JPS60175316A - Method of producing conductive transparent thin film - Google Patents
Method of producing conductive transparent thin filmInfo
- Publication number
- JPS60175316A JPS60175316A JP3178584A JP3178584A JPS60175316A JP S60175316 A JPS60175316 A JP S60175316A JP 3178584 A JP3178584 A JP 3178584A JP 3178584 A JP3178584 A JP 3178584A JP S60175316 A JPS60175316 A JP S60175316A
- Authority
- JP
- Japan
- Prior art keywords
- thin film
- film
- vapor
- glass plate
- conductivity
- 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.)
- Pending
Links
- 239000010409 thin film Substances 0.000 title claims description 15
- 238000000034 method Methods 0.000 title description 23
- 239000010408 film Substances 0.000 claims description 29
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 16
- 239000000758 substrate Substances 0.000 claims description 14
- 238000010438 heat treatment Methods 0.000 claims description 13
- 229910052721 tungsten Inorganic materials 0.000 claims description 13
- 239000010937 tungsten Substances 0.000 claims description 13
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 238000001704 evaporation Methods 0.000 claims description 4
- 239000011521 glass Substances 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 238000002834 transmittance Methods 0.000 description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 238000000151 deposition Methods 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 238000007740 vapor deposition Methods 0.000 description 4
- 230000008021 deposition Effects 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 229910003437 indium oxide Inorganic materials 0.000 description 2
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 238000007736 thin film deposition technique Methods 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- -1 tin halide Chemical class 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 238000005019 vapor deposition process Methods 0.000 description 1
Landscapes
- Non-Insulated Conductors (AREA)
- Manufacturing Of Electric Cables (AREA)
- Physical Vapour Deposition (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】 (技術分野)。[Detailed description of the invention] (Technical field).
本発明はタングステンおよびその酸化物を主成分とする
被膜を基板上に形成する導電性透明薄膜の製造方法に関
する。The present invention relates to a method for manufacturing an electrically conductive transparent thin film in which a film containing tungsten and its oxide as a main component is formed on a substrate.
(従来技術)
ガラスやプラスチックなどの透明基板上に透明な導電性
薄膜を形成したものは液晶表示素子や太陽電池などの電
気光学素子をはじめ防曇ガラスや静電防止材としてその
需要が増大している。(Prior art) Demand for transparent conductive thin films formed on transparent substrates such as glass or plastic is increasing for use in electro-optical devices such as liquid crystal display elements and solar cells, as well as anti-fog glass and antistatic materials. ing.
可視域において透明でかつ高い電気伝導性をもつ透明導
電性膜を得る方法として1例えば、刊行物〔表面) V
ol 18. N[L8第440頁「透明導電性フィル
ムJ (1980)に記載されているように、■金やパ
ラジウムなどの金属薄膜をごく薄く蒸着する方法;およ
び■酸化スズや酸化インジウムなど導電性のある酸化半
導体を被覆する方法が知られている。■の金属薄膜蒸着
法では導電性は良好であるが、透明性に劣る。■の酸化
半導体被覆法には。As a method for obtaining a transparent conductive film that is transparent and has high electrical conductivity in the visible region, 1, for example, Publication [Surface] V
ol 18. N[L8, p. 440, "Transparent Conductive Film J (1980)" describes the following methods: ■ method of depositing a very thin metal film such as gold or palladium; Methods for coating oxide semiconductors are known.The metal thin film deposition method (2) has good conductivity but poor transparency.The method (2) for coating oxide semiconductors has good conductivity but poor transparency.
さらに、導電性付与剤としてハロゲン化スズなどの水溶
液を基板上に噴霧する方法や酸化スズ、酸化インジウム
などを真空蒸着する方法(特公昭51−37667号公
報、特公昭49−18447号公報)がある。チタンを
蒸着した後にこれを強制酸化して。Furthermore, there are methods of spraying an aqueous solution of tin halide or the like onto the substrate as a conductivity imparting agent, and methods of vacuum evaporating tin oxide, indium oxide, etc. (Japanese Patent Publication No. 51-37667, Japanese Patent Publication No. 49-18447). be. After titanium is vapor-deposited, it is forcibly oxidized.
適当な抵抗値の酸化チタン膜を得る方法も知られている
。しかし、水溶液噴霧方法では均一な導電膜を形成する
ことが難しい。また、真空蒸着法においても、蒸着条件
が不安定で工程が繁雑であるため、透明性と導電性とを
あわせもつ優れた膜を再現性よく製造することは至難の
ことである。また、酸化インジウム等は高価である欠点
もある。A method for obtaining a titanium oxide film with an appropriate resistance value is also known. However, it is difficult to form a uniform conductive film using the aqueous solution spraying method. Furthermore, even in the vacuum deposition method, since the deposition conditions are unstable and the process is complicated, it is extremely difficult to produce a film with excellent transparency and conductivity with good reproducibility. In addition, indium oxide and the like also have the disadvantage of being expensive.
(発明の目的)
本発明の目的は、優れた導電性と透明性とを有する薄膜
の製造方法を提供することにある。本発明の他の目的は
、安価で、均一な導電性を有する透明薄膜の製造方法を
提供することにある。本発明のさらに他の目的は、複雑
な工程を経ることなく基板表面に優れた導電性と透明性
とを有する薄膜を形成する方法を提供することにある。(Objective of the Invention) An object of the present invention is to provide a method for producing a thin film having excellent conductivity and transparency. Another object of the present invention is to provide a method for manufacturing a transparent thin film that is inexpensive and has uniform conductivity. Still another object of the present invention is to provide a method for forming a thin film having excellent conductivity and transparency on a substrate surface without going through complicated steps.
(発明の構成)
本発明は適当な減圧水蒸気雰囲気下で金属タングステン
を蒸発させることにより基板上に形成される薄膜が透明
でかつ高い導電率を示す、という発明者の知見にもとづ
いて完成された。それゆえ。(Structure of the Invention) The present invention was completed based on the inventor's knowledge that a thin film formed on a substrate by evaporating metallic tungsten in an appropriate reduced pressure steam atmosphere is transparent and exhibits high conductivity. . therefore.
本発明の導電性透明薄膜の製造方法は、M圧水蒸気雰囲
気下で金属タングステンを加熱し蒸発させてタングステ
ンおよびその酸化物を主成分とする被膜を基板上に形成
させることを包含し、そのことにより上記目的が達成さ
れる。The method for producing a conductive transparent thin film of the present invention includes heating and evaporating metallic tungsten in an M-pressure steam atmosphere to form a film containing tungsten and its oxides as main components on a substrate. The above objective is achieved.
本発明に用いられる基板としては9例えば透明ガラスや
透明プラスチックがある。しかしこれに限られることは
なく、セラミック、布9紙など種々の素材が用いられる
。これら基板に、水蒸気を導入しながら金属タングステ
ンを加熱蒸発させ。Examples of substrates used in the present invention include transparent glass and transparent plastic. However, the material is not limited to this, and various materials such as ceramic, cloth, and paper may be used. Tungsten metal is heated and evaporated onto these substrates while introducing water vapor.
透明な薄膜を形成する。具体的には、真空槽内に上記基
板を入れ真空槽を真空ポンプで排気しながら、金属タン
グステンを抵抗加熱、電子銃加熱などの既知の加熱方法
で加熱する。抵抗加熱による方法では、タングステンワ
イアに直接通電することによりどの真空度においてもタ
ングステン原子を蒸発させることができる。この方法は
装置も簡単であるので好適である。電子銃加熱による方
法では真空度が5 X 10−’Torrを上まわるこ
とが好ましい。このような高真空領域においては蒸着速
度が速くなる。しかし、これを下まわると放電がおこり
、フィラメントの消耗が激しいため加熱が不可能となる
。基板は特に加熱を必要としないが。Forms a transparent thin film. Specifically, the substrate is placed in a vacuum chamber, and while the vacuum chamber is evacuated by a vacuum pump, metal tungsten is heated by a known heating method such as resistance heating or electron gun heating. In the resistance heating method, tungsten atoms can be evaporated at any degree of vacuum by directly applying current to the tungsten wire. This method is suitable because the apparatus is simple. In the method using electron gun heating, the degree of vacuum is preferably greater than 5 x 10-'Torr. In such a high vacuum region, the deposition rate becomes faster. However, if the temperature is lower than this, electric discharge occurs and the filament is severely consumed, making heating impossible. Although the substrate does not require any particular heating.
加熱をすれば蒸着薄膜の導電率が高くなる傾向にある。Heating tends to increase the conductivity of the deposited thin film.
加熱により発生ずる金属タングステンの蒸気の一部と水
蒸気とが反応しタングステンおよびその酸化物を主成分
とする薄膜が基板上に形成されると推定される。このと
き雰囲気ガスの主な分圧が水であればよく、このほかに
酸素、窒素、水素などのガスが多少混入していてもよい
。例えばペルジャーのような蒸着装置の内部をあらかじ
め1O−5Torr程度の高真空にしておき、ここに外
部から水を導入して適切な真空度とする。ロータリーポ
ンプや油拡散ポンプなどの真空ポンプで所定の真空度を
達成すれば残留ガスの大部分は水蒸気である。It is presumed that a portion of the metallic tungsten vapor generated by heating reacts with the water vapor, and a thin film containing tungsten and its oxides as main components is formed on the substrate. At this time, it is sufficient that the main partial pressure of the atmospheric gas is water, and other gases such as oxygen, nitrogen, and hydrogen may also be mixed to some extent. For example, the interior of a vapor deposition apparatus such as a Pelger is brought to a high vacuum of about 10-5 Torr in advance, and water is introduced from the outside to create an appropriate degree of vacuum. If a predetermined degree of vacuum is achieved using a vacuum pump such as a rotary pump or an oil diffusion pump, most of the residual gas will be water vapor.
それゆえ、特に水蒸気を導入しなくてもよい。しかし水
蒸気圧を一定に制御するために蒸着の過程において、必
要に応じて外部から水蒸気を導入することも可能である
。Therefore, it is not necessary to particularly introduce water vapor. However, in order to control the water vapor pressure at a constant level, water vapor can be introduced from the outside as necessary during the vapor deposition process.
槽内の水蒸気分圧は形成される蒸着膜の透明性および導
電率に大きな影響を与える。通常2X10−’〜I X
10””Torrに設定される。真空度がlXl0−
’Torrを上まわると蒸着膜が青色に着色し、導電率
が低下する。2 X 10−’Torrを下まわると透
明性は向上するが導電性が極端に低下する。このとき抵
抗加熱法を用いると蒸着速度が極端に遅くなる。The partial pressure of water vapor in the tank has a large effect on the transparency and conductivity of the deposited film. Normally 2X10-'~I
It is set to 10””Torr. The degree of vacuum is lXl0-
When the temperature exceeds 'Torr, the deposited film is colored blue and the conductivity decreases. When the value is less than 2 x 10-'Torr, transparency improves, but conductivity extremely decreases. If a resistance heating method is used at this time, the deposition rate will be extremely slow.
蒸着膜の厚さは1通常、500〜2000人の範囲に選
ばれる。膜の厚さは使用目的に応じて適宜選択される。The thickness of the deposited film is usually selected in the range of 500 to 2000. The thickness of the film is appropriately selected depending on the purpose of use.
膜が厚ずぎると表面抵抗は小さいが透明性が低下する。If the film is too thick, the surface resistance will be low but the transparency will be reduced.
膜が薄すぎると透明性に優れるが表面抵抗が大きくなる
。得られた蒸着膜は表面抵抗値が0.1〜10にΩ/a
d、である。また、可視領域における全光線透過率は7
5%以上であり、生成条件を選択することにより全光線
透過率が85%以上の蒸着膜を得ることも可能である。If the film is too thin, it will have excellent transparency but will have a high surface resistance. The obtained vapor deposited film has a surface resistance value of 0.1 to 10 Ω/a.
d. In addition, the total light transmittance in the visible region is 7
It is 5% or more, and by selecting the production conditions, it is also possible to obtain a deposited film with a total light transmittance of 85% or more.
本発明で得られる蒸着膜の基板との密着性はJ 1.
S DO202に基づく試験により良好であることが確
認されている。The adhesion of the vapor deposited film obtained in the present invention to the substrate is J1.
It has been confirmed that it is good in a test based on S DO202.
(実施例) 以下に本発明を実施例について説明する。(Example) The present invention will be described below with reference to Examples.
大施拠↓
洗浄したガラス板を真空槽内に配置した。槽内をあらか
じめI X 10−’Torrに排気したのち、8×1
0−’Torrの水蒸気を導入し、タングステンを通電
加熱して100人/IIkin、の速度で500人の厚
さに蒸着した。このときのガラス板の温度は100℃で
あった。蒸着膜が形成されたガラス板の表面抵抗値は3
にΩ/cnl、そして、600nmにおける全光線透過
率は85%であった。蒸着前のガラス板の全光線透過率
は96%であった。Large facility ↓ The cleaned glass plate was placed in a vacuum chamber. After evacuating the inside of the tank to I x 10-'Torr in advance,
Water vapor at 0-'Torr was introduced, and tungsten was heated with electricity to deposit it to a thickness of 500 mm at a rate of 100 mm/IIkin. The temperature of the glass plate at this time was 100°C. The surface resistance value of the glass plate on which the vapor deposited film was formed is 3.
Ω/cnl, and the total light transmittance at 600 nm was 85%. The total light transmittance of the glass plate before vapor deposition was 96%.
叉族炎↓
I X 10−”Torrの水蒸気を導入したこと以外
は実施例1と同様である。蒸着膜が形成されたガラス板
の表面抵抗値は1.5にΩ/ail、そして全光線透過
率は75%であった。The process is the same as in Example 1 except that water vapor of 10-'' Torr was introduced.The surface resistance value of the glass plate on which the vapor-deposited film was formed was 1.5Ω/ail, and the total light beam was Transmittance was 75%.
犬里炭ニ
ガラス板を赤外線ヒーターで加熱して200℃としたこ
と以外は実施例1と同様である。蒸着膜が形成されたガ
ラス板の表面抵抗値は0.8 KΩ/cot。The procedure was the same as in Example 1 except that the Inusato charcoal and glass plate was heated to 200° C. with an infrared heater. The surface resistance value of the glass plate on which the vapor deposited film was formed was 0.8 KΩ/cot.
そして全光線透過率は80%であった。The total light transmittance was 80%.
叉旌炭↓
槽内をあらかじめロータリーポンプにより1×1O−2
Torrに排気し、水蒸気を導入しなかったこと以外は
実施例1と同様である。蒸着膜が形成されたガラス板の
表面抵抗値は5にΩ/ad、そして全光線透過率は75
%であった。Charcoal↓ 1×1O−2 in the tank using a rotary pump in advance
The procedure was the same as in Example 1 except that the exhaust gas was evacuated to Torr and no water vapor was introduced. The surface resistance value of the glass plate on which the vapor deposited film was formed is 5Ω/ad, and the total light transmittance is 75.
%Met.
ル較炭土
8 X 10−’Torrの酸素を導入したこと以外は
実施例1と同様である。蒸着膜が形成されたガラス板の
表面抵抗値は10’Ω/cd以上、そして全光線透過率
は95%であった。The procedure was the same as in Example 1 except that 8 x 10 Torr of oxygen was introduced. The surface resistance value of the glass plate on which the vapor deposited film was formed was 10'Ω/cd or more, and the total light transmittance was 95%.
止較炎蛮
8 X 10−’Torrの窒素を導入したこと以外は
実施例1と同様に操作を行ったが膜の成長速度が遅く1
00人/min、の速度では蒸着できなかった。10人
/min、の速度で厚さ300人の蒸着膜を形成させた
。The operation was carried out in the same manner as in Example 1 except that nitrogen of 8 x 10-' Torr was introduced, but the growth rate of the film was slow.
Vapor deposition could not be performed at a rate of 0.00 people/min. A deposited film with a thickness of 300 layers was formed at a rate of 10 layers/min.
蒸着膜が形成されたガラス板の表面抵抗値は108Ω/
己以上であり、そして全光線透過率は95%以上であっ
た。The surface resistance value of the glass plate on which the vapor deposited film was formed was 108Ω/
and the total light transmittance was 95% or more.
此J2U建走
窒素の代わりに水素を導入したこと以外は比較例2と同
様である。蒸着膜が形成されたガラス板の表面抵抗値は
108Ω/e11!以上であり、そして全光線透過率は
95%以上であった。This J2U was the same as Comparative Example 2 except that hydrogen was introduced instead of nitrogen. The surface resistance value of the glass plate on which the vapor deposited film was formed was 108Ω/e11! The total light transmittance was 95% or more.
ル較桝土
洗浄したガラス板を真空槽内に配置した。槽内をあらか
じめI X 10−’Torrに排気したのち、8×1
0−”Torrの水蒸気を導入し、錫をタングステンボ
ート内で加熱して100人/min、の速度で500人
の厚さに蒸着した。 このときのガラス板の温度は10
0℃であった。形成された蒸着膜は不透明であり、全光
線透過率は10%以下であった。蒸着前のガラス板の全
光線透過率は96%であった。蒸着膜のガラス板との密
着性も悪く、指でこすると簡単にガラス板から剥離した
。The washed glass plate was placed in a vacuum chamber. After evacuating the inside of the tank to I x 10-'Torr in advance,
Water vapor at 0-'' Torr was introduced, and tin was heated in a tungsten boat and deposited to a thickness of 500 mm at a rate of 100 mm/min. At this time, the temperature of the glass plate was 10 mm.
It was 0°C. The deposited film formed was opaque and had a total light transmittance of 10% or less. The total light transmittance of the glass plate before vapor deposition was 96%. The adhesion of the deposited film to the glass plate was also poor, and it easily peeled off from the glass plate when rubbed with fingers.
(発明の効果)
本発明によれば、このように、高い導電性を示し、かつ
透明性に優れた蒸着薄膜が得られる。蒸着層は均一であ
り、したがって導電性も均一である。基板との密着性に
おいても優れている。さらに、用いられるタングステン
は必ずしも高純度である必要はなく、市販のタングステ
ンワイアが使用されうる。このため薄膜は安価に調製さ
れうる。(Effects of the Invention) According to the present invention, a vapor-deposited thin film exhibiting high conductivity and excellent transparency can be obtained. The deposited layer is uniform and therefore the conductivity is also uniform. It also has excellent adhesion to the substrate. Furthermore, the tungsten used does not necessarily have to be of high purity; commercially available tungsten wire can be used. Therefore, thin films can be prepared at low cost.
また、複雑な操作も不要である。この導電性透明薄膜は
電気光学素子や発熱素子としてのみならず防滴・防曇ガ
ラスなどにも有効に利用されうる。Further, no complicated operations are required. This conductive transparent thin film can be effectively used not only as electro-optical elements and heating elements, but also as drip-proof and anti-fog glass.
Claims (1)
発させてタングステンおよびその酸化物を主成分とする
被膜を基板上に形成させることを包含する導電性透明薄
膜の製造方法。(2) A method for producing a conductive transparent thin film, which includes heating and evaporating metallic tungsten in a reduced pressure steam atmosphere to form a film containing tungsten and its oxides as main components on a substrate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3178584A JPS60175316A (en) | 1984-02-21 | 1984-02-21 | Method of producing conductive transparent thin film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3178584A JPS60175316A (en) | 1984-02-21 | 1984-02-21 | Method of producing conductive transparent thin film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS60175316A true JPS60175316A (en) | 1985-09-09 |
Family
ID=12340709
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3178584A Pending JPS60175316A (en) | 1984-02-21 | 1984-02-21 | Method of producing conductive transparent thin film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60175316A (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5170492A (en) * | 1974-12-16 | 1976-06-18 | Kogyo Gijutsuin | Teiteikono sankainjiumudodenmakuno seizoho |
JPS5179296A (en) * | 1974-12-28 | 1976-07-10 | Citizen Watch Co Ltd | Tomeidodenmakuno seizohoho |
JPS51107497A (en) * | 1975-03-18 | 1976-09-24 | Sharp Kk | SANKABUTSU HANDOTAIMAKUSEIZOSOCHI |
JPS55104013A (en) * | 1979-02-05 | 1980-08-09 | Nitto Electric Ind Co | Method of fabricating transparent conductive membrane |
JPS58206008A (en) * | 1982-05-26 | 1983-12-01 | コニカ株式会社 | Method of forming transparent conductive laminate |
-
1984
- 1984-02-21 JP JP3178584A patent/JPS60175316A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5170492A (en) * | 1974-12-16 | 1976-06-18 | Kogyo Gijutsuin | Teiteikono sankainjiumudodenmakuno seizoho |
JPS5179296A (en) * | 1974-12-28 | 1976-07-10 | Citizen Watch Co Ltd | Tomeidodenmakuno seizohoho |
JPS51107497A (en) * | 1975-03-18 | 1976-09-24 | Sharp Kk | SANKABUTSU HANDOTAIMAKUSEIZOSOCHI |
JPS55104013A (en) * | 1979-02-05 | 1980-08-09 | Nitto Electric Ind Co | Method of fabricating transparent conductive membrane |
JPS58206008A (en) * | 1982-05-26 | 1983-12-01 | コニカ株式会社 | Method of forming transparent conductive laminate |
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