JP2013175444A - Sensitizing dye for photoelectric conversion and photoelectric conversion element using the same, and dye-sensitized solar cell - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a sensitizing dye with a new structure allowing for effectively taking electric current out, a good photoelectric conversion element using the dye, and a dye-sensitized solar cell.SOLUTION: A sensitizing dye for photoelectric conversion is represented by the formula (I). (In the formula, Rto Rrepresent an alkyl group with a carbon atom number of 1 to 6 which may have a substituent or represents a substituted or unsubstituted aryl group. Rto Rmay be the same or different and represent a hydrogen atom, a halogen atom, a substituted or unsubstituted aryl group, and the like. Rto Rmay be the same or different and represent a hydrogen atom, an alkyl group with a carbon atom number of 1 to 6 which may have a substituent, and the like. m represents an integer number of 0 to 4 and n represents an integer number of 0 to 4. Provided that m + n is within the range of 0 to 4. Y is an adsorbing group having a heterocycle comprising nitrogen and sulfur or an adsorbing group having a cyano olefin moiety.)

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 was reported by Prof. Gretzel et al. Of Lausanne University of Technology in Switzerland (see Non-Patent Document 1, for example). 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 the most dominant, 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 5). reference).

Although the organic dyes described in Patent Documents 1 to 5 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 Patent Laid-Open No. 11-214730 JP 11-238905 A JP 2009-16158 A JP 2009-48925 JP 2009-205890 A International Publication No. 2012/014500

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. Is to provide.

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 (I).

Wherein represents R ₁ to R ₃ which may have a substituent alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group. R _{4 to} R ₉ may be the same or different, and may be a hydrogen atom, a halogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group, an amino group, Represents a monosubstituted amino group or a disubstituted amino group. R _{10 to} R ₁₅ 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 having 2 carbon atoms. Represents an alkenyl group of ˜6. Here, R ₁₀ and R ₁₁ , R ₁₂ and R ₁₃ , R ₁₄ and R ₁₅ may be bonded to each other to form a ring. 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. When a plurality of R _{10 to} R ₁₃ are present (when m = 2 to 4), R ₁₀ , R ₁₁ , R ₁₂ , and R ₁₃ may be the same or different. When a plurality of R ₁₄ and R ₁₅ are present (when n = 2 to 4), R ₁₄ and R ₁₅ may be the same as or different from each other. Y is an adsorptive group represented by the following general formula (I-1) or (I-2).

In the formula, R ₁₆ and R ₁₇ may be the same or different and each represents an alkyl group having 1 to 3 carbon atoms substituted with an acidic group or an unsubstituted alkyl group having 2 to 4 carbon atoms. However, at least one of R _{16 and} R ₁₇ is an alkyl group having 1 to 3 carbon atoms substituted with an acidic group. p represents an integer of 0 to 2. When two R ₁₆ exist (when p = 2), each may be the same as or different from each other.

In the formula, R ₁₈ represents an acidic group.

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

Wherein represents R ₁ to R ₃ which may have a substituent alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group. R _{4 to} R ₉ may be the same or different, and may be a hydrogen atom, a halogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group, an amino group, Represents a monosubstituted amino group or a disubstituted amino group. R _{10 to} R ₁₅ 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 having 2 carbon atoms. Represents an alkenyl group of ˜6. Here, R ₁₀ and R ₁₁ , R ₁₂ and R ₁₃ , R ₁₄ and R ₁₅ may be bonded to each other to form a ring. R ₁₆ and R ₁₇ may be the same or different and each represents an alkyl group having 1 to 3 carbon atoms substituted with an acidic group or an unsubstituted alkyl group having 2 to 4 carbon atoms. However, at least one of R _{16 and} R ₁₇ is an alkyl group having 1 to 3 carbon atoms substituted with an acidic group. 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 a plurality of R _{10 to} R ₁₃ are present (when m = 2 to 4), R ₁₀ , R ₁₁ , R ₁₂ , and R ₁₃ may be the same or different. When a plurality of R ₁₄ and R ₁₅ are present (when n = 2 to 4), R ₁₄ and R ₁₅ may be the same as or different from each other. When a plurality of R ₁₆ are present (when p = 2), each may be the same as or different from each other.

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

Wherein represents R ₁ to R ₃ which may have a substituent alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group. R _{4 to} R ₉ may be the same or different, and may be a hydrogen atom, a halogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group, an amino group, Represents a monosubstituted amino group or a disubstituted amino group. R ₁₆ and R ₁₇ may be the same or different and each represents an alkyl group having 1 to 3 carbon atoms substituted with an acidic group or an unsubstituted alkyl group having 2 to 4 carbon atoms. However, at least one of R _{16 and} R ₁₇ is an alkyl group having 1 to 3 carbon atoms substituted with an acidic group. m represents 0 or 1, n represents 0 or 1, and p represents 0 or 1.

4). In the general formula (1) or (2), at least one of R _{16 and} R ₁₇ is an alkyl group having 1 to 3 carbon atoms substituted with a carboxyl group, 4. The sensitizing dye for photoelectric conversion according to any one of 3 above.

5. In the general formula (1) or (2), at least one of R _{16 and} R ₁₇ is a carboxymethyl group, the increase for photoelectric conversion according to any one of 2 to 4 above, Sensitive dye.

6). In the general formula (1) or (2), R ₁₆ and R ₁₇ are groups selected from a carboxymethyl group, a 1,2-dicarboxyethyl group or an ethyl group, and at least R ₁₆ or R ₁₇ Any one of these is a carboxymethyl group or a 1, 2- dicarboxyethyl group, The sensitizing dye for photoelectric conversion of any one of said 2-5 characterized by the above-mentioned.

7). In the general formula (1) or (2), R ₁ is a substituted or unsubstituted phenyl group, R ₂ and R ₃ are methyl groups, and all of R _{4 to} R ₉ are hydrogen atoms. The sensitizing dye for photoelectric conversion according to any one of 2 to 6, wherein:

8). 2. The sensitizing dye for photoelectric conversion according to 1 above, wherein the sensitizing dye for photoelectric conversion represented by the general formula (I) is represented by the following general formula (3).

Wherein represents R ₁ to R ₃ which may have a substituent alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group. R _{4 to} R ₉ may be the same or different, and may be a hydrogen atom, a halogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group, an amino group, Represents a monosubstituted amino group or a disubstituted amino group. R _{10 to} R ₁₅ 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 having 2 carbon atoms. Represents an alkenyl group of ˜6. Here, R ₁₀ and R ₁₁ , R ₁₂ and R ₁₃ , R ₁₄ and R ₁₅ may be bonded to each other to form a ring. R ₁₈ represents an acidic group. 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. When a plurality of R _{10 to} R ₁₃ are present (when m = 2 to 4), R ₁₀ , R ₁₁ , R ₁₂ , and R ₁₃ may be the same or different. When a plurality of R ₁₄ and R ₁₅ are present (when n = 2 to 4), R ₁₄ and R ₁₅ may be the same as or different from each other.

9. 9. The sensitizing dye for photoelectric conversion according to 8, wherein the sensitizing dye for photoelectric conversion represented by the general formula (3) is represented by the following general formula (4).

Wherein represents R ₁ to R ₃ which may have a substituent alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group. R _{4 to} R ₉ may be the same or different, and may be a hydrogen atom, a halogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group, an amino group, Represents a monosubstituted amino group or a disubstituted amino group. R ₁₈ represents an acidic group. m represents 0 or 1, and n represents 0 or 1.

10. In the general formula (3) or (4), R ₁ is a substituted or unsubstituted phenyl group, R ₂ and R ₃ are methyl groups, and all of R _{4 to} R ₉ are hydrogen atoms. 10. The sensitizing dye for photoelectric conversion as described in any one of 8 or 9 above.

11. 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 described in any one of 1 to 10 above is supported on a semiconductor layer. A photoelectric conversion element obtained.

12 12. The photoelectric conversion element as described in 11 above, wherein 4-tert-butylpyridine is contained in the electrolyte layer in the photoelectric conversion element.

13. 13. A dye-sensitized solar cell obtained by modularizing the photoelectric conversion element according to any one of 11 and 12 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 1-22 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 pigment | dye which has the structure of the said general formula (I) or (1)-(4) is demonstrated concretely below, this invention is not limited to these.

“An optionally substituted alkyl group having 1 to 6 carbon atoms” represented by R _{1 to} R ₉ in the general formula (I) or (1) to (4) or “substituted or unsubstituted” Specific examples of the “alkyl group having 1 to 6 carbon atoms” or the “aryl group” in the “aryl group” include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, and t-butyl group. And linear or branched alkyl groups having 1 to 6 carbon atoms such as n-hexyl group; aryl groups such as phenyl group, naphthyl group, anthryl group and pyrenyl group. Here, the aryl group represents an aromatic hydrocarbon group and a condensed polycyclic aromatic group.

The “optionally substituted alkyl group having 1 to 6 carbon atoms” or “substituted aryl group” represented by R _{1 to} R ₉ in the general formula (I) or (1) to (4) Specific examples of the “substituent” in the above are halogen atoms such as fluorine atom, chlorine atom, bromine atom; methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, t-butyl group, hexyl group Linear or branched alkyl groups having 1 to 6 carbon atoms such as phenyl groups, naphthyl groups, anthryl groups, pyrenyl groups and the like; amino groups; methylamino groups, ethylamino groups, t-butylamino groups Group, monosubstituted amino group such as phenylamino group; disubstituted amino group such as dimethylamino group, diethylamino group, di-t-butylamino group, diphenylamino group; hydroxyl group, optionally esterified group Examples include ruboxyl group, cyano group; ethenyl group such as phenylethenyl group and diphenylethenyl group; alkoxy group such as methoxy group, ethoxy group and propoxy group. Although the number of these substituents may be one or more, R _{1 to} R ₉ are more preferably groups having no substituent.

Specific examples of the “halogen atom”, “monosubstituted amino group”, or “disubstituted amino group” represented by R _{4 to} R ₉ in the general formula (I) or (1) to (4) include fluorine. Halogen atoms such as atoms, chlorine atoms, bromine atoms; methylamino groups, ethylamino groups, t-butylamino groups, phenylamino groups, dimethylamino groups, diethylamino groups, di-t-butylamino groups, diphenylamino groups, etc. Examples thereof include a monosubstituted amino group or a disubstituted amino group having a substituent selected from a linear or branched alkyl group having 1 to 6 carbon atoms and an aryl group.

The “optionally substituted alkyl group having 1 to 6 carbon atoms” represented by R _{10 to} R ₁₅ in the general formula (I), (1) or (3) or “having a substituent. Specific examples of the “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” include a methyl group and an ethyl group. , N-propyl group, isopropyl group, n-butyl group, t-butyl group, n-hexyl group and the like linear or branched alkyl groups having 1 to 6 carbon atoms; vinyl group, allyl group, isopropenyl And an alkenyl group having 2 to 6 carbon atoms such as a group, 2-butenyl group and 1-hexenyl group. R ₁₀ and R ₁₁ , R ₁₂ and R ₁₃ , R ₁₄ and R ₁₅ may be bonded to each other to form a ring.

The “optionally substituted alkyl group having 1 to 6 carbon atoms” represented by R _{10 to} R ₁₅ in the general formula (I), (1) or (3) or “having a substituent. Specific examples of the “substituent” in the “optionally alkenyl group having 2 to 6 carbon atoms” include halogen atoms such as fluorine atom, chlorine atom and bromine atom; methyl group, ethyl group, n-propyl group, Linear or branched alkyl groups having 1 to 6 carbon atoms such as isopropyl group, n-butyl group, t-butyl group and hexyl group; aryl groups such as phenyl group, naphthyl group, anthryl group and pyrenyl group; Amino group; monosubstituted amino group such as methylamino group, ethylamino group, t-butylamino group, phenylamino group; disubstituted amino group such as dimethylamino group, diethylamino group, di-t-butylamino group, diphenylamino group, etc. Examples include mino group; hydroxyl group, optionally esterified carboxyl group, cyano group; alkoxy group such as methoxy group, ethoxy group, and propoxy group. Although the number of these substituents may be one or plural, it is particularly preferable that R _{10 to} R ₁₅ are groups having no substituent.

Formula (I-1), (1) or (2) in the represented by _{R 16} or _{R 17,} the number of "carbon atoms in the" alkyl group having 1 to 3 carbon atoms substituted with an acidic group "1 Specific examples of the “3 alkyl group” 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. Among these, a linear alkyl group having 1 to 3 carbon atoms is preferable, and a methyl group or an ethyl group is more preferable.

As the “acidic group” in the “alkyl group having 1 to 3 carbon atoms substituted with an acidic group” represented by R ₁₆ or R ₁₇ in the general formula (I-1), (1) or (2), Specific examples 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. Among these, a carboxyl group or a phosphonic acid group is preferable, and a carboxyl group is more preferable. In addition, the number of “acidic groups” may be one or two or more, but one or two is preferable, and it is more preferable that one of the acidic groups is substituted at the terminal of the alkyl group. When two or more acidic groups are substituted, each acidic group may be the same or different.

Specific examples of the “alkyl group having 1 to 3 carbon atoms substituted with an acidic group” represented by R ₁₆ or R ₁₇ in the general formula (I-1), (1) or (2) include carboxy Methyl group, 1-carboxyethyl group, 2-carboxyethyl group, 1,2-dicarboxyethyl group, 3-carboxypropyl group, 1,3-dicarboxypropyl group; sulfomethyl group, 2-sulfoethyl group; phosphomethyl group, 2-phosphoethyl group, 1-methyl-2-phosphoethyl group; other examples include an alkyl group substituted with a carboxyl group, a sulfonic acid group, a phosphoric acid group, a hydroxamic acid group, a phosphonic acid group, a boric acid group, or a phosphinic acid group. be able to. Among these, an alkyl group having 1 to 3 carbon atoms substituted with a carboxyl group or a phosphonic acid group is preferable, a methyl group or an ethyl group substituted with a carboxyl group is more preferable, a carboxymethyl group or a 1,2-dioxy group. A carboxyethyl group is particularly preferred.

Specific examples of the “unsubstituted alkyl group having 2 to 4 carbon atoms” represented by R ₁₆ or R ₁₇ in the general formula (I-1), (1) or (2) include an ethyl group, n Examples thereof include linear or branched alkyl groups having 2 to 4 carbon atoms such as -propyl group, isopropyl group, n-butyl group and t-butyl group. Among these, an ethyl group or an n-propyl group is preferable, and an ethyl group is more preferable.

In the general formula (I-1), (1) or (2), at least one of R _{16 and} R ₁₇ is an alkyl group having 1 to 3 carbon atoms substituted with an acidic group. . When p = 0, R ₁₆ does not exist, so R ₁₇ is an alkyl group having 1 to 3 carbon atoms substituted with an acidic group.

Specific examples of the acidic group represented by R ₁₈ in the general formula (I-2), (3), or (4) include a carboxyl group, a sulfonic acid group, a phosphoric acid group, a hydroxamic acid group, a phosphonic acid group, Examples thereof include an 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.

R ₁ is preferably a substituted or unsubstituted aryl group, and more preferably a substituted or unsubstituted phenyl group. R ₂ and R ₃ are preferably an optionally substituted alkyl group having 1 to 6 carbon atoms, more preferably an unsubstituted alkyl group having 1 to 6 carbon atoms, and particularly preferably a methyl group. R _{4 to} R ₉ are preferably a hydrogen atom or a disubstituted amino group, and particularly preferably a hydrogen atom. R _{10 to} R ₁₅ are preferably a hydrogen atom or an optionally substituted alkyl group having 1 to 6 carbon atoms, more preferably a hydrogen atom or a hexyl group, and particularly preferably a hydrogen atom. m is preferably an integer of 0 to 4, more preferably 0 or 1. n is preferably an integer of 0 to 4, more preferably 0 or 1. p is preferably an integer of 0 to 2, more preferably 0 or 1.

In general formula (I), Y is an adsorbing group represented by general formula (I-1) or (I-2). In the sensitizing dye for photoelectric conversion of the present invention, in the general formulas (I-1), (1) and (2), R ₁₆ or / and R ₁₇ are carboxymethyl group, 1,2-dicarboxyethyl group or ethyl group. When p is 0 or 1, or in the general formulas (I-2), (3), and (4), when R ₁₈ is a carboxyl group or a phosphonic acid group, on the surface of the semiconductor layer This is preferable because it can be easily adsorbed. In addition, it is preferable that R ₁ is a substituted or unsubstituted phenyl group, R ₂ and R ₃ are methyl groups, and R _{4 to} R ₉ are all hydrogen atoms because a particularly efficient photoelectric conversion element can be obtained.

The sensitizing dye for photoelectric conversion of the present invention represented by the general formula (I) or (1) to (4) includes all possible stereoisomers. Any isomer can be suitably used as a sensitizing dye for photoelectric conversion in the present invention. For example, when p = 0 in the general formula (1), the sensitizing dye for photoelectric conversion of the present invention includes compounds represented by the following general formulas (5) and (6), and when p = 1 Includes compounds represented by the following general formulas (7) to (10). Moreover, the sensitizing dye for photoelectric conversion of this invention represented by General formula (3) shall include the compound represented by following General formula (11) and (12). In addition, the sensitizing dye for photoelectric conversion of the present invention may be a mixture of two or more selected from these stereoisomers.

  Specific examples of the sensitizing dye for photoelectric conversion represented by the general formula (I) of the present invention 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 represented by the general formula (I) or (1) to (4) can be synthesized using a known method. For example, in the general formula (1), when m = 0 and n = 0, the aryl lithium generated by the metal halogen exchange between the corresponding bromo compound (B-1) and butyllithium is captured by DMF. Formyl body (B-2) is obtained. Then, the sensitizing dye for photoelectric conversion of the present invention can be synthesized by performing a condensation reaction with a rhodanine compound such as rhodanine-3-acetic acid. In the general formula (1), when m = 1 to 4 and n = 0, the corresponding bromo compound (B-1) and a boronic acid having a formyl group such as 4-formylphenylboronic acid (B— Using 3), a formyl body (B-4) is obtained by performing a cross-coupling reaction such as Suzuki coupling. Then, it can synthesize | combine by performing condensation reaction of the obtained formyl body (B-4) and rhodanine compounds, such as rhodanine-3-acetic acid. Further, in the general formula (1), when m = 1 to 4 and n = 1 to 4, it has a corresponding bromo compound (B-5) and a formyl group such as 5-formyl-2-thiopheneboronic acid. Formyl body (B-7) can be obtained by performing a cross coupling reaction such as Suzuki coupling using boronic acid (B-6). Thereafter, the sensitizing dye for photoelectric conversion of the present invention can be synthesized by performing a condensation reaction with a rhodanine compound such as rhodanine-3-acetic acid.

The sensitizing dye for photoelectric conversion of the present invention represented by the general formula (3) can also be synthesized by the same method as the sensitizing dye for photoelectric conversion of the present invention represented by the general formula (1). That is, for example, by using cyanoacetic acid or cyanomethylphosphonic acid instead of rhodanine compound such as rhodanine-3-acetic acid, a condensation reaction with formyl (B-2), (B-4), (B-7) is carried out. By doing so, it can be synthesized. In addition, about the bromo body (B-1) or (B-5) used as a starting material, it is compoundable by a well-known method (for example, refer patent document 6). For example, N- (9,9-dimethylfluoren-2-yl) -2-bromoaniline is synthesized by a reaction of 2-bromoaniline and 9,9-dimethyl-2-iodofluorene, and a cyclization reaction is performed. Thus, 12,12-dimethyl-10,12-dihydro-indeno [2,1-b] carbazole can be synthesized. Subsequently, 12,12-dimethyl-10-phenyl-10,12-dihydroindeno [2,1-b] carbazole can be synthesized by performing a condensation reaction such as an Ullmann reaction with iodobenzene. Furthermore, 7-bromo-12,12-dimethyl-10-phenyl-10,12-dihydroindeno [2,1-b] carbazole can be synthesized by bromination with N-bromosuccinimide or the like. it can. Here, by using 2-bromoaniline, 2-iodofluorene, or an iodo compound substituted with a corresponding substituent as a raw material, a bromo compound (B-1) having various substituents can be synthesized.

  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, the above general formula (I) or ( Sensitizing dyes other than 1) to (4) can 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.

  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, acetonitrile, and N, N-dimethylformamide 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 Examples include, but are not limited to, organic hole transport materials such as phenylamine derivatives, pyrazoline derivatives, fluorenone derivatives, hydrazone compounds, and stilbene compounds.

  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, and phenoxy resin. 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. The dye-sensitized solar cell of the present invention is a module in which the photoelectric conversion element containing the sensitizing dye represented by the general formula (I) or (1) to (4) is a cell, and the required number of cells are arranged. Obtained by providing predetermined electrical wiring.

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-5) 20 ml of toluene, 5 ml of ethanol, and 5 ml of water were added to a reaction vessel, and 12,12-dimethyl-10-phenyl-10,12-dihydro was added thereto. 0.50 g of the following compound (C-1) obtained by brominating indeno [2,1-b] carbazole with N-bromosuccinimide, 0.22 g of 4-formylphenylboronic acid, and 0.47 g of potassium carbonate. In addition, after stirring, depressurization, degassing, and nitrogen substitution in the reaction vessel were repeated 5 times. Next, 0.07 g of tetrakis (triphenylphosphine) palladium was added, and the mixture was stirred with heating at 73 ° C. for 5 hours. After the reaction solution was cooled to room temperature, extraction operation was performed by adding 10 ml of toluene and 20 ml of water. The organic layer was dried over magnesium sulfate and then concentrated under reduced pressure to obtain a crude product. The obtained crude product was purified by silica gel column chromatography (developing solvent: toluene) and dried under reduced pressure to obtain 0.41 g (yield 77%) of the following compound (C-2) as a yellow solid.

To the reaction vessel were added 26 ml of toluene, 0.40 g of compound (C-2), 0.18 g of rhodanine-3-acetic acid, and 0.11 g of piperidine, and the mixture was heated and stirred at 110 ° C. for 3 hours. After cooling to room temperature, the solid was collected by filtration. The obtained solid was dissolved in 50 ml of chloroform, and extraction operation was performed by adding 100 ml of 1M hydrochloric acid. The organic layer was dried over sodium sulfate and concentrated under reduced pressure to obtain 0.38 g (yield 69%) of an orange powder of a sensitizing dye for photoelectric conversion (A-5).

  The structure of the obtained orange 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) = 1.47-1.57 (6H), 4.92-4.98 (2H), 7.27-7.33 (1H), 7.35-7.47 (4H), 7 .52-7.58 (1H), 7.60-7.72 (7H), 7.84-7.91 (4H), 8.45-8.52 (2H).

[Synthesis Example 2] Synthesis of sensitizing dye for photoelectric conversion (A-6) 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, a crude product was obtained by concentrating the solution obtained by adding 20 ml of chloroform under reduced pressure. The obtained crude product was purified by silica gel column chromatography (developing solvent: hexane / ethyl acetate = 3/1) and dried under reduced pressure to obtain 5.56 g of the following compound (C-3) (yield 32%). Of a yellow solid was obtained.

To the reaction vessel, 5.00 g of compound (C-3), 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-4) as a yellow powder.

To the reaction vessel were added 25 ml of toluene, 0.27 g of compound (C-4), 0.40 g of compound (C-2) obtained in Synthesis Example 1, and 0.18 g of piperidine, and the mixture was heated and stirred at 103 ° C. for 2 hours. After cooling to room temperature, the solid was collected by filtration. The obtained solid was dissolved in 50 ml of chloroform, and extraction operation was performed by adding 100 ml of 1M hydrochloric acid. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure to obtain 0.63 g (yield 96%) of an orange powder of a sensitizing dye for photoelectric conversion (A-6).

[Synthesis Example 3] Synthesis of sensitizing dye for photoelectric conversion (A-31) 25 ml of dimethyl sulfoxide, 0.58 g of the compound (C-1), 0.26 g of 5-formyl-2-thiopheneboronic acid, acetic acid After adding 0.16 g of potassium and 0.02 g of palladium acetate and stirring, the pressure reduction, deaeration, and nitrogen substitution in the reaction vessel were repeated four times. Next, 0.07 g of butylbis (1-adamantyl) phosphine was added, and the mixture was heated and stirred at 80 ° C. for 3 hours. After cooling the reaction solution to room temperature, extraction operation was performed by adding 200 ml of chloroform and 100 ml of water. The organic layer was dried over magnesium sulfate and then concentrated under reduced pressure to obtain a crude product. The obtained crude product was purified by silica gel column chromatography (developing solvent: hexane / ethyl acetate = 5/1) and dried under reduced pressure to give 0.46 g (74% yield) of the following compound (C-5). Of a yellow solid was obtained.

To the reaction vessel were added 40 ml of toluene, 0.60 g of compound (C-5), 0.30 g of rhodanine-3-acetic acid, and 0.17 g of piperidine, and the mixture was heated and stirred at 60 ° C. for 2 hours. After cooling to room temperature, the solid was collected by filtration. The obtained solid was dissolved in 50 ml of chloroform, and extraction operation was performed by adding 100 ml of 1M hydrochloric acid. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure to obtain 0.57 g (yield 70%) of a yellow powder of a sensitizing dye for photoelectric conversion (A-31).

[Synthesis Example 4] Synthesis of a sensitizing dye for photoelectric conversion (A-85) 30 ml of toluene, 0.40 g of the compound (C-2) obtained in Synthesis Example 1, 0.08 g of cyanoacetic acid, 0. 11 g was added and stirred with heating at 105 ° C. for 3 hours. After cooling to room temperature, the solid was collected by filtration. The obtained solid was dissolved in 50 ml of chloroform, and extraction operation was performed by adding 100 ml of 1M hydrochloric acid. The organic layer was dried over sodium sulfate and concentrated under reduced pressure to obtain 0.46 g (yield 75%) of a yellow powder of a sensitizing dye for photoelectric conversion (A-85).

[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-5) obtained in Synthesis Example 1 is dissolved in a mixed solvent of acetonitrile / tert-butyl alcohol = 1/1 to prepare 50 ml of a 100 μM concentration solution. 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 2 to 11]
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-5) 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 1-2]
As the sensitizing dye for photoelectric conversion, in place of (A-5), it was carried out except that the sensitizing dye for photoelectric conversion shown in the following (D-1) and (D-2) not belonging to the present invention was used. 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.

[Example 12]
As a sensitizing dye for photoelectric conversion, (A-6) is used instead of (A-5), and as a solvent for dissolving the sensitizing dye for photoelectric conversion, a mixed solvent of acetonitrile / tert-butyl alcohol = 1/1 A photoelectric conversion element was prepared in the same manner as in Example 1 except that tetrahydrofuran was used instead, 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 2.

[Examples 13 to 22]
A photoelectric conversion element was prepared in the same manner as in Example 12 except that the sensitizing dye shown in Table 2 was used instead of (A-6) 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 2.

[Comparative Examples 3 to 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-3) and (D-4) not belonging to the present invention was used instead of (A-6). A photoelectric conversion element was produced in the same manner as in Example 12, 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 2.

From the results of Table 1 and Table 2, by using the sensitizing dye for photoelectric conversion of the present invention, a photoelectric conversion element that has high photoelectric conversion efficiency and can maintain high photoelectric conversion efficiency even if light irradiation is continued for a long time. It turned out to be obtained. Among Examples 1 to 11 using a mixed solvent of acetonitrile / tert-butyl alcohol as a solvent for dissolving the sensitizing dye for photoelectric conversion, the photoelectric conversion elements obtained in Examples 1 to 5, 10 and 11 were used. The photoelectric conversion efficiency was particularly excellent. Moreover, in Examples 12-22 using tetrahydrofuran as a solvent for dissolving the sensitizing dye for photoelectric conversion, the photoelectric conversion efficiency of the photoelectric conversion elements obtained in Examples 12-17, 21, and 22 is particularly excellent. It was. 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 (13)

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

Wherein represents R ₁ to R ₃ which may have a substituent alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group. R _{4 to} R ₉ may be the same or different, and may be a hydrogen atom, a halogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group, an amino group, Represents a monosubstituted amino group or a disubstituted amino group. R _{10 to} R ₁₅ 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 having 2 carbon atoms. Represents an alkenyl group of ˜6. Here, R ₁₀ and R ₁₁ , R ₁₂ and R ₁₃ , R ₁₄ and R ₁₅ may be bonded to each other to form a ring. 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. When a plurality of R _{10 to} R ₁₃ are present (when m = 2 to 4), R ₁₀ , R ₁₁ , R ₁₂ , and R ₁₃ may be the same or different. When a plurality of R ₁₄ and R ₁₅ are present (when n = 2 to 4), R ₁₄ and R ₁₅ may be the same as or different from each other. Y is an adsorptive group represented by the following general formula (I-1) or (I-2).

In the formula, R ₁₆ and R ₁₇ may be the same or different and each represents an alkyl group having 1 to 3 carbon atoms substituted with an acidic group or an unsubstituted alkyl group having 2 to 4 carbon atoms. However, at least one of R _{16 and} R ₁₇ is an alkyl group having 1 to 3 carbon atoms substituted with an acidic group. p represents an integer of 0 to 2. When two R ₁₆ exist (when p = 2), each may be the same as or different from each other.

In the formula, R ₁₈ represents an acidic group. 2. The sensitizing dye for photoelectric conversion according to claim 1, wherein the sensitizing dye for photoelectric conversion represented by the general formula (I) is represented by the following general formula (1).

Wherein represents R ₁ to R ₃ which may have a substituent alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group. R _{4 to} R ₉ may be the same or different, and may be a hydrogen atom, a halogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group, an amino group, Represents a monosubstituted amino group or a disubstituted amino group. R _{10 to} R ₁₅ 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 having 2 carbon atoms. Represents an alkenyl group of ˜6. Here, R ₁₀ and R ₁₁ , R ₁₂ and R ₁₃ , R ₁₄ and R ₁₅ may be bonded to each other to form a ring. R ₁₆ and R ₁₇ may be the same or different and each represents an alkyl group having 1 to 3 carbon atoms substituted with an acidic group or an unsubstituted alkyl group having 2 to 4 carbon atoms. However, at least one of R _{16 and} R ₁₇ is an alkyl group having 1 to 3 carbon atoms substituted with an acidic group. 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 a plurality of R _{10 to} R ₁₃ are present (when m = 2 to 4), R ₁₀ , R ₁₁ , R ₁₂ , and R ₁₃ may be the same or different. When a plurality of R ₁₄ and R ₁₅ are present (when n = 2 to 4), R ₁₄ and R ₁₅ may be the same as or different from each other. When a plurality of R ₁₆ are present (when p = 2), each may be the same as or different from each other. The sensitizing dye for photoelectric conversion represented by the general formula (1) is represented by the following general formula (2).

Wherein represents R ₁ to R ₃ which may have a substituent alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group. R _{4 to} R ₉ may be the same or different, and may be a hydrogen atom, a halogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group, an amino group, Represents a monosubstituted amino group or a disubstituted amino group. R ₁₆ and R ₁₇ may be the same or different and each represents an alkyl group having 1 to 3 carbon atoms substituted with an acidic group or an unsubstituted alkyl group having 2 to 4 carbon atoms. However, at least one of R _{16 and} R ₁₇ is an alkyl group having 1 to 3 carbon atoms substituted with an acidic group. m represents 0 or 1, n represents 0 or 1, and p represents 0 or 1. The general formula (1) or (2) is characterized in that at least one of R _{16 and} R ₁₇ is an alkyl group having 1 to 3 carbon atoms substituted with a carboxyl group. Or the sensitizing dye for photoelectric conversion of any one of Claim 3. 5. The photoelectric device according to claim 2, wherein in the general formula (1) or (2), at least one of R _{16 and} R ₁₇ is a carboxymethyl group. Sensitizing dye for conversion. In the general formula (1) or (2), R ₁₆ and R ₁₇ are groups selected from a carboxymethyl group, a 1,2-dicarboxyethyl group or an ethyl group, and at least R ₁₆ or R ₁₇ Any one of these is a carboxymethyl group or a 1, 2- dicarboxyethyl group, The sensitizing dye for photoelectric conversion of any one of Claims 2-5 characterized by the above-mentioned. In the general formula (1) or (2), R ₁ is a substituted or unsubstituted phenyl group, R ₂ and R ₃ are methyl groups, and all of R _{4 to} R ₉ are hydrogen atoms. The sensitizing dye for photoelectric conversion according to any one of claims 2 to 6, wherein: 2. The sensitizing dye for photoelectric conversion according to claim 1, wherein the sensitizing dye for photoelectric conversion represented by the general formula (I) is represented by the following general formula (3).

Wherein represents R ₁ to R ₃ which may have a substituent alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group. R _{4 to} R ₉ may be the same or different, and may be a hydrogen atom, a halogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group, an amino group, Represents a monosubstituted amino group or a disubstituted amino group. R _{10 to} R ₁₅ 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 having 2 carbon atoms. Represents an alkenyl group of ˜6. Here, R ₁₀ and R ₁₁ , R ₁₂ and R ₁₃ , R ₁₄ and R ₁₅ may be bonded to each other to form a ring. R ₁₈ represents an acidic group. 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. When a plurality of R _{10 to} R ₁₃ are present (when m = 2 to 4), R ₁₀ , R ₁₁ , R ₁₂ , and R ₁₃ may be the same or different. When a plurality of R ₁₄ and R ₁₅ are present (when n = 2 to 4), R ₁₄ and R ₁₅ may be the same as or different from each other. The sensitizing dye for photoelectric conversion represented by the general formula (3) is represented by the following general formula (4).

Wherein represents R ₁ to R ₃ which may have a substituent alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group. R _{4 to} R ₉ may be the same or different, and may be a hydrogen atom, a halogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group, an amino group, Represents a monosubstituted amino group or a disubstituted amino group. R ₁₈ represents an acidic group. m represents 0 or 1, and n represents 0 or 1. In the general formula (3) or (4), R ₁ is a substituted or unsubstituted phenyl group, R ₂ and R ₃ are methyl groups, and all of R _{4 to} R ₉ are hydrogen atoms. The sensitizing dye for photoelectric conversion according to claim 8, wherein the sensitizing dye is for photoelectric conversion. 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 claims 1 to 10 is supported on the semiconductor layer. A photoelectric conversion element obtained by The photoelectric conversion element according to claim 11, 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 11 and 12 and providing predetermined electrical wiring.

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