JPH06263442A - Production of powdery agins2 and agins2 film - Google Patents

Production of powdery agins2 and agins2 film

Info

Publication number
JPH06263442A
JPH06263442A JP5079014A JP7901493A JPH06263442A JP H06263442 A JPH06263442 A JP H06263442A JP 5079014 A JP5079014 A JP 5079014A JP 7901493 A JP7901493 A JP 7901493A JP H06263442 A JPH06263442 A JP H06263442A
Authority
JP
Japan
Prior art keywords
powder
agins
film
agins2
heat treatment
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.)
Withdrawn
Application number
JP5079014A
Other languages
Japanese (ja)
Inventor
Keiichiro Uenae
圭一郎 植苗
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.)
Maxell Holdings Ltd
Original Assignee
Hitachi Maxell 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 Hitachi Maxell Ltd filed Critical Hitachi Maxell Ltd
Priority to JP5079014A priority Critical patent/JPH06263442A/en
Publication of JPH06263442A publication Critical patent/JPH06263442A/en
Withdrawn legal-status Critical Current

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Classifications

    • 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
    • Y02E10/541CuInSe2 material PV cells

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  • Surface Treatment Of Glass (AREA)
  • Photovoltaic Devices (AREA)

Abstract

PURPOSE:To provide powdery AgInS2 and an AgInS2 film useful as the material of a photoelectric conversion element of a solar cell, etc. CONSTITUTION:Powdery silver or powdery silver sulfide is mixed with powdery indium or powdery indium sulfide and powdery sulfur and the resulting mixture is heat-treated to produce the objective rowdery AgInS2 powder. This powdery AgInS2 is impasted by mixing with a solvent and the resulting pasty mixture is applied on a substrate and heat-treated to produce the objective AgInS2 film.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は、太陽電池に代表される
光電変換素子の材料として使用されるAgInS2 (銀
インジウム硫化物)の粉末およびその膜の製造方法に関
する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a powder of AgInS 2 (silver indium sulfide) used as a material for a photoelectric conversion element represented by a solar cell and a method for producing a film thereof.

【0002】[0002]

【従来の技術】光電変換素子に使用される半導体材料
は、一般にチョクラルスキー法や引上げ法などに代表さ
れる結晶成長法によって製造されてきた。
2. Description of the Related Art Semiconductor materials used for photoelectric conversion elements have generally been manufactured by a crystal growth method represented by the Czochralski method and the pulling method.

【0003】これは、CuInSe2 、AgInS2
どに代表されるI−III−VI属材料についても同様
であり、例えば“1992年秋季応用物理学会予稿集
p.1125”によれば、何件かの固相結晶成長法の試
みが報じられている。
This also applies to I-III-VI group materials represented by CuInSe 2 , AgInS 2 and the like. For example, according to "Autumn Society of Applied Physics, 1992 Proceedings, p. 1125", there are several cases. The solid phase crystal growth method has been reported.

【0004】しかし、それらは、いずれも、結晶の成長
条件の抑制を厳密にしなければならなかったり、ワンバ
ッチで製造できる量が少なかったりで、実用化がむつか
しいという問題があった。
However, each of them has a problem that it is difficult to put them into practical use because it is necessary to strictly control the growth conditions of crystals and the amount that can be produced in one batch is small.

【0005】また、特開昭64−64369号公報に
は、各成分粉末または化合物を機械的に混合することに
よってCuInSe2 粉末を得ることが報告されてい
る。しかし、それはCuInSe2 に限られていて、A
gInS2 についてはまったく触れられておらず、した
がって、AgInS2 については実用性に優れた製造方
法が確立されていない。
Further, Japanese Patent Laid-Open No. 64-64369 reports that CuInSe 2 powder is obtained by mechanically mixing each component powder or compound. However, it is limited to CuInSe 2 and
not mention at all about the GINS 2, therefore excellent production method for practical use has not been established for AgInS 2.

【0006】[0006]

【発明が解決しようとする課題】本発明は、従来のAg
InS2 の製造方法における問題点を解決し、生産性の
優れたAgInS2 粉末およびAgInS2 膜の製造方
法を提供することを目的とする。
The present invention is based on the conventional Ag method.
It is an object of the present invention to solve the problems in the method for producing InS 2 and to provide a method for producing an AgInS 2 powder and an AgInS 2 film having excellent productivity.

【0007】[0007]

【課題を解決するための手段】本発明は、Ag(銀)粉
末またはAg硫化物粉末と、In(インジウム)粉末ま
たはIn硫化物粉末と、硫黄粉末とを混合し、得られた
混合物を熱処理することによってAgInS2 粉末を製
造し、また得られたAgInS2 粉末を溶剤と混合して
ペースト状にし、そのペースト状混合物を基板上に塗布
し、熱処理することによってAgInS2 膜を製造する
ことにより、上記目的を達成したものである。
According to the present invention, Ag (silver) powder or Ag sulfide powder, In (indium) powder or In sulfide powder, and sulfur powder are mixed, and the resulting mixture is heat treated. by manufacture AgInS 2 powder, also AgInS 2 powder was mixed with a solvent into a paste, coating the paste mixture onto a substrate to produce a AgInS 2 film by heat treatment by The above-mentioned object is achieved.

【0008】上記製造方法を詳細に説明すると、AgI
nS2 粉末の製造にあたっては、まず、各成分を製造し
たいAgInS2 の組成と同一組成になるように秤量
し、それらを混合する。その際の混合方法としては、あ
る程度のエネルギーを有する方法でないと充分に均一な
混合が行なわれず、熱処理による合成が円滑に進行しな
くなるので、ボールミルやサンドミルなどの機械的な混
合方法を採用することが好ましい。
The above manufacturing method will be described in detail.
In producing the nS 2 powder, first, each component is weighed so as to have the same composition as AgInS 2 to be produced, and they are mixed. As a mixing method at that time, unless the method has a certain amount of energy, sufficiently uniform mixing cannot be performed, and the synthesis by heat treatment will not proceed smoothly.Therefore, use a mechanical mixing method such as a ball mill or a sand mill. Is preferred.

【0009】混合時の回転速度を一定にすると、混合時
間に伴って混合物の粒径は小さくなるので、混合時間は
長いほどよいが、通常は50〜200時間程度が採用さ
れる。
If the rotation speed during mixing is kept constant, the particle size of the mixture becomes smaller with the mixing time, so the longer the mixing time is, the better, but usually about 50 to 200 hours is adopted.

【0010】混合直後の粉末はAgInS2 以外にAg
In5 8 が生成していたり、In硫化物が残存してい
ることがあるが、それらは次の熱処理によって消滅す
る。
Immediately after mixing, the powder was AgInS 2 as well as Ag.
In 5 S 8 may be generated or In sulfide may remain, but they disappear by the next heat treatment.

【0011】熱処理時の温度は高温になるほどAgIn
2 の合成に好適となり、700℃以上ではX線回折に
よってもAg硫化物、In硫化物、AgIn5 8 など
がまったく観察されなくなり、通常700〜850℃程
度の温度で熱処理される。また、熱処理時間は熱処理温
度にもよるが1〜10時間程度が好ましい。
As the temperature during heat treatment increases, the AgIn
It is suitable for the synthesis of S 2 , and Ag sulfide, In sulfide, AgIn 5 S 8 and the like are not observed at all by X-ray diffraction at 700 ° C. or higher, and heat treatment is usually performed at a temperature of 700 to 850 ° C. The heat treatment time is preferably about 1 to 10 hours, though it depends on the heat treatment temperature.

【0012】そして、この熱処理は、AgInS2 やそ
の原料成分の酸化を防止するために、例えばN2 (窒
素)雰囲気、H2 (水素)雰囲気、あるいはAr(アル
ゴン)雰囲気などの不活性ガス雰囲気など、酸素を含ま
ない雰囲気中で行なうのが好ましい。
In order to prevent the oxidation of AgInS 2 and its raw material components, this heat treatment is carried out in an inert gas atmosphere such as N 2 (nitrogen) atmosphere, H 2 (hydrogen) atmosphere or Ar (argon) atmosphere. It is preferable to carry out in an atmosphere containing no oxygen.

【0013】AgInS2 の製造にあたり、Ag(銀)
成分としてはAg粉末またはAg硫化物粉末が用いられ
るが、そのAg硫化物としては例えばAg2 Sなどが挙
げられる。また、In(インジウム)成分としてはIn
粉末またはIn硫化物粉末が用いられるが、そのIn硫
化物としては例えばInS、In2 3 などが挙げられ
る。
In manufacturing AgInS 2 , Ag (silver)
Ag powder or Ag sulfide powder is used as the component, and examples of the Ag sulfide include Ag 2 S and the like. In addition, as the In (indium) component, In
Powder or In sulfide powder is used, and examples of the In sulfide include InS and In 2 S 3 .

【0014】Ag粉末またはAg硫化物粉末と、In粉
末またはIn硫化物粉末と、硫黄粉末との混合割合は、
化学量論的にAgInS2 になるのが最も適正である
が、10%程度ずれてもよい。
The mixing ratio of Ag powder or Ag sulfide powder, In powder or In sulfide powder, and sulfur powder is
The most suitable is stoichiometrically AgInS 2 , but it may be shifted by about 10%.

【0015】上記のようにして得られたAgInS2
末を用いてのAgInS2 膜の製造は、上記AgInS
2 粉末に適当な溶剤、例えばプロピレングリコールなど
を加えて混合してペースト状にし、そのペースト状混合
物を例えばガラス板、Al23 セラミックスなどに代
表されるように700℃以上で成分がAgInS2 に拡
散しない基板上にスクリーン印刷法などにより塗布し、
熱処理することによって行なわれる。そして、基板上に
形成されたAgInS2 は基板から剥がして使用に供し
てもよいし、また基板上に形成した状態でその基板と共
に使用に供してもよい。
The AgInS 2 film is produced by using the AgInS 2 powder obtained as described above.
2 powder in a suitable solvent, for example, mixed with the propylene glycol to form a paste, the paste mixture, for example a glass plate, Al 2 O 3 component 700 ° C. or higher, as typified by ceramics AgInS 2 It is applied by a screen printing method on a substrate that does not diffuse into
It is performed by heat treatment. The AgInS 2 formed on the substrate may be peeled off from the substrate for use, or may be formed on the substrate for use together with the substrate.

【0016】上記溶剤との混合にあたってAgInS2
粉末は、粒径が小さいほどペースト状混合物の塗布性が
良好になり、平均粒径5μm以下になると平滑な塗布膜
が得られるようになる。
In mixing with the above solvent, AgInS 2
The smaller the particle size of the powder, the better the coatability of the paste mixture, and when the average particle size is 5 μm or less, a smooth coating film can be obtained.

【0017】塗布後の熱処理は、AgInS2 と基板と
の密着性を高めたり、AgInS2を焼結させて膜強度
を高めるためのものであるが、この塗布後の熱処理温度
がAgInS2 粉末製造時の熱処理温度より高い場合は
AgInS2 が結晶成長して粒子形状が大きく変化し膜
内応力が大きくなって膜剥がれが生じるようになるた
め、塗布後の熱処理温度はAgInS2 粉末の製造時の
熱処理温度以下、つまりAgInS2 粉末製造時の熱処
理温度と同温かまたはそれより低い温度であることが必
要である。
The heat treatment after coating is intended to enhance the adhesion between AgInS 2 and the substrate or to sinter AgInS 2 to enhance the film strength. The heat treatment temperature after coating is the AgInS 2 powder production. If the temperature is higher than the heat treatment temperature at that time, the crystal growth of AgInS 2 causes a large change in the particle shape and the stress in the film increases, causing film peeling. Therefore, the heat treatment temperature after coating is the same as that at the time of manufacturing AgInS 2 powder. It is necessary that the temperature is equal to or lower than the heat treatment temperature, that is, the same as or lower than the heat treatment temperature at the time of producing the AgInS 2 powder.

【0018】この塗布後の熱処理温度、つまりAgIn
2 膜製造時の熱処理温度は700℃以上であることが
好ましく、また基板が熱に耐え、かつAgInS2 粉末
製造時の熱処理温度以下であることが必要である。そし
て、この際の熱処理時間としては1〜10時間が好まし
い。
The heat treatment temperature after coating, that is, AgIn
The heat treatment temperature during the production of the S 2 film is preferably 700 ° C. or higher, and it is necessary that the substrate withstand the heat and be equal to or lower than the heat treatment temperature during the production of AgInS 2 powder. The heat treatment time at this time is preferably 1 to 10 hours.

【0019】上記したようなAgInS2 粉末やAgI
nS2 膜の製造方法によれば、混合に用いるミル(混合
装置)や熱処理装置は容易に大型化でき、またAgIn
2膜の形成にあたってのスクリーン印刷などが固相結
晶成長法による場合のスパッタリングなどの乾式膜形成
方法とは異なり設備が簡単で、生産性に富んでいるの
で、その結果として、安価なAgInS2 粉末やAgI
nS2 膜を提供することができる。
As described above, AgInS 2 powder and AgI
According to the nS 2 film manufacturing method, the mill (mixing device) and the heat treatment device used for mixing can be easily increased in size, and AgIn
Unlike the dry film forming method such as sputtering in which the solid-phase crystal growth method is used for the screen printing for forming the S 2 film, the equipment is simple and the productivity is high. As a result, the inexpensive AgInS 2 film is formed. Powder and AgI
An nS 2 film can be provided.

【0020】上記のようにして得られたAgInS2
末やAgInS2 膜は、主として光電変換素子の材料と
して用いられるが、同じ3元系のCuInS2 などに比
べると融点が870℃と低いため(CuInS2 は10
90℃)、低温で加工しやすいというメリットがある。
The AgInS 2 powder or AgInS 2 film obtained as described above is mainly used as a material for a photoelectric conversion element, but its melting point is 870 ° C. lower than that of the same ternary CuInS 2 ( CuInS 2 is 10
90 ° C), which has the advantage of being easy to process at low temperatures.

【0021】また、現在盛んに研究されているp型Cu
InSe2 との積層として太陽電池を形成する場合、C
uInS2 がp型、n型のコントロールがむつかしいの
に対して、AgInS2 は良好なn型を示すというメリ
ットがあり、またバンドキャップの点からもCuInS
2 の1.1eVと最も高効率が期待される1.7〜
1.9eVのバンドキャップ(AgInS2 は1.9e
V)を有しており、同じAg系のAgInSe2 (1.
2eV)、AgGaS2 (2.8eV)に比べても有利
である。
Further, p-type Cu, which is currently being actively studied,
When forming a solar cell as a stack with InSe 2 , C
UInS 2 is p-type, whereas the n-type controls are Mutsukashii, there is a merit that AgInS 2 shows a good n-type, also in terms of band gap CuInS
The highest efficiency of 1.1 eV of e 2 is expected to be 1.7 to
1.9 eV band cap (AgInS 2 is 1.9 eV)
V), and the same Ag-based AgInSe 2 (1.
2 eV) and AgGaS 2 (2.8 eV) are also advantageous.

【0022】[0022]

【実施例】つぎに、実施例を挙げて本発明をより具体的
に説明する。ただし、本発明はそれらの実施例のみに限
定されるものではない。
EXAMPLES Next, the present invention will be described more specifically with reference to examples. However, the present invention is not limited to only those examples.

【0023】実施例1 Ag粉末、In粉末、硫黄粉末をそれぞれ0.05mo
l、0.05mol、0.1mol用意し、それらをボ
ールミル容器に仕込み、該容器をボールミルにセットし
た。100時間混合後、ミルから取り出し、得られた混
合物粉末を乳鉢で軽く粉砕した後、750℃に設定した
2 雰囲気中で2時間熱処理し、熱処理後、乳鉢で再度
粉砕してAgInS2 粉末を得た。
Example 1 Ag powder, In powder, and sulfur powder were each added in an amount of 0.05 mo.
1, 0.05 mol, 0.1 mol were prepared, these were charged in a ball mill container, and the container was set in a ball mill. After mixing 100 hours, removed from the mill, was lightly grinding the mixture powder obtained in a mortar, then heat-treated for 2 hours in a N 2 atmosphere was set to 750 ° C., after heat treatment, the AgInS 2 powder was ground again in a mortar Obtained.

【0024】上記のようにして得られたAgInS2
末を1g秤量し、それを400kg/cm2 の圧力でコ
ールドプレスし、直径8mm、厚さ1mmのAgInS
2 ペレットを得た。
1 g of the AgInS 2 powder obtained as described above was weighed and cold pressed at a pressure of 400 kg / cm 2 to obtain AgInS having a diameter of 8 mm and a thickness of 1 mm.
2 pellets were obtained.

【0025】このAgInS2 ペレットの一方の面に溶
融したIn−Ga(重量比1:1)合金を塗布し、Ag
ペーストでニッケル線を固定し、最後に他面側からガラ
ス基板にエポキシ樹脂で固定した。
Molten In-Ga (weight ratio 1: 1) alloy was applied to one surface of the AgInS 2 pellet to form Ag.
A nickel wire was fixed with a paste, and finally, a glass substrate was fixed with an epoxy resin from the other surface side.

【0026】このようにして得られた半導体電極を用
い、対極には白金板を用い、電解液には0.05mol
/lの水酸化カリウム水溶液を用いてセルを作製した。
The semiconductor electrode thus obtained is used, a platinum plate is used as the counter electrode, and the electrolyte solution is 0.05 mol.
A cell was prepared using a potassium hydroxide aqueous solution of 1 / l.

【0027】光源には300Wキセノンランプを用い、
上記セルに光照射し、その照射時の電流と電圧を測定し
た。その結果を非照射時に測定した電流値および電圧値
と併せて図1に示す。
A 300 W xenon lamp is used as a light source,
The cell was irradiated with light and the current and voltage during the irradiation were measured. The result is shown in FIG. 1 together with the current value and voltage value measured during non-irradiation.

【0028】図1において、「光オン」とは光照射時を
示し、「光オフ」とは非照射時を示すが、この図1に示
すように、+側の同電圧で比較したときの光照射時(光
オン)の電流値は非照射時(光オフ)の電流値より大き
く、得られたAgInS2 粉末を用いて作製した半導体
電極から光電流が取り出せることが判明した。
In FIG. 1, “light on” indicates the time when light is irradiated, and “light off” indicates the time when light is not irradiated. As shown in FIG. 1, when comparing at the same voltage on the + side, The current value during light irradiation (light on) was larger than the current value during non-irradiation (light off), and it was found that a photocurrent can be extracted from the semiconductor electrode manufactured using the obtained AgInS 2 powder.

【0029】なお、得られたAgInS2 の結晶性はX
線回折で調べたところ(121)主配向の斜方晶であっ
た。
The crystallinity of the obtained AgInS 2 is X.
When examined by line diffraction, it was an orthorhombic crystal with a (121) main orientation.

【0030】実施例2 Ag粉末、In粉末、硫黄粉末をそれぞれ0.05mo
l、0.05mol、0.1mol用意し、それらをボ
ールミル容器に仕込み、該容器をボールミルにセットし
た。100時間混合後、ミルから取り出し、得られた混
合物粉末を乳鉢で軽く粉砕した後、800℃に設定した
2 雰囲気中で2時間熱処理し、熱処理後、乳鉢で再度
粉砕してAgInS2 粉末を得た。
Example 2 Ag powder, In powder, and sulfur powder were each added in an amount of 0.05 mo.
1, 0.05 mol, 0.1 mol were prepared, these were charged in a ball mill container, and the container was set in a ball mill. After mixing 100 hours, removed from the mill, was lightly grinding the mixture powder obtained in a mortar, then heat-treated for 2 hours in a N 2 atmosphere was set to 800 ° C., after heat treatment, the AgInS 2 powder was ground again in a mortar Obtained.

【0031】得られたAgInS2 粉末の粒径を測定し
たところ平均粒径4μmであった。このAgInS2
末を4g秤量し、これにポリプロピレングリコールを
0.8ml添加し、充分に混合してペースト状にした。
得られたペースト混合物をスクリーン印刷法によってガ
ラス基板〔Corning7059(商品名)ガラス〕
上に塗布した。
The particle size of the obtained AgInS 2 powder was measured and found to be 4 μm in average particle size. 4 g of this AgInS 2 powder was weighed, 0.8 ml of polypropylene glycol was added thereto, and they were mixed sufficiently to form a paste.
The paste mixture thus obtained was screen-printed onto a glass substrate [Corning 7059 (trade name) glass].
Applied on top.

【0032】塗布膜を焼結させるため、800℃に設定
したN2 雰囲気中で2時間熱処理した。熱処理温度はA
gInS2 の結晶性とガラス基板との密着性を考慮して
決定されるが、本実施例のようにガラス基板としてCo
rning7059(商品名)ガラスを用いた場合には
800℃が最適であった。
In order to sinter the coating film, it was heat-treated in an N 2 atmosphere set at 800 ° C. for 2 hours. Heat treatment temperature is A
It is determined in consideration of the crystallinity of gInS 2 and the adhesiveness with the glass substrate.
When using running7059 (trade name) glass, 800 ° C. was optimum.

【0033】AgInS2 膜の製造にあたって使用した
AgInS2 粉末の結晶構造は(121)主配向の斜方
晶であったが、AgInS2 膜におけるAgInS2
結晶構造は膜製造時の熱処理によって(112)主配向
の正方晶(カルコパイライト構造)に変化していた。
[0033] AgInS 2 crystal structure of AgInS 2 powder used in the production of film was the orthorhombic main orientation (121), the crystal structure of AgInS 2 in AgInS 2 film by heat treatment during film production (112 ) It changed into the tetragonal crystal (chalcopyrite structure) of the main orientation.

【0034】[0034]

【発明の効果】以上説明したように、本発明では、Ag
粉末またはAg硫化物粉末と、In粉末またはIg硫化
物粉末と、硫黄粉末を混合し、得られた混合物を熱処理
することによって、AgInS2 粉末を容易に製造する
ことができるようになった。
As described above, according to the present invention, Ag
By mixing powder or Ag sulfide powder, In powder or Ig sulfide powder, and sulfur powder, and heat-treating the obtained mixture, AgInS 2 powder can be easily manufactured.

【0035】このような本発明の方法によれば、従来の
固相結晶成長法に比べて生産性が優れており、太陽電池
などの光電変換素子用の材料として有望なAgInS2
粉末を安価に提供することができるようになった。
According to the method of the present invention as described above, the productivity is excellent as compared with the conventional solid phase crystal growth method, and AgInS 2 which is promising as a material for photoelectric conversion elements such as solar cells.
The powder can now be provided at low cost.

【0036】また、上記AgInS2 粉末を用いて製造
したAgInS2 膜を光電変換素子に用いることによ
り、太陽電池の最も重要課題である低コストが可能にな
る。
Further, by using the AgInS 2 film produced by using the above AgInS 2 powder for the photoelectric conversion element, it becomes possible to reduce the cost which is the most important issue of the solar cell.

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

【図1】AgInS2 ペレットを用いた半導体電極と、
白金板からなる対極を備え、電解液として0.05mo
l/lの水酸化カリウム水溶液を用いたセルの電流−電
圧特性を示す図である。
FIG. 1 is a semiconductor electrode using AgInS 2 pellets,
Equipped with a counter electrode consisting of a platinum plate, with an electrolyte of 0.05mo
It is a figure which shows the current-voltage characteristic of the cell which used the 1 / l potassium hydroxide aqueous solution.

Claims (8)

【特許請求の範囲】[Claims] 【請求項1】 Ag粉末またはAg硫化物粉末と、In
粉末またはIn硫化物粉末と、硫黄粉末とを混合し、得
られた混合物を熱処理することを特徴とするAgInS
2 粉末の製造方法。
1. Ag powder or Ag sulfide powder and In
Powder or In sulfide powder, and sulfur powder are mixed, and the obtained mixture is heat-treated.
2 Powder manufacturing method.
【請求項2】 混合をボールミルやサンドミルなどの機
械的混合によって行なうことを特徴とする請求項1記載
のAgInS2 粉末の製造方法。
2. The method for producing AgInS 2 powder according to claim 1, wherein the mixing is performed by mechanical mixing such as a ball mill or a sand mill.
【請求項3】 熱処理を酸素を含まない雰囲気中で行な
うことを特徴とする請求項1記載のAgInS2 粉末の
製造方法。
3. The method for producing AgInS 2 powder according to claim 1, wherein the heat treatment is performed in an atmosphere containing no oxygen.
【請求項4】 熱処理を700℃以上で行なうことを特
徴とする請求項1記載のAgInS2 粉末の製造方法。
4. The method for producing AgInS 2 powder according to claim 1, wherein the heat treatment is performed at 700 ° C. or higher.
【請求項5】 請求項1記載のAgInS2 粉末を溶剤
と混合してペースト状にし、そのペースト状混合物を基
板上に塗布し、熱処理することを特徴とするAgInS
2 膜の製造方法。
5. The AgInS 2 powder according to claim 1, which is mixed with a solvent to form a paste, and the paste mixture is applied onto a substrate and heat-treated.
2 Membrane manufacturing method.
【請求項6】 溶剤がプロピレングリコールであること
を特徴とする請求項5記載のAgInS2 膜の製造方
法。
6. The method for producing an AgInS 2 film according to claim 5, wherein the solvent is propylene glycol.
【請求項7】 AgInS2 膜製造時の熱処理温度がA
gInS2 粉末製造時の熱処理温度以下であることを特
徴とする請求項5記載のAgInS2 膜の製造方法。
7. The heat treatment temperature at the time of manufacturing the AgInS 2 film is A
The method for producing an AgInS 2 film according to claim 5, wherein the temperature is not higher than the heat treatment temperature at the time of producing the gInS 2 powder.
【請求項8】 溶剤と混合するAgInS2 粉末の平均
粒径が5μm以下であることを特徴とする請求項5記載
のAgInS2 膜の製造方法。
8. The method for producing an AgInS 2 film according to claim 5, wherein the AgInS 2 powder mixed with the solvent has an average particle size of 5 μm or less.
JP5079014A 1993-03-12 1993-03-12 Production of powdery agins2 and agins2 film Withdrawn JPH06263442A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5079014A JPH06263442A (en) 1993-03-12 1993-03-12 Production of powdery agins2 and agins2 film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5079014A JPH06263442A (en) 1993-03-12 1993-03-12 Production of powdery agins2 and agins2 film

Publications (1)

Publication Number Publication Date
JPH06263442A true JPH06263442A (en) 1994-09-20

Family

ID=13678097

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5079014A Withdrawn JPH06263442A (en) 1993-03-12 1993-03-12 Production of powdery agins2 and agins2 film

Country Status (1)

Country Link
JP (1) JPH06263442A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6852657B2 (en) 2001-08-22 2005-02-08 Schott Glas Optical colored glasses
US7960306B2 (en) 2008-05-28 2011-06-14 Industrial Technology Research Institute Photo-energy transformation catalysts and methods for fabricating the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6852657B2 (en) 2001-08-22 2005-02-08 Schott Glas Optical colored glasses
US7960306B2 (en) 2008-05-28 2011-06-14 Industrial Technology Research Institute Photo-energy transformation catalysts and methods for fabricating the same

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