JPH07321330A - Electron part - Google Patents

Electron part

Info

Publication number
JPH07321330A
JPH07321330A JP11615994A JP11615994A JPH07321330A JP H07321330 A JPH07321330 A JP H07321330A JP 11615994 A JP11615994 A JP 11615994A JP 11615994 A JP11615994 A JP 11615994A JP H07321330 A JPH07321330 A JP H07321330A
Authority
JP
Japan
Prior art keywords
electrode
potential
metal
conductive particles
electrodes
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.)
Granted
Application number
JP11615994A
Other languages
Japanese (ja)
Other versions
JP3148515B2 (en
Inventor
Yoshiko Mino
美子 美濃
Ikunori Kobayashi
郁典 小林
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP11615994A priority Critical patent/JP3148515B2/en
Publication of JPH07321330A publication Critical patent/JPH07321330A/en
Application granted granted Critical
Publication of JP3148515B2 publication Critical patent/JP3148515B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To prevent corrosion and disconnection of an electrode under a high temperature and high humidity by a method wherein, in an electrode connecting with other electrodes by using conductive adhesives containing conductive particles, a metal having a higher oxide potential than the reduction potential of these conductive particles is used. CONSTITUTION:In an electrode connecting with other electrodes by using conductive adhesives containing conductive particles, a metal having a higher oxide potential than a reduction potential of conductive particles is used. Particularly, when the conductive particles of conductive adhesives are composed of Ni or Au, zirconium is added to aluminum as a metal having a higher oxide potential than a reduction potential of Ni or Au and such aluminum is used as an electrode. For example, mounting electrodes 2a, 3a of a TFT array are formed with Al to which zirconium being a high melting point metal reducing a corrosion current is added. Incidently, excellent effects are exhibited in the range where content of Zr included in Al is 0.3 to 10.0%.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】この発明は、液晶表示装置等に用
いられる電子部品に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to electronic parts used in liquid crystal display devices and the like.

【0002】[0002]

【従来の技術】近年、液晶表示装置のスイッチング素子
として用いられている薄膜トランジスタ(TFT)にお
いて、工程簡略化や実装抵抗の軽減等からゲート配線や
ソース配線を直接実装部へ引き出すアレイ構成が用いら
れている。この従来の液晶表示装置に用いられるTFT
アレイのゲート配線およびソース配線と各実装電極の概
略斜視図を図3に示す。
2. Description of the Related Art Recently, in a thin film transistor (TFT) used as a switching element of a liquid crystal display device, an array structure in which a gate wiring and a source wiring are directly drawn to a mounting portion is used in order to simplify the process and reduce mounting resistance. ing. TFT used in this conventional liquid crystal display device
FIG. 3 shows a schematic perspective view of the gate wiring and the source wiring of the array and each mounting electrode.

【0003】TFTアレイは、透明基板1上に、マトリ
クス状に画素電極10が配置され、各画素電極10にT
FTのドレイン電極が接続され、ゲート配線2とソース
配線3が絶縁層(図示せず)を介して交差して形成され
ている。そして、ゲート配線2およびソース配線3の各
延長部には実装電極2a,3aが設けられている。つぎ
に、図3のTFTアレイにTAB実装を施した従来のメ
タル構成を図4,図5を用いて以下に説明する。図4は
実装電極2a,3a上にTAB材を実装した平面図であ
り、図5は図4におけるA−A’線の断面図である。
In the TFT array, the pixel electrodes 10 are arranged in a matrix on the transparent substrate 1, and each pixel electrode 10 has a T-shaped pattern.
The drain electrode of the FT is connected, and the gate wiring 2 and the source wiring 3 are formed to intersect each other with an insulating layer (not shown) interposed therebetween. Mounting electrodes 2a and 3a are provided on the respective extension portions of the gate wiring 2 and the source wiring 3. Next, a conventional metal structure in which the TFT array of FIG. 3 is TAB mounted will be described below with reference to FIGS. 4 and 5. 4 is a plan view in which a TAB material is mounted on the mounting electrodes 2a and 3a, and FIG. 5 is a cross-sectional view taken along the line AA ′ in FIG.

【0004】TFTアレイの実装電極2a,3aは、ゲ
ートおよびソース配線材である例えばAlやAl化合物
で形成されている。実装電極2a,3aの上部は液晶駆
動用ICとのコンタクトを得るために、TFTの最終工
程として絶縁保護膜4を開口している。なお、図5はゲ
ート配線2の実装電極2a部分の断面図であるが、ソー
ス配線3の実装電極3a部分の断面構成も図5と同様で
ある。一方、TAB材5はポリイミドフィルムにTAB
電極6が配置され、TAB電極6は例えば配線材にAu
やSnメッキが施されている。
The mounting electrodes 2a and 3a of the TFT array are formed of, for example, Al or Al compound which is a gate and source wiring material. In order to obtain contact with the liquid crystal driving IC, the upper part of the mounting electrodes 2a and 3a has an insulating protective film 4 opened as a final step of the TFT. Although FIG. 5 is a sectional view of the mounting electrode 2a portion of the gate wiring 2, the sectional configuration of the mounting electrode 3a portion of the source wiring 3 is the same as that in FIG. On the other hand, TAB material 5 is TAB on a polyimide film.
The electrode 6 is arranged, and the TAB electrode 6 is made of, for example, Au as a wiring material.
And Sn plating are applied.

【0005】そして、TFTアレイの実装電極2a,3
aとTAB電極6とを導電性接着材8で電気的・機械的
に接続している。導電性接着材8は、導電性粒子8aを
含有した接着材であり、導電性粒子8aとしては、例え
ばNi粒子や、樹脂ボールにNiやAuメッキされたも
のである。また、露出した実装電極2a,3aを保護す
るために保護材9が塗布形成されている。このようにし
てTFT実装パネルが完成する。
Then, the mounting electrodes 2a, 3 of the TFT array
a and the TAB electrode 6 are electrically and mechanically connected to each other with a conductive adhesive material 8. The conductive adhesive 8 is an adhesive containing conductive particles 8a, and the conductive particles 8a are, for example, Ni particles, or resin balls plated with Ni or Au. Further, a protective material 9 is applied and formed to protect the exposed mounting electrodes 2a and 3a. In this way, the TFT mounting panel is completed.

【0006】このようなTFTアレイのアレイ電極メタ
ルとTAB材メタルとの相関を電気化学法により評価し
た。まず、ポテンシオガルバノスタットを用いた評価系
を図6に示す。図6において、21は動作電極、22は
参照電極、23は対極、24は電界液、25は電流計I
と電圧計Vを有する測定器である。参照電極22にAg
・AgCl、対極23にPt、電解液24にNa2 SO
4水溶液(0.01M/l)を用いた。そして、動作電
極21として、TAB電極6のメッキ材であるAu,S
n、導電性接着材8の導電性粒子8aを構成するAu,
Ni、TFTアレイの実装電極2a,3aとなる純Al
を用いて、動作電極21,参照電極22および対極23
に電圧を印加して純Al,Au,Ni,Snの各メタル
の電位を測定した。この測定による分極曲線を図7に示
す。図7の横軸は電圧計Vの電圧値であり、Ag・Ag
Clの参照電極22の電位に対する動作電極21の電位
を示す。縦軸は電流計Iの電流値である。
The correlation between the array electrode metal of such a TFT array and the TAB material metal was evaluated by an electrochemical method. First, FIG. 6 shows an evaluation system using a potentiogalvanostat. In FIG. 6, 21 is a working electrode, 22 is a reference electrode, 23 is a counter electrode, 24 is an electrolytic solution, and 25 is an ammeter I.
And a voltmeter V. Ag on the reference electrode 22
・ AgCl, Pt for counter electrode 23, Na 2 SO for electrolyte 24
4 aqueous solution (0.01 M / l) was used. Then, as the working electrode 21, Au, S which is the plating material of the TAB electrode 6 is used.
n, Au constituting the conductive particles 8a of the conductive adhesive 8,
Ni, pure Al to be the mounting electrodes 2a and 3a of the TFT array
By using the working electrode 21, the reference electrode 22 and the counter electrode 23.
A voltage was applied to the electrodes to measure the potentials of the pure Al, Au, Ni, and Sn metals. The polarization curve obtained by this measurement is shown in FIG. The horizontal axis of FIG. 7 is the voltage value of the voltmeter V, and Ag · Ag
The potential of the working electrode 21 with respect to the potential of the reference electrode 22 of Cl is shown. The vertical axis represents the current value of the ammeter I.

【0007】その結果、Au,Sn,Niを50mv/
secでカソード分極すると、参照電極22に対するA
uの平衡電位は+1.83v、Niでは+1.22v、
Snでは−0.334vであり、Au,NiはSnより
低印加電圧で還元電流が流れ出す。一方、参照電極22
に対する純Alの平衡電位は−0.58vであり、50
mv/secでアノード分極すると、Alの溶出に伴う
酸化電流が流れる。図7に示すように、TAB材メタル
(Au,Sn)とアレイ電極メタル(Al)との相関に
おいて、特に導電性粒子8aの構成要素であるAuやN
iがAlに接触した場合には、AuとAl間、NiとA
l間において電池反応が進行してAlが腐食しやすい状
態にあることがわかる。
As a result, Au, Sn, and Ni were added at 50 mv /
When cathode polarization is performed in sec, A to the reference electrode 22
The equilibrium potential of u is + 1.83v, Ni is + 1.22v,
In Sn, it is −0.334v, and in Au and Ni, the reducing current starts flowing at a lower applied voltage than Sn. On the other hand, the reference electrode 22
The equilibrium potential of pure Al is -0.58v,
When anodic polarization is performed at mv / sec, an oxidation current flows along with the elution of Al. As shown in FIG. 7, in the correlation between the TAB material metal (Au, Sn) and the array electrode metal (Al), in particular, Au or N which is a constituent element of the conductive particle 8a.
When i contacts Al, between Au and Al, Ni and A
It can be seen that the cell reaction progresses during the interval of 1 and Al is easily corroded.

【0008】[0008]

【発明が解決しようとする課題】したがって、上記従来
のTFT実装パネルを高温高湿下にさらすと、TFTア
レイの実装電極2a,3aとTAB電極6との間に電池
反応を生じ、局部腐食を生じる。腐食は進行度によって
電極配線の腐食断線に至るものがある。この発明の目的
は、高温高湿下においても電極間の接続部における電池
反応を抑制して、電極の腐食および断線を防止すること
のできる電子部品を提供することである。
Therefore, when the above-mentioned conventional TFT mounting panel is exposed to high temperature and high humidity, a battery reaction occurs between the mounting electrodes 2a and 3a of the TFT array and the TAB electrode 6 to cause local corrosion. Occurs. Corrosion may lead to corrosion breakage of electrode wiring depending on the degree of progress. An object of the present invention is to provide an electronic component capable of suppressing a battery reaction at a connection portion between electrodes even under high temperature and high humidity, and preventing corrosion and disconnection of the electrodes.

【0009】[0009]

【課題を解決するための手段】請求項1記載の電子部品
は、導電性粒子を含有する導電性接着材を用いて他の電
極と接続する電極に、前記導電性粒子の還元電位よりも
高い酸化電位を有する金属を用いたことを特徴とする。
請求項2記載の電子部品は、請求項1記載の電子部品に
おいて、他の電極に接続する電極に用いる金属は、腐食
電流が小さくなる高融点金属を添加したアルミニウムか
らなるものである。
According to another aspect of the present invention, there is provided an electronic component, in which an electrode connected to another electrode by using a conductive adhesive containing conductive particles is higher than a reduction potential of the conductive particles. It is characterized by using a metal having an oxidation potential.
According to a second aspect of the present invention, in the electronic component according to the first aspect, the metal used for an electrode connected to another electrode is aluminum to which a refractory metal having a small corrosion current is added.

【0010】請求項3記載の電子部品は、請求項2記載
の電子部品において、アルミニウムに添加する高融点金
属としてジルコニウムを用いたものである。
According to a third aspect of the present invention, in the electronic component according to the second aspect, zirconium is used as the refractory metal added to aluminum.

【0011】[0011]

【作用】この発明の構成によれば、導電性粒子を含有す
る導電性接着材を用いて他の電極と接続する電極に、導
電性粒子の還元電位よりも高い酸化電位を有する金属を
用いたことにより、高温高湿下においても、電極間にお
いてそれぞれ電位差を保持して、電池反応を抑制し、電
極の腐食および断線を防止することができる。
According to the structure of the present invention, a metal having an oxidation potential higher than the reduction potential of the conductive particles is used for the electrode connected to the other electrode by using the conductive adhesive containing the conductive particles. As a result, even under high temperature and high humidity, it is possible to maintain the potential difference between the electrodes, suppress the battery reaction, and prevent corrosion and disconnection of the electrodes.

【0012】特に、導電性接着材の導電性粒子がNiや
Auよりなる場合に、NiやAuの還元電位よりも高い
酸化電位を有する金属としてジルコニウムを添加したア
ルミニウムを電極に用いることにより、電池反応を抑制
し、電極の腐食および断線を防止することができる。
In particular, when the conductive particles of the conductive adhesive are made of Ni or Au, by using aluminum containing zirconium as a metal having an oxidation potential higher than the reduction potential of Ni or Au for the electrode, a battery can be obtained. The reaction can be suppressed, and the corrosion and disconnection of the electrode can be prevented.

【0013】[0013]

【実施例】この発明の一実施例について説明する。この
実施例では、従来例の図3〜図5におけるTFTアレイ
の実装電極2a,3aを、腐食電流が小さくなる高融点
金属であるジルコニウム(Zr)を添加したAl(Al
Zr)で形成したことを特徴とし、その他の構成は従来
と同様である。
EXAMPLE An example of the present invention will be described. In this embodiment, the mounting electrodes 2a and 3a of the TFT array shown in FIGS. 3 to 5 of the conventional example are made of Al (Al) to which zirconium (Zr) which is a refractory metal having a small corrosion current is added.
It is characterized in that it is formed of Zr), and the other structure is the same as the conventional one.

【0014】Zr添加量によってAlZrの実装電極2
a,3aの電位は変化する。純Alとの比較を含めAl
Zrについて、図6に示す従来例と同様にして電気化学
法により測定した分極曲線を図1に示す。図1の横軸は
図6に示す電圧計Vの電圧値であり、Ag・AgClを
用いた参照電極22の電位に対する動作電極21の電位
を示す。縦軸は電流計Iの電流値である。なお、図1中
の各E0 の値はこの実施例での参照電極22に対する純
Al,Al−Zr0.7at%,Al−Zr1.4at
%の各メタルの平衡電位である。
AlZr mounting electrode 2 depending on the amount of Zr added
The potentials of a and 3a change. Al including comparison with pure Al
A polarization curve of Zr measured by an electrochemical method in the same manner as in the conventional example shown in FIG. 6 is shown in FIG. The horizontal axis of FIG. 1 is the voltage value of the voltmeter V shown in FIG. 6, and shows the potential of the working electrode 21 with respect to the potential of the reference electrode 22 using Ag / AgCl. The vertical axis represents the current value of the ammeter I. The values of E 0 in FIG. 1 are pure Al, Al-Zr 0.7 at% and Al-Zr 1.4 at for the reference electrode 22 in this embodiment.
% Is the equilibrium potential of each metal.

【0015】図1に示すように、純Alは−0.5vで
は既に酸化電流が測定されている。しかし、Zr添加の
AlZrは−0.5vよりも高いところで酸化電流が測
定されており、また、Zr濃度の高いAlZr(Al−
Zr1.4at%)の方が、Zr濃度の低いAlZr
(Al−Zr0.7at%)より高いところで酸化電流
が測定されている。
As shown in FIG. 1, the oxidation current of pure Al was already measured at -0.5v. However, the oxidation current of AlZr added with Zr is higher than -0.5v, and the oxidation current is measured at a high Zr concentration.
Zr1.4at%) has a lower Zr concentration than AlZr
The oxidation current is measured at a higher temperature than (Al-Zr 0.7 at%).

【0016】このZr濃度が0.7%と1.4%のAl
Zrを、図3〜図5のゲートおよびソースの実装電極2
a,3aに用い、実装電極部のメタル構成を従来例同
様、図6に示す電気化学法により評価した結果を図2に
示す。なお、従来例でも説明したように、TAB電極6
は配線材にAuやSnメッキが施されてあり、導電性接
着材8は、Ni粒子や、NiやAuメッキした樹脂ボー
ルからなる導電性粒子8aを含有した接着材である。
Al having Zr concentrations of 0.7% and 1.4%
Zr is the mounting electrode 2 for the gate and the source in FIGS.
FIG. 2 shows the results of evaluation of the metal structure of the mounting electrode portions used for a and 3a by the electrochemical method shown in FIG. 6 as in the conventional example. As described in the conventional example, the TAB electrode 6
The wiring material is plated with Au or Sn, and the conductive adhesive 8 is an adhesive containing Ni particles and conductive particles 8a made of resin balls plated with Ni or Au.

【0017】図2から、実装関連材であるAuやNiや
Snの還元電位とTFT電極であるAlZrの酸化電位
の相関において、Zr濃度0.7at%,1.4at%
のAlZrどちらも酸化電流の流れ始める酸化電位はS
n,Ni各還元電位よりも高く、したがってAlZrと
Sn間およびAlZrとNi間ではそれぞれが接触して
も電池反応は生じにくいことが判った。また、Zr濃度
0.7at%のAlZrの酸化電位はAuの還元電位よ
り低く、電池反応が生じる。しかし、Zr濃度1.4a
t%のAlZrの酸化電位はAuの還元電位より高く、
したがってAlZrとAu間ではZrが高濃度であれば
それぞれが接触しても電池反応は生じにくいことが判っ
た。
From FIG. 2, in the correlation between the reduction potential of Au, Ni, and Sn which are mounting-related materials and the oxidation potential of AlZr which is a TFT electrode, the Zr concentrations are 0.7 at% and 1.4 at%.
In both AlZr, the oxidation potential at which the oxidation current starts to flow is S
It was found that the cell potential is higher than the reduction potentials of n and Ni, so that a cell reaction is unlikely to occur between AlZr and Sn and between AlZr and Ni even if they come into contact with each other. Further, the oxidation potential of AlZr having a Zr concentration of 0.7 at% is lower than the reduction potential of Au, and a battery reaction occurs. However, Zr concentration 1.4a
The oxidation potential of t% AlZr is higher than the reduction potential of Au,
Therefore, it was found that between Zr and Au, if the Zr concentration is high, the battery reaction is unlikely to occur even if they contact each other.

【0018】また、この実施例によるTFTアレイを温
度85℃,湿度85%の環境下で放置試験し、光学顕微
鏡による観察を行った。その結果、AlZrは純Alと
比べてメタル露出部での腐食が少なく、かつ純Alは腐
食の大きな拡がりが見られたのに対して、AlZrはピ
ンホールレベルの形状で、その数も少なかった。以上の
ようにこの実施例によれば、実装部材であるAuやNi
やSnの還元電位よりも高い酸化電位を有するAlZr
を実装電極2a,3aに用いることにより、電極電位差
を大きく保持して、実装部材とAlZr間の電池反応を
抑制し、Al腐食を防止でき、信頼性の向上を図ること
ができる。
Further, the TFT array according to this example was subjected to a standing test in an environment of a temperature of 85 ° C. and a humidity of 85%, and observed by an optical microscope. As a result, AlZr was less corroded in the exposed metal part than pure Al, and a large spread of corrosion was seen in pure Al, whereas AlZr was pinhole level shape and the number was small. . As described above, according to this embodiment, the mounting members Au and Ni are used.
AlZr having an oxidation potential higher than the reduction potential of Sn and Sn
By using the as the mounting electrodes 2a and 3a, a large electrode potential difference can be maintained, a battery reaction between the mounting member and AlZr can be suppressed, Al corrosion can be prevented, and reliability can be improved.

【0019】また、この実施例では、図5に示す構成に
おいて、TFTアレイの実装電極2a,3aとなる電極
材料にAlZrを用いたが、液晶駆動用ICを載置する
TAB材5の実装電極であるTAB電極6にAlZrを
用いることにより効果を得ることができる。また、液晶
駆動用ICの実装電極にAlZrを用いることもでき
る。
Further, in this embodiment, in the structure shown in FIG. 5, AlZr is used as the electrode material for the mounting electrodes 2a and 3a of the TFT array, but the mounting electrode of the TAB material 5 on which the liquid crystal driving IC is mounted is mounted. The effect can be obtained by using AlZr for the TAB electrode 6 which is Also, AlZr can be used for the mounting electrodes of the liquid crystal driving IC.

【0020】なお、電極材料であるAlに含有されるZ
rの含有量は、0.3〜10.0%の範囲においてより
良い効果がある。TFTアレイの配線材は、液晶表示装
置としての表示特性上、細線,薄膜が望まれる。したが
って、Zr濃度の上限(10.0%)は前記配線材のデ
バイス設計上の比抵抗値で規定され、Zr濃度の下限
(0.3%)は本発明の目的とするAl防食効果が得ら
れ、かつ成膜ターゲットのつくりやすさ(均一濃度分布
等)から規定した。
Z contained in Al which is an electrode material
The content of r has a better effect in the range of 0.3 to 10.0%. The wiring material of the TFT array is desired to be a thin line or a thin film in view of display characteristics as a liquid crystal display device. Therefore, the upper limit (10.0%) of the Zr concentration is defined by the specific resistance value of the wiring material in the device design, and the lower limit (0.3%) of the Zr concentration provides the Al anticorrosion effect which is the object of the present invention. And the ease of forming the film-forming target (uniform concentration distribution, etc.).

【0021】また、この実施例では、電極材料として、
Alに含有する高融点金属としてZrを用いたが、スカ
ンジウム(Sc)やタングステン(W)を用いても同様
の効果を得ることができる。以上の実施例から明らかな
ように、この発明を適用する電子部品として、スイッチ
ング素子としてTFTを有する液晶表示装置があり、ゲ
ートおよびソース・ドレイン電極の実装電極をAlZr
で形成することにより、実装部材であるAuやNiやS
nの還元電位とTFT電極であるAlZrの酸化電位と
の間に電極電位差を大きく保持して、高温高湿下におい
ても、実装部材とAlZr間の電池反応を抑制し、Al
腐食を防止でき、信頼性の向上を図ることができる。ま
た、Al腐食については、AuメッキされたTAB電極
との相関において特に有効であり、信頼性の高い液晶表
示装置を得ることができる。
In this embodiment, the electrode material is
Although Zr is used as the refractory metal contained in Al, the same effect can be obtained by using scandium (Sc) or tungsten (W). As is clear from the above embodiments, there is a liquid crystal display device having a TFT as a switching element as an electronic component to which the present invention is applied, and the mounting electrodes for the gate and source / drain electrodes are AlZr.
By being formed with, the mounting members Au, Ni, S
A large electrode potential difference is maintained between the reduction potential of n and the oxidation potential of AlZr, which is the TFT electrode, to suppress the battery reaction between the mounting member and AlZr even under high temperature and high humidity.
Corrosion can be prevented and reliability can be improved. Further, Al corrosion is particularly effective in correlation with the Au-plated TAB electrode, and a highly reliable liquid crystal display device can be obtained.

【0022】[0022]

【発明の効果】この発明によれば、導電性粒子を含有す
る導電性接着材を用いて他の電極と接続する電極に、導
電性粒子の還元電位よりも高い酸化電位を有する金属を
用いたことにより、高温高湿下においても、電極間にお
いてそれぞれ電位差を保持して、電池反応を抑制し、電
極の腐食および断線を防止することができ、信頼性の向
上を図ることができる。
According to the present invention, a metal having an oxidation potential higher than the reduction potential of the conductive particles is used for the electrode connected to another electrode by using the conductive adhesive containing the conductive particles. As a result, even under high temperature and high humidity, the potential difference can be held between the electrodes, the battery reaction can be suppressed, the electrodes can be prevented from corrosion and disconnection, and the reliability can be improved.

【0023】特に、導電性接着材の導電性粒子がNiや
Auよりなる場合に、NiやAuの還元電位よりも高い
酸化電位を有する金属としてジルコニウムを添加したア
ルミニウムを電極に用いることにより、電池反応を抑制
し、電極の腐食および断線を防止することができ、信頼
性の向上を図ることができる。
In particular, when the conductive particles of the conductive adhesive are made of Ni or Au, by using aluminum containing zirconium as a metal having an oxidation potential higher than the reduction potential of Ni or Au for the electrode, The reaction can be suppressed, the electrodes can be prevented from corroding and breaking, and the reliability can be improved.

【図面の簡単な説明】[Brief description of drawings]

【図1】この発明の実施例を説明するためのAlZrに
ついて電気化学法により測定した分極曲線を示す図であ
る。
FIG. 1 is a diagram showing a polarization curve measured by an electrochemical method for AlZr for explaining an example of the present invention.

【図2】この発明の実施例における実装関連材を電気化
学法により測定した分極曲線を示す図である。
FIG. 2 is a diagram showing a polarization curve of a mounting-related material in an example of the present invention measured by an electrochemical method.

【図3】液晶表示装置に用いられるTFTアレイの斜視
図である。
FIG. 3 is a perspective view of a TFT array used in a liquid crystal display device.

【図4】従来のTAB材をTFTアレイに装着した平面
図である。
FIG. 4 is a plan view in which a conventional TAB material is mounted on a TFT array.

【図5】図4におけるA−A’線の断面図である。5 is a cross-sectional view taken along the line A-A ′ in FIG.

【図6】電気化学法による評価系を示す図である。FIG. 6 is a diagram showing an evaluation system by an electrochemical method.

【図7】従来例における実装関連材を電気化学法により
測定した分極曲線を示す図である。
FIG. 7 is a diagram showing a polarization curve of a mounting-related material in a conventional example measured by an electrochemical method.

【符号の説明】[Explanation of symbols]

2a 実装電極 5 TAB材 6 TAB電極 8 導電性接着材 8a 導電性粒子 2a Mounting electrode 5 TAB material 6 TAB electrode 8 Conductive adhesive 8a Conductive particle

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 H01L 21/60 311 R 6918−4M ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification number Office reference number FI technical display location H01L 21/60 311 R 6918-4M

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 導電性粒子を含有する導電性接着材を用
いて他の電極と接続する電極に、前記導電性粒子の還元
電位よりも高い酸化電位を有する金属を用いたことを特
徴とする電子部品。
1. A metal having an oxidation potential higher than the reduction potential of the conductive particles is used for an electrode connected to another electrode by using a conductive adhesive containing conductive particles. Electronic components.
【請求項2】 他の電極に接続する電極に用いる金属
は、腐食電流が小さくなる高融点金属を添加したアルミ
ニウムからなる請求項1記載の電子部品。
2. The electronic component according to claim 1, wherein the metal used for an electrode connected to another electrode is aluminum to which a refractory metal having a small corrosion current is added.
【請求項3】 アルミニウムに添加する高融点金属とし
てジルコニウムを用いた請求項2記載の電子部品。
3. The electronic component according to claim 2, wherein zirconium is used as the refractory metal added to aluminum.
JP11615994A 1994-05-30 1994-05-30 Liquid crystal display and electronic components Expired - Fee Related JP3148515B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11615994A JP3148515B2 (en) 1994-05-30 1994-05-30 Liquid crystal display and electronic components

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11615994A JP3148515B2 (en) 1994-05-30 1994-05-30 Liquid crystal display and electronic components

Publications (2)

Publication Number Publication Date
JPH07321330A true JPH07321330A (en) 1995-12-08
JP3148515B2 JP3148515B2 (en) 2001-03-19

Family

ID=14680242

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11615994A Expired - Fee Related JP3148515B2 (en) 1994-05-30 1994-05-30 Liquid crystal display and electronic components

Country Status (1)

Country Link
JP (1) JP3148515B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120200985A1 (en) * 2009-10-30 2012-08-09 Masashi Shoji Electrode foil and capacitor using same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120200985A1 (en) * 2009-10-30 2012-08-09 Masashi Shoji Electrode foil and capacitor using same
US8749954B2 (en) * 2009-10-30 2014-06-10 Panasonic Corporation Electrode foil and capacitor using same

Also Published As

Publication number Publication date
JP3148515B2 (en) 2001-03-19

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