JP2014049426A - Method of manufacturing organic solar cell element module - Google Patents

Abstract

PROBLEM TO BE SOLVED: To manufacture an organic solar cell element module in an easy method.SOLUTION: A method of manufacturing an organic solar cell element module includes: a first electrode base material forming process of forming a first electrode base material 10 by forming a plurality of first electrode layers 12 which are formed in stripes on a first base material and each have a connection part, including both ends of each stripe, formed; a substrate preparation process for a second electrode base material of preparing one second electrode base material substrate 20' which has at least a second electrode layer and can have a plurality of striped second electrode base materials 20 cut; a function layer formation process of carrying out of one of a process of forming a function layer on the first electrode base material on the side of the first electrode layers and a process of continuously forming a function layer on the second electrode base material substrate on the side of the second electrode layer; a cutting process for the second electrode base material substrate; a sticking process of sticking the first electrode layer side of the first electrode base material and the second electrode layer side of the second electrode base material together; and a connection process of electrically connecting a first electrode layer of one organic solar cell element 2 and a second electrode layer of another organic solar cell element adjoining it.

Description

  The present invention relates to a method for producing an organic solar cell element module that can produce an organic solar cell element module with high production efficiency and at low cost.

  Currently used solar cells are classified in various ways depending on the material of the light absorption layer and its application. Among them, the organic solar cell is a solar cell in which an organic compound having electron donating and electron accepting functions is arranged between two different electrodes, compared with an inorganic solar cell typified by silicon. In view of the fact that the manufacturing method is easy, the area can be increased at a low cost, and colorability and flexibility can be imparted.

Moreover, the organic solar cell mainly utilizes a dye-sensitized solar cell that obtains photovoltaic power using an organic dye and an organic thin-film solar cell that uses an organic semiconductor.
In order to put the organic solar cell into practical use, a larger output voltage is required. Therefore, it has been attempted to connect a plurality of organic solar cell elements to form an organic solar cell element module. Yes.

  As a manufacturing method of the organic solar cell element module described above, for example, Patent Documents 1 and 2 propose the following manufacturing method.

For example, in Patent Document 1, as a method for manufacturing an organic thin film solar cell element module, a first conductive layer and a photoelectric conversion layer are formed in a pattern on a support base, and a second conductive layer and carrier transport are formed on a flexible film. A layer is formed in a pattern, the photoelectric conversion layer and the carrier transport layer are brought into contact with each other, and the first conductive layer and the second conductive layer are brought into partial contact so as to be connected in series. The manufacturing method which manufactures an organic thin-film solar cell element module by bonding a conductive film is shown.
However, the above-described manufacturing method has a problem in that the manufacturing process becomes complicated because it is necessary to form a pattern for each layer constituting the organic thin-film solar cell element module.

Further, for example, in Patent Document 2, as a method for producing a dye-sensitized solar cell element module, a solid electrolyte layer is formed on an oxide semiconductor electrode substrate having a porous layer carrying an electrode base material and a sensitizing dye. A production method for producing a dye-sensitized solar cell module by forming a plurality of dye-sensitized solar cell elements by bonding them to a counter electrode substrate having a counter electrode layer, and connecting them It is shown.
However, in the above-described manufacturing method, the number of steps is increased because the method includes a step of creating a plurality of dye-sensitized solar cell elements and a step of connecting the dye-sensitized solar cell elements to each other. There was a problem.
Moreover, since the dye-sensitized solar cell element module manufactured by the above-described manufacturing method has a configuration in which dye-sensitized solar cell elements formed separately are connected, the strength may not be sufficient. There was a problem.

Patent Document 3 discloses, as a method for producing a dye-sensitized solar cell element, a pseudo solid electrolyte that includes a partition layer provided around the porous layer of the oxide semiconductor electrode substrate described above, and includes a conductive carbon material and a solvent. Is applied to the partition wall layer, the solvent is removed to form a pseudo solid electrolyte layer, and this is bonded to a counter electrode substrate to produce a dye-sensitized solar cell element.
In Patent Document 4 and Patent Document 5, as a method for producing a dye-sensitized solar cell element, a partition wall is provided on the counter electrode substrate described above, and a gel electrolyte layer is formed inside the partition wall. The manufacturing method which manufactures a dye-sensitized solar cell element by bonding together with an oxide semiconductor electrode substrate is shown.

  However, when the manufacturing method of the dye-sensitized solar cell element shown in Patent Document 3, Patent Document 4, and Patent Document 5 described above is applied to the manufacturing method of the dye-sensitized solar cell element module, the partition wall described above A process for forming a layer or a partition wall is required, and a high accuracy is required for alignment of the counter electrode substrate and the oxide semiconductor electrode substrate, which causes a problem that the manufacturing process becomes complicated.

  Therefore, since the conventional method for manufacturing an organic solar cell element module described above has complicated steps, a method for manufacturing an organic solar cell element module that can be manufactured with higher productivity is required. Yes.

By the way, in an organic type solar cell element module, in order to improve workability, the structure which can provide high flexibility is calculated | required.
Here, as a configuration of a conventional organic solar cell element module having flexibility, for example, a configuration in which a plurality of organic solar cell elements are formed between two flexible substrates.
However, when bending is performed on the organic solar cell element module having the above-described configuration, the two flexible base materials have different curvatures, so that it is difficult to exhibit a desired bendability. In some cases, the organic solar cell element module deteriorates due to bending.

  Therefore, in Patent Document 6, as a method for producing a dye-sensitized solar cell element module, a first electrode base material in which a plurality of first electrode layers are formed on a single first base material, and a second electrode A plurality of second electrode substrates each having a layer, the plurality of first electrode layers formed on one first electrode substrate and the second electrode layers of each second electrode substrate facing each other Manufacturing to manufacture a dye-sensitized solar cell module by injecting an electrolyte after being disposed between the first electrode layer and the second electrode layer using a sealant or an adhesive A method is disclosed. According to the manufacturing method described above, a configuration in which the second electrode layers formed on each second electrode substrate face each other in accordance with the plurality of first electrode layers formed on one first electrode substrate. Therefore, a dye-sensitized solar cell element module having high flexibility can be obtained.

  However, the manufacturing method described above requires a step of injecting an electrolyte after the first electrode base material and the second electrode base material are bonded together, so that it takes time to manufacture a large area cell. There was a problem. Further, in order to bond the first electrode base material and the second electrode base material, it is necessary to provide an adhesive part, an insulating part, etc., but in the dye-sensitized solar cell module, the above-mentioned adhesive part, insulating part Etc. cannot contribute to power generation, and the power generation efficiency of the dye-sensitized solar cell module module is reduced by reducing the entire power generation area of the dye sensitized solar cell module. there were.

  In addition, also in the organic thin film solar cell element module, the manufacturing method which can provide favorable flexibility has not been discovered.

JP 2002-319689 A JP 2009-193705 A JP 2010-153348 A JP 2007-294696 A JP 2007-33545 A JP 2006-32110 A

  The present invention has been made in view of the above circumstances, and an organic solar cell element module having a plurality of organic solar cell elements connected to each other and having excellent processability can be manufactured by a simple method. The main object is to provide a method for producing an organic solar cell element module.

  In order to solve the above-described problems, the present invention has one first base material and two connection portions formed in a stripe shape on the first base material and including both end portions of each stripe. A first electrode substrate having a plurality of first electrode layers, a plurality of strip-shaped second electrode substrates having at least a second electrode layer and having two connection portions at both ends, and the above An organic solar cell element formed between the first electrode layer and the second electrode layer, having a plurality of functional layers containing an organic substance, and having the first electrode layer, the second electrode layer, and the functional layer Are connected to each other, and the first electrode layer of one of the organic solar cell elements and the second electrode layer of the other organic solar cell element adjacent to the one organic solar cell element are the respective electrodes. The two connection parts formed at both ends of the A method of manufacturing an organic solar cell element module connected to each other, wherein the organic solar cell element module is formed in a stripe shape on the first base material and has two connection portions including both end portions of each stripe. A first electrode base material forming step for forming the first electrode base material, and cutting out a plurality of strip-shaped second electrode base materials having at least the second electrode layer and having two connection portions at both ends. A second electrode substrate substrate preparing step for preparing one second electrode substrate substrate capable of performing the above, and the functional layer on the first electrode layer side of the first electrode substrate. A functional layer forming step of performing any one of a step of forming a pattern corresponding to the pattern of the step, or a step of continuously forming the functional layer on the second electrode layer side of the second electrode base substrate, By cutting the substrate for the second electrode base material, A number of second electrode substrates, the first electrode layer side of the first electrode substrate and the second electrode layer side of the second electrode substrate are opposed to each other, and the functional layer is A bonding step of bonding the first electrode substrate and the second electrode substrate by sticking them as an interface, the first electrode layer of the one organic solar cell element, and the one organic solar cell A connection step of electrically connecting the second electrode layer of the other organic solar cell element adjacent to the element at the two connection portions formed at both ends of each electrode. An organic solar cell module manufacturing method is provided.

  The manufacturing method of the organic solar cell element module of the present invention includes a plurality of first electrode layers formed on one first base material via a functional layer containing an organic substance, and a plurality of second electrode base materials. Since the formed 2nd electrode layer can be bonded together, there exists an effect that it becomes possible to manufacture the organic type solar cell element module which has a shape excellent in workability by a simple method.

  In particular, according to the present invention, the first electrode layer of one organic solar cell element and the second electrode layer of another organic solar cell element adjacent to the one organic solar cell element include: By being electrically connected between the two connection portions formed at both ends of each electrode, it becomes possible to produce the organic solar cell element module having excellent electrical connection reliability, The path through which the current flows is shortened, and it becomes possible to manufacture the organic solar cell element module with high efficiency in which current loss due to resistance at the electrode is reduced.

It is the schematic which shows an example of the dye-sensitized solar cell element module manufactured in the manufacturing method of the organic type solar cell element module of this invention. It is a schematic sectional drawing which shows the other example of the dye-sensitized solar cell element module manufactured in the manufacturing method of the organic type solar cell element module of this invention. It is process drawing which shows an example of the 1st electrode base material formation process in the manufacturing method of the organic type solar cell element module of this invention. It is process drawing which shows an example of the board | substrate preparation process for 2nd electrode base materials, a porous layer formation process, a functional layer formation process, and a cutting process in the manufacturing method of the organic solar cell element module of this invention. It is process drawing which shows the other example of the board | substrate preparation process for 2nd electrode base materials in the manufacturing method of the organic type solar cell element module of this invention, a porous layer formation process, a functional layer formation process, and a cutting process. It is a schematic plan view which shows an example of the 1st electrode base material formed in the manufacturing method of the organic type solar cell element module of this invention. It is a schematic sectional drawing which shows an example of the organic thin film solar cell element module manufactured in the manufacturing method of the organic type solar cell element module of this invention. It is process drawing which shows the other example of the 1st electrode base material formation process in the manufacturing method of the organic type solar cell element module of this invention. It is process drawing which shows the other example of the board | substrate preparation process for 2nd electrode base materials, a functional layer formation process, and a cutting process in the manufacturing method of the organic solar cell element module of this invention.

  Hereinafter, the manufacturing method of the organic solar cell element module of the present invention will be described.

  The method for producing an organic solar cell element module of the present invention has one first base material and two connection portions formed in a stripe shape on the first base material and including both end portions of each stripe. A first electrode substrate having a plurality of first electrode layers formed as described above, a plurality of strip-shaped second electrode substrates having at least a second electrode layer and having two connection portions at both ends, and An organic solar cell formed between the first electrode layer and the second electrode layer, having a plurality of functional layers containing an organic substance, and having the first electrode layer, the second electrode layer, and the functional layer A plurality of elements are connected, and the first electrode layer of one organic solar cell element and the second electrode layer of another organic solar cell element adjacent to the one organic solar cell element are The above two formed on both ends of each electrode A method for manufacturing an organic solar cell element module that is electrically connected between connection portions, wherein two connection portions that are formed in a stripe shape on the first base material and include both ends of each stripe are provided. A first electrode base material forming step of forming the first electrode base material by forming the plurality of first electrode layers formed so as to have at least the second electrode layer, and two at both ends. A second electrode base material substrate preparation step for preparing a single second electrode base material substrate capable of cutting out a plurality of strip-shaped second electrode base materials having connecting portions, and the first electrode base material Forming the functional layer on the first electrode layer side in a pattern corresponding to the pattern of the first electrode layer, or continuing the functional layer on the second electrode layer side of the second electrode substrate. Functional layer for performing any one of the processes Forming step, cutting the second electrode base material substrate to form the plurality of second electrode base materials, the first electrode layer side of the first electrode base material, and the second electrode base material. A bonding step of bonding the first electrode substrate and the second electrode substrate by facing the second electrode layer side of the electrode substrate and sticking the functional layer as an interface, and one of the above The first electrode layer of the organic solar cell element and the second electrode layer of the other organic solar cell element adjacent to the one organic solar cell element are formed at both ends of each electrode. And a connecting step of electrically connecting the two connecting portions.

  In the organic solar cell element module manufactured according to the present invention, at least one of the first electrode base material or the second electrode base material serves as a light receiving surface for sunlight. The organic solar cell element module is manufactured so that at least one of the electrode substrate and the second electrode substrate is a transparent substrate.

Here, the transparency of the “substrate having transparency” is such that the organic solar cell element module produced by the production method of the present invention can exhibit its function by receiving sunlight. The light transmittance is not particularly limited as long as it can transmit sunlight, but the total light transmittance is preferably 50% or more. In addition, the transparency is JIS K7
It is a value measured by a measuring method based on 361-1: 1997.

In the functional layer forming step of the present invention, “form a functional layer on the first electrode layer side” or “form a functional layer on the second electrode layer side” means the first electrode layer or the second electrode layer. This is a concept including not only the case where the functional layer is directly formed on the surface of the film but also the case where the functional layer is formed via another layer.
Further, “the functional layer is formed in a pattern corresponding to the pattern of the first electrode layer” means that each organic solar cell element constituting the organic solar cell element module manufactured by the manufacturing method of the present invention functions. It refers to forming each functional layer on each first electrode layer formed in a pattern so as to have a layer. Specifically, it means that one functional layer is formed in a pattern that can be continuously formed on the first electrode layer.

  Moreover, in the bonding step in the present invention, “the first electrode layer side of the first electrode substrate and the second electrode layer side of the second electrode substrate are opposed to each other, and the functional layer is adhered as an interface” Not only when the first electrode layer and the second electrode layer are adhered to each other with the functional layer as an interface, but when another layer is formed on the surface of the first electrode layer or the second electrode layer, This is a concept including the case where the outermost surface layer of the first electrode layer and the outermost surface layer of the second electrode layer are brought into close contact with each other as an interface.

  According to this invention, since it has a bonding process, since the functional layer containing an organic substance can be used as an interface, the adhesion between the first electrode substrate and the second electrode substrate can be made sufficient. It becomes possible.

  According to the present invention, the first electrode layer of one organic solar cell element and the second electrode layer of another organic solar cell element adjacent to the one organic solar cell element include: By being electrically connected at the two connection portions formed at both ends of each electrode, it becomes possible to produce the organic solar cell element module with excellent electrical connection reliability, This makes it possible to produce a highly efficient organic solar cell element module with reduced current loss due to resistance at the electrodes.

Moreover, according to this invention, there exist the following effects by having the functional layer formation process mentioned above.
For example, when the functional layer is formed on the first electrode layer side of the first electrode base material, the width of the functional layer can be formed wider than the width of the first electrode layer formed in a pattern. When it is set as a solar cell element module, the contact of the 1st electrode layer and 2nd electrode layer in one organic type solar cell element can be prevented, and generation | occurrence | production of an internal short circuit can be suppressed.
On the other hand, for example, when the functional layer is formed on the second electrode layer side of the second electrode base substrate, the functional layer is continuously formed on the second electrode base substrate, and the desired cutting step is performed thereafter. Since it can be cut into a shape, it is not necessary to form the functional layer in a pattern corresponding to the pattern of each first electrode layer, so that the functional layer forming step can be simplified. Further, since it is not necessary to form the functional layer in a pattern corresponding to the pattern of each first electrode layer, it is possible to reduce waste of materials used for the functional layer.

  In addition, according to the present invention, an organic solar cell element module having one first electrode base material and a plurality of second electrode base materials can be manufactured. For example, the first electrode base material and the second electrode base material By using a flexible base material for each of the electrode base materials, it becomes possible to manufacture an organic solar cell element module that is easy to bend and has high strength and high workability.

Here, the manufacturing method of the organic solar cell element module of the present invention is roughly divided into two modes depending on the type of the organic solar cell element module to be manufactured.
Specifically, the organic solar cell element module contains metal oxide semiconductor fine particles in which a dye sensitizer is supported on the surface of either the first electrode layer or the second electrode layer. A dye-sensitized solar cell module comprising a plurality of dye-sensitized solar cells each having a porous layer and the functional layer being a solid electrolyte layer containing a polymer compound and a redox pair An organic thin-film solar cell element module configured by connecting a plurality of organic thin-film solar cell elements each having a photoelectric conversion layer between the certain aspect (first aspect) and the first electrode layer and the second electrode layer, And an embodiment (second embodiment) in which the functional layer is a layer containing an organic substance formed between the first electrode layer and the second electrode layer.

  Hereinafter, each aspect will be described.

I. 1st aspect The 1st aspect of the manufacturing method of the organic solar cell element module of this invention is the metal by which the dye sensitizer was carry | supported on the surface of either one of the said 1st electrode layer or the said 2nd electrode layer. Dye sensitization comprising a plurality of dye-sensitized solar cell elements each having a porous layer containing oxide semiconductor fine particles and the functional layer being a solid electrolyte layer containing a polymer compound and a redox couple It is a manufacturing method which manufactures a sensitive solar cell element module.
In the following description, the organic solar cell element module is referred to as a dye-sensitized solar cell element module.

  Moreover, in the dye-sensitized solar cell element module manufactured by the manufacturing method of this aspect, the electrode layer in which the porous layer is formed is usually an oxide semiconductor in the first electrode layer or the second electrode layer. An electrode layer that is used as an electrode layer and is not formed with a porous layer is used as a counter electrode layer.

Here, the dye-sensitized solar cell element module manufactured by the manufacturing method of this embodiment will be described with reference to the drawings. Fig.1 (a) is a schematic plan view which shows an example of the dye-sensitized solar cell element module manufactured by the manufacturing method of this aspect, FIG.1 (b) is the sectional view on the AA line of Fig.1 (a). FIG.
As shown in FIGS. 1A and 1B, the dye-sensitized solar cell element module 100 manufactured by the manufacturing method of this aspect is formed on one first base material 11 and first base material 11. Formed on the first electrode substrate 10 having the plurality of first electrode layers 12 formed in a pattern, the plurality of second electrode substrates 20 having at least the second electrode layer 22, and the second electrode layer 22. A porous layer 3, and a solid electrolyte layer 4 formed between the first electrode layer 12 of the first electrode substrate 10 and the porous layer 3 formed on the second electrode substrate 20. It is.
In the dye-sensitized solar cell element module 100, it is preferable that the catalyst layer 5 be formed between the first electrode layer 12 and the solid electrolyte layer 4.
The dye-sensitized solar cell module 100 includes a plurality of dye-sensitized solar cell elements 1 each having the first electrode layer 12, the catalyst layer 5, the solid electrolyte layer 4, the porous layer 3, and the second electrode layer 22. It is configured to be connected.

  Further, in the dye-sensitized solar cell module 100 shown in FIG. 1A, the first electrode layer 12 is formed in a stripe shape, and the second electrode substrate having the second electrode layer 22 is a strip. It is formed in a shape. Furthermore, the dye-sensitized solar cell element module 100 has two connection portions a and a ′ including both end portions of each stripe of the first electrode layer 12, and is provided at both end portions of the strip of each second electrode layer 22. It has two connection portions b and b ′, and is adjacent to the connection portions a and a ′ of the first electrode layer 12 of one dye-sensitized solar cell element 1 and the one dye-sensitized solar cell element 1. In this case, the connection portions b and b ′ of the second electrode layer 22 of the other dye-sensitized solar cell element 1 are electrically connected by direct contact.

As shown in FIG. 2, in the manufacturing method of this aspect, the dye-sensitized solar cell module 100 in which the porous layer 3 is formed in a pattern on the first electrode layer 12 may be manufactured. it can. In this case, the catalyst layer 5 is preferably formed between the second electrode layer 22 and the solid electrolyte layer 4.
FIG. 2 is a schematic cross-sectional view showing another example of the dye-sensitized solar cell module manufactured by the manufacturing method of this embodiment, and the reference numerals not described are the same as those in FIG. Since it is possible, description here is abbreviate | omitted.

  As described above, since the dye-sensitized solar cell module manufactured by the manufacturing method of this aspect has a porous layer as an essential component, in this aspect, in addition to the above-described steps, A porous layer forming step of forming a porous layer on the surface of either the first electrode layer or the second electrode layer is an essential step.

  More specifically, in the method for manufacturing a dye-sensitized solar cell element module according to this aspect, the first electrode base material is formed by forming the plurality of first electrode layers on the first base material. An electrode base material forming step and a second electrode base material for preparing a second electrode base material substrate having at least the second electrode layer and capable of cutting out the plurality of second electrode base materials. Porous for forming a porous layer containing metal oxide semiconductor fine particles carrying a dye sensitizer on the surface of either the first electrode layer or the second electrode layer on the substrate preparation step A layer forming step and a step of forming the functional layer in a pattern corresponding to the pattern of the first electrode layer on the first electrode layer side of the first electrode substrate, or the second electrode substrate substrate One of the steps of continuously forming the functional layer on the second electrode layer side is performed. A functional layer forming step; a cutting step of forming the plurality of second electrode base materials by cutting the second electrode base material substrate; the first electrode layer side of the first electrode base material; A bonding step of bonding the first electrode substrate and the second electrode substrate by facing the second electrode layer side of the second electrode substrate and sticking the functional layer as an interface; Electrically connecting the first electrode layer of the two dye-sensitized solar cell elements and the second electrode layer of another dye-sensitized solar cell element adjacent to the one dye-sensitized solar cell element. And a connecting step for connecting.

  Here, the manufacturing method of the dye-sensitized solar cell element module of this aspect is demonstrated using figures. 3 (a) to 3 (d) and FIGS. 4 (a) to 4 (e) are process diagrams illustrating an example of a method for producing the dye-sensitized solar cell module of this embodiment, and FIG. It is a figure shown about the example which manufactures the dye-sensitized solar cell element module shown to (b).

First, the 1st electrode base material formation process in this aspect is demonstrated. As shown in FIGS. 3A and 3B, in the first electrode base material forming step, the first electrode layer 12 is continuously formed on the first base material 11. In the first electrode base material forming step, the catalyst layer 5 may be formed. In this case, the catalyst layer 5 is continuously formed and laminated on the first electrode layer 12. 3A shows an example of the first base material 11 in which the first electrode layer 12 and the catalyst layer 5 are continuously formed from the top surface. FIG. 3B shows the example of FIG. BB line cross section is shown.
Next, as shown in FIGS. 3C and 3D, the first electrode layer 12 and the catalyst layer 5 are patterned into a predetermined pattern by an etching process or the like, thereby forming a single first base material 11. Then, the first electrode substrate 10 having a plurality of first electrode layers 12 and catalyst layers 5 formed in a pattern is formed. In FIG. 3C, the first electrode layer 12 and the catalyst layer 5 are formed in a stripe shape, and each of the first electrode layer 12 and the catalyst layer 5 includes two connection portions a including both ends of each stripe. , A ′ is shown as an example.
In addition, in FIG.3 (c), an example of the 1st electrode base material 10 formed by the 1st electrode base material formation process is shown from the upper surface, and in FIG.3 (d), B 'of FIG.3 (c) is shown. -B 'line cross section is shown.

Next, the second electrode substrate substrate preparation step and the porous layer forming step in this embodiment will be described. As shown in FIGS. 4A and 4B and FIGS. 5A and 5B, in the second electrode base material substrate preparation step, the second electrode base material having the second electrode layer 22 is provided. A substrate 20 ′ is prepared. Next, in the porous layer forming step, the porous layer 3 containing the metal oxide semiconductor fine particles carrying the dye sensitizer on the second electrode layer 22 is continuously formed. As shown in FIGS. 4 (a) and 4 (b), portions b and b ′ (the connecting portions of the second electrode layer 22 in the second electrode base material cut out from the second electrode base material substrate 20 ′). Hereinafter, the porous layer 3 is preferably formed continuously in a portion other than the connection portion b or b ′ of the second electrode substrate 20 ′.
4A shows an example of the second electrode base material substrate on which the porous layer 3 is formed by the porous layer forming step, and FIG. 4B shows an example of FIG. ) Is a cross-sectional view taken along the line CC of FIG.

Further, as shown in FIGS. 5A and 5B, in the porous layer forming step, the porous layer 3 may be continuously formed in a predetermined pattern shape. FIG. 5A shows an example in which the porous layer 3 is continuously formed in a stripe shape in portions other than the connection portions b and b ′ of the second electrode substrate 20 ′. .
In FIG. 5A, another example of the second electrode substrate 20 ′ having the porous layer 3 formed by the porous layer forming step is shown from the top, and in FIG. 5B, The DD sectional view of Drawing 5 (a) is shown.

  Although not shown, in the porous layer forming step, a porous layer may be formed on the first electrode layer.

Next, the functional layer formation process in this aspect is demonstrated.
As shown in FIGS. 4C and 4D, and FIGS. 5C and 5D, in the functional layer forming step, the porous layer 3 of the second electrode base substrate 20 ′ described above is formed. The solid electrolyte layer 4 including the polymer compound and the redox couple is continuously formed.
In FIG. 4C, an example of the second electrode substrate 20 ′ having the solid electrolyte layer 4 formed thereon is shown from the top, and in FIG. 4D, C ′ in FIG. -C 'line cross section is shown. Further, FIG. 5C shows another example of the second electrode substrate 20 ′ on which the solid electrolyte layer 4 is formed from the top surface, and FIG. 5D shows the example of FIG. D'-D 'line cross section is shown.

  Although not shown, in the functional layer forming step, the solid electrolyte layer may be formed on the first electrode layer of the first electrode base material in a pattern corresponding to the pattern of the first electrode layer.

Next, the cutting process in this embodiment will be described.
As shown in FIGS. 4E and 5E, in the cutting step, the second electrode substrate 20 is formed by cutting the second electrode substrate 20 ′ into a desired shape. 4 (e) and 5 (e), when the dye-sensitized solar cell element module is used, the second electrode substrate is so shaped that the adjacent second electrode substrate 20 does not contact. An example in which 20 is formed is shown.

  Next, the bonding process and the connection process in this embodiment will be described. In the bonding step, the solid electrolyte layer is adhered as an interface so that the catalyst layer formed on the first electrode substrate and the porous layer formed on the second electrode substrate face each other. The first electrode substrate and the second electrode substrate are bonded together. In the bonding step, for example, two connection portions including both ends of each stripe of the first electrode layer formed in a stripe shape of one dye-sensitized solar cell element, and the one dye-sensitized type The first electrode substrate and the second electrode substrate are arranged so that the two connection portions at both ends of the strip-shaped second electrode layer of another dye-sensitized solar cell element adjacent to the solar cell element are in contact with each other. A bonding process can be performed simultaneously by pasting. In addition, the specific example of a bonding process and a connection process is mentioned later.

  By performing the above steps, the dye-sensitized solar cell element module shown in FIGS. 1A and 1B can be manufactured.

  According to this aspect, since the solid electrolyte layer is used as the functional layer, a sealing material, an adhesive, and the like that are necessary when a liquid electrolyte is used are not necessary, and thus the manufacturing cost can be reduced. It becomes possible to manufacture a dye-sensitized solar cell module by a simple method. In addition, by eliminating the need for sealing materials and adhesives, it is possible to increase the area that contributes to power generation, making it possible to manufacture dye-sensitized solar cell module with high power generation efficiency. It becomes.

  Hereinafter, each process of the manufacturing method of the dye-sensitized solar cell element module of this aspect is demonstrated.

1. 1st electrode base material formation process The 1st electrode base material formation process of this mode was formed on the 1st base material in stripes, and was formed so that it might have two connection parts including the both ends of each stripe In this step, the first electrode base material is formed by forming a plurality of first electrode layers.
Here, the 1st electrode base material formed by this process is demonstrated.

  The 1st electrode base material formed by this process has a 1st base material and the 1st electrode layer formed on the 1st base material.

As a 1st electrode base material, the base material which has transparency may be sufficient, and the base material which does not have transparency may be sufficient, The light reception of the dye-sensitized solar cell element module manufactured by this aspect It is appropriately selected depending on the surface.
When the second electrode substrate is a substrate having transparency, the first electrode substrate formed in this step may be a substrate having transparency, or a group having no transparency. It may be a material.
On the other hand, when the 2nd electrode substrate is a substrate which does not have transparency, the 1st electrode substrate formed in this process is a substrate which has transparency.
Each will be described below.

(1) Substrate having transparency When the first electrode substrate is a substrate having transparency, the first electrode substrate is usually a transparent substrate as a first substrate and a first electrode layer. And a transparent electrode layer formed on the transparent substrate.

(A) 1st base material When the said 1st electrode base material is a base material which has transparency, as above-mentioned, a transparent base material is used as a 1st base material.
The said transparent base material supports the transparent electrode layer mentioned later.
As such a transparent substrate, for example, an inorganic transparent substrate or a resin substrate can be used. Among these, the resin base is preferable because it is lightweight, has excellent processability, and can reduce manufacturing costs.

  Examples of the resin base material include ethylene / tetrafluoroethylene copolymer film, biaxially stretched polyethylene terephthalate (PET), polyethersulfone (PES), polyetheretherketone (PEEK), and polyetherimide (PEI). ), Polyimide (PI), polyester naphthalate (PEN), polycarbonate (PC), and the like. In particular, in this embodiment, biaxially stretched polyethylene terephthalate (PET), polyester naphthalate. It is preferable to use a substrate made of a resin such as (PEN) or polycarbonate (PC).

  Examples of the inorganic transparent substrate include a synthetic quartz substrate and a glass substrate.

  The thickness of the transparent substrate used in this embodiment can be appropriately selected according to the use of the dye-sensitized solar cell element module, and is usually in the range of 5 μm to 2000 μm. In particular, it is preferably in the range of 10 μm to 500 μm, and more preferably in the range of 25 μm to 200 μm.

  The form of the transparent substrate used in this embodiment is not particularly limited as long as it can obtain a desired dye-sensitized solar cell element module. More preferably, it is a long base material having flexibility. Since the transparent substrate is in the above-described form, the step of forming the solid electrolyte layer on the first electrode substrate side can be performed by the R to R process in this step and the functional layer forming step described later. Therefore, it becomes possible to manufacture with high manufacturing efficiency.

  In addition, as the flexibility of the transparent substrate, as long as it can be wound in a roll shape and can impart desired workability to the dye-sensitized solar cell element module to be manufactured. There is no particular limitation. Specifically, the flexibility of the transparent base material described above refers to bending when a force of 5 KN is applied in the fine ceramic bending test method of JIS R1601.

Moreover, it is preferable that the transparent base material used for this aspect is excellent in heat resistance, a weather resistance, water vapor | steam, and other gas barrier properties. This is because when the transparent substrate has gas barrier properties, for example, the temporal stability of the dye-sensitized solar cell of this embodiment can be increased. In particular, in this embodiment, oxygen permeability is 1 cc / m ² / day · atm or less under conditions of a temperature of 23 ° C. and a humidity of 90%, and a water vapor transmission rate of 1 g under conditions of a temperature of 37.8 ° C. and a humidity of 100% It is preferable to use a transparent substrate having a gas barrier property of / m ² / day or less. In this aspect, in order to achieve such gas barrier properties, a material in which an arbitrary gas barrier layer is provided on the transparent substrate may be used. The oxygen permeability is a value measured using an oxygen gas permeability measuring device (manufactured by Modern Control Co., Ltd., OX-TRAN 2/20: trade name). The water vapor transmission rate is a value measured using a water vapor transmission rate measuring device (manufactured by Modern Control Co., Ltd., PERMATRAN-W 3/31: trade name).

(B) 1st electrode layer When the said 1st electrode base material is a base material which has transparency, as above-mentioned, a transparent electrode layer is used as a 1st electrode layer.
A transparent electrode layer is formed in pattern shape on the transparent electrode base material mentioned above. The transparent electrode layer is not particularly limited as long as it has transparency enough to receive sunlight, and may be a transparent electrode, or a transparent electrode and an auxiliary electrode are laminated. It may be.

(I) Transparent electrode The transparent electrode used in this embodiment is not particularly limited as long as it has transparency and predetermined conductivity. Examples of the material used for such a transparent electrode include metal oxides and conductive polymer materials.

Examples of the metal oxide include SnO ₂ , ZnO, a compound in which tin is added to indium oxide (ITO), a compound in which zinc oxide is added to indium oxide (IZO), and the like. In this embodiment, any of these metal oxides can be suitably used, but among these, fluorine-doped SnO ₂ (hereinafter referred to as FTO) and ITO are preferably used. This is because FTO and ITO are excellent in both conductivity and sunlight permeability.
On the other hand, examples of the conductive polymer material include polythiophene, polyaniline (PA), polypyrrole, polyethylenedioxythiophene (PEDOT), and derivatives thereof. Moreover, these can also be used in mixture of 2 or more types.

The total light transmittance of the transparent electrode in the present invention is preferably 85% or more, more preferably 90% or more, and particularly preferably 92% or more. This is because when the total light transmittance of the transparent electrode is within the above range, light can be sufficiently transmitted through the transparent electrode and light can be efficiently absorbed by the porous layer.
The total light transmittance is a value measured using an SM color computer (model number: SM-C) manufactured by Suga Test Instruments Co., Ltd. in the visible light region.

The sheet resistance of the transparent electrode in the present invention is preferably 500Ω / □ or less, more preferably 300Ω / □ or less, and particularly preferably 50Ω / □ or less. This is because if the sheet resistance is larger than the above range, the generated charge may not be sufficiently transmitted to the external circuit.
In addition, the said sheet resistance is measured based on JIS R1637 (Resistance test method of fine ceramics thin film: Measurement method by 4 probe method) using a surface resistance meter (Loresta MCP: Four-terminal probe) manufactured by Mitsubishi Chemical Corporation. It is the value.

  The transparent electrode used in this embodiment may have a single layer structure or a structure in which a plurality of layers are laminated. Examples of the configuration in which a plurality of layers are stacked include a mode in which layers made of materials having different work functions are stacked, and a mode in which layers made of different metal oxides are stacked.

The thickness of the transparent electrode used in this embodiment is not particularly limited as long as desired conductivity can be achieved in accordance with the use of the dye-sensitized solar cell element module. In particular, the film thickness of the transparent electrode in this embodiment is usually preferably in the range of 5 nm to 2000 nm, and particularly preferably in the range of 10 nm to 1000 nm. If the thickness is thicker than the above range, it may be difficult to form a homogeneous transparent electrode layer, or the total light transmittance may be lowered and it may be difficult to obtain good photoelectric conversion efficiency. If the thickness is thinner than the above range, the conductivity of the transparent electrode layer may be insufficient.
In addition, the said thickness shall point out the total thickness which totaled the thickness of all the layers, when a transparent electrode is comprised from a several layer.

  The pattern shape of the transparent electrode is not particularly limited as long as a desired dye-sensitized solar cell element module can be produced, and the use of the dye-sensitized solar cell module is first described in the connection step described later. Although it is appropriately selected depending on the connection method of the electrode layer and the second electrode layer, a stripe shape is preferable. This is because the transparent electrode is easily formed when formed in a pattern. Moreover, it is because it becomes easy to form the porous layer, solid electrolyte layer, etc. which are formed in the process after this process.

Moreover, it is preferable to set it as the pattern shape which has a connection part with a 2nd electrode layer as a pattern shape of a transparent electrode.
As shown in FIG. 3C, the connecting portion is preferably formed with two connecting portions a and a ′ including both end portions of the striped transparent electrode. In the case of a dye-sensitized solar cell module, the contact area between the first electrode layer and the second electrode layer can be increased, connection failure can be prevented, and two connections By having a portion, the above-mentioned organic solar cell element module with excellent electrical connection reliability can be manufactured, and the current flow path is shortened, and the current loss due to the resistance at the electrode is reduced. This is because the organic solar cell element module can be manufactured.

  The method for forming the transparent electrode is not particularly limited as long as it is a method capable of forming a transparent electrode that can be used as a plurality of first electrode layers in a predetermined pattern on the above-described transparent substrate. A method of forming the transparent electrode layer using a metal mask using a vapor deposition method such as a sputtering method, a method of forming the transparent electrode layer material film on the entire surface of the transparent substrate, and etching the film into a predetermined pattern, Examples thereof include a method in which the transparent electrode layer material is a metal paste, and the metal paste is printed on a transparent substrate.

(Ii) Auxiliary electrode In this step, as described above, the transparent electrode layer may be formed by laminating the above-described transparent electrode and auxiliary electrode.
Here, the auxiliary electrode is an electrode formed in a mesh shape using a conductive material. By using the auxiliary electrode together with the transparent electrode described above, it is possible to increase the power generation efficiency of the dye-sensitized solar cell module manufactured according to this aspect.

  The position where the auxiliary electrode is formed is not particularly limited as long as the power generation efficiency of the dye-sensitized solar cell element module manufactured according to the present embodiment can be increased by using the auxiliary electrode together with the transparent electrode. It may be formed on the transparent electrode formed on the transparent substrate, or may be formed between the transparent substrate and the transparent electrode. In this embodiment, it is more preferable that the auxiliary electrode is formed between the transparent substrate and the transparent electrode. When the solid electrolyte layer to be described later contains iodide ions, compared to the case where the auxiliary electrode is formed on the transparent electrode formed on the transparent substrate, iodide ions in the solid electrolyte layer It is because it becomes difficult to contact.

The material for the auxiliary electrode used in this embodiment is not particularly limited as long as it is a material that can increase the power generation efficiency of the dye-sensitized solar cell of this embodiment.
Specific examples of materials used for such auxiliary electrodes include titanium, tungsten, molybdenum, chromium, platinum, etc., and aluminum, nickel, copper, iron, silver, and alloys thereof. It can be used by applying anti-corrosion surface treatment to typical metal species.

(2) Substrate not having transparency When the first electrode substrate is a substrate not having transparency, the transparency as described in the above-mentioned “substrate having transparency” is used. Although it will not specifically limit if it is a base material which is not shown, Usually, it has a 1st base material and the metal layer formed in the pattern form on the 1st base material.

(A) First base material The first base material may be a transparent base material or a first base material having no transparency. About a transparent base material, since it can be made to be the same as that of what was described in the item of "(1) Base material which has transparency" mentioned above, description here is abbreviate | omitted.
On the other hand, a resin-made base material can be mentioned as a 1st base material which does not have transparency.
In addition, about the resin material used for a resin-made base material, since it can be the same as that of the material used for the transparent resin-made base material mentioned above, description here is abbreviate | omitted.

  Further, the specific thickness, form, etc. of the first base material having no transparency can be the same as those described in the above-mentioned section “(1) Transparency base material”. Explanation here is omitted.

(B) 1st electrode layer When the said 1st electrode base material is a base material which does not have transparency, as above-mentioned, a metal layer is used as a 1st electrode layer.
Further, the metal layer is not particularly limited as long as it can be formed in a predetermined pattern shape on the above-described first base material, but preferably has flexibility. This is because when the metal layer has flexibility, the processability of the dye-sensitized solar cell element module manufactured according to this embodiment can be further improved.

  Specific examples of the metal used for the metal layer include copper, aluminum, titanium, chromium, tungsten, molybdenum, platinum, tantalum, niobium, zirconium, zinc, various stainless steels, and alloys thereof. Chromium, tungsten, various stainless steels and their alloys are desirable.

  Further, the thickness of the metal layer is not particularly limited as long as it functions as the first electrode layer of the dye-sensitized solar cell element module, but it is usually preferably in the range of 5 μm to 1000 μm, and 10 μm to 500 μm. More preferably, it is in the range of 20 μm to 200 μm.

  About the pattern shape of the said metal layer, since it can be made to be the same as that of the pattern shape of the transparent electrode mentioned above, description here is abbreviate | omitted.

The method for forming the metal layer can be the same as the method for forming a general metal layer.
For example, after a metal film is formed on the first substrate by vapor deposition or the like, a metal layer having a predetermined pattern shape is formed by etching, or pattern vapor deposition on the first substrate using a metal mask or the like. Examples of the method include forming a metal layer.

(3) Other configurations The first electrode substrate formed in this step is not particularly limited as long as it has the first substrate and the first electrode layer, and has other configurations as necessary. It may be.

  For example, when a porous layer is formed on the second electrode substrate substrate side in the porous layer forming step described later, a catalyst layer is formed on the first electrode layer of the first electrode substrate formed in this step. Is preferably formed.

The catalyst layer has a function that contributes to the improvement of the luminous efficiency of the dye-sensitized solar cell element module.
Examples of such a catalyst layer include, for example, an embodiment in which Pt is vapor-deposited on the first electrode layer, polyethylene dioxythiophene (PEDOT), polypyrrole (PP), polyaniline (PA), and derivatives thereof and these An embodiment in which the catalyst layer is formed from a mixture of these may be mentioned, but this is not restrictive.

  The film thickness of such a catalyst layer is preferably in the range of 5 nm to 500 nm, more preferably in the range of 10 nm to 300 nm, and particularly preferably in the range of 15 nm to 100 nm.

  The method for forming the catalyst layer is not particularly limited as long as the catalyst layer can be formed with a desired thickness on the first electrode layer described above. The method for forming a catalyst layer in a general dye-sensitized solar cell element and Since it can be the same, description here is abbreviate | omitted.

The catalyst layer 5 formed in this step may be formed on the entire surface of the first electrode layer 12 as shown in FIGS. 3C and 3D. As shown in FIG. A part of the first electrode layer 12 may be formed in a pattern.
In addition, when the catalyst layer is formed in a pattern, it is preferably formed so as to correspond to the pattern shape of the solid electrolyte layer described later. In addition, since the pattern shape of a solid electrolyte layer is mentioned later, description here is abbreviate | omitted.

(4) 1st electrode base material As a 1st electrode base material formed in this process, although any of the base material which has transparency mentioned above and the base material which does not have transparency may be sufficient, it is transparent. It is preferable that the substrate has a property.
Here, in the porous layer forming step described later, a porous layer is formed either on the first electrode layer of the first electrode base material or on the second electrode layer of the second electrode base material substrate described later. However, when the porous layer is formed on the second electrode layer, the porous layer can be continuously formed, and the production method of this embodiment can be made a simpler method. Become.
Moreover, as a formation method of a porous layer, it is preferable to use the method of using a metal layer as a 2nd electrode layer, and baking and forming a porous layer on a metal layer.
Therefore, since it is preferable to use a substrate having no transparency as the second electrode substrate, the first electrode substrate formed in this step is preferably a substrate having transparency. .

2. Second electrode base material preparation step The second electrode base material preparation step in this aspect includes the second electrode layer and can cut out the plurality of second electrode base materials having two connection portions at both ends. This is a step of preparing a single second electrode substrate.

The substrate for the second electrode substrate may be a substrate having transparency or a substrate having no transparency, and may be a dye-sensitized type produced by the production method of this embodiment. It is appropriately selected depending on the light receiving surface of the solar cell element module.
In the case where the first electrode base material formed in the first electrode base material forming step is a transparent base material, the second electrode base material substrate may be a transparent base material. The base material which does not have transparency may be sufficient. On the other hand, when the first electrode substrate is a substrate having no transparency, a substrate having transparency is used as the second electrode substrate.

  Such a substrate for the second electrode base material is not limited as long as it has a function as an electrode and can be cut into a desired shape by a cutting process described later to form the second electrode base material. It may be composed of a second electrode layer, and may have a second electrode layer and a second base material for supporting the second electrode layer.

When the second electrode substrate is composed of the second electrode layer, specifically, a single metal layer, that is, a metal substrate is used as the second electrode substrate.
Further, the form of the metal substrate is not particularly limited as long as a desired second electrode substrate can be formed, but may be a long shape having flexibility wound up in a roll shape. preferable.
In addition, as flexibility of a metal base material, specifically, the metal material bending test method of JIS Z 2248 indicates that it bends when a force of 5 KN is applied.

  About the metal used for the said metal base material, since it can be set as the same as the metal layer used for the 1st electrode base material mentioned above, description here is abbreviate | omitted.

  In addition, the thickness of the metal substrate is not particularly limited as long as it is a thickness that can be cut in a cutting step described later, and can be equal to the thickness of the metal layer used for the first electrode substrate described above. .

On the other hand, when the substrate for the second electrode base material has the second electrode layer and the second base material, the second electrode layer has been described in the first electrode base material forming step described above. A transparent electrode layer or a metal layer can be used, and as the second base material, the transparent base material or the resin base material described in the section of the first electrode base material forming step described above can be used.
In addition, as a board | substrate for 2nd electrode base materials, the 2nd electrode layer is normally formed in the 2nd base material whole surface.

  About a transparent base material, a resin base material, a transparent electrode layer, and a metal layer, since it can be set as the thing demonstrated by the term of the 1st electrode base material formation process mentioned above, description here is abbreviate | omitted.

The second electrode substrate for substrate prepared in this step can have other configurations as necessary.
For example, when a porous layer is formed on the first electrode layer of the first electrode substrate described above in the porous layer forming step described later, it is preferable to form a catalyst layer on the second electrode layer.
Note that the catalyst layer can be the same as that described in the section of the first electrode base material forming step described above, and thus the description thereof is omitted here.

  The substrate for the second electrode base material prepared in this step is more preferably a second electrode layer, that is, a metal base material. As explained in the section of the first electrode base material forming step described above, in the porous layer forming step described later, it is preferable to form a porous layer on the second electrode layer of the second electrode base material substrate. Because.

3. Porous layer forming step In the porous layer forming step in this embodiment, the metal oxide semiconductor fine particles having a dye sensitizer carried on either one of the plurality of first electrode layers or the second electrode layer are provided. It is the process of forming the porous layer to contain.
Hereinafter, the porous layer formed in this step and the method for forming the porous layer will be described.

(1) Porous layer The porous layer contains metal oxide semiconductor fine particles carrying a dye sensitizer. Hereinafter, the metal oxide semiconductor fine particles and the dye sensitizer used in the porous layer will be described.

(A) Metal oxide semiconductor fine particle The metal oxide semiconductor fine particle is not particularly limited as long as it is made of a metal oxide having semiconductor characteristics. Examples of the metal oxide constituting the metal oxide semiconductor fine particles include TiO ₂ , ZnO, SnO ₂ , ITO, ZrO ₂ , MgO, Al ₂ O ₃ , CeO ₂ , Bi ₂ O ₃ , Mn ₃ O ₄ , Y ₂ O ₃ , WO ₃ , Ta ₂ O ₅ , Nb ₂ O ₅ , La ₂ O _{3 and the} like can be mentioned.
Among these, in this embodiment, it is most preferable to use metal oxide semiconductor fine particles made of TiO ₂ . This is because TiO ₂ is particularly excellent in semiconductor characteristics.

The average particle diameter of the metal oxide semiconductor fine particles is usually preferably in the range of 1 nm to 10 μm, particularly preferably in the range of 10 nm to 1000 nm.
The average particle size of the metal oxide semiconductor fine particles means the primary particle size.

(B) Dye sensitizer The dye sensitizer is not particularly limited as long as it can absorb light and generate an electromotive force. Examples of such a dye sensitizer include organic dyes and metal complex dyes. Examples of the organic dyes include acridine, azo, indigo, quinone, coumarin, merocyanine, phenylxanthene, indoline, and carbazole dyes. In the present invention, among these organic dyes, a coumarin dye is preferably used. Further, as the metal complex dye, it is preferable to use a ruthenium dye, and it is particularly preferable to use a ruthenium bipyridine dye and a ruthenium terpyridine dye which are ruthenium complexes. This is because such a ruthenium complex has a wide wavelength range of light to be absorbed, so that the wavelength range of light that can be photoelectrically converted can be greatly expanded.

(C) Optional component The porous layer may contain an optional component in addition to the metal oxide semiconductor fine particles. As an arbitrary component used for this process, resin can be mentioned, for example. It is because the brittleness of the porous layer formed in this step can be improved by containing the resin in the porous layer.

  Examples of the resin that can be used for the porous layer in this step include polyvinyl pyrrolidone, ethyl cellulose, caprolactan, and the like.

(D) Porous layer The thickness of the porous layer formed in this step can be appropriately determined according to the use of the dye-sensitized solar cell module produced by the production method of this embodiment, It is not limited. In particular, the thickness of the porous layer in the present invention is usually preferably in the range of 1 μm to 100 μm, and particularly preferably in the range of 3 μm to 30 μm.

  In this step, the porous layer is formed on either the plurality of first electrode layers of the first electrode base material or the second electrode layer of the second electrode base material substrate.

Here, in the connection step described later, it is preferable that a porous layer does not exist in two connection portions at both ends of the first electrode layer and the second electrode layer.
Therefore, in this case, as shown in FIG. 6, it is preferable that the porous layer 4 is not formed at the connection portions a and a ′ of the first electrode layers 12. Further, as shown in FIGS. 4A and 5A, it is preferable to continuously form a porous layer in a portion other than the connection portions b and b ′ of the second electrode substrate 20 ′. .

  When the porous layer 4 is formed on the first electrode layer 12, the porous layer 4 is formed so that the width of the porous layer 4 is larger than the width of the first electrode layer 12 as shown in FIG. 6. It is preferable. Thereby, in the dye-sensitized solar cell element module manufactured according to this aspect, the occurrence of an internal short circuit due to the contact between the first electrode layer and the second electrode layer in one dye-sensitized solar cell element. This is because it can be prevented.

FIG. 6 is a top view showing an example of a first electrode base material in which a porous layer is formed on the first electrode layer side in this step. In FIG. 6, a region indicated by a one-dot chain line indicates a region where the first electrode layer is formed.

(2) Formation method of porous layer As a formation method of the porous layer used in this step, it is desired on the plurality of first electrode layers of the first electrode substrate or the second electrode layer of the second electrode substrate. The method is not particularly limited as long as the porous layer can be formed with a thickness of 5 mm.

In addition, when the form of the said 1st base material or the form of the board | substrate for 2nd electrode base materials is the elongate shape wound up by the roll shape mentioned above, this process is performed by R to R process. It is more preferable. This is because a dye-sensitized solar cell module can be manufactured with higher manufacturing efficiency.
Therefore, it is preferable that an R to R process can be applied as a method for forming the porous layer used in this step.

  In this step, it is preferable to form a porous layer on the second electrode layer of the second electrode substrate. In this case, since it becomes possible to form a porous layer continuously, it is a simpler method compared with the case where a porous layer is formed in a pattern on the first electrode layer of the first electrode substrate. This is because a porous layer can be formed.

In addition, as a formation method of a porous layer, the following method can be mentioned more specifically.
First, a coating liquid for forming a porous layer comprising at least the metal oxide semiconductor fine particles, a binder resin, and a solvent described above is prepared. Next, using the metal layer as the second electrode layer, the porous layer forming coating solution prepared on the metal layer is applied with a desired film thickness to form a porous layer forming coating film, The porous layer forming layer is formed by firing the porous layer forming coating film and thermally decomposing the binder resin. Next, the porous layer is formed by attaching the above-described dye sensitizer to the surface of the porous layer forming layer.
The binder resin and the solvent used in the porous layer forming coating solution can be the same as those used in a general porous layer forming method, and thus description thereof is omitted here. Moreover, as a coating liquid for porous layer formation, a dispersing agent can also be added as needed other than the component mentioned above.
Moreover, since it can be made to be the same as that of the thing used with the formation method of a general porous layer also about the application method of a coating liquid for porous layer formation, baking conditions, etc., description here is abbreviate | omitted.

Moreover, as a formation method of a porous layer, it is also possible to use the following method.
First, the porous layer forming composition including the metal oxide semiconductor fine particles and the solvent described above is applied on the second electrode layer and dried to form the porous layer forming layer, and then the porous layer forming layer is formed. A porous layer is formed by attaching a dye sensitizer to the layer. The solvent used in the porous layer forming composition, the coating method of the porous layer forming composition, and the drying conditions are the same as those used in the general porous layer forming method. The description here is omitted.
This method can also be used when a porous layer is formed on the first electrode layer of the first electrode substrate.

Moreover, as a formation method of a porous layer, it is also possible to use the following method.
Using a method similar to the method of firing and forming the porous layer on the second electrode layer described above, after forming the release layer on the heat-resistant substrate, the porous layer is disposed on the release layer, A porous layer is formed by bonding to the second electrode layer and then peeling off the heat-resistant substrate.
This method can also be used when a porous layer is formed on the first electrode layer of the first electrode substrate.

4). Functional layer formation process The functional layer formation process in this aspect is a pattern corresponding to the pattern of the first electrode layer with the solid electrolyte layer containing the polymer compound and the redox couple on the first electrode layer side of the first electrode substrate. Or a step of continuously forming the solid electrolyte layer on the second electrode layer side of the second electrode substrate.
In the present embodiment, “the solid electrolyte layer is formed in a pattern corresponding to the pattern of the first electrode layer” means that each organic solar cell constituting the organic solar cell element module manufactured by the manufacturing method of the present invention is used. It refers to forming each solid electrolyte layer on each first electrode layer formed in a pattern so that the battery element has a solid electrolyte layer. More specifically, it means that one solid electrolyte layer is formed in a pattern that can be continuously formed on one first electrode layer.

  Here, the solid electrolyte layer formed in this step contains a polymer compound and a redox couple and does not exhibit fluidity. In the present invention, the solid electrolyte layer is a concept including a gel electrolyte layer.

(1) Material of solid electrolyte layer The material of the solid electrolyte layer in this embodiment contains a polymer compound and a redox couple.

(A) Polymer Compound The polymer compound used for the solid electrolyte layer will be described.

  Examples of the polymer compound in the solid electrolyte layer include polyether, polymethacrylic acid, polyacrylic acid alkyl ester, polymethacrylic acid alkyl ester, polycaprolactone, polyhexamethylene carbonate, polysiloxane, polyethylene oxide, polypropylene oxide, and polyacrylonitrile. Polyvinylidene fluoride, polyvinyl fluoride, polyhexafluoropropylene, polyfluoroethylene, polyethylene, polypropylene, polystyrene, a polymer having a main chain of polyacrylonitrile, or a copolymer of two or more of these monomer components is preferably used. Can do.

  Moreover, as a high molecular compound used for the said solid electrolyte layer, a cellulose resin can be mentioned. Since the cellulosic resin has high heat resistance, the electrolyte layer solidified with the cellulosic resin does not leak even at high temperatures and has high thermal stability. Specifically, cellulose such as cellulose, cellulose acetate, cellulose diacetate, and cellulose triacetate (CA), cellulose acetate butyrate (CAB), cellulose acetate propionate (CAP), cellulose acetate phthalate, cellulose such as cellulose nitrate Examples thereof include cellulose ethers such as esters, methylcellulose, ethylcellulose, benzylcellulose, cyanoethylcellulose, hydroxymethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose, and carboxymethylcellulose. Any of these cellulose resins may be used alone, or two or more thereof may be used in combination.

  Among cellulose resins, a cationic cellulose derivative is particularly preferably used from the viewpoint of compatibility with the electrolyte solution. The cationic cellulose derivative means a product obtained by cationization by reacting a cellulose or an OH group of the derivative with a cationizing agent. By containing the cationic cellulose derivative, it is possible to obtain a solid electrolyte layer that is excellent in retention of the electrolytic solution, and that has no leakage of the electrolytic solution, particularly at high temperature or under pressure, and excellent in thermal stability.

  The molecular weight of the cellulose-based resin as described above varies depending on the type of the cellulose-based resin and is not particularly limited. However, from the viewpoint of obtaining good film-forming properties when forming the electrolyte layer, the mass average molecular weight is 10,000 or more. (Polystyrene conversion), and particularly preferably within the range of 100,000 to 200,000. For example, when ethyl cellulose is used as the cellulosic resin, it is a value obtained by dissolving ethyl cellulose at 2% by mass in water and measuring the viscosity at 30 ° C., within a range of 5 mPa · s to 1000 mPa · s, particularly 10 mPa. -It is preferable to set it as the molecular weight which shows the viscosity in the range of s-500mPa * s.

  The glass transition temperature of the cellulose resin is preferably in the range of 80 ° C. to 150 ° C. in order to obtain sufficient thermal stability of the electrolyte layer.

  The polymer compound used in the present invention is preferably a transparent compound. When the polymer compound has transparency, the transparency of the solid electrolyte layer can be further improved. Further, by improving the transparency of the solid electrolyte layer, the appearance of the dye-sensitized solar cell module manufactured by the manufacturing method of this embodiment can be improved. Moreover, since it becomes possible to prevent light from being blocked by the solid electrolyte layer when the solid electrolyte layer penetrates into the porous layer, the dye-sensitized solar cell module manufactured according to the present aspect The performance can be improved.

  The content of such a polymer compound is appropriately set in consideration of the above because the thermal stability of the solid electrolyte layer is lowered when it is too low, and the photoelectric conversion efficiency of the solar cell is lowered when it is too high. The Specifically, it is preferable to contain 5 mass%-60 mass% in the material which comprises a solid electrolyte layer. If the polymer compound in the material constituting the solid electrolyte layer has a proportion lower than the above range, sufficient adhesion to the porous layer described later may not be obtained, and the solid electrolyte layer itself This is not preferable because it may lead to a decrease in the mechanical strength. On the other hand, if the ratio is higher than the above range, a large amount of insulating polymer compound is present, which is not preferable because the function of transporting charges may be hindered.

(B) Redox Pair Next, the redox couple used for the solid electrolyte layer will be described.
In the solid electrolyte layer formed in this step, the redox couple is not particularly limited as long as it is generally used in the electrolyte layer of a dye-sensitized solar cell. Specifically, a combination of iodine and iodide and a combination of bromine and bromide are preferable. For example, as a combination of iodine and iodide, a combination of metal iodide such as LiI, NaI, KI, and CaI ₂ and I ₂ can be mentioned. Further, examples of the combination of bromine and bromide include a combination of a metal bromide such as LiBr, NaBr, KBr, and CaBr ₂ and Br ₂ .

  Moreover, as content of the said oxidation reduction pair, the ratio of the oxidation reduction pair which occupies for a solid electrolyte layer exists in the range of 1 mass%-50 mass%, especially within the range of 5 mass%-35 mass%. Is preferred.

(C) Other components In addition to the polymer compound and the redox couple described above, necessary components can be appropriately added to the solid electrolyte layer used in the present invention. An example of such a component is an ionic liquid.

(2) Solid electrolyte layer The thickness of the solid electrolyte layer formed by this step is preferably in the range of 10 nm to 100 µm, more preferably in the range of 1 µm to 50 µm, and particularly preferably in the range of 5 µm to 30 µm. This is because when the thickness of the solid electrolyte layer is less than the above range, the solid electrolyte layer does not function sufficiently and the power generation efficiency of the dye-sensitized solar cell module may be reduced. Moreover, when the film thickness of the said solid electrolyte layer exceeds the said range, it is because it will become difficult to form the dye-sensitized solar cell element module manufactured by the manufacturing method of this aspect in a thin film.

  When the solid electrolyte layer is formed on the first electrode substrate side, the pattern shape of the solid electrolyte layer is a porous layer formed on the first electrode layer in the porous layer forming step described above. The pattern shape is preferably the same.

Further, when the solid electrolyte layer is formed on the second electrode substrate substrate side, the solid electrolyte layer is usually formed continuously. The solid electrolyte layer is formed by providing a portion where the solid electrolyte layer is not formed at two connection portions at both ends of the second electrode layer.
The specific shape of the solid electrolyte layer can be the same as the shape of the porous layer formed on the second electrode layer in the porous layer forming step described above.

(3) Method for forming solid electrolyte layer In this step, when the solid electrolyte layer described above is formed in a pattern on the first electrode layer side of the first electrode base material, The method is not particularly limited as long as it can form a solid electrolyte layer having a desired pattern with a desired thickness on the electrode layer, and a known method can be used.
In addition, when the form of the 1st base material used for the said 1st electrode base material is the elongate shape wound up by the roll shape mentioned above, it is more preferable that this process is performed by a R to R process. This is because a dye-sensitized solar cell module can be manufactured with higher manufacturing efficiency.

On the other hand, also in the case where the above-described solid electrolyte layer is continuously formed on the second electrode substrate side of the second electrode substrate, in this step, the solid electrolyte layer may be formed with a desired thickness as a method for forming the solid electrolyte layer. If a layer can be formed, it will not specifically limit, A well-known coating method can be used.
Moreover, when the form of the said 2nd electrode base-material board | substrate is the elongate shape wound up by the roll shape mentioned above, it is more preferable that this process is performed by a R to R process. This is because a dye-sensitized solar cell module can be manufactured with higher manufacturing efficiency.

5. Cutting Step The cutting step in this aspect is a step of forming the plurality of second electrode base materials by cutting the second electrode base material substrate.

  The shape of the second electrode substrate formed by this step is particularly limited as long as the adjacent second electrode substrates are not in contact with each other in the dye-sensitized solar cell element module manufactured according to this aspect. First, it can be selected and determined as appropriate depending on the use of the dye-sensitized solar cell module.

Moreover, in the connection process mentioned later, when electrically connecting the 1st electrode layer and 2nd electrode layer of an adjacent dye-sensitized solar cell element, the shape of the 2nd electrode base material formed in this process For example, it is preferable that the second electrode layer has a shape having a connection portion with the first electrode layer.
When the second electrode substrate has a strip shape, the connection portions are formed with connection portions b and b ′ including the ends of the short sides of the strip as shown in FIGS. 4 (e) and 5 (e). It is preferable. In the case of a dye-sensitized solar cell module, the contact area between the first electrode layer and the second electrode layer can be increased, connection failure can be prevented, and two connections By having a portion, the above-mentioned organic solar cell element module with excellent electrical connection reliability can be manufactured, and the current flow path is shortened, and the current loss due to the resistance at the electrode is reduced. This is because the organic solar cell element module can be manufactured.

  Moreover, when the porous layer and solid electrolyte layer mentioned above are formed on the 2nd electrode base-material board | substrate, the porous layer and solid electrolyte layer which the 2nd electrode base material formed by this process normally has The second electrode base material substrate is cut so as to have a pattern corresponding to the pattern of the first electrode layer described above.

  The method for cutting the second electrode base material substrate used in this step is not particularly limited as long as it is a method capable of cutting out the second electrode base material having a desired shape from the second electrode base material substrate. First, a known method can be used.

6). Bonding step The bonding step in this embodiment is such that the first electrode layer side of the first electrode substrate and the second electrode layer side of the second electrode substrate are opposed to each other, and the solid electrolyte layer is used as an interface. In this step, the first electrode substrate and the second electrode substrate are bonded together.

In this step, when a porous layer is formed on the plurality of first electrode layers of the first electrode base material described above, the porous layer and the second electrode layer are opposed to each other to form a solid The electrolyte layer is adhered as an interface. On the other hand, when the porous layer is formed on the second electrode layer of the second electrode substrate described above, the first electrode layer and the porous layer are opposed to each other, and the solid electrolyte layer is used as an interface. Let
Further, when the catalyst layer is formed on the electrode layer on the side where the porous layer is not formed, the porous layer and the catalyst layer are opposed to each other, and the solid electrolyte layer is adhered as an interface.

Here, this step will be described with reference to the drawings.
In this step, for example, the catalyst layer 5 formed on the plurality of first electrode layers 12 of the first electrode substrate 10 shown in FIG. 3D and the plurality of second layers shown in FIG. The porous layer 3 formed on the second electrode layer of the electrode base material is opposed to the solid electrolyte layer 4 as an interface. Thereby, in this process, the structure of the dye-sensitized solar cell element module 100 shown by FIG. 1 (a), (b) can be obtained.

  The bonding method used in this step is not particularly limited as long as it is a bonding method capable of satisfactorily bringing the first electrode layer and the porous layer into close contact with the solid electrolyte layer as an interface. It is preferable to use a roll laminating method or a vacuum laminating method. It is because it is easy to bond so that air may not enter into the contact surface.

7). Connection process The connection process in this aspect includes the first electrode layer of one dye-sensitized solar cell element and the other dye-sensitized solar cell elements adjacent to the one dye-sensitized solar cell element. This is a step of electrically connecting the second electrode layer.

  As a method for connecting the first electrode layer and the second electrode layer in this step, at both ends of the first electrode layer and the second electrode layer of the dye-sensitized solar cell element adjacent to each other in the dye-sensitized solar cell element module. The method is not particularly limited as long as it is a method capable of electrically connecting the two formed connection portions. For example, the first electrode layer and the second electrode layer of the adjacent dye-sensitized solar cell element are directly in contact with each other, or a conductive layer is formed between the first electrode layer and the second electrode layer and connected. The method of electrically connecting inside the dye-sensitized solar cell element module, such as making it possible, is mentioned. This is because the connection method is simpler than the method of electrically connecting outside the dye-sensitized solar cell module.

In this step, it is preferable to use a method in which a conductive layer is formed and connected between the first electrode layer and the second electrode layer of adjacent dye-sensitized solar cell elements. This is because a connection failure in the dye-sensitized solar cell module manufactured according to this aspect can be prevented more appropriately.
As a material for the conductive layer, a general conductive adhesive or the like can be used.

Here, a connection method using the connection portion will be specifically described with reference to the drawings.
In this step, for example, the catalyst layer 5 formed on the plurality of first electrode layers 12 of the first electrode substrate 10 shown in FIG. 3D and the plurality of second layers shown in FIG. When the porous layer 3 formed on the second electrode layer 22 of the electrode base material 20 is opposed and bonded with the solid electrolyte layer 4 as an interface, both ends of each stripe of the first electrode layer 12 are bonded. As shown in FIG. 1 (a), two adjacent connecting portions a and a 'and two connecting portions b and b' at both ends of the strip of the second electrode layer 22 are brought into direct contact with each other. The first electrode layer 11 and the second electrode layer 22 of the sensitized solar cell element can be electrically connected.

8). Other Steps The method for producing the dye-sensitized solar cell element module of the present embodiment is not particularly limited as long as it is a production method having the above-described steps, and necessary steps can be appropriately selected and added. .
As such a process, for example, after preparing a dye-sensitized solar cell element module, a transparent resin film or a metal laminate is formed on the first electrode substrate and the second electrode substrate of the dye-sensitized solar cell element module. A process of arranging and packaging the form can be exemplified.

  Further, for example, a plurality of dye-sensitized solar cell element modules are produced by performing the above-described steps, and a larger dye-sensitized solar cell is obtained by combining the plurality of dye-sensitized solar cell element modules. The process of forming a battery element module can be mentioned.

II. 2nd aspect The 2nd aspect of the manufacturing method of the organic type solar cell element module of this invention is a plurality of organic thin-film solar cell elements each having a photoelectric conversion layer connected between the first electrode layer and the second electrode layer. It is a manufacturing method for manufacturing an organic thin-film solar cell element module, in which the functional layer is a layer containing an organic substance formed between the first electrode layer and the second electrode layer.
In the following description, the organic solar cell element module will be referred to as an organic thin film solar cell element module.

  In addition, in the organic thin film solar cell element module manufactured by the manufacturing method of this aspect, either the first electrode layer or the second electrode layer is an electrode (hole) for extracting holes generated in the photoelectric conversion layer. The other electrode is used as an electrode (electron extraction electrode) for taking out electrons generated in the photoelectric conversion layer.

Here, the organic thin-film solar cell element module manufactured by the manufacturing method of this aspect is demonstrated using figures. FIG. 7 is a schematic cross-sectional view showing an example of an organic thin-film solar cell element module manufactured by the manufacturing method of this aspect. The schematic plan view of FIG. 7 can be the same as the schematic plan view of the dye-sensitized solar cell element module shown in FIG.
As shown in FIG. 7, the organic thin-film solar cell element module 200 manufactured by the manufacturing method of this aspect includes a plurality of first substrates 11 formed in a pattern on the first substrate 11 and the first substrate. Formed between the first electrode substrate 10 having the electrode layer 12, the plurality of second electrode substrates 20 having at least the second electrode layer 22, and the first electrode layer 12 of the first electrode substrate 10. The photoelectric conversion layer 6 is included.
Moreover, the organic thin-film solar cell element module 2 has a hole extraction layer formed on one of the first electrode layer and the second electrode layer, and the electrode layer on which the hole extraction layer is not formed. It is preferable that an electron extraction layer is formed thereon. FIG. 7 shows an example in which the hole extraction layer 7 is formed on the first electrode layer 12 and the electron extraction layer 8 is formed on the second electrode layer 22.
The organic thin film solar cell element module 200 includes a plurality of organic thin film solar cell elements 2 each having the first electrode layer 12, the hole extraction layer 7, the photoelectric conversion layer 6, the electron extraction layer 8, and the second electrode layer 22. Is configured.

Moreover, as a functional layer in the organic thin-film solar cell element module manufactured by this aspect, it is a layer containing the organic substance formed between a 1st electrode layer and a 2nd electrode layer, a 1st electrode base material and a 2nd If it is a layer which can make the 1st electrode base material and the 2nd electrode base material adhere | attach favorably by setting it as the interface at the time of bonding an electrode base material, it will not specifically limit.
Specific examples of the functional layer include a photoelectric conversion layer or a hole extraction layer mainly composed of polyethylenedioxythiophene-polystyrenesulfonic acid (PEDOT / PSS).

  More specifically, the manufacturing method of the organic thin-film solar cell element module according to the present aspect includes a first electrode base on which the first electrode base is formed by forming the plurality of first electrode layers on the first base. A second electrode base material substrate preparation for preparing a second electrode base material substrate having at least a second electrode layer and capable of cutting out the plurality of second electrode base materials; And a step of forming a functional layer in a pattern corresponding to the pattern of the first electrode layer on the first electrode layer side of the first electrode substrate, or the second electrode of the second electrode substrate. A functional layer forming step of performing any one of the steps of continuously forming the functional layer on the layer side, and cutting to form the plurality of second electrode substrates by cutting the second electrode substrate. Steps of the first electrode layer side of the first electrode base material and the second electrode base material A bonding step of bonding the first electrode base material and the second electrode base material by facing the second electrode layer side and closely contacting the functional layer as an interface, and one organic thin film solar cell A connection step of electrically connecting the first electrode layer of the element and the second electrode layer of the other organic thin film solar cell element adjacent to the one organic thin film solar cell element.

  In addition, the said organic thin film solar cell element module makes a photoelectric conversion layer an essential structure. Therefore, in the manufacturing method of the organic thin-film solar cell element module according to this aspect, when the photoelectric conversion layer is not formed in the functional layer forming step, the surface of either the first electrode layer or the second electrode layer is separately provided. It shall have the process of forming a photoelectric converting layer.

  Here, the manufacturing method of the organic thin film solar cell element module of this aspect is demonstrated using figures. 8 (a) to 8 (d) and FIGS. 9 (a) to 9 (e) are process diagrams showing an example of a method for producing the organic thin-film solar cell element module of the present embodiment, and the organic shown in FIG. It is a figure shown about the example which manufactures a thin film solar cell element module.

First, the 1st electrode base material formation process in this aspect is demonstrated. As shown in FIGS. 8A and 8B, in the first electrode base material forming step, the first electrode layer 12 is continuously formed on the first base material 11. In the first electrode base material forming step, either the hole extraction layer or the electron extraction layer may be formed according to the use of the first electrode layer. 8A and 8B show an example in which the hole extraction layer 7 is formed. In this case, the hole extraction layer 7 is continuously formed and laminated on the first electrode layer 12. FIG. 8A shows an example of the first base material 11 on which the hole extraction layer 7 is continuously formed from the upper surface, and FIG. 8B shows E ′ in FIG. 8A. -E 'line cross section is shown.
Next, as shown in FIGS. 8C and 8D, the first electrode layer 12 and the hole extraction layer 7 are patterned into a predetermined pattern by etching or the like, so that one sheet of the first substrate 11 is formed. Then, the first electrode substrate 10 having the plurality of first electrode layers 12 and the hole extraction layer 7 formed in a pattern is formed. In FIG. 8C, the first electrode layer 12 and the hole extraction layer 7 are formed in a stripe shape, and each of the first electrode layer 12 and the hole extraction layer 7 includes two ends including both ends of the stripe. An example in which connection portions a and a ′ are formed is shown.
In addition, in FIG.8 (c), an example of the 1st electrode base material 10 formed by the 1st electrode base material formation process is shown from the upper surface, FIG.8 (d) shows E 'of FIG.8 (c). -E 'line cross section is shown.

Next, the 2nd electrode base-material board | substrate preparation process in this aspect is demonstrated. As shown in FIGS. 9A and 9B, in the second electrode substrate substrate preparation step, a second electrode substrate substrate 20 ′ having the second electrode layer 22 is prepared. In addition, in the prepared second electrode substrate 20 ′, a hole extraction layer or an electron extraction layer may be formed on the second electrode layer 22 according to the use of the second electrode layer 22. . 9A and 9B show an example in which the electron extraction layer 8 is formed.
Note that FIG. 9A shows an example of the second electrode substrate 20 ′ on which the electron extraction layer 8 is formed from the top, and FIG. 9B shows the FF in FIG. 9A. A line section is shown.

Next, the functional layer formation process in this aspect is demonstrated.
As shown in FIGS. 9C and 9D, in the functional layer forming step, the photoelectric conversion layer 6 is continuously formed on the electron extraction layer 8 of the second electrode base substrate 20 ′ described above. . In the connection step described later, when the first electrode layer and the second electrode layer of the adjacent organic thin-film solar cell elements are electrically connected, as shown in FIG. It is preferable that the photoelectric conversion layer 6 is continuously formed in a portion other than the connection portions b and b ′ of the substrate 20 ′.
In addition, in FIG.9 (c), an example of 2nd electrode base-material board | substrate 20 'in which the photoelectric converting layer 6 was formed is shown from the upper surface, FIG.9 (d) shows F' of FIG.9 (c). -F 'line cross section is shown.
Although not shown, in the functional layer forming step, the photoelectric conversion layer may be formed in a pattern on the first electrode layer side of the first electrode base material.

Next, the cutting process in this embodiment will be described.
As shown in FIG. 9 (e), in the cutting step, the second electrode substrate 20 is formed by cutting the second electrode substrate 20 'to a desired size. In addition, in FIG.9 (e), when it is set as an organic thin film solar cell element module, about the example in which the 2nd electrode base material 20 is formed so that it may become a shape where the adjacent 2nd electrode base material 20 does not contact. Show.

  Next, the bonding process and the connection process in this embodiment will be described. Although not shown, in the bonding step, the photoelectric conversion layer is formed so that the hole extraction layer formed on the first electrode substrate and the electron extraction layer formed on the second electrode substrate face each other. Are adhered as an interface to bond the first electrode substrate and the second electrode substrate. Moreover, in the bonding step, so that two connection portions at both ends of the first electrode layer of two adjacent organic thin film solar cell elements and two connection portions at both ends of the second electrode layer are in contact with each other, By bonding the first electrode substrate and the second electrode substrate, the connection step can be performed simultaneously.

  By performing the above steps, the organic thin-film solar cell element module shown in FIG. 6 can be manufactured.

  According to this aspect, an organic thin film solar cell element module having one first electrode base material and a plurality of second electrode base materials can be manufactured. Therefore, an organic thin film excellent in workability A solar cell element module can be manufactured.

  Hereinafter, each process of the manufacturing method of the organic thin film solar cell element module of this aspect is demonstrated.

1. 1st electrode base material formation process The 1st electrode base material formation process of this aspect is a process of forming a 1st electrode base material by forming a some 1st electrode layer on a 1st base material.
Here, the 1st electrode base material formed by this process is demonstrated.

The first substrate formed by this step has one first substrate and the first electrode layer formed on the first substrate.
The first electrode layer may be an electrode for extracting holes generated in the photoelectric conversion layer (hole extraction electrode), or an electrode for extracting electrons generated in the photoelectric conversion layer (electron extraction electrode). It may be.

As a 1st electrode base material, the base material which has transparency may be sufficient, and the base material which does not have transparency may be sufficient by the light-receiving surface of the organic thin-film solar cell element module manufactured by this aspect. It is appropriately selected.
When the second electrode substrate is a substrate having transparency, the first electrode substrate formed in this step may be a substrate having transparency, or a group having no transparency. It may be a material.
On the other hand, when the 2nd electrode substrate is a substrate which does not have transparency, the 1st electrode substrate formed in this process is a substrate which has transparency.

(1) Substrate having transparency When the first electrode substrate formed in this step is a substrate having transparency, a transparent substrate is usually used as the first substrate, and the first electrode layer A transparent electrode is used.

  The transparent base material can be the same as that described in the above-mentioned section “1. First aspect”, and thus the description thereof is omitted here.

  Further, the transparent electrode is not particularly limited as long as it has conductivity and transparency, and those generally used as a transparent electrode can be used. For example, In—Zn—O (IZO), In—Sn—O (ITO), ZnO—Al, Zn—Sn—O, and the like can be given.

  Since the total light transmittance, thickness, pattern shape, and formation method of the transparent electrode can be the same as those described in the first aspect, the description thereof is omitted here.

  Further, when the first electrode layer is a transparent electrode, an auxiliary electrode may be further laminated. The auxiliary electrode can be the same as that described in the above-mentioned section “1. First aspect”, and thus the description thereof is omitted here.

(2) Substrate not having transparency When the first electrode substrate formed in this step is a substrate not having transparency, the above-mentioned “1. The 1st base material demonstrated by the term of the aspect is used, and the electroconductive layer which does not have transparency is used as a 1st electrode layer.

The constituent material of the conductive layer is not particularly limited as long as it has conductivity, but it is preferably selected as appropriate in consideration of the work function of the constituent material of the second electrode layer. For example, when the constituent material of the second electrode layer is a material having a low work function, the constituent material of the first electrode layer is preferably a material having a high work function. Examples of the material having a high work function include Au, Ag, Co, Ni, Pt, C, ITO, SnO ₂ , fluorine-doped SnO ₂ , and ZnO.
On the other hand, when the constituent material of the second electrode layer is a material having a high work function, the discretion of the first electrode layer is preferably a material having a low work function.
Examples of the material having a low work function include Li, In, Al, Ca, Mg, Sm, Tb, Yb, Zr, and LiF. Examples of the reflective material include Al, Ag, Cu, and Au.

  In addition, about the thickness of a conductive layer, a pattern shape, etc., since it can be the same as that of the transparent electrode mentioned above, description here is abbreviate | omitted.

(3) Other configurations The first electrode base material formed in this step is not particularly limited as long as it includes the first electrode base material and the first electrode layer described above, and other necessary materials are also available. Can have a configuration.
Examples of such a configuration include a hole extraction layer and an electron extraction layer.

(A) Hole extraction layer When using the 1st electrode layer of the 1st electrode base material formed in this process as a hole extraction electrode, it is preferred to form a hole extraction layer on the 1st electrode layer.
The hole extraction layer is a layer provided so that holes can be easily extracted from the photoelectric conversion layer to the hole extraction electrode (transparent electrode layer). Thereby, since the hole extraction efficiency from the photoelectric conversion layer to the hole extraction electrode is increased, the photoelectric conversion efficiency can be improved.

The material used for the hole extraction layer in the present invention is not particularly limited as long as it is a material that stabilizes the extraction of holes from the photoelectric conversion layer to the hole extraction electrode. Specifically, doped polyaniline, polyphenylene vinylene, polythiophene, polypyrrole, polyparaphenylene, polyacetylene, conductive organic compounds such as triphenyldiamine (TPD), or electron donation such as tetrathiofulvalene, tetramethylphenylenediamine, etc. An organic material that forms a charge transfer complex composed of an organic compound and an electron-accepting compound such as tetracyanoquinodimethane and tetracyanoethylene. Also, a thin film of metal such as Au, In, Ag, Pd, etc. can be used. Furthermore, a thin film of metal or the like may be formed alone or in combination with the above organic material.
Among these, polyethylenedioxythiophene (PEDOT), polyethylenedioxythiophene-polystyrenesulfonic acid (PEDOT / PSS), polyaniline, and polypyrrole that can be dispersed in water are preferably used.

In this embodiment, the material used for the hole extraction layer is preferably polyethylene dioxythiophene-polystyrene sulfonic acid (PEDOT / PSS). This is because the PEDOT / PSS can exhibit high adhesion to the photoelectric conversion layer when the first electrode substrate and the second electrode substrate are brought into close contact in the bonding step described later. Moreover, it is because it is possible to mix the adhesion improving material as mentioned later for improving adhesiveness into PEDOT / PSS which is an aqueous dispersion.
In addition, when a hole extraction layer has PEDOT / PSS as a main component, you may form in the functional layer formation process mentioned later.

The hole extraction layer in the present invention is made of the above-mentioned material, but may contain an adhesion improving material capable of improving the adhesion with the photoelectric conversion layer, if necessary. . This is because, when the laminating method as described above is used, the adhesion between the photoelectric conversion layer and the hole extraction layer can be improved.
Such an adhesion improving material is not particularly limited as long as it does not hinder the function of the hole extraction layer, and a sugar chain or the like can be preferably used. This is because the adhesiveness is excellent and the cost can be reduced.
Further, as the sugar chain, specifically, D-sorbitol or the like can be used.

  The content of the adhesion improving material is not particularly limited as long as it does not hinder the function of the hole extraction layer, and 0.1 mass in the material constituting the hole extraction layer. % To 5% by mass, preferably 0.5% to 3% by mass, especially 1% to 2% by mass. Is preferred. It is because it can be made more excellent in adhesiveness when the content is within the above range.

  The film thickness of the hole extraction layer in the present invention is preferably in the range of 10 nm to 200 nm when the organic material is used, and in the range of 0.1 nm to 5 nm in the case of the metal thin film. It is preferable that

  The method for forming the hole extraction layer in the present invention is not particularly limited as long as the hole extraction layer can be formed with high accuracy. Specifically, it is possible to use a method in which a coating solution for hole extraction layer containing the above material is applied, dried and then fired.

(B) Electron extraction layer When the first electrode layer of the first electrode substrate formed in this step is used as an electron extraction electrode, it is preferable to form an electron extraction layer on the first electrode layer.
The electron extraction layer is a layer provided so that holes can be easily extracted from the photoelectric conversion layer to the electron extraction electrode. Thereby, since the electron extraction efficiency from the photoelectric conversion layer to the electron extraction electrode is increased, the photoelectric conversion efficiency can be improved.

The material used for the electron extraction layer is not particularly limited as long as it is a material that stabilizes the extraction of electrons from the photoelectric conversion layer to the electron extraction electrode, and as described above, depending on the type of the photoelectric conversion unit. It is selected appropriately. Specifically, inorganic materials such as alkaline earth metals such as Ca, alkali metals such as LiF and CaF ₂ or fluorides of alkaline earth metals, metal oxides such as titanium oxide and zinc oxide, and doped polyaniline , Conductive organic compounds such as polyphenylene vinylene, polythiophene, polypyrrole, polyparaphenylene, polyacetylene, triphenyldiamine (TPD), or electron donating compounds such as tetrathiofulvalene, tetramethylphenylenediamine, and tetracyanoquinodimethane And organic materials that form a charge transfer complex composed of an electron-accepting compound such as tetracyanoethylene. Moreover, the metal dope layer with an alkali metal or alkaline-earth metal is mentioned. Preferable examples include bathocuproin (BCP) or bathophenantrone (Bphen) and a metal doped layer such as Li, Cs, Ba, and Sr.

  The electron extraction layer is preferably made of titanium oxide among the materials described above. This is because titanium oxide is unlikely to be deteriorated even when held in the atmosphere, and the electron extraction efficiency is also unlikely to decrease, so that an organic thin film solar cell element module having excellent battery characteristics can be obtained.

The surface roughness Ra of the electron extraction layer in the present invention is not particularly limited as long as it can be stably used as an organic thin film solar cell element module, but is preferably 1.0 μm or less. Especially, it is preferable that it is 0.5 micrometer or less, and it is especially more preferable that it is 0.3 micrometer or less.
When the surface roughness is in the above-described range, it is more stable that the first electrode layer and the second electrode layer of one organic thin film solar cell element in the organic thin film solar cell element module are in contact with each other to cause an internal short circuit. This is because it can be prevented.
In addition, the said surface roughness Ra can be calculated | required by the method prescribed | regulated to JISB0601-1994.

In addition, the thickness of the electron extraction layer in the present invention is not particularly limited as long as electrons can be easily extracted from the photoelectric conversion layer to the first electrode layer. And preferably within a range of 50 nm to 5000 nm. Especially, it is preferable to exist in the range of 50 nm-1000 nm, and it is especially preferable to exist in the range of 50 nm-300 nm.
This is because when the film thickness is within the above range, the electron extraction layer can have few pinholes or the like. Further, it is possible to sufficiently cover the surface of the first electrode layer.

  The formation position of the electron extraction layer in the present invention in plan view is not particularly limited as long as it includes a region where the first electrode layer and a photoelectric conversion layer described later overlap in plan view. The first electrode layer and the photoelectric conversion layer are preferably all regions that overlap in plan view. This is because the photoelectric conversion efficiency can be improved.

  The method for forming the electron extraction layer is not particularly limited as long as the electron extraction layer can be formed in a pattern and can be uniformly formed to a predetermined film thickness. Any of the methods can be used, and is appropriately selected depending on the material.

(4) Formation method of 1st electrode base material As a formation method of the 1st electrode base material used for this process, forming the 1st electrode base material which can obtain a desired organic thin-film solar cell element module is formed. Although it will not specifically limit if it is a method which can be formed, It is preferable to form using a R to R process.

2. Second electrode base material preparation step The second electrode base material preparation step in this aspect includes the second electrode layer, and a single second electrode base material capable of cutting out the plurality of second electrode base materials. This is a step of preparing a substrate for use.

Here, the 2nd electrode base-material board | substrate prepared by this process is demonstrated.
The second electrode layer of the second electrode base material substrate in this step is an electrode facing the first electrode layer. The second electrode layer may be an electrode for extracting holes generated in the photoelectric conversion layer (hole extraction electrode), or an electrode for extracting electrons generated in the photoelectric conversion layer (electron extraction electrode). May be.

  The substrate for the second electrode base material may or may not have transparency, and is appropriately selected according to the light receiving surface of the organic thin film solar cell module. When the second electrode base material side is the light receiving surface, the second electrode base material substrate needs to have transparency. On the other hand, when the first electrode layer side is the light receiving surface, the second electrode substrate may or may not have transparency. Moreover, when it is set as a see-through type organic thin film solar cell module, the board | substrate for 2nd electrode base materials needs to have transparency.

  The substrate for the second electrode substrate may be composed of a second electrode layer, or may have a second electrode layer and a second substrate.

  When the substrate for the second electrode substrate has the second electrode layer and the second substrate, the second electrode layer and the second substrate are the same as the first electrode layer and the first substrate described above. Can be used.

When the second electrode substrate is composed of the second electrode layer, a single metal layer, that is, a metal substrate is usually used.
The metal used for the metal substrate is not particularly limited as long as it has conductivity, but is preferably selected in consideration of the work function of the constituent material of the first electrode layer.
Specifically, since it can be the same as the metal described in the section of the first electrode base material forming step described above, description thereof is omitted here.

  About the form of the board | substrate for 2nd electrode base materials, since it can be the same as that of the form of the board | substrate for 2nd electrode base materials demonstrated in the term of the 1st aspect mentioned above, description here is abbreviate | omitted.

The substrate for the second electrode base material prepared in this step can have a configuration other than the configuration described above.
For example, when the second electrode layer is used as a hole extraction electrode, it is preferable to form a hole extraction layer on the second electrode layer. On the other hand, when the second electrode layer is used as an electron extraction electrode, it is preferable to form an electron extraction layer on the second electrode layer.
Note that the hole extraction layer and the electron extraction layer can be the same as those described in the section of the first electrode base material formation step described above, and thus description thereof is omitted here.

3. Functional layer forming step The functional layer forming step in this embodiment is a step of forming a functional layer in a pattern corresponding to the pattern of the first electrode layer on the first electrode layer side of the first electrode substrate, or the second electrode. This is a step of performing any one of the steps of continuously forming the functional layer on the second electrode layer side of the base substrate.
In the present embodiment, “the functional layer is formed in a pattern corresponding to the pattern of the first electrode layer” means that each organic thin film solar cell constituting the organic thin film solar cell element module manufactured by the manufacturing method of the present embodiment. It means that a functional layer is formed on each first electrode layer so that the element has a functional layer.

As described above, the functional layer formed in this step is a layer including an organic substance that is formed between the first electrode layer and the second electrode layer. More specifically, a photoelectric conversion layer and a hole extraction layer mainly composed of PEDOT / PSS can be exemplified.
Therefore, in this step, the functional layer to be formed is a photoelectric conversion layer (first embodiment) and the functional layer to be formed is a hole extraction layer (hereinafter referred to as functionally correct layer) mainly composed of PEDOT / PSS. In some cases, it may be referred to as a hole extraction layer.) (Second embodiment).
Each embodiment will be described below.

(1) 1st embodiment The functional layer formation process of this embodiment forms the photoelectric conversion layer in a pattern corresponding to the pattern of the first electrode layer on the first electrode layer side of the first electrode base material, Or it is the process of performing any one of the processes of forming a photoelectric converting layer continuously in the said 2nd electrode layer side of the said 2nd electrode base-material board | substrate.
Here, the photoelectric conversion layer formed in this step will be described.

(A) Photoelectric conversion layer The photoelectric conversion layer used in this embodiment is formed between the first electrode layer and the second electrode layer in the organic thin-film solar cell element module manufactured by the manufacturing method of this embodiment. Is. In addition, the photoelectric converting layer in this invention means the member which contributes to electric charge separation of an organic thin film solar cell element, and conveys the produced | generated electron and a hole toward the electrode of an opposite direction, respectively.

The photoelectric conversion layer used in this embodiment may be a single layer having both an electron accepting function and an electron donating function (embodiment A), or an electron accepting function having an electron accepting function. A layer and an electron donating layer having an electron donating function may be laminated (embodiment B).
Hereinafter, each aspect will be described.

(I) A Mode A mode A of the photoelectric conversion layer in this embodiment is a single layer having both electron accepting and electron donating functions, and contains an electron accepting material and an electron donating material. Is. In this photoelectric conversion layer, since charge separation occurs using a pn junction formed in the photoelectric conversion layer, it functions as a photoelectric conversion layer alone.

The electron donating material of the photoelectric conversion layer is not particularly limited as long as it has a function as an electron donor, but it is preferable that the film can be formed by a wet coating method. A donating conductive polymer material is preferable.
The conductive polymer is a so-called π-conjugated polymer, which is composed of a π-conjugated system in which double bonds or triple bonds containing carbon-carbon or hetero atoms are alternately linked to single bonds, and exhibits semiconducting properties. It is. In the conductive polymer material, since π conjugation is developed in the polymer main chain, charge transport in the main chain direction is basically advantageous.
In addition, since the electron transfer mechanism of the conductive polymer is mainly hopping conduction between molecules by π stacking, charge transport not only in the main chain direction of the polymer but also in the film thickness direction of the photoelectric conversion layer is advantageous. It is. Furthermore, the conductive polymer material can be easily formed by a wet coating method by using a coating solution in which the conductive polymer material is dissolved or dispersed in a solvent. Therefore, there is an advantage that the cost can be reduced in the manufacturing process without requiring expensive equipment.

  Examples of the electron-donating conductive polymer material include polyphenylene, polyphenylene vinylene, polysilane, polythiophene, polycarbazole, polyvinyl carbazole, porphyrin, polyacetylene, polypyrrole, polyaniline, polyfluorene, polyvinyl pyrene, polyvinyl anthracene, and these Derivatives and copolymers thereof, or phthalocyanine-containing polymers, carbazole-containing polymers, organometallic polymers, and the like can be given.

Among the above, thiophene-fluorene copolymer, polyalkylthiophene, phenylene ethynylene-phenylene vinylene copolymer, phenylene ethynylene-thiophene copolymer, phenylene ethynylene-fluorene copolymer, fluorene-phenylene vinylene copolymer A thiophene-phenylene vinylene copolymer is preferably used. This is because the energy level difference is appropriate for many electron-accepting materials.
For example, a phenylene ethynylene-phenylene vinylene copolymer (Poly [1,4-phenyleneethynylene-1,4-(2,5-dioctadodecyloxyphenylene) -1,4-phenyleneethene-1,2-diyl-1,4- ( 2,5-dioctadodecyloxyphenylene) ethene-1,2-diyl]) is detailed in Macromolecules, 35, 3825 (2002) and Micromol. Chem. Phys., 202, 2712 (2001).

  Next, the electron-accepting material is not particularly limited as long as it has a function as an electron acceptor. However, it is preferable that the material can be formed by a wet coating method. It is preferable that the conductive conductive polymer material. This is because the conductive polymer material has the advantages as described above.

Examples of the electron-accepting conductive polymer material used in this embodiment include polyphenylene vinylene, polyfluorene, and derivatives thereof, and copolymers thereof, carbon nanotubes, fullerene derivatives, CN groups, or CF _3. Examples thereof include group-containing polymers and —CF ₃ substituted polymers thereof. Specific examples of polyphenylene vinylene derivatives include CN-PPV (poly [2-methoxy-5- (2′-ethylhexyloxy) -1,4- (1-cyanovinylene]), MEH-CN-PPV (poly [2-methoxy -5- (2'-ethylhexyloxy) -1,4- (1-cyanoinylene]) and the like.

  Further, an electron accepting material doped with an electron donating compound, an electron donating material doped with an electron accepting compound, or the like can be used. Among these, a conductive polymer material doped with an electron donating compound or an electron accepting compound is preferably used. The above conductive polymer material is basically advantageous in charge transport in the direction of the main chain because π conjugation is developed in the polymer main chain, and doped with an electron donating compound or an electron accepting compound. This is because electric charges are generated in the π-conjugated main chain, and the electrical conductivity can be greatly increased.

Examples of the electron-accepting conductive polymer material doped with the electron-donating compound include the above-described electron-accepting conductive polymer material. In addition, as the electron-donating compound to be doped, for example, a Lewis base such as an alkali metal such as Li, K, Ca, or Cs or an alkaline earth metal can be used. The Lewis base acts as an electron donor.
Examples of the electron-donating conductive polymer material doped with the electron-accepting compound include the above-described electron-donating conductive polymer material. As the electron-accepting compound to be doped, for example, a Lewis acid such as FeCl ₃ (III), AlCl ₃ , AlBr ₃ , AsF ₆ or a halogen compound can be used. In addition, Lewis acid acts as an electron acceptor.

  The mixing ratio of the electron-donating material and the electron-accepting material in this embodiment is appropriately adjusted to an optimal mixing ratio depending on the type of material used.

As the film thickness of the photoelectric conversion layer in this embodiment, the film thickness generally employed in bulk heterojunction organic thin film solar cells can be employed. Specifically, it is preferably set within a range of 0.2 nm to 3000 nm, and more preferably within a range of 1 nm to 600 nm.
This is because when the film thickness is larger than the above range, the volume resistance in the photoelectric conversion layer may be increased. On the other hand, if the film thickness is thinner than the above range, light may not be sufficiently absorbed.

  The method for forming the photoelectric conversion layer in this embodiment is not particularly limited as long as it can be uniformly formed in a predetermined film thickness, but a wet coating method is preferably used. This is because if the wet coating method is used, the photoelectric conversion layer can be formed in the atmosphere, the cost can be reduced, and the area can be easily increased.

The method for applying the photoelectric conversion layer coating liquid in this embodiment is not particularly limited as long as it can be applied uniformly to apply the photoelectric conversion layer forming coating liquid. , Spin coating method, dip coating method, roll coating method, bead coating method, spray coating method, bar coating method, gravure coating method, ink jet method, screen printing method, offset printing method and the like.
Especially, it is preferable that the coating method of the coating liquid for photoelectric conversion layer formation is a method which can adjust thickness mainly according to a coating amount. As a method capable of adjusting the thickness mainly depending on the coating amount, for example, a die coating method, a bead coating method, a bar coating method, a gravure coating method, an ink jet method, a screen printing method, an offset printing method, or the like. Can be mentioned. The printing method is suitable for increasing the area of the organic thin film solar cell.

After the application of the photoelectric conversion layer forming coating solution, a drying treatment for drying the formed coating film may be performed. It is because productivity can be improved by removing the solvent etc. which are contained in the coating liquid for photoelectric conversion layer formation at an early stage.
As a drying method, for example, a general drying method such as heat drying, air drying, vacuum drying, infrared heat drying, or the like can be used.

(Ii) Aspect B In the photoelectric conversion layer B in this embodiment, an electron accepting layer having an electron accepting function and an electron donating layer having an electron donating function are laminated. .
Hereinafter, the electron-accepting layer and the electron-donating layer will be described.

(Electron-accepting layer)
The electron-accepting layer used in this embodiment has an electron-accepting function and contains an electron-accepting material.

  Such an electron-accepting material is not particularly limited as long as it has a function as an electron acceptor, but is preferably a material that can be formed into a film by a wet coating method. The conductive polymer material is preferable. This is because the conductive polymer material has the advantages as described above. Specific examples include the same electron-accepting conductive polymer materials used for the photoelectric conversion layer of the first aspect.

  As the film thickness of the electron-accepting layer in this embodiment, a film thickness generally employed in a bilayer organic thin film solar cell can be employed. Specifically, it can be set within a range of 0.1 nm to 1500 nm, and preferably within a range of 1 nm to 300 nm. This is because if the film thickness is larger than the above range, the volume resistance in the electron-accepting layer may increase. On the other hand, if the film thickness is thinner than the above range, light may not be sufficiently absorbed.

  The method for forming the electron-accepting layer in this embodiment can be the same as the method for forming the photoelectric conversion layer of the first embodiment.

(Electron donating layer)
The electron donating layer used in this embodiment has an electron donating function and contains an electron donating material.

  The electron donating material in this embodiment is not particularly limited as long as it has a function as an electron donor, but it is preferable that the material can be formed by a wet coating method. The conductive polymer material is preferable. This is because the conductive polymer material has the advantages as described above. Specific examples include the same electron donating conductive polymer materials used for the photoelectric conversion layer of the first aspect.

  As the film thickness of the electron donating layer in this embodiment, a film thickness generally employed in a bilayer type organic thin film solar cell can be employed. Specifically, it can be set within a range of 0.1 nm to 1500 nm, and preferably within a range of 1 nm to 300 nm. This is because if the film thickness is larger than the above range, the volume resistance in the electron donating layer may be increased. On the other hand, if the film thickness is thinner than the above range, light may not be sufficiently absorbed.

  The method for forming the electron donating layer in this embodiment can be the same as the method for forming the photoelectric conversion layer of the first embodiment.

(B) Method for forming photoelectric conversion layer In this step, when the photoelectric conversion layer is formed in a pattern on the first electrode substrate side, the photoelectric conversion layer is continuously formed on the second electrode substrate substrate side. In any case, it is preferable to form the photoelectric conversion layer by using an R to R process.

(2) Second Embodiment In the functional layer forming step of the present embodiment, the functional hole extraction layer is formed in a pattern corresponding to the pattern of the first electrode layer on the first electrode layer side of the first electrode substrate. Or a step of continuously forming a functional hole extraction layer on the second electrode layer side of the second electrode substrate.
In addition, in the manufacturing method of the organic thin-film solar cell element module of this aspect, when performing the functional layer formation process of a 2nd embodiment, the photoelectric conversion layer demonstrated in the item of the above-mentioned "(1) 1st aspect" is 1st. A step of forming on the surface of either the first electrode layer or the second electrode layer is performed separately.

  The functional hole extraction layer formed by this step is mainly composed of PEDOT / PSS. Note that the functional hole extraction layer can be the same as that described in the section of the first electrode base material formation step described above, and a description thereof will be omitted here.

  Further, in this step, the functional hole extraction layer is an electrode used for the hole extraction electrode among the first electrode layer of the first electrode substrate or the second electrode layer of the second electrode substrate. When the photoelectric conversion layer is formed on an electrode layer that is not used for the hole extraction electrode in the first electrode layer or the second electrode layer, the photoelectric conversion layer It may be formed on top.

  In this step, when the functional hole extraction layer is formed in a pattern on the first electrode base material side, the functional hole extraction layer is continuously formed on the second electrode base material substrate side. However, it is preferable to form the functional layer using an R to R process.

4). Cutting Step The cutting step in this aspect is a step of forming the plurality of second electrode base materials by cutting the second electrode base material substrate.

  About the cutting process in this aspect, since it can be made to be the same as that of the process described by the term of the 1st aspect mentioned above, description here is abbreviate | omitted.

5. Bonding step The bonding step in this embodiment is such that the first electrode layer side of the first electrode base material and the second electrode layer side of the second electrode base material face each other, and the functional layer is used as an interface. This is a step of bonding the first electrode substrate and the second electrode substrate.

  In this step, for example, when a photoelectric conversion layer is used as an interface as a functional layer, it is formed on the surface of either the first electrode layer of the first electrode base material or the second electrode layer of the second electrode base material. The first electrode base material and the second electrode base material are bonded together with the photoelectric conversion layer thus formed facing the electrode layer on the side where the photoelectric conversion layer is not formed. Note that either the hole extraction layer or the electron extraction layer may be formed in the first electrode layer or the second electrode layer as described above.

  Also, in this step, for example, when the functional hole extraction layer is used as the interface as the functional layer, either the first electrode layer of the first electrode base material or the second electrode layer of the second electrode base material is selected. A first electrode base material, wherein a functional hole extraction layer formed on a photoelectric conversion layer formed on one surface is opposed to an electrode layer on which the functional hole extraction layer is not formed. And a 2nd electrode base material is bonded.

  In this step, for example, when the photoelectric conversion layer and the functional hole extraction layer are used as the interface as the functional layer, the first electrode layer of the first electrode substrate and the second electrode layer of the second electrode substrate Among them, the photoelectric conversion layer formed on one of the surfaces and the functional hole extraction layer formed on the electrode layer on the side where the photoelectric conversion layer is not formed are opposed to each other to form the first electrode group. The material and the second electrode substrate are bonded together.

  As a bonding method of the first electrode substrate and the second electrode substrate used in this step, the first electrode substrate and the second electrode substrate can be adhered to each other with the functional layer as an interface. If it does not specifically limit.

  Further, in this step, when the functional hole extraction layer described above is bonded as an interface, PEDOT / PSS exhibits excellent adhesiveness in a predetermined temperature range, and thus it is preferable to perform thermocompression bonding. .

The temperature range for thermocompression bonding is not particularly limited as long as the above-described PEDOT / PSS can exhibit adhesiveness, but it is preferably in the range of 100 ° C to 150 ° C. Especially, it is preferable that it exists in the range of 110 to 140 degreeC, and it is more preferable that it is in the range of 120 to 130 degreeC especially.
When the temperature is lower than the above temperature range, PEDOT / PSS may not be able to exhibit adhesiveness that can make the first electrode base material and the second electrode base material have sufficient adhesion. . On the other hand, when higher than the said temperature range, the 1st base material of a 1st electrode base material may deteriorate.

The pressure for thermocompression bonding is usually a pressure that allows the first electrode substrate and the second electrode substrate to be brought into close contact with each other due to the adhesiveness exhibited by PEDOT / PSS within the temperature range described above. Although not particularly limited, it is preferably within a range of 0.1 MPa to 1 MPa. Especially, it is preferable to be in the range of 0.2 MPa to 0.8 MPa, and it is more preferable to be in the range of 0.4 MPa to 0.5 MPa.
If it is lower than the above range, the adhesion of the first electrode base material and the second electrode base material may be insufficient. On the other hand, if it is higher than the above range, the first electrode base material and the second electrode base material There is a possibility that the battery characteristics of the organic thin-film solar cell are deteriorated due to an excessive change in the structure of the laminate of the two-electrode base material.

  The atmosphere for thermocompression bonding is not particularly limited as long as the characteristics of the constituent layers of the first electrode substrate and the second electrode substrate do not deteriorate. For example, vacuum, nitrogen, air, etc. Is mentioned. Of these, vacuum, nitrogen and the like are preferable.

6). Connection process The connection process in this aspect includes the first electrode layer of one organic thin film solar cell element and the second electrode layer of another organic thin film solar cell element adjacent to the one organic thin film solar cell element. Are electrically connected.

  Since the connection process in this aspect can be the same as the process described in the first aspect, the description is omitted here.

7). Other Steps The method for producing the organic thin-film solar cell element module of the present embodiment is not particularly limited as long as it has the respective steps described above, and other necessary configurations can be appropriately selected and added. is there. Specifically, since it can be the same as the process described in the section of “I. First aspect”, the description here is omitted.

  The present invention is not limited to the above embodiment. The above-described embodiment is an exemplification, and the technical idea described in the claims of the present invention has substantially the same configuration and exhibits the same function and effect regardless of the case. It is included in the technical scope of the invention.

  Hereinafter, the present invention will be described more specifically with reference to examples.

(Example 1)
(Dye-sensitized solar cell module)
<Preparation of first electrode substrate>
A transparent conductive film having an ITO film (first electrode layer) formed on a PEN film (first base material) is prepared, and platinum (catalyst layer) is laminated on the ITO film with a thickness of 13 mm (transmittance 72%). I let you. A plurality of layers formed by forming an insulating portion by laser scribing on the manufactured first electrode layer and platinum laminate and having two connection portions formed in a stripe shape and including both end portions of each stripe. A first electrode layer was prepared. The stripe part of the first electrode layer was 100 mm in the long direction and 12 mm in the short direction. Thereby, the 1st electrode base material which has two connection parts including the both ends in which the some 1st electrode layer and catalyst layer were formed on the 1st base material of 1 sheet was obtained.

<Preparation of composition for porous layer>
5 g of porous titanium oxide fine particles (manufactured by Nippon Aerosil Co., Ltd., trade name: P25) were added to 16.7 g of ethanol, and 0.25 g of acetylacetone and 20 g of zirconia beads (φ1.0 mm) were added to a paint shaker. Then, 0.25 g of polyvinylpyrrolidone (manufactured by Nippon Shokubai Co., Ltd., trade name: K-30) was added as a binder to prepare a porous layer composition.

<Formation of porous layer>
The prepared composition for a porous layer is formed on a titanium foil (second electrode substrate), which is a conductive substrate, with an area of 10 cm width by a doctor blade method, leaving two connection portions at both ends. It was applied and then dried at 120 ° C. to form a 9 μm thick layer containing a large number of fine titanium oxide particles. A pressure of 0.1 t / cm ² was applied to the titanium oxide fine particle layer with a press. After the pressing, the porous layer forming layer was formed by firing at 500 ° C. for 30 minutes.

<Dye adsorption>
Next, an organic dye (trade name: D358, manufactured by Mitsubishi Paper Industries Co., Ltd.) is used as a dye sensitizer, and the volume ratio of acetonitrile and tert-butyl alcohol is 1: 3 so that the concentration is 3.0 × 10 ⁻⁴ mol / l. A dye-supporting coating solution was prepared by dissolving in 1 solution. The layer for forming a porous layer formed on the above-described conductive substrate was immersed in this dye-carrying coating solution for 3 hours. Thereafter, the pigment-carrying coating solution was pulled up from the pigment-carrying coating solution, washed with acetonitrile, and then air-dried. As a result, the porous layer was formed by supporting the dye sensitizer on the pore surface of the titanium oxide fine particles.

<Preparation of electrolyte layer forming coating solution>
0.043 g of potassium iodide was added to a solution prepared by dissolving 0.14 g of cationic hydroxycellulose (manufactured by Daicel Chemical Industries, Ltd., trade name: Gelner QH200) in 2.72 g of ethanol, and the mixture was dissolved by stirring. Next, 0.18 g of 1-ethyl-3-methylimidazolium tetracyanoborate (EMIm-B (CN) 4), 0.5 g of 1-propyl-3-methylimidazolium iodide (PMIm-I), And 0.025 g of I ₂ was added and dissolved by stirring. This prepared the coating liquid for electrolyte layer formation which can be coated.

<Formation of solid electrolyte layer>
On the porous layer (10 cm width), an electrolyte layer forming coating solution was applied by a doctor blade method and dried at 100 ° C. to form an electrolyte layer.

<Cutting of substrate for second electrode base material>
The second electrode substrate was formed into a strip shape having a width of 10 mm, with both ends of the substrate for the second electrode substrate, on which the electrolyte layer was formed, on which the porous layer was not formed as ends in the longitudinal direction.

<Preparation of dye-sensitized solar cell module>
Of the second electrode base material cut out on the strip, after forming a conductive adhesive on the connecting portion of both ends where the porous layer is not formed, both ends of the first electrode layer adjacent to the conductive adhesive The first electrode base material and the second electrode base material were bonded to each other so as to be connected to the connection portion, thereby producing a module.

<Connection>
A dye-sensitized solar cell element module was produced by connecting ITO and Ti at the connecting portions at both ends of adjacent cells with a conductive adhesive.

<Sealing>
The produced dye-sensitized solar cell module was sandwiched between fillers and laminated at 150 ° C. for sealing.

<Evaluation of battery performance>
About the produced dye-sensitized solar cell element module, artificial sunlight (AM1.5, incident light intensity of 100 mW / cm ² ) is used as a light source, is incident from the counter electrode side, and a source measure unit (Keutley 2400 type) is used. Current-voltage characteristics due to voltage application were measured. As a result, when the short-circuit current 23 (mA), the open circuit voltage 6.1 (V), the fill factor 0.24, and the maximum output 32 mW are shown, and the fluorescent lamp (500 lux) is used as the light source, the short-circuit current 0.25 ( mA), open circuit voltage 4.7 (V), fill factor 0.70, and maximum output 0.8 mW.

(Example 2)
(Organic thin film solar cell module)
<Preparation of electron extraction layer>
A transparent conductive film in which an ITO film (first electrode layer) is formed on a PEN film (first base material) is prepared, and a conductive polymer paste (poly-) having sorbitol added at a solid content ratio of 2 wt% on the film. (3,4-Ethylenedioxythiophene) dispersion)
It was dried at 50 degrees for 30 minutes to form an electron extraction layer. The obtained substrate was patterned by laser processing, and 10 first electrode layers having two connection portions including both end portions with an electrode area of 100 mm × 12 mm were produced.

<Preparation of photoelectric conversion layer>
Next, the coating liquid for photoelectric conversion layers was adjusted. Mixing polythiophene (P3HT: poly (3-hexylthiophene-2,5-diyl)) and electron-receiving fullerene (PCBN ([6,6] -pheny-C61-butyric acid methyl ester)) at a weight ratio of 5: 2. Then, a chlorobenzene solution having a solid content concentration of 1.0 wt% was prepared. Finally, this solution was filtered with a filter paper to prepare a photoelectric conversion layer coating solution.
Next, the same solution was applied on a Ti foil having a thickness of 30 μm by applying a doctor blade method in an area of 10 cm width, leaving two connection portions at both ends, thereby forming a photoelectric conversion layer (film thickness 150 nm).
Subsequently, the obtained Ti foil having the photoelectric conversion layer was cut into a strip shape with a width of 10 mm, and a plurality of second electrode substrates (photoelectric conversion electrode substrates) were produced.

<Lamination>
Next, after forming the conductive adhesive on the connecting portions at both ends of the produced plurality of photoelectric conversion electrode substrates, the conductive adhesive is connected to the connecting portions at both ends of the adjacent first electrode layer. The laminate was laminated on the patterned electron extraction layer, and laminated by a roll laminator under the conditions of a laminating pressure of 4 kgf / cm ² and a laminating temperature of 130 ° C., and a plurality of cells were produced on the substrate.

<Connection>
The organic thin film solar cell element module was produced by connecting ITO and Ti foil of the connection part of the both ends of an adjacent cell with a conductive adhesive.

<Sealing>
Finally, the organic thin film solar cell element module was sealed with a sealing glass material and an adhesive sealing material.

<Evaluation of battery performance>
About the produced organic thin-film solar cell module, by using pseudo sunlight (AM1.5, incident light intensity 100 mW / cm ² ) as a light source, it is incident from the counter electrode side, and voltage is applied using a source measure unit (Keutley 2400 type). Current-voltage characteristics were measured. As a result, a short-circuit current of 30 (mA), an open-circuit voltage of 7.0 (V), a fill factor of 0.24, and a maximum output of 50.4 mW are exhibited. The characteristics of 30 (mA), open circuit voltage 5.0 (V), fill factor 0.71, and maximum output 1.1 mW were obtained.

DESCRIPTION OF SYMBOLS 1 ... Dye-sensitized solar cell element 2 ... Organic thin film solar cell element 3 ... Porous layer 4 ... Solid electrolyte layer 5 ... Catalyst layer 6 ... Photoelectric conversion layer 7 ... Hole extraction layer 8 ... Electron extraction layer 10 ... 1st Electrode substrate 11 ... First substrate 12 ... First electrode layer 20 ... Second electrode substrate 20 '... Substrate for second electrode substrate 100 ... Dye-sensitized solar cell module 200 ... Organic thin film solar cell module

Claims (6)

A first substrate having one first substrate and a plurality of first electrode layers formed in a stripe shape on the first substrate and having two connection portions including both ends of each stripe. A plurality of strip-shaped second electrode substrates having one electrode substrate, at least a second electrode layer, and two connecting portions at both ends; and between the first electrode layer and the second electrode layer Having a plurality of functional layers formed and containing organic matter,
A plurality of organic solar cell elements having the first electrode layer, the second electrode layer, and the functional layer are connected to each other, and the first electrode layer and the one organic layer of one organic solar cell element are configured. The organic solar cell in which the second electrode layer of another organic solar cell element adjacent to the solar cell element is electrically connected between the two connection portions formed at both ends of each electrode layer A battery element module manufacturing method comprising:
On the first base material, the first electrode base material is formed by forming the plurality of first electrode layers formed in a stripe shape and having two connection portions including both end portions of each stripe. Forming a first electrode base material,
Preparing a second substrate for a second electrode substrate capable of cutting out a plurality of strip-shaped second electrode substrates having at least the second electrode layer and having two connecting portions at both ends; An electrode substrate substrate preparation step;
Forming the functional layer in a pattern corresponding to the pattern of the first electrode layer on the first electrode layer side of the first electrode substrate, or the second electrode layer side of the second electrode substrate. A functional layer forming step of performing any one of the steps of continuously forming the functional layer;
A cutting step of forming the plurality of second electrode base materials by cutting the second electrode base material substrate;
The first electrode substrate and the second electrode substrate side of the first electrode substrate and the second electrode layer side of the second electrode substrate are opposed to each other, and the functional layer is brought into close contact as an interface. A bonding step of bonding the second electrode substrate;
The first electrode layer of one organic solar cell element and the second electrode layer of another organic solar cell element adjacent to the one organic solar cell element are formed at both ends of each electrode. And a connecting step of electrically connecting the two connecting portions. The method of manufacturing an organic solar cell element module.   The first base material is a long base material having flexibility that is wound up in a roll shape, and the first electrode base material forming step and the first electrode base side of the first electrode base material The method for producing an organic solar cell module according to claim 1, wherein the functional layer forming step of forming the functional layer is performed by a roll to roll process.   The function of forming the functional layer on the second electrode layer side of the second electrode base material is a long substrate having flexibility in which the second electrode base material substrate is wound in a roll shape. The method for producing an organic solar cell element module according to claim 1, wherein the layer forming step is performed by a roll to roll process.   The organic solar cell element module has a porous layer containing metal oxide semiconductor fine particles carrying a dye sensitizer on the surface of either the first electrode layer or the second electrode layer. And the functional layer is a dye-sensitized solar cell module formed by connecting a plurality of dye-sensitized solar cell elements, each of which is a solid electrolyte layer containing a polymer compound and a redox pair. The manufacturing method of the organic solar cell element module according to any one of claims 1 to 3.   The method for manufacturing an organic solar cell element module according to claim 4, wherein the second electrode layer is a metal layer, and the porous layer is formed on the metal layer.   The organic solar cell element module is an organic thin film solar cell module configured by connecting a plurality of organic thin film solar cell elements each having a photoelectric conversion layer between the first electrode layer and the second electrode layer, The organic according to any one of claims 1 to 3, wherein the functional layer is a layer containing an organic substance formed between the first electrode layer and the second electrode layer. Of manufacturing a solar cell element module.

Images