WO2006046397A1 - 薄膜光電変換装置用基板およびそれを用いた集積型薄膜光電変換装置 - Google Patents
薄膜光電変換装置用基板およびそれを用いた集積型薄膜光電変換装置 Download PDFInfo
- Publication number
- WO2006046397A1 WO2006046397A1 PCT/JP2005/018674 JP2005018674W WO2006046397A1 WO 2006046397 A1 WO2006046397 A1 WO 2006046397A1 JP 2005018674 W JP2005018674 W JP 2005018674W WO 2006046397 A1 WO2006046397 A1 WO 2006046397A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- photoelectric conversion
- thin film
- substrate
- conversion device
- film photoelectric
- Prior art date
Links
- 239000000758 substrate Substances 0.000 title claims abstract description 120
- 239000010409 thin film Substances 0.000 title claims abstract description 110
- 238000006243 chemical reaction Methods 0.000 claims abstract description 171
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims abstract description 49
- 239000011787 zinc oxide Substances 0.000 claims abstract description 24
- 239000002245 particle Substances 0.000 claims description 50
- 239000010408 film Substances 0.000 claims description 44
- 238000000926 separation method Methods 0.000 claims description 11
- 229910044991 metal oxide Inorganic materials 0.000 claims description 4
- 150000004706 metal oxides Chemical class 0.000 claims description 4
- 239000011521 glass Substances 0.000 abstract description 25
- 238000002834 transmittance Methods 0.000 abstract description 9
- 239000010410 layer Substances 0.000 description 187
- 239000010419 fine particle Substances 0.000 description 24
- 238000000034 method Methods 0.000 description 23
- 239000004065 semiconductor Substances 0.000 description 21
- 229910021419 crystalline silicon Inorganic materials 0.000 description 19
- 229910021417 amorphous silicon Inorganic materials 0.000 description 14
- 230000000694 effects Effects 0.000 description 12
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 8
- 229910021424 microcrystalline silicon Inorganic materials 0.000 description 8
- 229910052710 silicon Inorganic materials 0.000 description 8
- 239000010703 silicon Substances 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000013078 crystal Substances 0.000 description 5
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 5
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 5
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 5
- 238000004506 ultrasonic cleaning Methods 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 229910052814 silicon oxide Inorganic materials 0.000 description 4
- 238000004544 sputter deposition Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LEVVHYCKPQWKOP-UHFFFAOYSA-N [Si].[Ge] Chemical compound [Si].[Ge] LEVVHYCKPQWKOP-UHFFFAOYSA-N 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000005229 chemical vapour deposition Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 230000031700 light absorption Effects 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000002230 thermal chemical vapour deposition Methods 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- 229910000577 Silicon-germanium Inorganic materials 0.000 description 2
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- LHJQIRIGXXHNLA-UHFFFAOYSA-N calcium peroxide Chemical compound [Ca+2].[O-][O-] LHJQIRIGXXHNLA-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- HQWPLXHWEZZGKY-UHFFFAOYSA-N diethylzinc Chemical compound CC[Zn]CC HQWPLXHWEZZGKY-UHFFFAOYSA-N 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- BPUBBGLMJRNUCC-UHFFFAOYSA-N oxygen(2-);tantalum(5+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ta+5].[Ta+5] BPUBBGLMJRNUCC-UHFFFAOYSA-N 0.000 description 2
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 2
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000002310 reflectometry Methods 0.000 description 2
- 229910001936 tantalum oxide Inorganic materials 0.000 description 2
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 2
- 229960001763 zinc sulfate Drugs 0.000 description 2
- 229910000368 zinc sulfate Inorganic materials 0.000 description 2
- 229910001928 zirconium oxide Inorganic materials 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 241000652704 Balta Species 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- -1 ITO Chemical compound 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 235000019402 calcium peroxide Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000006059 cover glass Substances 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- WSUTUEIGSOWBJO-UHFFFAOYSA-N dizinc oxygen(2-) Chemical compound [O-2].[O-2].[Zn+2].[Zn+2] WSUTUEIGSOWBJO-UHFFFAOYSA-N 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- SCCCLDWUZODEKG-UHFFFAOYSA-N germanide Chemical compound [GeH3-] SCCCLDWUZODEKG-UHFFFAOYSA-N 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 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
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- ORUIBWPALBXDOA-UHFFFAOYSA-L magnesium fluoride Chemical compound [F-].[F-].[Mg+2] ORUIBWPALBXDOA-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002488 metal-organic chemical vapour deposition Methods 0.000 description 1
- 239000013081 microcrystal Substances 0.000 description 1
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910000484 niobium oxide Inorganic materials 0.000 description 1
- URLJKFSTXLNXLG-UHFFFAOYSA-N niobium(5+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Nb+5].[Nb+5] URLJKFSTXLNXLG-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910021332 silicide Inorganic materials 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000005361 soda-lime glass Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 239000013598 vector Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor 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
- H01L31/02—Details
- H01L31/0224—Electrodes
- H01L31/022466—Electrodes made of transparent conductive layers, e.g. TCO, ITO layers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor 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
- H01L31/02—Details
- H01L31/0224—Electrodes
- H01L31/022466—Electrodes made of transparent conductive layers, e.g. TCO, ITO layers
- H01L31/022483—Electrodes made of transparent conductive layers, e.g. TCO, ITO layers composed of zinc oxide [ZnO]
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor 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
- H01L31/02—Details
- H01L31/0236—Special surface textures
- H01L31/02363—Special surface textures of the semiconductor body itself, e.g. textured active layers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor 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
- H01L31/02—Details
- H01L31/0236—Special surface textures
- H01L31/02366—Special surface textures of the substrate or of a layer on the substrate, e.g. textured ITO/glass substrate or superstrate, textured polymer layer on glass substrate
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor 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
- H01L31/0248—Semiconductor 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 characterised by their semiconductor bodies
- H01L31/036—Semiconductor 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 characterised by their semiconductor bodies characterised by their crystalline structure or particular orientation of the crystalline planes
- H01L31/0392—Semiconductor 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 characterised by their semiconductor bodies characterised by their crystalline structure or particular orientation of the crystalline planes including thin films deposited on metallic or insulating substrates ; characterised by specific substrate materials or substrate features or by the presence of intermediate layers, e.g. barrier layers, on the substrate
-
- 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
Definitions
- the present invention relates to a substrate for a thin film photoelectric conversion device and an improvement in performance of an integrated thin film photoelectric conversion device using the same.
- Such a thin film photoelectric conversion device generally includes a transparent electrode layer, one or more photoelectric conversion units, and a back electrode layer that are sequentially stacked on an insulating translucent substrate.
- the photoelectric conversion unit is generally formed by stacking a P-type layer, an i-type layer, and an n-type layer in this order or vice versa, and the i-type photoelectric conversion layer that occupies the main part is amorphous.
- One is called an amorphous photoelectric conversion unit, and one whose i-type layer is crystalline is called a crystalline photoelectric conversion unit.
- the thin-film photoelectric conversion device can make the photoelectric conversion unit thinner than the conventional photoelectric conversion device using Balta single crystal or polycrystalline silicon. There is a problem that it is limited by the film thickness. Therefore, in order to use light incident on the photoelectric conversion unit including the photoelectric conversion layer more effectively, the surface of the transparent electrode layer in contact with the photoelectric conversion unit is made uneven (textured), and light is scattered at the interface. Later, the light path length is extended by making it enter the photoelectric conversion unit, and the amount of light absorption in the photoelectric conversion unit is increased. This technology is called “optical confinement” and is an important elemental technology for practical use of thin film photoelectric conversion devices with high photoelectric conversion efficiency.
- An amorphous silicon photoelectric conversion device which is an example of a thin film photoelectric conversion device, is made of a transparent material such as glass.
- Oxidized tin (SnO) film formed on an insulating substrate and having surface irregularities as a transparent electrode layer
- the surface unevenness of the transparent electrode layer effectively contributes to light confinement in the photoelectric conversion unit.
- a glass substrate with a SnO film formed by thermal chemical vapor deposition (thermal CVD) as a transparent electrode layer with surface irregularities effective for light confinement thermal chemical vapor deposition (thermal CVD) as a transparent electrode layer with surface irregularities effective for light confinement
- the SnO film uses hydrogen, which has low plasma resistance.
- SnO film is reduced in the deposition environment of the photoelectric conversion unit with a large plasma density
- zinc oxide (ZnO) is widely used as a transparent electrode layer material.
- No. 2 is less expensive than indium tin oxide (ITO) and has high plasma resistance, and is suitable as a transparent electrode layer material for thin film photoelectric conversion devices.
- ITO indium tin oxide
- thin film polycrystalline silicon which uses a larger amount of hydrogen than the deposition conditions used during the formation of amorphous silicon and requires a large plasma density, is converted into crystalline silicon such as microcrystalline silicon. It is effective for the crystalline silicon thin film photoelectric conversion device used as a part.
- crystalline and “microcrystal” in the specification of the present application partially include amorphous, and also include those.
- the method of forming a ZnO film disclosed in Patent Document 1 is a low-temperature organic metal CVD method (low-temperature MOCVD method) of 200 ° C or lower. It is preferable as a method for forming a transparent electrode layer of a thin film photoelectric conversion device because it can be formed at a film formation speed that is one digit faster than the sputtering method and the utilization efficiency of raw materials is high. . Therefore, in order to increase the photoelectric conversion efficiency of the thin film crystalline photoelectric conversion device, the thin film photoelectric conversion device using the light confinement effect due to the surface irregularity shape using low-temperature formed ZnO as disclosed in Patent Document 1. High efficiency is being studied.
- the substrate for a photoelectric conversion device including a glass substrate provided with a transparent electrode layer is used on the light incident side in the photoelectric conversion device, the transparent electrode layer contributing to the light confinement effect In addition to the uneven surface shape, a high light transmittance is desired.
- Patent Document 2 in order to improve the photoelectric conversion efficiency of a photoelectric conversion device including a solar cell, which is limited only by improvement of the transparent electrode layer itself used for the transparent electrode layer, a glass and a transparent electrode layer are used.
- a substrate for a photoelectric conversion device that employs a configuration in which two films of a high refractive index film and a low refractive index film are formed therebetween is disclosed.
- a 28 nm thick SnO film and a 24 nm silicon oxide (SiO 2) film are formed sequentially from the glass substrate side by thermal CVD.
- the SnO film is applied to the transparent electrode layer because the thermal energy at the time of glass molding can be used to form the transparent electrode layer.
- a high-temperature process of about 570 ° C or higher is used to form a multilayer film between and a transparent electrode layer formed thereon.
- Patent Document 1 Japanese Patent Laid-Open No. 2000-252501
- Patent Document 2 Japanese Patent Laid-Open No. 2001-036117
- Patent Document 2 shows that the reflection loss reduction structure between the glass substrate and the transparent electrode layer is effective in improving the photoelectric conversion efficiency of the thin film photoelectric conversion device. Therefore, in a thin film photoelectric conversion device substrate using ZnO as a transparent electrode layer, it is important to consider providing a reflection loss reduction structure between the glass and the transparent electrode layer as a technology that leads to improved photoelectric conversion efficiency. A simple method is required.
- the present invention improves the light transmittance of a thin film photoelectric conversion device substrate using a transparent insulating substrate such as a glass substrate and ZnO that can be formed at a low temperature as a transparent electrode layer, and thin film photoelectric conversion.
- the object is to improve the photoelectric conversion efficiency of the device.
- a substrate for a thin film photoelectric conversion device of the present invention has a transparent insulating substrate, an intermediate layer deposited thereon, and a transparent electrode layer containing at least zinc oxide zinc.
- the refractive index in the intermediate layer changes smoothly from the translucent insulating substrate side toward the transparent electrode layer side, and the convex portion of the intermediate layer has a curved surface force at the interface on the transparent electrode layer side.
- the surface is characterized by having irregularities.
- the intermediate layer includes high refractive index particles having a refractive index of 1.8 to 2.6 and low refractive index particles having a refractive index of 1.4 to 1.7
- the translucent insulating substrate side force can also be directed to the transparent electrode layer side to effectively change the refractive index of the intermediate layer.
- the particle diameter of the high refractive index particles contained in the intermediate layer is preferably 1Z4 to 3Z4, which is smaller than the particle diameter of the low refractive index particles. This is because, by reducing the particle size, highly refractive particles can be accumulated on the translucent insulating substrate side in the intermediate layer, and a refractive index gradient can be effectively formed.
- the average film thickness of the intermediate layer is preferably in the range of 50 to 200 nm.
- the translucent insulating substrate force due to an increase in the internal stress of the transparent electrode layer is a force that may cause the transparent electrode layer to peel off. This is particularly preferable because film peeling can be suppressed by the anchor effect due to the surface irregularities of the intermediate layer.
- At least one photoelectric conversion unit and a back electrode layer form a plurality of photoelectric conversion cells on the substrate for the thin film photoelectric conversion device.
- the plurality of cells are separated by a plurality of separation grooves, and the plurality of cells are electrically connected in series to each other through a connection groove.
- a thin film photoelectric conversion device substrate having improved light transmittance can be supplied, and a thin film photoelectric conversion device having high photoelectric conversion efficiency can be provided.
- FIG. 1 is a schematic cross-sectional view showing an example of a substrate for a thin film photoelectric conversion device according to the present invention.
- FIG. 2 is a schematic plan view showing an element surface of a typical example of an integrated thin film photoelectric conversion device.
- FIG. 3 Schematic section showing an enlarged view of the laminated structure in the area surrounded by the ellipse 2A in Fig. 2. Plan view.
- FIG. 4 A schematic cross-sectional view showing an example of the thin film photoelectric conversion device according to the present invention in an enlarged manner in a region surrounded by an ellipse 3A in FIG.
- FIG. 1 shows a schematic cross-sectional view of a thin film photoelectric conversion device substrate according to an embodiment of the present invention.
- an intermediate layer 101 and a transparent electrode layer 102 are sequentially deposited on a translucent insulating substrate 100. Since the translucent insulating substrate 100 is positioned on the light incident side of the thin film photoelectric conversion device, it transmits more sunlight and absorbs it into the photoelectric conversion unit. It is preferable that it is as transparent as possible.
- high-efficiency thin-film photoelectric conversion devices can be achieved by applying a non-reflective coating to the light incident surface of the substrate so as to reduce the light reflection loss at the light incident surface of sunlight (h V). obtain.
- a general-purpose glass plate or film used as the light-transmitting insulating substrate 100 generally has a smooth surface
- a transparent electrode there is a high possibility that the transparent electrode layer 102 is peeled from the light-transmitting insulating substrate 100 due to the internal stress of the layer 102 and the semiconductor layer further deposited thereon. Therefore, as the thin film photoelectric conversion device substrate 10 of the present invention, the intermediate layer 101 is formed on the translucent substrate 100 having a smooth surface, and the transparent electrode layer 102 is deposited by the intermediate layer 101. It is preferable to provide fine surface irregularities on the side.
- the fine concavo-convex convex portion formed on the transparent electrode layer 102 side of the intermediate layer 101 is a curved surface. Since the convex part is a curved surface, it is possible to prevent an increase in crystal grain boundaries starting from the shape of the intermediate layer 101 during the crystal growth of the thin film sequentially deposited thereon, and to suppress the deterioration of the electrical characteristics of the thin film. Because.
- the intermediate layer 101 formed in the present invention is preferably made of a metal oxide film containing two or more kinds of particles having different refractive indexes. This is because the apparent refractive index of the intermediate layer can be adjusted by the mixing ratio of particles having different refractive indexes.
- the particles having different refractive indexes used in the intermediate layer should be a combination of high refractive index particles having a refractive index of 1.8 to 2.6 and low refractive index particles having a refractive index of 1.4 to 1.7.
- the particles having different refractive indexes used in the intermediate layer should be a combination of high refractive index particles having a refractive index of 1.8 to 2.6 and low refractive index particles having a refractive index of 1.4 to 1.7.
- Examples of the high refractive index particles include ZnO, SnO, ITO, indium oxide (In ⁇ ), titanium oxide (
- TiO aluminum oxide
- Al 2 O 3 zirconium oxide
- ZrO 2 zirconium oxide
- Nb 2 O 3 niobium oxide
- Tantalum oxide Ti 2 O 3
- zinc sulfate ZnS
- cerium oxide CeO 2
- silicon oxide SiO 2
- magnesium fluoride MgF 2
- fluorine fluorine
- the particle diameter of the high refractive index particles contained in the intermediate layer is preferably smaller than the particle diameter of the low refractive index particles, and is preferably 1Z4 to 3Z4 of the particle diameter of the low refractive index particles. It is more preferably 1Z2. If the particle size is in this range, it is possible to use two or more types of particles with different refractive indices.
- the apparent refractive index of the intermediate layer 101 can be a value between the translucent insulating substrate 100 and the transparent electrode layer 102. In addition, if the particle size is within this range, the gap between the low refractive index particles having a relatively large particle size, or the gap between the low refractive index particle and the translucent insulating substrate should be filled with the high refractive index particles. Is preferable.
- the average film thickness of the intermediate layer 101 is preferably in the range of 50 to 200 nm. The reason is that if the intermediate layer is too thin, the refractive index gradient in the intermediate layer cannot be sufficiently formed, so that the effect of the intermediate layer is not exerted. If the intermediate layer is too thick, the intermediate layer is formed on the transparent electrode layer side. This is because the surface irregularities formed are too large, affecting the crystal growth of the transparent electrode layer and the photoelectric conversion unit sequentially deposited on the surface, and reducing the photoelectric conversion efficiency.
- the method for forming the intermediate layer 101 containing fine particles on the surface of the translucent insulating substrate 100 is not particularly limited. However, a method of coating with a binder forming material containing a solvent is desirable.
- the adhesive layer that plays a role in improving the adhesion strength between fine particles and between the fine particles and the translucent insulating substrate 100 is an inorganic material considering long-term reliability and durability against photoelectric conversion unit formation conditions (especially temperature). Is preferred. Specific examples include metal oxides such as silicon oxide, aluminum oxide, titanium oxide, zirconium oxide, and tantalum oxide. In particular, when attaching SiO fine particles to a glass substrate, the same silicon
- a silicon oxide containing silicon as the main component for the adhesive layer because the adhesion is strong due to the formation of a silicide bond, the transparency is good, and the refractive index is close to that of the substrate or fine particles.
- Examples of the method for applying the coating solution to the surface of the translucent insulating substrate 100 include a dating method, a spin coat method, a bar coat method, a spray method, a die coat method, a roll coat method, and a flow coat method.
- a roll coat method is preferably used.
- the coated thin film is dried by heating. Since the film thus formed contains fine particles, the shape of the convex portion is a curved surface.
- the intermediate layer in which fine particles are densely deposited since most of the particles are formed so as to be in contact with the light-transmitting insulating substrate 100, high-refractive-index particles having a small particle diameter are larger than those of the transparent electrode layer 102.
- the light deposits on the translucent insulating substrate 100 side. Therefore, the refractive index of the intermediate layer 101 has a tendency that the translucent insulating substrate 100 side force gradually decreases toward the transparent electrode layer 102. This crouch The change in the refractive index is preferable in order to reduce the reflection loss of incident light generated between the translucent insulating substrate 100 and the transparent electrode layer 102.
- the translucent insulating substrate 100 When soda lime glass is used as the translucent insulating substrate 100, there is a concern that the aluminum component from the glass may enter the transparent electrode layer 102 or the semiconductor layer formed thereon.
- the intermediate layer 101 has an average film thickness of 50 to 200 nm and functions as an alkali barrier film because there is a binder that also has metal oxide strength between the particle surface and the particles.
- the thin film photoelectric conversion device substrate on which the transparent electrode layer 102 is formed is a layered body of transparent thin film, and therefore has a tendency to cause uneven color due to light interference. When the layer 101 is interposed, color unevenness due to interference is also reduced.
- the photoelectric conversion unit 110 is a thin film photoelectric conversion device having a crystalline photoelectric conversion layer. It is suitable for those.
- the ZnO transparent electrode layer 102 of the thin film photoelectric conversion device substrate of the present invention is formed by a CVD method under a reduced pressure condition at a substrate temperature of 200 ° C.
- the substrate temperature here refers to the temperature of the surface where the substrate is in contact with the heating part of the film forming apparatus.
- the average thickness of the ZnO film is preferably 0.7 to 5 m, and preferably 1 to 3 m. Is more preferable. This is because if the ZnO film is too thin, it will be difficult to sufficiently provide the unevenness that effectively contributes to the light confinement effect, and if the ZnO film is too thick to obtain the necessary conductivity for the transparent electrode layer, the ZnO film This is because the light absorption by itself reduces the amount of light that passes through ZnO and reaches the photoelectric conversion unit, thereby reducing efficiency. Furthermore, when it is too thick, the film forming cost increases due to an increase in the film forming time.
- a large area capable of producing a high output at a high voltage like a power thin film photoelectric conversion device When manufacturing a thin film photoelectric conversion device, a thin film photoelectric conversion device formed on a large substrate is required in order to improve the yield without using a plurality of thin film photoelectric conversion devices formed on a large substrate connected in series. Generally, it is divided into a plurality of cells, and these cells are connected in series to be integrated. In particular, in a thin-film photoelectric conversion device of the type in which light is incident from the glass substrate side, a semiconductor layer is sequentially formed on the glass substrate, and then the loss due to the resistance of the transparent conductive oxide (TCO) electrode on the glass substrate is reduced. In order to reduce this, the transparent electrode layer is generally processed into a strip with a predetermined width by a laser scribing method, and cells are connected in series in a direction perpendicular to the longitudinal direction of the strip to integrate them. is there.
- TCO transparent conductive oxide
- FIG. 2 a typical example of the element surface of the integrated thin film photoelectric conversion device is shown in a schematic plan view.
- FIG. 3 schematically shows an enlarged cross-sectional structure of the region surrounded by the ellipse 2A in FIG.
- FIG. 4 is a schematic cross-sectional view further enlarging the more detailed laminated structure in the region surrounded by the ellipse 3A in FIG.
- FIG. 4 an integrated thin film photoelectric conversion device according to an embodiment of the present invention is shown in a schematic cross-sectional view.
- This thin film photoelectric conversion device includes an intermediate layer 101, a transparent electrode layer 102, a photoelectric conversion unit 110, and a back electrode layer 120 that are sequentially deposited on a translucent insulating substrate 100.
- the photoelectric conversion unit 110 includes a p-type or n-type conductive layer 111, a substantially intrinsic semiconductor photoelectric conversion layer 112, and a reverse conductivity type layer 113, which are sequentially deposited.
- sunlight (h v) to be subjected to photoelectric conversion is incident from the translucent insulating substrate 100 side.
- a separation groove 103 is formed by laser scribing so as to be separated into a plurality of regions corresponding to a plurality of integrated photoelectric conversion cells. These separation grooves 103 extend linearly in a direction perpendicular to the paper surface of FIG.
- the residue after scribing is removed by ultrasonic cleaning using water or an organic solvent.
- a cleaning method a method of removing residues using an adhesive or a jet gas is also possible.
- a photoelectric conversion unit 110 that is a semiconductor layer cover is formed on the transparent electrode layer 102 in which the separation groove 103 is formed.
- the photoelectric conversion unit 110 includes a one conductivity type layer 111, an intrinsic photoelectric conversion layer 112, and a reverse conductivity type layer 113.
- the photoelectric conversion unit may be a single unit as illustrated, or a plurality of units may be stacked.
- the photoelectric conversion unit 110 the solar Those having absorption in the main wavelength region (400 to 1200 nm) of light are preferred, for example, a unit having an amorphous silicon thin film or a crystalline silicon thin film as the photoelectric conversion layer 112.
- silicon-based materials also include semiconductor materials containing 50% or more of silicon, such as silicon carbide and silicon germanium.
- the photoelectric conversion unit 110 which is an amorphous silicon-based thin film photoelectric conversion unit or a crystalline silicon-based thin film photoelectric conversion unit, is formed by stacking each semiconductor layer by a plasma CVD method in the order of, for example, a pin type.
- a p-type microcrystalline silicon layer 111 doped with boron which is a conductivity type determining impurity atom, of 0.01 atomic% or more, an intrinsic amorphous silicon layer or intrinsic crystalline silicon serving as a photoelectric conversion layer.
- the layer 112 and the n-type microcrystalline silicon layer 113 doped with 0.01 atomic% or more of phosphorus, which is a conductivity-determining impurity atom, may be deposited in this order.
- these layers are not limited to the above.
- an amorphous silicon film may be used as the p-type layer.
- an alloy material such as amorphous or microcrystalline silicon carbide or silicon germanium may be used for the p-type layer.
- the film thickness of the conductive type (p-type, n-type) microcrystalline silicon-based layer is preferably 3 nm or more and lOOnm or less, more preferably 5 nm or more and 50 nm or less.
- the intrinsic photoelectric conversion layer 112 is an intrinsic crystalline silicon layer, it is preferably formed by a plasma CVD method at a substrate temperature of 300 ° C or lower. It is preferable to contain many hydrogen atoms that terminate and inactivate defects in crystal grain boundaries and grains by forming them at a low temperature. Specifically, the hydrogen content of the photoelectric conversion layer is preferably in the range of 1 to 30 atomic%. This layer is preferably formed as a thin film that is substantially an intrinsic semiconductor having a conductivity type determining impurity atom density of 1 ⁇ 10 18 cm 3 or less.
- the crystal grains contained in the intrinsic crystalline silicon layer 112 grow in a columnar shape from the transparent electrode layer 102 side, and have a (110) preferential orientation plane with respect to the film plane.
- the film thickness of the intrinsic crystalline silicon layer 112 is preferably 1 m or more in order to obtain sufficient light absorption, and the viewpoint power for suppressing peeling due to internal stress of the crystalline thin film is preferably 10 m or less.
- the thin-film crystalline photoelectric conversion unit 110 preferably has absorption in the main wavelength region of sunlight (400 to 1200 nm)
- the crystalline silicon carbide layer that is an alloy material instead of the intrinsic crystalline silicon layer (For example, crystalline silicon containing 10 atomic percent or less of carbon Force also becomes crystalline silicon carbide layer) or crystalline silicon germanium layer (e.g. 30 atomic 0/0 less crystalline silicon force becomes crystalline silicon germanide containing germanium - ⁇ beam layer) may be formed.
- the photoelectric conversion units 110 stacked in this way are divided into a plurality of strip-shaped semiconductor regions by the semiconductor layer dividing grooves 104 formed by laser scribing as in the case of the transparent electrode layer 102.
- These semiconductor dividing grooves 104 also extend linearly in a direction perpendicular to the paper surface of FIG. Since the semiconductor dividing groove 104 is used to electrically connect the transparent electrode layer 102 and the back electrode 120 between adjacent cells, it is not a problem even if a sliver residue remains partially. First, ultrasonic cleaning may be omitted.
- a back electrode layer 120 is formed on the laser patterned semiconductor layer 110.
- the back electrode layer 120 it is preferable to form at least one metal layer 122 having at least one material force selected from Al, Ag, Au, Cu, Pt and Cr by sputtering or vapor deposition. Further, between the photoelectric conversion unit 110 and the metal layer 122, ITO, SnO
- the transparent conductive layer 121 has a function of improving the adhesion between the photoelectric conversion unit 110 and the metal layer 122, increasing the light reflectance of the metal layer 122, and preventing a chemical change of the photoelectric conversion unit 110.
- the back electrode layer 120 is patterned by laser scribing similar to that of the semiconductor layer 110, and after the plurality of back electrode separation grooves 105 are formed by locally blowing the back electrode layer 120 together with the semiconductor layer 110, Ultrasonic cleaned. As a result, a plurality of strip-shaped thin film photoelectric conversion device cells are formed, and these cells are electrically connected in series to each other through the connection grooves. Finally, although not shown, the back side of the thin film photoelectric conversion device is protected by a sealing resin.
- a tandem thin film photoelectric conversion device in which an amorphous silicon photoelectric conversion unit and a crystalline silicon photoelectric conversion unit are sequentially stacked on the transparent electrode layer 102 can be given.
- the amorphous silicon photoelectric conversion unit is sensitive to light of about 360 to 800 nm, and the crystalline silicon photoelectric conversion unit can photoelectrically convert light up to about 1200 nm longer than that.
- the thin film photoelectric conversion device is a thin film photoelectric conversion device that can effectively use incident light in a wider range. Therefore, the substrate for a thin film photoelectric conversion device of the present invention is also preferable for a tandem thin film photoelectric conversion device including such a crystalline photoelectric conversion unit.
- Example 1 a thin film photoelectric conversion device substrate as shown in FIG.
- SiO fine particles and TiO fine particles are contained on a glass substrate 101 having a thickness of 0.7 mm and a 125 mm square.
- the coating solution used to form the intermediate layer 101 is a spherical silica dispersion with an average particle size of 1 OOnm, a spherical acid-titanium dispersion with an average particle size of 30 nm (rutile type), water, and an ethyl acetate solve.
- the mixture was prepared by adding tetraethoxysilane and further adding hydrochloric acid. Tetraethoxysilane is hydrolyzed by hydrochloric acid, and the binder SiO
- Spherical silica (SiO fine particles) and spherical titanium oxide (TiO fine particles) are in a weight ratio of 5: 2.
- the spherical material and the binder were in a weight ratio of 4: 1.
- a transparent electrode layer 102 having a ZnO force was formed on the obtained intermediate layer 101.
- the transparent electrode layer 102 is formed by a CVD method under a reduced pressure condition by setting the substrate temperature to 160 ° C., supplying diethyl zinc (DEZ) and water as source gases, and diborane gas as a dopant gas.
- the thickness of the transparent electrode layer 102 made of the obtained ZnO film was 1.6 ⁇ m, the sheet resistance was about 9 ⁇ Z, and the haze ratio was 23%.
- the haze ratio is expressed by (diffuse transmittance Z total light transmittance) X 100 as described in JIS K7136.
- the relative reflectance of the substrate was measured with a spectrophotometer upon incidence of glass side force light. It was. At this time, direct reflected light having a reflection angle of 8 ° was measured with an integrating sphere with respect to the substrate to be measured. In order to reduce the effect of reflected light on the uneven surface force of the transparent electrode layer located on the back surface during measurement, an adjustment liquid with a refractive index of 1.7 (Jodium Methane) is provided on the uneven surface side of the transparent electrode layer. Was applied and protected with a cover glass. The relative reflectance at 550 nm was 8.6%.
- Comparative Example 1 a transparent electrode layer 102 made of ZnO was directly formed on a glass substrate 101 having a thickness of 0.7 mm and a 125 mm square in substantially the same manner as in Example 1. Compared to Example 1, the difference is that the intermediate layer 101 does not exist.
- the obtained substrate had a sheet resistance of about 9 ⁇ Z and a haze ratio of 19%.
- the relative reflectance of this thin film photoelectric conversion device substrate was 9.0% at 550 nm.
- FIG. 5 shows the relative reflectance vectors of the thin film photoelectric conversion device substrates obtained in Example 1 and Comparative Example 1. From this figure, it can be seen that, in the region of 400 to 700 nm, the substrate for the thin film photoelectric conversion device to which the intermediate layer of Example 1 is applied is lower than that of Comparative Example 1 and shows a reflectivity. .
- Example 2 a substrate for a thin film photoelectric conversion device was produced in the same manner as in Example 1. However, the difference from Example 1 is that the SiO fine particles and the TiO fine particles are mixed at a weight ratio of 3: 1.
- the sheet resistance of the thin film photoelectric conversion device substrate formed under the conditions was about 9 ⁇ Z, the haze ratio was 24%, and the relative reflectance at 550 nm was 8.3%.
- Example 3 a substrate for a thin film photoelectric conversion device was produced in the same manner as in Example 1. However, the difference from Example 1 is that low-refractive-index fine particles are SiO fine particles having an average particle diameter of 80 nm and high refractive index.
- SnO fine particles with an average particle diameter of 25 nm were mixed at a weight ratio of 2: 1.
- the sheet resistance of the thin film photoelectric conversion device substrate formed under these conditions was about 9 ⁇ Z, the haze ratio was 23%, and the relative reflectance at 550 nm was 8.7%.
- Example 4 a substrate for a thin film photoelectric conversion device was produced in the same manner as in Example 3. However, the difference from Example 3 is that SiO fine particles with an average particle size of 80 nm and SnO fine particles with an average particle size of 25 nm are 5: The point of mixing at a weight ratio of 2.
- the substrate for the thin film photoelectric conversion device formed under these conditions had a sheet resistance of about 9 ⁇ , a haze ratio of 22%, and a relative reflectance at 550 nm of 8.5%.
- Table 1 shows the main characteristics of the thin film photoelectric conversion device substrate in Examples 1 to 4 and Comparative Example 1 described above.
- the force of each of Examples 1 to 4 shows a lower relative reflectance than Comparative Example 1, as shown in the component force.
- the haze ratio of the substrate is higher than that of Comparative Example 1 when the intermediate layer of the present invention is inserted. Since the haze ratio is expressed by (diffuse transmittance Z total light transmittance) X 100, an increase in the haze ratio value due to the application of the intermediate layer can be expected to improve the light confinement effect in the thin film photoelectric conversion device.
- the transparent electrode layer 102 is separated into a strip-shaped transparent electrode layer having a width W of about 10 mm and a length L of 10 cm by forming a transparent electrode layer separation groove 103 having a width of about 100 ⁇ m by laser scribing. .
- the residue after scribing was removed by ultrasonic cleaning using water.
- An amorphous silicon photoelectric conversion unit 110 composed of a microcrystalline silicon layer 113 was sequentially formed by a plasma CVD method. After forming the semiconductor dividing groove 104 by laser scribing, a 90-nm-thick A1 doped ZnO 121 and a 200-nm-thick Ag 122 were sequentially formed as a back electrode 120 by a sputtering method. When the back electrode separation groove 105 was subjected to ultrasonic cleaning after laser scribing, the film peeling area on the substrate was not confirmed. After integration, the number of cells connected in series was 10.
- the integrated silicon thin film photoelectric conversion device obtained as described above was irradiated with light of AMI. 5 at a light amount of 1 OOmWZcm 2 to measure the output characteristics.
- Table 2 shows the open circuit voltage (Voc), short circuit current density CFsc), fill factor (FF), and conversion efficiency obtained for each substrate.
- Example 9 an integrated tandem thin film photoelectric conversion device was produced using the thin film photoelectric conversion device substrate of Example 1.
- An amorphous silicon photoelectric conversion unit was formed by plasma CVD as in Example 5.
- a P-type microcrystalline silicon layer having a thickness of 15 nm and an intrinsic crystalline material having a thickness of 1.6 m were formed by plasma CVD.
- Silicon photoelectric conversion layer and thickness A crystalline silicon photoelectric conversion unit composed of an n-type microcrystalline silicon layer having a thickness of 15 nm was formed.
- 90 nm thick A1-doped ZnO 121 and 200 nm thick Ag 122 were sequentially formed as the back electrode 120 by sputtering.
- ultrasonic cleaning was performed after laser scribing the back electrode separation groove 105, the film peeling region on the substrate was not confirmed even though the film thickness of the semiconductor layer portion was thicker than in Examples 5 to 8. I helped.
- the output characteristics were measured by irradiating the obtained silicon-based tandem-type thin film photoelectric converter with AMI. 5 light at a light intensity of lOOmWZcm 2 . 2 , FF power 71.2%, and conversion efficiency was 13.1%.
- an intermediate layer that can be easily formed, has a curved surface at the interface on the transparent electrode layer side, and has a changed refractive index.
- a high-performance integrated thin film photoelectric conversion device can be provided by using the substrate for a thin film photoelectric conversion device.
Landscapes
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Electromagnetism (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Photovoltaic Devices (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006542332A JPWO2006046397A1 (ja) | 2004-10-28 | 2005-10-11 | 薄膜光電変換装置用基板およびそれを用いた集積型薄膜光電変換装置 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004-314433 | 2004-10-28 | ||
JP2004314433 | 2004-10-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2006046397A1 true WO2006046397A1 (ja) | 2006-05-04 |
Family
ID=36227641
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2005/018674 WO2006046397A1 (ja) | 2004-10-28 | 2005-10-11 | 薄膜光電変換装置用基板およびそれを用いた集積型薄膜光電変換装置 |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPWO2006046397A1 (ja) |
WO (1) | WO2006046397A1 (ja) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009107517A1 (ja) * | 2008-02-27 | 2009-09-03 | シャープ株式会社 | 薄膜太陽電池およびその製造方法 |
WO2010004811A1 (ja) * | 2008-07-07 | 2010-01-14 | 三菱電機株式会社 | 薄膜太陽電池およびその製造方法 |
WO2010016468A1 (ja) * | 2008-08-05 | 2010-02-11 | 旭硝子株式会社 | 透明導電膜基板およびこの基板を用いた太陽電池 |
WO2011161632A1 (fr) * | 2010-06-23 | 2011-12-29 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Substrat comprenant une couche d'oxyde transparent conducteur et son procede de fabrication |
JP2012089712A (ja) * | 2010-10-20 | 2012-05-10 | Mitsubishi Electric Corp | 薄膜太陽電池およびその製造方法 |
CN102646726A (zh) * | 2011-02-22 | 2012-08-22 | 三菱综合材料株式会社 | 带有太阳能电池用复合膜的透明基板及其制造方法 |
KR101592576B1 (ko) | 2009-03-31 | 2016-02-05 | 엘지이노텍 주식회사 | 태양전지 및 이의 제조방법 |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6048920B2 (ja) * | 2012-02-23 | 2016-12-21 | 国立大学法人島根大学 | 光散乱膜及びその製造方法、太陽電池 |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02180081A (ja) * | 1988-12-30 | 1990-07-12 | Taiyo Yuden Co Ltd | 非晶質半導体太陽電池 |
JPH10326903A (ja) * | 1997-05-23 | 1998-12-08 | Sharp Corp | 微粒子塗布膜およびそれを用いた光電変換素子と光拡散体 |
JPH11135817A (ja) * | 1997-10-27 | 1999-05-21 | Sharp Corp | 光電変換素子およびその製造方法 |
JP2000183376A (ja) * | 1998-12-17 | 2000-06-30 | Nisshin Steel Co Ltd | 太陽電池用絶縁基板及びその製造方法 |
JP2000261013A (ja) * | 1999-03-09 | 2000-09-22 | Nippon Sheet Glass Co Ltd | 透明導電膜付きガラス基板 |
JP2001278637A (ja) * | 1999-12-13 | 2001-10-10 | Nippon Sheet Glass Co Ltd | 低反射ガラス物品 |
WO2003019676A1 (en) * | 2001-08-23 | 2003-03-06 | Pacific Solar Pty Limited | Glass beads coating process |
JP2003243676A (ja) * | 2002-02-19 | 2003-08-29 | Kanegafuchi Chem Ind Co Ltd | 薄膜光電変換装置 |
-
2005
- 2005-10-11 WO PCT/JP2005/018674 patent/WO2006046397A1/ja active Application Filing
- 2005-10-11 JP JP2006542332A patent/JPWO2006046397A1/ja active Pending
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02180081A (ja) * | 1988-12-30 | 1990-07-12 | Taiyo Yuden Co Ltd | 非晶質半導体太陽電池 |
JPH10326903A (ja) * | 1997-05-23 | 1998-12-08 | Sharp Corp | 微粒子塗布膜およびそれを用いた光電変換素子と光拡散体 |
JPH11135817A (ja) * | 1997-10-27 | 1999-05-21 | Sharp Corp | 光電変換素子およびその製造方法 |
JP2000183376A (ja) * | 1998-12-17 | 2000-06-30 | Nisshin Steel Co Ltd | 太陽電池用絶縁基板及びその製造方法 |
JP2000261013A (ja) * | 1999-03-09 | 2000-09-22 | Nippon Sheet Glass Co Ltd | 透明導電膜付きガラス基板 |
JP2001278637A (ja) * | 1999-12-13 | 2001-10-10 | Nippon Sheet Glass Co Ltd | 低反射ガラス物品 |
WO2003019676A1 (en) * | 2001-08-23 | 2003-03-06 | Pacific Solar Pty Limited | Glass beads coating process |
JP2003243676A (ja) * | 2002-02-19 | 2003-08-29 | Kanegafuchi Chem Ind Co Ltd | 薄膜光電変換装置 |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009206279A (ja) * | 2008-02-27 | 2009-09-10 | Sharp Corp | 薄膜太陽電池およびその製造方法 |
WO2009107517A1 (ja) * | 2008-02-27 | 2009-09-03 | シャープ株式会社 | 薄膜太陽電池およびその製造方法 |
JP5127925B2 (ja) * | 2008-07-07 | 2013-01-23 | 三菱電機株式会社 | 薄膜太陽電池およびその製造方法 |
WO2010004811A1 (ja) * | 2008-07-07 | 2010-01-14 | 三菱電機株式会社 | 薄膜太陽電池およびその製造方法 |
WO2010016468A1 (ja) * | 2008-08-05 | 2010-02-11 | 旭硝子株式会社 | 透明導電膜基板およびこの基板を用いた太陽電池 |
JPWO2010016468A1 (ja) * | 2008-08-05 | 2012-01-26 | 旭硝子株式会社 | 透明導電膜基板およびこの基板を用いた太陽電池 |
KR101592576B1 (ko) | 2009-03-31 | 2016-02-05 | 엘지이노텍 주식회사 | 태양전지 및 이의 제조방법 |
US20130092230A1 (en) * | 2010-06-23 | 2013-04-18 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Substrate comprising a transparent conductive oxide film and its manufacturing process |
CN102947943A (zh) * | 2010-06-23 | 2013-02-27 | 原子能与替代能源委员会 | 包含透明的导电氧化物膜的基底及其制造方法 |
FR2961952A1 (fr) * | 2010-06-23 | 2011-12-30 | Commissariat Energie Atomique | Substrat comprenant une couche d'oxyde transparent conducteur et son procede de fabrication |
JP2013529845A (ja) * | 2010-06-23 | 2013-07-22 | コミサリア ア レネルジィ アトミーク エ オ ゼネ ルジイ アルテアナティーフ | 透明導電性酸化膜を備える基体及びその製造方法 |
WO2011161632A1 (fr) * | 2010-06-23 | 2011-12-29 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Substrat comprenant une couche d'oxyde transparent conducteur et son procede de fabrication |
CN102947943B (zh) * | 2010-06-23 | 2016-11-09 | 原子能与替代能源委员会 | 包含透明的导电氧化物膜的基底及其制造方法 |
JP2012089712A (ja) * | 2010-10-20 | 2012-05-10 | Mitsubishi Electric Corp | 薄膜太陽電池およびその製造方法 |
CN102646726A (zh) * | 2011-02-22 | 2012-08-22 | 三菱综合材料株式会社 | 带有太阳能电池用复合膜的透明基板及其制造方法 |
JP2012174899A (ja) * | 2011-02-22 | 2012-09-10 | Mitsubishi Materials Corp | 太陽電池用複合膜付き透明基板およびその製造方法 |
TWI552363B (zh) * | 2011-02-22 | 2016-10-01 | Mitsubishi Materials Corp | Transparent substrate for composite film for solar cell, and method of manufacturing the same |
CN102646726B (zh) * | 2011-02-22 | 2017-09-08 | 三菱综合材料株式会社 | 带有太阳能电池用复合膜的透明基板及其制造方法 |
Also Published As
Publication number | Publication date |
---|---|
JPWO2006046397A1 (ja) | 2008-05-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5600660B2 (ja) | 薄膜太陽電池用基板および薄膜太陽電池の製造方法 | |
US8203073B2 (en) | Front electrode for use in photovoltaic device and method of making same | |
JP5069790B2 (ja) | 薄膜光電変換装置用基板とそれを含む薄膜光電変換装置、並びに薄膜光電変換装置用基板の製造方法 | |
JP2005311292A (ja) | 薄膜太陽電池用基板、及びその製造方法、並びにそれを用いた薄膜太陽電池 | |
JP4222500B2 (ja) | シリコン系薄膜光電変換装置 | |
US20080223436A1 (en) | Back reflector for use in photovoltaic device | |
US20080105293A1 (en) | Front electrode for use in photovoltaic device and method of making same | |
US20080105298A1 (en) | Front electrode for use in photovoltaic device and method of making same | |
US20080302414A1 (en) | Front electrode for use in photovoltaic device and method of making same | |
WO2006046397A1 (ja) | 薄膜光電変換装置用基板およびそれを用いた集積型薄膜光電変換装置 | |
EP2351110A2 (en) | Method of making front electrode of photovoltaic device having etched surface and corresponding photovoltaic device | |
JP3706835B2 (ja) | 薄膜光電変換装置 | |
JP2000252500A (ja) | シリコン系薄膜光電変換装置 | |
WO2008063305A2 (en) | Front electrode for use in photovoltaic device and method of making same | |
JPH07321362A (ja) | 光起電力装置 | |
CN201222505Y (zh) | 太阳能电池结构 | |
JP5469298B2 (ja) | 光電変換装置用透明導電膜、及びその製造方法 | |
EP2503602B1 (en) | Thin-film photoelectric conversion device, and process for production of thin-film photoelectric conversion device | |
WO2011105171A1 (ja) | 太陽電池およびその製造方法 | |
KR101327089B1 (ko) | 태양전지 모듈 및 이의 제조방법 | |
JP2012038956A (ja) | 薄膜太陽電池モジュール | |
KR20120122798A (ko) | 박막 두께 조절로 광 투과율을 개선한 화합물 태양전지 및 이의 제조방법 | |
JP2013042084A (ja) | 薄膜光電変換装置の製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BW BY BZ CA CH CN CO CR CU CZ DK DM DZ EC EE EG ES FI GB GD GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV LY MD MG MK MN MW MX MZ NA NG NO NZ OM PG PH PL PT RO RU SC SD SG SK SL SM SY TJ TM TN TR TT TZ UG US UZ VC VN YU ZA ZM |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): GM KE LS MW MZ NA SD SZ TZ UG ZM ZW AM AZ BY KG MD RU TJ TM AT BE BG CH CY DE DK EE ES FI FR GB GR HU IE IS IT LU LV MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2006542332 Country of ref document: JP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 05793706 Country of ref document: EP Kind code of ref document: A1 |