JP2013065527A - Dye for dye-sensitized solar cell, semiconductor electrode, and dye-sensitized solar cell - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a dye for a dye-sensitized solar cell, having a color tone of blue purple to blue, and having an excellent photoelectric conversion characteristic, to provide a semiconductor electrode sensitized by the dye for a dye-sensitized solar cell, and to provide a dye-sensitized solar cell using the semiconductor electrode.SOLUTION: A tertiary nitrogen atom of an indoline ring acts as an electron donative portion (donor) and a quaternary nitrogen atom of a benzothiazolium ring acts as an electron-withdrawing portion (acceptor), and both of them have a structure coupled by conjugated double bond. The semiconductor electrode, sensitized with a dye having the above-mentioned chemical structure and the dye-sensitized solar cell, formed by using the semiconductor electrode, are provided.

Description

  The present invention relates to a dye for a dye-sensitized solar cell, a semiconductor electrode, and a dye-sensitized solar cell.

  Global warming due to the increase in carbon dioxide concentration caused by the use of large amounts of fossil fuels, and the increase in energy demand accompanying population growth are recognized as problems related to the survival of humankind. Therefore, in recent years, the use of sunlight that does not generate infinite and harmful substances has been energetically studied. Examples of solar energy that is currently used as a clean energy source include residential single crystal silicon, polycrystalline silicon, amorphous silicon, and inorganic solar cells such as cadmium telluride and indium copper selenide.

  However, these inorganic solar cells also have drawbacks. For example, a silicon system is required to have a very high purity. Naturally, the purification process is complicated, the number of processes is large, and the manufacturing cost is high. In addition, there is a demand for weight reduction and the like, and in particular, it is disadvantageous in that payback to the user is long, and there is a problem in the spread.

  On the other hand, many solar cells using organic materials have been proposed. As an organic solar cell, a Schottky photoelectric conversion element that joins a p-type organic semiconductor and a metal having a low work function, a p-type organic semiconductor and an n-type inorganic semiconductor, or a p-type organic semiconductor and an electron-accepting organic compound are joined. There are heterojunction photoelectric conversion elements and the like, and organic semiconductors used are synthetic dyes and pigments such as chlorophyll and perylene, conductive polymer materials such as polyacetylene, or composite materials thereof. These are thinned by a vacuum deposition method, a casting method, a dipping method or the like to form a battery material. Although organic materials have advantages such as low cost and easy area enlargement, there are many problems that the photoelectric conversion efficiency is as low as 1% or less, and the durability is poor.

  Under such circumstances, a solar cell exhibiting good characteristics has been reported by Dr. Gretzell of Switzerland (see, for example, Non-Patent Document 1). This document also discloses materials and manufacturing techniques necessary for battery fabrication. This solar cell is called a dye-sensitized solar cell or a Gretzel solar cell, and is a wet solar cell using a titanium oxide porous thin film spectrally sensitized with a ruthenium complex (hereinafter referred to as Ru complex) as a working electrode. The advantage of this method is that it is not necessary to purify an inexpensive semiconductor such as titanium oxide to a high purity, so that the manufacturing cost can be reduced compared to the inorganic solar cell described above, and the available light is in the visible light region. Because it is widespread, it is possible to effectively convert sunlight, which has a high energy intensity in the visible light region, into electricity.

  However, since noble metal Ru, which has resource limitations, is used, there is a possibility that a problem may occur in the stable supply of the Ru complex when a dye-sensitized solar cell is put into practical use. In addition, due to this resource limitation, the Ru complex itself is expensive, and there may be a problem in terms of cost during mass production. In order to solve such a problem, various proposals have been made for the purpose of changing at least part of the Ru complex to a cheaper organic dye. For example, various merocyanine dyes, cyanine dyes, 9-phenylxanthene dyes, coumarin dyes, and the like have been disclosed, but these are considerably inferior to Ru complexes in terms of photoelectric conversion characteristics, and are practical. Most of them were poor (see, for example, Patent Documents 1 to 4).

  In addition, since organic dyes have clear colors such as yellow, red, and blue, which are not found in ruthenium complexes, many applications have been proposed for design applications that make use of the colors (for example, Non-Patent Document 2). reference). Among them, various styryl dyes, squarylium ring-containing dyes, and the like have been proposed as dyes having a blue-violet to blue color tone (see, for example, Patent Documents 5 and 6), but have sufficient photoelectric conversion characteristics. There is almost no pigment, and further improvements are required.

  On the other hand, JP 2005-82678 A (Patent Document 7) and JP 2010-49990 A (Patent Document 8) are derived from an indoline ring having a specific structure and a nitrogen-containing heterocyclic quaternary salt. Hemicyanine dyes are disclosed. However, although these publications have some examples of the substituents of the tertiary nitrogen atom of the indoline ring, details regarding the influence of these substituents and the substitution position on the photoelectric conversion characteristics of the hemicyanine dye are detailed. There is no description. Therefore, with respect to the hemicyanine dye, it has not been possible to predict how the photoelectric conversion characteristics of the dye can be improved by manipulation of the substituent of the tertiary nitrogen atom of the indoline ring.

JP 11-238905 A JP 2001-76773 A Japanese Patent Laid-Open No. 10-92477 JP 2002-164089 A JP 2003-234133 A JP 2007-70509 A JP 2005-82678 A JP 2010-49990 A

Nature, 353, 737 (1991) Applied Physics, Vol. 73, No. 12, 1549 (2004)

  An object of the present invention is to provide a dye-sensitized solar cell dye having a color tone of bluish purple to blue and having excellent photoelectric conversion characteristics, a semiconductor electrode sensitized by the dye-sensitized solar cell dye, and The object is to provide a dye-sensitized solar cell using the semiconductor electrode.

  As a result of intensive studies to solve the above-mentioned problems, the present inventors have found that a dye for a dye-sensitized solar cell represented by the general formula (1) (hereinafter referred to as “dye”), a semiconductor sensitized by this dye These goals could be achieved by a dye-sensitized solar cell using an electrode and a semiconductor electrode.

In the general formula (1), R ₁ is a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group, a cyano group, a carbamoyl group, an alkoxycarbonyl group, an aryloxycarbonyl group, a 2-oxazolinyl group, or 5,6-dihydro-4H. A substituent selected from any of -1,3-oxazin-2-yl groups is shown. R ₂ and R ₃ represent a hydrogen atom or an alkyl group, and both may be linked to form a cyclopentane ring or a cyclohexane ring. L ₁ and L _{2 each} represent a conjugated methine group unit. L ₃ represents an alkylene group. R ₄ represents an electron donating group in which Hammett's substituent constant σp value is negative. R ₅ represents an acidic group having a pKa of less than 6. X ⁻ represents a counter anion.

  The dye represented by the general formula (1) has a vivid blue-violet to blue color tone and excellent photoelectric conversion characteristics. By sensitizing with this dye, the blue-violet to blue color tone is obtained. A semiconductor electrode having excellent photoelectric conversion efficiency and a dye-sensitized solar cell using the semiconductor electrode can be obtained.

The dye of the present invention is described in detail below. In the general formula (1), R ₁ represents a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group, a cyano group, a carbamoyl group (for example, a carbamoyl group, an N-methylcarbamoyl group, an N-ethylcarbamoyl group, an N-propyl group). Carbamoyl group, N-butylcarbamoyl group, N-pentylcarbamoyl group, N-hexylcarbamoyl group, N-heptylcarbamoyl group, N-octylcarbamoyl group, N-decylcarbamoyl group, N, N-dimethylcarbamoyl group, N, N -Diethylcarbamoyl group, N, N-dipropylcarbamoyl group, N-methyl-N-ethylcarbamoyl group, N-methyl-N-propylcarbamoyl group, N-methyl-N-butylcarbamoyl group, N-ethyl-N- Propylcarbamoyl group, N-ethyl-N-butylcarba Moyl group, N, N-pentamethylenecarbamoyl group, N, N-hexamethylenecarbamoyl group, N-phenylcarbamoyl group, N- (1-naphthyl) carbamoyl group, N- (2-naphthyl) carbamoyl group, N- ( 2-pyridyl) carbamoyl group, N- (3-pyridyl) carbamoyl group, N- (4-pyridyl) carbamoyl group, N-methyl-N-phenylcarbamoyl group, N-ethyl-N-phenylcarbamoyl group, N, N -Diphenylcarbamoyl group, etc.), alkoxycarbonyl group (eg, methoxycarbonyl group, ethoxycarbonyl group, propoxycarbonyl group, butoxycarbonyl group, pentyloxycarbonyl group, hexyloxycarbonyl group, octyloxycarbonyl group, decyloxycarbonyl group, etc.) , Aryloxycar Nyl group (for example, phenoxycarbonyl group, 1-naphthyloxycarbonyl group, 2-naphthyloxycarbonyl group, etc.), 2-oxazolinyl group, 5,6-dihydro-4H-1,3-oxazin-2-yl group The substituent selected from these is shown. The carbamoyl group, alkoxycarbonyl group and aryloxycarbonyl group described above may further have various substituents if possible. Examples of the substituent include aliphatic groups (for example, methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, decyl group, undecyl group, dodecyl group, tetradecyl group, Alkyl groups such as pentadecyl groups, alkenyl groups such as allyl groups and butenyl groups, alkynyl groups such as propargyl groups, benzyl groups, phenethyl groups, phenylpropyl groups, phenylbutyl groups, 1-naphthylmethyl groups, 2-naphthylmethyl groups, etc. Aralkyl groups, etc.), aromatic groups (eg, phenyl, tolyl, naphthyl, etc.), heterocyclic groups (eg, indolyl, pyridyl, furyl, thienyl, etc.), amino groups, vinyl groups, alkoxy Group, aryloxy group, alkylthio group, arylthio group, hydroxy group, carboxy group, alkoxycarbo Group, an aryloxycarbonyl group, there are halogen atoms or the like, and may further have a substituent, if they are possible. In addition, it is preferable that the above-described benzene ring to which R ₁ is bonded has no substituent other than R ₁ .

R ₂ and R ₃ are each a hydrogen atom or an alkyl group (for example, methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, decyl group, undecyl group, dodecyl group, tetradecyl group, Pentadecyl group or the like), and both may be linked to form a cyclopentane ring or a cyclohexane ring. Among them, preferred are those in which they are linked to form a cyclopentane ring or a cyclohexane ring, and particularly preferred are those in which both are linked to form a cyclopentane ring.

L ₁ and L _{2 each} represent a conjugated methine group unit. This conjugated methine group unit is composed of a conjugated methine chain having an odd number of carbon atoms. The number of carbon atoms is preferably 1 or 3, and particularly preferred are L ₁ and L ₂ having 1 carbon atom.

L ₃ represents an alkylene group (for example, a methylene group, an ethylene group, a propylene group, a tetramethylene group, a hexamethylene group, etc., which may be a linear structure or a branched structure). Of these, those having 1 to 4 carbon atoms are preferred, and those having 1 or 2 carbon atoms are particularly preferred.

R ₄ represents an electron donating group in which Hammett's substituent constant σp value is negative. The Hammett's σp value is described in various books. For example, “Structure-activity relationship of drugs—Guidelines for drug design and mechanism of action research” (Chemistry domain, extra number 122; Nankodo ( 1979)), Chem. Rev. 91, 165 (1991). Specific examples of these electron donating groups include alkyl groups (for example, methyl group, ethyl group, n-propyl group, n-butyl group, iso-butyl group, etc.), alkoxy groups (for example, methoxy group, ethoxy group). N-propoxy group, iso-propoxy group, n-butoxy group, n-hexyloxy group, n-octyloxy group, benzyloxy group, etc.), amino group (for example, amino group, methylamino group, ethylamino group, Dimethylamino group, diethylamino group, di-n-propylamino group, di-n-butylamino group, phenylamino group, diphenylamino group, acetylamino group, etc.), hydrazino group, ureido group, hydroxy group and the like. Of course, it is not limited to these. Of these, preferred are an alkyl group, an alkoxy group, a dialkyl-substituted amino group, a hydroxy group and the like, and among them, a dialkyl-substituted amino group, an alkoxy group and a hydroxy group are particularly preferred. Further, if possible, the above-described substituent may be further substituted with various substituents as long as the electron-donating factor of the substituent is not deactivated. Moreover, it is preferable that substituents other than the above-mentioned R ₄ do not exist on the benzothiazolium ring.

R ₅ represents an acidic group having a pKa of less than 6. Examples of the acidic group having a pKa of less than 6 include, for example, a carboxy group, a sulfo group, a sulfino group, a sulfeno group, a phosphono group, and a phosphinico group, and among them, a carboxy group is particularly preferable. These acidic groups may be free acids, such as salts (for example, ammonium salts such as ammonium salt, trimethylammonium salt, triethylammonium salt, tetra-n-butylammonium salt, lithium salt, sodium salt, potassium salt, etc. Alkali metal salts, etc.).

X ⁻ represents a counter anion. Examples thereof include halogen ions (for example, chloride, bromide, iodide, etc.), alkyl sulfate ions (for example, methyl sulfate ion, ethyl sulfate ion, etc.), organic sulfonate ions (for example, methanesulfonate, p-toluenesulfonate). Etc.) and perchlorate ions. Further, when the dye molecule forms an inner salt, this counter anion does not exist.

In the stilbene structure site in the general formula (1) described above, Z-type and E-type geometric isomers may be generated. In the present invention, any of these geometric isomers may be used. In addition, regarding the conjugated methine group units of L ₁ and L ₂ , geometrical isomers (cis type and trans type) of each conjugated carbon double bond may be generated. Any combination of geometric isomerism may be used.

When R ₂ and R ₃ in the general formula (1) are both alkyl groups, the carbon atoms at the 2-position and 3-position of the indoline ring to which R ₂ and R ₃ are respectively bonded are asymmetric carbons, There is a possibility that optical isomers of each site may be generated, but in the present invention, any combination of these optical isomers may be used.

  In the dye represented by the general formula (1) of the present invention, the tertiary nitrogen atom of the indoline ring is an electron donating site (donor), and the quaternary nitrogen atom of the benzothiazolium ring is an electron withdrawing site (acceptor). And has a structure in which both are linked by a conjugated double bond. In general, when molecularly designing a sensitizing dye in a photoelectric conversion material, in order to perform electron injection from the dye to the semiconductor more efficiently, an acid that promotes the adsorptivity to the semiconductor in the vicinity of the acceptor site into which electrons flow. Introduce a group. The dye adsorbs on the semiconductor via an acidic group that promotes adsorptivity. After the electron is injected into the semiconductor, the dye becomes a dye cation, and then regenerates as a dye by receiving electron injection from an electrolyte described later. The dye-sensitized solar cell exhibits a function as a battery by repeating the electron transfer cycle of the dye.

  Although the specific example of the pigment | dye of this invention is given to the following, this invention is not limited to these.

  These compounds can be easily synthesized with reference to known synthesis methods described in, for example, JP-A-2005-82678.

  The dye-sensitized solar cell includes a conductive support, a semiconductor layer (semiconductor electrode) sensitized with a dye provided on the surface of the conductive support, a charge transfer layer, and a counter electrode. The semiconductor layer may be a single layer structure or a stacked structure, and is designed according to the purpose. In addition, at the boundary of this element such as the boundary between the conductive layer and the semiconductor layer of the conductive support, the boundary between the semiconductor layer and the moving layer, the constituent components of each layer may be diffused or mixed with each other.

  As the conductive support, there can be used a support made of glass or plastic having a conductive layer containing a conductive agent on its surface, such as a metal having a conductive property in itself. In the latter case, the conductive agent is a metal oxide such as platinum, gold, silver, copper, aluminum or the like, carbon or indium-tin composite oxide (hereinafter abbreviated as “ITO”), fluorine-doped tin oxide or the like. (Hereinafter abbreviated as “FTO”) and the like. The conductive support preferably has a transparency that transmits light of 10% or more, and more preferably transmits 50% or more. Among these, conductive glass in which a conductive layer made of ITO or FTO is deposited on glass is particularly preferable.

  A metal lead wire may be used for the purpose of reducing the resistance of the transparent conductive substrate. Examples of the material of the metal lead wire include metals such as aluminum, copper, silver, gold, platinum, and nickel. A metal lead wire is installed on a transparent conductive support by vapor deposition, sputtering, pressure bonding, etc., and a method of providing ITO or FTO thereon, or a method of installing a metal lead wire on a transparent substrate having conductivity on the surface. is there.

  Examples of the semiconductor contained in the semiconductor layer include a single semiconductor such as silicon and germanium, a compound semiconductor typified by a metal chalcogenide, or a compound having a perovskite structure. Metal chalcogenides include titanium, tin, zinc, iron, tungsten, zirconium, hafnium, strontium, indium, cerium, yttrium, lanthanum, vanadium, niobium, or tantalum oxides, cadmium, zinc, lead, silver, antimony, bismuth. And sulfides, cadmium, selenide of lead, telluride of cadmium, and the like. Other compound semiconductors are preferably phosphides such as zinc, gallium, indium, cadmium, gallium arsenide, copper-indium-selenide, copper-indium-sulfide, and the like. As the compound having a perovskite structure, strontium titanate, calcium titanate, sodium titanate, barium titanate, potassium niobate and the like are preferable.

  The semiconductor used in the present invention may be single crystal or polycrystalline. From the viewpoint of photoelectric conversion efficiency, a single crystal is preferable, but from the viewpoint of manufacturing cost, securing raw materials, etc., polycrystalline is preferable. The particle size of the semiconductor is preferably 2 nm or more and 1 μm or less.

  Examples of a method for forming a semiconductor layer on a conductive support include a method in which a dispersion or colloidal solution of semiconductor fine particles is applied on a conductive support, a sol-gel method, and the like. As a method for preparing the dispersion, a sol-gel method, a method of mechanically pulverizing with a mortar, etc., a method of dispersing while pulverizing using a mill, or precipitating as fine particles in a solvent when synthesizing a semiconductor, The method of using as it is is mentioned.

  In the case of a dispersion prepared by mechanical pulverization or pulverization using a mill, the dispersion is prepared by dispersing at least semiconductor fine particles alone or a mixture of semiconductor fine particles and a resin in water or an organic solvent. Resins used include polymers and copolymers of vinyl compounds such as styrene, vinyl acetate, acrylic acid esters, methacrylic acid esters, silicone resins, phenoxy resins, polysulfone resins, polyvinyl butyral resins, polyvinyl formal resins, polyester resins. , Cellulose ester resin, cellulose ether resin, urethane resin, phenol resin, epoxy resin, polycarbonate resin, polyarylate resin, polyamide resin, polyimide resin and the like.

  As a medium for dispersing the semiconductor fine particles, alcohol media such as water, methanol, ethanol, or isopropyl alcohol, ketone media such as acetone, methyl ethyl ketone, or methyl isobutyl ketone, ethyl formate, ethyl acetate, or n-butyl acetate, etc. Ester media such as diethyl ether, dimethoxyethane, tetrahydrofuran, dioxolane, or dioxane, and amide media such as N, N-dimethylformamide, N, N-dimethylacetamide, or N-methyl-2-pyrrolidone , Dichloromethane, chloroform, bromoform, methyl iodide, dichloroethane, trichloroethane, trichloroethylene, chlorobenzene, o-dichlorobenzene, fluorobenzene, bromobenzene, iodine Halogenated hydrocarbon media such as debenzene or 1-chloronaphthalene, n-pentane, n-hexane, n-octane, 1,5-hexadiene, cyclohexane, methylcyclohexane, cyclohexadiene, benzene, toluene, o-xylene, Examples thereof include hydrocarbon-based media such as m-xylene, p-xylene, ethylbenzene, and cumene. These can be used alone or as a mixed medium of two or more.

  Examples of the dispersion application method include a roller method, a dip method, an air knife method, a blade method, a wire bar method, a slide hopper method, an extrusion method, a curtain method, a spin method, and a spray method.

  The semiconductor layer may be a single layer or multiple layers. In the case of multiple layers, a dispersion of semiconductor fine particles having different particle diameters can be applied in multiple layers, or different types of semiconductors, and application layers having different compositions of resins and additives can be applied in multiple layers. In addition, when the film thickness is insufficient with a single coating, the multilayer coating is an effective means.

  In general, as the thickness of the semiconductor layer increases, the amount of supported dye increases per unit projected area and the light capture rate increases. However, the diffusion distance of the generated electrons also increases, and the recombination of charges also increases. End up. Therefore, the film thickness of the semiconductor layer is preferably 0.1 to 100 μm, and more preferably 1 to 30 μm.

The semiconductor fine particles may or may not be heat-treated after being coated on the conductive support. However, heat treatment is preferred from the viewpoints of electronic contact between fine particles, improvement in coating film strength, and improvement in adhesion to the support. Further, microwave irradiation, press treatment, or electron beam irradiation may be performed. These treatments may be performed alone or in combination of two or more. In the heat treatment, the heating temperature is preferably 40 to 700 ° C, more preferably 80 to 600 ° C. The heating time is preferably 5 minutes to 50 hours, and more preferably 10 minutes to 20 hours. Microwave irradiation may be performed from the semiconductor layer forming side of the semiconductor electrode or from the back side. Although there is no restriction | limiting in particular in irradiation time, It is preferable to carry out within 1 hour. The press treatment is preferably performed at 9.8 × 10 ⁶ N / m ² or more, and more preferably at 9.8 × 10 ⁷ N / m ² or more. The pressing time is not particularly limited, but is preferably within 1 hour.

  The semiconductor fine particles preferably have a large surface area so that many dyes can be adsorbed. For this reason, it is preferable that the surface area in the state which coated the semiconductor layer on the support body is 10 times or more with respect to a projection area, and it is more preferable that it is 100 times or more.

  The dye-sensitized solar cell dye represented by the general formula (1) of the present invention may be used alone or in combination of two or more. In addition, for the purpose of reducing the amount of Ru used in a dye-sensitized solar cell that also uses a ruthenium (Ru) complex, the dye of the present invention and a Ru complex may be used in combination. Other merocyanine dyes, cyanine dyes, 9-phenylxanthene dyes, coumarin dyes, phthalocyanine dyes, naphthalocyanine dyes and the like may be used in combination.

  As a method of adsorbing the dye to the semiconductor layer, a method of immersing a working electrode containing semiconductor fine particles in a dye solution or a dye dispersion, or a method of applying a dye solution or a dispersion to the semiconductor layer and adsorbing it is used. Can do. In the former case, dipping method, dipping method, roller method, air knife method, etc. can be used, and in the latter case, wire bar method, slide hopper method, extrusion method, curtain method, spin method, spray method, etc. Can be used.

  When adsorbing the dye, a condensing agent may be used in combination. The condensing agent may be either catalytically acting that physically or chemically binds the dye to the inorganic surface, or one that acts stoichiometrically to favorably shift the chemical equilibrium. . Furthermore, you may add a thiol or a hydroxy compound as a condensation adjuvant.

  The medium for dissolving or dispersing the pigment is water, methanol, ethanol, isopropyl alcohol, alcohol-based media such as t-butyl alcohol, ketone-based media such as acetone, methyl ethyl ketone, or methyl isobutyl ketone, ethyl formate, ethyl acetate, or Ester media such as n-butyl acetate, ether media such as diethyl ether, dimethoxyethane, tetrahydrofuran, dioxolane, or dioxane, nitrile media such as acetonitrile and propionitrile, N, N-dimethylformamide, N, N- Amide-based media such as dimethylacetamide or N-methyl-2-pyrrolidone, dichloromethane, chloroform, bromoform, methyl iodide, dichloroethane, trichloroethane, trichloroethylene, Halogenated hydrocarbon media such as lobenzene, o-dichlorobenzene, fluorobenzene, bromobenzene, iodobenzene, or 1-chloronaphthalene, n-pentane, n-hexane, n-octane, 1,5-hexadiene, cyclohexane, Examples thereof include hydrocarbon-based media such as methylcyclohexane, cyclohexadiene, benzene, toluene, o-xylene, m-xylene, p-xylene, ethylbenzene, and cumene. These can be used alone or in admixture of two or more.

  The temperature for adsorbing the dye is preferably -50 ° C or higher and 200 ° C or lower. Further, the adsorption may be performed while stirring. Examples of the stirring method include, but are not limited to, a stirrer, a ball mill, a paint conditioner, a sand mill, an attritor, a disperser, and ultrasonic dispersion. The time required for adsorption is preferably 5 seconds to 1000 hours, more preferably 10 seconds to 500 hours, and even more preferably 1 minute to 150 hours.

  In the present invention, when the dye is adsorbed on the semiconductor layer, a steroidal compound may be used in combination and co-adsorbed.

  Specific examples of the steroidal compound include those shown in E-1 to E-10 below. The amount of the steroidal compound is preferably 0.01 to 1000 parts by mass and more preferably 0.1 to 100 parts by mass with respect to 1 part by mass of the pigment.

  After adsorbing the dye, or after co-adsorbing the dye and the steroidal compound, basic compounds such as t-butylpyridine, 2-picoline, 2,6-lutidine, or phosphoric acid, phosphate ester, alkyl You may immerse in the organic solvent containing acidic compounds, such as phosphoric acid, an acetic acid, and propionic acid.

  As the charge transfer layer, an electrolytic solution in which a redox couple is dissolved in an organic solvent, a gel electrolyte in which a polymer matrix is impregnated with a liquid in which the redox couple is dissolved in an organic solvent, a molten salt containing a redox couple, a solid electrolyte, an inorganic A hole transport material, an organic hole transport material, or the like can be used.

  The electrolytic solution is preferably composed of an electrolyte, a solvent, and an additive. Preferred electrolytes are metal iodide-iodine combinations such as lithium iodide, sodium iodide, potassium iodide, cesium iodide, and calcium iodide, and quaternary compounds such as tetraalkylammonium iodide, pyridinium iodide, and imidazolium iodide. Iodine salt of ammonium compound-iodine combination, metal bromide-bromine combination such as lithium bromide, sodium bromide, potassium bromide, cesium bromide, calcium bromide, quaternary ammonium such as tetraalkylammonium bromide, pyridinium bromide Bromine-bromine combinations of compounds, metal complexes such as ferrocyanate-ferricyanate, ferrocene-ferricinium ions, sulfur compounds such as sodium polysulfide, alkylthiol-alkyldisulfides, viologen Dye, hydroquinone - quinones, and the like. The above-mentioned electrolytes may be a single combination or a mixture. Further, a molten salt in a molten state at room temperature can also be used as the electrolyte. When this molten salt is used, it is not necessary to use a solvent.

  The electrolyte concentration in the electrolytic solution is preferably 0.05 to 20M, and more preferably 0.1 to 15M. Solvents used for the electrolyte include carbonate solvents such as ethylene carbonate and propylene carbonate, heterocyclic compounds such as 3-methyl-2-oxazolidinone, ether solvents such as dioxane, diethyl ether and ethylene glycol dialkyl ether, methanol, ethanol Alcohol solvents such as polypropylene glycol monoalkyl ether, nitrile solvents such as acetonitrile and benzonitrile, aprotic polar solvents such as dimethyl sulfoxide and sulfolane are preferred. Further, basic compounds such as t-butylpyridine, 2-picoline, and 2,6-lutidine may be used in combination.

  The electrolyte can also be gelled by techniques such as polymer addition, oil gelling agent addition, polymerization including polyfunctional monomers, and polymer crosslinking reaction. Preferable polymers in the case of gelation by polymer addition include polyacrylonitrile, polyvinylidene fluoride and the like. Preferred gelling agents for gelation by adding an oil gelling agent include dibenzylidene-D-sorbitol, cholesterol derivatives, amino acid derivatives, trans- (1R, 2R) -1,2-cyclohexanediamine alkylamide derivatives, alkyl Examples include urea derivatives, N-octyl-D-gluconamide benzoate, double-headed amino acid derivatives, quaternary ammonium derivatives, and the like.

  Preferred monomers for polymerization with a polyfunctional monomer include divinylbenzene, ethylene glycol dimethacrylate, ethylene glycol diacrylate, diethylene glycol dimethacrylate, triethylene glycol dimethacrylate, pentaerythritol triacrylate, trimethylolpropane triacrylate, and the like. be able to. Furthermore, esters and amides derived from acrylic acid such as acrylamide and methyl acrylate and α-alkyl acrylic acid, esters derived from maleic acid and fumaric acid such as dimethyl maleate and diethyl fumarate, butadiene, cyclohexane and the like. Dienes such as pentadiene, aromatic vinyl compounds such as styrene, p-chlorostyrene and sodium styrene sulfonate, vinyl esters, acrylonitrile, methacrylonitrile, vinyl compounds having a nitrogen-containing heterocyclic ring, vinyl having a quaternary ammonium salt A monofunctional monomer such as a compound, N-vinylformamide, vinylsulfonic acid, vinylidene fluoride, vinyl alkyl ethers, N-phenylmaleimide may be contained. 0.5-70 mass% is preferable and the polyfunctional monomer which occupies for the monomer whole quantity has more preferable 1.0-50 mass%.

  The above-mentioned monomers can be polymerized by radical polymerization. The monomer for gel electrolyte that can be used in the present invention can be radically polymerized by heating, light, electron beam or electrochemical. The polymerization initiator used when the crosslinked polymer is formed by heating is 2,2'-azobisisobutyronitrile, 2,2'-azobis (2,4-dimethylvaleronitrile), dimethyl-2 An azo initiator such as 2,2'-azobis (2-methylpropionate) and a peroxide initiator such as benzoyl peroxide are preferable. The addition amount of these polymerization initiators is preferably 0.01 to 20% by mass and more preferably 0.1 to 10% by mass with respect to the total amount of monomers.

  When the electrolyte is gelled by a polymer crosslinking reaction, it is desirable to use a polymer containing a reactive group necessary for the crosslinking reaction and a crosslinking agent in combination. Preferable examples of the reactive group necessary for the crosslinking reaction include nitrogen-containing heterocycles such as pyridine, imidazole, thiazole, oxazole, triazole, morpholine, piperidine and piperazine. Preferred cross-linking agents include bifunctional or higher functional reagents capable of electrophilic reaction with nitrogen atoms such as alkyl halides, halogenated aralkyls, sulfonic acid esters, acid anhydrides, acid chlorides, and isocyanates.

  When an inorganic hole transport material is used instead of the electrolyte, copper iodide, copper thiocyanide, or the like can be introduced into the electrode by a casting method, a coating method, a spin coating method, a dipping method, electrolytic plating, or the like.

  It is also possible to use an organic charge transport material instead of the electrolyte. Charge transport materials include hole transport materials and electron transport materials. Examples of the former include, for example, oxadiazoles disclosed in Japanese Patent Publication No. 34-5466, triphenylmethanes disclosed in Japanese Patent Publication No. 45-555, and Japanese Patent Publication No. 52-4188. Pyrazolines shown in the above, hydrazones shown in JP-B-55-42380, oxadiazoles shown in JP-A-56-123544, etc., JP-A-54-58445 And tetrasylbenzidines disclosed in JP-A No. 58-65440, and stilbenes disclosed in JP-A No. 60-98437. Among them, examples of the charge transport material used in the present invention are shown in JP-A-60-24553, JP-A-2-96767, JP-A-2-183260, and JP-A-2-226160. Particularly preferred are the hydrazones described, and the stilbenes shown in JP-A-2-51162 and JP-A-3-75660. Moreover, these can be used individually or in mixture of 2 or more types.

  On the other hand, examples of the electron transport material include chloranil, tetracyanoethylene, tetracyanoquinodimethane, 2,4,7-trinitro-9-fluorenone, 2,4,5,7-tetranitro-9-fluorenone, 2,4 , 5,7-tetranitroxanthone, 2,4,8-trinitrothioxanthone, 1,3,7-trinitrodibenzothiophene, 1,3,7-trinitrodibenzothiophene-5,5-dioxide, etc. . These electron transport materials can be used alone or as a mixture of two or more.

  Further, for the purpose of improving the charge transfer efficiency in the charge transfer layer, a certain electron withdrawing compound can be added to the charge transfer layer. Examples of the electron-withdrawing compound include quinones such as 2,3-dichloro-1,4-naphthoquinone, 1-nitroanthraquinone, 1-chloro-5-nitroanthraquinone, 2-chloroanthraquinone, and phenanthrenequinone, 4-nitro Aldehydes such as benzaldehyde, ketones such as 9-benzoylanthracene, indandione, 3,5-dinitrobenzophenone, or 3,3 ', 5,5'-tetranitrobenzophenone, phthalic anhydride, 4-chloronaphthalic anhydride Acid anhydrides such as terephthalalmalononitrile, 9-anthrylmethylidenemalononitrile, 4-nitrobenzalmalononitrile, or cyano compounds such as 4- (p-nitrobenzoyloxy) benzalmalononitrile, 3-benzalphthalide , 3- (α-cyano- - Nitorobenzaru) phthalide, or 3- (alpha-cyano -p- Nitorobenzaru) -4,5,6,7 can be mentioned phthalides such as tetrachloro phthalide like.

  When forming a charge transfer layer using a charge transport material, a resin may be used in combination. When resin is used in combination, polystyrene resin, polyvinyl acetal resin, polysulfone resin, polycarbonate resin, polyester resin, polyphenylene oxide resin, polyarylate resin, acrylic resin, methacrylic resin, phenoxy resin and the like can be mentioned. Among these, polystyrene resin, polyvinyl acetal resin, polycarbonate resin, polyester resin, and polyarylate resin are preferable. These resins may be used alone or as a copolymer in combination of two or more.

  There are two main methods for forming the charge transfer layer. One is a method in which a counter electrode is first bonded onto a semiconductor layer that has adsorbed a dye, and a liquid charge transfer layer is sandwiched in the gap. The other is a method in which a charge transfer layer is provided directly on a semiconductor layer adsorbed with a dye. In the latter case, a counter electrode is newly provided on the charge transfer layer.

  In the former case, examples of the method for sandwiching the charge transfer layer include a normal pressure process using a capillary phenomenon due to immersion and a vacuum process in which the gas phase is replaced with a liquid phase at a pressure lower than normal pressure. In the latter case, in the wet charge transfer layer, it is necessary to provide a counter electrode without being dried to prevent liquid leakage at the edge portion. In the case of a gel electrolyte, there is a method in which it is applied in a wet manner and solidified by a method such as polymerization. In that case, you may provide a counter electrode after drying and fixing. In addition to the electrolytic solution, the organic charge transport material solution and gel electrolyte can be applied in the same manner as the semiconductor layer and pigment application, as well as the immersion method, roller method, dipping method, air knife method, extrusion method, slide Examples thereof include a hopper method, a wire bar method, a spin method, a spray method, a casting method, and various printing methods.

  The counter electrode can be used on a support having a conductive layer in the same manner as the substrate having conductivity on the surface, but the support is not necessarily required when the conductive layer itself has sufficient strength and sealing properties. Specific examples of the material used for the counter electrode include metals such as platinum, gold, silver, copper, aluminum, rhodium and indium, carbon compounds, and conductive metal oxides such as ITO and FTO. There is no particular limitation on the thickness of the counter electrode.

  In order for light to reach the semiconductor layer, at least one of the conductive substrate and the counter electrode on the surface holding the semiconductor layer must be substantially transparent. In the photoelectric conversion element of the present invention, a method in which the conductive substrate is transparent on the surface holding the semiconductor fine particle layer and sunlight is incident from the conductive substrate side holding the semiconductor layer is preferable. In this case, a material that reflects light is preferably used for the counter electrode, and a metal, glass, plastic, or metal thin film on which a conductive oxide is deposited is preferable.

  As described above, there are two types of coating of the counter electrode: when applied on the charge transfer layer and when applied on the semiconductor layer. In either case, the counter electrode material can be appropriately formed on the charge transfer layer or the semiconductor layer by a technique such as coating, laminating, vapor deposition, or bonding depending on the type of the counter electrode material or the type of the charge transfer layer. When the charge transfer layer is solid, the counter electrode can be directly formed on the charge transfer layer by a technique such as coating, vapor deposition, or chemical vapor deposition (CVD).

  EXAMPLES Next, although an Example demonstrates this invention still in detail, this invention is not limited to these at all.

(Synthesis Example 1: Synthesis of Dye D-1)
Intermediate A: 0.50 g, Intermediate B: 0.42 g, and 20 ml of methanol were mixed and heated under reflux for 2 hours. Subsequently, the mixture was cooled to room temperature, and the precipitated solid was collected by filtration, further washed with 15 ml of methanol and dried to obtain 0.48 g of a crude product. This was purified by silica gel column chromatography (developing solvent: chloroform / methanol = 10/1 (volume ratio)) to obtain 0.25 g of dye D-1.
Absorption maximum (methanol solution): 556 nm

Example 1
<Preparation of dye-sensitized solar cell>
Paint conditioner (2 g titanium oxide (Nippon Aerosil Co., Ltd., trade name: P-25), 0.2 g acetylacetone, 0.3 g surfactant (trade name: Triton X-100, made by Aldrich Co.) together with 6.5 g water (Red Devil) for 6 hours. Further, 0.2 g of concentrated nitric acid, 0.4 ml of ethanol, and 1.2 g of polyethylene glycol (# 20,000) were added to 4.0 g of this dispersion to prepare a paste. This paste was applied on a FTO glass substrate so as to have a film thickness of 10 μm, dried at room temperature, and then baked at 100 ° C. for 1 hour and further at 550 ° C. for 1 hour to obtain a semiconductor electrode.

  The dye of the present invention shown in Table 1 and the dye of the following comparison were each dissolved in a mixed solution of t-butyl alcohol / acetonitrile (1/1 = volume ratio) to prepare a dye solution having a concentration of 0.3 mM. A semiconductor electrode prepared previously was immersed in these dye solutions at room temperature for 3 hours to perform an adsorption treatment, thereby preparing a dye-adsorbing semiconductor electrode (working electrode). As the counter electrode, a titanium plate on which platinum was sputtered was used. Both electrodes were placed so as to face each other, and an electrolyte was injected between them to produce a dye-sensitized solar cell. The electrolyte was 3-methoxypropionitrile of lithium iodide 0.1M, iodine 0.05M, 1,2-dimethyl-3-n-propylimidazolium iodide 0.5M, 4-t-butylpyridine 0.05M. The solution was used.

<Evaluation of photoelectric conversion efficiency>
Pseudo sunlight (AM1.5G, irradiation intensity) generated from a solar simulator (manufactured by Yamashita Denso Co., Ltd., device name: YSS-40S) as a light source from the working electrode side of the dye-sensitized solar cell thus produced. 100mW / cm < ² >) was irradiated, and the photoelectric conversion characteristic was measured using the electrochemical measuring device (The solartron company make, apparatus name: SI-1280B). About the photoelectric conversion efficiency of each dye-sensitized solar cell produced using the present invention and the comparative dye obtained as described above, the relative value when the photoelectric conversion efficiency of the comparative dye C-1 is 100 As evaluated. Moreover, the color tone of the working electrode was visually evaluated. The results are shown in Table 1.

(Example 2)
The dyes of the present invention (D-1, D-5, D-7, D-10, D-16) and the comparative dyes (C-1, C-2) were mixed with t-butyl alcohol / acetonitrile (1/1 = A dye solution having a concentration of 0.3 mM was prepared by dissolving in a mixed solution of (volume ratio). The steroid compound (E-1) was dissolved in this dye solution at a concentration of 0.6 mM. Subsequently, the semiconductor electrode produced in Example 1 was immersed in this dye solution for 3 hours at room temperature to perform an adsorption treatment. Hereinafter, photoelectric conversion characteristics were evaluated in the same manner as in Example 1. About the photoelectric conversion efficiency of each dye-sensitized solar cell produced using the present invention and the comparative dye obtained as described above, the relative value when the photoelectric conversion efficiency of the comparative dye C-1 is 100 As evaluated. Moreover, the color tone of the working electrode was visually evaluated. The results are shown in Table 2.

  As is clear from the results of Tables 1 and 2, the photoelectric conversion material using the compound of the present invention has a color tone of bluish purple to blue, has a higher photoelectric conversion efficiency than the comparative compound, and has excellent photoelectric conversion characteristics. You can see that it has.

  The dye for a dye-sensitized solar cell of the present invention can be used for an optical sensor sensitive to light of a specific wavelength in addition to a dye-sensitized solar cell.

Claims (3)

A dye for a dye-sensitized solar cell represented by the following general formula (1).

(In the general formula (1), R ₁ represents a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group, a cyano group, a carbamoyl group, an alkoxycarbonyl group, an aryloxycarbonyl group, a 2-oxazolinyl group, 5,6-dihydro- 4H-1,3-oxazin-2-yl represents a substituent selected from any of the following groups: R ₂ and R ₃ represent a hydrogen atom or an alkyl group, and they are linked to form a cyclopentane ring or a cyclohexane ring. They may be linked to form a cyclopentane ring or a cyclohexane ring, L ₁ and L _{2 each} represent a conjugated methine group unit, L ₃ represents an alkylene group, and R ₄ represents a Hammett substitution. .X .R ₅ to group constant σp value is a negative value and becomes an electron-donating group showing an acidic group of less than pKa of 6 ^- represents a counter anion )   A semiconductor electrode sensitized with the dye for a dye-sensitized solar cell according to claim 1.   A dye-sensitized solar cell using the semiconductor electrode according to claim 2.