WO2011024408A1 - 拡散剤組成物、不純物拡散層の形成方法、および太陽電池 - Google Patents
拡散剤組成物、不純物拡散層の形成方法、および太陽電池 Download PDFInfo
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- WO2011024408A1 WO2011024408A1 PCT/JP2010/005093 JP2010005093W WO2011024408A1 WO 2011024408 A1 WO2011024408 A1 WO 2011024408A1 JP 2010005093 W JP2010005093 W JP 2010005093W WO 2011024408 A1 WO2011024408 A1 WO 2011024408A1
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- impurity diffusion
- agent composition
- diffusing agent
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F10/00—Individual photovoltaic cells, e.g. solar cells
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- H10P32/16—
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/22—Diffusion of impurity materials, e.g. doping materials, electrode materials, into or out of a semiconductor body, or between semiconductor regions; Interactions between two or more impurities; Redistribution of impurities
- H01L21/228—Diffusion of impurity materials, e.g. doping materials, electrode materials, into or out of a semiconductor body, or between semiconductor regions; Interactions between two or more impurities; Redistribution of impurities using diffusion into or out of a solid from or into a liquid phase, e.g. alloy diffusion processes
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/22—Diffusion of impurity materials, e.g. doping materials, electrode materials, into or out of a semiconductor body, or between semiconductor regions; Interactions between two or more impurities; Redistribution of impurities
- H01L21/2225—Diffusion sources
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F10/00—Individual photovoltaic cells, e.g. solar cells
- H10F10/10—Individual photovoltaic cells, e.g. solar cells having potential barriers
- H10F10/14—Photovoltaic cells having only PN homojunction potential barriers
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F71/00—Manufacture or treatment of devices covered by this subclass
- H10F71/121—The active layers comprising only Group IV materials
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- H10P32/14—
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- H10P32/19—
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- 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
- Y02E10/547—Monocrystalline silicon PV cells
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- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Definitions
- the present invention relates to a diffusing agent composition, a method for forming an impurity diffusion layer, and a solar cell.
- a diffusing agent In the manufacture of solar cells, spin coating is often used as a method for applying a diffusing agent to the surface of a semiconductor substrate, but attempts have been made to employ screen printing, roll coating, or the like.
- screen printing method first, a screen (printing plate) made of mesh-like silk, synthetic resin, stainless steel or the like is stretched on a frame, and a portion where a diffusing agent passes and a portion where it does not pass are formed on the screen.
- a diffusing agent is applied to the screen, and the applied diffusing agent is extruded onto the surface of the semiconductor substrate with a squeegee. Then, the diffusing agent is transferred to the surface of the semiconductor substrate, whereby a coating film of the diffusing agent including a predetermined pattern or line is formed on the surface of the semiconductor substrate.
- a printing roller (printing plate) in which grooves are formed along the circumference and a pressing roller for pressing the semiconductor substrate against the printing roller are arranged to face each other with a slight distance therebetween.
- the printing roller and the pressing roller are rotated in opposite directions, and the semiconductor substrate is passed between them.
- the printing roller and the semiconductor substrate come into contact with each other with pressure, and the diffusing agent filled in the groove of the printing roller is transferred to the surface of the semiconductor substrate, thereby including a predetermined pattern or line on the surface of the semiconductor substrate.
- a coating of agent is formed.
- Patent Document 1 describes a dopant paste (diffusing agent composition) intended to be used in these printing methods.
- a diffusing agent that can be suitably used in these methods has not been known. That is, in the above-described screen printing method and roll coat printing method, since the diffusing agent is applied to the mesh-shaped or roll-shaped printing plate, the diffusing agent needs to have a predetermined viscosity. In order to impart viscosity to the diffusing agent, the conventional diffusing agent has a solid content concentration set to be somewhat high, but this makes the diffusing agent easy to dry. When the diffusing agent applied to the printing plate is dried, printing blur occurs on the semiconductor substrate, and a good coating film cannot be formed.
- the diffusing agent used in the screen printing method or roll coat printing method has been required to have a predetermined viscosity but be difficult to dry.
- the diffusing agent can form an accurate coating film shape (pattern) when applied to the surface of the semiconductor substrate, that is, the coating film formability and evenly diffuse and diffuse in a predetermined area of the semiconductor substrate.
- the resistance value of a region to a desired value that is, to improve the diffusibility.
- the present invention has been made on the basis of such recognition by the inventor, and the purpose thereof is an diffusion film that has excellent coating film forming properties and diffusibility, and that can be suitably employed in screen printing methods and roll coat printing methods. It is providing the agent composition, the formation method of the impurity diffusion layer using the said diffusing agent composition, and a solar cell.
- an aspect of the present invention is a diffusing agent composition
- the diffusing agent composition is a diffusing agent composition used for printing an impurity diffusing component on a semiconductor substrate.
- Component (A) binder resin (B) that disappears by thermal decomposition at a temperature lower than the temperature at which impurity diffusion component (A) starts thermal diffusion, SiO 2 fine particles (C), and a boiling point of 100 ° C. or higher
- a diffusing agent composition that has excellent coating film forming properties and diffusibility, and can be suitably employed in screen printing methods and roll coat printing methods.
- Another embodiment of the present invention is a method for forming an impurity diffusion layer.
- the method for forming an impurity diffusion layer includes a coating film forming step of forming a coating film by printing the diffusing agent composition of the above embodiment, and a diffusing agent composition.
- the impurity diffusion layer can be formed with higher accuracy.
- Still another embodiment of the present invention is a solar cell, and the solar cell includes a semiconductor substrate having an impurity diffusion layer formed by the impurity diffusion layer forming method of the above embodiment.
- the diffusing agent composition which can be employ
- 1A to 1D are process cross-sectional views for explaining a method for manufacturing a solar cell including a method for forming an impurity diffusion layer according to an embodiment.
- 2A to 2D are process cross-sectional views for explaining a method for manufacturing a solar cell including a method for forming an impurity diffusion layer according to an embodiment.
- the diffusing agent composition according to the present embodiment is a diffusing agent composition used for printing an impurity diffusing component on a semiconductor substrate, and includes an impurity diffusing component (A), a binder resin (B), and SiO 2 fine particles ( C) and an organic solvent (D).
- an impurity diffusing component A
- a binder resin B
- SiO 2 fine particles C
- an organic solvent D
- the impurity diffusion component (A) is a compound generally used as a dopant for the production of solar cells.
- the impurity diffusion component (A) is an N-type impurity diffusion component containing a group V (group 15) element compound or a P-type impurity diffusion component containing a group III (group 13) element compound.
- an N-type or P-type impurity diffusion layer (impurity diffusion region) can be formed in the semiconductor substrate.
- An N-type impurity diffusion component containing a group V element compound can form an N-type impurity diffusion layer in a P-type semiconductor substrate in the step of forming an electrode in a solar cell.
- An N + -type (high-concentration N-type) impurity diffusion layer can be formed therein.
- the group V element compound contained in the impurity diffusion component (A) include P 2 O 5 , Bi 2 O 3 , Sb (OCH 2 CH 3 ) 3 , SbCl 3 , As (OC 4 H 9 ) 3 and the like.
- the impurity diffusion component (A) contains one or more of these compounds.
- the P-type impurity diffusion component containing a Group III element compound can form a P-type impurity diffusion layer in the N-type semiconductor substrate in the step of forming the electrode in the solar cell.
- a P + -type (high concentration P-type) impurity diffusion layer can be formed in the semiconductor substrate.
- the group III element compound contained in the impurity diffusion component (A) include B 2 O 3 and Al 2 O 3 , and the impurity diffusion component (A) contains one or more of these compounds. .
- the amount of the impurity diffusion component (A) added is appropriately adjusted according to the thickness of the impurity diffusion layer formed on the semiconductor substrate.
- the amount of the impurity diffusion component (A) added is based on the total mass of the solid components of the impurity diffusion component (A), the binder resin (B), and the SiO 2 fine particles (C) (when the solid component is 100). ), Preferably 5 to 60% by mass, more preferably 15 to 50% by mass.
- the addition amount of the impurity diffusion component (A) is 5% by mass or more, better diffusibility is obtained, and when the addition amount of the impurity diffusion component (A) is 60% by mass or less, a more stable solution Good film formability is obtained.
- Binder resin (B) The binder resin (B) has a characteristic that the impurity diffusion component (A) is well dispersed. Therefore, the binder resin (B) plays a role of uniformly dispersing the impurity diffusion component (A) in the diffusing agent composition, thereby uniformly dispersing the impurity diffusion component (A) on the surface of the semiconductor substrate.
- the binder resin (B) is a resin that is thermally decomposed and disappears at a temperature lower than the temperature at which the impurity diffusion component (A) starts thermal diffusion.
- the impurity diffusion component (A) when the impurity diffusion component (A) is thermally diffused, no carbon remains on the surface of the semiconductor substrate, and as a result, the carbon diffuses into the semiconductor substrate together with the thermal diffusion of the impurity diffusion component (A) to obtain a desired resistance value. It is possible to avoid situations such as disappearance or variation in resistance value.
- the diffusibility of the diffusing agent composition can be improved, and the resistance value in the region where the diffusing agent composition of the semiconductor substrate is diffused is accurately adjusted to a desired value.
- the “temperature at which thermal diffusion starts” is a temperature at which the entry of impurity diffusion components from the surface of the semiconductor substrate into the semiconductor substrate begins.
- the impurity diffusion components are composed of the semiconductor substrate and the diffusing agent composition.
- the temperature when entering from the interface with the object about 10 nm, preferably about 1 nm.
- the “disappearing by thermal decomposition” means, for example, that the binder resin disappears about 95%, preferably about 99%, more preferably 100% of the total mass of the binder resin.
- the binder resin (B) As the binder resin (B), a resin whose thermal decomposition temperature is less than 200 ° C. lower than the temperature at which the impurity diffusion component (A) starts thermal diffusion, or a resin whose thermal decomposition temperature is less than 400 ° C. Is preferred.
- the binder resin (B) is preferably a resin that is thermally decomposed by 80% by mass or more at a heating temperature of 500 ° C. According to these, it is possible to more reliably avoid a state in which there is a carbon residue during thermal diffusion of the impurity diffusion component (A).
- the “thermal decomposition temperature” is a temperature when the mass reduction of the binder resin starts, for example, when the mass of the binder resin is reduced by about 5%, preferably about 1% of the total mass of the binder resin. Temperature.
- the binder resin (B) is preferably a non-silicon resin.
- the diffusing agent composition adheres to the printing plate when the diffusing agent composition attached to the printing plate of the screen printing machine or roll coater dries. There is a case.
- hydrofluoric acid HF
- the hydrofluoric acid adhering to the printing plate becomes a metal part of the printing machine. There is a risk of adhesion and corrosion of these metal parts.
- hydrofluoric acid is a deleterious substance, the danger accompanying the removal work of a diffusing agent composition will increase.
- the diffusing agent composition dried on the printing plate can be washed with an organic solvent such as acetone or isobutanol. Therefore, the diffusing agent composition according to the present embodiment is easy to handle.
- the binder resin (B) includes an acrylic resin.
- the acrylic resin contained in the binder resin (B) preferably has a butyral group.
- Specific examples of the binder resin (B) include methyl methacrylate (MMA), methacrylic acid (MAA), isobutyl methacrylate (i-BMA), tertiary butyl methacrylate (t-BMA), acrylic acid, ethyl acrylate, methyl acrylate, Examples thereof include acrylic resins composed of polymerizable monomers such as butyl acrylate, hydroxyethyl acrylate, hydroxypropyl acrylate, isobutyl acrylate, ethyl methacrylate, butyl methacrylate, and hydroxypropyl methacrylate.
- the addition amount of the binder resin (B) is preferably 5 to 60% by mass with respect to the total mass of the solid component of the impurity diffusion component (A), the binder resin (B), and the SiO 2 fine particles (C), More preferably, it is 15 to 50% by mass.
- the addition amount of the binder resin (B) is 5% by mass or more, the coating film formability is further improved and a uniform coating film (printed film) can be formed, thereby obtaining good diffusibility.
- the addition amount of the binder resin (B) is 60% by mass or less, a more stable solution and good diffusibility can be obtained.
- SiO 2 fine particles (C) are added as a filler, and the compatibility of the impurity diffusion component (A) and the binder resin (B) can be improved by adding the SiO 2 fine particles (C).
- the impurity diffusion component (A) can be uniformly applied to the surface of the semiconductor substrate, and as a result, the impurity diffusion component (A) is more uniformly applied to the semiconductor substrate. Can diffuse. Therefore, the diffusibility of the diffusing agent composition can be improved by the SiO 2 fine particles (C).
- the average particle size is preferably about 1 ⁇ m or less.
- SiO 2 fine particles (C) include fumed silica.
- the addition amount of SiO 2 fine particles (C) is an impurity diffusion component (A), relative to the total weight of the solid content of the binder resin (B), and SiO 2 particles (C), preferably 5 to 60 mass% More preferably, it is 15 to 50% by mass.
- the addition amount of the SiO 2 fine particles (C) is 5% by mass or more, a more stable solution can be obtained and better diffusibility can be obtained.
- the added amount of the SiO 2 fine particles (C) is 60% by mass or less, better coating film formability is obtained, and better diffusibility is obtained.
- the SiO 2 fine particles (C) are not added, the solution is difficult to stabilize, and the coating film has a mottled pattern, making it difficult to obtain good diffusibility.
- Organic solvent (D) contains an organic solvent (D1) having a boiling point of 100 ° C. or higher. Since the boiling point of the organic solvent (D1) is 100 ° C. or higher, drying of the diffusing agent composition can be suppressed. Therefore, when a diffusing agent composition is applied to a printing plate used in a roll coat printing method or a screen printing method, it can be avoided that the diffusing agent composition is dried and fixed on the printing plate. Therefore, by containing the organic solvent (D), it is possible to prevent printing blurring from occurring in the coating film printed on the semiconductor substrate. That is, the coating film formability of the diffusing agent composition is improved by the organic solvent (D).
- an organic solvent (D) contains an organic solvent (D1) so that it may become 10 mass% or more with respect to the total mass of an organic solvent (D).
- the content of the organic solvent (D1) with respect to the organic solvent (D) is less than 10% by mass, the obtained drying suppression effect is small, and printing blur may occur in the coating film formed on the surface of the semiconductor substrate.
- Examples of the organic solvent (D1) include ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monopropyl ether, ethylene glycol monobutyl ether, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, ethylene glycol dipropyl ether, propylene glycol monomethyl ether, Propylene glycol monoethyl ether, propylene glycol monopropyl ether, propylene glycol monobutyl ether, propylene glycol dimethyl ether, propylene glycol diethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monophenyl ether, diethylene glycol Dimethyl ether, diethylene glycol diethyl ether, triethylene glycol monomethyl ether, triethylene glycol monoethyl ether, triethylene glycol dimethyl ether, triethylene glycol diethyl ether, tripropylene glycol monomethyl
- Examples of the organic solvent (D) include a mixture of the above-mentioned organic solvent (D1) and ethanol, isopropanol, methyl ethyl ketone, acetone, ethyl acetate, methanol, n-hexane, cyclohexane and the like.
- the concentration of the metal impurity contained in the diffusing agent composition is preferably 500 ppm or less. Thereby, the fall of the efficiency of the photovoltaic effect which arises by containing metal impurities can be suppressed.
- the diffusing agent composition of the present embodiment may contain a general surfactant, antifoaming agent, and the like as other additives.
- the ratio of the solid component to the total mass of the diffusing agent composition can be appropriately changed depending on the printing method, but is preferably 5 to 90% by mass.
- FIGS. 1 and 2 a method of forming an impurity diffusion layer on a semiconductor substrate using a roll coat printing method or a screen printing method, and a solar cell including the semiconductor substrate on which the impurity diffusion layer is formed thereby A manufacturing method will be described.
- 1A to 1D and FIGS. 2A to 2D are steps for explaining a method for manufacturing a solar cell including a method for forming an impurity diffusion layer according to an embodiment. It is sectional drawing.
- a method for forming an N-type impurity diffusion layer in a P-type semiconductor substrate will be described as an example.
- the present invention is not limited to this.
- a P-type impurity diffusion layer is formed in an N-type semiconductor substrate. You can also.
- the method for forming an impurity diffusion layer according to the present embodiment includes a step of printing the above diffusing agent composition containing the impurity diffusing component (A) on a semiconductor substrate to form a coating film, Diffusing the impurity diffusion component (A) into the semiconductor substrate.
- a P-type semiconductor substrate 1 such as a silicon substrate is prepared.
- a texture portion 1a having a fine concavo-convex structure is formed on one main surface of the semiconductor substrate 1 using a known wet etching method. Reflection of light on the surface of the semiconductor substrate 1 is prevented by the texture portion 1a.
- the above-described diffusing agent composition 2 containing the N-type impurity diffusion component (A) is applied to the main surface of the semiconductor substrate 1 on the textured portion 1a side.
- the diffusing agent composition 2 is applied to the surface of the semiconductor substrate 1 by a roll coat printing method or a screen printing method. That is, in the case of the roll coat printing method, the diffusing agent composition 2 is filled in a printing roller provided in a well-known roll coater, and the semiconductor substrate 1 is interposed between the printing roller and a roller disposed opposite to the printing roller. The diffusing agent composition 2 is printed on the semiconductor substrate 1.
- the diffusing agent composition 2 is applied to a screen provided in a known screen printing machine, and the diffusing agent composition 2 is extruded onto the surface of the semiconductor substrate 1 with a squeegee.
- the diffusing agent composition 2 is printed on 1. After forming the coating film in this manner, the applied diffusing agent composition 2 is dried using a known means such as an oven.
- the semiconductor substrate 1 coated with the diffusing agent composition 2 is placed in an electric furnace and baked. After firing, the N-type impurity diffusion component (A) in the diffusing agent composition 2 is diffused from the surface of the semiconductor substrate 1 into the semiconductor substrate 1 in an electric furnace. Instead of the electric furnace, the semiconductor substrate 1 may be heated by conventional laser irradiation. In this way, the N-type impurity diffusion component (A) is diffused into the semiconductor substrate 1 to form the N-type impurity diffusion layer 3.
- the diffusing agent composition 2 is removed by a known etching method.
- a silicon nitride film SiN film
- CVD method chemical vapor deposition method
- a passivation film 4 made of a film is formed. This passivation film 4 also functions as an antireflection film.
- the surface electrode 5 is patterned on the main surface of the semiconductor substrate 1 on the side of the passivation film 4 by screen printing a silver (Ag) paste.
- the surface electrode 5 is formed in, for example, a comb pattern in order to increase the efficiency of the solar cell.
- the back electrode 6 is formed on the other main surface of the semiconductor substrate 1 by screen printing an aluminum (Al) paste.
- the semiconductor substrate 1 on which the back electrode 6 is formed is placed in an electric furnace and baked, and then the aluminum on which the back electrode 6 is formed is transferred into the semiconductor substrate 1. To diffuse. Thereby, the electrical resistance on the back electrode 6 side can be reduced.
- the solar cell 10 according to the present embodiment can be manufactured through the above steps.
- the diffusing agent composition according to the present embodiment includes the impurity diffusion component (A) and the binder that decomposes and disappears at a temperature lower than the temperature at which the impurity diffusion component (A) starts thermal diffusion.
- the diffusing agent composition according to the present embodiment has almost no carbon residue during thermal diffusion of the impurity diffusing component (A), has high diffusibility, and is difficult to dry, so there is little printing blur and high coating film formation
- the diffusing agent composition according to the present embodiment can be easily removed with an organic solvent for washing even when dried, it can be suitably employed in a screen printing method or a roll coat printing method.
- the impurity diffusion layer can be formed with higher accuracy.
- the coating film with higher accuracy can be formed by using this diffusing agent composition, the reliability of the solar cell can be improved.
- the binder resin (B) a resin having a thermal decomposition temperature lower than 200 ° C. lower than the temperature at which the impurity diffusion component (A) starts thermal diffusion, or a thermal decomposition temperature lower than 400 ° C.
- the resin having it is possible to further reduce the possibility of the presence of carbon residue when the impurity diffusion component (A) starts thermal diffusion, and to further improve the diffusibility of the diffusing agent composition. Can do.
- the binder resin (B) is a non-silicon resin, it can be easily removed by washing with an organic solvent having low toxicity, that is, the apparatus cleaning property can be improved.
- the organic solvent (D) contains the organic solvent (D1) so as to be 10% by mass or more with respect to the total mass of the organic solvent (D), the possibility of printing blurring being further reduced. Therefore, the film-forming property of the diffusing agent composition can be further improved.
- an impurity diffusion region can be selectively provided at a desired location. Therefore, compared with the conventional method, consumption of a diffusing agent composition can be suppressed without requiring a complicated process. Thereby, the manufacturing cost of a solar cell can be held down.
- the diffusing agent composition is printed on the semiconductor substrate by the roll coat printing method or the screen printing method, but other methods such as spin-on method, spray printing method, ink jet printing method, letterpress printing method, intaglio printing method, etc. A printing method may be adopted.
- MMA Methyl methacrylate
- MAA Methacrylic acid
- i-BMA Isobutyl methacrylate
- ACA 200M Acrylic resin (manufactured by Daicel Cytec)
- Macromelt OM652 Polyamide resin (Henkel)
- Macromelt 6900 Polyamide resin (Henkel)
- AEROSIL200 Fumed silica (manufactured by Nippon Aerosil Co., Ltd.)
- the ratio (mass%) of each component is a ratio with respect to the total mass of the diffusing agent composition.
- the diffusing agent compositions of Examples 1 to 3, 7, 8, 12 to 17, and Comparative Examples 3 to 5 were screen-printed on a P-type semiconductor substrate using a screen printer (MT2030 type (manufactured by Murakami Techno Co., Ltd.)). did.
- the diffusing agent compositions of Examples 9 to 11 were screen-printed on an N-type semiconductor substrate using the same screen printer.
- the printing conditions were a printing pressure of 4.2 kgf / cm 2 , a squeegee speed of 3.52 cm / sec, and a squeegee hardness of 70 °.
- the diffusing agent compositions of Examples 1 to 7 and Comparative Examples 1, 2, and 4 were roll coat printed on a P-type semiconductor substrate using a roll coater (RC-353-P (Dainippon Screen Mfg. Co., Ltd.)). did.
- the semiconductor substrate was placed on a hot plate and dried at 150 ° C. for 3 minutes. Subsequently, the semiconductor substrate was placed in an electric furnace, and the semiconductor substrate was baked by heating at 600 ° C. for 30 minutes in an O 2 atmosphere. Thereafter, this semiconductor substrate was heated at 900 ° C. for 30 minutes in an N 2 atmosphere for Examples 1 to 8, 12 to 17 and Comparative Examples 1 to 5, and 950 for Examples 9 to 11 in an N 2 atmosphere.
- the impurity diffusion component (A) was thermally diffused by heating at 0 ° C. for 30 minutes. Then, the phosphorous silicate glass film (PSG film) formed on the surface of the semiconductor substrate by thermal diffusion was peeled off with hydrofluoric acid (hydrogen fluoride).
- the binder resin (B) having a thermal decomposition temperature of less than 400 ° C. corresponds to a binder resin that decomposes and disappears at a temperature lower than the temperature at which the impurity diffusion component (A) starts thermal diffusion, This corresponds to a binder resin having a thermal decomposition temperature lower than 200 ° C. lower than the temperature at which the impurity diffusion component (A) starts thermal diffusion.
- the diffusing agent composition adhering to the screen used for screen printing or the printing roll used for roll coat printing is washed with an organic solvent that does not corrode the metal parts of the printing press. It was visually evaluated whether or not it was removed (O: removed, x: residue was not removed).
- the organic solvents used are as shown in Tables 1 to 4.
- the results of Examples 1 to 7 are shown in Table 1, the results of Examples 8 to 14 are shown in Table 2, the results of Examples 15 to 17 are shown in Table 3, and the results of Comparative Examples 1 to 5 are shown in Table 4.
- the content of the organic solvent (D1) is 10% by mass.
- the diffusing agent composition of Example 7 which is less than 8% (8%)
- better results were obtained for drying properties.
- the binder resin (B) of Comparative Example 3 was a silane compound, no carbon residue was observed.
- the present invention can be used for a diffusing agent composition, a method for forming an impurity diffusion layer, and a solar cell.
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Abstract
Description
不純物拡散成分(A)は、一般にドーパントとして太陽電池の製造に用いられる化合物である。不純物拡散成分(A)は、V族(15族)元素の化合物を含むN型の不純物拡散成分、またはIII族(13族)元素の化合物を含むP型の不純物拡散成分であり、太陽電池における電極を形成する工程において、半導体基板内にN型またはP型の不純物拡散層(不純物拡散領域)を形成することができる。V族元素の化合物を含むN型の不純物拡散成分は、太陽電池における電極を形成する工程において、P型の半導体基板内にN型の不純物拡散層を形成することができ、N型の半導体基板内にN+型(高濃度N型)の不純物拡散層を形成することができる。不純物拡散成分(A)に含まれるV族元素の化合物としては、例えば、P2O5、Bi2O3、Sb(OCH2CH3)3、SbCl3、As(OC4H9)3などが挙げられ、不純物拡散成分(A)にはこれらの化合物が1種類以上含まれる。また、III族元素の化合物を含むP型の不純物拡散成分は、太陽電池における電極を形成する工程において、N型の半導体基板内にP型の不純物拡散層を形成することができ、P型の半導体基板内にP+型(高濃度P型)の不純物拡散層を形成することができる。不純物拡散成分(A)に含まれるIII族元素の化合物としては、例えば、B2O3、Al2O3などが挙げられ、不純物拡散成分(A)にはこれらの化合物が1種類以上含まれる。
バインダー樹脂(B)は、不純物拡散成分(A)が良好に分散する特性を有する。そのため、バインダー樹脂(B)は、不純物拡散成分(A)を拡散剤組成物中に均一に分散させ、これにより不純物拡散成分(A)を半導体基板表面に均一に分散させる役割を果たす。バインダー樹脂(B)は、不純物拡散成分(A)が熱拡散を開始する温度未満の温度で熱分解して消失する樹脂である。そのため、不純物拡散成分(A)の熱拡散時に、半導体基板表面にカーボンが残らず、これにより不純物拡散成分(A)の熱拡散とともにカーボンが半導体基板内に拡散して所望の抵抗値が得られなくなったり、抵抗値のばらつきが生じるといった事態を回避することができる。
SiO2微粒子(C)はフィラーとして添加され、SiO2微粒子(C)の添加によって不純物拡散成分(A)とバインダー樹脂(B)との相溶性を向上させることができる。不純物拡散成分(A)とバインダー樹脂(B)との相溶性が向上すると、不純物拡散成分(A)を半導体基板表面により均一に塗布でき、その結果、不純物拡散成分(A)を半導体基板により均一に拡散させることができる。そのため、SiO2微粒子(C)によって、拡散剤組成物の拡散性を向上させることができる。SiO2微粒子(C)の大きさは、平均粒径が約1μm以下であることが好ましい。
有機溶剤(D)は、沸点が100℃以上の有機溶剤(D1)を含有する。有機溶剤(D1)の沸点が100℃以上であるため、拡散剤組成物の乾燥を抑制することができる。そのため、ロールコート印刷法やスクリーン印刷法で用いられる印刷版に拡散剤組成物を塗布した際に、拡散剤組成物が印刷版上で乾燥して固着してしまうのを回避することができる。したがって、有機溶剤(D)を含有することで、半導体基板に印刷された塗膜に印刷カスレが生じるのを防ぐことができる。すなわち、有機溶剤(D)によって拡散剤組成物の塗膜形成性が向上する。有機溶剤(D)は、有機溶剤(D1)を、有機溶剤(D)の全質量に対して10質量%以上となるように含むことが好ましい。有機溶剤(D)に対する有機溶剤(D1)の含有量が10質量%未満の場合には、得られる乾燥抑制効果が小さく、半導体基板表面に形成した塗膜に印刷カスレが生じる可能性がある。
図1および図2を参照して、半導体基板にロールコート印刷法またはスクリーン印刷法を用いて不純物拡散層を形成する方法と、これにより不純物拡散層が形成された半導体基板を備えた太陽電池の製造方法について説明する。図1(A)~図1(D)、および図2(A)~図2(D)は、実施の形態に係る不純物拡散層の形成方法を含む太陽電池の製造方法を説明するための工程断面図である。なお、ここではP型の半導体基板にN型の不純物拡散層を形成する方法を例として説明するが、特にこれに限定されず、例えばN型の半導体基板にP型の不純物拡散層を形成することもできる。
下記表1~4に記載の成分および含有比に従って、不純物拡散成分(A)、バインダー樹脂(B)、SiO2微粒子(C)、および有機溶剤(D)を混合して各成分を均一に分散させて、実施例1~17、および比較例1~5に係る拡散剤組成物を得た。
MMA:メチルメタクリレート
MAA:メタクリル酸
i-BMA:イソブチルメタクリレート
ACA 200M:アクリル樹脂(ダイセルサイテック社製)
マクロメルトOM652:ポリアミド樹脂(ヘンケル社製)
マクロメルト6900:ポリアミド樹脂(ヘンケル社製)
AEROSIL200:ヒュームドシリカ(日本アエロジル株式会社製)
各構成成分の割合(質量%)は、拡散剤組成物の全質量に対する割合である。
実施例1~3、7、8、12~17、比較例3~5の拡散剤組成物は、スクリーン印刷機(MT2030型(ムラカミテクノ株式会社製))を用いてP型半導体基板にスクリーン印刷した。また、実施例9~11の拡散剤組成物は、同じスクリーン印刷機を用いてN型半導体基板にスクリーン印刷した。印刷条件は、印圧を4.2kgf/cm2、スキージ速度を3.52cm/sec、スキージ硬度を70°とした。また、実施例1~7、比較例1、2、4の拡散剤組成物は、ロールコーター(RC-353-P(大日本スクリーン製造社製))を用いてP型半導体基板にロールコート印刷した。各拡散剤組成物の印刷後、半導体基板をホットプレート上に載置して、150℃で3分間乾燥させた。続いて、半導体基板を電気炉内に載置し、O2雰囲気下、600℃で30分間加熱して半導体基板を焼成した。その後、この半導体基板を、実施例1~8、12~17、比較例1~5についてはN2雰囲気下、900℃で30分間加熱し、実施例9~11についてはN2雰囲気下、950℃で30分間加熱して、不純物拡散成分(A)を熱拡散させた。そして、熱拡散によって半導体基板表面に形成されたリンシリケートガラス膜(PSG膜)をフッ酸(フッ化水素)で剥離した。なお、ここでは、熱分解温度が400℃未満のバインダー樹脂(B)が、不純物拡散成分(A)が熱拡散を開始する温度未満の温度で熱分解して消失するバインダー樹脂に相当し、また、熱分解温度が不純物拡散成分(A)が熱拡散を開始する温度よりも200℃低い温度未満であるバインダー樹脂に相当する。
スクリーン印刷に使用されたスクリーン、あるいはロールコート印刷に使用された印刷ロールに付着した拡散剤組成物を、印刷機の金属部品を腐食させない有機溶剤を用いて洗浄し、付着した拡散剤組成物が除去されたか否かを目視で評価した(○:除去された、×:除去されずに残渣が残った)。使用した有機溶剤は、表1~4の通りである。実施例1~7の結果を表1に、実施例8~14の結果を表2に、実施例15~17の結果を表3に、比較例1~5の結果を表4に示す。
拡散剤組成物が印刷機上で乾燥した場合には、印刷した塗膜に印刷カスレが生じる。そこで、半導体基板に形成された塗膜に印刷カスレが見られるか否かを目視で確認して、拡散剤組成物の印刷機上での乾燥性を評価した(◎:印刷カスレがない、○:わずかに印刷カスレが見られるが太陽電池の製造において許容できる程度である、×:許容できない程度の印刷カスレがある)。実施例1~7、比較例1、2、4は、ロールコーター上での乾燥性を、実施例8~17、比較例3、5は、スクリーン印刷機上での乾燥性を評価した。実施例1~7の結果を表1に、実施例8~14の結果を表2に、実施例15~17の結果を表3に、比較例1~5の結果を表4に示す。なお、前記「太陽電池の製造において許容できる程度」、および「許容できない程度」は、当業者が実験等によって適宜設定することができる。
不純物拡散成分(A)を熱拡散させた後、半導体基板表面にカーボン残渣が見られるか、目視で評価した。評価は、カーボン残渣が見られた場合を「有り」、カーボン残渣が見られなかった場合を「無し」とした。実施例1~7の結果を表1に、実施例8~14の結果を表2に、実施例15~17の結果を表3に、比較例1~5の結果を表4に示す。
半導体基板に形成された不純物拡散層のシート抵抗値を、シート抵抗測定器(VR-70(国際電気株式会社製))を用いて四探針法により測定した。実施例1~7の結果を表1に、実施例8~14の結果を表2に、実施例15~17の結果を表3に、比較例1~5の結果を表4に示す。
Claims (10)
- 半導体基板への不純物拡散成分の印刷に用いられる拡散剤組成物であって、
不純物拡散成分(A)と、
前記不純物拡散成分(A)が熱拡散を開始する温度未満の温度で熱分解して消失するバインダー樹脂(B)と、
SiO2微粒子(C)と、
沸点が100℃以上の有機溶剤(D1)を含む有機溶剤(D)と、
を含有することを特徴とする拡散剤組成物。 - 前記バインダー樹脂(B)は、その熱分解温度が、前記不純物拡散成分(A)が熱拡散を開始する温度よりも200℃低い温度未満であることを特徴とする請求項1に記載の拡散剤組成物。
- 前記バインダー樹脂(B)は、その熱分解温度が400℃未満であることを特徴とする請求項1または2に記載の拡散剤組成物。
- 前記バインダー樹脂(B)は、非シリコン系樹脂であることを特徴とする請求項1乃至3のいずれか1項に記載の拡散剤組成物。
- 前記バインダー樹脂(B)は、アクリル系樹脂を含むことを特徴とする請求項1乃至4のいずれか1項に記載の拡散剤組成物。
- 前記アクリル系樹脂は、ブチラール基を有することを特徴とする請求項5に記載の拡散剤組成物。
- 前記有機溶剤(D)は、前記有機溶剤(D1)を、有機溶剤(D)の全質量に対して10質量%以上となるように含むことを特徴とする請求項1乃至6のいずれか1項に記載の拡散剤組成物。
- 半導体基板に、請求項1乃至7のいずれか1項に記載の拡散剤組成物を印刷して塗膜を形成する塗膜形成工程と、
前記拡散剤組成物の不純物拡散成分(A)を前記半導体基板に拡散させる拡散工程と、
を含むことを特徴とする不純物拡散層の形成方法。 - 前記塗膜形成工程において、ロールコート印刷法またはスクリーン印刷法により、半導体基板に拡散剤組成物を印刷することを特徴とする請求項8に記載の不純物拡散層の形成方法。
- 請求項8または9に記載の不純物拡散層の形成方法により不純物拡散層が形成された半導体基板を備えたことを特徴とする太陽電池。
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- 2010-08-18 US US13/391,907 patent/US9620367B2/en active Active
- 2010-08-18 KR KR1020127007502A patent/KR101442356B1/ko active Active
- 2010-08-18 EP EP10811467.9A patent/EP2472569B1/en active Active
- 2010-08-20 TW TW099127953A patent/TWI508140B/zh active
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Cited By (12)
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| EP2545583A4 (en) * | 2010-03-08 | 2014-07-30 | Dynaloy Llc | METHOD AND COMPOSITIONS FOR DOPING SILICON SUBSTRATES WITH MOLECULAR MONOSLAYS |
| WO2013005738A1 (ja) * | 2011-07-05 | 2013-01-10 | 日立化成工業株式会社 | n型拡散層形成組成物、n型拡散層の製造方法及び太陽電池素子の製造方法 |
| JP5176158B1 (ja) * | 2011-07-05 | 2013-04-03 | 日立化成株式会社 | n型拡散層形成組成物、n型拡散層の製造方法及び太陽電池素子の製造方法 |
| CN103650111A (zh) * | 2011-07-05 | 2014-03-19 | 日立化成株式会社 | n型扩散层形成用组合物、n型扩散层的制造方法以及太阳能电池元件的制造方法 |
| CN103839787A (zh) * | 2011-07-05 | 2014-06-04 | 日立化成株式会社 | n型扩散层形成用组合物、n型扩散层的制造方法以及太阳能电池元件的制造方法 |
| CN105006429A (zh) * | 2011-07-05 | 2015-10-28 | 日立化成株式会社 | n型扩散层形成用组合物、n型扩散层的制造方法以及太阳能电池元件的制造方法 |
| CN105551947A (zh) * | 2011-07-05 | 2016-05-04 | 日立化成株式会社 | n型扩散层形成用组合物、n型扩散层的制造方法以及太阳能电池元件的制造方法 |
| WO2013011986A1 (ja) * | 2011-07-19 | 2013-01-24 | 日立化成工業株式会社 | n型拡散層形成組成物、n型拡散層の製造方法、及び太陽電池素子の製造方法 |
| JP5176159B1 (ja) * | 2011-07-19 | 2013-04-03 | 日立化成株式会社 | n型拡散層形成組成物、n型拡散層の製造方法、及び太陽電池素子の製造方法 |
| CN103794478A (zh) * | 2011-07-19 | 2014-05-14 | 日立化成株式会社 | n型扩散层形成用组合物、n型扩散层的制造方法以及太阳能电池元件的制造方法 |
| CN103387777A (zh) * | 2012-05-07 | 2013-11-13 | 东京应化工业株式会社 | 扩散剂组合物及杂质扩散层的形成方法 |
| CN103387777B (zh) * | 2012-05-07 | 2018-05-25 | 东京应化工业株式会社 | 扩散剂组合物及杂质扩散层的形成方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR101442356B1 (ko) | 2014-09-18 |
| EP2472569B1 (en) | 2018-01-03 |
| CN102473613A (zh) | 2012-05-23 |
| CN102473613B (zh) | 2015-09-02 |
| KR20120059579A (ko) | 2012-06-08 |
| JP2011071489A (ja) | 2011-04-07 |
| US20120160306A1 (en) | 2012-06-28 |
| US9620367B2 (en) | 2017-04-11 |
| TW201125024A (en) | 2011-07-16 |
| EP2472569A4 (en) | 2013-05-22 |
| TWI508140B (zh) | 2015-11-11 |
| EP2472569A1 (en) | 2012-07-04 |
| JP5815215B2 (ja) | 2015-11-17 |
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