JPS5835989A - Amorphous photo-semiconductor device - Google Patents

Amorphous photo-semiconductor device

Info

Publication number
JPS5835989A
JPS5835989A JP56135690A JP13569081A JPS5835989A JP S5835989 A JPS5835989 A JP S5835989A JP 56135690 A JP56135690 A JP 56135690A JP 13569081 A JP13569081 A JP 13569081A JP S5835989 A JPS5835989 A JP S5835989A
Authority
JP
Japan
Prior art keywords
metal film
film
amorphous
back metal
amorphous semiconductor
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
JP56135690A
Other languages
Japanese (ja)
Other versions
JPH0458710B2 (en
Inventor
Takeo Fukatsu
深津 猛夫
Soichi Sakai
総一 酒井
Takashi Shibuya
澁谷 尚
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.)
Sanyo Electric Co Ltd
Sanyo Denki Co Ltd
Original Assignee
Sanyo Electric Co Ltd
Sanyo Denki 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 Sanyo Electric Co Ltd, Sanyo Denki Co Ltd filed Critical Sanyo Electric Co Ltd
Priority to JP56135690A priority Critical patent/JPS5835989A/en
Publication of JPS5835989A publication Critical patent/JPS5835989A/en
Publication of JPH0458710B2 publication Critical patent/JPH0458710B2/ja
Granted legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10FINORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F77/00Constructional details of devices covered by this subclass
    • H10F77/30Coatings
    • H10F77/306Coatings for devices having potential barriers

Landscapes

  • Photovoltaic Devices (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】 本発明は非晶質光半導体装置に関する。[Detailed description of the invention] The present invention relates to an amorphous optical semiconductor device.

太陽光を電気エネルギーに変換する太陽電池及び光信号
を電気信号として検出する光tンサ等の光半導体装置に
従来の単結晶半導体に換って非晶質半導体を具えたもの
が出現するに至って来た。
Optical semiconductor devices such as solar cells that convert sunlight into electrical energy and optical sensors that detect optical signals as electrical signals are now equipped with amorphous semiconductors instead of conventional single crystal semiconductors. It's here.

斯る非晶質半導体は単結晶半導体に比べ全く異なったプ
ラズマ放電法等の製造方法によって形成され、その製造
エネルギーや工程が簡単で、連続的に大量生産が可能で
あり、しかも使用材料が少なくてすむなどの数多くの優
れた特長点を有している。
Such amorphous semiconductors are formed using a manufacturing method such as a plasma discharge method that is completely different from single crystal semiconductors, and their manufacturing energy and processes are simple, allowing for continuous mass production, and they use fewer materials. It has many excellent features such as ease of use.

第1@は非晶質半導体を具えた従来の光半導体装置を示
し、(1)はガフヌ・耐熱性樹脂等の絶縁体から我る透
光性基板、(2)は該基板(1)の−主面に被着され友
酸化スズ5nOv・酸化インジウムInzO5・酸化イ
ンシウムスズエn20s−8nO2等の透明電極膜、(
31ut!IN明N*Ml (21上Vc シフンE3
1Hs雰囲気中でのデフズマ放電により形成された非晶
質yyコン(a−8i)等の非晶質半導体膜で、該半導
体膜(3)はVポフンB2H6@7rヌフインPH1等
の不純物を適宜5IHs雰囲気に添加することによって
P型N型制御が可能でこの従来例に於いてはP型・T型
・Nfilの各層を積層せしめた5層構造を収している
。(4)は上記非晶質半導体@ (3)上に!!着され
た7/Mfi:17AAl、金Au等の裏面金属膜、(
5)は該裏面金属膜(4)に超音波ポンディング着しく
け銀ペーストへ導電性接着剤によって固着された第1の
リード線、 (6)dllll第1のリード11(5)
と同様に超音波ボンディング、導電性接着剤によってA
1、Au等の電極パッド(7)を介して透明電極膜(2
)に接続された第2のリート線、(8)は上記裏面金属
’!II(41等を覆うエポキシ系のモーμド体である
The first @ shows a conventional optical semiconductor device comprising an amorphous semiconductor, (1) is a transparent substrate made of an insulator such as a heat-resistant resin, and (2) is the substrate (1). - A transparent electrode film of tin friend oxide 5nOv, indium oxide InzO5, indium tin oxide n20s-8nO2, etc. deposited on the main surface, (
31ut! IN Ming N * Ml (21 upper Vc Shihun E3
The semiconductor film (3) is an amorphous semiconductor film such as amorphous yycon (a-8i) formed by defsumer discharge in a 1Hs atmosphere, and the semiconductor film (3) is impurities such as VpofunB2H6@7rnufuinPH1 and the like for 5IHs. By adding it to the atmosphere, it is possible to control P-type and N-type, and this conventional example has a five-layer structure in which P-type, T-type, and Nfil layers are laminated. (4) is above the amorphous semiconductor @ (3)! ! Applied 7/Mfi: 17AAl, back metal film such as gold Au, (
5) a first lead wire fixed to the back metal film (4) by ultrasonic bonding and silver paste with a conductive adhesive; (6) dlllll first lead 11 (5);
A by ultrasonic bonding, conductive adhesive as well as
1. Transparent electrode film (2) via electrode pad (7) made of Au etc.
), (8) is connected to the back metal '! II (41 etc.) is an epoxy-based mode μ mode body.

斯る構造の非晶質光半導体装置に透光性基板(1)並び
に透明電[!II(z)を、透過して非晶質半導体層(
3)に光が照射されると、該半導体層(3)内に於いて
ホール及び又は電子が発生し透明電極膜(2)と裏面金
属膜(4)との間に光起電力が生起される。そして。
In the amorphous optical semiconductor device having such a structure, a transparent substrate (1) and a transparent electrode [! II(z) is transmitted through the amorphous semiconductor layer (
When 3) is irradiated with light, holes and/or electrons are generated in the semiconductor layer (3), and a photovoltaic force is generated between the transparent electrode film (2) and the back metal film (4). Ru. and.

上記光起電力は第1及び第2のり−ド@ (51(6)
を介して外部に取り出される。
The above photovoltaic force is the first and second glued @ (51(6)
It is taken out to the outside via.

然し乍ら斯る構造によると、透光性基板(1)の光照射
面から見て非晶質半導体層(3)の裏面に存在する裏面
金IEII(4)の−rIljはモールド体部)によっ
て覆われてセいるものの、!1!モー〜ド体(8)は長
期的なスケールで見ると僅かではあるが水分を透過せし
める為に上記裏面金属膜(4)が腐食せしめられる危惧
を有しτいた。特に裏面金属膜(4)の他の一面が被着
する非晶質半導体膜(31は単結晶半導体に比べ格子欠
陥が多く通かに結晶性に欠は多孔質であると共!IC,
@厚は通常ミクロンオーダ若しくはそれ以下の薄膜状を
成している。従って第2図に模式的に示す如く裏面釡属
11(4)の一部に水分により腐食を招くと、該腐食部
(9)を浸透し声水分h ’lI−/、買手導体層(3
)の多孔質及び薄膜状によって該半導体層(1)と裏面
金属膜(4)との8rNJ全域に拡散し上記裏面金属膜
(4)を界面方向からも浸食し始める。即ち、裏面金属
11(4)は露出面及び界面の両面から水分によって腐
食されることになり、従来の単結晶半導体に比べ信頼性
の点でかなり問題となる欠点を有していた。
However, according to such a structure, -rIlj of the back surface gold IEII (4) present on the back surface of the amorphous semiconductor layer (3) when viewed from the light irradiation surface of the transparent substrate (1) is covered by the mold body). Although it is difficult to understand! 1! When viewed on a long-term scale, the mode body (8) allows moisture to pass therethrough, albeit to a small extent, so there is a risk that the metal film on the rear surface (4) may be corroded. In particular, the amorphous semiconductor film (31) to which the other side of the back metal film (4) is adhered has more lattice defects than a single crystal semiconductor, generally lacks crystallinity, and is porous! IC,
@The thickness is usually on the order of microns or less, forming a thin film. Therefore, as schematically shown in FIG. 2, if a part of the back pot 11 (4) is corroded by moisture, the moisture permeates through the corroded part (9) and the buyer conductor layer (3
) due to its porous and thin film shape, it diffuses over the entire area of 8rNJ between the semiconductor layer (1) and the back metal film (4), and begins to erode the back metal film (4) from the interface direction as well. In other words, the back metal 11(4) is corroded by moisture from both the exposed surface and the interface, and has a disadvantage in terms of reliability compared to conventional single crystal semiconductors.

本発明は斯る点に艦みて為されたものであって以下に:
1lI311以降tv#照して本発明の一実施例につき
詳述する。
The present invention has been made in consideration of these points, and is as follows:
An embodiment of the present invention will be described in detail with reference to 1lI311 and tv#.

第3因は本発明の一実施例を示す断面図であって第1図
の従来例と対応しており同じものについてFir14w
号が付しである。即ち、(1)は透光性基板。
The third factor is a sectional view showing an embodiment of the present invention, which corresponds to the conventional example shown in FIG.
A number is attached. That is, (1) is a transparent substrate.

(2)は透明電[11,(3)は非晶質半導体膜、(4
)は裏面金属膜、(5)は第1のリード線、(6)は第
2のリード線、(7)は電極パッド、侶lrjモーμド
体で、異なるところは新たに上記裏面金属!(4)を水
分くよる腐食を防止すべく該裏面金属膜(4)より耐湿
性に冨む保護金属膜αG″′C被覆したところにある。
(2) is a transparent film [11, (3) is an amorphous semiconductor film, (4
) is the back metal film, (5) is the first lead wire, (6) is the second lead wire, (7) is the electrode pad, and is different from the above back metal! (4) is coated with a protective metal film αG'''C which is more moisture resistant than the back metal film (4) in order to prevent corrosion due to moisture.

この様に本発明は裏面金属I!(4)及び保接金属膜(
至)を形成する金属組成の耐湿性が問題となってくる。
In this way, the present invention is based on the back metal I! (4) and insulation metal film (
The moisture resistance of the metal composition that forms the

そこで本発明者は上紀両金属膜(4)(2)を形成可能
な金属アルミニワムAl、金Au、銀Ag、銅Ou、=
yケIvNi、スズSn、鉛p’b、yンチモンSb、
fiiZn、インジウムエn、チタンT1、モリブデン
MO%タングステンW%について経験的に耐湿性の良い
ものから第1グループ(以下G1と略す)〜第4グルー
プ(以下G4と略す]に下表の如く分類した。
Therefore, the present inventor has developed metal aluminum Al, gold Au, silver Ag, copper Ou, which can form both metal films (4) and (2).
yke IvNi, tin Sn, lead p'b, yke IvNi, tin Sb,
FiiZn, Indium En, Titanium T1, Molybdenum MO% Tungsten W% are empirically classified into Groups 1 (hereinafter abbreviated as G1) to Group 4 (hereinafter abbreviated as G4) based on those with good moisture resistance as shown in the table below. did.

G5の中から保護金属膜aoの材料を適宜選択すれば良
く、またG2のAut−裏面金属膜(4)として使用す
ればG1の中から選択すれば良い。他の組合せ例として
、裏面金属膜(4)t−Al−で構成し、保護金属@顛
をA1と01〜G3内の金属との合金例えば、Al−T
i、Al−Au等で形成しても良く、更に他の合金Ti
−Ag、Mo−Ag等であっても良い。
The material of the protective metal film ao may be appropriately selected from G5, and if used as the Out-back metal film (4) of G2, it may be selected from G1. As another example of a combination, the back metal film (4) is made of t-Al-, and the protective metal is an alloy of A1 and the metals in 01 to G3, for example, Al-T
It may be formed of Ti, Al-Au, etc., and may also be formed of other alloys such as Ti.
-Ag, Mo-Ag, etc. may be used.

この様に裏面金属膜(4)及び保護金属膜αOは裏面金
属all(4)を形成する金属に比べ保護金属膜αOが
耐湿性に冨む金属であれば該金属の単体及び合金であっ
ても構わない。更に、保護金属膜α0rs一層に限らず
多層にしても良く、この場合積層する順序はオーミック
性が良ければ例えば裏面金属膜(4)力;A1で、保護
金属at(2)がMO,Sn多層構造の如(MOとSn
との耐湿性が逆であっても良い。
In this way, the back metal film (4) and the protective metal film αO can be made of a single substance or an alloy of the metal if the protective metal film αO is a metal with higher moisture resistance than the metal forming the back metal all (4). I don't mind. Furthermore, the protective metal film α0rs is not limited to one layer, but may be multilayered. In this case, if the ohmic properties are good, the order of lamination is, for example, backside metal film (4) force; A1, protective metal at (2) MO, Sn multilayer. Structure (MO and Sn
The moisture resistance may be reversed.

尚、E#13G1〜G40金属は真空蒸着、電子ビーム
蒸着或いはスパー/ 9 リング等の方法により適宜選
択形成される。
Incidentally, the E#13G1 to G40 metals are appropriately selected and formed by a method such as vacuum evaporation, electron beam evaporation, or spar/9 ring.

次に本発明の具体的実施例を第4図に示す。第4図の本
発明非晶質光半導体装置は一主面にPINIP合型a−
Slの非晶質半導体膜(3)を具えると共に、Alから
殴る裏面金属膜(4)と、MO層(10a)Sn層(1
0b)を嘔次積層した多層構造の保護金属膜(至)を有
している。上記非晶質半導体膜(3)t!−主面に工n
tos−8nOz 03m明電極電極(2)を被1セし
めたガラスから匝る透光性基板(1)をプラズマ反応炉
の電極間に配置し、SiH4ガスにB2H6を添加する
ことによって厚み50〜100A程度の2層(5p)を
、Sir゛4ガスのみで5000〜7000A程度の工
1層(31)を m後にSj、HaガスKPH5を添加
することによって500A以下のN層(3n)を、上記
透光性基板(1)上に堆積形成せしめることができる。
Next, a specific embodiment of the present invention is shown in FIG. The amorphous optical semiconductor device of the present invention shown in FIG. 4 has a PINIP composite a-
It includes an amorphous semiconductor film (3) of Sl, a back metal film (4) made of Al, an MO layer (10a), and a Sn layer (1).
It has a protective metal film (to) with a multilayer structure in which 0b) is laminated in sequence. The above amorphous semiconductor film (3) t! - Machining on main surface
TOS-8nOz 03m Bright Electrode A transparent substrate (1) made of glass covered with an electrode (2) is placed between the electrodes of the plasma reactor, and by adding B2H6 to SiH4 gas, a thickness of 50~ 2 layers (5p) of about 100A, 1 layer (31) of about 5000 to 7000A using only Sir4 gas, and N layer (3n) of 500A or less by adding Sj and Ha gas KPH5 after m. It can be deposited on the light-transmitting substrate (1).

そして、A1の裏面金属膜(4)は真空蒸着法によって
厚み1μjllK形成され、MO層(10aJmびKS
n層(I Qb) O保1[i金JII膜ωは電子ビー
ム蒸着法及び又d真空蒸着法によって夫々厚み2000
〜3000A、3000〜5000A積層される。
Then, the back metal film (4) of A1 is formed with a thickness of 1μJllK by vacuum evaporation method, and the MO layer (10aJm and KS
n-layer (I Qb) O 1 [i Gold JII film ω was deposited with a thickness of 2000 mm by electron beam evaporation method and d vacuum evaporation method, respectively.
~3000A, 3000~5000A stacked.

本発1’[ffl斯るMOMl(IQa)並びに5nl
II(101))の多層構造から成る保護金属WIIa
IJを具えた本発明装置と上記保護金属膜ωが存在しな
い従来装置とを比較するために、gi度60℃、湿度9
0%の恒温恒湿雰囲兜中に長期間放置せしめる信頼性実
験を施したところ下記のような結果を得た。
This issue 1' [ffl such MOMl (IQa) and 5nl
Protective metal WIIa consisting of a multilayer structure of II (101))
In order to compare the device of the present invention equipped with an IJ and the conventional device without the above-mentioned protective metal film ω, a gi degree of 60°C and a humidity of 9
A reliability experiment was conducted in which the device was left in a constant temperature and humidity atmosphere of 0% for a long period of time, and the following results were obtained.

この様に本発明は放置時間1000時間を経過しても不
良は発生せず、また2000時間、4000時間に於い
ても従来装置の1/3 以下に不良率を抑圧することが
できる。
As described above, in the present invention, no defects occur even after 1000 hours of standing time, and even after 2000 hours and 4000 hours, the defective rate can be suppressed to 1/3 or less of that of the conventional device.

ところで従来装置に於ける第1・第2のり一ドj1(S
)(@)fllE1m属IIII(4)及び電極パッド
(7)に対して超音波ボンディング若しくげ導電性接着
剤により固着せしめられておL #[IPJlのリード
線(5)げ薄S伏の非晶質半導体@ r3)上の裏面金
属膜(4)に超f波ボンディングされる際、超f渡擾動
により1下の上記非晶質半導体層(3)が破壊される虞
があった。これは非晶質半導体#(1)がミクロンオー
f若しくはそれ以下の薄膜であることに起因しており、
上記*m例に示した叩く太陽電池として用いる場合dミ
クロン以下の極薄膜の時変僕効率が最高になることが確
認されているので、該太陽電池の破壊確率社光センサ等
他の40に比べ高くなっている。
By the way, in the conventional device, the first and second glue dots j1 (S
) (@) fllE1m III (4) and the electrode pad (7) are fixed by ultrasonic bonding or a conductive adhesive. When performing ultra-f wave bonding to the back metal film (4) on the amorphous semiconductor@r3), there was a risk that the amorphous semiconductor layer (3) below the amorphous semiconductor layer (3) would be destroyed due to the ultra-f vibration. This is due to the fact that the amorphous semiconductor #(1) is a thin film of micron ohm or less.
It has been confirmed that the time-varying efficiency of an ultra-thin film of d microns or less is the highest when used as a solar cell as shown in the *m example above. It is relatively high.

一方、導電性接着剤を用いるものは大変作業性が悪い。On the other hand, those using conductive adhesive have very poor workability.

ところが本発明によれば、保護金属膜αGの最上層KS
n、Ag、Ni、等半田付が可能な金属を配置すること
Kよって半田付による第1のリード線(5)の固着を行
なわしめることができ、薄膜状の非晶質半導体@ (3
)を破壊する仁となく、また作業性を損うことなく機械
的に強固に両者を結合せしめることができる。この場合
第3図及び第4図に示す如く電極パッド(7)上に保護
金属膜αGと同じ材料から成る金属膜α1)を形成すれ
ば、第2のリード線(6)と電極パッド(7)との接続
にりいても第1のy −ド線(6)と同様半田付が可能
となる。
However, according to the present invention, the uppermost layer KS of the protective metal film αG
By disposing a solderable metal such as n, Ag, Ni, etc., the first lead wire (5) can be fixed by soldering, and a thin film-like amorphous semiconductor @ (3
), it is possible to firmly connect the two mechanically without damaging the joints or impairing workability. In this case, if a metal film α1) made of the same material as the protective metal film αG is formed on the electrode pad (7) as shown in FIGS. 3 and 4, the second lead wire (6) and the electrode pad (7) ) can be soldered in the same way as the first y-domain wire (6).

本発明非晶質光半導体装1iti以上の説明から明らか
な如く、非晶質半導体膜上に積層せしめた裏Iff金属
膜を該裏面金属膜より耐湿性に冨む保護金属膜で!lI
覆するので、裏面金属膜の水分による腐食を防止するこ
とができ信頼性の高い装置を得ることができる。
As is clear from the above description of the amorphous optical semiconductor device of the present invention, the back Iff metal film laminated on the amorphous semiconductor film is a protective metal film that is more moisture resistant than the back metal film! lI
Since the metal film on the back surface is covered with water, corrosion due to moisture can be prevented and a highly reliable device can be obtained.

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

第1(2)は従来装置の断面図、第2図は従来装置の欠
点を説明する為の模式図、第6図d本発明装置の一実施
例断面図、第4図は他の賽施例断面図、を夫々示してい
る。 (1)・・・−・透光性基板、(3)・・・・・・薄膜
状非晶質半導体膜、(41−−−−−−裏面金属膜、α
υ・・・・・・保護金属膜。
1(2) is a sectional view of the conventional device, FIG. 2 is a schematic diagram for explaining the drawbacks of the conventional device, FIG. 6d is a sectional view of an embodiment of the device of the present invention, and FIG. Example cross-sectional views are shown, respectively. (1)...---Transparent substrate, (3)...Thin film-like amorphous semiconductor film, (41----back metal film, α
υ・・・Protective metal film.

Claims (1)

【特許請求の範囲】[Claims] (1)  ii光性基叛の一主面に少なくとも薄膜状非
晶質半導体膜及び裏面金属膜を順次積層せしめると共に
、該裏面金属膜より耐湿性に富む保護金属膜で上記裏面
金属膜を被覆することを特徴とし九非晶質光半導体装置
(1) ii. At least a thin amorphous semiconductor film and a back metal film are sequentially laminated on one main surface of the photosensitive substrate, and the back metal film is covered with a protective metal film having higher moisture resistance than the back metal film. Nine amorphous optical semiconductor devices characterized by:
JP56135690A 1981-08-28 1981-08-28 Amorphous photo-semiconductor device Granted JPS5835989A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56135690A JPS5835989A (en) 1981-08-28 1981-08-28 Amorphous photo-semiconductor device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56135690A JPS5835989A (en) 1981-08-28 1981-08-28 Amorphous photo-semiconductor device

Publications (2)

Publication Number Publication Date
JPS5835989A true JPS5835989A (en) 1983-03-02
JPH0458710B2 JPH0458710B2 (en) 1992-09-18

Family

ID=15157629

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56135690A Granted JPS5835989A (en) 1981-08-28 1981-08-28 Amorphous photo-semiconductor device

Country Status (1)

Country Link
JP (1) JPS5835989A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59167072A (en) * 1983-03-12 1984-09-20 Agency Of Ind Science & Technol Series-connected type thin film solar battery
JPS6032352A (en) * 1983-08-01 1985-02-19 Matsushita Electric Ind Co Ltd Solar battery module
JPH01129471A (en) * 1987-11-16 1989-05-22 Fuji Electric Corp Res & Dev Ltd Thin-film solar cell
US5034417A (en) * 1987-05-29 1991-07-23 Fujisawa Pharmaceutical Co., Ltd. New alkanesulfonanilide derivatives, processes for preparation thereof and pharmaceutical composition comprising the same
LT4329B (en) 1995-10-05 1998-04-27 Helsinn Healthcare S.A. EXTERNAL USE PRE-FIRE AGENT

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55108780A (en) * 1979-02-14 1980-08-21 Sharp Corp Thin film solar cell

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55108780A (en) * 1979-02-14 1980-08-21 Sharp Corp Thin film solar cell

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59167072A (en) * 1983-03-12 1984-09-20 Agency Of Ind Science & Technol Series-connected type thin film solar battery
JPS6032352A (en) * 1983-08-01 1985-02-19 Matsushita Electric Ind Co Ltd Solar battery module
US5034417A (en) * 1987-05-29 1991-07-23 Fujisawa Pharmaceutical Co., Ltd. New alkanesulfonanilide derivatives, processes for preparation thereof and pharmaceutical composition comprising the same
JPH01129471A (en) * 1987-11-16 1989-05-22 Fuji Electric Corp Res & Dev Ltd Thin-film solar cell
LT4329B (en) 1995-10-05 1998-04-27 Helsinn Healthcare S.A. EXTERNAL USE PRE-FIRE AGENT

Also Published As

Publication number Publication date
JPH0458710B2 (en) 1992-09-18

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