JP5363690B1 - Sensitizing dye for photoelectric conversion, photoelectric conversion element using the same, and dye-sensitized solar cell - Google Patents

Abstract

The present invention provides a sensitizing dye for photoelectric conversion represented by the following general formula (1); a dye-sensitized photoelectric conversion element in which at least a semiconductor layer and an electrolyte layer are provided between a pair of opposed electrodes. A photoelectric conversion element having a photoelectric conversion sensitizing dye supported on the semiconductor layer; and a dye-sensitized solar cell having the photoelectric conversion element, wherein the photoelectric conversion element is modularized, and predetermined electrical wiring is The present invention relates to a provided dye-sensitized solar cell.
[Chemical 1]

Description

  The present invention relates to a sensitizing dye used for a dye-sensitized photoelectric conversion element, a photoelectric conversion element using the same, and a dye-sensitized solar cell.

  In recent years, carbon dioxide generated from fossil fuels such as coal, oil, and natural gas has caused global warming as a greenhouse gas, environmental destruction due to global warming, and increased global energy consumption accompanying population growth. There is a concern that environmental destruction on a global scale will continue to progress. Under such circumstances, the use of solar energy, which is unlikely to be depleted unlike fossil fuels, has been energetically studied. Since solar power generation can be expected to prevent global warming and save energy costs, solar energy is being developed and used rapidly, especially in Europe and Japan.

  As a means for photovoltaic power generation, a solar cell using a photoelectric conversion element that converts sunlight energy into electric energy has attracted attention. As solar cells, inorganic solar cells such as single crystal, polycrystal, amorphous silicon, gallium arsenide, cadmium sulfide, indium copper selenide and other compound semiconductors have been mainly studied, some of which are for residential use. Have been put to practical use. However, these inorganic solar cells have problems such as high manufacturing costs and difficulty in securing raw materials.

  On the other hand, organic solar cells using organic materials are said to be advantageous in terms of manufacturing cost, increase in area, and securing raw materials. As an organic solar cell, a Schottky junction type organic solar cell using generation of electromotive force at a contact interface between an organic semiconductor and a metal has been known, but it is recognized that there is a limit in improving photoelectric conversion efficiency. It came to be. Therefore, a pn heterojunction organic solar cell using a contact interface between two organic semiconductors or a contact interface between an organic semiconductor and an inorganic semiconductor has been expected. However, the photoelectric conversion efficiency of these organic solar cells is significantly lower than that of inorganic solar cells, and there is a problem that durability is poor.

  Under such circumstances, a dye-sensitized solar cell exhibiting high photoelectric conversion efficiency has been reported by Professor Gretzel et al. Of Lausanne University of Technology in Switzerland (for example, Non-Patent Document 1). The proposed dye-sensitized solar cell is a wet solar cell composed of a titanium oxide porous thin film electrode, a ruthenium complex dye, and an electrolytic solution. Dye-sensitized solar cells have a simpler device structure than other solar cells, and can be manufactured without large-scale manufacturing facilities, and are comparable to amorphous silicon solar cells already in practical use. In recent years, it has attracted attention as a next-generation solar cell because high photoelectric conversion efficiency is expected.

  As the sensitizing dye used in the dye-sensitized solar cell, from the point of photoelectric conversion efficiency, ruthenium complex is considered to be most advantageous, but ruthenium is a noble metal, which is disadvantageous in terms of production cost, and When practical use requires a large amount of ruthenium complex, resource constraints also become a problem. Therefore, research on dye-sensitized solar cells using organic dyes that do not contain noble metals such as ruthenium as sensitizing dyes has been actively conducted. As organic dyes not containing a noble metal, coumarin dyes, cyanine dyes, merocyanine dyes, rhodacyanine dyes, phthalocyanine dyes, porphyrin dyes, xanthene dyes and the like have been reported (for example, Patent Documents 1 to 3). ).

  Although the organic dyes described in Patent Documents 1 to 3 have the advantages that they are inexpensive, have a large extinction coefficient, and can control the absorption characteristics due to the variety of structures, in terms of photoelectric conversion efficiency and stability over time, The present situation is that a product that sufficiently satisfies the required characteristics has not been obtained.

Japanese Unexamined Patent Publication No. 11-214730 Japanese Unexamined Patent Publication No. 11-238905 Japanese Unexamined Patent Publication No. 2010-31204

Nature (Vol. 353, 737-740, 1991)

  The problem to be solved by the present invention is to provide a sensitizing dye having a novel structure capable of efficiently taking out an electric current, and further using the sensitizing dye, a photoelectric conversion element having good photoelectric conversion and a dye sensitization It is to provide a solar cell.

  In order to solve the above problems, the inventors have intensively studied on improving the photoelectric conversion characteristics of a sensitizing dye, and as a result, by using a sensitizing dye having a specific structure, a highly efficient and highly durable photoelectric conversion element is obtained. I found out that That is, the present invention has the following contents.

  The present invention provides a sensitizing dye for photoelectric conversion represented by the following general formula (1).

In formula, R < ₁ > and R < ₂ > represents the C1-C6 alkyl group which may have a substituent, or a substituted or unsubstituted aryl group. R ₃ represents an alkyl group having 1 to 6 carbon atoms which may have a substituent. R _{4 to} R ₇ may be the same or different and each represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms which may have a substituent. m represents an integer of 2 to 8, and n represents an integer of 1 to 3. When n is 2 or 3, a plurality of R _{4 to} R ₇ may be the same as or different from each other. A represents a monovalent group represented by any one of the following general formulas (2) to (4).

In the formula, R ₈ represents an acidic group.

In the formula, R ₉ represents an alkyl group having 1 to 6 carbon atoms having an acidic group as a substituent or an unsubstituted alkyl group having 1 to 6 carbon atoms. R _{10 to} R ₁₃ may be the same or different and each has a hydrogen atom, a halogen atom, an acidic group, an alkyl group having 1 to 6 carbon atoms which may have a substituent, or a substituent. Or an alkenyl group having 2 to 6 carbon atoms. However, at least one of R _{9 to} R ₁₃ is an alkyl group having 1 to 6 carbon atoms (in the case of R ₉ ) or an acidic group (in the case of R _{10 to} R ₁₃ ) having an acidic group as a substituent. It shall be. R _{10 to} R ₁₃ may be bonded to each other through a single bond between adjacent groups to form a ring. X represents a sulfur atom, an oxygen atom, or C (CH ₃ ) ₂ . Y represents an anion.

In the formula, R ₁₄ and R ₁₅ may be the same or different and each represents an alkyl group having 1 to 6 carbon atoms or an unsubstituted alkyl group having 1 to 6 carbon atoms having at least two acidic groups as substituents. Represent. However, at least one of R _{14 and} R ₁₅ is an alkyl group having 1 to 6 carbon atoms having at least two acidic groups as substituents. p represents an integer of 0 to 2. When p is 2, two R ₁₄ may be the same as or different from each other.

In the general formula (1), R ₁ is preferably a substituted or unsubstituted aryl group.

  In the general formula (1), m is preferably 3 or 4.

In the general formula (1), R ₂ and R ₃ are preferably methyl groups.

In the general formula (1), R _{4 to} R ₇ are preferably hydrogen atoms and n is preferably 1.

  The present invention also provides a dye-sensitized photoelectric conversion element in which at least a semiconductor layer and an electrolyte layer are provided between a pair of opposing electrodes, and the photoelectric conversion sensitizing dye is supported on the semiconductor layer. A photoelectric conversion element is provided.

  In the photoelectric conversion element, it is preferable that the electrolyte layer contains 4-tert-butylpyridine.

  The present invention also provides a dye-sensitized solar cell having a photoelectric conversion element, wherein the photoelectric conversion element is modularized and provided with predetermined electrical wiring.

  According to the present invention, it is possible to obtain a sensitizing dye for photoelectric conversion capable of efficiently taking out current. Moreover, by using the sensitizing dye for photoelectric conversion, a highly efficient and highly durable photoelectric conversion element and a dye-sensitized solar cell can be obtained.

FIG. 1 is a schematic cross-sectional view illustrating configurations of photoelectric conversion elements of Examples 1 to 20 and Comparative Examples 1 to 4 of the present invention.

  Hereinafter, embodiments of the present invention will be described in detail. The sensitizing dye for photoelectric conversion of the present invention is used as a sensitizer in a dye-sensitized photoelectric conversion element. In the photoelectric conversion element of the present invention, for example, a photoelectrode obtained by adsorbing a dye to a semiconductor layer on a conductive support and a counter electrode are arranged to face each other with an electrolyte layer interposed therebetween.

  Although the sensitizing dye for photoelectric conversion represented by the general formula (1) will be specifically described below, the present invention is not limited to these.

Specific examples of the “aryl group” in the “substituted or unsubstituted aryl group” represented by R ₁ or R ₂ in the general formula (1) include carbons such as a phenyl group, a naphthyl group, an anthryl group, and a pyrenyl group. An aryl group having 6 to 20 atoms can be exemplified. Here, the aryl group includes an aromatic hydrocarbon group and a condensed polycyclic aromatic group.

Specific examples of the “substituent” in the “substituted or unsubstituted aryl group” represented by R ₁ or R ₂ in the general formula (1) include halogen atoms such as fluorine atom, chlorine atom and bromine atom; A linear or branched alkyl group having 1 to 6 carbon atoms such as a group, ethyl group, n-propyl group, isopropyl group, n-butyl group, t-butyl group, hexyl group; methoxy group, ethoxy group, A linear or branched alkoxy group having 1 to 6 carbon atoms such as propoxy group, t-butoxy group, pentyloxy group; dimethylamino group, diethylamino group, ethylmethylamino group, methylpropylamino group, di-t -A linear or branched alkyl group having 1 to 6 carbon atoms, such as a butylamino group or a diphenylamino group, an aromatic hydrocarbon group, a condensed polycyclic aromatic group, or A disubstituted amino group having a selected substituent; a hydroxyl group; a carboxyl group that may be esterified such as a carboxyl group, a methyl ester group, and an ethyl ester group; a straight chain having 1 to 6 carbon atoms substituted with the carboxyl group; Examples thereof include a chain or branched alkoxy group; an ethenyl group such as a phenylethenyl group and a diphenylethenyl group; a cyano group. The number of these substituents may be one or more.

As the “alkyl group having 1 to 6 carbon atoms” in the “optionally substituted alkyl group having 1 to 6 carbon atoms” represented by R _{1 to} R ₇ in the general formula (1), Specifically, a linear or branched alkyl group having 1 to 6 carbon atoms such as methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, t-butyl group, and n-hexyl group. Can give.

Specific examples of the “substituent” in the “optionally substituted alkyl group having 1 to 6 carbon atoms” represented by R _{1 to} R ₇ in the general formula (1) include a fluorine atom, Halogen atoms such as chlorine atom and bromine atom; linear or branched alkoxy groups having 1 to 6 carbon atoms such as methoxy group, ethoxy group, propoxy group, t-butoxy group and pentyloxy group; phenyl group and naphthyl group Aryl groups such as a group, anthryl group and pyrenyl group; a dimethylamino group, a diethylamino group, an ethylmethylamino group, a methylpropylamino group, a di-t-butylamino group, a diphenylamino group, etc. A disubstituted amino group having a substituent selected from a linear or branched alkyl group, an aromatic hydrocarbon group, and a condensed polycyclic aromatic group; a hydroxyl group; a carboxyl , Methyl ester, ethyl ester esterified carboxyl group which may be such as group; and the like cyano group. The number of these substituents may be one or more, but when R _{1 to} R ₇ are an optionally substituted alkyl group having 1 to 6 carbon atoms, an alkyl having no substituent It is preferably a group (unsubstituted alkyl group).

  In the general formula (1), A represents a monovalent adsorption group represented by any one of the general formulas (2) to (4).

Specific examples of the “acidic group” represented by R ₈ in the general formula (2) include a carboxyl group, a sulfonic acid group, a phosphoric acid group, a hydroxamic acid group, a phosphonic acid group, a boric acid group, a phosphinic acid group, and a silanol. Group. Among these, a carboxyl group or a phosphonic acid group is preferable, and a carboxyl group is more preferable.

Specific examples of the “alkyl group having 1 to 6 carbon atoms” in the “alkyl group having 1 to 6 carbon atoms having an acidic group as a substituent” represented by R ₉ in the general formula (3) include methyl Examples thereof include linear or branched alkyl groups having 1 to 6 carbon atoms such as a group, ethyl group, n-propyl group, isopropyl group, butyl group, t-butyl group and n-hexyl group. Among these, a linear or branched alkyl group having 1 to 3 carbon atoms is preferable, and a methyl group or an ethyl group is more preferable.

Specific examples of the “acidic group” in the “alkyl group having 1 to 6 carbon atoms having an acidic group as a substituent” represented by R ₉ in the general formula (3) include a carboxyl group, a sulfonic acid group, phosphorus Examples thereof include an acid group, a hydroxamic acid group, a phosphonic acid group, a boric acid group, a phosphinic acid group, and a silanol group. Among these, a carboxyl group or a phosphonic acid group is preferable, and a carboxyl group is more preferable. Although the number of “acidic groups” may be one or more, it is preferably one. The substitution position of the “acidic group” is preferably the terminal of the alkyl group.

As the “alkyl group having 1 to 6 carbon atoms having an acidic group as a substituent” represented by R ₉ in the general formula (3), the number of carbon atoms is 1 to 1 having a carboxyl group or a phosphonic acid group as a substituent. 3 linear or branched alkyl groups are preferred, and a methyl group or ethyl group having a carboxyl group as a substituent is more preferred.

Specific examples of the “unsubstituted alkyl group having 1 to 6 carbon atoms” represented by R ₉ in the general formula (3) include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, and an n-butyl group. And a straight-chain or branched alkyl group having 1 to 6 carbon atoms such as t-butyl group and n-hexyl group. Among these, a linear or branched alkyl group having 1 to 3 carbon atoms is preferable, and a methyl group or an ethyl group is more preferable.

Specific examples of the “acidic group” represented by R _{10 to} R ₁₃ in the general formula (3) include a carboxyl group, a sulfonic acid group, a phosphoric acid group, a hydroxamic acid group, a phosphonic acid group, a boric acid group, and a phosphinic acid. Group, silanol group and the like. Among these, a carboxyl group or a phosphonic acid group is preferable, and a carboxyl group is more preferable.

In the general formula (3), at least one of R _{9 to} R ₁₃ is an alkyl group having 1 to 6 carbon atoms (in the case of R ₉ ) or an acidic group (R _{10 to} R ₁₃ ) having an acidic group as a substituent. ₁₃ ). Here, when R ₉ is an unsubstituted alkyl group having 1 to 6 carbon atoms, at least one of R _{10 to} R ₁₃ is an acidic group, and all of R _{10 to} R ₁₃ are not acidic groups, R ₉ is an alkyl group having 1 to 6 carbon atoms having an acidic group as a substituent.

Specific examples of the “halogen atom” represented by R _{10 to} R ₁₃ in the general formula (3) include a fluorine atom, a chlorine atom, and a bromine atom. The “optionally substituted alkyl group having 1 to 6 carbon atoms” represented by R _{10 to} R ₁₃ in the general formula (3) or “the number of carbon atoms optionally having a substituent” Specific examples of the “alkyl group having 1 to 6 carbon atoms” and the “alkenyl group having 2 to 6 carbon atoms” in the “2-6 alkenyl group” include a methyl group, an ethyl group, an n-propyl group, and an isopropyl group. A linear or branched alkyl group having 1 to 6 carbon atoms such as n-butyl group, t-butyl group and n-hexyl group; and vinyl group, allyl group, isopropenyl group, 2-butenyl group, Examples thereof include straight-chain or branched alkenyl groups having 2 to 6 carbon atoms such as 1-hexenyl group. R _{10 to} R ₁₃ may be bonded to each other through a single bond between adjacent groups to form a ring.

The “optionally substituted alkyl group having 1 to 6 carbon atoms” represented by R _{10 to} R ₁₃ in the general formula (3) or “the number of carbon atoms optionally having a substituent” Specific examples of the “substituent” in the “2-6 alkenyl group” include halogen atoms such as fluorine atom, chlorine atom and bromine atom; alkoxy groups such as methoxy group, ethoxy group and propoxy group; phenyl group, naphthyl group, Aryl groups such as anthryl group and pyrenyl group; linear or branched alkyl groups having 1 to 6 carbon atoms such as dimethylamino group, diethylamino group, di-t-butylamino group and diphenylamino group, aromatic Examples thereof include a disubstituted amino group having a substituent selected from a hydrocarbon group and a condensed polycyclic aromatic group. Although the number of these substituents may be one or more, R _{10 to} R ₁₃ are preferably groups having no substituent.

In the general formula (3), X represents a sulfur atom, an oxygen atom, or C (CH ₃ ) ₂ . Among these, a sulfur atom or C (CH ₃ ) ₂ is preferable. Further, as the “anion” represented by Y in the general formula (3), specifically, iodide ion, bromide ion, chloride ion, hexafluorophosphate ion, tetrafluoroborate ion, perchlorine Acid ions can be raised. Among these, iodide ion, bromide ion, hexafluorophosphate ion or perchlorate ion is preferable, and iodide ion or bromide ion is more preferable.

As “an alkyl group having 1 to 6 carbon atoms” in “an alkyl group having 1 to 6 carbon atoms having at least two acidic groups as a substituent” represented by R ₁₄ or R ₁₅ in the general formula (4) Is specifically a linear or branched group having 1 to 6 carbon atoms such as methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, t-butyl group and n-hexyl group. An alkyl group can be mentioned. Among these, a linear or branched alkyl group having 1 to 3 carbon atoms is preferable, an ethyl group or an n-propyl group is more preferable, and an ethyl group is particularly preferable.

Specific examples of the “acid group” in the “alkyl group having 1 to 6 carbon atoms having at least two acid groups as a substituent” represented by R ₁₄ or R ₁₅ in the general formula (4) include a carboxyl group. Sulfonic acid group, phosphoric acid group, hydroxamic acid group, phosphonic acid group, boric acid group, phosphinic acid group, and the like. Among these, a carboxyl group or a phosphonic acid group is preferable, and a carboxyl group is more preferable. The number of “acidic groups” is two or more, but preferably two. The plurality of acidic groups may be the same or different.

The “C1-C6 alkyl group having at least two acidic groups as a substituent” represented by R ₁₄ or R ₁₅ in the general formula (4) is a carbon atom having a carboxyl group or a phosphonic acid group. A linear or branched alkyl group of 1 to 3 is preferable, and an ethyl group or an n-propyl group having a carboxyl group or a phosphonic acid group is more preferable. Specifically, a 1,2-dicarboxyethyl group or a 1,3-dicarboxypropyl group is more preferable, and a 1,2-dicarboxyethyl group is particularly preferable.

Specific examples of the “unsubstituted alkyl group having 1 to 6 carbon atoms” represented by R ₁₄ or R ₁₅ in the general formula (4) include an ethyl group, an n-propyl group, an isopropyl group, and an n-butyl group. And a straight-chain or branched alkyl group having 1 to 6 carbon atoms such as t-butyl group and n-hexyl group. Among these, a linear or branched alkyl group having 2 to 4 carbon atoms is preferable, a linear alkyl group having 2 to 4 carbon atoms is more preferable, and an ethyl group or an n-propyl group is more preferable. An ethyl group is particularly preferred.

In the general formula (4), at least one of R _{14 and} R ₁₅ is an alkyl group having 1 to 6 carbon atoms having at least two acidic groups as substituents. When p is 0, since R ₁₄ does not exist, R ₁₅ is an alkyl group having 1 to 6 carbon atoms having at least two acidic groups as substituents. Moreover, when p is 2, any one of R <_14> and R < ₁₅ > which exists two should just be a C1-C6 alkyl group which has an at least 2 acidic group as a substituent.

In the general formula (1), R ₁ is preferably a substituted or unsubstituted aryl group, and more preferably a substituted or unsubstituted phenyl group. R ₂ is preferably an unsubstituted alkyl group having 1 to 6 carbon atoms or an unsubstituted aryl group, more preferably an unsubstituted alkyl group having 1 to 3 carbon atoms or an unsubstituted phenyl group, and particularly preferably a methyl group. R ₃ is preferably an unsubstituted alkyl group having 1 to 3 carbon atoms, and more preferably a methyl group. R _{4 to} R ₇ are preferably a hydrogen atom or a hexyl group, and more preferably a hydrogen atom.

In the general formula (1), m represents an integer of 2 to 8, and the ring containing (CH ₂ ) _m is formed from m CH ₂ (methylene group) and two carbon atoms on the indoline ring. Represents a ring structure. m is preferably an integer of 2 to 6, more preferably 3 (5-membered ring) or 4 (6-membered ring). In the general formula (1), n represents an integer of 1 to 3, preferably 1 or 2, and more preferably 1.

In General Formula (3), R ₉ is preferably an alkyl group having 1 to 3 carbon atoms having an acidic group as a substituent, and more preferably a methyl group or an ethyl group having a carboxyl group or a phosphonic acid group. R _{10 to} R ₁₃ are preferably a hydrogen atom, an acidic group, or an alkenyl group having 2 to 6 carbon atoms that may have a substituent, and may have a hydrogen atom, a carboxyl group, or a substituent. A good alkenyl group having 2 to 6 carbon atoms is more preferred.

  In General formula (4), p is an integer of 0-2, and 0 or 1 is preferable.

Among the sensitizing dyes for photoelectric conversion of the present invention represented by the general formula (1), the sensitizing dye for photoelectric conversion in which m is 3 or 4 and R ₂ and R ₃ are methyl groups is particularly efficient. Since a high photoelectric conversion element is obtained, it is preferable. Furthermore, the sensitizing dye for photoelectric conversion of the present invention represented by the general formula (1) can easily adsorb the sensitizing dye on the surface of the semiconductor layer by having a carboxyl group or a phosphonic acid group. This leads to improvement of photoelectric conversion characteristics.

  The sensitizing dye for photoelectric conversion of the present invention represented by the general formula (1) includes all possible stereoisomers. Any isomer can be suitably used as a sensitizing dye for photoelectric conversion in the present invention. For example, in the general formula (1), the sensitizing dye for photoelectric conversion of the present invention when A is a monovalent group represented by the general formula (2) is represented by the following general formula (5) or (6). It is intended to include such compounds. In the general formula (1), when A is a monovalent group represented by the general formula (4) and p is 0, the sensitizing dye for photoelectric conversion of the present invention has the following general formula ( The compound represented by 7) or (8) is included. In addition, it may be a mixture of two or more selected from these stereoisomers.

  Specific examples of the sensitizing dye for photoelectric conversion of the present invention represented by the general formula (1) are shown below, but the present invention is not limited thereto. The following exemplary compounds show examples of possible stereoisomers, and include all other stereoisomers. Moreover, each may be a mixture of two or more stereoisomers.

  These compounds were purified by column chromatography, adsorption purification using silica gel, activated carbon, activated clay, etc., recrystallization or crystallization using a solvent, and the like. These compounds were identified by NMR analysis.

  The sensitizing dye for photoelectric conversion of the present invention can be synthesized using a known method. For example, when A is a sensitizing dye for photoelectric conversion represented by the general formula (2) in the general formula (1), it can be synthesized as follows. A bromo compound (B-1) represented by the following general formula (B-1) and a boronic acid (B-2) represented by the following general formula (B-2) having a formyl group such as 4-formylphenylboronic acid -2), a formyl body (B-3) represented by the following general formula (B-3) can be obtained by performing a cross-coupling reaction such as Suzuki coupling. Then, the sensitizing dye for photoelectric conversion of this invention is compoundable by performing condensation reaction with the obtained formyl body (B-3), cyanoacetic acid, etc. The sensitizing dye for photoelectric conversion in which A is represented by the general formula (3) or (4) in the general formula (1) can also be synthesized by the same method. In addition, about the bromo body (B-1) represented by general formula (B-1), it is compoundable using a well-known method. For example, it can be synthesized by bromination of hexahydrocarbazole substituted at the corresponding 9-position with an aryl group with bromine or N-bromosuccinimide.

  The sensitizing dye for photoelectric conversion of the present invention may be used alone or in combination of two or more. The sensitizing dye for photoelectric conversion of the present invention can be used in combination with other sensitizing dyes not belonging to the present invention. Specific examples of other sensitizing dyes include ruthenium complexes, coumarin dyes, cyanine dyes, merocyanine dyes, rhodacyanine dyes, phthalocyanine dyes, porphyrin dyes, xanthene dyes, represented by the general formula (1). Examples of the sensitizing dye other than the sensitizing dye for photoelectric conversion may be mentioned. When the sensitizing dye for photoelectric conversion of the present invention and these other sensitizing dyes are used in combination, the amount of the other sensitizing dye used for the sensitizing dye for photoelectric conversion of the present invention is 10 to 200% by mass. It is preferable to set it to 20 to 100% by mass.

  In the present invention, a method for producing a dye-sensitized photoelectric conversion element is not particularly limited. A semiconductor layer is formed on a conductive support (electrode), and the photoelectric conversion sensitizing dye of the present invention is formed on the semiconductor layer. A method of adsorption is preferred. As a method for adsorbing the dye, a method of immersing the semiconductor layer in a solution obtained by dissolving the dye in a solvent is generally used. When using two or more types of the sensitizing dye for photoelectric conversion of the present invention in combination, or when using the sensitizing dye for photoelectric conversion of the present invention in combination with other sensitizing dyes, prepare a mixed solution of all the dyes to be used. The semiconductor layer may be immersed, or a separate solution may be prepared for each dye, and the semiconductor layer may be sequentially immersed in each solution.

  In the present invention, in addition to the metal plate, a glass substrate or a plastic substrate provided with a conductive layer having a conductive material on the surface can be used as the conductive support. Specific examples of the conductive material include metals such as gold, silver, copper, aluminum, and platinum, conductive transparent oxide semiconductors such as fluorine-doped tin oxide and indium-tin composite oxide, and carbon. However, it is preferable to use a glass substrate coated with a fluorine-doped tin oxide thin film.

  Specific examples of the semiconductor forming the semiconductor layer in the present invention include metals such as titanium oxide, zinc oxide, tin oxide, indium oxide, zirconium oxide, tungsten oxide, tantalum oxide, iron oxide, gallium oxide, nickel oxide, and yttrium oxide. Oxides: titanium sulfide, zinc sulfide, zirconium sulfide, copper sulfide, tin sulfide, indium sulfide, tungsten sulfide, cadmium sulfide, silver sulfide and other metal sulfides; titanium selenide, zirconium selenide, indium selenide, tungsten selenide And metal selenides such as silicon and germanium. These semiconductors can be used alone or in combination of two or more. In the present invention, it is preferable to use titanium oxide, zinc oxide, or tin oxide as the semiconductor.

  Although the aspect of the semiconductor layer in the present invention is not particularly limited, it is preferably a thin film having a porous structure composed of fine particles. When the substantial surface area of the semiconductor layer increases due to the porous structure and the like, and the amount of dye adsorbed on the semiconductor layer increases, a highly efficient photoelectric conversion element can be obtained. The semiconductor particle diameter is preferably 5 to 500 nm, and more preferably 10 to 100 nm. The film thickness of the semiconductor layer is usually 2 to 100 μm, more preferably 5 to 20 μm. As a method for forming a semiconductor layer, a paste containing semiconductor fine particles is applied on a conductive substrate by a wet coating method such as a spin coating method, a doctor blade method, a squeegee method, or a screen printing method, and then a solvent or additive is baked. Examples thereof include, but are not limited to, a method for forming a film by removing the film, and a method for forming a film by sputtering, vapor deposition, electrodeposition, electrodeposition, microwave irradiation, and the like.

  In the present invention, the paste containing semiconductor fine particles may be a commercially available product, or a paste prepared by dispersing a commercially available semiconductor fine powder in a solvent. Specific examples of the solvent used in preparing the paste include alcohol solvents such as water, methanol, ethanol, isopropyl alcohol, ketone solvents such as acetone, methyl ethyl ketone, methyl isobutyl ketone, n-hexane, cyclohexane, benzene, Hydrocarbon solvents such as toluene can be mentioned, but are not limited to these. These solvents can be used alone or as a mixed solvent of two or more.

  In the present invention, when the semiconductor fine powder is dispersed in a solvent, it may be ground with a mortar or the like, or a dispersing machine such as a ball mill, a paint conditioner, a vertical bead mill, a horizontal bead mill, or an attritor may be used. When preparing the paste, it is preferable to add a surfactant or the like in order to prevent aggregation of the semiconductor fine particles, and it is preferable to add a thickener such as polyethylene glycol to increase the viscosity.

  Adsorption of the sensitizing dye for photoelectric conversion of the present invention onto the surface of the semiconductor layer is performed by immersing the semiconductor layer in the dye solution and leaving it at room temperature for 30 minutes to 100 hours or under heating conditions for 10 minutes to 24 hours. However, it is preferable to leave at room temperature for 10 to 20 hours. The dye concentration in the dye solution is preferably 10 to 2000 μM, more preferably 50 to 500 μM.

  Specific examples of the solvent used when the photoelectric conversion sensitizing dye of the present invention is adsorbed on the surface of the semiconductor layer include alcohol solvents such as methanol, ethanol, isopropyl alcohol, and tert-butyl alcohol, acetone, methyl ethyl ketone, and methyl. Ketone solvents such as isobutyl ketone, ester solvents such as ethyl formate, ethyl acetate and n-butyl acetate, ether solvents such as diethyl ether, 1,2-dimethoxyethane, tetrahydrofuran and 1,3-dioxolane, N, N -Amide solvents such as dimethylformamide, N, N-dimethylacetamide, N-methyl-2-pyrrolidone, nitrile solvents such as acetonitrile, methoxyacetonitrile, propionitrile, dichloromethane, chloroform, bromoform, o-dichlorobenzene, etc. C Gen hydrocarbon solvents, n- hexane, cyclohexane, benzene, may be mentioned hydrocarbon solvents such as toluene, but are not limited to. These solvents are used alone or as a mixed solvent of two or more. Among these solvents, methanol, ethanol, tert-butyl alcohol, acetone, methyl ethyl ketone, tetrahydrofuran and acetonitrile are preferable.

  When adsorbing the sensitizing dye for photoelectric conversion of the present invention on the surface of the semiconductor layer, a cholic acid derivative such as cholic acid or deoxycholic acid, chenodeoxycholic acid, lysocholic acid, and dehydrocholic acid is dissolved in the dye solution, It may be co-adsorbed with the dye. By using cholic acid or a cholic acid derivative, association between the dyes is suppressed, and electrons can be efficiently injected from the dye into the semiconductor layer in the photoelectric conversion element. When cholic acid or cholic acid derivatives are used, their concentration in the dye solution is preferably from 0.1 to 100 mM, more preferably from 1 to 10 mM.

  The counter electrode (electrode) used in the photoelectric conversion element of the present invention is not particularly limited as long as it has conductivity, but a conductive material having catalytic ability is used to promote the redox ion oxidation-reduction reaction. It is preferable to do this. Specific examples of the conductive material include, but are not limited to, platinum, rhodium, ruthenium, carbon, and the like. In the present invention, it is particularly preferable to use as a counter electrode a platinum thin film formed on a conductive support. As a method for forming a conductive thin film, a paste containing a conductive material is applied onto a conductive substrate by a wet coating method such as a spin coating method, a doctor blade method, a squeegee method, or a screen printing method, and then fired. Examples thereof include a method for forming a film by removing a solvent and additives, and a method for forming a film by a sputtering method, a vapor deposition method, an electrodeposition method, an electrodeposition method, a microwave irradiation method, and the like, but are not limited thereto.

  In the photoelectric conversion element of the present invention, an electrolyte is filled between a pair of opposed electrodes to form an electrolyte layer. As the electrolyte to be used, a redox electrolyte is preferable. Examples of redox electrolytes include, but are not limited to, redox ion pairs such as iodine, bromine, tin, iron, chromium, and anthraquinone. Among these, iodine-based electrolytes and bromine-based electrolytes are preferable. In the case of an iodine-based electrolyte, for example, a mixture of potassium iodide, lithium iodide, dimethylpropylimidazolium iodide and the like and iodine is used. In the present invention, it is preferable to use an electrolytic solution obtained by dissolving these electrolytes in a solvent. 0.05-5M is preferable and, as for the density | concentration of the electrolyte in electrolyte solution, 0.2-1M is more preferable.

  Solvents for dissolving the electrolyte include nitrile solvents such as acetonitrile, methoxyacetonitrile, propionitrile, 3-methoxypropionitrile, benzonitrile, ether solvents such as diethyl ether, 1,2-dimethoxyethane, tetrahydrofuran, N Amide solvents such as N, N-dimethylformamide and N, N-dimethylacetamide, carbonate solvents such as ethylene carbonate and propylene carbonate, and lactone solvents such as γ-butyrolactone and γ-valerolactone. It is not limited to. These solvents are used alone or as a mixed solvent of two or more. Of these solvents, nitrile solvents are preferred.

  In the present invention, 4-tert-butylpyridine, 4-methylpyridine, 2-vinylpyridine, N, N-dimethyl-4-aminopyridine, N, N-dimethylaniline, N-methylbenzimidazole, etc. An amine compound, particularly 4-tert-butylpyridine, may be contained. The concentration of the amine compound in the electrolytic solution is preferably 0.05 to 5M, and more preferably 0.2 to 1M. The inclusion of an amine compound in the electrolytic solution is particularly preferable because the open-circuit voltage and fill factor of the dye-sensitized photoelectric conversion element are increased.

  In the present invention, a gel electrolyte obtained by adding a gelling agent, a polymer or the like to the electrolytic solution may be used. Further, a solid electrolyte using a polymer such as a polyethylene oxide derivative may be used instead of the electrolytic solution containing the redox electrolyte. By using a gel electrolyte or a solid electrolyte, volatilization of the electrolytic solution can be reduced.

  In the photoelectric conversion element of the present invention, a solid charge transport layer may be formed between the pair of opposed electrodes instead of the electrolyte. The charge transport material contained in the solid charge transport layer is preferably a hole transport material. Specific examples of the charge transport material include inorganic hole transport materials such as copper iodide, copper bromide and copper thiocyanide, polypyrrole, polythiophene, poly-p-phenylene vinylene, polyvinyl carbazole, polyaniline, oxadiazole derivatives, tri Organic hole transport materials such as phenylamine derivatives, pyrazoline derivatives, fluorenone derivatives, hydrazone compounds, and stilbene compounds are exemplified, but not limited thereto.

  In the present invention, when forming a solid charge transport layer using an organic hole transport material, it is preferable to use a film-forming binder resin in combination. Specific examples of the film-forming binder resin include polystyrene resin, polyvinyl acetal resin, polycarbonate resin, polysulfone resin, polyester resin, polyphenylene oxide resin, polyarylate resin, alkyd resin, acrylic resin, phenoxy resin, and the like. However, it is not limited to these. These resins can be used alone or as a copolymer in combination of one or more. 20-1000 mass% is preferable and the usage-amount with respect to the organic hole transport material of these binder resin is more preferable 50-500 mass%.

  In the photoelectric conversion element of the present invention, an electrode (photoelectrode) provided with a semiconductor layer to which a sensitizing dye is adsorbed is an anode, and a counter electrode is a cathode. Light such as sunlight may be irradiated from either the photoelectrode side or the counter electrode side, but irradiation from the photoelectrode side is preferable. By irradiation with sunlight or the like, the dye absorbs light and becomes excited to emit electrons. The electrons flow to the outside via the semiconductor layer and move to the counter electrode. On the other hand, the dye that has been in an oxidized state by emitting electrons returns to the ground state by receiving electrons supplied from the counter electrode via ions in the electrolyte. By this cycle, a current flows and functions as a photoelectric conversion element.

When evaluating the characteristics of the photoelectric conversion element of the present invention, short-circuit current, open-circuit voltage, fill factor, and photoelectric conversion efficiency are measured. The short circuit current represents the current per 1 cm ² flowing between the two terminals when the output terminal is short-circuited, and the open circuit voltage represents the voltage between the two terminals when the output terminal is opened. The fill factor is a value obtained by dividing the maximum output (product of current and voltage) by the product of the short-circuit current and the open-circuit voltage, and mainly depends on the internal resistance. The photoelectric conversion efficiency is obtained as a percentage value obtained by multiplying the value obtained by dividing the maximum output (W) by the light intensity (W) per 1 cm ² by 100.

  The photoelectric conversion element of the present invention can be applied to a dye-sensitized solar cell, various optical sensors, and the like. In the dye-sensitized solar cell of the present invention, the photoelectric conversion element containing the sensitizing dye represented by the general formula (1) becomes a cell, and the required number of the cells are arranged to be modularized, and predetermined electrical wiring is provided. Can be obtained.

  EXAMPLES Hereinafter, although an Example demonstrates this invention concretely, this invention is not limited to a following example.

[Synthesis Example 1] Synthesis of sensitizing dye for photoelectric conversion (A-1) To a reaction vessel, 100 ml of toluene, 25 ml of ethanol, and 10 ml of water were added, and a compound (C-1) represented by the following formula (C-1) was added thereto. ) 4.00 g, 4-formylphenylboronic acid 2.40 g, and potassium carbonate 4.70 g were added and stirred. After stirring, 0.65 g of tetrakis (triphenylphosphine) palladium was added and heated to reflux for 1 hour. After cooling to room temperature, extraction operation was performed, the organic layer was dried over magnesium sulfate, and the solvent was distilled off to obtain a crude product. The obtained crude product was purified by silica gel column chromatography and dried under reduced pressure to obtain 1.40 g (yield 33%) of a yellow solid of compound (C-2) represented by the following formula (C-2). Got.

  To the reaction vessel were added 20 ml of toluene, 0.45 g of compound (C-2), 0.25 g of cyanoacetic acid, and 0.52 ml of piperidine, and the mixture was heated to reflux for 7 hours. After cooling to room temperature, 30 ml of 1M hydrochloric acid and chloroform were added to the reaction solution for extraction, and 100 ml of 1M hydrochloric acid was added to the resulting organic layer to perform extraction again. The organic layer was dried over magnesium sulfate, and the solvent was distilled off to obtain a crude product. After dissolving the crude product in 50 ml of chloroform, 100 ml of hexane was added and the precipitated solid was collected by filtration and dried at 60 ° C. under reduced pressure to obtain 0.30 g of sensitizing dye for photoelectric conversion (A-1) (recovery). A reddish brown powder having a rate of 52%) was obtained.

  The structure of the obtained reddish brown powder was identified by NMR analysis.

The following 27 hydrogen signals were detected by 1H-NMR (CDCl ₃ ) (carboxyl group hydrogen was not observed). δ (ppm) = 1.3-1.13 (3H), 1.17-1.26 (3H), 1.28-1.66 (7H), 1.91-2.01 (1H), 6 .41-6.48 (1H), 7.24-7.32 (3H), 7.41-7.48 (3H), 7.55-7.60 (1H), 7.82-7.88 (2H), 8.05-8.12 (2H), 8.30-8.35 (1H).

[Synthesis Example 2] Synthesis of sensitizing dye for photoelectric conversion (A-5) 20 ml of ethanol in a reaction vessel, 0.45 g of compound (C-2) obtained in Synthesis Example 1, 0.36 g of diethyl cyanophosphonate, piperidine 0.35 ml was added and heated to reflux for 4 hours. After cooling to room temperature, the solvent was distilled off and the resulting solid was dissolved in toluene, and 100 ml of 1M hydrochloric acid was added to carry out a liquid separation operation. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled off to obtain a crude product. The crude product was purified by silica gel column chromatography to obtain 0.44 g (yield 69%) of orange oil of the compound (C-3) represented by the following formula (C-3).

  To the reaction vessel were added 0.34 g of the above compound (C-3), 15 ml of acetonitrile, and 1.70 ml of trimethylsilyl bromide, and the mixture was heated and stirred at 65 ° C. for 4 hours. After cooling to room temperature, 150 ml of a mixture of methanol / water = 2/1 was added to the reaction mixture, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was dried over anhydrous magnesium sulfate, and the solvent was distilled off to obtain 0.27 g (yield 90%) of an orange powder of a sensitizing dye for photoelectric conversion (A-5).

[Synthesis Example 3] Synthesis of sensitizing dye for photoelectric conversion (A-17) 10 ml of ethanol in a reaction vessel, 0.36 g of compound (C-2) obtained in Synthesis Example 1, and represented by the following formula (C-4) The compound (C-4) 0.27g was added, and it heated and refluxed for 17 hours. After cooling to room temperature, the solvent was distilled off to obtain a crude product. The crude product was purified by silica gel column chromatography to obtain 0.47 g (yield 76%) of purple powder of sensitizing dye for photoelectric conversion (A-17).

[Synthesis Example 4] Synthesis of sensitizing dye for photoelectric conversion (A-46) 30 ml of acetonitrile in a reaction vessel, 0.50 g of compound (C-2) obtained in Synthesis Example 1, and represented by the following formula (C-5) The compound (C-5) 0.33g and piperidine 0.22g were added, and it heated and refluxed for 2 hours. After cooling to room temperature, 30 ml of chloroform and 10 ml of ethyl acetate were added to the reaction solution and washed with 50 ml of 1M hydrochloric acid and 25 ml of water. The organic layer was dried over magnesium sulfate, and the solvent was distilled off to obtain a crude product. The crude product was dissolved in 30 ml of ethyl acetate, washed with 30 ml of saturated brine, and the organic layer was dried over anhydrous sodium acetate. After distilling off the solvent, 0.51 g (63% yield) of a sensitizing dye for photoelectric conversion (A-46) was obtained by crystallization using 16 ml of chloroform, 0.8 ml of ethyl acetate and 80 ml of n-hexane. A reddish brown powder was obtained.

  The structure of the obtained reddish brown powder was identified by NMR analysis.

The following 30 hydrogen signals were detected by 1H-NMR (CDCl ₃ ) (carboxyl group hydrogen was not observed). δ (ppm) = 1.6-1.12 (3H), 1.18-1.25 (3H), 1.29-1.63 (7H), 1.90-2.01 (1H), 3 .23-3.58 (2H), 5.90-6.13 (1H), 6.43-6.49 (1H), 7.23-7.34 (3H), 7.39-7.48 (3H), 7.53-7.57 (1H), 7.65-7.72 (2H), 7.80-7.90 (3H).

[Synthesis Example 5] Synthesis of sensitizing dye for photoelectric conversion (A-47) 20 ml of ethanol in a reaction vessel, 0.50 g of compound (C-2) obtained in Synthesis Example 1, and represented by the following formula (C-6) Compound (C-6) 0.35 g and piperidine 0.34 g were added and heated to reflux for 1 hour. After cooling to room temperature, the solvent was distilled off, and 50 ml of ethyl acetate was added and dissolved. After sequentially washing with 50 ml of 1M hydrochloric acid, 50 ml of water and 25 ml of saturated brine, the organic layer was dried over anhydrous sodium acetate and the solvent was distilled off. The obtained crude product was crystallized using 10 ml of chloroform and 90 ml of n-hexane to obtain 0.56 g (yield 69%) of reddish brown powder of sensitizing dye for photoelectric conversion (A-47).

[Example 1]
A titanium oxide paste (manufactured by Solaronix, Ti-Nanoxide D) was applied to a glass substrate coated with a fluorine-doped tin oxide thin film by a squeegee method. After drying at 110 ° C. for 1 hour, baking was performed at 450 ° C. for 30 minutes to obtain a titanium oxide thin film having a thickness of 5 μm. Next, the sensitizing dye for photoelectric conversion (A-1) obtained in Synthesis Example 1 is dissolved in a mixed solvent of acetonitrile / tert-butyl alcohol = 1/1 to prepare 50 ml of a solution having a concentration of 100 μM. Inside, a glass substrate coated with titanium oxide and sintered was immersed for 15 hours at room temperature to adsorb the pigment, thereby obtaining a photoelectrode.

  A platinum thin film having a thickness of 15 nm was formed on a glass substrate coated with a fluorine-doped tin oxide thin film by a sputtering method using an auto fine coater (JFC-1600 manufactured by JEOL Ltd.) as a counter electrode. Next, a spacer (heat-sealing film) having a thickness of 60 μm is sandwiched between the photoelectrode and the counter electrode, and bonded together by heat sealing. After the electrolyte is injected from the hole previously formed in the counter electrode, the hole is sealed. And the photoelectric conversion element was produced. As the electrolytic solution, a 3-methoxypropionitrile solution of lithium iodide 0.1M, dimethylpropylimidazolium iodide 0.6M, iodine 0.05M, and 4-tert-butylpyridine 0.5M was used.

From the photoelectrode side of the photoelectric conversion element, light generated by a pseudo-sunlight irradiation device (OTENTO-SUN III type manufactured by Spectrometer Co., Ltd.) is irradiated, and a source meter (Model 2400 General-Purpose SourceMeter manufactured by KEITHLEY) is irradiated. Was used to measure current-voltage characteristics. The intensity of light was adjusted to 100 mW / cm ² . In addition, the photoelectric conversion efficiency was measured after 20 hours of irradiation with light, and the change in characteristics was evaluated. The measurement results are summarized in Table 1.

[Examples 2 to 20]
A photoelectric conversion element was prepared in the same manner as in Example 1 except that the sensitizing dye shown in Table 1 was used instead of (A-1) as the sensitizing dye for photoelectric conversion, and current-voltage characteristics were measured. . In addition, the photoelectric conversion efficiency was measured after 20 hours of irradiation with light, and the change in characteristics was evaluated. The measurement results are summarized in Table 1.

[Comparative Examples 1-4]
As the sensitizing dye for photoelectric conversion, it was carried out except that the sensitizing dye for photoelectric conversion shown in the following (D-1) to (D-4) not belonging to the present invention was used instead of (A-1). A photoelectric conversion element was produced in the same manner as in Example 1, and current-voltage characteristics were measured. In addition, the photoelectric conversion efficiency was measured after 20 hours of irradiation with light, and the change in characteristics was evaluated. The measurement results are summarized in Table 1. In addition, the outline of a structure of the photoelectric conversion element produced in Examples 1-20 and Comparative Examples 1-4 is shown in FIG.

  From the results of Table 1, by using the sensitizing dye for photoelectric conversion of the present invention, it is possible to obtain a photoelectric conversion element that has high photoelectric conversion efficiency and maintains high photoelectric conversion efficiency even if light irradiation is continued for a long time. There was found. On the other hand, the photoelectric conversion efficiency of the photoelectric conversion element using the sensitizing dye for photoelectric conversion of the comparative example was insufficient.

  This application is based on Japanese Patent Application 2012-111120 filed on May 15, 2012 and Japanese Patent Application 2013-011391 filed on January 24, 2013, the contents of which are incorporated herein by reference.

  The solar cell using the sensitizing dye for photoelectric conversion of the present invention is useful as a dye-sensitized solar cell that can efficiently convert sunlight energy into electric energy, and can provide clean energy.

DESCRIPTION OF SYMBOLS 1 Conductive support body 2 Dye carrying | support semiconductor layer 3 Electrolyte layer 4 Counter electrode 5 Conductive support body

Claims (8)

Sensitizing dye for photoelectric conversion represented by the following general formula (1):

In the formula, R ₁ and R ₂ each represents an optionally substituted alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group; R ₃ has a substituent. Represents an optionally substituted alkyl group having 1 to 6 carbon atoms; R _{4 to} R ₇ may be the same as or different from each other, and may be a hydrogen atom or a substituent having 1 to 6 carbon atoms; M represents an integer of 2 to 8; n represents an integer of 1 to 3, and when n is 2 or 3, a plurality of R _{4 to} R ₇ may be the same as or different from each other. Well; A represents a monovalent group represented by any one of the following general formulas (2) to (4):

In which R ₈ represents an acidic group;

In the formula, R ₉ represents an alkyl group having 1 to 6 carbon atoms having an acidic group as a substituent or an unsubstituted alkyl group having 1 to 6 carbon atoms; and R _{10 to} R ₁₃ may be the same or different. Or a hydrogen atom, a halogen atom, an acidic group, an alkyl group having 1 to 6 carbon atoms which may have a substituent, or an alkenyl group having 2 to 6 carbon atoms which may have a substituent. Provided that at least one of R _{9 to} R ₁₃ is an alkyl group having 1 to 6 carbon atoms (in the case of R ₉ ) or an acidic group (of R _{10 to} R ₁₃ ) having an acidic group as a substituent. And R _{10 to} R ₁₃ may be bonded to each other through a single bond between adjacent groups to form a ring; X is a sulfur atom, an oxygen atom, or C (CH ₃ ) represents ₂ ; Y represents an anion;

In the formula, R ₁₄ and R ₁₅ may be the same or different and each represents an alkyl group having 1 to 6 carbon atoms or an unsubstituted alkyl group having 1 to 6 carbon atoms having at least two acidic groups as substituents. Wherein at least one of R _{14 and} R ₁₅ is an alkyl group having 1 to 6 carbon atoms having at least two acidic groups as substituents; p represents an integer of 0 to 2 In the case where p is 2, two R _{14 s} may be the same as or different from each other; The sensitizing dye for photoelectric conversion according to claim 1, wherein in the general formula (1), R ₁ is a substituted or unsubstituted aryl group.   The sensitizing dye for photoelectric conversion according to claim 1 or 2, wherein m is 3 or 4 in the general formula (1). The sensitizing dye for photoelectric conversion according to any one of claims 1 to ₃ , wherein, in the general formula (1), R ₂ and R ₃ are methyl groups. The sensitizing dye for photoelectric conversion according to any one of claims 1 to 4, wherein, in the general formula (1), R _{4 to} R ₇ are hydrogen atoms and n is 1.   In the dye-sensitized photoelectric conversion element in which at least a semiconductor layer and an electrolyte layer are provided between a pair of opposing electrodes, the sensitizing dye for photoelectric conversion according to any one of claims 1 to 5 is provided. A photoelectric conversion element carried on the semiconductor layer.   The photoelectric conversion element according to claim 6, wherein the electrolyte layer contains 4-tert-butylpyridine.   A dye-sensitized solar cell having a photoelectric conversion element, wherein the photoelectric conversion element according to claim 6 or 7 is modularized and provided with predetermined electrical wiring.

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