
JP5228595B2 (en) * 2008-04-21 2013-07-03 ソニー株式会社 SEMICONDUCTOR LIGHT EMITTING ELEMENT AND METHOD FOR MANUFACTURING SAME, LAMINATED STRUCTURE AND METHOD FOR FORMING THE SAME
KR101531688B1 (en) * 2008-11-12 2015-06-26 솔브레인 주식회사 Etchant for transparent conductive ITO films
JP2010242124A (en) * 2009-04-01 2010-10-28 Tosoh Corp Composition for etching, and etching method
CN102803562B (en) * 2009-06-25 2015-09-30 3M创新有限公司 The method of Wet-type etching self-assembled monolayer patterned substrate and metal pattern goods
CN104630775B (en) * 2015-02-15 2017-06-09 东南大学 A kind of large-scale preparation method of heat exchanger aluminium foil fins set super hydrophobic surface
CN104893728B (en) * 2015-04-10 2018-11-27 深圳新宙邦科技股份有限公司 A kind of etching solution of the low-tension for ITO/Ag/ITO film
CN107099799A (en) * 2017-03-31 2017-08-29 李世华 A kind of chlorination copper etchant solution and preparation method thereof
CN112852429B (en) * 2021-01-08 2022-09-09 绵阳艾萨斯电子材料有限公司 Silver metal thin film layer etching solution and preparation and application thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003031688A1 (en) * 2001-10-09 2003-04-17 Nagase Chemtex Corporation Etchant composition
JP2004137586A (en) * 2002-10-21 2004-05-13 Mitsubishi Chemicals Corp Etching liquid, and etching method
JP2004176115A (en) * 2002-11-26 2004-06-24 Kanto Chem Co Inc Liquid composition for etching metallic thin film consisting essentially of silver
JP2004238656A (en) * 2003-02-04 2004-08-26 Kobe Steel Ltd Etching liquid for silver thin film, and etching method and pattern forming method for silver thin film using the etching liquid
JP2005206903A (en) * 2004-01-23 2005-08-04 Kanto Chem Co Inc Etchant composition

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5759917A (en) * 1996-12-30 1998-06-02 Cabot Corporation Composition for oxide CMP
CN100371809C (en) * 2001-07-06 2008-02-27 三星电子株式会社 An etchant for a wire, a method for manufacturing the wire and a method for manufacturing a thin film transistor array panel including the method
TW593765B (en) * 2001-07-23 2004-06-21 Sony Corp Etching method and etching liquid
US20030168431A1 (en) * 2002-02-25 2003-09-11 Ritdisplay Corporation Etchant composition for silver alloy

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003031688A1 (en) * 2001-10-09 2003-04-17 Nagase Chemtex Corporation Etchant composition
JP2004137586A (en) * 2002-10-21 2004-05-13 Mitsubishi Chemicals Corp Etching liquid, and etching method
JP2004176115A (en) * 2002-11-26 2004-06-24 Kanto Chem Co Inc Liquid composition for etching metallic thin film consisting essentially of silver
JP2004238656A (en) * 2003-02-04 2004-08-26 Kobe Steel Ltd Etching liquid for silver thin film, and etching method and pattern forming method for silver thin film using the etching liquid
JP2005206903A (en) * 2004-01-23 2005-08-04 Kanto Chem Co Inc Etchant composition

Also Published As

Publication number Publication date
JP2006253473A (en) 2006-09-21
CN101033549A (en) 2007-09-12
CN100543188C (en) 2009-09-23
KR101299254B1 (en) 2013-08-22
TW200634134A (en) 2006-10-01
TWI402330B (en) 2013-07-21
KR20060098328A (en) 2006-09-18

Similar Documents

Publication Publication Date Title
JP4528164B2 (en) Etching solution composition
KR101391603B1 (en) Echant for silver pattern
KR101608873B1 (en) Etchant for metal wire and method for manufacturing metal wire using the same
CN109234736B (en) Long-life copper-molybdenum etching solution and etching method
KR101749634B1 (en) Etching liquid for film of multilayer structure containing copper layer and molybdenum layer
JP2006077241A (en) Etching liquid composition for indium oxide-based transparent conductive film and etching method using the composition
KR20110129880A (en) Etching solution compositions for metal laminate films
KR20150052396A (en) Manufacturing method of an array substrate for liquid crystal display
JP2009076910A (en) Etching fluid composition for metal wiring formation for tft-lcd
KR20140005411A (en) Etchant for metal wire and method for manufacturing metal wire using the same
JP2004176115A (en) Liquid composition for etching metallic thin film consisting essentially of silver
KR20150045220A (en) Etchant composition for metal wire and method for preparing metal wire using the same
KR20130045190A (en) Etching solution composition for metalfilm comprising copper layer and/or copper alloy layer, and etching method using same
KR20110123025A (en) Etchant for metal wire and method for manufacturing metal wire using the same
TW201336972A (en) Etchant composition and etching method
JP6078394B2 (en) Etching solution composition and etching method
JP2009007634A (en) Etching method for silver alloy film, and etching solution
CN110295368B (en) Indium tin oxide/silver multi-layer film etching liquid composition containing no phosphate
TW201503331A (en) Method of manufacturing array substrate for liquid crystal display
JP2005206903A (en) Etchant composition
JP2012129346A (en) Etchant composition
KR20140028446A (en) Etchant composition for etching metal wire and method for preparing metal wire using the same
CN108950527A (en) A kind of crystallite nickel-phosphorus alloy chemical plating fluid and preparation method thereof
KR20090081937A (en) Etchant composition for an Indium based oxide layer and method for fabricating metal pattern
KR102300540B1 (en) Etching liquid composition and etching method

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20080304

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20100215

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20100223

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20100421

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20100518

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20100604

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130611

Year of fee payment: 3

R150 Certificate of patent or registration of utility model

Ref document number: 4528164

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

Free format text: JAPANESE INTERMEDIATE CODE: R150

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250