JP3229705B2 - Photovoltaic device - Google Patents
Photovoltaic deviceInfo
- Publication number
- JP3229705B2 JP3229705B2 JP10387493A JP10387493A JP3229705B2 JP 3229705 B2 JP3229705 B2 JP 3229705B2 JP 10387493 A JP10387493 A JP 10387493A JP 10387493 A JP10387493 A JP 10387493A JP 3229705 B2 JP3229705 B2 JP 3229705B2
- Authority
- JP
- Japan
- Prior art keywords
- conductive metal
- metal oxide
- photovoltaic device
- oxygen concentration
- oxide layer
- 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.)
- Expired - Lifetime
Links
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)
Description
【0001】[0001]
【産業上の利用分野】この発明は光起電力装置に関し、
特に半導体層上に光入射側の透明電極を形成した、いわ
ゆる逆タイプ構造の光起電力装置に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a photovoltaic device,
In particular, the present invention relates to a so-called inverted type photovoltaic device in which a transparent electrode on the light incident side is formed on a semiconductor layer.
【0002】[0002]
【従来の技術】この種の逆タイプ構造において、出力電
流の向上を図る手段として、高反射金属を用いた背面電
極と半導体層との界面に透明導電膜を挿入して、半導体
−金属界面での反射率の低下を防ぐ構造が特公昭60−
41878号に示されている。2. Description of the Related Art In a reverse type structure of this type, as a means for improving output current, a transparent conductive film is inserted into an interface between a back electrode using a highly reflective metal and a semiconductor layer, and a semiconductor-metal interface is used. Is a structure that prevents the reflectance of
No. 41878.
【0003】[0003]
【発明が解決しようとする課題】しかし、半導体層を形
成するときは、多くの場合、水素を多く含むプラズマの
ような還元性の強い雰囲気を用いるが、このような逆タ
イプ構造において導電性金属酸化物膜を形成する場合に
は、下地金属との反応を避けるために、蒸着法やスパッ
タ法などに形成法が限られてしまい、還元雰囲気に対す
る耐性の優れた導電性金属酸化物膜の形成は困難であっ
た。However, when a semiconductor layer is formed, a strongly reducing atmosphere such as a plasma containing a large amount of hydrogen is often used. When an oxide film is formed, the formation method is limited to an evaporation method, a sputtering method, or the like in order to avoid a reaction with a base metal, and a conductive metal oxide film having excellent resistance to a reducing atmosphere is formed. Was difficult.
【0004】また、還元雰囲気に対する耐性の優れた導
電性金属酸化物膜は導電性が劣るため、これを使用した
場合には光起電力装置の直列抵抗(Rs)が増加し、変
換効率(η)の低下を招いてしまうという問題があっ
た。さらには、プロセスの増加を伴うために、コストが
増加してしまう。それゆえに、この発明の主たる目的
は、還元雰囲気にさらされても導電性金属酸化物膜での
光の透過率の減少を抑制し、それによって低コストで高
効率の光起電力装置を提供することである。[0004] Further, since a conductive metal oxide film having excellent resistance to a reducing atmosphere has poor conductivity, when it is used, the series resistance (Rs) of the photovoltaic device increases and the conversion efficiency (η) increases. ) Is caused. Further, the cost is increased due to the increase in the number of processes. Therefore, a main object of the present invention is to provide a low-cost and high-efficiency photovoltaic device that suppresses a decrease in light transmittance of a conductive metal oxide film even when exposed to a reducing atmosphere. That is.
【0005】[0005]
【課題を解決するための手段】第1発明は、導電性金属
酸化物膜で被覆された基板上に形成された半導体層およ
び半導体層上に形成された光入射側透明電極を有する光
起電力装置であって、導電性金属酸化物膜を一方の電極
またはその一部としたものにおいて、基板と半導体層と
の間に存在する導電性金属酸化物層の厚み方向において
半導体層に隣接する領域の第1の酸素濃度を他の領域の
第2の酸素濃度より高くすると共に、半導体層に隣接す
る領域における導電性金属酸化物層の厚みを10Å〜1
00Åの範囲としたことを特徴とする、光起電力装置で
ある。According to a first aspect of the present invention, there is provided a photovoltaic device having a semiconductor layer formed on a substrate covered with a conductive metal oxide film and a light incident side transparent electrode formed on the semiconductor layer. In the device, in which the conductive metal oxide film is used as one electrode or a part thereof, a region adjacent to the semiconductor layer in a thickness direction of the conductive metal oxide layer existing between the substrate and the semiconductor layer The first oxygen concentration of the other region is higher than the second oxygen concentration of the other region, and the first region is adjacent to the semiconductor layer.
The thickness of the conductive metal oxide layer in the region
A photovoltaic device characterized by having a range of 00 ° .
【0006】[0006]
【0007】[0007]
【作用】還元性雰囲気などにさらされる可能性のある導
電性金属酸化物膜の表面付近の酸素濃度を、他の導電性
金属酸化物膜の主たる部分よりも高くすることで、還元
性雰囲気に対する耐性が強くなり、導電性金属酸化物膜
での光透過率の減少が抑制される。また、表面付近のみ
の酸素濃度を高くするために、光起電力装置の直列抵抗
の増加はほとんど生じない。By making the oxygen concentration near the surface of the conductive metal oxide film that may be exposed to a reducing atmosphere, etc., higher than the main part of the other conductive metal oxide films, The resistance is increased, and a decrease in light transmittance in the conductive metal oxide film is suppressed. Further, since the oxygen concentration only near the surface is increased, the series resistance of the photovoltaic device hardly increases.
【0008】この効果により、光起電力装置の出力電流
を向上させることが可能である。また、導電性酸化物膜
は1度のプロセスで作製できるため、他の材料でコーテ
ィングする場合に比べて低コスト化が可能である。[0008] The effect of this, it is possible to improve the output current of the photovoltaic device. Further, since the conductive oxide film can be manufactured in one process, the cost can be reduced as compared with the case where the conductive oxide film is coated with another material.
【0009】[0009]
【発明の効果】この発明によれば、低コストで、高効率
の光起電力装置が得られる。この発明の上述の目的,そ
の他の目的,特徴および利点は、図面を参照して行う以
下の実施例の詳細な説明から一層明らかとなろう。According to the present invention, a low-cost and high-efficiency photovoltaic device can be obtained. The above and other objects, features and advantages of the present invention will become more apparent from the following detailed description of embodiments with reference to the drawings.
【0010】[0010]
【実施例】図1に示す実施例の光起電力装置10は、絶
縁性プラスチック基板12を含み、この絶縁性プラスチ
ック基板12上に、公知のRFスパッタリング法を用い
て、表1に示す条件により、それぞれAgおよびITO
からなる高反射金属電極層14および導電性金属酸化物
層16を形成した。導電性金属酸化物層16は最初の9
50Å(以下、第1導電性金属酸化物層16aと称す)
をArのみの雰囲気で形成し、その後50Å(以下、第
2導電性金属酸化物層16bと称す)をArにO2 を添
加して形成した。DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS A photovoltaic device 10 according to an embodiment shown in FIG. 1 includes an insulating plastic substrate 12, and is formed on the insulating plastic substrate 12 by a known RF sputtering method under the conditions shown in Table 1. , Ag and ITO respectively
, A highly reflective metal electrode layer 14 and a conductive metal oxide layer 16 were formed. The conductive metal oxide layer 16 comprises the first 9
50 ° (hereinafter, referred to as first conductive metal oxide layer 16a)
Was formed in an atmosphere containing only Ar, and then 50 ° (hereinafter, referred to as a second conductive metal oxide layer 16b) was formed by adding O 2 to Ar.
【0011】この上に、表2に示す条件で非晶質半導体
層18を、n層,i層,p層の順に、公知のプラズマC
VD法により形成した。その後、光入射側透光性電極層
20としてITOを表1に示す条件により、RFスパッ
タリング法を用いて形成した。さらに、集電金属層22
として、公知の抵抗加熱蒸着法により、くし型Ag電極
を形成した。On this, an amorphous semiconductor layer 18 is formed under the conditions shown in Table 2 in the order of an n-layer, an i-layer, and a p-layer by a known plasma C method.
It was formed by the VD method. Thereafter, ITO was formed as the light incident side translucent electrode layer 20 by RF sputtering under the conditions shown in Table 1. Further, the current collecting metal layer 22
A comb-shaped Ag electrode was formed by a known resistance heating evaporation method.
【0012】[0012]
【表1】 [Table 1]
【0013】[0013]
【表2】 [Table 2]
【0014】比較のために、導電性金属酸化物層16を
第1導電性金属酸化物層16aと同じ条件のみで100
0Å形成し、他は全て同じ条件としたものを比較例と
し、両者の特性を表3に示す。For comparison, the conductive metal oxide layer 16 is formed under the same conditions as those of the first conductive metal oxide layer 16a.
0 ° was formed, and the other conditions were all the same.
【0015】[0015]
【表3】 [Table 3]
【0016】なお、第1導電性金属酸化物層16aの酸
素濃度は61%であり、第2導電性金属酸化物層16b
の酸素濃度は65%(第1導電性金属酸化物層16aの
酸素濃度の107%)であった。このとき、第1導電性
金属酸化物層16aの屈折率は2.1であり、第2導電
性金属酸化物層16bの屈折率は2.0(第1導電性金
属酸化物層16aの屈折率の95%)であった。The first conductive metal oxide layer 16a has an oxygen concentration of 61% and the second conductive metal oxide layer 16b
Was 65% (107% of the oxygen concentration of the first conductive metal oxide layer 16a). At this time, the refractive index of the first conductive metal oxide layer 16a is 2.1, and the refractive index of the second conductive metal oxide layer 16b is 2.0 (the refractive index of the first conductive metal oxide layer 16a). 95% of the rate).
【0017】次に、この実施例において、第2導電性金
属酸化物層16bの膜厚を変化させたときの光起電力装
置10の変換効率の変化の様子を図2に示す。図2を参
照すると、第2導電性金属酸化物層16bの膜厚が10
Åから100Åの範囲で効率が向上している。これは、
10Å以下の領域では非晶質半導体層18を形成する際
の還元性雰囲気に対する耐性が十分ではないために、効
率の向上が見られず、100Å以上の領域では第2導電
性金属酸化物層16bの抵抗成分が大きくなってしまう
ために曲線因子の低下を招き、結果として効率が低下し
てしまうからである。Next, FIG. 2 shows how the conversion efficiency of the photovoltaic device 10 changes when the thickness of the second conductive metal oxide layer 16b is changed in this embodiment. Referring to FIG. 2, the second conductive metal oxide layer 16b has a thickness of 10
The efficiency is improved in the range of Å to 100Å. this is,
In the region below 10 °, the efficiency is not improved because the resistance to the reducing atmosphere when forming the amorphous semiconductor layer 18 is not sufficient, and in the region above 100 °, the second conductive metal oxide layer 16b is formed. This is because the resistance component becomes large, causing a decrease in the fill factor, and as a result, the efficiency is reduced.
【0018】さらに、第2導電性金属酸化物層16bの
膜厚は50Åで一定とし、第1導電性金属酸化物層16
aの酸素濃度に対する第2導電性金属酸化物16bの酸
素濃度の比を変えたときの光起電力装置10の変換効率
の変化の様子を図3に示す。なお、第2導電性金属酸化
物層16bの酸素濃度は形成時の酸素分圧により制御し
た。Further, the thickness of the second conductive metal oxide layer 16b is fixed at 50 ° and the first conductive metal oxide layer 16b is
FIG. 3 shows how the conversion efficiency of the photovoltaic device 10 changes when the ratio of the oxygen concentration of the second conductive metal oxide 16b to the oxygen concentration of a is changed. Note that the oxygen concentration of the second conductive metal oxide layer 16b was controlled by the oxygen partial pressure during formation.
【0019】第1導電性金属酸化物層16aの酸素濃度
に対する第2導電性金属酸化物層16bの酸素濃度の比
が105%から110%の範囲で変換効率の向上が見ら
れる。これは、105%以下の領域では非晶質半導体層
18を形成する際の還元性雰囲気に対する耐性が十分で
はないために、効率の向上が見られず、110%以上の
領域では導電性金属酸化物層16bの抵抗成分が大きく
なってしまうために曲線因子の低下を招き、結果として
効率が低下してしまう。The conversion efficiency is improved when the ratio of the oxygen concentration of the second conductive metal oxide layer 16b to the oxygen concentration of the first conductive metal oxide layer 16a is in the range of 105% to 110%. This is because the resistance to a reducing atmosphere when the amorphous semiconductor layer 18 is formed is not sufficient in the region of 105% or less, so that the efficiency is not improved. Since the resistance component of the material layer 16b is increased, the fill factor is reduced, and as a result, the efficiency is reduced.
【0020】導電性金属酸化物層16aの酸素濃度に対
する導電性金属酸化物層16bの酸素濃度の比で105
%および110%というのは、屈折率でいえばそれぞれ
96.5%および93%に相当する。なお、上述の実施
例では、導電性金属酸化物層の形成にスパッタリング法
を用いたが、これ以外の方法、たとえば熱CVD法やM
OCVD法やEB蒸着法などを用いてもよい。The ratio of the oxygen concentration of the conductive metal oxide layer 16b to the oxygen concentration of the conductive metal oxide layer 16a is 105
% And 110% correspond to a refractive index of 96.5% and 93%, respectively. In the above embodiment, the sputtering method was used to form the conductive metal oxide layer. However, other methods, such as the thermal CVD method and the M
OCVD, EB vapor deposition, or the like may be used.
【0021】また、導電性金属酸化物層としては、上で
述べた酸化錫(SnO2 ),酸化インジウム錫(IT
O)以外の導電性金属酸化物、たとえば酸化亜鉛(Zn
O)や酸化カドミウム(CdO)などが用いられてもよ
いのはもちろんである。As the conductive metal oxide layer, tin oxide (SnO 2 ) and indium tin oxide (IT
O), other conductive metal oxides such as zinc oxide (Zn)
Of course, O) or cadmium oxide (CdO) may be used.
【図1】この発明の一実施例を示す断面構造図である。FIG. 1 is a sectional structural view showing one embodiment of the present invention.
【図2】第2導電性金属酸化物層の膜厚を変化させたと
きの光起電力装置の変換効率の変化を示すグラフであ
る。FIG. 2 is a graph showing a change in the conversion efficiency of the photovoltaic device when the thickness of the second conductive metal oxide layer is changed.
【図3】第1導電性金属酸化物層の酸素濃度に対する第
2導電性金属酸化物の酸素濃度の比を変化させたときの
光起電力装置の変換効率の変化を示すグラフである。FIG. 3 is a graph showing a change in the conversion efficiency of the photovoltaic device when the ratio of the oxygen concentration of the second conductive metal oxide to the oxygen concentration of the first conductive metal oxide layer is changed.
10 …光起電力装置 12 …基板 14 …高反射金属電極 16a …第1導電性金属酸化物層 16b …第2導電性金属酸化物層 18 …非晶質半導体層 20 …光入射側透明電極 DESCRIPTION OF SYMBOLS 10 ... Photovoltaic device 12 ... Substrate 14 ... High reflective metal electrode 16a ... First conductive metal oxide layer 16b ... Second conductive metal oxide layer 18 ... Amorphous semiconductor layer 20 ... Light incident side transparent electrode
フロントページの続き (56)参考文献 特開 平5−13790(JP,A) 特開 平1−205474(JP,A) 特開 昭58−80877(JP,A) 特開 昭59−119875(JP,A) (58)調査した分野(Int.Cl.7,DB名) H01L 31/04 - 31/078 Continuation of the front page (56) References JP-A-5-13790 (JP, A) JP-A-1-205474 (JP, A) JP-A-58-80877 (JP, A) JP-A-59-119875 (JP) , A) (58) Fields investigated (Int. Cl. 7 , DB name) H01L 31/04-31/078
Claims (2)
形成された半導体層および前記半導体層上に形成された
光入射側透明電極を有する光起電力装置であって、前記
導電性金属酸化物膜を一方の電極またはその一部とした
ものにおいて、 前記基板と前記半導体層との間に存在する導電性金属酸
化物層の厚み方向において前記半導体層に隣接する領域
の第1の酸素濃度を他の領域の第2の酸素濃度より高く
すると共に、 前記半導体層に隣接する領域における前記導電性金属酸
化物層の厚みを10Å〜100Åの範囲としたこと を特
徴とする、光起電力装置。1. A photovoltaic device comprising: a semiconductor layer formed on a substrate covered with a conductive metal oxide film; and a light incident side transparent electrode formed on the semiconductor layer. In the case where the metal oxide film is used as one electrode or a part thereof, a first portion of a region adjacent to the semiconductor layer in a thickness direction of the conductive metal oxide layer existing between the substrate and the semiconductor layer Oxygen concentration higher than the second oxygen concentration in other areas
And the conductive metal acid in a region adjacent to the semiconductor layer
A photovoltaic device, wherein the thickness of the oxide layer is in the range of 10 to 100 degrees .
に対して105%以上かつ110%以下である、請求項
1記載の光起電力装置。2. The photovoltaic device according to claim 1, wherein said first oxygen concentration is not less than 105% and not more than 110% with respect to said second oxygen concentration.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10387493A JP3229705B2 (en) | 1993-04-30 | 1993-04-30 | Photovoltaic device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10387493A JP3229705B2 (en) | 1993-04-30 | 1993-04-30 | Photovoltaic device |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH06314804A JPH06314804A (en) | 1994-11-08 |
| JP3229705B2 true JP3229705B2 (en) | 2001-11-19 |
Family
ID=14365589
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10387493A Expired - Lifetime JP3229705B2 (en) | 1993-04-30 | 1993-04-30 | Photovoltaic device |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3229705B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101000057B1 (en) * | 2008-02-04 | 2010-12-10 | 엘지전자 주식회사 | Method for manufacturing a solar cell having a multilayer transparent conductive layer |
| JP2009231505A (en) * | 2008-03-21 | 2009-10-08 | Sanyo Electric Co Ltd | Solar battery |
| JP2010225735A (en) * | 2009-03-23 | 2010-10-07 | Mitsubishi Electric Corp | Photosensor and manufacturing method thereof |
| JP2011228733A (en) * | 2011-06-29 | 2011-11-10 | Mitsubishi Electric Corp | Photosensor and method of manufacturing the same |
-
1993
- 1993-04-30 JP JP10387493A patent/JP3229705B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH06314804A (en) | 1994-11-08 |
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