JPS5932179A - Manufacture of solar battery - Google Patents

Manufacture of solar battery

Info

Publication number
JPS5932179A
JPS5932179A JP57143022A JP14302282A JPS5932179A JP S5932179 A JPS5932179 A JP S5932179A JP 57143022 A JP57143022 A JP 57143022A JP 14302282 A JP14302282 A JP 14302282A JP S5932179 A JPS5932179 A JP S5932179A
Authority
JP
Japan
Prior art keywords
layer
electrode
aluminum
back surface
paste
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
JP57143022A
Other languages
Japanese (ja)
Other versions
JPH023310B2 (en
Inventor
Yuuji Tawara
裕滋 田原
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.)
Hoxan Corp
Hokusan Co Ltd
Original Assignee
Hoxan Corp
Hokusan 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 Hoxan Corp, Hokusan Co Ltd filed Critical Hoxan Corp
Priority to JP57143022A priority Critical patent/JPS5932179A/en
Publication of JPS5932179A publication Critical patent/JPS5932179A/en
Publication of JPH023310B2 publication Critical patent/JPH023310B2/ja
Granted legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L31/00Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
    • H01L31/18Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof
    • H01L31/1804Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof comprising only elements of Group IV of the Periodic System
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L31/00Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
    • H01L31/02Details
    • H01L31/0224Electrodes
    • H01L31/022408Electrodes for devices characterised by at least one potential jump barrier or surface barrier
    • H01L31/022425Electrodes for devices characterised by at least one potential jump barrier or surface barrier for solar cells
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/547Monocrystalline silicon PV cells
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50Manufacturing or production processes characterised by the final manufactured product

Abstract

PURPOSE:To shorten the working time of manufacturing a solar battery and to reduce the cost of materials to be used by forming by baking a p<+> type layer after printing with aluminum paste and forming an aluminum back surface electrode of the aluminum paste layer. CONSTITUTION:An n<+> type layer which is covered with an Si oxidized film on the entire surface of a p type Si wafer by diffusing phosphorus or boron in the wafer. Then, the peripheral side part of the n<+> type layer is removed, and an aluminum layer A is printed on the back surface part of the n<+> type layer. Then, this is baked in the air. The aluminum paste is diffused in the p type layer of the Si wafer by this baking, a p<+> type layer is formed, and a back surface field which becomes an n<+>-P-P<+> type junction is advanced. In this manner, an aluminum back surface electrode A' with the layer A remains adjacent to the p<+> type layer. In this case, an aluminum passage oxidized layer A'' is formed on the surface of the electrode A'. Subsequently, this is etched with HF, an SiO2 layer is removed, and the layer A'' is also removed. Then, a surface electrode B is formed on the exposed surface.

Description

【発明の詳細な説明】 本発明はl)型シリコンウェハによって、114P  
1)−1接合とした入隅′IIL/llIケ製造4−る
ための方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides 114P
1) It relates to a method for manufacturing an inner corner 'IIL/llI' which is a -1 joint.

従来から効率のよいB S F (1’1ack 5u
rfaceFielcl )化された太陽電池が用いら
れているが、との種電池の製造は、次の如き1稈を経て
実施されている。
Traditionally efficient B S F (1'1ack 5u
rfaceFielcl) solar cells are used, but the production of seed cells is carried out through one culm as follows.

すなわちO51図の1.、稈説、明図か示す通り、先4
゛(イ)の141 < m 、GされたP型シリコンウ
ェハにダJし既′f−11のり11り燐等を拡散さぜる
ことにより、(ロ)のようにP型シリコンウェハの全表
面にn”層乞J[モ成し71 P ++ ’  接合を
得るが、この際11 ”層はシリコン酸化膜に上って覆
われている0次1仁1”、 ilt+ )拡iik済I
)型シリコンウェハにおける裏面および1011面部分
の04 層を除ノl−るのであるが、このためには当該
n +?jに1114酸性レジス1インクをイ゛ノ2(
」μmn11・ざJ77稈たけスクリーン印11ilI
 L −C”j’t、 t’4さナタ後、II F−I
t N 031f+W、’、カII F−11N(J、
、 −CI13 C00II溶Q Ic テゴノ千7グ
処理ずろが、研磨紙1仁よる機械研磨″!(1+ili
すように1.て第2す、がくして同図e・)の如きく、
σ〕か?!)r嘗1ろ。
In other words, 1 in diagram O51. , culm theory, as shown in the clear diagram, first 4
゛(A) 141 < m, by dipping onto the G-treated P-type silicon wafer and diffusing phosphorus, etc., the entire P-type silicon wafer as shown in (B). An n'' layer is formed on the surface to obtain a junction, but at this time the 11'' layer is covered by a silicon oxide film of 0th order 1'', ilt+) expanded I
) type silicon wafer, the 04 layer on the back surface and the 1011 side portion is removed, but for this purpose, the n+? Add 1114 Acid Resist 1 ink to Ino 2 (
”μmn11・zaJ77 culm screen mark 11ilI
L -C"j't, after t'4, II F-I
t N 031f+W,', Ka II F-11N (J,
, -CI13 C00II Melting Q Ic Tegono 1,700g process is mechanically polished with 1 layer of abrasive paper''! (1+ili
1. The second step is as shown in the same figure (e).
σ〕? ! )r嘗1ro.

次にI: Hj:のもグ月仁つき、表面側におζプるシ
リ=+ >酸化11’J %: If F rこよりエ
ツチング処理[−て、これ4除去した後、そのP層裏面
側にA17/f、着h’i tl) ’z同図の使)に
示す通り1′(空蒸着により形成し、これを空気中にて
1.l’A成することで、当該へl、を1)層に(広1
1にさせ、これ1こよってPF層を形成してn”  P
  I)→接合とする133 F化処理を行なうのであ
る。
Next, I: Hj: Nomoguzuki etched, zeta on the surface = + > Oxidation 11'J A17/f on the side, attached h'i tl) 'z As shown in the same figure, 1' (formed by empty evaporation, and by forming 1.l'A in air, l' , into 1) layer (wide 1
1 and form a PF layer by this 1 to form n”P
I) → 133 F conversion treatment is performed.

上記1(S J”化処理により1.11層の裏面に04
1着残存し、た(へ)に示すAt−酸化11S! +2
1を、tl Ct 。
04 on the back side of the 1.11 layer by the above 1 (S J” processing)
One piece remained, At-oxidized 11S shown in ta(f)! +2
1, tl Ct.

N a OH溶f1.+仁より除去して(1・)の状態
とな12、次て(チウ(l刀に示す通り、真空蒸着法に
よってP+層にはi’i −Pd−AgまたはTi−A
gによる裏面電極(3)を・ n+層には1’i−Ag
による表面電極(4)を形成し、さらに要すれば両′市
極f31 +411こ、プイノビングによろハンダ層(
!’il +51 ’ を被着すると共に、表面?!f
 4ifi f4rにはさらに反射防電11か(6)を
被装することになる。
N a OH solution f1. The P+ layer is removed by vacuum evaporation to form a state of (1・).
1'i-Ag for the n+ layer.
If necessary, form a surface electrode (4) by applying a solder layer (
! As well as applying 'il +51', the surface? ! f
4ifi f4r will be further coated with reflective protection 11(6).

このように、−上記(DAt蒸着1c」:るn S l
”化人陽電池の製造方法番こよれば、■]型シリコンウ
ェハの拡散処理により得られた。−I一層につき、その
裏面部分の全面にわたって、これを除去した後、B11
−化処理を行なうから、当該除ノミ作業に可成りの労力
と時間とを明することNなり、4rc11F工7チング
処理と1lcA4;Q:はNa011による処理を夫々
施さねばならないだけでなく、別途Δgj−用いて11
1極をLiX空蒸着するため、このためにも相当の作S
’s ll& 1iJl ’;z ′J”j、 L、か
つ使用資1’ 1.高6111につくため、太陽電池の
安6111な提供ができ斤い欠陥があ7、。
Thus, - the above (DAt evaporation 1c': n S l
According to the manufacturing method of ``Kajin solar cell,'' it was obtained by diffusion treatment of a type silicon wafer.
Since the flea removal process requires considerable effort and time, 4rc11F and 1lcA4;Q: not only have to be treated with Na011, but also separately. Δgj-using 11
Since one pole is vacuum-deposited with LiX, a considerable amount of work is required for this purpose.
's ll & 1iJl '; z 'J"j, L, and used resources 1' 1. Due to the height of 6111, there are defects that prevent us from providing solar cells at a cheap price7.

これに対し0′12図の1稈説明図に示す、AIベース
トを用いたBSF化太陽WL池の製ヌ省方法(i、II
” iff: )7法の難点をl」成り改善し得るもの
となっている。
On the other hand, the method for manufacturing a BSF solar WL pond using AI base (i, II
``if: )'' The disadvantages of the 7 methods can be improved.

1なわら同θくでは、(イ)(I:I)か前記方法の(
イ)(ロ)と1゛<同じであり、次にll’il l1
11X1〜分の+11゛層のみ丘除ノ、してeうq) 
IJいくなし、l欠に11 Fエツチングに」、り表裏
面のツリー1ン酸化暎を除去し7た(二)に対し、−C
1その裏面lll1目こAtベース)・層(1)′ を
スクリーン印bill して(ホ)のtil+ <なし
、当該ベース1の溶媒を千備1111熱により蒸発させ
た後、空気中にて填:II9.するのである。
1, but in the same θ, (I) (I:I) or (I) of the above method.
A) (B) and 1゛< are the same, then ll'il l1
11X1~min +11゛ layer only hill removed, then euq)
In contrast to (2), which removed the tree oxidation on the front and back surfaces, -C
1. On the back side of the base 1), screen mark the layer (1)' and til + <None. After evaporating the solvent of the base 1 with Senbi 1111 heat, fill it in air. :II9. That's what I do.

この焼成処理によって、Atペーストは裏面11+ll
 ノn ’ 層を突き破ってI)型シリコンウェハの1
)層に拡11(シて7Jき、この結果同図(へ)に示す
通り、I’1IVi+仁隣接1−、た1トド層を形成す
ることができるのであり、このようにしてn”’ P 
 I’+接合となるT3 S l・”化処理を進行させ
、この際T、) −1層の面にはA、 1ペー スト酸
化層(21′ が形成される0 次でこのΔtペースト酸化層(21′  をII (:
 t、Na011溶液にて除去し、得られた(1・)に
71シて、¥5面屯極f31’ 、表面?l(極t41
’、ハンダ層tr+# tr、+///そして反射時1
11模(6)′が形成されて行く(勇(IJlG)の1
稈は1)iI記JJ法と同]2である。
By this baking process, the At paste becomes 11+ll on the back side.
1 of the I) type silicon wafer by breaking through the non' layer.
) layer is expanded by 7J, and as a result, as shown in the same figure (f), it is possible to form a layer of I'1IVi + adjacent 1-, t1, and in this way n"' P
At this time, this Δt paste oxidation process is carried out to form an I'+ junction, and this Δt paste oxidation layer (21') is formed on the surface of the T,)-1 layer. Layer (21' to II (:
t, removed with Na011 solution, 71 points on the obtained (1.), ¥5 surface polarity f31', surface? l (pole t41
', solder layer tr+# tr, +/// and 1 when reflected
11 models (6)' are formed (Yu (IJlG)'s 1
The culm is 1) iI same as JJ method] 2.

−[、記のA、 tペーヌトによるB S+”化入隅電
池の製造によilげ、Ail方法の如<n”  層の#
!’n1部分除にL稈が省略され、これにより可成りそ
の一作猶時間を短縮することができるもの\、や(iす
5I02の除去とAtペ−〕1酸重層化21′ の除去
とが必要であるだけでなく、Ag、Ti−Ag′4fを
用いての電極形成が不可欠であるため、作急性の向にに
も限度があり、かつ屯イ販j1ぞ成のために貴金属が用
いられるため前価な入隅’flL iffとなる点につ
いての改善(、、tなされていない。
- [, A of the above, according to the production of B S+'' layer cells by t paint, # of the <n'' layer according to the Ail method.
! The L culm is omitted in the 'n1 partial removal, which can considerably shorten the time required for one crop. Not only is it necessary, but it is also essential to form electrodes using Ag or Ti-Ag'4f, so there is a limit to how quickly they can be made, and precious metals are not used for the purpose of local sales. Improvements have not been made regarding the point where the input corner 'flLiff' becomes a predetermined value.

本発明は上記の如き問題点に忽み、Atべ−スト印刷後
の焼成処理によって、I)十層を形成すると共に、当該
Atペースト尼1によってAt。
In view of the above-mentioned problems, the present invention forms 1) 10 layers by a firing process after At base printing, and at the same time, the At paste layer 1 forms At.

裏面宙、極が116成されるようにし、しがも、ノリー
rン酸化IF・3とAtペースト酸化層の除去を同時(
C?1ない?IFるようにして、111記従来法の介意
を解消し、ようとするもので、その!待機とするところ
は、117(4)シリ7ンウェハに対して燐等(こよる
1広ft’<り匹丁甲褒J+i!iずこと(こより、当
月1ンエハの全表面にノリーIン酸化11%’jでDゎ
〕したn ” 層5:)ヒ成1〜、当該「1)層の周側
部分を除ノてして、同I+ ”層の裏面部分にAtベー
ストを印111すし、これを′;3気中にて焼1j’2
.することにより、Atベーストを、シリ−ノン酸化+
1ttH111罎−Piの裏面部分から前記ll型シリ
:7ンウエハの11層に拡11(させ■臼層をIte 
;Iv、 、l Z、 c トT、1111)I)I 
接合とするI(St”化処理%h?+“ない、仁れによ
ってP+層に41着されたM記A /−ペーフ日仁よる
At裏面電極を残仔彫成ぜ17め、次にこれを弗化水素
溶液にてエツチング処Jlp 、−4ろこと((Lす、
−1L記八を裏面電極47) 45面に11(成さJl
ているAtペースト酸化層と、n11記シリ:jン酸化
膜とを除去して、当該At裏面電極と11−ト層の表n
+i i“i1X分を一箸Vさせ、当該表面1115分
(仁は表面屯4i@を常法に上り形成1することにある
On the back side, the electrode was formed at 116, and the Noreen oxidation IF-3 and the At paste oxide layer were removed at the same time (
C? Isn't there 1? This is an attempt to eliminate the intervention of the conventional law in Article 111 by making it IF. On standby, 117 (4) silicon 7 wafers are oxidized with phosphorus, etc. n'' layer 5 with Dゎ] of 11%'j:) Remove the peripheral part of the layer 1~, and mark the At base on the back side of the layer 111. , Bake this in the air for 1j'2
.. By doing so, the At base is converted into silicon-non oxidized +
1ttH111 - Expand the 11 layer from the back side of the Pi to the 11 layers of the 7-inch wafer.
;Iv, ,l Z, c トT, 1111)I)I
I (St) processing to be bonded %h? was etched with a hydrogen fluoride solution.
-1L record 8 to back electrode 47) 11 (made Jl) to 45th side
The At paste oxide layer and the silicon oxide film of n11 are removed, and the At back electrode and the surface of the 11-t layer are removed.
+i i "i1X minute is made one chopstick V, and the said surface 1115 minutes (Jin is to climb the surface tun 4i@ in the usual manner and form 1.

本発明を1133図に示ずL稈説明図C仁よってliT
細t細説C説示ば、例えば同図(イ)の妬く直径3イン
チ、厚す:(OOμn+slΩαのll型シリコンウェ
ハを用aル、従来例の如く燐拡散に上って同図(に)の
よ月こ、当該ウェハの↑而にゎたり11+層を形成する
のであり、この際形成さiまたn+flの面抵抗は5o
Ω、/、  、 I¥さは02μ??+であった。
The present invention is not shown in Figure 1133, but is shown in Figure 1.
For example, using a silicon wafer with a diameter of 3 inches and a thickness of (OOμn+slΩα) as shown in the same figure (A), phosphorus is diffused as in the conventional example. Noyotsuki forms an 11+ layer on the ↑ side of the wafer, and at this time, the sheet resistance of the formed layer i and n+fl is 5o.
Ω、/、、I¥さは02μ? ? It was +.

イして上記拡1枚処理により、そのn’ I(’Iiは
5102であるシリコン酸化h′つにより覆ゎ)するこ
と\なるが、次1.稈では当該1’l ’1  層の周
側部分だけを従来例と同じく化学エツチング、柄挿研磨
等の1段により除去し、て、同図()うの状態とする。
Then, by the above-mentioned enlarging process, the n'I ('Ii is covered with silicon oxide h' which is 5102) is formed, but the following 1. In the culm, only the circumferential portion of the 1'l'1 layer is removed by one step of chemical etching, handle polishing, etc., as in the conventional example, resulting in the state shown in FIG.

さらにに)に示ず[稈番こあって、n”Kの裏面部分す
なわち、そのシリコン酸化層面にAtペースト層Aを、
スクリーン印刷するのであるが、このν□111J2川
したす1該ベースI・としては、200〜300メツシ
ユの−fルミニウム粉であす、印11i!lにより?:
tらi?たぞのlb21rfit 80〜] 20μm
と+iJ戒りjワく形成しておき、印11i11後は2
00℃程度で10〜15分間、予備IJ11熱すること
で溶媒を蒸発させておく。
Furthermore, (not shown in ) [there is an At paste layer A on the back surface of n''K, that is, on the silicon oxide layer surface,
I am going to screen print this ν□111J2 River Shitasu 1 The base I is 200 to 300 mesh of -f luminium powder, marked 11i! By l? :
tra i? Tazo's lb21rfit 80~] 20μm
And +iJ commandment jwawa form, after mark 11i11 is 2
The solvent is evaporated by heating the preliminary IJ11 at about 00°C for 10 to 15 minutes.

さらに1−記のものを、空気中にて825℃〜875℃
の温度、望ましくは850℃にて4〜6分間焼成ずろ〇 この焼成17.lj処理こよって、A /、ベース]・
は裏面部 0)11に13ける5i02、n  層を突き破って、
■)欅」シリ:1ンウエハのP層に拡散して行き、この
結束同図の(ホ)ICiJt ’4−通り、P層に隣接
したP +に’i S: 1141にづ−るこhができ
るのであり、かくして1111・ (ン 接合と斤る1
3 S F化処理が4A行するが、本発明てはAtペー
スト層Aが、すべて118 F fじに消費されてしオ
うのではなく、P+層に隣接してへtベース1層へによ
るAt裏面電極Δ′が残存形1)見されるのであり、こ
の際At裏面電極A′の面にはAtべ〜スト酸化層Δ“
が形成さiする。
Furthermore, 825°C to 875°C in the air
17. Baking at a temperature of 4 to 6 minutes, preferably 850°C. Due to lj processing, A/, base]・
Breaks through the back surface 0) 11 to 13 5i02, n layer,
■) Keyaki's silicon: Diffuses into the P layer of the 1-n wafer, and as shown in the same figure, it spreads to the P + adjacent to the P layer as shown in the same figure. Thus, 1111.
3 SF processing is performed in 4A rows, but in the present invention, the At paste layer A is not completely consumed as 118 F f, but is instead consumed in one layer adjacent to the P+ layer. The At back electrode Δ' can be seen in the residual form 1), and at this time, an At base oxide layer Δ" is formed on the surface of the At back electrode A'.
is formed.

次に上記の(ホ)につきrt ト’エツチング処理を施
すのであるが、これには50%の弗化水素水溶液に約1
0分間浸漬すればよく、当該処理により表面側のSiO
□ と裏面側に残存するSiO□とがll′I!失され
るだけでなく、Atは両性金属で酸、アルカリの双方と
灰地、するから、II P+こ」、すΔLベースト酸化
層A”も除去されることになる。
Next, regarding (e) above, an RT etching process is performed, which involves adding approximately 1.
It is sufficient to immerse for 0 minutes, and this treatment removes the SiO on the surface side.
□ and SiO□ remaining on the back side are ll'I! In addition to being removed, since At is an amphoteric metal and reacts with both acids and alkalis, the oxide layer based on ΔL is also removed.

面上記エツチング処理によるA4ペースト酸化層A ”
の除去を、より完全なものとするたぬ、さらに約5分間
稈度超?1波洗浄処理を行なうようにするのが望ましく
、これによってAt裏面11極八′の面と11−1 層
の表面部分にあ・(Jる而とが謹聴され、(へ)−こ示
ずものが得られる。
A4 paste oxide layer A” by etching process above the surface
To make the removal more complete, leave the culm for about 5 minutes. It is desirable to perform a single-wave cleaning process, so that the surface of the At back surface 11 pole 8' and the surface area of the layer 11-1 are carefully cleaned, and the You can get something.

次で」−記n ”層の表面部分に、常法に↓す1’ i
 −A gによる表面電極13を形成し、さらに図示例
では、At裏面亀@A’ と表面電極13とに鍍金属c
、c’ を夫々施すようにしており、こハ、にはバッグ
メツ”t、Znゾソキ、SnメツA雪かbf滴で1V、
す、ハングメ゛ツキをh(口せハAt裏面電極の+l1
il fl’!−1’i i向十できるとj+、に、直
列抵lI+5−・1・さくてき、7,11メツキの場合
には、さらに+TI+4候性を1着火L TOること\
な粋、S nメッキで+:iバッグ(11−1かb1能
lため太陽電池の接続時(C1その作!i4 (’1.
がよくなる。
Next, write 1'i on the surface of the layer in the usual manner.
-A surface electrode 13 is formed by A g, and furthermore, in the illustrated example, the At back surface @A' and the surface electrode 13 are plated with metal c.
, c' are applied respectively, and in this case, 1V is applied with bag mettsu't, Zn soki, Sn mettsu A snow or bf drops,
Then, set the hang plate to +l1 of the back electrode.
il fl'! -1'i If it is possible to move towards i, then to j+, the series resistor lI+5-・1・cut, and in the case of 7,11 plating, further add +TI+4 weatherability to 1 ignition L TO\
Nice, S n plating +: i bag (11-1 or b1 function) when connecting solar cells (C1 work! i4 ('1.
gets better.

尚表面’H’h +4 +3についてはi)(全処理で
はなく、−Yイ、ノビン法(こよりハンダを(1着でき
乙ので、回fJぐ+r−J−リハ7・ダ1A7i ’;
7形成4−ろ、にうにしで噂、よく、さ1−1ic・仔
9yに1芯[5従来法と同1つく表面電極1λにji 
”、tt防+t、 lj’、+4 l) f 11ic
ずようにし妹ものか、同図(ト)(こ7I:されている
As for the surface 'H'h +4 +3, i) (not all processing, -Y, Novin method (soldering from this) (because one piece can be soldered, 1A7i');
Rumor has it that 7 formation 4-ro, 2 sea urchins, 1 core for 1-1ic, 1 core for 9y [5 same as the conventional method, 1 surface electrode 1λ for ji]
", tt defense + t, lj', +4 l) f 11ic
Is it a younger sister or something like that?

奉イ色明け1−ふ: fD i屯り、Atペースト層八
へS l(,12のl二からIt −i  層(こ印刷
して焼]y、するようbT、 L斤から、広い而Jul
にわたってのII−’層のドロア去1稈をイて要に−4
ろことができ、これ(こよつでiij成l)のイ′ll
!l′、時間台′f5.−縮できるだ(・Jでなく、I
Q ++7.によるH S t’化処理を施すことに1
つτpH,・i %: ij)ると同時に、Δl裏面T
往極A′忙も形成してし1つようにしたから、改めてA
g。
1-F: From fD i to At paste layer 8, S l (, 12 l2 to It -i layer (print and bake) y, so that bT, from L loaf, wide Jul
After removing the 1st culm of the II-' layer, the main point is -4.
I'll be able to do this, and I'll be able to do this.
! l', timetable'f5. -It can be reduced (I, not J)
Q++7. 1 to perform H S t' processing by
τpH,・i %: ij) At the same time, Δl back surface T
Since I had already formed the last A′ busy, I decided to write A again.
g.

TiAg等+1.1: /:+ ni fi+7) 7
i M I稈’fr: Jilfj ス’II 9もな
くなり、この結果作業時間の短縮はもとより、使用され
る質相からも、その(R: +jl−化を図ることかで
きろ。
TiAg etc.+1.1: /:+ ni fi+7) 7
i M I culm'fr: Jilfj Su'II 9 will also be eliminated, and as a result, not only will the work time be shortened, but also from the quality used, it will be possible to make it (R: +jl-).

さら1こまたS i O□ とA1ベースI・榮″化層
A ”との除九をII Fにより ・度にTiなうより
にしたので、この点からも作業1−稈の簡易化と能率向
上が実現できること\なり、実際−)〕第1図の方法I
Cよるときは40枚72時間:ろ0分、弔21ン10ノ
5法では40枚、/1時間のtt(・1であったものか
、40枚/ :30分となった0 また本発明によって得られた製品につき、その l−V
 ’に性力\ら、 その’D、) 4’6 Iu Ml
、 開1jK ’t’lf、 lj−、%求めtところ
、F表のη+1<第2図のJ〕法による製品よりく5、
優れた特性を示し、また1、稈の1′簡略化(こも拘ら
ず第1図の方法による製品と同℃もしくはそれり−1−
の結果を得ることかできたO尚i)ij記したノ・ンダ
鍍金1C」、りへl裏面電極をジノル[7たものにつき
、90℃、湿度1 (1(1%による(i1頼性試験f
、 200時間行なった結果、異常は認められなかった
In addition, the division of S i O Efficiency improvement can be achieved \Actually-)〕Method I in Figure 1
According to C, 40 sheets 72 hours: 0 minutes, in the funeral 21-10-5 method, 40 sheets, / 1 hour tt (・1, 40 sheets / : 30 minutes 0. For the product obtained by the invention, its l-V
'ni sexual power\ra, so'D,) 4'6 Iu Ml
, Open 1jK 't'lf, lj-, % tWhere, from the product by the method η+1 in F table <J in Figure 2] 5,
It exhibits excellent properties, and also 1. 1' simplification of the culm (despite this, the temperature is the same or lower than that of the product produced by the method shown in Figure 1).
I was able to obtain the results of the following results.I) The back electrode was heated to 90°C and the humidity was 1% (by 1% (i1 reliability). exam f
After 200 hours of testing, no abnormalities were found.

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

第1図はA /、 l’!空蒸H+コ、t:るB S 
F化’r’ i −Ag 71を極入隅i1i、池の製
造l稈説明図、第2図はへLベースト印11i111こ
↓る+38 +”化”L’ i −A g電イ七太陽電
池の製造1.稈説明図、第:3図は本発明ic係る太陽
電池の製造I稈説明図である〇八 ・・・・・Δtベー
スl一層 A′ ・・・・・A、 を裏面?lHf1A″ ・−・
−・Atペースト酸化11/i■3  ・・・・・表面
電極 特許出願人 代理人 弁理1  月 爪6   誠 第1図   第2図 第3図 395−
Figure 1 shows A/, l'! Air steam H + Ko, t:ru B S
F conversion 'r' i -Ag 71 is placed in the corner i1i, Pond production l culm explanatory diagram, Figure 2 is L base mark 11i111 ↓ + 38 + "Cation"L' i -A g electric seven suns Manufacturing of batteries 1. Culm explanatory diagram, Figure 3 is an explanatory diagram of I culm for manufacturing a solar cell according to the present invention. lHf1A″・−・
-・At paste oxidation 11/i■3...Surface electrode patent applicant's attorney Patent attorney 1 Month Nail 6 Makoto Fig. 1 Fig. 2 Fig. 3 395-

Claims (1)

【特許請求の範囲】 (II  +1 +ll++シリニ]ンウ「ハ(こ燐、
ボロン等による拡11(処理をIjiliずこと1仁よ
り、当該ウェハの全表面にシリコン酸化11≧で伯われ
た11+層を形成し、当該■1一層の周側部分を除去し
て、同111層の裏面部分子こAtペーストを印16す
し、これを空気中(こて焼成することにより、Atペ−
]ltシリコン酸化膜、111  層の裏面部分から前
記“1)型シリコンウェハのP層に拡散さぜ1)1  
層’tl杉1況することで、ロー1−  p  p ト
接合とする+3 S F比処理を行ない、これに上ッテ
l”−’ 層に11着された前記Atペーストニ」、る
Δl裏面電極を残存形成せしめ、次にこfL、%:弗化
水素溶71々にてエッヂング処理することにより、ヒ記
A、 を裏面電極の表面に形成さ:h テイルへlベー
スi・酸化病と、前記シリコン酸化1トキとを除ノ、し
て、当該At裏面電イ賑とを常法に5しり形成したこと
を特徴とする太陽電池の製造1ノ法。 (2)  弗化水累溶1(1,+こよろエソイング処理
の後に、J、71音波洗滌を施して、Atベース1酸化
層の除去を補完させるよりにしたことを4’!l′徴と
する特+i’F 、llI!求の範囲第1項記載の太陽
111.池の製J2r力法。 +31AA裏面電極に、ハンダ、Zn、S n等による
鍍金処理が施される特i′1.!I11求の範囲;1〜
1項記載の太陽電池の製造方法。
[Scope of Claims] (II +1 +ll++Sirini)
An enlarged 11+ layer with silicon oxide 11≧ is formed on the entire surface of the wafer using boron, etc., and the peripheral part of the 11 layer is removed. Mark 16 pieces of molecular At paste on the back side of the layer and heat it in the air (by firing it with a trowel).
]lt silicon oxide film, 111 Diffusion from the back side of the layer to the P layer of the "1) type silicon wafer1)1
By forming the first layer, a +3 SF ratio treatment is performed to form a low 1-pp joint, and on top of this, the above-mentioned At paste is applied to the 11th layer, and the back surface of the Δl After the electrode is formed and then etched with a hydrogen fluoride solution, marks A and A are formed on the surface of the back electrode. , the silicon oxide layer is removed, and the At back surface electrode layer is formed in a conventional manner. (2) After the fluoride water cumulative solution 1 (1, + Koyoro Esoing treatment), J, 71 sonic cleaning was performed to complement the removal of the At-based 1 oxide layer. The special +i'F, llI! Range of requirements The Taiyo 111. Ike's J2r force method described in item 1. The special i'1 where the +31AA back electrode is plated with solder, Zn, Sn, etc. .!I11 Search range; 1~
A method for manufacturing a solar cell according to item 1.
JP57143022A 1982-08-18 1982-08-18 Manufacture of solar battery Granted JPS5932179A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57143022A JPS5932179A (en) 1982-08-18 1982-08-18 Manufacture of solar battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57143022A JPS5932179A (en) 1982-08-18 1982-08-18 Manufacture of solar battery

Publications (2)

Publication Number Publication Date
JPS5932179A true JPS5932179A (en) 1984-02-21
JPH023310B2 JPH023310B2 (en) 1990-01-23

Family

ID=15329094

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57143022A Granted JPS5932179A (en) 1982-08-18 1982-08-18 Manufacture of solar battery

Country Status (1)

Country Link
JP (1) JPS5932179A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4703553A (en) * 1986-06-16 1987-11-03 Spectrolab, Inc. Drive through doping process for manufacturing low back surface recombination solar cells
DE19758712B4 (en) * 1996-12-20 2007-02-15 Mitsubishi Denki K.K. Silicon solar cell or semiconductor device production - involves electrical separation of p-n junction using glass-based material
JP2007201007A (en) * 2006-01-24 2007-08-09 Sharp Corp Photoelectric conversion element
EP1906455A1 (en) * 2005-06-22 2008-04-02 Kyocera Corporation Solar cell element and solar cell element manufacturing method

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4703553A (en) * 1986-06-16 1987-11-03 Spectrolab, Inc. Drive through doping process for manufacturing low back surface recombination solar cells
DE19758712B4 (en) * 1996-12-20 2007-02-15 Mitsubishi Denki K.K. Silicon solar cell or semiconductor device production - involves electrical separation of p-n junction using glass-based material
EP1906455A1 (en) * 2005-06-22 2008-04-02 Kyocera Corporation Solar cell element and solar cell element manufacturing method
EP1906455A4 (en) * 2005-06-22 2010-12-01 Kyocera Corp Solar cell element and solar cell element manufacturing method
JP2007201007A (en) * 2006-01-24 2007-08-09 Sharp Corp Photoelectric conversion element

Also Published As

Publication number Publication date
JPH023310B2 (en) 1990-01-23

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