The present invention relates to a technology of wavelength conversion film: In particular, the present invention relates to a technology of enhancing the conversion efficiency of solar batteries in which a fluorescent substance is excited upon being irradiated with near ultraviolet light to blue light and causes light emission, thereby achieving wavelength conversion.
In general, the quantum efficiency of solar battery is lower in an ultraviolet light to blue light region than that in a green light to near infrared light region. Inconsequence, the efficiency of solar battery can be enhanced by wavelength-converting light having a wavelength of ultraviolet light to blue light of wavelength components of light reaching the solar battery to light of green light to near infrared light, thereby increasing the light in a wavelength region having high quantum efficiency of the solar battery. It has hitherto been known that the efficiency of solar battery is enhanced by setting up a wavelength conversion film in a route where light reaches the solar battery.
For example, in PTL 1, a fluorescent coloring agent is used as a wavelength conversion material. In addition, in PTL 2, a rare earth complex-containing ORMOSIL composite is used. In addition, in NPL 1, an organic metal complex is used. However, the above-described fluorescent coloring agent and organic metal complex are insufficient in terms of durability, and hence, they are difficult to keep a function as a wavelength conversion material for solar batteries over a long period of time. In addition, in PTL 3, a wavelength conversion material for solar batteries using a fluorescent substance is described. However, in PTL 3, specific numerical values of the efficiency enhancement amount are not described. In addition, in PTL 4, though a configuration in which monocrystalline silicon is interposed by a sealing agent having a conversion material capable of converting absorbed light into a light having a longer wavelength than that of the absorbed light is described, a specific configuration of the wavelength conversion material such as a fluorescent substance, etc. is not described. In addition, in PTL 5, it is described that a design to confine light from a light-emitting material in the inside of a solar battery by providing the light-emitting material with alignment is applied. However, PTL 5 does not describe the length of the light-emitting material, does not describe a composition of the light-emitting material, and does not describe a manufacturing method for providing the alignment.
PTL 1: JP-A-2001-7377
PTL 2: JP-A-2000-327715
PTL 3: JP-A-2003-218379
PTL 4: JP-A-7-202243
PTL 5: JP-T-2008-536953
NPL 1: Proceedings of the 58th Japan Society of Coordination Chemistry, 1PF-011
For the wavelength conversion material for solar batteries, grappling with use of an organic metal complex and a fluorescent substance as an inorganic compound as a wavelength conversion material for solar batteries is made. However, in the conventional wavelength conversion materials for solar batteries, the direction of light emitted from the light-emitting material is isotropic, and therefore, there are more components of light transmitting into the side on which sunlight is incident without going toward the solar battery cell. Accordingly, the conventional wavelength conversion materials have not sufficiently enhanced the photoelectric conversion efficiency of the solar batteries yet, and hence, it is demanded to more enhance the photoelectric conversion efficiency.
Under such circumstances, the present invention has been made, and an object thereof is to provide a technology for increasing the amount of light going toward a solar battery cell among lights emitted from a wavelength conversion material, thereby enabling the photoelectric conversion efficiency of the solar batteries to be enhanced.
Among the inventions disclosed in the present application, summaries of those which are representative are briefly described as follows. That is, a solar battery module in one embodiment of the present invention has a front glass, a transparent resin, a solar battery cell, and a back sheet. In addition, the front glass is a semi-tempered glass for solar batteries, and there may be the case where the front glass has an antireflection film.
The transparent resin is incorporated with a fluorescent substance capable of emitting visible light to near infrared light upon being excited with near ultraviolet light to blue light. In the present invention, the wavelength conversion material is either a fluorescent substance having a needle form or a needle resin having a fluorescent substance sealed therein. Since this wavelength conversion material is in a needle form, the outgoing light from the wavelength conversion material has anisotropy.
By disposing the needle fluorescent substance or the needle resin having a fluorescent substance sealed therein in a horizontal direction against the principal plane of the solar battery cell, it is possible to make the amount of light going toward the solar battery cell large. That is, by using the above-described wavelength conversion film for solar batteries, it is possible to fabricate a solar battery module having high photoelectric conversion efficiency.
According to the present invention, the outgoing light which has been subjected to wavelength conversion with a fluorescent substance or the like is able to make the amount of light going toward the battery cell side large, and hence, it is possible to enhance the photoelectric conversion efficiency of solar batteries.
A structure of a solar battery module according to the present invention is shown in
The sealing material 3 has a role as a protective material and is disposed so as to cover the solar battery cell 4 capable of converting light energy into electric energy. In addition, as for the sealing material, in addition to EVA (ethylene-vinyl acetate copolymer), silicon potting materials, polyvinyl butyral, and the like can also be used.
As for the solar battery cell 4, a variety of solar battery cells such as monocrystalline silicon solar batteries, polycrystalline silicon solar batteries, thin film compound semiconductor solar batteries, amorphous silicon solar batteries, etc. can be used. This solar battery cell 4 is disposed singly or plurally within the solar battery module 1, and in the case where the solar battery cell 4 is disposed plurally, they are electrically connected to each other with an inter connector. As for the back sheet 5, in order to bring about weather resistance, high insulation, and strength, the back sheet 5 can contain a metal layer and a plastic film layer.
As shown in
The wavelength conversion layer is acceptable so long as it is present until at least sunlight is incident into the solar battery cell 4, and the wavelength conversion layer is acceptable so long as it is present at least either on the light-receiving surface of the front glass 2 or between the front glass 2 and the solar battery cell 4. In addition, since the wavelength conversion layer is acceptable so long as it is able to absorb only light which is incident into the solar battery cell, the wavelength conversion layer may exist at a position at which the converted light can be supplied into at least an incident part of sunlight into the solar battery cell 4, and it may not exist uniformly in the same area as the surface area of the solar battery module 1.
In consequence, as for the structure of the solar battery module, in addition to the configuration shown in
As shown in
In the light of above, as for the solar battery having a structure in which a material containing a fluorescent substance is set up in a route where light reaches the solar battery, there may be considered a method of mixing the material containing a fluorescent substance in the material of the front glass 2 or the sealing material 3; a method of blending the wavelength conversion material 7 in an appropriate solvent and coating the solution on a desired place; and the like. All of these methods may be adopted so long as the absorption of sunlight in the solar battery cell 4 is not hindered, and the function of the wavelength conversion material 7 is not impaired. Above all, the method of using the wavelength conversion material 7 shown in
In the case of using a fluorescent substance material as the wavelength conversion material, when the fluorescent substance is spherical, the light emission from the fluorescent substance is isotropic, and components of light transmitting into the side on which sunlight is incident without going toward the solar battery cell are produced. As shown in
In
The needle fluorescent substance or the wavelength conversion material having a fluorescent substance sealed in a needle resin can bring about directional properties of the light emission. That is, in the case where the shape of the wavelength conversion material is vertically oriented, a proportion of the component of light going toward the vertical direction is larger than a proportion of the component of light going toward the horizontal direction. This is because the refractive index of the inorganic fluorescent substance is from about 1.5 to 2.0, a value of which is larger than the refractive index (1.5) of the sealing material.
In consequence, the vertically oriented fluorescent substance material or wavelength conversion material having a fluorescent substance sealed in a needle resin is arranged at an angle higher than 41.8°, namely the major axis of the wavelength conversion material is made coincident with the parallel direction to the surface on which sunlight is incident. According to this, in the light produced from the light-emitting material, a proportion of the component of light which does not go toward the solar battery cell can be significantly reduced.
Here, when the vertical length of the needle fluorescent substance or the light-emitting material having a fluorescent substance sealed in a needle resin, namely the long diameter, is defined as “a”, and the horizontal length, namely the short diameter, is defined as “b”, there is a relation of “a>b”; and when the thickness of the wavelength conversion film is defined as “c”, a relation of “a>c” is preferable. In order to set up the needle fluorescent substance and the light-emitting material having a fluorescent substance sealed in a needle resin at an angle higher than 41.8°, the relation is set up at “a>1.34c”. Incidentally, a ratio of the long diameter (a) of the needle fluorescent substance or the light-emitting material having a fluorescent substance sealed in a needle resin to the short diameter (b) thereof is more preferably “a>2b”.
By adopting such a configuration, the raw material of the sealing material and the needle fluorescent substance or the light-emitting material having a fluorescent substance sealed in a needle resin are kneaded and molded into a film form, whereby a wavelength conversion film having the light-emitting material mixed therein can be easily manufactured at a desired angle. In that case, the light-emitting material is randomly set up in the sealing material at an angle of from 41.8° to 90°.
In addition, the wavelength conversion film in which the needle fluorescent substance or the light-emitting material having a fluorescent substance sealed in a needle resin is mixed may be a single layer, or can be formed so as to have a multilayered structure upon being superimposed. When a multilayered structure is formed, even in the case where the long diameter (a) of the needle fluorescent substance and the light-emitting material having a fluorescent substance sealed in a needle resin is short, the thickness for protecting the solar battery cell can be ensured without impairing the function of the sealing material by making the thickness of a single layer of the wavelength conversion film thin and superimposing those wavelength conversion films to form a multilayered structure. In addition, as for the needle resin for sealing the fluorescent substance therein, though polymers of an acrylic acid ester or a methacrylic acid ester are preferable, transparent materials such as a silicon resin, a glass, etc. are acceptable so long as they do not impair the function of wavelength convention.
The long diameter (a) or short diameter (b) of the needle fluorescent substance or the needle resin having a fluorescent substance sealed therein as described above is a diameter in the case of applying a statistical treatment as described later because it varies depending upon the individual particle.
In general, the quantum efficiency of solar battery becomes low as the light is turned from blue light to near ultraviolet light, and the wavelength of the incident light becomes shorter. On the other hand, a material in which the quantum efficient of a fluorescent substance is from about 0.7 to 0.9 is used as the wavelength conversion material. Results obtained by making a trial calculation of an increase of generated electric power in the case of changing the excitation edge wavelength on the long wavelength side of a fluorescent substance having an excitation band at 300 nm or more where a spectral intensity of sunlight is present are shown in
When the quantum efficiency is from 0.6 to 0.9, the increase of generated electric power by the wavelength conversion is seen at an excitation edge wavelength of from 350 to 670 nm. When the excitation edge wavelength is from 430 to 500 nm, the increase of generated electric power is the largest. That is, so long as the quantum efficiency of the wavelength conversion material is from 0.6 to 0.9, by using a wavelength conversion material having an excitation edge wavelength falling within the range of from 430 to 500 nm, the generated electric power of solar battery can be enhanced at a maximum. When the quantum efficiency is from 0.7 to 0.9, by using the wavelength conversion material having the excitation edge wavelength falling within the range of from 450 to 500 nm, the generated electric power of solar battery can be enhanced at a maximum. In addition, in the case where the quantum efficiency of the wavelength conversion material is 0.7 or more, even when a material further having an excitation edge wavelength of from 410 to 600 nm is used, the generated electric power of solar battery can be enhanced as compared with the case of wavelength conversion using a conventional organic complex (quantum efficiency: about 0.6).
On the other hand, in the fluorescent substance, there is also a loss due to optical scattering, and its degree is related to the particle diameter and the addition concentration. As for the relation between the particle diameter of the wavelength conversion material and the light scattering intensity, when the wavelength of sunlight is 500 nm, the light scattering intensity becomes maximum at a particle diameter of 250 nm, a value of which is a half of the wavelength of sunlight, due to the Mie scattering. The relation between light scattering intensity and particle diameter is shown in
Next, as for the addition concentration of the wavelength conversion material into the sealing material, it is desirable that at least one fluorescent substance particle is present on the side on which sunlight is incident, and the fluorescent substance mixed in the sealing material evenly gets the sunlight. When the addition concentration is in excess, the optical scattering increases, whereas when the addition concentration is too low, the light passing therethrough without being subjected to wavelength conversion increases. Accordingly, in the case of a fluorescent substance having an average particle diameter of 2.3 μm, the addition concentration is 2% by weight. In addition, in the case of a fluorescent substance having an average particle diameter of 5.8 μm, the addition concentration is 5% by weight. In addition, in the case of a fluorescent substance having an average particle diameter of 1.2 μm, the addition concentration is 1% by weight. In consequence, in the case where the average particle diameter of the fluorescent substance is from 1 to 5 μm, the addition concentration is from 1 to 5% by weight. However, such a value is a result obtained by calculating the necessary amount of the fluorescent substance, and an optimum concentration is present around this amount.
In consequence, when an average particle diameter of the fluorescent substance is defined as A (μm), as for an optimum concentration range B (% by weight), the effect starts to become apparent at about 1/200 times of the optimum concentration 2A/2.3, and the effect is found until about 10 times. In consequence, the concentration of the fluorescent substance is favorably in the range of (0.004A≦B≦8.7A), and when stopping of light and light scattering are taken into consideration, more preferably, the effect of the wavelength conversion is high in the range of from about 1/100 times to about 5 times of the optimum concentration 2A/2.3. In consequence, it may be considered that the concentration of the fluorescent substance is optimum in the range of (0.008A≦B≦4.3A).
As for the wavelength conversion material, a material capable of converting near ultraviolet light to blue light of not more than 500 nm into green light to near infrared light of from 500 nm to 1,100 nm and making the converted light incident into the solar battery cell is preferable. In particular, a material having an excitation band at 300 nm or more where a spectral intensity of sunlight is present, a quantum efficiency of 0.7 or more, and an excitation edge wavelength of from 410 to 600 nm is preferable. A material having an excitation edge wavelength of from 430 to 500 nm is the most preferable. Furthermore, from the standpoints of luminance lifetime and moisture resistance, an inorganic fluorescent substance material which is used for a variety of displays, lamps, and white LED, and the like is preferable. However, the material is limited to one whose excitation band is distributed in near ultraviolet light to blue light.
From these viewpoints, in the present invention, a fluorescent substance material composition having an excitation band in near ultraviolet light to blue light and having high light conversion efficiency was chosen. Examples of such a fluorescent substance include a fluorescent substance represented by MMgAl10O17:Eu,Mn, wherein M is one kind or a plural kind of elements of Ba, Sr, and Ca; a fluorescent substance whose parent material contains any one of (Ba, Sr)2SiO4 (Ba, Sr, Ca)2SiO4, Ba2SiO4, Sr3SiO5, (Sr, Ca, Ba)3SiO5, (Ba, Sr, Ca)3MgSi2O8, Ca3Si2O7, Ca2ZnSi2O7, Ba3Sc2Si3O12, and Ca3Sc2Si3O12; and a fluorescent substance whose parent material is represented by MAlSiN3, wherein M is any one kind or a plural kind of elements of Ba, Sr, Ca, and Mg. In addition, a rare earth element such as Eu, Ce, etc. is used as a light-emitting central element.
In addition, an average particle diameter of the fluorescent substance which is used in the present invention is from 10 nm to 20 μm. Here, the average particle diameter of the fluorescent substance can be specified as follows. Examples of a method of examining the average particle diameter of the particle (fluorescent substance particle) include a method of the measurement with a particle size distribution analyzer; a method of the direct observation with an electron microscope; and the like. When the case of examining the average particle diameter with an electron microscope is taken as an example, the average particle diameter can be calculated as follows. Each of sections of variables of the particle diameter of the particle ( . . . , 0.8 to 1.2 μm, 1.3 to 1.7 μm, 1.8 to 2.2 μm, . . . , 6.8 to 7.2 μm, 7.3 to 7.7 μm, 7.8 to 8.2 μm, . . . , etc.) is expressed by a class value ( . . . , 1.0 μm, 1.5 μm, 2.0 μm, . . . , 7.0 μm, 7.5 μm, 8.0 μm, . . . , etc.), and this is defined as xi. Then, when the frequency of each of the variables observed by an electron microscope is expressed by fi, an average value A is expressed as follows.
A=Σx
i
f
i
/Σf
i
=Σx
i
f
i
/N
However, Σfi=N. In the fluorescent substance of the present invention, since the excitation edge wavelength is adaptive as a wavelength conversion material, an excellent effect as a wavelength conversion material for solar batteries can be obtained.
In the case where the fluorescent substance is in a needle form having a long diameter (a) and a short diameter (b), an average particle diameter obtained by the above-described measurement is adopted with respect to each of the long diameter (a) and the short diameter (b). Namely, in the present description, the long diameter (a) refers to an average long diameter (a), and the short diameter (b) refers to an average short diameter (b). Then, when the particle diameter of the needle fluorescent substance is referred to, it means “(a+b)/2”. The long diameter (a) or the short diameter (b) in the needle resin having a fluorescent substance sealed therein is a value obtained by performing the same statistical treatment. Namely, in the present description, the long diameter (a) of the needle resin having a fluorescent substance sealed therein refers to an average long diameter (a), and the short diameter (b) refers to an average short diameter (b).
A variety of solar battery modules using the foregoing wavelength conversion material were fabricated. Examples thereof are hereunder described.
To a transparent resin (EVA), small amounts of an organic peroxide, a crosslinking auxiliary, and an adhesion enhancer were added; a needle acrylic resin (vertical length a=680 μm, horizontal length b=20 μm) having a (Ba,Ca,Sr)MgAl10O17:Eu,Mn fluorescent substance (particle diameter: 6 μm) sealed therein was mixed in a proportion of 0.5% by weight; the contents were kneaded using a roll mill heated at 80° C.; and the kneaded material was then interposed between two sheets of polyethylene terephthalate using a press, thereby fabricating a sealing material 3 composed mainly of EVA and having a thickness of 500 μm. In addition, as for the above-described fluorescent substance composition, one kind composition or a mixture of plural kinds of compositions may be used.
Subsequently, this sealing material 3 was allowed to stand for cooling to room temperature; the polyethylene terephthalate film was released; the resultant was laminated together with a front glass 2, a solar battery cell 4, and a back sheet 5 as shown in
To a transparent resin (EVA), small amounts of an organic peroxide, a crosslinking auxiliary, and an adhesion enhancer were added; a needle acrylic resin (vertical length a=200 μm, horizontal length b=20 μm) having a (Ba,Ca,Sr)MgAl10O17:Eu,Mn fluorescent substance (particle diameter: 50 μm) sealed therein was mixed in a proportion of 1% by weight; the contents were kneaded using a roll mill heated at 80° C.; and the kneaded material was then interposed between two sheets of polyethylene terephthalate using a press, thereby fabricating a sealing material 3 composed mainly of EVA and having a thickness of 166 μm. In addition, as for the above-described fluorescent substance composition, one kind composition or a mixture of plural kinds of compositions may be used.
Subsequently, this sealing material 3 was allowed to stand for cooling to room temperature; the polyethylene terephthalate film was released; three sheets of the sealing material 3 were superimposed together with a front glass 2, a solar battery cell 4, and a back sheet 5 to form a multilayered structure and laminated as shown in
To a transparent resin (EVA), small amounts of an organic peroxide, a crosslinking auxiliary, and an adhesion enhancer were added; a (Ba, Ca, Sr)MgAl10O17:Eu, Mn fluorescent substance (vertical length: 60 μm, horizontal length: 5 μm) was mixed in a proportion of 0.5% by weight; the contents were kneaded using a roll mill heated at 80° C.; and the kneaded material was then interposed between two sheets of polyethylene terephthalate using a press, thereby fabricating a sealing material 3 composed mainly of EVA and having a thickness of 50 μm. In addition, as for the above-described fluorescent substance composition, one kind composition or a mixture of plural kinds of compositions may be used.
Subsequently, this sealing material 3 was allowed to stand for cooling to room temperature; the polyethylene terephthalate film was released; ten sheets of the sealing material 3 were superimposed together with a front glass 2, a solar battery cell 4, and a back sheet 5 to form a multilayered structure and laminated as shown in
To a transparent resin (EVA), small amounts of an organic peroxide, a crosslinking auxiliary, and an adhesion enhancer were added; a (Ba,Sr)2SiO4:Eu fluorescent substance (vertical length: 60 μm, horizontal length: 5 μm) was mixed in a proportion of 0.5% by weight; the contents were kneaded using a roll mill heated at 80° C.; and the kneaded material was then interposed between two sheets of polyethylene terephthalate using a press, thereby fabricating a sealing material 3 composed mainly of EVA and having a thickness of 50 μm. In addition, as for the above-described fluorescent substance composition, one kind composition or a mixture of plural kinds of compositions may be used.
Subsequently, this sealing material 3 was allowed to stand for cooling to room temperature; the polyethylene terephthalate film was released; ten sheets of the sealing material 3 were superimposed together with a front glass 2, a solar battery cell 4, and a back sheet 5 to form a multilayered structure and laminated as shown in
To a transparent resin (EVA), small amounts of an organic peroxide, a crosslinking auxiliary, and an adhesion enhancer were added; a (Ba,Sr,Ca)2SiO4:Eu fluorescent substance (vertical length: 60 μm, horizontal length: 5 μm) was mixed in a proportion of 0.5% by weight; the contents were kneaded using a roll mill heated at 80° C.; and the kneaded material was then interposed between two sheets of polyethylene terephthalate using a press, thereby fabricating a sealing material 3 composed mainly of EVA and having a thickness of 50 μm. In addition, as for the above-described fluorescent substance composition, one kind composition or a mixture of plural kinds of compositions may be used.
Subsequently, this sealing material 3 was allowed to stand for cooling to room temperature; the polyethylene terephthalate film was released; ten sheets of the sealing material 3 were superimposed together with a front glass 2, a solar battery cell 4, and a back sheet 5 to form a multilayered structure and laminated as shown in
To a transparent resin (EVA), small amounts of an organic peroxide, a crosslinking auxiliary, and an adhesion enhancer were added; a CaAlSiN3:Eu fluorescent substance (vertical length: 60 μm, horizontal length: 5 μm) was mixed in a proportion of 0.5 by weight; the contents were kneaded using a roll mill heated at 80° C.; and the kneaded material was then interposed between two sheets of polyethylene terephthalate using a press, thereby fabricating a sealing material 3 composed mainly of EVA and having a thickness of 50 μm. In addition, as for the above-described fluorescent substance composition, one kind composition or a mixture of plural kinds of compositions may be used.
Subsequently, this sealing material 3 was allowed to stand for cooling to room temperature; the polyethylene terephthalate film was released; ten sheets of the sealing material 3 were superimposed together with a front glass 2, a solar battery cell 4, and a back sheet 5 to form a multilayered structure and laminated as shown in
Subsequently, a solar battery module was fabricated using the above-described wavelength conversion material. To a transparent resin (EVA), small amounts of an organic peroxide, a crosslinking auxiliary, and an adhesion enhancer were added; a needle acrylic resin (vertical length a=680 μm, horizontal length b=20 μm) having a (Ba, Sr)2SiO4:Eu fluorescent substance (particle diameter: 10 μm) sealed therein was mixed in a proportion of 0.5% by weight; and the contents were kneaded using a roll mill heated at 80° C.; the kneaded material was then interposed between two sheets of polyethylene terephthalate using a press, thereby fabricating a sealing material 3 composed mainly of EVA and having a thickness of 500 μm. In addition, as for the above-described fluorescent substance composition, one kind composition or a mixture of plural kinds of compositions may be used.
Subsequently, this sealing material 3 was allowed to stand for cooling to room temperature; the polyethylene terephthalate film was released; the resultant was laminated together with a front glass 2, a solar battery cell 4, and a back sheet 5 as shown in
To a transparent resin (EVA), small amounts of an organic peroxide, a crosslinking auxiliary, and an adhesion enhancer were added; a needle acrylic resin (vertical length a=680 μm, horizontal length b=30 μm) having a (Ba,Sr,Ca)2SiO4:Eu fluorescent substance (particle diameter: 20 μm) sealed therein was mixed in a proportion of 0.5% by weight; the contents were kneaded using a roll mill heated at 80° C.; the kneaded material was then interposed between two sheets of polyethylene terephthalate using a press, thereby fabricating a sealing material 3 composed mainly of EVA and having thickness of 500 μm. In addition, as for the above-described fluorescent substance composition, one kind composition or a mixture of plural kinds of compositions may be used.
Subsequently, this sealing material 3 was allowed to stand for cooling to room temperature; the polyethylene terephthalate film was released; the resultant was laminated together with a front glass 2, a solar battery cell 4, and a back sheet 5 as shown in
To a transparent resin (EVA), small amounts of an organic peroxide, a crosslinking auxiliary, and an adhesion enhancer were added; a needle acrylic resin (vertical length a=680 μm, horizontal length b=20 μm) having a CaAlSiN3:Eu fluorescent substance (particle diameter: 15 μm) sealed therein was mixed in a proportion of 0.5% by weight; the contents were kneaded using a roll mill heated at 80° C.; the kneaded material was then interposed between two sheets of polyethylene terephthalate using a press, thereby fabricating a sealing material 3 composed mainly of EVA and having a thickness of 500 μm. In addition, as for the above-described fluorescent substance composition, one kind composition or a mixture of plural kinds of compositions may be used.
Subsequently, this sealing material 3 was allowed to stand for cooling to room temperature; the polyethylene terephthalate film was released; the resultant was laminated together with a front glass 2, a solar battery cell 4, and a back sheet 5 as shown in
The foregoing Examples are concerned with the case of mixing a wavelength conversion material in a sealing material. However, as shown in
The same is also applicable to the case where separately from the antireflection film 6, the wavelength conversion film 8 having, as the wavelength conversion material 7, a needle fluorescent substance or a needle resin having a fluorescent substance sealed therein is disposed outside the front glass 2 as shown in
1: Solar battery module
2: Front glass
3: Sealing material
4: Solar battery cell
5: Back sheet
6: Antireflection film
7: Wavelength conversion material
8: Wavelength conversion film
9: Condensing lens
10: Supporting frame
11: Substrate
20: Fluorescent substance
30: Needle resin
Number | Date | Country | Kind |
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2010 292389 | Dec 2010 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/JP2011/078486 | 12/8/2011 | WO | 00 | 9/6/2013 |