JP2013191477A - Sensitizing dye for photoelectric conversion, and photoelectric conversion element and dye-sensitized solar cell using the same - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a sensitizing dye of a new structure capable of efficiently extracting a current, and to provide a good photoelectric conversion element and a good dye-sensitized solar cell using the sensitizing dye.SOLUTION: The sensitizing dye for photoelectric conversion is represented by general formula (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 and environmental destruction due to global warming as a greenhouse gas. There is a concern that environmental destruction on a global scale will continue to progress. In such a situation, unlike fossil fuels, studies using solar energy that is unlikely to be exhausted are energetically conducted. The introduction of photovoltaic power generation makes it possible to prevent global warming and save energy costs, and so solar energy development and use is rapidly progressing year by year mainly 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, compound semiconductors such as gallium arsenide, cadmium sulfide, and indium copper selenide have been mainly researched and put into practical use for residential use. Some are. 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 that uses 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. became. Therefore, a pn heterojunction type utilizing a contact interface between two kinds of organic semiconductors or a contact interface between an organic semiconductor and an inorganic semiconductor has been expected. However, there is a problem that the photoelectric conversion efficiency is much lower than that of the inorganic solar cell and the 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 noble metals, 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 4). ).

Although the organic dyes described in Patent Documents 1 to 4 have the advantages of being inexpensive, having a large extinction coefficient, and capable of controlling 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 Patent Laid-Open No. 11-214730 JP 11-238905 A JP 2004-139755 A JP 2006-156212 A

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 current, and further to provide a good photoelectric conversion element and dye-sensitized solar cell using the sensitizing dye. It is to be.

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.

1. A sensitizing dye for photoelectric conversion represented by the following general formula (1).

In the formula, R _{1 to} R ₅ may be the same or different, and may be a hydrogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, or an optionally substituted carbon atom. The alkoxy group of number 1-6, or a substituted or unsubstituted aryl group is represented. R ₆ and R ₇ may be the same or different and each represents a hydrogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, or a substituted or unsubstituted aryl group. R _{8 to} R ₁₃ may be the same or different and each represents a hydrogen atom or an optionally substituted alkyl group having 1 to 6 carbon atoms. m represents an integer of 0 to 4, and n represents an integer of 0 to 4. However, m + n shall be in the range of 0-4. p represents an integer of 0 to 2. When m = 2 to 4, a plurality of R _{8 to} R ₁₁ may be the same or different from each other in R ₈ , R ₉ , R ₁₀ , and R ₁₁ . For n = 2 to 4, _{R 12, R 13} to plural present, the _{R 12 together, R 13} to each other may be the same as or different from each other to each other. A represents a monovalent group represented by any one of the following general formulas (2) to (4).

In the formula, R ₁₄ represents an acidic group.

In the formula, R ₁₅ represents an alkyl group having 1 to 3 carbon atoms having an acidic group or an unsubstituted alkyl group having 1 to 4 carbon atoms. R _{16 to} R ₁₉ 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 _{15 to} R ₁₉ is an acidic group or a group having an acidic group. R _{16 to} R ₁₉ 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 ₂₀ and R ₂₁ may be the same or different and each represents an alkyl group having 1 to 3 carbon atoms having an acidic group or an unsubstituted alkyl group having 2 to 4 carbon atoms. However, at least one of R ₂₀ or R ₂₁ is an alkyl group having 1 to 3 carbon atoms having an acidic group. q represents the integer of 0-2. When q = 2, a plurality of R ₂₀ may be the same as or different from each other.

2. 2. The sensitizing dye for photoelectric conversion according to 1 above, wherein the sensitizing dye for photoelectric conversion represented by the general formula (1) is represented by the following general formula (5).

In the formula, R ₃ represents an unsubstituted alkyl group having 1 to 6 carbon atoms or an unsubstituted alkoxy group having 1 to 6 carbon atoms, and R ₂₂ and R ₂₃ represent a hydrogen atom or 1 to 6 carbon atoms. An unsubstituted alkyl group is represented. m represents 0 or 1, n represents an integer of 0 to 3, and p represents 0 or 1. However, it is assumed that at least one of m or n is 0. A represents a monovalent group represented by any one of the general formulas (2) to (4).

3. 3. The sensitizing dye for photoelectric conversion as described in 1 or 2 above, wherein in the general formula (1) or (5), m and n are 0.

4). In the dye-sensitized photoelectric conversion element in which at least a semiconductor layer and an electrolyte layer are provided between the counter electrodes, the photoelectric conversion sensitizing dye according to any one of the above 1 to 3 is supported on the semiconductor layer. A photoelectric conversion element obtained.

5. 5. The photoelectric conversion element as described in 4 above, wherein 4-tert-butylpyridine is contained in the electrolyte layer in the photoelectric conversion element.

6). 6. A dye-sensitized solar cell obtained by modularizing the photoelectric conversion element according to any one of 4 and 5 and providing a 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.

It is a schematic sectional drawing showing the structure of the photoelectric conversion element of this invention Examples 4-14 and Comparative Examples 1-4.

  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, 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.

The “carbon” in the “optionally substituted alkyl group having 1 to 6 carbon atoms” or “substituted or unsubstituted aryl group” represented by R _{1 to} R ₇ in the general formula (1) Specific examples of the “alkyl group having 1 to 6 atoms” or “aryl group” include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, a t-butyl group, and an n-hexyl group. And a linear or branched alkyl group having 1 to 6 carbon atoms; an aryl group such as a phenyl group, a naphthyl group, an anthryl group, and a pyrenyl group. Here, the aryl group represents an aromatic hydrocarbon group and a condensed polycyclic aromatic group.

“Substitution” in the “optionally substituted alkyl group having 1 to 6 carbon atoms” or “substituted or unsubstituted aryl group” represented by R _{1 to} R ₇ in the general formula (1) Specific examples of the “group” include halogen atoms such as fluorine atom, chlorine atom and bromine atom; methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, t-butyl group, hexyl group and the like. Linear or branched alkyl group having 1 to 6 carbon atoms; linear or branched alkyl group having 1 to 6 carbon atoms such as methoxy group, ethoxy group, propoxy group, t-butoxy group, pentyloxy group, etc. Alkoxy group; aryl group such as phenyl group, naphthyl group, anthryl group, pyrenyl group; dimethylamino group, diethylamino group, ethylmethylamino group, methylpropylamino group, di-t-butylamino A disubstituted amino group having a substituent selected from a linear or branched alkyl group having 1 to 6 carbon atoms, an aromatic hydrocarbon group, a condensed polycyclic aromatic group, such as a diphenylamino group; Examples thereof include a hydroxyl group; a carboxyl group that may be esterified; a cyano group, and the like. Although the number of these substituents may be one or more, it is particularly preferable that R _{1 to} R ₇ are groups having no substituent (unsubstituted groups).

As “an alkoxy group having 1 to 6 carbon atoms” in “an alkoxy group having 1 to 6 carbon atoms which may have a substituent” represented by R _{1 to} R ₅ in the general formula (1) Specific examples include 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.

The “substituent” in the “optionally substituted alkoxy group having 1 to 6 carbon atoms” represented by R _{1 to} R ₅ in the general formula (1) is specifically fluorine. Halogen atoms such as atoms, chlorine atoms and bromine atoms; aryl groups such as phenyl groups, naphthyl groups, anthryl groups and pyrenyl groups; carbons such as dimethylamino groups, diethylamino groups, di-t-butylamino groups and diphenylamino groups A disubstituted amino group having a substituent selected from a linear or branched alkyl group having 1 to 6 atoms, an aromatic hydrocarbon group, a condensed polycyclic aromatic group; a hydroxyl group, even if esterified Good carboxyl group; cyano group and the like can be mentioned. Although the number of these substituents may be one or more, R _{1 to} R ₅ are particularly preferably groups having no substituent.

As “an alkyl group having 1 to 6 carbon atoms” in “an alkyl group having 1 to 6 carbon atoms which may have a substituent” represented by R _{8 to} R ₁₃ in the general formula (1) Is specifically a straight-chain or branched carbon atom number 1 to 6 such as methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, t-butyl group, n-hexyl group. An alkyl group.

The “substituent” in the “optionally substituted alkyl group having 1 to 6 carbon atoms” represented by R _{8 to} R ₁₃ in the general formula (1) is specifically 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 and propoxy group; phenyl group, naphthyl group, anthryl group, pyrenyl group, etc. Aryl groups such as dimethylamino group, diethylamino group, di-t-butylamino group, diphenylamino group, etc., linear or branched alkyl groups having 1 to 6 carbon atoms, aromatic hydrocarbon groups, condensed poly Examples thereof include a disubstituted amino group having a substituent selected from a ring aromatic group; a hydroxyl group, an optionally esterified carboxyl group, a cyano group, and the like. Although the number of these substituents may be one or more, R _{8 to} R ₁₃ are particularly preferably groups having no substituent.

As the “acidic group” represented by R ₁₄ in the general formula (2), specifically, carboxyl group, sulfonic acid group, phosphoric acid group, hydroxamic acid group, phosphonic acid group, boric acid group, phosphinic acid Group, silanol group, and the like.

As the “alkyl group having 1 to 3 carbon atoms” in the “alkyl group having 1 to 3 carbon atoms having an acidic group” represented by R ₁₅ in the general formula (3), specifically, a methyl group, Examples thereof include linear or branched alkyl groups having 1 to 3 carbon atoms, such as an ethyl group, an n-propyl group, and an isopropyl group. In addition, as the “alkyl group having 1 to 4 carbon atoms” in the “unsubstituted alkyl group having 1 to 4 carbon atoms” represented by R ₁₅ in the general formula (3), specifically, a methyl group, Examples thereof include linear or branched alkyl groups having 1 to 4 carbon atoms such as ethyl group, n-propyl group, isopropyl group, n-butyl group and t-butyl group.

Specific examples of the “acidic group” in the “alkyl group having 1 to 3 carbon atoms having an acidic group” represented by R ₁₅ in the general formula (3) include a carboxyl group, a sulfonic acid group, and a phosphoric acid group. And hydroxamic acid group, phosphonic acid group, boric acid group, phosphinic acid group, silanol group, and the like. Here, the alkyl group having 1 to 3 carbon atoms substituted with an acidic group is preferably linear rather than branched, has one acidic group, and the acidic group is a terminal of the alkyl group. Those substituted with are particularly preferred.

As the “acidic group” represented by R _{16 to} R ₁₉ in the general formula (3), specifically, carboxyl group, sulfonic acid group, phosphoric acid group, hydroxamic acid group, phosphonic acid group, boric acid group , Phosphinic acid groups, silanol groups, and the like. In addition, when R < ₁₅ > is a C1-C4 unsubstituted alkyl group, at least any one of R < ₁₆ > -R < ₁₉ > must be an acidic group.

Represented by R _{16 to} R ₁₉ in the general formula (3), “halogen atom”, “optionally substituted alkyl group having 1 to 6 carbon atoms” or “having a substituent” As the “halogen atom”, “alkyl group having 1 to 6 carbon atoms” or “alkenyl group having 2 to 6 carbon atoms” in the “optionally alkenyl group having 2 to 6 carbon atoms”, specifically, fluorine Halogen atoms such as atoms, chlorine atoms and bromine atoms; linear or branched carbon such as methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, t-butyl group and n-hexyl group Examples thereof include an alkyl group having 1 to 6 atoms; an alkenyl group having 2 to 6 carbon atoms such as a vinyl group, an allyl group, an isopropenyl group, a 2-butenyl group, and a 1-hexenyl group. R _{16 to} R ₁₉ 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 _{16 to} R ₁₉ in the general formula (3) or “optionally substituted carbon atom” Specific examples of the “substituent” in the “alkenyl group of 2 to 6” 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 and 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 And a disubstituted amino group having a substituent selected from an aromatic hydrocarbon group and a condensed polycyclic aromatic group. Although the number of these substituents may be one or more, R _{16 to} R ₁₉ are particularly preferably groups having no substituent.

Specific examples of the “anion” represented by Y in the general formula (3) include iodine ion, bromine ion, chlorine ion, hexafluorophosphate ion, tetrafluoroborate ion, and perchlorate ion. , Etc.

As the “alkyl group having 1 to 3 carbon atoms” in the “alkyl group having 1 to 3 carbon atoms having an acidic group” represented by R ₂₀ and R ₂₁ in the general formula (4), specifically, Examples thereof include linear or branched alkyl groups having 1 to 3 carbon atoms, such as a methyl group, an ethyl group, an n-propyl group, and an isopropyl group. Further, as the “alkyl group having 2 to 4 carbon atoms” in the “unsubstituted alkyl group having 2 to 4 carbon atoms” represented by R ₂₀ and R ₂₁ in the general formula (4), specifically, Examples thereof include linear or branched alkyl groups having 2 to 4 carbon atoms such as ethyl group, n-propyl group, isopropyl group, n-butyl group and t-butyl group.

As the “acidic group” in the “alkyl group having 1 to 3 carbon atoms having an acidic group” represented by R ₂₀ and R ₂₁ in the general formula (4), specifically, a carboxyl group, a sulfonic acid group, Examples thereof include a phosphoric acid group, a hydroxamic acid group, a phosphonic acid group, a boric acid group, a phosphinic acid group, and a silanol group. Here, at least one of R _{20 and} R ₂₁ is an alkyl group having 1 to 3 carbon atoms having an acidic group. The alkyl group having 1 to 3 carbon atoms having an acidic group is preferably linear rather than branched, has one acidic group, and the acidic group is substituted at the end of the alkyl group. Those are particularly preferred. Since the case of q = 0 _{R 20} is _{absent, R 21} is an alkyl group having 1 to 3 carbon atoms having an acidic group.

The “alkyl group having 1 to 6 carbon atoms” in the “unsubstituted alkyl group having 1 to 6 carbon atoms” represented by R ₂₂ and R ₂₃ in the general formula (5) is specifically a methyl group. Linear or branched alkyl groups having 1 to 6 carbon atoms, such as ethyl group, n-propyl group, isopropyl group, n-butyl group, t-butyl group and n-hexyl group. .

In the general formula (1), R ₁ , R ₂ , R ₄ and R ₅ are preferably a hydrogen atom or an unsubstituted alkyl group having 1 to 6 carbon atoms, and particularly preferably a hydrogen atom. R ₃ is preferably an unsubstituted alkyl group having 1 to 6 carbon atoms or an unsubstituted alkoxy group having 1 to 6 carbon atoms, more preferably an unsubstituted alkoxy group having 1 to 6 carbon atoms, and 1 carbon atom. Especially preferred are unsubstituted alkoxy groups of ~ 3. R ₆ and R ₇ are preferably a substituted or unsubstituted aryl group, particularly preferably a substituted or unsubstituted phenyl group. R _{8 to} R ₁₃ are preferably a hydrogen atom or a hexyl group, and particularly preferably a hydrogen atom.

In the general formula (2), R ₁₄ is preferably a carboxyl group or a sulfonic acid group, and particularly preferably a carboxyl group. In the general formula (3), R ₁₅ is preferably an alkyl group having 1 to 3 carbon atoms having a carboxyl group, and particularly preferably a carboxymethyl group or a carboxyethyl group. R _{16 to} R ₁₉ are preferably a hydrogen atom or an alkenyl group having 2 to 6 carbon atoms which may have a substituent, and particularly preferably a hydrogen atom. However, when R ₁₅ is an unsubstituted alkyl group, at least one of R _{16 to} R ₁₉ is an acidic group. X is preferably a sulfur atom or C (CH ₃ ) ₂ , and particularly preferably a sulfur atom. Y is preferably iodine ion, bromine ion, hexafluorophosphate ion or perchlorate ion, particularly preferably iodine ion or bromine ion. In the general formula (4), when R ₂₀ and R ₂₁ are an alkyl group having 1 to 3 carbon atoms having an acidic group, a carboxymethyl group or a carboxyethyl group is preferable, and a carboxymethyl group is preferable. Particularly preferred. When R ₂₀ and R ₂₁ are an unsubstituted alkyl group having 2 to 4 carbon atoms, an ethyl group or an n-propyl group is preferable, and an ethyl group is particularly preferable. m is preferably 0 or 1, particularly preferably 0. n is preferably an integer of 0 to 3, particularly preferably 0. p is preferably an integer of 0 to 2, particularly preferably 0 or 1. q is preferably an integer of 0 to 2, particularly preferably 0 or 1.

Among the sensitizing dyes for photoelectric conversion of the present invention represented by the general formula (1), the sensitizing dye for photoelectric conversion represented by the general formula (5) is preferable because a highly efficient photoelectric conversion element is obtained. . Furthermore, by having a carboxyl group as an acidic group, the sensitizing dye can be easily adsorbed on the surface of the semiconductor layer, leading to an improvement in photoelectric conversion characteristics.

The sensitizing dye for photoelectric conversion of the present invention represented by the general formula (1) includes all possible stereoisomers. For example, in the general formula (1), when p = 1 and A is a monovalent group represented by the general formula (2), compounds represented by the following general formulas (6) to (9) And all other possible stereoisomers. Moreover, the mixture of 2 or more types chosen from these stereoisomers may be sufficient. Any of the isomers can be suitably used as a sensitizing dye for photoelectric conversion in the present invention. When p is 1 or 2, one bonded to the 3-position carbon atom of indole (p = 1) Or, for two consecutive carbon-carbon double bonds (p = 2), trans is more preferable than cis. For example, among the compounds represented by the following general formulas (6) to (9), the following general formula (6) or (7) is particularly preferable.

  Specific examples of the sensitizing dye for photoelectric conversion represented by the general formula (1) of the present invention are shown in the following (A-1) to (A-115), but the present invention is not limited thereto. . The following (A-1) to (A-115) are 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 represented by the general formula (1) can be synthesized as follows. As an example, a case where p = 1 will be described. When m = 0 and n = 0, an intermediate is obtained by performing a Horner-Wadsworth-Emmons reaction using a 3-formylindole derivative (B-1) and a phosphonic acid derivative (B-2). (B-3) can be obtained. A formyl body (B-4) is obtained by conducting a Vilsmeier-Haack reaction between the obtained intermediate (B-3) and phosphorus oxychloride. Then, the sensitizing dye for photoelectric conversion of this invention is compoundable by performing condensation reaction with the obtained formyl body (B-4), cyanoacetic acid, etc. In the case of m = 1 to 4 and n = 0, the intermediate (B) -Boldsworth-Emmons reaction is performed using the bromo compound (B-5) and the phosphonic acid derivative (B-2). B-6) can be obtained. By performing cross coupling reaction such as Suzuki coupling using the obtained intermediate (B-6) and boronic acid (B-7) having a formyl group such as 4-formylphenylboronic acid, formyl A body (B-8) can be obtained. Then, the sensitizing dye for photoelectric conversion of this invention is compoundable by performing condensation reaction with the obtained formyl body (B-8), cyanoacetic acid, etc. When m = 0 and n = 1 to 4, the intermediate (B-6) and a boronic acid (B-9) having a formyl group such as 5-formyl-2-thiopheneboronic acid are used. The formyl body (B-10) can be obtained by carrying out a cross-coupling reaction such as Suzuki coupling. Thereafter, the sensitizing dye for photoelectric conversion of the present invention can be synthesized by performing a condensation reaction with cyanoacetic acid or the like.

In the case of p = 0 or 2 in the general formula (1), it can be synthesized in the same manner as in the case of p = 1.

  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, other than the general formula (1). Although a sensitizing dye etc. can be mention | raise | lifted, it is not limited to these. 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.

  The method for producing a dye-sensitized photoelectric conversion element in the present invention is not particularly limited, but a method of forming a semiconductor layer on a conductive support and allowing the semiconductor layer to adsorb the sensitizing dye for photoelectric conversion of the present invention. 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 used in the photoelectric conversion element of the present invention is not particularly limited as long as it has conductivity, but in order to promote the redox ion oxidation-reduction reaction, a conductive material having catalytic ability is used. preferable. 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 the counter 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, and carbonate solvents such as ethylene carbonate and propylene carbonate, but are not limited thereto. 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 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 counter 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, the photoelectrode formed by adsorbing the sensitizing dye to the semiconductor layer serves as an anode, and the counter electrode serves as 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-4) 250 ml of dimethylacetamide, 10.81 g of 3-formylindole, 11.58 g of 4-iodoanisole and 6.69 g of copper acetate were added, and 150 The mixture was stirred for 48 hours at ° C. The reaction solution was cooled to room temperature, diluted with 300 ml of ethyl acetate, added with 500 ml of a saturated aqueous ammonium chloride solution, and stirred for 2 hours. After performing the liquid separation operation, 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 to obtain 2.48 g (yield 20%) of the following compound (C-1) as a brown solid.

To the reaction vessel, 20 ml of 1,4-dioxane, 1.00 g of compound (C-1), 1.45 g of diethyl (3,3-diphenylallyl) phosphonate and 0.54 g of potassium tert-butoxide were added, and the mixture was stirred at room temperature for 30 minutes. did. The reaction was stopped by adding 50 ml of water, and then extraction with ethyl acetate was performed three times. 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 to obtain 1.35 g (yield 79%) of the following compound (C-2) as a yellow solid.

To the reaction vessel, 17 ml of N, N-dimethylformamide, 1.16 g of compound (C-2) and 0.5 ml of phosphorus oxychloride were added and stirred at room temperature for 90 minutes, and further stirred at 40 ° C. for 2 hours. The reaction was stopped by adding 40 ml of water while cooling the reaction solution to 0 ° C. by diluting with 50 ml of toluene. After adding 2 ml of 48% aqueous sodium hydroxide and stirring at 50 ° C. for 1 hour, extraction with toluene was performed three times. The organic layer was dried over magnesium sulfate, and the solvent was distilled off to obtain a crude product. The resulting crude product was purified by silica gel column chromatography to obtain 0.72 g (yield 89%) of the following compound (C-3) as a yellow solid.

To the reaction vessel were added 15 ml of toluene, 0.23 g of compound (C-3), 0.09 g of cyanoacetic acid, and 0.25 ml of piperidine, and the mixture was refluxed with heating for 6 hours. The reaction solution was cooled to room temperature, and the precipitated solid was collected by filtration. The obtained solid was dissolved in 30 ml of toluene, 80 ml of 1M hydrochloric acid was added, and the mixture was stirred for 30 minutes. Liquid separation operation was performed, the organic layer was dried over magnesium sulfate, and then the solvent was distilled off to obtain a crude product. The obtained crude product was purified by silica gel column chromatography to obtain 0.09 g (yield 34%) of reddish brown powder of a sensitizing dye for photoelectric conversion (A-4).

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

The following 25 hydrogen signals were detected by 1H-NMR (CDCl ₃ ) (carboxyl group hydrogen was not observed). δ (ppm) = 3.87 (3H), 6.83-6.93 (1H), 7.10-7.52 (20H), 7.93 (1H).

[Synthesis Example 2] Synthesis reaction vessel for photoelectric conversion sensitizing dye (A-57) 15 ml of toluene, 0.23 g of compound (C-3) obtained in Synthesis Example 1, and the following compound (C-4) 0. 15 g and piperidine 0.20 ml were added, and the mixture was heated and stirred at 100 ° C. for 6 hours. After cooling to room temperature, the precipitated solid was collected by filtration. The obtained solid was dissolved in 35 ml of toluene, 100 ml of 1M hydrochloric acid was added, and the mixture was stirred for 30 minutes. Liquid separation operation was performed, the organic layer was dried over magnesium sulfate, and then the solvent was distilled off to obtain a crude product. The obtained crude product was purified by silica gel column chromatography to obtain 0.11 g (yield 31%) of reddish brown powder of a sensitizing dye for photoelectric conversion (A-57).

[Synthesis Example 3] Synthesis of sensitizing dye for photoelectric conversion (A-97) 40 ml of acetonitrile, 8.00 g of 3-ethylrhodanine, 8.64 g of ethyl isothiocyanatoacetate, and 9.07 g of diazabicycloundecene were added to ice. After stirring under cooling, 8.30 g of ethyl bromoacetate was added, and the mixture was heated and stirred at 100 ° C. for 1 hour. After cooling to room temperature, the reaction solution obtained by adding 20 ml of chloroform was concentrated under reduced pressure to obtain a crude product. The obtained crude product was purified by silica gel column chromatography to obtain 5.56 g (yield 32%) of the following compound (C-5) as a yellow solid.

To the reaction vessel, 5.00 g of compound (C-5), 28 ml of acetic acid and 63 ml of concentrated hydrochloric acid were added, and the mixture was heated and stirred at 90 ° C. for 1 hour. After cooling to room temperature, the solid was collected by filtration and dispersed in 70 ml of water. After stirring the dispersion for a while, the crystals were collected by filtration to obtain 3.48 g (yield 76%) of the following compound (C-6) as a yellow powder.

To the reaction vessel were added 25 ml of toluene, 0.35 g of the compound (C-3) obtained in Synthesis Example 1, 0.25 g of the above compound (C-6), and 0.19 ml of piperidine, and the mixture was refluxed with heating for 3 hours. The reaction solution was cooled to room temperature, and the precipitated solid was collected by filtration. The obtained solid was dissolved in 80 ml of toluene, 80 ml of 1M hydrochloric acid was added, and the mixture was stirred for 30 minutes. Liquid separation operation was performed, the organic layer was dried over magnesium sulfate, and then the solvent was distilled off to obtain a crude product. The obtained crude product was purified by silica gel column chromatography to obtain 0.46 g (yield 78%) of reddish brown powder of a sensitizing dye for photoelectric conversion (A-97).

[Example 4]
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-4) 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 injecting the electrolyte from the hole of the counter electrode, the hole is sealed, and photoelectric conversion is performed. An 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 5 to 14]
A photoelectric conversion element was prepared in the same manner as in Example 4 except that the sensitizing dye shown in Table 1 was used instead of (A-4) 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-4). A photoelectric conversion element was produced in the same manner as in Example 4, 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.

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.

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 (6)

A sensitizing dye for photoelectric conversion represented by the following general formula (1).

In the formula, R _{1 to} R ₅ may be the same or different, and may be a hydrogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, or an optionally substituted carbon atom. The alkoxy group of number 1-6, or a substituted or unsubstituted aryl group is represented. R ₆ and R ₇ may be the same or different and each represents a hydrogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, or a substituted or unsubstituted aryl group. R _{8 to} R ₁₃ may be the same or different and each represents a hydrogen atom or an optionally substituted alkyl group having 1 to 6 carbon atoms. m represents an integer of 0 to 4, and n represents an integer of 0 to 4. However, m + n shall be in the range of 0-4. p represents an integer of 0 to 2. When m = 2 to 4, a plurality of R _{8 to} R ₁₁ may be the same or different from each other in R ₈ , R ₉ , R ₁₀ , and R ₁₁ . For n = 2 to 4, _{R 12, R 13} to plural present, the _{R 12 together, R 13} to each other may be the same as or different from each other to each other. A represents a monovalent group represented by any one of the following general formulas (2) to (4).

In the formula, R ₁₄ represents an acidic group.

In the formula, R ₁₅ represents an alkyl group having 1 to 3 carbon atoms having an acidic group or an unsubstituted alkyl group having 1 to 4 carbon atoms. R _{16 to} R ₁₉ 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 _{15 to} R ₁₉ is an acidic group or a group having an acidic group. R _{16 to} R ₁₉ 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 ₂₀ and R ₂₁ may be the same or different and each represents an alkyl group having 1 to 3 carbon atoms having an acidic group or an unsubstituted alkyl group having 2 to 4 carbon atoms. However, at least one of R ₂₀ or R ₂₁ is an alkyl group having 1 to 3 carbon atoms having an acidic group. q represents the integer of 0-2. When q = 2, a plurality of R ₂₀ may be the same as or different from each other. 2. The sensitizing dye for photoelectric conversion according to claim 1, wherein the sensitizing dye for photoelectric conversion represented by the general formula (1) is represented by the following general formula (5).

In the formula, R ₃ represents an unsubstituted alkyl group having 1 to 6 carbon atoms or an unsubstituted alkoxy group having 1 to 6 carbon atoms, and R ₂₂ and R ₂₃ represent a hydrogen atom or 1 to 6 carbon atoms. An unsubstituted alkyl group is represented. m represents 0 or 1, n represents an integer of 0 to 3, and p represents 0 or 1. However, it is assumed that at least one of m or n is 0. A represents a monovalent group represented by any one of the general formulas (2) to (4). The sensitizing dye for photoelectric conversion according to claim 1, wherein m and n are 0 in the general formula (1) or (5). In the dye-sensitized photoelectric conversion element in which at least a semiconductor layer and an electrolyte layer are provided between the counter electrodes, the semiconductor layer carries the photoelectric conversion sensitizing dye according to any one of claims 1 to 3. A photoelectric conversion element obtained by The photoelectric conversion element according to claim 4, wherein 4-tert-butylpyridine is contained in the electrolyte layer in the photoelectric conversion element. A dye-sensitized solar cell obtained by modularizing the photoelectric conversion element according to any one of claims 4 and 5 and providing predetermined electrical wiring.

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