JP4807020B2 - Method for producing binder composition for dispersing semiconductor fine particles - Google Patents

Description

The present invention relates to a method for producing a binder composition for dispersing semiconductor fine particles, and more specifically, a binder composition for dispersing fine semiconductor particles suitable for forming a porous semiconductor layer in a negative electrode of a dye-sensitized solar cell. It relates to the manufacturing method .

  Currently, there is great expectation for photovoltaic power generation from the viewpoint of global environmental problems and fossil energy resource depletion problems, and single crystal and polycrystalline silicon photoelectric conversion elements are put into practical use as solar cells. However, this type of solar cell is expensive and has a problem of supply of silicon raw materials, and the practical application of solar cells using materials other than silicon is desired.

  From the above viewpoint, recently, a dye-sensitized solar cell has attracted attention as a solar cell using a material other than silicon. As shown in FIG. 1, this dye-sensitized solar cell uses a transparent conductive film 1b (for example, ITO film) as an electrode substrate 1 on a transparent substrate 1a such as transparent glass or a transparent resin film. A porous film 3 made of a metal oxide semiconductor such as titanium dioxide is provided on the transparent conductive film 1b, and a sensitizing dye (for example, Ru dye) 5 is adsorbed on the surface of the porous film 3 as the negative electrode 7. Such a negative electrode 7 has a structure in which the positive electrode 10 is opposed to the electrolyte solution 8 therebetween.

  In the dye-sensitized solar cell having such a structure, when visible light is irradiated from the negative electrode 7 side, the dye 5 is excited and transitions from the ground state to the excited state. It is injected into the conduction band of the porous membrane 3 and moves to the positive electrode 10 through the external circuit 12. The electrons that have moved to the positive electrode 10 are carried by the ions in the electrolytic solution and return to the dye 5. Electric energy is extracted by repeating such a process. The power generation mechanism of such a dye-sensitized solar cell differs from that of a pn junction photoelectric conversion element in that light capture and electron conduction are performed at different locations, which is very similar to a plant photoelectric conversion process. ing.

By the way, the negative electrode 7 of the dye-sensitized solar cell as described above is obtained by applying a semiconductor particle slurry such as titanium oxide on the transparent conductive film 1b of the transparent substrate 1a and baking the semiconductor particle. It is manufactured by forming a porous film 3, applying a dye solution thereon, adsorbing the dye to the porous film 3, and then removing the solvent of the dye solution. Thus, when manufacturing the negative electrode of a dye-sensitized solar cell, the porous membrane 3 of the titanium oxide semiconductor is used as an organic solvent solution of titanium alkoxide as a binder, semiconductor fine particles are dispersed in the binder, and the titanium alkoxide is dispersed. There has been proposed a method of forming by a sol-gel method by hydrolyzing and condensing bismuth (Patent Documents 1 and 2).
Japanese Patent No. 2664194 Japanese Patent Publication 8-15097

  When a semiconductor porous film is produced by the sol-gel method as described above, the gelation product of titanium alkoxide functions as a binder for bonding the semiconductor fine particles, so that the conversion efficiency of the solar cell can be increased. However, according to the study by the present inventors, there has been a problem that the conversion efficiency varies widely and it is difficult to stably obtain a high conversion efficiency.

Accordingly, an object of the present invention is to form a semiconductor porous film that can be used to form a semiconductor porous film when producing a negative electrode of a dye-sensitized solar cell, and can ensure high conversion efficiency stably. It is providing the manufacturing method of the binder composition for semiconductor fine particle dispersion | distribution .

According to the present invention, it comprises tetraisopropoxytitanium and an organic solvent, and a part of the tetraisopropoxytitanium contains a modified product modified by reaction with the organic solvent, and at 130 ° C. for 2 hours. The solid content formed by gelation of the following formula :
A _600cm-1 / A _400cm-1
In the formula, A ₆₀₀ cm ⁻¹ is the peak height at a wave number of 600 cm ⁻¹ derived from TiO _2.
Indicate
A ₄₀₀ cm ⁻¹ is the peak height at a wave number of 400 cm ⁻¹ derived from TiOH.
Showing,
A method for producing a binder composition for dispersing semiconductor fine particles showing an infrared absorption spectrum in which the peak intensity ratio represented by
As the organic solvent, an organic compound having a functional group containing active hydrogen and forming the modified product by a substitution reaction between the functional group and isopropoxyl group, or a chelate with a titanium atom of tetraisopropoxy titanium And using an organic compound that forms the modified product by the chelate,
Tetraisopropoxytitanium in an amount of 0.1 to 3 mol / L at a temperature of 0 to 25 ° C. in an inert gas atmosphere at a rate of 0.01 to 1 ml / sec with stirring in the organic solvent. A method for producing a binder composition for dispersing semiconductor fine particles, characterized in that a part of tetraisopropoxytitanium is modified with an organic solvent by being dropped and reacted with the organic solvent .
In the method for producing a binder composition for dispersing semiconductor fine particles of the present invention, it is preferable to use a monovalent lower alcohol having 1, 2 or 4 carbon atoms, acetylacetone or ethylene glycol as the organic solvent.

In the binder composition for dispersing semiconductor fine particles produced by the present invention,
(1) The average composition of the titanium component contained in the binder composition is represented by the following formula (1):
^{_{Ti · (O- i C 3 H}} 7) 4-xn · R n (1)
In the formula, R is introduced into tetraisopropoxy titanium by reaction with an organic solvent.
A modifying group
x is the reaction valence of the organic solvent;
n is a number satisfying 0 <xn <4.
Represented by
(2) The organic solvent is lower alcohol , acetylacetone or ethylene glycol, and the average composition of the titanium component is represented by the following formula (1a), (1b) or (1c):
^{_{Ti · (O- i C 3 H}} 7) 4-n · (OR 1) n (1a)
In the formula, R ¹ is an alkyl group having 1, 2 or 4 carbon atoms,
n is a number 0 <n <4,
^{_{Ti · (O- i C 3 H}} 7) 4-n · (CH 3 COCHCOCH 3) n (1b)
Where n is a number 0 <n <4.
^{_{Ti · (O- i C 3 H}} 7) 4-2n · (OC 2 H 4) n (1c)
Where n is a number 0 <n <2.
In represented that,
Is preferred.

In the present invention, the semiconductor dispersing the binder composition, and semiconductor fine particles, is used as the semiconductor fine particle dispersion slurry boiling point is mixed with 200 ° C. or less of the organic solvent.
In the semiconductor fine particle-dispersed slurry, the semiconductor fine particles are preferably titanium dioxide.

A semiconductor porous film is obtained by baking the coating film formed by applying the semiconductor fine particle-dispersed slurry at a temperature of 200 ° C. or lower.

The binder composition for dispersing semiconductor fine particles produced by the method of the present invention (hereinafter sometimes simply referred to as “the binder composition for dispersing fine semiconductor particles of the present invention”) is a slurry in which semiconductor fine particles are dispersed (slurry for coating). The semiconductor porous film is formed by applying this slurry onto a predetermined transparent conductive substrate and baking it. The binder composition of the present invention used for the formation of such a semiconductor porous film is one in which tetraisopropoxytitanium is dissolved and dispersed in an organic solvent as a main component (binder component). Is an organic solvent reactive with tetraisopropoxy titanium (specifically, an organic solvent having an active hydrogen as a functional group or an organic compound capable of forming a chelate with a titanium atom of tetraisopropoxy titanium) And a part of tetraisopropoxytitanium is modified by reaction with this organic solvent. Therefore, in the binder composition of the present invention, the solid content formed by gelation is In the infrared absorption spectrum of
A _600cm-1 / A _400cm-1
The peak intensity ratio represented by is 1.09 or more. That is, A ₆₀₀ cm ⁻¹ indicates the peak height at a wave number of 600 cm ⁻¹ derived from TiO ₂ , A ₄₀₀ cm ⁻¹ indicates the peak height at a wave number of 400 cm ⁻¹ derived from TiOH, and the above peak intensity A ratio of 1.09 or more means that a modified product of tetraisopropoxytitanium (a part of the four alkoxyl groups bonded to Ti is contained in the organic solvent compound) in a certain amount or more. Reactive functional groups are substituted or Ti is formed into a chelate ), and thus the gelled product (solid content) has a large amount of TiO ₂ bonds due to condensation of tetraisopropoxy titanium. It means that it is generated. For example, when tetraisopropoxytitanium and an organic solvent are merely mixed, they are merely present in the same field, and water and tetraisopropoxy contained in the organic solvent are present. Only a slight amount of titanium will react to TiOH. Therefore, since the amount of TiO ₂ bonds is reduced, the peak intensity ratio is less than 1.09.

That is, in the binder composition for dispersing semiconductor fine particles of the present invention, the modified product is produced in such an amount that the peak intensity ratio is 1.09 or more. Therefore, the semiconductor fine particles are dispersed in the composition. When the slurry is prepared and the coating layer formed by applying this slurry is baked to form a porous semiconductor film, the conversion efficiency of the solar cell should be maintained at a stable and high level with little variation. Is possible. The reason why such a high conversion efficiency can be secured stably has not been precisely clarified, but probably in the semiconductor porous film formed using the binder composition of the present invention, the semiconductor particles are bonded to each other. It seems that TiO _{2 serving as a} binder is uniformly formed at a high density. For example, as understood from the experimental results of Examples and Comparative Examples described later, the binder of the present invention in which the modified product is formed so that the peak intensity ratio in the infrared absorption spectrum of the gelled product is 1.09 or more. When the composition is used (Example 1), the conversion efficiency of the obtained solar cell is in the range of 3.9 to 4.8%, the variation is small, and the average value is 4 % And extremely high value. On the other hand, in the binder composition (Comparative Example 1) in which the peak intensity ratio is as small as less than 1.09 and almost no modified product is generated, the gelled product contains a considerable amount of TiOH bonds, and the density of TiO _{2 serving as} a binder is low. For this reason, the conversion efficiency of the obtained solar cell has a high maximum value of 4.8%, but greatly varies in the range of 2 to 4.8%, and the average value is also considerably low at about 3%.

  Thus, according to the present invention, it is possible to produce a solar cell that stably exhibits high conversion efficiency.

(Binder composition for dispersing semiconductor fine particles)
Semiconductor fine particle dispersion binder composition produced by the present invention, the titanium tetraisopropoxide, was dispersed in the organic solvent, a portion of the titanium tetraisopropoxide are modified by reaction with organic solvent It is used as a material for forming the semiconductor porous film 3 in FIG.

The tetraisopropoxy titanium (and modified product) in this binder composition has a function as a binder for bonding the semiconductor particles in the film when the semiconductor porous film 3 is formed. TiO ₂ is formed, and this TiO ₂ functions as a binder.

The organic solvent that reacts with tetraisopropoxy titanium is, for example, an organic compound that contains an active hydrogen-containing functional group or an organic compound that can form a chelate with a titanium atom of tetraisopropoxy titanium. Has a functional group that releases active hydrogen and substitutes a part of the isopropoxy group of tetraisopropoxytitanium to form a modified product, the latter chelating with a titanium atom. Therefore, in the state in which such a modified product is formed, the average composition of the titanium component of the binder composition is represented by the following formula (1).
^{_{Ti · (O- i C 3 H}} 7) 4-xn · R n (1)
In the formula, R is introduced into tetraisopropoxy titanium by reaction with an organic solvent.
A modifying group
x is the reaction valence of the organic solvent;
n is a number satisfying 0 <xn <4.

  In the present invention, examples of the reactive organic solvent as described above include various aliphatic alcohols such as dihydric alcohols such as monohydric alcohols and glycols, β-diketones, β-ketoamines, β-ketoertels, and alkanolamines. Methanol, ethanol, n-butanol, sec-butanol, t-butanol from the viewpoint that they are reactive with tetraisopropoxy titanium and easily volatile and can be easily removed by heating at a relatively low temperature. C1, 2 or 4 lower alcohol, ethylene glycol and acetylacetone are preferably used.

For example, when a monovalent lower alcohol having 1, 2, or 4 carbon atoms is used as the organic solvent, the reaction valence is 1, and the lower alcohol is titanium isopropoxy as shown in the following formula. It reacts with do.
^{_{Ti · (O- i C 3 H}} 7) 4 + nR 1 OH
^{_{→ Ti · (O- i C 3}} H 7) 4-n · (OR 1) n + nC 3 H 7 OH
Therefore, the average composition of the titanium component of the binder composition is represented by the following formula (1a).
^{_{Ti · (O- i C 3 H}} 7) 4-n · (OR 1) n (1a)
In the formula, R ¹ is an alkyl group having 1, 2 or 4 carbon atoms,
n is a number 0 <n <4.

When acetylacetone is used as the organic solvent, the reaction valence is 1, and the lower alcohol reacts with titanium isopropoxide as shown in the following formula.
^{_{Ti · (O- i C 3 H}} 7) 4 + nCH 3 COCH 2 COCH 3
^{_{→ Ti · (O- i C 3}} H 7) 4-n · (CH 3 COCHCOCH 3) n + nC 3 H 7 OH
Therefore, the average composition of the titanium component of this binder composition is represented by the following formula (1b).
^{_{Ti · (O- i C 3 H}} 7) 4-n · (CH 3 COCHCOCH 3) n (1b)
In the formula, n is a number of 0 <n <4.

When ethylene glycol is used as the organic solvent, the reaction valence is 2, and the lower alcohol reacts with titanium isopropoxide as shown in the following formula.
^{_{Ti · (O- i C 3 H}} 7) 4 + nC 2 H 4 · (OH) 2
^{_{→ Ti · (O- i C 3}} H 7) 4-2n · (OC 2 H 4) n + 2nC 3 H 7 OH
Therefore, the average composition of the titanium component of this binder composition is represented by the following formula (1c).
^{_{Ti · (O- i C 3 H}} 7) 4-2n · (OC 2 H 4) n (1c)
In the formula, n is a number of 0 <n <2.

Of course, in the present invention, the organic solvents described above can be used alone or in combination of two or more. When a plurality of organic solvents described above are used, the average composition of the titanium component is equal to (O— per Ti element) by the amount of the substituted (O- ^iC ₃ H ₇ ) group that has been dropped off by the chelate. ^{The number of i} C ₃ H ₇ ) groups is less than 4.

In the binder composition of the present invention, the degree to which the above-described modified product is generated can be determined by an infrared absorption spectrum when gelled, and as shown in the examples described later, For the solid content formed by gelation after removing the solvent, the following formula:
A _600cm-1 / A _400cm-1
In the formula, A ₆₀₀ cm ⁻¹ indicates a peak height at a wave number of 600 cm ⁻¹ derived from TiO ₂ ,
A ₄₀₀ cm ⁻¹ indicates the peak height at a wave number of 400 cm ⁻¹ derived from TiOH.
It is necessary that the modified product is generated to such an extent that the peak intensity ratio represented by the formula is 1.09 or more, particularly 1.25 or more. That is, the larger this value is, the larger the amount of the modified product contained in the coating composition (the larger the value of n in the above formula (1) etc.), and the formed gelled product (solid content) contains TiO 2. ₂ it is indicative that there is a high density, since this result, the semiconductor porous film formed by using the binder composition, the semiconductor particles are dispersed density of the TiO ₂ as a binder, variation Therefore, high conversion efficiency can be stably obtained. The peak intensity ratio is usually about 3.0 at the maximum.

The amount of Ti element contained in the binder composition of the present invention (corresponding to the total amount of tetraisopropoxy titanium and its modified product) is 0.1 to 3 mol / L, particularly 0.5, in terms of tetraisopropoxy titanium. It is necessary to be in the range of 2 mol / L. That is, the amount of Ti element corresponds to the amount of tetraisopropoxytitanium used for the preparation of the binder composition. When the Ti component is contained at such a concentration, the tetraisopropoxytitanium is most efficiently used. Propoxy titanium can be modified, and at the same time, a semiconductor fine particle-dispersed slurry having a viscosity suitable for coating can be formed, and the organic solvent can be removed in a short time.

(Preparation of binder composition for dispersing semiconductor fine particles)
The binder composition described above is produced by dropping tetraisopropoxytitanium in an inert gas atmosphere at a temperature of 0 to 25 ° C. and dropping it into an organic solvent with stirring.

That is, in the production method of the present invention, in order to prevent tetraisopropoxytitanium from gelling, tetraisopropoxytitanium is dropped into the organic solvent in an inert gas atmosphere, and the temperature of the organic solvent is also 0. It is necessary to keep at a low temperature of ˜25 ° C.

Further, the dropping rate of tetraisopropoxy titanium needs to be in the range of 0.01 to 1 ml / sec . If the dropping rate is slower than the above range, the productivity is lowered, and if the dropping rate is made faster than the above range, the production amount of the reaction product is likely to vary and the characteristics become unstable. There is a fear. Furthermore, stirring is preferably performed at a shear rate of, for example, 100 rpm or more, particularly 300 to 5,000 rpm, in order to allow the reaction to proceed uniformly.

  The reaction time is such that the peak intensity ratio of the IR spectrum of the solid content is in the above-mentioned range, and varies depending on the amount of tetraisopropoxytitanium or reactive organic solvent used, but is usually about 0.5 to 4 hours. For example, it is preferable to set the reaction time by measuring in advance the peak intensity ratio of the solid content every time.

(Semiconductor fine particle dispersion slurry)
The semiconductor fine particle-dispersing binder prepared as described above is obtained by dispersing semiconductor fine particles therein to form a slurry, and coating and baking using the slurry, thereby forming a semiconductor porous film indicated by 3 in FIG. 3 is formed.

Semiconductor fine particles include those conventionally used in dye-sensitized solar cells, specifically, oxides of metals such as titanium, zirconium, hafnium, strontium, tantalum, chromium, molybdenum, tungsten, or these metals. For example, perovskite oxides such as SrTiO ₃ and CaTiO ₃ can be used. In the present invention, since TiO ₂ gel serves as a binder for semiconductor fine particles, titanium dioxide is most preferable in that a high conversion rate can be secured. Such semiconductor fine particles may have a particle size of 5 to 500 nm, particularly 5 to 350 nm in terms of porosity.

  Further, the semiconductor fine particles can be directly dispersed in the binder composition described above, but in order to uniformly disperse the binder composition in advance, the semiconductor fine particles are dispersed in an organic solvent by ultrasonic dispersion or the like in advance. It is desirable to mix this dispersion with the binder composition under stirring. Examples of the organic solvent used for preparing the dispersion include lower alcohols having 4 or less carbon atoms such as methanol, ethanol, isopropanol, n-butanol, sec-butanol, and t-butanol; ethylene glycol, propylene glycol (1,2 -Propanediol), aliphatic glycols such as 1,3-propanediol, 1,4-butanediol, 1,2-butanediol, 1,3-butanediol, 2-methyl-1,3-propanediol; Ketones such as methyl ethyl ketone; amines such as dimethyl ethyl amine can be used singly or in combination of two or more, and lower alcohols having 4 or less carbon atoms are particularly preferred. Such lower alcohols are easily volatile, can be easily volatilized and removed at low temperature, and have excellent dispersibility in titanium dioxide fine particles, and also have the reactivity used for the preparation of binder compositions. This is because it is compatible with organic solvents. In this case, the concentration of the semiconductor fine particles in the organic solvent dispersion is preferably about 10 to 50% by weight.

  When preparing the semiconductor fine particle-dispersed slurry in this manner, the amount of the binder composition to be used is generally 10 elements per 100 parts by weight of the semiconductor fine particles in terms of the amount of Ti element in the composition expressed in terms of tetraisopropoxy titanium. An amount of 40 to 40 parts by weight, particularly 10 to 30 parts by weight, is suitable for uniformly and stably dispersing the semiconductor fine particles and forming a uniform semiconductor porous film. That is, if the amount of the binder composition used is too large, the slurry becomes low viscosity due to an increase in the amount of solvent, and it becomes difficult to form a coating layer having a stable thickness due to dripping or the like, and the semiconductor in the semiconductor porous film Since the fine particle density is reduced, the conversion efficiency when the solar cell is formed may be reduced. Also, if the amount of the binder composition used is less than the above range, the paste becomes highly viscous and the workability decreases, and it is difficult to form a homogeneous semiconductor porous film due to uneven thickness of the porous film, etc. There is a risk.

  The semiconductor fine particle-dispersed slurry prepared as described above is used for forming a semiconductor porous film as follows, and is preferably used for producing a negative electrode of a dye-sensitized battery.

(Formation of semiconductor porous membrane and production of negative electrode)
Hereinafter, the formation process of the semiconductor porous film and the manufacturing process of the negative electrode in the dye-sensitized solar cell using the above-described semiconductor fine particle-dispersed slurry will be described with reference to FIG.

  First, the transparent electrode substrate 1 shown in FIG. 1 is prepared. This transparent electrode substrate 1 is obtained by providing a transparent conductive film 1b on a transparent substrate 1a, and a transparent glass plate or a transparent resin film is used as the transparent substrate 1a. As the transparent resin film, any film can be used as long as it is transparent. For example, low-density polyethylene, high-density polyethylene, polypropylene, poly-1-butene, poly-4-methyl-1-pentene, or ethylene, propylene, Polyolefin resins such as random or block copolymers of α-olefins such as 1-butene and 4-methyl-1-pentene; ethylene-vinyl acetate copolymer, ethylene-vinyl alcohol copolymer, ethylene-vinyl chloride Ethylene-vinyl compound copolymer resins such as copolymers; styrene resins such as polystyrene, acrylonitrile-styrene copolymers, ABS, α-methylstyrene-styrene copolymers; polyvinyl alcohol, polyvinyl pyrrolidone, polyvinyl chloride, Polyvinylidene chloride, vinyl chloride-vinyl chloride Vinyl resins such as den copolymers, polyacrylic acid, polymethacrylic acid, polymethyl acrylate and polymethyl methacrylate; polyamide resins such as nylon 6, nylon 6-6, nylon 6-10, nylon 11 and nylon 12 Polyester resins such as polyethylene terephthalate and polybutylene terephthalate; polycarbonates; polyphenylene oxide; cellulose derivatives such as carboxymethyl cellulose and hydroxyethyl cellulose; starches such as oxidized starch, etherified starch and dextrin; and resins composed of a mixture thereof. A film can be used. In general, a polyethylene terephthalate film is preferably used from the viewpoint of strength and heat resistance. Moreover, the thickness and size of the transparent substrate 1a are not particularly limited, and are appropriately determined according to the use of the dye-sensitized solar cell to be finally used.

  The transparent conductive film 1b is typically a film made of an indium oxide-tin oxide alloy (ITO film) or a film in which tin oxide is doped with fluorine (FTO film). Is preferred. These are formed on the transparent substrate 1a by vapor deposition, and the thickness is usually about 0.5 to 0.7 μm.

  Next, the above-described semiconductor fine particle dispersed slurry of the present invention is applied onto the transparent conductive film 1b of the transparent substrate 1 to form a coating layer. This coating layer forms the semiconductor porous film (titania porous film) 3 in FIG. 1 by baking.

The coating of the semiconductor fine particle-dispersed slurry can be performed by a known method such as a doctor blade method, a spin coating method, a screen printing method, or a spray coating method, and the thickness after baking is about 5 to 20 μm. Is preferably about 0.001 to 0.005 g / cm ² .

  After coating the semiconductor fine particle dispersed slurry of the present invention on the transparent conductive film 1b of the transparent substrate 1 as described above, baking is performed. Although this baking is performed at 200 ° C. or lower, as understood from the above description, the slurry is formed using a non-aqueous binder composition, and therefore, particularly has 4 or less carbon atoms as an organic solvent. When a lower alcohol is used, there is an advantage that the semiconductor porous film 3 can be formed by baking at a low temperature of less than 100 ° C., particularly 70 to 95 ° C. That is, since baking can be performed in such a low temperature region, the above-described transparent glass can surely prevent deformation during baking even when a transparent resin film is used as the transparent substrate 1a. Therefore, the resin film can also be suitably used as the substrate material.

Such firing may be performed to such an extent that the semiconductor fine particles in the slurry are appropriately sintered. For example, it may be densified so that the relative density by the Archimedes method reaches 50 to 90%. It takes about 30 minutes. In the semiconductor porous layer 3 formed by such firing, since the TiO ₂ having an IR intensity ratio of not less than a predetermined value (1.09) binds the semiconductor fine particles by using a dense gelled product as a binder, As a result, it is possible to stably ensure high conversion efficiency.

  In order to produce the negative electrode, the sensitizing dye 5 is adsorbed by bringing the dye solution into contact with the semiconductor porous film 3 formed as described above. The contact of the dye solution is usually performed by dipping, and the adsorption treatment time (immersion time) is usually about 30 minutes to 24 hours, and after adsorption, the solvent of the dye solution is removed by drying, The negative electrode 7 having the semiconductor porous film 3 having the sensitizing dye 5 formed on the surface can be obtained.

As the sensitizing dye to be used, those known per se having a bonding group such as a carboxylate group, a cyano group, a phosphate group, an oxime group, a dioxime group, a hydroxyquinoline group, a salicylate group, an α-keto-enol group are used. For example, a ruthenium complex, an osmium complex, an iron complex, etc. can be used without any limitation. Ruthenium-tris (2,2′-bispyridyl-4,4′-dicarboxylate), ruthenium-cis-diaqua-bis (2,2′-bispyridyl-4,4) in that it has a particularly broad absorption band. Ruthenium-based complexes such as' -dicarboxylate) are preferred. Such a dye solution of a sensitizing dye is prepared using an alcohol organic solvent such as ethanol or butanol as a solvent, and the dye concentration is usually about 3 × 10 ^{−4 to} 5 × 10 ⁻⁴ mol / l. It is.

  Further, in the above manufacturing process, the semiconductor fine particle dispersed slurry of the present invention is coated and the dye is adsorbed after firing, but when the semiconductor fine particle dispersed slurry of the present invention is used, it is 100 ° C. Since baking can also be performed in a low temperature region of less than, baking can be performed after the dye adsorption treatment. That is, it is possible to apply the semiconductor fine particle-dispersed slurry and dry it, then contact the dye solution by dipping or the like to adsorb the sensitizing dye, and then perform baking. The drying in this case may be natural drying simply by leaving it in the atmosphere, but may be heated to a temperature of less than 100 ° C. if necessary.

  As shown in FIG. 1, the negative electrode 7 obtained as described above is used as a dye-sensitized solar cell by facing the positive electrode 10 which is a counter electrode with an electrolyte solution 8 interposed therebetween. .

  As the electrolyte solution 8, various electrolyte solutions containing a cation such as lithium ion and an anion such as chlorine ion can be used. Further, in this electrolyte solution, it is preferable that an oxidation-reduction pair capable of reversibly taking an oxidized structure and a reduced structure exists, and examples of such an oxidized-reduced pair include iodine-iodine compounds, bromine- Examples thereof include bromine compounds and quinone-hydroquinone. The electrolyte solution 8 is generally sealed with an electrically insulating resin or the like so that it does not leak between the electrodes.

  In addition, the positive electrode 10 can use various electrode substrates regardless of whether they are transparent or opaque. For example, a transparent electrode layer such as a platinum layer or ITO is deposited on the surface of a transparent substrate such as a glass substrate or a transparent resin film. Alternatively, it is possible to adopt an arbitrary structure such as a transparent electrode layer such as ITO deposited on the transparent substrate surface and a platinum layer deposited thereon.

  Thus, in the dye-sensitized solar cell in which the negative electrode is formed, high conversion efficiency can be stably ensured as shown in the following examples.

The superior effect of the present invention is illustrated in the following examples.
In a nitrogen gas atmosphere, at a temperature of 5 ° C., 140 g of tetraisopyropoxide was dropped into 0.4 liter of butanol stirred at a speed of 1,000 rpm at a dropping speed of 0.2 ml / sec. A titanium alkoxide solution was prepared over 2 hours. When the solid content formed by gelling this titanium alkoxide solution (gelation conditions: 130 ° C. for 2 hours) was subjected to infrared spectroscopic analysis (IR), the following formula:
A _600cm-1 / A _400cm-1
In the formula, A ₆₀₀ cm ⁻¹ indicates a peak height at a wave number of 600 cm ⁻¹ derived from TiO ₂ ,
A ₄₀₀ cm ⁻¹ indicates the peak height at a wave number of 400 cm ⁻¹ derived from TiOH.
The peak intensity ratio represented by is 1.31.
The titanium alkoxide solution prepared above and titanium dioxide particles (general-purpose titania particles having a constituent particle diameter of 15 to 350 nm) are obtained by changing the amount of Ti element in terms of tetraisopropoxide in the titanium alkoxide solution to titanium dioxide fine particles 100. Titanium dioxide fine particle paste having a solid content concentration of 25% by weight was prepared by mixing so as to be 40 parts by weight per part by weight.

Then, the titanium dioxide paste prepared above is applied to a conductive film (product name “OTEC”, manufactured by Tobi Co., Ltd.) in which an ITO film is provided as a conductive film on a polyethylene terephthalate film, and then a chamber in an atmosphere under reduced pressure of 1 Torr. A sample coated with a titanium dioxide paste was placed therein, and heated at 110 ° C. for 10 minutes to obtain a porous film. The thickness of the semiconductor paste was about 5 μm, and the semiconductor weight was 0.0021 g / cm ² . Thereafter, ruthenium complex dye dispersed in a purity of 99.5% ethanol _{[Ru (dcbpy) 2 (NCS} ) 2] · 2H immersed for 16 hours in a dye solution consisting of ₂ O, and obtain a negative electrode.
Using the negative electrode obtained as described above, 4-tert-butyl pyridine was added to this and LiI / I ₂ 0.5 mol / 0.05 mol) dissolved in methoxypropionitrile. Thus, a dye-sensitized solar cell was fabricated by sandwiching the prepared electrolyte with a positive electrode composed of an ITO / PET film on which platinum was deposited. Ten batteries were prepared in the same manner, and the conversion efficiency was measured. When the conversion efficiency was 3.9% to 4.8%, the average was about 4%, and the variation could be suppressed and the average performance increased. It was confirmed.

In a nitrogen gas atmosphere, 140 g of tetraisopyropoxide was dropped into 0.4 liter of butanol stirred at a speed of 500 rpm at a temperature of 10 ° C. at a dropping rate of 0.5 ml / sec. Over 2 hours. A titanium alkoxide solution was prepared. When the solid content formed by gelling the titanium alkoxide solution in the same manner as in Example 1 was analyzed by infrared spectroscopy (IR), the following formula:
A _600cm-1 / A _400cm-1
The peak intensity ratio represented by is 1.09.
The titanium alkoxide solution prepared above and titanium dioxide particles (general-purpose titania particles having a constituent particle diameter of 15 to 350 nm) are obtained by changing the amount of Ti element in terms of tetraisopropoxide in the titanium alkoxide solution to titanium dioxide fine particles 100. Titanium dioxide fine particle paste having a solid content concentration of 25% by weight was prepared by mixing so as to be 40 parts by weight per part by weight.

Then, the titanium dioxide paste prepared above is applied to a conductive film (product name “OTEC”, manufactured by Tobi Co., Ltd.) in which an ITO film is provided as a conductive film on a polyethylene terephthalate film, and then a chamber in an atmosphere under reduced pressure of 1 Torr. A sample coated with a titanium dioxide paste was placed therein, and heated at 110 ° C. for 10 minutes to obtain a porous film. The thickness of the semiconductor paste was about 5 μm, and the semiconductor weight was 0.0021 g / cm ² . Thereafter, the resultant was immersed in a dye solution composed of a ruthenium complex dye [Ru (dcbpy) ₂ (NCS) ₂ ] · 2H ₂ O dispersed in ethanol having a purity of 99.5% for 16 hours to obtain a negative electrode.
Using the negative electrode obtained as described above, 4-tert-butyl pyridine was added to this and LiI / I ₂ 0.5 mol / 0.05 mol) dissolved in methoxypropionitrile. Thus, a dye-sensitized solar cell was fabricated by sandwiching the prepared electrolyte with a positive electrode composed of an ITO / PET film on which platinum was deposited. Ten batteries were prepared in the same manner, and the conversion efficiency was measured. When the conversion efficiency was 3.9% to 4.7%, the average was about 4%, and the variation could be suppressed and the average performance increased. It was confirmed.

In a nitrogen gas atmosphere, 140 g of tetraisopyropoxide was dropped into 0.4 liter of ethylene glycol at a temperature of 10 ° C. and stirred at a speed of 500 rpm at a dropping rate of 0.5 ml / sec. For 2 hours. To prepare a titanium alkoxide solution. When the solid content formed by gelling the titanium alkoxide solution in the same manner as in Example 1 was analyzed by infrared spectroscopy (IR), the following formula:
A _600cm-1 / A _400cm-1
And the peak intensity ratio was 1.17.
The titanium alkoxide solution prepared above and titanium dioxide particles (general-purpose titania particles having a constituent particle diameter of 15 to 350 nm) are obtained by changing the amount of Ti element in terms of tetraisopropoxide in the titanium alkoxide solution to titanium dioxide fine particles 100. A titanium dioxide fine particle paste having a solid content of 25% by weight was prepared by mixing so as to be 40 parts by weight per part by weight.

Then, the titanium dioxide paste prepared above is applied to a conductive film (product name “OTEC”, manufactured by Tobi Co., Ltd.) in which an ITO film is provided as a conductive film on a polyethylene terephthalate film, and then a chamber in an atmosphere under reduced pressure of 1 Torr. A sample coated with a titanium dioxide paste was placed therein, and heated at 110 ° C. for 10 minutes to obtain a porous film. The thickness of the semiconductor paste was about 5 μm, and the semiconductor weight was 0.0021 g / cm ² . Thereafter, the resultant was immersed in a dye solution composed of a ruthenium complex dye [Ru (dcbpy) ₂ (NCS) ₂ ] · 2H ₂ O dispersed in ethanol having a purity of 99.5% for 16 hours to obtain a negative electrode.
Using the negative electrode obtained as described above, 4-tert-butyl pyridine was added to this and LiI / I ₂ 0.5 mol / 0.05 mol) dissolved in methoxypropionitrile. Thus, a dye-sensitized solar cell was fabricated by sandwiching the prepared electrolyte with a positive electrode composed of an ITO / PET film on which platinum was deposited. Ten batteries were prepared in the same manner, and the conversion efficiency was measured. When the conversion efficiency was 3.9% to 4.8%, the average was about 4%, and the variation could be suppressed and the average performance increased. It was confirmed.

Comparative Example 1

In a nitrogen gas atmosphere, 140 g of tetraisopyropoxide was dropped into 0.4 liter of butanol stirred at a speed of 500 rpm at a temperature of 50 ° C. at a dropping rate of 0.5 ml / sec. Over 2 hours. A titanium alkoxide solution was prepared. When the solid content formed by gelling the titanium alkoxide solution in the same manner as in Example 1 was analyzed by infrared spectroscopy (IR), the following formula:
A _600cm-1 / A _400cm-1
The peak intensity ratio represented by 1.0 was 1.065.
The titanium alkoxide solution prepared above and titanium dioxide particles (general-purpose titania particles having a constituent particle diameter of 15 to 350 nm) are obtained by changing the amount of Ti element in terms of tetraisopropoxide in the titanium alkoxide solution to titanium dioxide fine particles 100. A titanium dioxide fine particle paste having a solid content of 25% by weight was prepared by mixing so as to be 40 parts by weight per part by weight.

Then, the titanium dioxide paste prepared above is applied to a conductive film (product name “OTEC”, manufactured by Tobi Co., Ltd.) in which an ITO film is provided as a conductive film on a polyethylene terephthalate film, and then a chamber in an atmosphere under reduced pressure of 1 Torr. A sample coated with a titanium dioxide paste was placed therein, and heated at 110 ° C. for 10 minutes to obtain a porous film. The thickness of the semiconductor paste was about 5 μm, and the semiconductor weight was 0.0021 g / cm ² . Thereafter, the resultant was immersed in a dye solution composed of a ruthenium complex dye [Ru (dcbpy) ₂ (NCS) ₂ ] · 2H ₂ O dispersed in ethanol having a purity of 99.5% for 16 hours to obtain a negative electrode.
Using the negative electrode obtained as described above, 4-tert-butyl pyridine was added to this and LiI / I ₂ 0.5 mol / 0.05 mol) dissolved in methoxypropionitrile. Thus, a dye-sensitized solar cell was fabricated by sandwiching the prepared electrolyte with a positive electrode composed of an ITO / PET film on which platinum was deposited. When 10 batteries were prepared in the same manner and the conversion efficiency was measured, the conversion efficiency was 2.0% to 4.4%, the average was about 2.6%, the variation range was large, and the average performance was also high. It will be lower.

Comparative Example 2

In a nitrogen gas atmosphere at a temperature of 10 ° C. and stirring at a speed of 50 rpm, 0.4 g of butanol was dropped at a dropping rate of 10 ml / sec. An alkoxide solution was prepared. When the solid content formed by gelling the titanium alkoxide solution in the same manner as in Example 1 was analyzed by infrared spectroscopy (IR), the following formula:
A _600cm-1 / A _400cm-1
And the peak intensity ratio was 1.07.
The titanium alkoxide solution prepared above and titanium dioxide particles (general-purpose titania particles having a constituent particle diameter of 15 to 350 nm) are obtained by changing the amount of Ti element in terms of tetraisopropoxide in the titanium alkoxide solution to titanium dioxide fine particles 100. Titanium dioxide fine particle paste having a solid content concentration of 25% by weight was prepared by mixing so as to be 40 parts by weight per part by weight.

Then, the titanium dioxide paste prepared above is applied to a conductive film (product name “OTEC”, manufactured by Tobi Co., Ltd.) in which an ITO film is provided as a conductive film on a polyethylene terephthalate film, and then a chamber in an atmosphere under reduced pressure of 1 Torr. A sample coated with a titanium dioxide paste was placed therein, and heated at 110 ° C. for 10 minutes to obtain a porous film. The thickness of the semiconductor paste was about 5 μm, and the semiconductor weight was 0.0021 g / cm ² . Thereafter, the resultant was immersed in a dye solution composed of a ruthenium complex dye [Ru (dcbpy) ₂ (NCS) ₂ ] · 2H ₂ O dispersed in ethanol having a purity of 99.5% for 16 hours to obtain a negative electrode.
Using the negative electrode obtained as described above, 4-tert-butyl pyridine was added to this and LiI / I ₂ 0.5 mol / 0.05 mol) dissolved in methoxypropionitrile. Thus, a dye-sensitized solar cell was fabricated by sandwiching the prepared electrolyte with a positive electrode composed of an ITO / PET film on which platinum was deposited. Ten batteries were prepared in the same manner, and the conversion efficiency was measured. The conversion efficiency was 2.9% to 4.8%, the average was about 3.1%, the variation range was large, and the average performance was also good. It will be lower.

The figure which shows schematic structure of a dye-sensitized solar cell.

Explanation of symbols

1: Transparent electrode substrate 1a: Transparent substrate 1b: Transparent conductive layer 3: Semiconductor porous film 5: Sensitizing dye 7: Negative electrode 8: Electrolyte solution 10: Positive electrode

Claims (2)

It consists of tetraisopropoxytitanium and an organic solvent, and part of the tetraisopropoxytitanium contains a modified product modified by reaction with the organic solvent, and is formed by gelation at 130 ° C. for 2 hours. that solids, the following formula:
A _600cm-1 / A _400cm-1
In the formula, A ₆₀₀ cm ⁻¹ is the peak height at a wave number of 600 cm ⁻¹ derived from TiO _2.
Indicate
A ₄₀₀ cm ⁻¹ is the peak height at a wave number of 400 cm ⁻¹ derived from TiOH.
Showing,
A method for producing a binder composition for dispersing semiconductor fine particles showing an infrared absorption spectrum in which the peak intensity ratio represented by
As the organic solvent, an organic compound having a functional group containing active hydrogen and forming the modified product by a substitution reaction between the functional group and isopropoxyl group, or a chelate with a titanium atom of tetraisopropoxy titanium And using an organic compound that forms the modified product by the chelate,
Tetraisopropoxytitanium in an amount of 0.1 to 3 mol / L at a temperature of 0 to 25 ° C. in an inert gas atmosphere at a rate of 0.01 to 1 ml / sec with stirring in the organic solvent. A method of producing a binder composition for dispersing semiconductor fine particles, wherein a part of tetraisopropoxytitanium is modified with an organic solvent by being dropped and reacted with the organic solvent. The method for producing a binder composition for dispersing semiconductor fine particles according to claim 1, wherein a monovalent lower alcohol having 1, 2 or 4 carbon atoms, acetylacetone or ethylene glycol is used as the organic solvent .

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