JPH03196680A - Manufacture of solar battery - Google Patents
Manufacture of solar batteryInfo
- Publication number
- JPH03196680A JPH03196680A JP1337369A JP33736989A JPH03196680A JP H03196680 A JPH03196680 A JP H03196680A JP 1337369 A JP1337369 A JP 1337369A JP 33736989 A JP33736989 A JP 33736989A JP H03196680 A JPH03196680 A JP H03196680A
- Authority
- JP
- Japan
- Prior art keywords
- electrode
- semiconductor film
- conductive pattern
- patterns
- conducting
- 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
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 239000004065 semiconductor Substances 0.000 claims abstract description 36
- 239000000758 substrate Substances 0.000 claims abstract description 10
- 238000000034 method Methods 0.000 claims description 17
- 230000008878 coupling Effects 0.000 claims description 3
- 238000010168 coupling process Methods 0.000 claims description 3
- 238000005859 coupling reaction Methods 0.000 claims description 3
- 230000001678 irradiating effect Effects 0.000 claims description 2
- 239000010408 film Substances 0.000 description 43
- 238000006243 chemical reaction Methods 0.000 description 6
- 229910021417 amorphous silicon Inorganic materials 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 238000000059 patterning Methods 0.000 description 5
- 238000010304 firing Methods 0.000 description 4
- 238000009413 insulation Methods 0.000 description 4
- 238000007650 screen-printing Methods 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 238000005530 etching Methods 0.000 description 3
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 2
- MARUHZGHZWCEQU-UHFFFAOYSA-N 5-phenyl-2h-tetrazole Chemical compound C1=CC=CC=C1C1=NNN=N1 MARUHZGHZWCEQU-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 2
- 239000011669 selenium Substances 0.000 description 2
- 150000003377 silicon compounds Chemical class 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- LEVVHYCKPQWKOP-UHFFFAOYSA-N [Si].[Ge] Chemical compound [Si].[Ge] LEVVHYCKPQWKOP-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- PZPGRFITIJYNEJ-UHFFFAOYSA-N disilane Chemical compound [SiH3][SiH3] PZPGRFITIJYNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- LQJIDIOGYJAQMF-UHFFFAOYSA-N lambda2-silanylidenetin Chemical compound [Si].[Sn] LQJIDIOGYJAQMF-UHFFFAOYSA-N 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910021424 microcrystalline silicon Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- FVZVCSNXTFCBQU-UHFFFAOYSA-N phosphanyl Chemical group [PH2] FVZVCSNXTFCBQU-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000012495 reaction gas Substances 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- ABTOQLMXBSRXSM-UHFFFAOYSA-N silicon tetrafluoride Chemical compound F[Si](F)(F)F ABTOQLMXBSRXSM-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
Landscapes
- Photovoltaic Devices (AREA)
Abstract
Description
【発明の詳細な説明】
(イ)産業上の利用分野
本発明は太陽光や人工照明の下で発電動作する太陽電池
の製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION (a) Field of Industrial Application The present invention relates to a method for manufacturing a solar cell that generates electricity under sunlight or artificial lighting.
(ロ)従来の技術
近年、太陽電池はクリーンなエネルギー源として多くの
関・じ1が寄せられ、ており、特にアモルファスシリコ
ンを以丁a−5iと記す)等の薄膜太陽電池は低コスト
化に有利なことから電力用のlIk有カー穴補として、
現在、変換効率の向」−や低コスト化の研究が盛んに行
なわれている。こうした状況のなかで、集積型薄膜太陽
電池のバターニングプロセスとして、受光面′I4.極
膜1ユに、絶縁ペースト及び導電性ペーストからなる!
8縁パターン及び導電パターンをスクリーン印刷し乾燥
、焼成後レーザを上記パターンtをパルス光で照射する
ことにより、絶縁パターン上で分離、導電パターン−L
で接続を行なう(特開昭62−33477号公報)方法
や、接続は導電パターンとレーザ、分離はエツチング(
米国特許第4,724,011号)を用いる方法等が開
発されている。(b) Conventional technology In recent years, solar cells have received a lot of attention as a clean energy source, and in particular, thin film solar cells such as amorphous silicon (hereinafter referred to as a-5i) have lower costs. Because it is advantageous, it is used as a lIk car hole supplement for electric power.
Currently, research is being actively conducted to improve conversion efficiency and reduce costs. Under these circumstances, the light-receiving surface 'I4. One polar film consists of insulating paste and conductive paste!
After screen printing the 8-edge pattern and the conductive pattern, drying, and baking, the above pattern t is irradiated with pulsed laser light to separate the conductive pattern on the insulating pattern.
(Japanese Unexamined Patent Publication No. 62-33477), connection is made using a conductive pattern and a laser, and separation is made by etching (
A method using U.S. Pat. No. 4,724,011) has been developed.
(ハ)発明が解決しようとする課題
しかるに接続はレーザ、分離はエツチングを用いる方法
は、レーザパターン方法とエツチング工程が複雑で低コ
スト化には不利であることや、また上記2つの方法とも
接続は、導電パターンと裏面電極との間に高抵抗なa−
5i膜が存在するため、レーザパワーか弱すぎると導電
パターンと裏面電極間の抵抗が高くなり、高出力が得ら
れず、信頼性もよくないという欠点があった。さらに接
続に用いられているレーザはパルス光であり、接続は点
で行なわれているため、発電の際には、レーザ光により
形成されたホールのみに電流が集中するため、発熱によ
り導電パターンのダメージが信頼性を低くする可能性が
あり、また逆にレーザパワーを強くすると、導電パター
ンを突きぬけて下層の受光面電極膜をも破壊してしまう
という欠点もあった。(c) Problems to be Solved by the Invention However, the method of using a laser for connection and etching for separation is disadvantageous in terms of cost reduction because the laser patterning method and etching process are complicated, and it is also difficult to connect with the above two methods. is a high-resistance a-
Due to the presence of the 5i film, if the laser power is too weak, the resistance between the conductive pattern and the back electrode increases, making it impossible to obtain high output and having poor reliability. Furthermore, the laser used for connection is pulsed light and the connection is made at points, so when generating electricity, the current concentrates only in the holes formed by the laser light, so the conductive pattern is damaged by heat generation. Damage may reduce reliability, and conversely, if the laser power is increased, it may penetrate through the conductive pattern and destroy the underlying light-receiving surface electrode film.
本発明はこのような欠点を解決せんとするらのである。The present invention seeks to solve these drawbacks.
(ニ)課題を解決するための手段
本発明は、上記課題を解決するために、基板の絶縁表面
に複数の第1!極を整列配置し、上記第1電極の隣接対
向間隔部の一方に近接して結合用導電パターンを形成し
、当該導電パターン及び第1電極を含んで上記基板上に
半導体膜を設け、L記導電パターンを覆う半導体膜に対
して露出面側からエネルギビームを照射して被照射部位
の半導体膜部分を連続的に除去し当該導電パターンを゛
ト導体膜から露出せしめた後、斯る導電パターンを含め
て半導体膜上に第2電極を配置することを特徴とする。(d) Means for Solving the Problems In order to solve the above problems, the present invention provides a plurality of first ! arranging the electrodes, forming a coupling conductive pattern close to one of the adjacent opposing spacing parts of the first electrode, and providing a semiconductor film on the substrate including the conductive pattern and the first electrode; After irradiating the semiconductor film covering the conductive pattern with an energy beam from the exposed surface side and continuously removing the irradiated portion of the semiconductor film to expose the conductive pattern from the conductive film, the conductive pattern is removed. The second electrode is arranged on the semiconductor film including the second electrode.
(ホ)作用
上述の如く第2電極を形成する前に、導電パターン上の
半導体膜部分がレーザビームの照射により連続的に除去
され当該導電パターンを露出した後、斯る導電パターン
を含めて半導体膜上に第2電極を配置することによって
、第2電極は連続的に直接接触する。(E) Function As mentioned above, before forming the second electrode, the semiconductor film portion on the conductive pattern is continuously removed by laser beam irradiation to expose the conductive pattern, and then the semiconductor film including the conductive pattern is removed. By placing the second electrode on the membrane, the second electrode is in continuous direct contact.
(へ)実施例
以下第1図乃至第7図を参照して、本発明製造方法を太
陽電池の製造方法に適用した実施例につき詳述する。(f) Examples Hereinafter, examples in which the manufacturing method of the present invention is applied to a solar cell manufacturing method will be described in detail with reference to FIGS. 1 to 7.
第1図の工程では、厚さl mm −5mm、面積10
cmX 10cm −5Qcmx 50cm程度の透明
なガラス等の絶縁材料からなる基板(1)上全面に、厚
さ約2000人−5000人の酸化錫(SnO,)、酸
化インジウム錫(I TO)に代表される透光性導電酸
化物(TCO)の単層型或いはそれらの積層型の透明電
極膜が被着された後、隣接間隔部(ab)(bc)がレ
ーザビーム(LB)の照射により除去されて、第1電極
として個別の各透明1極膜(2a ) (2b )
(2c ) −が分離形成される。使用されるレーザ
装置は基板(1)にほとんど吸収されることのない波長
が適当であり、上記ガラスに対しては0.35μm〜2
.5μmの波長のパルス出力型が好ましい。斯る好適な
実施例は、波長約1.06 pmエネルギ密度13J/
Cm’、パルス繰返し周波数3KHzのQスイッチ付き
Nd:YAGレーザであり、隣接間隔部(ab)の間隔
は約50〜100μmに設定される。In the process shown in Figure 1, the thickness is l mm -5 mm and the area is 10 mm.
cmX 10cm -5Qcmx 50cm The entire surface of the substrate (1) made of an insulating material such as transparent glass is coated with a layer of tin oxide (SnO) or indium tin oxide (ITO) with a thickness of approximately 2000 to 5000 mm. After a transparent electrode film of a single layer type or a laminated type of transparent conductive oxide (TCO) is deposited, the adjacent spacing parts (ab) and (bc) are removed by irradiation with a laser beam (LB). Then, each transparent monopolar film (2a) (2b) is used as the first electrode.
(2c) - is separated and formed. The laser device used is suitable for a wavelength that is hardly absorbed by the substrate (1), and for the above glass, the wavelength is 0.35 μm to 2 μm.
.. A pulse output type with a wavelength of 5 μm is preferable. Such a preferred embodiment has a wavelength of about 1.06 pm and an energy density of 13 J/
Cm', a Q-switched Nd:YAG laser with a pulse repetition frequency of 3 KHz, and the spacing between adjacent spacing parts (ab) is set to about 50 to 100 μm.
第2図の工程では、先の工程で分割配置された透明電極
膜(2a (2b)(2c)・・・の一方の隣接間隔
部(ab (bc)・・・の近傍に偏って該隣接間隔
部(ab’ (bc)・・・に近い側から導電パター
ン(3ab (3bc)・・・及び絶縁パターン(
4ab)(4bc)・・・が各々1本づつ平行に帯状に
形成される。例えば上記導電パターン(3ab)(3b
cJ・・・は銀(Ag)ペーストやその他の金属ペース
トをスクリーン印刷手法により高さ約1010−207
I幅約100−150 μmにパターニングされた後、
約550℃の温度にて焼成される。また絶縁パターン(
4ab)(4bC)・・・としては後工程で形成され半
導体光活性層として動作する非晶質半導体膜に拡散した
りすることのない材料、例えば二酸化シリコン(SiO
!)粉末をペースト状にしたS+Otペーストやその他
の無機材料が選択され、上記Agペーストと同様スクリ
ーン印刷手法により所定の箇所に高さ約110−20p
、幅約100−150μmにパターニングされ、これも
同様に約550℃の温度にて焼成される。In the process shown in FIG. The conductive pattern (3ab (3bc))... and the insulating pattern (
4ab) (4bc)... are formed in parallel strips, one each. For example, the conductive patterns (3ab) (3b)
cJ... is approximately 1010-207 cm in height by screen printing silver (Ag) paste or other metal paste.
After patterning to an I width of about 100-150 μm,
It is fired at a temperature of about 550°C. Also, the insulation pattern (
4ab) (4bC)... is a material that is formed in a later process and does not diffuse into the amorphous semiconductor film that acts as a semiconductor photoactive layer, such as silicon dioxide (SiO
! ) S+Ot paste made from powder into a paste or other inorganic material is selected, and is printed at a predetermined location to a height of about 110-20p using the same screen printing method as the Ag paste above.
, is patterned to have a width of approximately 100-150 μm, and is similarly fired at a temperature of approximately 550°C.
この様にAgペーストの焼成温度とSin。In this way, the firing temperature of Ag paste and Sin.
ペーストの焼成温度とが等しい場合、両者の焼成は基本
的には同一に行なわれる。然し、両者を同時に焼成する
に際しては、両者を同時にスクリーン印刷できないため
に、先ずAgペースト或いはS10.ペーストのスクリ
ーン印刷を行ない、次にこのペーストに対し予備焼成或
は予備乾燥を施した後、残りの5iOrペースト或いは
Agペーストをスクリーン印刷する必要がある。When the firing temperatures of the pastes are the same, the firing of both pastes is basically performed in the same manner. However, when firing both at the same time, since both cannot be screen printed at the same time, Ag paste or S10. After screen printing the paste and then pre-baking or pre-drying the paste, it is necessary to screen print the remaining 5iOr paste or Ag paste.
第3図の工程では、各透明電極膜(2a)<2b)(2
c)・−・、1記導電パターン(3ab:1j 3 b
C>−−−及び絶縁パターン(4ab) (4bC
)・・・の表面を含んで基板(1)上のほぼ全面に充電
変換に有効に寄与する厚さ4000人〜7000人の非
晶質シリコン(a−5i)等の非晶質半導体膜(3)が
モノシラン(S i H4) 、ジシラン(S i 、
H,) 、四弗化シリコン(SiF、)、モノ70ロシ
ラン(SiH,F)等のシリコン化合物ガスを主ガスと
し適宜価電子制御用のジボラン(B、H6)、ホスフイ
ノ(P)(S)のドーピングガスが添加された反応ガス
中でのプラズマCVD法や光CVD法により形成される
。斯る半導体膜(5)は上記B、H,やPH,の添加に
よりその内部に膜面に平行なpin接合を含み、従って
より具体的には、上記シリコン化合物ガスにB * H
s、更にはメタン(CH,)、エタン(C,H,)等の
水素化炭素ガスの添加によりプラズマCV D法や光C
VD法によりp型の非晶質シリコンカーバイド(a−5
iC)が被着され、次いでi型(ノンドープ)のa−5
i及びn型のa−5i或いは微結晶シリコン(μc−5
i)が順次積層被着される。In the process shown in FIG. 3, each transparent electrode film (2a) < 2b) (2
c) ---, 1 conductive pattern (3ab:1j 3 b
C>--- and insulation pattern (4ab) (4bC
)..., an amorphous semiconductor film such as amorphous silicon (a-5i) with a thickness of 4,000 to 7,000 thick, which effectively contributes to charge conversion, is spread over almost the entire surface of the substrate (1), including the surface of the substrate (1). 3) is monosilane (S i H4), disilane (S i ,
The main gas is silicon compound gas such as silicon tetrafluoride (SiF, ), mono-70rosilane (SiH, F), and diborane (B, H6), phosphino (P) (S) for controlling valence electrons as appropriate. It is formed by a plasma CVD method or a photo CVD method in a reaction gas to which a doping gas of . Such a semiconductor film (5) contains a pin junction parallel to the film surface due to the addition of B, H, or PH, and therefore, more specifically, B*H is added to the silicon compound gas.
Furthermore, by adding hydrogenated carbon gas such as methane (CH,) or ethane (C,H,), plasma CVD method or optical
P-type amorphous silicon carbide (a-5
iC) is deposited, then i-type (non-doped) a-5
i and n type a-5i or microcrystalline silicon (μc-5
i) are deposited in a layered manner.
尚、半導体光活性層として動作する半導体は上記a−3
i系の半導体に限らず硫化カドミウム(CdS)、テル
ル化カドミウム(Cd T e )、セレン(Se)等
の膜状半導体であっても良いが、工業的には上記a−5
i、a−5iC1更には非晶質シリコンゲルマニウム<
a−5iGe)、非晶質シリコン錫(a−5iSn)等
に代表されるa−5j系半導体が好ましい。Note that the semiconductor that operates as the semiconductor photoactive layer is a-3 above.
In addition to i-based semiconductors, film semiconductors such as cadmium sulfide (CdS), cadmium telluride (CdTe), and selenium (Se) may also be used, but industrially, the above a-5
i, a-5iC1 and further amorphous silicon germanium <
Preferred are a-5j semiconductors represented by a-5iGe), amorphous silicon tin (a-5iSn), and the like.
第一1図の工程では、上記導電パターン(3ab)(3
bc)を覆う非晶質半導体膜(5)に対して、その露出
面側からレーザビーム或いは電子ビームの如きエネルギ
ビームを照射して、被照射部位の半導体膜部分(5)′
が上記エネルギビームの走査方向に連続的、即ち線状に
除去される。使用されるエネルギビームは例えば波長1
、06 pmのQスイッチ付きNd:YAGレーザか
らパルス状に出射されるレーザビームであり、上記半導
体膜部分(5)°が連続的に除去されるべくレーザパル
スの一部が重なるように走査される。このとき照射され
るレーザビーム(LB、)は、半導体膜に直接照射され
ると共に下層に膜厚十分な導電パターン(3ab)(3
bc)が存在することから、多少大きなエネルギ密度を
持ったとしても、更に下層の透明導を膜(2a)(2b
)(2c)・・・を直撃するに至らない。その結果、非
晶質半導体膜(5a)(5b)(5c)は導電パターン
(3ab)(3bc)表面を連続的に露出せしめた状態
で個別に分割される。In the process shown in FIG. 11, the conductive pattern (3ab) (3
bc) is irradiated with an energy beam such as a laser beam or an electron beam from the exposed surface side of the amorphous semiconductor film (5) covering the semiconductor film portion (5)' of the irradiated area.
is removed continuously, ie, linearly, in the scanning direction of the energy beam. The energy beam used is e.g.
, 06 pm is a laser beam emitted in a pulsed manner from a Q-switched Nd:YAG laser, and the laser beam is scanned so that a portion of the laser pulse overlaps in order to continuously remove the semiconductor film portion (5)°. Ru. The laser beam (LB, ) irradiated at this time is directly irradiated onto the semiconductor film, and the conductive pattern (3ab) (3
bc), even if it has a somewhat large energy density, the transparent conductor in the lower layer is further removed from the film (2a) (2b
) (2c)... cannot be directly hit. As a result, the amorphous semiconductor films (5a) (5b) (5c) are individually divided with the surfaces of the conductive patterns (3ab) (3bc) continuously exposed.
第5図の工程では、半導体膜(5)及びこの半導体膜(
5)から露出した導電パターン(3a b)(3bc)
を含んで基板(1)のほぼ全面にAl、Ti、TiAg
、Ni等の単層或いは積層構造の第2電極としての裏面
電極膜(6)が被着される。In the process shown in FIG. 5, the semiconductor film (5) and this semiconductor film (
5) Conductive patterns exposed from (3a b) (3bc)
Al, Ti, TiAg on almost the entire surface of the substrate (1) including
A back electrode film (6) as a second electrode of a single layer or a laminated structure made of , Ni, etc. is deposited.
第6図の最終工程では、絶縁パターン(4ab)(4b
c)・・・の表面上に位置する非晶質半導体v(5a)
(5bン (5cン及び裏面電極膜(6)の積層体部分
にこの積層体部分の表面側からレーザビームCL B
1)が照射される。斯る絶縁パターン(4ab)(4b
c)・・・上の積層体部分に照射されるレーザビーム(
LB、)は、斯る積層体部分を除去するに足りる十分な
エネルギ密度を備えている。即ち、レーザビーム(L
B 、)が照射される積層体部分は複数の光電変換領域
(7a)(7b)(7c)・・・に跨って一様に連なっ
た裏面電極膜(6)及び個別の半導体膜(5a)(5b
)<5c)の積層体を上記各領域(7a)(7b)(7
c)・・・毎に分割せんがために除去される箇所であり
、多少大きなエネルギ密度を持ったとしてら、L記積層
体部分の直下には厚み(高さ)が1分な絶縁パターン(
4ab)(4bc)・・・が存在する結果、斯る絶縁パ
ターン(4ab)(4bC)・・・の表面を僅かに除去
するだけであり、下層・\の第2レーザビーム(LBt
)の到達は阻止される。この第2のレーザビーム(LB
*)の照射によって、上記積層体を電気的に且つ物理的
に分離する分離溝(8ab)(8bc)・・・が形成さ
れる。In the final step in FIG. 6, insulation patterns (4ab) (4b
c) Amorphous semiconductor v (5a) located on the surface of...
(5b) A laser beam CL B is applied to the laminate part of the back electrode film (6) from the surface side of this laminate part.
1) is irradiated. Such insulation patterns (4ab) (4b
c)... Laser beam irradiated to the upper layered body part (
LB,) has sufficient energy density to remove such a portion of the stack. That is, the laser beam (L
The laminate portion to which B, ) is irradiated is a back electrode film (6) uniformly connected across a plurality of photoelectric conversion regions (7a) (7b) (7c)... and individual semiconductor films (5a). (5b
) < 5c) in each of the above regions (7a) (7b) (7
c) It is a part that is removed for division drilling every time, and assuming that it has a somewhat large energy density, there is an insulating pattern (with a thickness (height) of 1 minute) directly under the laminate part marked L (
4ab) (4bc)..., the surface of the insulating pattern (4ab) (4bC)... is only slightly removed, and the second laser beam (LBt) of the lower layer
) is prevented from reaching the destination. This second laser beam (LB
By the irradiation of *), separation grooves (8ab) (8bc), . . . that electrically and physically separate the laminate are formed.
その結果、相隣り合う光電変換領域(7a)(7b l
(7c )−の裏面電極膜(6a)C6b)・・・
と透明電極膜(2b)(2c)・・・は、上記分離溝<
8 a b ) (8b c ) −より裏面tt
L極膜(6a ) (6b ) (6c )−の隣
接間隔#(ab)(bc)・・・に近い側において導電
パターン(3ab)(3bc)・・・を介して直接結合
することとなる。As a result, adjacent photoelectric conversion regions (7a) (7b l
(7c) - Back electrode film (6a)C6b)...
and the transparent electrode films (2b), (2c)... are in the above separation groove <
8 a b ) (8 b c ) - Back side tt
L electrode films (6a) (6b) (6c)- are directly coupled via conductive patterns (3ab) (3bc) on the side closer to adjacent spacing #(ab)(bc)... .
斯る製造方法に基づき製造された太陽電池に対して、そ
の出力特性を測定したところ、透明電極膜(2b)(2
c)上の導電パターン(3ab)(3bc)と、隣接す
る充電変換領域の裏面電極膜(6a) (6b)とを
、半導体膜(5)及び裏面電極膜(6)積層後レーザビ
ームの照射を施した従来の結合(溶着)構造を持つ太陽
電池に比して、フィルファクタ及び開放電圧の向上が確
認され、短絡電流についてはほぼ同等の値が得られた。When we measured the output characteristics of the solar cells manufactured based on this manufacturing method, we found that the transparent electrode film (2b) (2
c) After laminating the semiconductor film (5) and the back electrode film (6), the upper conductive patterns (3ab) (3bc) and the back electrode film (6a) (6b) of the adjacent charge conversion region are irradiated with a laser beam. Compared to solar cells with a conventional bonded (welded) structure, improvements in fill factor and open circuit voltage were confirmed, and almost the same values for short circuit current were obtained.
その結果、出力電力の上昇が図れた。斯る特性改善は、
導電パターンと裏面電極膜の結合構造が溶着による間接
的なものではなく、直接的なものによるところが大きい
。As a result, the output power was increased. Such characteristic improvement is
The bonding structure between the conductive pattern and the back electrode film is not indirect due to welding, but is largely due to direct bonding.
第7図は本発明製造方法を実施した太陽電池に対する信
頼性試験をまとめたものである。信頼性試験は、初期値
の出力電力に吋する出力電力の時間的変動を示している
。信頼性試験は、90℃の高温試験、60℃、95%の
恒温恒温試験、−40℃の低温試験、−20℃〜80℃
の温度サイクル試験である。信頼性試験の結果は、−4
0℃の低温試験では1000時間経過後若干の出力特性
が見られた他は、初期値より出力特性が向上した。斯る
出力特性の向上は、高温処理に基づくアニーリング効果
によるものと思われる。FIG. 7 summarizes reliability tests on solar cells manufactured using the manufacturing method of the present invention. The reliability test shows the temporal variation of the output power from the initial value to the output power. Reliability tests include a high temperature test at 90°C, a constant temperature test at 60°C, 95%, a low temperature test at -40°C, and -20°C to 80°C.
This is a temperature cycle test. The reliability test result is -4
In the low-temperature test at 0° C., the output characteristics were improved from the initial values, except that some output characteristics were observed after 1000 hours. It is believed that such improvement in output characteristics is due to an annealing effect based on high temperature treatment.
第8図及び第9図は本発明製造方法の他の実施例を示し
ている。即ち、この実施例では、絶縁ペーストからなる
絶縁パターンが省略され、透明電極膜(2a)(2b)
上には導電ペーストからなる導電パターン(3ab)(
3bc)・・・のみが形成されている。FIGS. 8 and 9 show other embodiments of the manufacturing method of the present invention. That is, in this example, the insulating pattern made of insulating paste is omitted, and the transparent electrode films (2a) (2b)
On top is a conductive pattern (3ab) made of conductive paste (
3bc)... are formed.
その結果、第9図の工程では、裏面電極膜の選択パター
ニングをレーザビームの照射により施すことができない
ので、当該裏面電極膜(6a)(6b)(6c)・・・
のパターニングは、膜形成時に、不要部をマスクで覆う
方法により同時に行なわれる。マスク法によるパターニ
ングは微細加工性の点で問題があるが、裏面電極膜(6
a)(6b) <6C)・・・に対しては微細加工が施
されなくても、充電変換領域(7a ) (,7b
) (7c ) −の有効面積を縮少するものではな
い。As a result, in the process shown in FIG. 9, selective patterning of the back electrode film cannot be performed by laser beam irradiation, so the back electrode films (6a) (6b) (6c)...
The patterning is carried out at the same time as the film is formed by covering unnecessary parts with a mask. Patterning using a mask method has problems in terms of microfabrication, but the back electrode film (6
a) (6b) <6C)... Even if no microfabrication is performed, the charge conversion region (7a) (,7b
) (7c) - does not reduce the effective area of -.
この方法によっても初期特性の向上と、高い信頼性試験
の結果が得られた。This method also improved the initial characteristics and yielded high reliability test results.
(ト)発明の効果
本発明は以上の説明から明らかな如く、第2電極は導電
パターンと連続的に直接接触するので、信頼性の高い高
出力特性の太陽電池を製造することができる。(g) Effects of the Invention As is clear from the above description, in the present invention, since the second electrode is in continuous direct contact with the conductive pattern, a highly reliable solar cell with high output characteristics can be manufactured.
第1図乃至第6図は本発明製造方法の一実施例を工程順
示し、第1図乃至第3図、第5図及び第6図は断面図、
第4図は一部断面斜視図、第7図は信頼性特性図、第8
図及び第9図は本発明製造方法の他の実施例の要部の工
程を示す断面図である。1 to 6 show an example of the manufacturing method of the present invention in the order of steps, and FIGS. 1 to 3, 5 and 6 are cross-sectional views,
Figure 4 is a partially sectional perspective view, Figure 7 is a reliability characteristic diagram, and Figure 8 is a reliability characteristic diagram.
9 and 9 are cross-sectional views showing the main steps of another embodiment of the manufacturing method of the present invention.
Claims (1)
上記第1電極の隣接対向間隔部の一方に近接して結合用
導電パターンを形成し、当該導電パターン及び第1電極
を含んで上記基板上に半導体膜を設け、上記導電パター
ンを覆う半導体膜に対して露出面側からエネルギビーム
を照射して被照射部位の半導体膜部分を連続的に除去し
当該導電パターンを半導体膜から露出せしめた後、斯る
導電パターンを含めて半導体膜上に第2電極を配置する
ことを特徴とする太陽電池の製造方法。(1) Arranging a plurality of first electrodes on the insulating surface of the substrate,
A conductive pattern for coupling is formed close to one of the adjacent opposing spacing portions of the first electrode, a semiconductor film is provided on the substrate including the conductive pattern and the first electrode, and a semiconductor film covering the conductive pattern is provided with a conductive pattern for coupling. After irradiating the exposed surface side with an energy beam to successively remove the irradiated portion of the semiconductor film and expose the conductive pattern from the semiconductor film, a second conductive pattern is placed on the semiconductor film including the conductive pattern. A method for manufacturing a solar cell, comprising arranging electrodes.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1337369A JP2771655B2 (en) | 1989-12-26 | 1989-12-26 | Solar cell manufacturing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1337369A JP2771655B2 (en) | 1989-12-26 | 1989-12-26 | Solar cell manufacturing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03196680A true JPH03196680A (en) | 1991-08-28 |
| JP2771655B2 JP2771655B2 (en) | 1998-07-02 |
Family
ID=18307974
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1337369A Expired - Fee Related JP2771655B2 (en) | 1989-12-26 | 1989-12-26 | Solar cell manufacturing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2771655B2 (en) |
-
1989
- 1989-12-26 JP JP1337369A patent/JP2771655B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP2771655B2 (en) | 1998-07-02 |
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