WO2007060743A1 - 太陽電池セル - Google Patents
太陽電池セル Download PDFInfo
- Publication number
- WO2007060743A1 WO2007060743A1 PCT/JP2005/021782 JP2005021782W WO2007060743A1 WO 2007060743 A1 WO2007060743 A1 WO 2007060743A1 JP 2005021782 W JP2005021782 W JP 2005021782W WO 2007060743 A1 WO2007060743 A1 WO 2007060743A1
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- WIPO (PCT)
- Prior art keywords
- electrode
- back surface
- silver
- silver electrode
- aluminum
- Prior art date
Links
- 238000006243 chemical reaction Methods 0.000 claims abstract description 26
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 197
- 229910052709 silver Inorganic materials 0.000 claims description 197
- 239000004332 silver Substances 0.000 claims description 197
- 229910052782 aluminium Inorganic materials 0.000 claims description 89
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 89
- 230000002093 peripheral effect Effects 0.000 abstract description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 67
- 229910052710 silicon Inorganic materials 0.000 description 66
- 239000010703 silicon Substances 0.000 description 66
- 239000000758 substrate Substances 0.000 description 62
- 238000004519 manufacturing process Methods 0.000 description 24
- 229910045601 alloy Inorganic materials 0.000 description 22
- 239000000956 alloy Substances 0.000 description 22
- 238000000034 method Methods 0.000 description 21
- 238000009792 diffusion process Methods 0.000 description 19
- 239000000463 material Substances 0.000 description 11
- 230000000694 effects Effects 0.000 description 10
- 238000007650 screen-printing Methods 0.000 description 9
- 238000010304 firing Methods 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 239000004065 semiconductor Substances 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000007639 printing Methods 0.000 description 6
- 230000008602 contraction Effects 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- 239000007772 electrode material Substances 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000010248 power generation Methods 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000006117 anti-reflective coating Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000005304 joining Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 101100520660 Drosophila melanogaster Poc1 gene Proteins 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 101100520662 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) PBA1 gene Proteins 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000002003 electrode paste Substances 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 1
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910000679 solder Inorganic materials 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
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
- H01L31/022408—Electrodes for devices characterised by at least one potential jump barrier or surface barrier
- H01L31/022425—Electrodes for devices characterised by at least one potential jump barrier or surface barrier for solar cells
-
- 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
- H01L31/04—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 adapted as photovoltaic [PV] conversion devices
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/05—Electrical interconnection means between PV cells inside the PV module, e.g. series connection of PV cells
- H01L31/0504—Electrical interconnection means between PV cells inside the PV module, e.g. series connection of PV cells specially adapted for series or parallel connection of solar cells in a module
-
- 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 solar battery cell, and more particularly to a solar battery cell in which the occurrence of electrode peeling is prevented.
- Solar power generation is a clean power generation method that generates power using light energy, which is infinite energy, and does not emit harmful substances.
- This solar power generation uses a solar cell that is a photoelectric conversion element that generates electric power by converting light energy from the sun into electrical energy.
- an electrode on the back surface of a light receiving surface in a generally produced solar cell is obtained by printing silver paste and aluminum paste on the back surface of a silicon substrate by screen printing, and then drying and firing. It is formed.
- aluminum formed on almost the entire back surface of the silicon substrate serves as a positive electrode.
- a silver electrode force is formed on the back surface of the silicon substrate as an output output electrode so that the silver electrode and the aluminum electrode partially overlap (for example, see Patent Document 1 and Patent Document 2).
- the aluminum electrode for increasing the output and the silver electrode for taking out the output are formed so as to partially overlap each other.
- the three kinds of metals, silicon of the silicon substrate, aluminum of the aluminum electrode, and silver of the silver electrode are partially alloyed.
- Patent Document 1 Japanese Patent Application Laid-Open No. 2003-273378
- Patent Document 2 Japanese Patent Laid-Open No. 10-335267
- this overlapping portion is used for rapid heating and cooling during firing. However, it is very brittle due to the stress that seems to be generated due to the difference in thermal expansion coefficient of each member. For this reason, after baking, for example, when the silver electrode is overlapped on the aluminum electrode, the corner of the silver electrode may peel off at the overlapped portion.
- the present invention has been made in view of the above, and an object thereof is to obtain a solar battery cell in which electrode peeling is effectively prevented.
- a solar battery cell includes a photoelectric conversion layer, a first electrode formed on one surface side of the photoelectric conversion layer, and a photoelectric conversion.
- the second electrode formed on the other surface side of the layer, and the other surface side of the photoelectric conversion layer in the in-plane direction of the photoelectric conversion layer, the outer edge portion overlaps with the second electrode and the corner portion is rounded And a third electrode for taking out the output of the second electrode force.
- a solar battery cell according to the present invention is formed on a photoelectric conversion layer and one surface side of the photoelectric conversion layer.
- a third electrode for taking out the second electrode force output provided on the other surface side of the photoelectric conversion layer, and the outer edge of the third electrode is a second electrode.
- the third electrode and the second electrode can be reliably bonded even at the corner of the third electrode by providing the corner with a rounded portion and a substantially rectangular shape. There is an effect that it is possible to realize a solar battery cell that effectively prevents the third electrode from being peeled off.
- the solar battery cell that is effective in the present embodiment has rounded corners of the third electrode, the area of the third electrode is reduced, and the amount of electrode material used can be reduced. it can. As a result, the solar battery cell according to the present embodiment has an effect that the material cost can be reduced and an inexpensive solar battery cell can be realized.
- FIG. 1-1 is a sectional view showing a schematic configuration of the solar battery cell according to the first embodiment of the present invention.
- FIG. 1-2 is a plan view showing a schematic configuration of the front surface side ((light receiving surface side) of the solar cell according to the first embodiment of the present invention.
- FIG. 1-3 is a plan view showing a schematic configuration of the back surface side (the surface side opposite to the light receiving surface) of the solar cell according to the first embodiment of the present invention.
- Fig. 1-4 shows an enlarged view of the periphery of an alloy part in which three types of metals, silicon, aluminum, and silver, are partially alloyed in the solar cell according to the first embodiment of the present invention. It is a figure.
- FIG. 1-5 shows the periphery of region B and region C in which the aluminum electrode and the back surface silver electrode provided on the back surface of the photovoltaic cell according to Embodiment 1 of the present invention partially overlap each other. It is sectional drawing which expands and shows a part.
- FIG. 2 shows an aluminum electrode and a backside silver electrode provided on the backside of a conventional solar cell.
- FIG. 5 is an enlarged cross-sectional view of a peripheral portion of a region B ′ and a region C ′ partially overlapping with poles.
- FIG. 3-1 is a cross-sectional view for explaining the method for manufacturing the solar cell according to the first embodiment of the present invention.
- FIG. 3-2 is a cross-sectional view for explaining the method for manufacturing the solar cell according to the first embodiment of the present invention.
- FIG. 3-3 is a cross-sectional view for explaining the method for manufacturing the solar cell according to the first embodiment of the present invention.
- FIGS. 3-4 are cross-sectional views illustrating the method for manufacturing the solar battery cell according to the first embodiment of the present invention.
- FIG. 3-5 is a cross-sectional view for explaining the method for manufacturing the solar cell according to the first embodiment of the present invention.
- FIG. 3-6 is a cross-sectional view for explaining the method for manufacturing the solar cell according to the first embodiment of the present invention.
- FIG. 3-7 is a plan view showing an example of a screen mask used for printing silver paste in the production of the solar battery cell according to the first embodiment of the present invention.
- FIG. 3-8 is a cross-sectional view showing an example of a screen mask used for printing silver paste in the production of the solar cell according to the first embodiment of the present invention.
- FIGS. 3-9 are cross-sectional views for explaining the method for manufacturing the solar cell according to the first embodiment of the present invention.
- FIG. 3-10 is a cross-sectional view illustrating the method of manufacturing the solar battery cell according to the first embodiment of the present invention.
- FIG. 4 1 is a plan view for explaining dimensions on the back surface side (surface side opposite to the light receiving surface) in a specific solar cell to which Embodiment 1 of the present invention is applied. It is.
- FIG. 42 is a plan view for explaining the shape and dimensions of the back surface silver electrode in a specific solar battery cell to which the first embodiment of the present invention is applied.
- FIG. 5-1 is a plan view showing a schematic configuration of the back surface side (surface side facing the light receiving surface) of the solar cell according to the second embodiment of the present invention.
- Fig. 5-2 shows an enlarged view of the periphery of an alloy part in which three types of metals, silicon, aluminum, and silver, are partially alloyed in the solar cell according to the second embodiment of the present invention. It is a figure.
- Fig. 5-3 shows the periphery of region D and region E in which the aluminum electrode and the back surface silver electrode provided on the back surface of the solar cell according to Embodiment 2 of the present invention partially overlap each other. It is sectional drawing which expands and shows a part.
- Fig. 6-1 is a plan view for explaining the dimensions of the back surface side (surface side opposite to the light receiving surface) in a specific solar cell to which Embodiment 2 of the present invention is applied.
- FIG. 6-1 is a plan view for explaining the dimensions of the back surface side (surface side opposite to the light receiving surface) in a specific solar cell to which Embodiment 2 of the present invention is applied.
- Fig. 6-2 is a plan view for explaining the shape and dimensions of the back surface silver electrode in a specific solar cell to which the second embodiment of the present invention is applied.
- FIGS. 1-1 to 1-3 are diagrams showing a schematic configuration of the solar cell according to the first embodiment of the present invention
- FIG. 1-1 shows a schematic configuration of the solar cell according to the first embodiment
- FIG. FIG. 1-2 is a plan view showing a schematic configuration of the front surface side (light-receiving surface side) of the solar cell according to the first embodiment
- FIG. 1-3 is a back surface of the solar cell according to the first embodiment.
- It is a top view which shows schematic structure of the side (surface side facing a light-receiving surface).
- Figure 11 is a cross-sectional view taken along line AA in Figure 1-3.
- the solar cell according to the present embodiment includes a p-type layer 11 that is a p-type silicon substrate as a semiconductor substrate, and the surface of the p-type layer 11.
- An n-type diffusion layer 13 in which the conductivity type is inverted a p + layer (BSF layer: Back Surface Field) 14 containing high-concentration impurities, a semiconductor layer portion 10 that is a photoelectric conversion layer that also has a force, and the semiconductor layer portion 10
- An antireflection film 15 provided on the light receiving surface of the semiconductor layer portion 10 to prevent reflection of incident light, a surface silver electrode 21 which is a light receiving surface electrode portion provided in a substantially rod shape on the light receiving surface of the semiconductor layer 10, and
- An aluminum electrode 17 which is a back electrode part provided on almost the entire back surface of the semiconductor layer part 10 for the purpose of extraction and reflection of incident light, and an extraction electrode part for taking out power from the aluminum electrode 17 A back surface silver electrode 19.
- FIG. 1-3 and FIG. 1-4 in the solar cell that works in the present embodiment, the aluminum electrode 17 and the back surface silver electrode 19 partially overlap on the p + layer 14.
- Fig.1-4 is an enlarged view showing the periphery of the backside silver electrode 19 in the plan view of Fig.1-3.
- the aluminum electrode 17 and the backside silver electrode 19 provided on the back side of the solar cell cell partially overlap each other.
- FIG. FIG. 1-5 is an enlarged view of the periphery of the back surface silver electrode 19 in the cross-sectional view of FIG. 1-1.
- the aluminum electrode 17 and the back surface silver electrode 19 provided on the back surface of the solar battery cell are partially shown.
- FIG. 6 is an enlarged cross-sectional view of the peripheral portion of region B and region C that overlap each other.
- the back surface silver electrode 19 extends in the in-plane direction of the silicon substrate, and is substantially rectangular (rectangular). ).
- the back silver electrode 19 exhibits a curved shape at the corners of a substantially rectangular shape (rectangle). Specifically, the back silver electrode 19 has a substantially rectangular (rectangular) corner rounded.
- the shape of the back surface silver electrode 19 is substantially rectangular (rectangular) in the in-plane direction of the silicon substrate, and the corners of the substantially rectangular (rectangular) are substantially straight. It is said to be a horn.
- the region B ′ in which the aluminum electrode 17 and the back surface silver electrode 19 partially overlap and It has area C ′.
- this overlapping portion is generated due to a difference in coefficient of thermal expansion of each member, which occurs in a rapid heating process and a cooling process during firing during manufacturing. Due to the possible stress, it is very fragile. Therefore, after firing, in the region B ′ and the region C where the aluminum electrode 17 and the back surface silver electrode 19 partially overlap, the back surface is formed at the corner of the back surface silver electrode 19 as shown in the region C ′ of FIG.
- the silver electrode 19 may peel off from the aluminum electrode 17 in some cases. This stress tends to concentrate on the sharp corners of the backside silver electrode 19. That is, due to the concentration of the stress, the alloy portion 23 is not normally formed in the sharp corner portion of the back surface silver electrode 19, and peeling of the back surface silver electrode 19 tends to occur from the right corner portion.
- the corners are rounded to eliminate the sharp corners of the backside silver electrode 19 so that stress is not concentrated on the corners of the backside silver electrode 19. It is taken as a taking part.
- the stress concentrated on the corners of the back surface silver electrode 19 can be relaxed, and as shown in FIG. In the region B and the region C where the back surface silver electrode 19 partially overlaps, the alloy part 23 is reliably formed, the bonding force between the aluminum electrode 17 and the back surface silver electrode 19, the aluminum electrode 17 and the back surface silver electrode. 19 substrate bonding force is improved.
- the back surface silver electrode 19 and the aluminum electrode 17 are securely bonded even at the corners of the back surface silver electrode 19, and the back surface silver electrode 19 is peeled off. It is possible to realize a solar battery cell that effectively prevents the above-described effect.
- the rounding dimension R is larger than the dimension of the alloy part 23, a part of the alloy part of the aluminum electrode 17 and the back surface silver electrode 19 cannot be formed, which is not suitable as the back surface silver electrode 19. It is right. Therefore, as shown in FIG. 1-4, the dimensions Ll, L3, and the dimension of the part where the aluminum electrode 17 and the backside silver electrode 19 overlap in the long side direction of the backside silver electrode 19 that determines the dimensions of the alloy part 23. In addition, the dimension L5 and L7 of the portion where the aluminum electrode 17 and the back surface silver electrode 19 overlap in the short side direction of the back surface silver electrode 19 is such that the alloy part 23 can be formed reliably. Need to be determined. In addition, the dimensions of the aluminum electrode 17 and the backside silver electrode 19 are determined in consideration of the force formed by screen printing, as described later, and the misalignment during printing of the aluminum paste and silver paste. Should.
- the solar cell according to the present embodiment even when a thin silicon substrate is used to reduce the cost of the solar cell, a large number of substrates are used in the silicon substrate as in the past. It is possible to cope with the occurrence of cracks and to increase the degree of freedom in selecting the type of silver paste that can be used.
- the back surface silver electrode is used as the round portion.
- the area of the surface silver electrode 19 is reduced, and the amount of silver paste used for the back surface silver electrode 19 is reduced. Therefore, according to the solar battery cell which is effective in the present embodiment, it is possible to reduce the material cost and to realize an effect of realizing an inexpensive solar battery cell. The specific reduction effect of the silver paste will be described later.
- a method for manufacturing a solar battery cell that works as described above in the present embodiment will be described.
- a solar cell that is effective in the present embodiment, first, as shown in FIG. 3-1, for example, a p-type single crystal silicon ingot manufactured by a pulling method or a forging method is used.
- a p-type silicon substrate 1 1 ′ is sliced from the polycrystalline silicon ingot.
- caustic soda or carbonated caustic soda of several wt% to 20 wt% is etched away to a thickness of about 10 m to 20 m to remove the damage layer and contamination on the silicon surface that occurs when slicing.
- the substrate is washed with a mixed solution of hydrochloric acid and hydrogen peroxide to remove heavy metals such as iron adhering to the substrate surface.
- anisotropic etching is performed with a solution obtained by adding IPA (isopropyl alcohol) to a similar alkali low-concentration solution to form a texture so that, for example, the silicon (111) surface appears.
- IPA isopropyl alcohol
- the n-type diffusion layer 13a is formed in order to form a pn junction.
- oxyphosphorus chloride (POC1) is used, and a nitrogen gas of 800 ° C to 900 ° C is used.
- N-type diffusion layer 13a is formed on the entire surface of silicon substrate 11 'by conducting diffusion treatment in a mixed gas atmosphere of oxygen and oxygen, and thermally diffusing phosphorus as shown in Fig. 3-2 to reverse the conductivity type.
- the sheet resistance of the 11-type diffusion layer 13 & is about several tens (30 to 80 to 07), and the depth of the n-type diffusion layer 13a is, for example, about 0.3 ⁇ m to 0.5 ⁇ m. It is.
- a polymer resist paste is printed and dried by a screen printing method to form a resist.
- the n-type diffusion layer 13a formed on the back and side surfaces of the silicon substrate 11 ′ is removed by immersing in a 20 wt% potassium hydroxide solution for several minutes. Thereafter, the resist is removed with an organic solvent to obtain a silicon substrate 11 ′ having an n-type diffusion layer 13 formed on the entire surface (light receiving surface) as shown in FIG.
- an antireflection film 15 such as a silicon oxide film, a silicon nitride film, or an oxide titanium film is formed on the surface of the n-type diffusion layer 13 with a uniform thickness.
- Anti-reflective coating 15 For example, in the case of a silicon oxide film, the plasma CVD method is used to generate SiH gas and NH gas.
- the film is formed under reduced pressure at a heating temperature of 300 ° C or higher.
- the refractive index is, for example, about 2.0 to 2.2, and the optimum film thickness of the antireflection film 15 is 70 ⁇ ! ⁇ 90nm.
- an aluminum paste containing glass is printed and dried on the entire back surface (the surface opposite to the light receiving surface) of the silicon substrate 11 'as shown in Fig. 3-5.
- An aluminum paste layer 17a is formed on the entire back surface of the silicon substrate 11.
- an opening is provided corresponding to the site where the back surface silver electrode 19 is formed.
- the coating thickness of the aluminum paste can be adjusted by the diameter of the screen mask and the thickness of the emulsion.
- a silver paste for the back surface silver electrode 19 is formed on the back surface (surface opposite to the light receiving surface) of the silicon substrate 11 'on which the aluminum electrode 17 is formed as shown in Fig. 3-6. Is dried to form a silver paste layer 19a.
- the shape of the silver paste layer 19a is a substantially quadrangle (rectangle) with rounded corners as shown in FIG. 1-3.
- the silver paste can be printed, for example, using a screen mask patterned with emulsion 27 on mesh 25 as shown in FIGS. 3-7 and 3-8.
- the silver paste printed on the surface silver electrode 21 is dried on the surface (light-receiving surface) of the silicon substrate 11 'on which the antireflection film 15 is formed, and is shown in Fig. 3-9.
- a silver paste layer 21a is formed.
- the coating thickness of the silver paste can also be adjusted according to the wire diameter of the mesh forming the screen mask and the emulsion thickness.
- the front and back electrode paste layers are simultaneously fired at 600 ° C. to 900 ° C. for several minutes to several tens of minutes.
- the silver base layer is baked to form the surface silver electrode 21 as shown in FIG. 3-10, but the antireflection film 15 is melted.
- the silver material contained in the silver paste comes into contact with the silicon of the silicon substrate 11 ′ and resolidifies. As a result, conduction between the surface silver electrode 21 and silicon is ensured. Such a process is commonly called a fire-through method.
- the aluminum paste layer is baked to become the aluminum electrode 17 as shown in FIG. 3-10, and the silver paste layer is baked. As shown in Fig. 3-10, this is the back silver electrode 19.
- the aluminum paste Aluminum reacts with silicon on the silicon substrate 11 to form a p + layer 14 immediately below the aluminum electrode 17. This layer is generally called the BSF (Back Surface Field) layer and contributes to improving the energy conversion efficiency of solar cells.
- the region force-type layer 11 is sandwiched between the n-type diffusion layer 13 and the p + layer 14.
- the silver paste reacts directly with the silicon of the silicon substrate 11 where it is in direct contact with the silicon substrate 11, and the silicon and aluminum paste of the silicon substrate 11 1 when it is in contact with the aluminum paste.
- Aluminum electrode 17 Aluminum, backside silver electrode 19 silver 3 types of metal force Partly forms an alloy.
- the above-described solar cell can be realized only by changing the shape of the back surface silver electrode, and at the time of screen printing of the silver paste for the back surface silver electrode without changing the existing equipment. This can be realized only by changing the mask shape.
- Omm 19 Table 1 shows the reduction area and silver paste reduction rate.
- Embodiment 2 another embodiment of the solar battery cell according to the present invention will be described.
- the basic configuration of the solar cell according to the second embodiment is the same as that of the solar cell according to the first embodiment described above. Accordingly, the following description will be made on differences of the solar battery cell according to the second embodiment from the solar battery cell according to the first embodiment.
- members similar to those of the solar battery cell according to the first embodiment are denoted by the same reference numerals as those in the first embodiment.
- FIGS. 5-1 to 5-3 are diagrams showing a schematic configuration of the solar battery cell according to the second embodiment of the present invention.
- FIG. 5-1 is a diagram corresponding to FIG. 1-3, and is a plan view showing a schematic configuration of the back surface side (surface side opposite to the light receiving surface) of the solar cell according to the second embodiment.
- FIG. 5-2 is a view corresponding to FIG. 14 and is an enlarged view showing the periphery of the back surface silver electrode 31 in the plan view of FIG. 5-1, and shows aluminum provided on the back surface of the solar battery cell.
- FIG. 4 is an enlarged view showing a part where an electrode 17 and a back surface silver electrode 31 partially overlap.
- FIG. 5-3 is a diagram corresponding to Fig. 1-5, and is an enlarged view of the periphery of the back surface silver electrode 31.
- FIG. 4 is an enlarged cross-sectional view of a peripheral portion of a region D and a region E where and are partially overlapped. Since the cross-sectional structure of the solar battery cell according to the first embodiment and the schematic configuration on the light receiving surface side (front surface side) of the solar battery cell are the same as those in the first embodiment, FIG. 11 and FIG. Refer to
- the back surface silver electrode 31 in the present embodiment corresponds to the back surface silver electrode 19 in Embodiment 1, and the corners are rounded as shown in FIGS. 5-1 and 5-2. This is different from the first embodiment in that it is a chamfered portion instead of a portion.
- the back surface silver electrode 31 extends in the in-plane direction of the silicon substrate and is substantially rectangular (rectangular). ).
- the back silver electrode 31 has a substantially square (rectangular) corner as a chamfer.
- the corners are chamfered so as to eliminate the sharp corners of the back surface silver electrode 31 so that stress is not concentrated on the corners of the back surface silver electrode 31. ! /
- the stress concentrated on the corners of the back surface silver electrode 31 can be relaxed.
- the back surface silver electrode 19 and the aluminum electrode 17 are securely bonded even at the corners of the back surface silver electrode 19 to effectively prevent the back surface silver electrode 19 from peeling. There is an effect that a positive battery cell can be realized.
- the dimension of the portion where the aluminum electrode 17 and the backside silver electrode 31 overlap in the long side direction of the backside silver electrode 31, which determines the dimensions of the alloy part 33 is L21. , L23, and the dimensions L25 and L27 of the portion where the aluminum electrode 17 and the backside silver electrode 31 overlap in the short side direction of the backside silver electrode 31 must be determined so that the alloy part 33 can be formed reliably.
- the dimensions of the aluminum electrode 17 and the backside silver electrode 31 are as follows, taking into account the force formed by screen printing as described later, and the misalignment during printing of the aluminum paste and silver paste. Should be decided.
- the bonding between the aluminum electrode 17 and the back surface silver electrode 31 and the bonding between the aluminum electrode 17 and the back surface silver electrode 31 with the substrate are ensured.
- the conventional solar battery cell uses a sharp corner portion where the back surface silver electrode should exist as a chamfered portion.
- the area of the silver electrode is reduced, and the amount of silver paste used for the back surface silver electrode 31 is reduced. Therefore, even in the solar battery cell that is useful in the present embodiment, it is possible to reduce the material cost, and it is possible to realize an inexpensive solar battery cell.
- the solar battery cell that is useful in the present embodiment has a substantially rectangular shape (rectangular shape) with chamfered corners as shown in Fig. 5-1, when the silver paste layer is screen-printed. Except for the above, it can be manufactured in the same process as in Embodiment 1. And this embodiment The solar cell can be realized only by changing the shape of the backside silver electrode, and only by changing the mask shape during screen printing of the silver paste for the backside silver electrode without changing the existing equipment. Can be realized.
- the chamfer dimension C of the chamfered portion of the back surface silver electrode 31 is 1.
- Table 3 shows the reduction area of the backside silver electrode 31 and the reduction rate of the silver paste when it is changed in increments of 0.5mm from ⁇ 3mm.
- the reduction area (mm 2 ) of the back surface silver electrode 31 from 2. Omm 2 to 18. as the chamfer dimension C of the chamfered portion of the back surface silver electrode 31 increases to 1. Omm force 3. Om m. It has increased up to 0 mm 2.
- the amount of the silver paste for the back surface silver electrode 31 can be reduced, and the material cost can be reduced for the solar battery cell which is effective in the present embodiment. Realize inexpensive solar cells You can!
- the solar battery cell according to the first embodiment and the second embodiment is an example of the embodiment of the present invention, and the present invention is not limited by the above description, and the present invention is not limited thereto. Without departing from the scope, it can be changed as appropriate within the scope.
- the solar cell according to the present invention is useful for a solar cell having a structure in which an aluminum electrode and a silver electrode for output extraction partially overlap.
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- Condensed Matter Physics & Semiconductors (AREA)
- Electromagnetism (AREA)
- General Physics & Mathematics (AREA)
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Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05809633.0A EP1870942B1 (en) | 2005-11-28 | 2005-11-28 | Solar cell |
US11/547,656 US20080105297A1 (en) | 2005-11-28 | 2005-11-28 | Solar Cell |
JP2006517869A JP4343225B2 (ja) | 2005-11-28 | 2005-11-28 | 太陽電池セル |
CN2005800174534A CN101088167B (zh) | 2005-11-28 | 2005-11-28 | 太阳能电池单元 |
PCT/JP2005/021782 WO2007060743A1 (ja) | 2005-11-28 | 2005-11-28 | 太陽電池セル |
EP10001436.4A EP2219227B1 (en) | 2005-11-28 | 2005-11-28 | Solar cell |
HK08102548.5A HK1111807A1 (en) | 2005-11-28 | 2008-03-05 | Solar cell |
US12/756,388 US8173895B2 (en) | 2005-11-28 | 2010-04-08 | Solar cell |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP2005/021782 WO2007060743A1 (ja) | 2005-11-28 | 2005-11-28 | 太陽電池セル |
Related Child Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP10001436.4A Previously-Filed-Application EP2219227B1 (en) | 2005-11-28 | 2005-11-28 | Solar cell |
US11/547,656 A-371-Of-International US20080105297A1 (en) | 2005-11-28 | 2005-11-28 | Solar Cell |
US12/756,388 Division US8173895B2 (en) | 2005-11-28 | 2010-04-08 | Solar cell |
Publications (1)
Publication Number | Publication Date |
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WO2007060743A1 true WO2007060743A1 (ja) | 2007-05-31 |
Family
ID=38066985
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2005/021782 WO2007060743A1 (ja) | 2005-11-28 | 2005-11-28 | 太陽電池セル |
Country Status (6)
Country | Link |
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US (2) | US20080105297A1 (ja) |
EP (2) | EP1870942B1 (ja) |
JP (1) | JP4343225B2 (ja) |
CN (1) | CN101088167B (ja) |
HK (1) | HK1111807A1 (ja) |
WO (1) | WO2007060743A1 (ja) |
Cited By (7)
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WO2009017174A1 (ja) * | 2007-07-30 | 2009-02-05 | Kyocera Corporation | 太陽電池モジュール |
WO2009122977A1 (ja) * | 2008-03-31 | 2009-10-08 | シャープ株式会社 | 太陽電池、太陽電池ストリングおよび太陽電池モジュール |
WO2009157053A1 (ja) * | 2008-06-23 | 2009-12-30 | 三菱電機株式会社 | 光起電力装置およびその製造方法 |
WO2011010373A1 (ja) * | 2009-07-22 | 2011-01-27 | 三菱電機株式会社 | 太陽電池セルおよびその製造方法 |
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US20080105297A1 (en) * | 2005-11-28 | 2008-05-08 | Mitsubishi Electric Corporation | Solar Cell |
JPWO2009139390A1 (ja) * | 2008-05-15 | 2011-09-22 | 株式会社アルバック | 薄膜太陽電池モジュール及びその製造方法 |
JP5154516B2 (ja) * | 2009-05-22 | 2013-02-27 | シャープ株式会社 | 太陽電池モジュール及び太陽電池モジュールの製造方法 |
DE102011001999A1 (de) | 2011-04-12 | 2012-10-18 | Schott Solar Ag | Solarzelle |
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DE102013212845A1 (de) * | 2013-07-02 | 2015-01-08 | Solarworld Industries Sachsen Gmbh | Photovoltaikmodul |
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JPWO2012115006A1 (ja) * | 2011-02-21 | 2014-07-07 | シャープ株式会社 | スクリーンおよび太陽電池の製造方法 |
Also Published As
Publication number | Publication date |
---|---|
CN101088167A (zh) | 2007-12-12 |
HK1111807A1 (en) | 2008-08-15 |
US20080105297A1 (en) | 2008-05-08 |
EP2219227A2 (en) | 2010-08-18 |
US20100193028A1 (en) | 2010-08-05 |
EP2219227B1 (en) | 2017-06-07 |
JP4343225B2 (ja) | 2009-10-14 |
EP1870942A1 (en) | 2007-12-26 |
US8173895B2 (en) | 2012-05-08 |
EP2219227A3 (en) | 2010-12-08 |
EP1870942B1 (en) | 2016-08-24 |
EP1870942A4 (en) | 2010-09-15 |
JPWO2007060743A1 (ja) | 2009-05-07 |
CN101088167B (zh) | 2011-07-06 |
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