Patent Application
20130008502
The present invention relates to an electrolyte for photoelectric conversion elements, and a photoelectric conversion element and a dye-sensitized solar cell using the electrolyte.
In recent years, environmental issues such as global warming and the like that are attributed to increases in carbon dioxide have become serious. As a result, non-silicon solar cells have gained attention as solar cells that have little environmental impact and that also allow for reduced manufacturing costs; and research and development of such is moving forward.
Among non-silicon solar cells, the dye-sensitized solar cell developed by Graetzel et al. in Switzerland has attracted attention as a new type of solar cell. As a solar cell using organic materials, these solar cells have advantages such as high photoelectric conversion efficiency and lower manufacturing costs than silicon solar cells.
However, dye-sensitized solar cells are electrochemical cells, and therefore use organic electrolytic solutions, ionic liquids and the like as electrolytes. In cases where organic electrolytic solutions are used, there is a problem in that electrical efficiency decreases due to volatilization and depletion during long-term use. Additionally, in cases where ionic liquids are used, while volatilization and depletion that occur during long-term use can be prevented, there are durability problems such as structural degradation caused by liquid leakage.
Therefore, research is being conducted regarding converting the electrolyte from a liquid to a gel or solid for the purpose of preventing the volatilization and liquid leakage of the electrolytic solution and ensuring the long-term stability and durability of the solar cell.
For example, Patent Document 1 describes an electrolyte for a photoelectric conversion element comprising (i) a lamellar clay mineral and/or an organically modified lamellar clay mineral and (ii) an ionic liquid (claim 1).
The present inventors discovered, as a result of investigating the photoelectric conversion element using the electrolyte for a photoelectric conversion element described in Patent Document 1, that when allowed to sit at rest at about 85% RH (relative humidity) for about 200 hours or longer, there are cases where the photoelectric conversion efficiency declines.
This is thought to be due to the electrolyte or sensitizing dye being altered by moisture or humidity that has entered the photoelectric conversion element.
Therefore, an object of the present invention is to provide an electrolyte for a photoelectric conversion element that can achieve superior moisture resistance, and a photoelectric conversion element and a dye-sensitized solar cell using the electrolyte.
As a result of diligent research, the present inventors discovered that an electrolyte for a photoelectric conversion element including an ionic liquid and a lamellar clay mineral having an alkylsilyl group can achieve superior moisture resistance, and thus arrived at the present invention.
Specifically, the present invention provides the following (a) to (d).
(a) An electrolyte for a photoelectric conversion element including an ionic liquid (A) and a lamellar clay mineral (B), wherein
the lamellar clay mineral (B) contains an alkylsilyl group.
(b) The electrolyte for a photoelectric conversion element according to (a), wherein the ionic liquid (A) includes a cation that is expressed by the following Formula (1) or (2).
In Formula (1), R1 is a hydrocarbon group having from 1 to 20 carbons that may contain a hetero atom, and may include a substituent having 1 to 20 carbons that may contain a hetero atom. R2 and R3 are each independently a hydrogen atom or a hydrocarbon group having from 1 to 20 carbons, and may include a hetero atom. However, the R3 moiety is absent if the nitrogen atom contains a double bond. In formula (2), Q is a nitrogen, oxygen, phosphorus, or sulfur atom; and R4, R5, R6, and R7 are each independently a hydrogen atom or a hydrocarbon group having 1 to 8 carbons that may include a hetero atom. However, the R7 moiety is absent if Q is an oxygen or a sulfur atom and, if Q is a sulfur atom, R4 and R5 may be linked.
(c) A photoelectric conversion element including: a photoelectrode having a transparent conductive film and a metal oxide semiconductor porous film;
a counterelectrode disposed opposite the photoelectrode; and
an electrolyte layer disposed between the photoelectrode and the counterelectrode, wherein
the electrolyte layer is the electrolyte for a photoelectric conversion element described in (a) or (b).
(d) A dye-sensitized solar cell including the photoelectrode described in (c) carrying a photosensitized dye.
As described below, the present invention is useful for providing an electrolyte for a photoelectric conversion element that can achieve superior moisture resistance, and a photoelectric conversion element and a dye-sensitized solar cell using the electrolyte.
Additionally, because moisture resistance is superior, the dye-sensitized solar cell of the present invention is extremely useful in that it can be applied, for example, to usage environments exposed to outside air where humidity fluctuates greatly.
The present invention is explained in further detail below.
An electrolyte for a photoelectric conversion element of the present invention (hereinafter also referred to simply as “the electrolyte of the present invention”) includes an ionic liquid (A) and a lamellar clay mineral (B). Additionally, the lamellar clay mineral (B) contains an alkylsilyl group.
The electrolyte of the present invention preferably further includes an organic solvent (C) having a boiling point of not less than 150° C. and a relative dielectric constant of not less than 20 because the moisture resistance of a photoelectric conversion element using the electrolyte of the present invention (hereinafter also referred to as “the photoelectric conversion element of the present invention”) will be better.
Next, each constituent of the electrolyte of the present invention will be described in detail.
The ionic liquid (A) for use in the electrolyte of the present invention is not particularly limited, and any ionic liquid conventionally used in an electrolyte can be used.
For example, quaternary ammonium salts, imidazolium salts, pyridinium salts, pyrrolidinium salts, piperidinium salts, and similar organic salt compounds described in, “Ionic Liquids: The Front and Future of Material Development”, edited by Hiroyuki OHNO, CMC Publishing Co., Ltd., 2003; “Functional Creation and Applications of Ionic Liquids”, NTS Inc., 2004; and the like can be used.
Additionally, for example, a single type of organic salt compound that is solid at room temperature can be used as the ionic liquid (A); or a mixture of two or more different types of solid organic salt compounds that are melted at a high temperature can be used as the ionic liquid (A), provided that the mixture is a liquid at room temperature.
Note that when the hereinafter described organic solvent (C) is included, an organic salt compound that is solid at room temperature (e.g. tetraethylammonium iodide and the like) can be used as the ionic liquid (A) because the organic salt compound may be liquefied in the electrolyte system by the organic solvent (C).
The ionic liquid (A) includes cations and, as counterions thereto, anions.
Specific examples of preferred cations include the cations expressed by Formula (1) or (2) below.
In Formula (1), R1 is a hydrocarbon group having from 1 to 20 carbons that may contain a hetero atom, and may include a substituent having 1 to 20 carbons that may contain a hetero atom. R2 and R3 are each independently a hydrogen atom or a hydrocarbon group having from 1 to 20 carbons, and may include a hetero atom. However, the R3 moiety is absent if the nitrogen atom contains a double bond.
In formula (2), Q is a nitrogen, oxygen, phosphorus, or sulfur atom; and R4, R5, R6, and R7 are each independently a hydrogen atom or a hydrocarbon group having 1 to 8 carbons that may include a hetero atom. However, the R7 moiety is absent if Q is an oxygen or a sulfur atom and, if Q is a sulfur atom, R4 and R5 may be linked.
The hydrocarbon group in Formula (1) having from 1 to 20 carbons that may contain a hetero atom, R1, preferably has a ring structure along with the nitrogen atom (ammonium ion) in Formula (1).
Next, preferable examples of the substituent, having from 1 to 20 carbons and that may contain a hetero atom that R1 in Formula (1) may include, include alkyl groups having from 1 to 20 carbons (e.g. a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, an ethylhexyl group, a nonyl group, a decyl group, a dodecyl group, an undecyl group, a hexadecyl group, an octadecyl group, a trifluoroethyl group, and the like); alkenyl groups having from 2 to 15 carbons (e.g. a vinyl group, an allyl group, and the like); aryl groups having from 6 to 20 carbons (e.g. a phenyl group, a tolyl group, and the like); aralkyl groups having from 7 to 20 carbons (e.g. a benzyl group, a phenylethyl group, a phenylpropyl group, and the like); alkoxy groups having from 1 to 20 carbons (e.g. a methoxy group, an ethoxy group, an n-propoxy group, an iso-propoxy group, an n-butoxy group, a tert-butoxy group, a sec-butoxy group, an n-pentoxy group, an n-hexoxy group, a 1,2-dimethylbutoxy group, a heptoxy group, an octoxy group, and the like); and alkylalkoxy groups having from 2 to 20 carbons (e.g. a methylene methoxy group (—CH2OCH3), an ethylene methoxy group (—CH2CH2OCH3), an n-propylene-iso-propoxy group (—CH2CH2CH2OCH(CH3)2), a methylene-t-butoxy group (—CH2—O—C(CH3)3), a butylene methoxy group, a pentylene methoxy group, a hexylene methoxy group, a heptylene methoxy group, an octylene methoxy group, a methylene ethoxy group, an ethylene ethoxy group, a propylene ethoxy group, a butylene ethoxy group, a pentylene ethoxy group, a hexylene ethoxy group, an ethylene ethoxy methoxy group, and the like). Additionally, R2 in Formula (1) may include two or more of these substituents.
Specific examples of the hydrocarbon group, having from 1 to 20 carbons and that may contain a hetero atom, R2 and R3, in Formula (1) include alkyl groups having from 1 to 20 carbons (e.g. a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, an ethylhexyl group, a nonyl group, a decyl group, a dodecyl group, an undecyl group, a hexadecyl group, an octadecyl group, a trifluoroethyl group, and the like); alkenyl groups having from 2 to 15 carbons (e.g. a vinyl group, an allyl group, and the like); aryl groups having from 6 to 20 carbons (e.g. a phenyl group, a tolyl group, and the like); aralkyl groups having from 7 to 20 carbons (e.g. a benzyl group, a phenylethyl group, a phenylpropyl group, and the like); alkoxy groups having from 1 to 20 carbons (e.g. a methoxy group, an ethoxy group, an n-propoxy group, an iso-propoxy group, an n-butoxy group, a tert-butoxy group, a sec-butoxy group, an n-pentoxy group, an n-hexoxy group, a 1,2-dimethylbutoxy group, a heptoxy group, an octoxy group, and the like); alkylalkoxy groups having from 2 to 20 carbons (e.g. a methylene methoxy group (—CH2OCH3), an ethylene methoxy group (—CH2CH2OCH3), an n-propylene-iso-propoxy group (—CH2CH2CH2OCH(CH3)2), a methylene-t-butoxy group (—CH2—O—C(CH3)3), a butylene methoxy group, a pentylene methoxy group, a hexylene methoxy group, a heptylene methoxy group, an octylene methoxy group, a methylene ethoxy group, an ethylene ethoxy group, a propylene ethoxy group, a butylene ethoxy group, a pentylene ethoxy group, a hexylene ethoxy group, an ethylene ethoxy methoxy group, and the like); and the like.
Additionally, specific examples of the hydrocarbon group, having from 1 to 8 carbons and that may contain a hetero atom, R4, R5, R6, and R7, in Formula (2) include alkyl groups having from 1 to 8 carbons (e.g. a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, and the like), alkoxy groups having from 1 to 8 carbons (e.g. a methoxy group, an ethoxy group, an n-propoxy group, an iso-propoxy group, an n-butoxy group, a tert-butoxy group, a sec-butoxy group, an n-pentoxy group, an n-hexoxy group, a 1,2-dimethylbutoxy group, and the like), alkylalkoxy groups having from 2 to 8 carbons (e.g. a methylene methoxy group (—CH2OCH3), an ethylene methoxy group (—CH2CH2OCH3), an n-propylene-iso-propoxy group (—CH2CH2CH2OCH(CH3)2), a methylene-t-butoxy group (—CH2—O—C(CH3)3, and the like), and the like.
Examples of the cations expressed by Formula (1) include imidazolium ions, pyridinium ions, pyrrolidinium ions, piperidinium ions, and the like.
Specific examples of preferred cations include the cations expressed by any of Formulas (3) to (6) below.
Of these, the cations expressed by the following Formulas (3) and (5) are preferable because the photoelectric conversion efficiency of the photoelectric conversion element of the present invention tends to be better.
In Formulas (3) to (6), R are each independently a hydrogen atom or a hydrocarbon group having from 1 to 20 carbons that may include a nitrogen atom.
More specific examples include the following cations.
Examples of the cations of Formula (2) include organic cations such as ammonium ions, sulfonium ions, phosphonium ions, and the like.
Specific examples of preferable cations are listed below.
Of these, aliphatic quarternary ammonium ions (particularly tetraalkyl ammonium ions) and sulfonium ions (particularly thiophenium ions) are preferable because the photoelectric conversion efficiency of the photoelectric conversion element of the present invention tends to be better.
On the other hand, specific examples of preferable anions included in the ionic liquid (A) include I−, Br−, AlCl4−, Al2Cl7−, NO3−, BF4−, PF6−, CH3COO−, CF3COO−, CF3SO3−, (CN)4B−, SCN−, (CF3SO2)2N−, (CN)2N−, (CF3SO2)3C−, (CN)3C−, AsF6−, SbF6−, F(HF)n−, CF3CF2CF2CF2SO3−, (CF3CF2SO2)2N−, CF3CF2CF2COO−, and the like.
Of these, the anions are preferably bromine ions (Br−) or iodine ions (I−) and more preferably iodine ions (I−) because the photoelectric conversion efficiency of the photoelectric conversion element of the present invention tends to be better.
Examples of the ionic liquid (A) include combinations and the like of the cations and anions described above.
Of these, the ionic liquid (A) is preferably an ionic liquid including imidazolium ions, pyrrolidinium ions, or tetraalkyl ammonium ions as the cations and iodine ions as the anions.
In the present invention, a synthesis method of the ionic liquid (A) is not particularly limited, and various types of ionic liquids obtained from combinations of the cations and the anions described above can be synthesized by a conventionally known method.
Synthesized products can be used as the ionic liquid (A) such as 1-methyl-3-methyl imidazolium iodide, 1-ethyl-3-methyl imidazolium iodide, 1-methyl-3-pentyl imidazolium iodide, 1-hexyl-3-methyl imidazolium iodide, 1-((2-methoxyethoxy)ethyl)-3-((2-methoxyethoxy)ethyl)imidazolium iodide, 1-methyl-1-butyl pyrrolidinium thiocyanate, 1-methyl-1-ethyl pyrrolidinium thiocyanate, and the like; and also commercially available products can be used. Specific examples of commercially available products that can be used as the ionic liquid (A) include 1-methyl-3-propyl imidazolium iodide (manufactured by Tokyo Chemical Industry Co., Ltd.), 1-methyl-3-butyl imidazolium iodide (manufactured by Tokyo Chemical Industry Co., Ltd.), 1-methyl-1-methyl-pyrrolidinium iodide (manufactured by Sigma-Aldrich Co. LLC.), tetrapropyl ammonium iodide (manufactured by Tokyo Chemical Industry Co., Ltd.), tetrabutyl ammonium iodide (manufactured by Tokyo Chemical Industry Co., Ltd.), 1-ethyl-3-methyl imidazolium tetracyanoborate (manufactured by Merck), 1-ethyl-3-methyl imidazolium thiocyanate (manufactured by Merck), 1-methyl-3-butyl imidazolium thiocyanate (manufactured by BASF), tetrapropyl ammonium thiocyanate (manufactured by Merck), 1-ethyl-3-methyl imidazolium bis(trifluoromethylsulphonyl)imide (manufactured by Solvent Innovation), and the like.
Note that as some of the ionic liquid display tautomerism, the ionic liquid (A) of the present invention includes tautomers thereof.
Specifically, for example, for 1-methyl-3-pentyl imidazolium iodide, a tautomer thereof, namely, 1-pentyl-3-methyl imidazolium iodide is included; and, for 1-ethyl-3-methyl imidazolium thiocyanate, a tautomer thereof, namely, 1-methyl-3-ethyl imidazolium thiocyanate is included.
In the present invention, a content of the ionic liquid (A) described above is preferably from 50 to 95 mass %, and more preferably from 65 to 95 mass % of a total mass of the electrolyte of the present invention. If the content is within this range, the photoelectric conversion efficiency of the photoelectric conversion element of the present invention will be better.
The lamellar clay mineral (B) used in the electrolyte of the present invention is not particularly limited, provided that it is a lamellar clay mineral containing an alkylsilyl group, and may, for example, be a reaction product of the lamellar clay mineral (b1) and an organosilane compound (b2) described hereinafter; a commercially available product described below; or the like.
Lamellar Clay Mineral (b1)
The lamellar clay mineral (b1) used in the preparation of the lamellar clay mineral (B) is not particularly limited, and is preferably a phyllosilicate having a silicic acid tetrahedron bonded in a bi-dimensional sheet-like form. Specific examples thereof include smectite-based clay minerals such as montmorillonite, saponite, beidellite, nontronite, hectorite, stevensite, and the like; vermiculite-based clay minerals such as vermiculite and the like; mica-based clay minerals such as muscovite, phlogopite, mica, and the like; and the like. One of these may be used alone, or two or more may be used in combination.
Additionally, the lamellar clay mineral (b1) may be a natural product or a synthesized product.
Of these, smectite-based clay minerals that expand in water and have cation exchange capacity or expanding mica is preferable.
Here, a cation exchange capacity of the lamellar clay mineral is preferably from 10 to 300 milliequivalents/100 g.
Preferable examples of commercially available product that can be used as such a lamellar clay mineral (b1) include natural montmorillonite (trade name: Kunipia F, manufactured by Kunimine Industries Co., Ltd.; average particle size: 0.1 to 1 μm), synthetic smectite (trade name: Sumecton SA, manufactured by Kunimine Industries Co., Ltd.; average particle size: 20 nm), synthetic expanding mica (trade name: Somasif ME-100, manufactured by Co-op Chemical Co., Ltd.; average particle size: 1 to 3 μm); synthetic smectite (trade name: Lucentite SWN, manufactured by Co-op Chemical Co., Ltd.; average particle size: 0.02 μm); and synthetic smectite (trade name: Lucentite SWF, manufactured by Co-op Chemical Co., Ltd.; average particle size: 0.02 μm).
In the present invention, an organically modified lamellar clay mineral can be used as the lamellar clay mineral (b1).
The organically modified lamellar clay mineral can be obtained by regular inter-layer cation-exchanging and, for example, can be obtained by adding organic onium ions to a water-based slurry of the lamellar clay mineral described above and mixing in order to induce a reaction.
Here, the “organic onium ions” are ions that are generated from an organic onium compound produced by coordinate bonding a proton or another cationic reagent, or the like to a lone electron pair in a compound including an element such as oxygen, sulfur, nitrogen, and the like that has a lone electron pair.
Additionally, conditions for organically modifying using the organic onium ions are not particularly limited, and the reaction is preferably induced using an amount of the organic onium ions 0.3 to 2.0 times, and more preferably induced using an amount of the organic onium ions 0.5 to 1.5 times the cation exchange capacity of the lamellar clay mineral, and the reaction is preferably induced at a temperature of from 10 to 95° C.
Examples of the organic onium ions include ammonium ions, phosphonium ions, oxonium ions, sulfonium ions, and the like.
Of these, ammonium ions are the most common, and specific examples thereof include aliphatic ammonium ions, pyridinium ions, quinolinium ions, imidazolium ions, pyrrolidinium ions, piperidinium ions, betaines, lecithin, cation dyes (pigments), and the like.
Additionally, the aliphatic ammonium ions expressed by Formulas (I) and (II) below are preferable, and specific examples thereof include hydroxypolyoxyethylene trialkylammonium, hydroxypolyoxypropylene trialkylammonium, di(hydroxypolyoxyethylene)dialkylammonium, di(hydroxypolyoxypropylene)dialkylammonium, dimethyldioctylammonium, dimethyldidodecylammonium, methylethyldioctylammonium, methylethyldioctylammonium, methyltrioctylammonium, methyltridodecylammonium, benzylmethyldioctylammonium, benzylmethyldidodecylammonium, benzylethyldioctylammonium, benzylethyldioctylammonium, benzyltrioctylammonium, benzyltridodecylammonium, and the like.
In Formula (I), R1 is a hydrocarbon group having from 1 to 30 carbons; R2 and R3 are each independently a polyoxyethylene group (—(CH2OH2O)n—H), a polyoxypropylene group (—(CH2CH(CH3)O)n—H, —(CH2CH2CH2O)n—H), or a hydrocarbon group having from 1 to 10 carbons; and R4 is a polyoxyethylene group (—(CH2CH2O)n—H) or a polyoxypropylene group (—(CH2CH(CH3)O)n—H, —(CH2OH2CH2O)n—H). Moreover, n is from 1 to 50.
In Formula (II), R1 is a methyl group or a benzyl group; R2 is a hydrocarbon group having from 1 to 3 carbons or a hydrocarbon group having from 6 to 15 carbons; and R3 and R4 are each independently a hydrocarbon group having from 6 to 15 carbons.
Examples of commercially available products that can be used as such an organically modified lamellar clay mineral include S-BEN NX, S-BEN WX, Organite, and Organite D (all manufactured by Hojun Co., Ltd.); Lucentite SEN, Lucentite SPN, Lucentite SAN, Lucentite STN, Somasif MAE, Somasif MEE, Somasif MPE, and Somasif MTE (all manufactured by Co-op Chemical Co., Ltd.); and the like.
Organosilane Compound (b2)
Examples of the organosilane compound (b2) used in the preparation of the lamellar clay mineral (B) include compounds expressed by Formula (7) below.
R8n—Si—R94-n (7)
In Formula (7), R8 is a monovalent hydrocarbon group that may be branched, having from 1 to 25 carbons, and may contain a hetero atom. R9 is a hydrolyzable group, and n is an integer from 1 to 3. When n is 2 or 3, the plurality of R8 moieties may be the same or different, and when n is 1 or 2, the plurality of R9 moieties may be the same or different.
Examples of the monovalent hydrocarbon group that may be branched, having from 1 to 25 carbons in Formula (7), R8, include methyl groups, ethyl groups, propyl groups, isopropyl groups, n-butyl groups, isobutyl groups, sec-butyl groups, tert-butyl groups, n-pentyl groups, isopentyl groups, neopentyl groups, tert-pentyl groups, 1-methylbutyl groups, 2-methylbutyl groups, 1,2-dimethylpropyl groups, hexyl groups, heptyl groups, octyl groups, nonyl groups, decyl groups, dodecyl groups, tridecyl groups, tetradecyl groups, hexadecyl groups, octadecyl groups, cyclohexyl groups, vinyl groups, allyl groups, phenyl groups, tolyl groups, styryl groups, α-methylstyryl groups, and the like; functional groups (e.g. chloromethyl groups, chloropropyl groups, trifluoropropyl groups, and the like) wherein part or all of the hydrogen atoms bonded to the carbon atoms of the groups described above are substituted with a halogen atom (e.g. fluorine, chlorine and the like); and the like.
Moreover, examples of the hydrolyzable group in Formula (7), R9, include alkoxy groups, acyl groups, halogen groups, and the like.
Examples of the compound expressed by Formula (7) include methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, n-propyltrimethoxysilane, n-propyltriethoxysilane, i-propyltrimethoxysilane, i-propyltriethoxysilane, n-butyltrimethoxysilane, n-butyltriethoxysilane, n-pentyltrimethoxysilane, n-pentyltriethoxysilane, cyclohexyltrimethoxysilane, phenyltrimethoxysilane, hexyltrimethoxysilane, octyltriethoxysilane, nonyltriethoxysilane, decyltriethoxysilane, dodecyltriethoxysilane, tridecyltriethoxysilane, tetradecyltriethoxysilane, pentadecyltriethoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, diethyldimethoxysilane, diethyldiethoxysilane, di-n-propyldimethoxysilane, di-i-propyldimethoxysilane, di-n-butyldimethoxysilane, n-pentyl.methyldimethoxysilane, cyclohexyl.methyldiethoxysilane, phenyl.methyldimethoxysilane, di-n-pentyldimethoxysilane, di-n-hexyldimethoxysilane, di-n-heptyldimethoxysilane, di-n-octyldimethoxysilane, dicyclohexyldimethoxysilane, diphenyldimethoxysilane, trimethylmethoxysilane, triethylmethoxysilane, tri-n-propylmethoxysilane, tri-i-propylmethoxysilane, tri-n-butylmethoxysilane, tri-n-pentylmethoxysilane, tri-cyclohexylmethoxysilane, triphenylmethoxysilane, tri-n-hexylmethoxysilane, tri-n-heptylmethoxysilane, tri-n-octylmethoxysilane, tricyclohexylmethoxysilane, triphenylmethoxysilane, tridecylmethoxysilane, vinyltrichlorosilane, vinyltrimethoxysilane, vinyltriethoxysilane, vinyl-tris(methoxyethoxy)silane, vinyltriisopropoxysilane, 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldiethoxysilane, 3-glycidoxypropyltriethoxysilane, p-styryltrimethoxysilane, 3-methacryloxypropylmethyldimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-acryloxypropyltrimethoxysilane, 3-mercaptopropylmethyldimethoxysilane, 3-mercaptopropyltrimethoxysilane, bis(triethoxysilylpropyl)disulfide, bis(triethoxysilylpropyl)tetrasulfide, methyltrichlorosilane, methyldichlorosilane, dimethyldichlorosilane, trimethylchlorosilane, phenyltrichlorosilane, diphenyldichlorosilane, octyldimethylchlorosilane, trifluoropropyltrichlorosilane, cyclohexylmethyldimethoxysilane, trifluoropropyltrimethoxysilane, triphenylsilanol, hexamethyldisilazane, methyltriphenoxysilane, and the like. One of these may be used alone, or two or more may be used in combination.
Of these, from the perspective of being able to suppress hygroscopicity of the electrolyte in an element, methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, n-propyltrimethoxysilane, n-propyltriethoxysilane, i-propyltrimethoxysilane, i-propyltriethoxysilane, n-butyltrimethoxysilane, n-butyltriethoxysilane, n-pentyltrimethoxysilane, n-pentyltriethoxysilane, cyclohexyltrimethoxysilane, phenyltrimethoxysilane, hexyltrimethoxysilane, octyltriethoxysilane, nonyltriethoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, diethyldimethoxysilane, diethyldiethoxysilane, di-n-propyldimethoxysilane, di-i-propyldimethoxysilane, di-n-butyldimethoxysilane, n-pentyl.methyldimethoxysilane, cyclohexyl.methyldiethoxysilane, phenyl.methyldimethoxysilane, diphenyldimethoxysilane, trimethylmethoxysilane, trimethylethoxysilane, triethylmethoxysilane, tri-n-propylmethoxysilane, tri-i-propylmethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, 3-mercaptopropyltrimethoxysilane, bis(triethoxysilylpropyl)disulfide, bis(triethoxysilylpropyl)tetrasulfide, cyclohexylmethyldimethoxysilane, trifluoropropyltrimethoxysilane, hexamethyldisilazane, dimethoxymethyl trifluoropropylsilane, nonafluoro hexyltrichlorosilane, trifluoropropyl trichlorosilane, and methyltrifluoropropyl dichlorosilane are preferable.
Additionally, examples that can be used as the organosilane compound (b2) include condensation products of the compounds expressed by Formula (7) including organopolysiloxane such as dimethylpolysiloxane, methylphenylpolysiloxane, methylhydrogenpolysiloxane, and the like.
Furthermore, organodisilazanes such as hexamethyldisilazane, divinyltetramethyldisilazane, and the like can be used as the organosilane compound (b2).
In the present invention, the reaction of the lamellar clay mineral (b1) and the organosilane compound (b2) described above is not particularly limited, and the lamellar clay mineral (B) containing an alkylsilyl group can be prepared by stirring these in an organic solvent such as methanol or the like at a temperature from about 0 to 250° C., thereby reacting the hydroxy group contained in the lamellar clay mineral (b1) and the hydrolyzable group contained in the organosilane compound (b2).
Here, “the hydroxy group contained in the lamellar clay mineral (b1)” refers to the hydroxy group generally contained in the crystalline layer (in most cases, the end face) of a known lamellar clay mineral such as montmorillonite, smectite, or the like. However, in the reaction described above, all of the hydroxy groups contained in the lamellar clay mineral (b1) need not be substituted by alkylsilyl groups.
Note that in the reaction described above, following or simultaneous with the reaction between the lamellar clay mineral (b1) and the organosilane compound (b2), a hydrolyzable group derived from the organosilane compound (b2) (the functional group unreacted with the lamellar clay mineral (b1)) may be hydrolyzed or condensed.
On the other hand, in the present invention, examples of products that can be preferably used as the lamellar clay mineral (B) containing an alkylsilyl group include commercially available products such as silane-treated montmorillonite treated with alkyltrialkoxysilane (Bengel S H, manufactured by Hojun Co., Ltd.), silane-treated organic bentonite treated with quaternary ammonium and alkyltrialkoxysilane (manufactured by Hojun Co., Ltd.), and the like.
In the present invention, by including the lamellar clay mineral (B) described above, a photoelectric conversion element having superior moisture resistance can be formed.
While the reasons why this is so are not specifically clear, it is thought that the lamellar clay mineral (B) can prevent the intrusion of atmospheric water vapor due to it being hydrophobized to a greater degree than conventionally known lamellar clay minerals.
In the present invention, a content of the lamellar clay mineral (B), indicated as a content of inorganic matter, is preferably from 1 to 250 parts by mass, and more preferably from 2 to 150 parts by mass per 100 parts by mass of the ionic liquid (A).
Here, “indicated as a content of inorganic matter” takes into account the content of the organically modified lamellar clay mineral, and, when using the organically modified lamellar clay mineral, refers to the mass excluding the inter-layer cations, specifically the organic onium ions described above. Note that lamellar clay mineral that is not organically modified is an inorganic material including inter-layer cations (e.g. Na+, K+, Li+ and the like). Therefore, the value of the content indicated as inorganic matter and the content indicated as the entire product are the same.
Furthermore, in the present invention, a lamellar clay mineral that does not contain an alkylsilyl group (hereinafter referred to as the “other lamellar clay mineral”) can be used in combination with the lamellar clay mineral (B).
Specific examples of the other lamellar clay mineral include the lamellar clay mineral (b1) described above.
Additionally, a content of the other lamellar clay mineral, when included, is preferably from 0.5 to 99.5 mass % and more preferably from 40 to 98 mass % of a total mass of the lamellar clay mineral (B) and the other lamellar clay mineral because the photoelectric conversion efficiency of the photoelectric conversion element of the present invention will be better.
The organic solvent (C) that is optionally included in the electrolyte of the present invention is not particularly limited, provided that it is an organic solvent having a boiling point of not less than 150° C. and a relative dielectric constant of not less than 20.
Here, “boiling point” refers to a boiling point at 1 atmosphere and “relative dielectric constant” refers to a value measured using a Liquid Dielectric Constant Meter (Liquid Dielectric Constant Meter Model M-870, manufactured by Nihon Rufuto, Co., Ltd.), having 25° C. and 10 kHz applied.
Specific examples of the organic solvent (C) include methoxypropionitrile (boiling point: 166° C., relative dielectric constant: 25), ethoxypropionitrile (boiling point: 171° C., relative dielectric constant: 22), butoxypropionitrile (boiling point: 206° C., relative dielectric constant: 20), dimethoxy propionitrile (boiling point: 195° C., relative dielectric constant: 28), glutaronitrile (boiling point: 286° C., relative dielectric constant: 20), ethylene glycol bis(propionitrile)ether (boiling point: 330° C., relative dielectric constant: 20), propylene carbonate (boiling point: 240° C., relative dielectric constant: 65), diethyl carbonate (boiling point: 240° C., relative dielectric constant: 65), ethylmethyl carbonate (boiling point: 240° C., relative dielectric constant: 65), γ-butyrolactone (boiling point: 205° C., relative dielectric constant: 65), γ-valerolactone (boiling point: ° C., relative dielectric constant: 58), dimethyl sulfoxide (boiling point: 189° C., relative dielectric constant: 47), ethyl isopropyl sulfone (boiling point: 250° C., relative dielectric constant: 32), sulfolane (boiling point: 285° C., relative dielectric constant: 38), methyl sulfolane (boiling point: 270° C., relative dielectric constant: 32), and the like. One of these may be used alone, or two or more may be used in combination. Note that when two or more of these are used in combination, for example, a high dielectric constant solvent (cyclic carbonates) such as ethylene carbonate, propylene carbonate, butylene carbonate, or the like; and a low viscosity solvent (chain carbonates) such as dimethyl carbonate, ethylmethyl carbonate, diethyl carbonate, ethyl-n-butyl carbonate, methyl-t-butyl carbonate, di-i-propyl carbonate, t-butyl-i-propyl carbonate, or the like may be appropriately mixed so long as the object of the present invention is not impaired.
Of these, methoxypropionitrile, ethoxy propionitrile, or butoxy propionitrile are preferably used because the photoelectric conversion efficiency of the photoelectric conversion element using the electrolyte of the present invention (hereinafter also referred to as the “photoelectric conversion element of the present invention”) will be better; propylene carbonate, diethyl carbonate, ethylmethyl carbonate, or γ-butyrolactone are preferably used because of being readily available and low cost; and ethyl isopropyl sulfone, sulfolane, or methyl sulfolane is preferably used because of being electrochemically stable and because little cracked gas is generated.
In the present invention, by including the organic solvent (C) described above, a photoelectric conversion element having superior moisture resistance can be formed.
While the reasons why this is so are not specifically clear, it is thought that this is a result of the hygroscopicity of the organic solvent (C) being lower than that of the ionic liquid (A), volatilization when used for an extended period of time being low, and solubility with respect to other electrolyte components being high.
Additionally, in the present invention, when the organic solvent (C) is included, a ratio (C/A) of the organic solvent (C) to the ionic liquid (A) is preferably from 29/71 to 0.5/99.5 and more preferably from 23/77 to 1/99 because the superior moisture resistance of the photoelectric conversion element of the present invention will be maintained and the elution of the photosensitized dye (particularly the organic dye) in the dye-sensitized solar cell of the present invention will be suppressed.
A redox couple can be added to the electrolyte of the present invention in order to further enhance the photoelectric conversion efficiency of the photoelectric conversion element of the present invention.
Any conventional product commonly used for, or that can be used for, dye-sensitized solar cells may be used as the redox couple so long as the object of the present invention is not impaired.
For example, iodine/iodide ions, bromine/bromide ions, and the like can be used. Specific examples thereof include iodine/iodide ion pairs such as metal iodides of iodine and LiI, NaI, KI, or the like, iodide salts of iodine and a quaternary imidazolium compound, iodide salts of iodine and a quaternary pyridinium compound, iodide salts of iodine and a tetralkylammonium compound, and the like; bromine/bromide ions such as metal bromides of bromine and LiBr, NaBr, KBr, and the like, bromide salts of bromine and a quaternary imidazolium compound, bromide salts of bromine and a quaternary pyridinium compound, bromide salts of bromine and a tetralkylammonium compound, and the like; metal complexes such as ferrocyanate-ferricyanate, ferrocene-ferricinium salt, and the like; sulfur compounds of a disulfide compound and a mercapto compound; hydroquinone; quinone; and the like. One of these may be used alone, or two or more may be used in combination.
Of these, iodine/iodide ions and bromine/bromide ions are preferable.
Additionally, an inorganic salt and/or an organic salt can be added to the electrolyte of the present invention in order to enhance short current of the photoelectric conversion element of the present invention.
Examples of the inorganic salt and/or organic salt include alkali metals, alkali earth metal salts, and the like, such as lithium iodide, sodium iodide, potassium iodide, magnesium iodide, calcium iodide, lithium trifluoroacetate, sodium trifluoroacetate, lithium thiocyanate, lithium tetrafluoroborate, lithium hexaphosphate, lithium perchlorate, lithium trifluoromethanesulfonate, lithium bis(trifluoromethanesulphonyl)imide, and the like. One of these may be used alone, or two or more may be used in combination.
An added amount of the inorganic salt and/or organic salt is not particularly limited and may be a conventional amount so long as the object of the present invention is not inhibited.
Additionally, pyridines and/or benzimidazoles can be added to the electrolyte of the present invention in order to enhance the open voltage of the photoelectric conversion element of the present invention.
Specific examples include alkylpyridines such as methylpyridine, ethylpyridine, propylpyridine, butylpyridine, and the like; alkylimidazoles such as methylimidazole, ethylimidazole, propylimidazole, and the like; alkylbenzimidazoles such as methylbenzimidazole, ethylbenzimidazole, butylbenzimidazole, propylbenzimidazole, and the like; and the like. One of these may be used alone, or two or more may be used in combination.
An added amount of the pyridines and/or the benzimidazoles is not particularly limited and can be a conventional amount, so long as the object of the present invention is not inhibited.
An organic solvent other than the organic solvent (C) may be added to the electrolyte of the present invention, and specific examples thereof include carbonate esters such as ethylene carbonate, propylene carbonate, and the like; ethers such as ethylene glycol dialkyl ether, propylene glycol dialkyl ether, and the like; alcohols such as ethylene glycol monoalkyl ether, propylene glycol monoalkyl ether, and the like; polyhydric alcohols such as ethylene glycol, propylene glycol, and the like; nitriles such as acetonitrile, propionitrile, methoxypropionitrile, cyanoethyl ether, glutaronitrile, valeronitrile, and the like; lactones such as γ-butyrolactone and the like; amides such as dimethylformamide, N-methylpyrrolidone, and the like; aprotic polar solvents such as dimethyl sulfoxide, sulfolane, and the like; and the like. One of these may be used alone, or two or more may be used in combination.
A content of the organic solvent is not particularly limited and can be a conventional amount so long as the object of the present invention is not inhibited.
A manufacturing method of the electrolyte of the present invention is not particularly limited and can, for example, be manufactured by mixing the ionic liquid (A) and the lamellar clay mineral (B), along with the optionally included other lamellar clay mineral, the organic solvent (C), and the like, and then thoroughly mixing and uniformly dispersing (kneading) using a ball mill, sand mill, pigment disperser, grinder, ultrasonic disperser, homogenizer, planetary mixer, Hobart mixer, roll, kneader, or the like at room temperature or under heat (e.g. from 40 to 150° C.).
Here, as necessary, an organic solvent (e.g. toluene or the like) can be mixed in with the mixture described above and, after the mixing, the organic solvent may be removed using vacuum distillation.
Next, the photoelectric conversion element and the dye-sensitized solar cell of the present invention will be described using
The photoelectric conversion element of the present invention includes a photoelectrode having a transparent conductive film and a metal oxide semiconductor porous film, a counterelectrode disposed so as to oppose the photoelectrode, and an electrolyte layer provided between the photoelectrode and the counterelectrode.
As illustrated in
Here, the transparent plate 1 preferably has excellent optical transparency, and specific examples include, in addition to glass plates, resin plates (films) such as polystyrene, polyethylene, polypropylene, polyethylene terephthalate, polyethylene naphthalate, polycarbonate, polyphenylene sulfide, cyclic olefin polymer, polyether sulfone, polysulfone, polyetherimide, polyarylate, triacetylcellulose, methyl polymethacrylate, and the like.
Additionally, specific examples of the transparent conductive film 2 include conductive metal oxides such as tin oxide doped with antimony or fluorine, zinc oxide doped with aluminum or gallium, indium oxide doped with tin, and the like.
Moreover, a thickness of the transparent conductive film 2 is preferably from about 0.01 to 1.0 μm.
Furthermore, the method for providing the transparent conductive film 2 is not particularly limited, and examples thereof include coating methods, sputtering methods, vacuum deposition methods, spray pyrolysis methods, chemical vapor deposition (CVD) methods, sol-gel methods, and the like.
Next, the oxide semiconductor porous film 3 is obtained by applying a dispersion of oxide semiconductor particles on the transparent conductive film 2.
Specific examples of the oxide semiconductor particles include titanium oxide, tin oxide, zinc oxide, tungsten oxide, zirconium oxide, hafnium oxide, strontium oxide, vanadium oxide, niobium oxide, and the like. One of these may be used alone, or two or more may be used in combination.
The dispersion is obtained by mixing the oxide semiconductor particles and a carrier medium using a disperser such as a sand mill, bead mill, ball mill, three-roll mill, colloid mill, ultrasonic homogenizer, Henschel mixer, jet mill, or the like.
Additionally, the dispersion, after being obtained by mixing using the disperser and immediately prior to use (application), is preferably subjected to ultrasonic treatment using an ultrasonic homogenizer or the like. By performing the ultrasonic treatment immediately prior to use, the photoelectric conversion efficiency of the photoelectric conversion element of the present invention will be better. Reasons for this are thought to be that the filling of the oxide semiconductor porous film, formed using the dispersion that has been subjected to ultrasonic treatment immediately prior to use, with the electrolyte of the present invention including the ionic liquid (A) described above is facilitated and the adsorption capacity of the dye is increased.
Furthermore, acetyl acetone, hydrochloric acid, nitric acid, surfactants, chelating agents, and the like may be added to the dispersion in order to prevent the oxide semiconductor particles in the dispersion from re-aggregating; and a polymeric or cellulose thickening agent such as polyethylene oxide, polyvinylalcohol, and the like may be added to increase the viscosity of the dispersion.
Examples of commercially available products that can be used as the dispersion include titanium oxide pastes SP100 and SP200 (both manufactured by Showa Denko K.K.), titanium oxide fine particle Ti-Nanoxide T (manufactured by Solaronix S.A.), Ti-Nanoxide D (manufactured by Solaronix S.A.), Ti-Nanoxide T/SP (manufactured by Solaronix S.A.), Ti-Nanoxide D/SP (manufactured by Solaronix S.A.), titania coating paste PECC01 (manufactured by Peccell Technologies, Inc.), titania particle pastes PST-18NR and PST-400C (both manufactured by Nikki Chemical Co., Ltd.), and the like.
A known wet film forming method, for example, can be used as the method for applying the dispersion on the transparent conductive film.
Specific examples of the wet film forming method include screen printing methods, ink jet printing methods, roll coating methods, doctor blade methods, spincoating methods, spraying methods, and the like.
Additionally, after applying the dispersion on the transparent conductive film, a heat treatment, chemical treatment, plasma, or ozone treatment is preferably performed in order to enhance electronic contact between the particles, enhance adhesion with the transparent conductive film, and enhance film strength.
A temperature of the heat treatment is preferably from 40° C. to 700° C. and more preferably from 40° C. to 650° C. Additionally, a duration of the heat treatment is not particularly limited, but is normally from about 10 seconds to 24 hours.
Specific examples of the chemical treatment include chemical plating using a titanium tetrachloride aqueous solution, chemisorption using a carboxylic acid derivative, electrochemical plating using a titanium trichloride aqueous solution, and the like.
As illustrated in
Examples of metals that can be used as the metal plate include platinum, gold, silver, copper, aluminum, indium, titanium, and the like. Examples of resin plates that can be used include, in addition to the plate (film) exemplified by the transparent plate 1 that constitutes the photoelectrode 4, common resin plates that are non-transparent or have limited transparency.
Additionally, examples of the conductive film provided on the surface include conductive metal oxides and the like such as metals such as platinum, gold, silver, copper, aluminum, indium, titanium, and the like; carbon; tin oxide; tin oxides doped with antimony or fluorine; zinc oxide; zinc oxides doped with aluminum or gallium; indium oxides doped with tin; and the like. A thickness and a forming method of the conductive film are the same as for the transparent conductive film 2 that constitutes the photoelectrode 4.
In the present invention, an electrode having a conductive polymeric film formed on a plate or a conductive polymeric film electrode can be used as a counterelectrode 5.
Specific examples of the conductive polymer include polythiophene, polypyrrole, polyaniline, and the like.
Examples of a method for forming the conductive polymeric film on the plate include a method in which a conductive polymeric film from a polymeric dispersion is formed on a plate using a conventionally known wet film forming method such as a dipping method or a spin coating method.
Examples of products that can be used as the conductive polymeric dispersion include a polyaniline dispersion described in Japanese Unexamined Patent Application Publication No. 2006-169291, commercially available products such as a polythiophene derivative aqueous dispersion (Baytron P, manufactured by Bayer), aquaSAVE (manufactured by Mitsubishi Rayon Co., Ltd., polyaniline derivative aqueous solution), and the like.
Additionally, when the plate is the conductive plate, in addition to the method described above, the conductive polymeric film can also be formed on the plate via an electrolysis polymerization method. The conductive polymeric film electrode can use a self-standing film wherein the conductive polymeric film formed on the electrode by the electrolysis polymerization method is peeled from the electrode, or a self-standing film formed using a casting method, a spin coating method, or the like that is conventionally known as a wet film forming method for forming a film from a conductive polymeric dispersion. Here, for convenience, a mixture of a state in which conductive polymeric particles are dispersed throughout the solvent and a state in which conductive polymers are dissolved in the solvent is referred to as the “conductive polymeric dispersion.”
As illustrated in
The photoelectric conversion element of the present invention can achieve superior moisture resistance because the electrolyte of the present invention described above is used.
The dye-sensitized solar cell of the present invention is a type of photoelectric conversion element wherein the photoelectrode constituting the photoelectric conversion element of the present invention described above carries a photosensitized dye.
Here, the photosensitized dye is not particularly limited so long as it is a dye having absorption in the visible light spectrum and/or infrared light spectrum, and a metal complex or an organic dye, or the like, can be used.
Examples of the metal complex include ruthenium complex dyes (see the following formula), iron complex dyes, osmium complex dyes, platinum complex dyes, iridium complex dyes, metal phthalocyanine, metal porphyrin, and the like on which a ligand having a bipyridine structure, a terpyridine structure, or the like is coordinated.
On the other hand, examples of the organic dye include porphyrin-based dyes, phthalocyanine-based dyes, cyanine-based dyes, melocyanine-based dyes, xanthene-based dyes, coumarin-based dyes, indole-based dyes, fluorene-based dyes, triphenylamine-based dyes, and the like.
A method for applying the photosensitized dye is not particularly limited and can be applied by dissolving the dye described above in, for example, water, an alcohol-based solvent, or a nitrile-based solvent, and then immersing the oxide semiconductor porous film 3 in the dye solution or coating the dye solution on the oxide semiconductor porous film 3.
The present invention will now be described in greater detail using the following examples, but is in no way limited to these examples.
An ionic liquid and the like, shown in Tables 1 and 2 (hereinafter abbreviated as “Table 1, etc.”) below, were stirred and mixed in a mixing container according to the composition ratios shown in Table 1, etc. to prepare the electrolyte.
Specifically, according to the composition ratios shown in Table 1, etc., lamellar clay mineral B1 and/or lamellar clay mineral 1 were added to the ionic liquids A1 to A3 shown in Table 1, etc. while stirring. Thus, a gel-like substance in which a lamellar clay mineral is pre-expanded and dispersed was obtained.
The iodine and N-methylbenzimidazole shown in Table 1, etc. were added and mixed with the obtained gel-like substance as the electrolyte component according to the composition ratios shown in Table 1, etc.
Note that when using the organic solvents shown in Table 1, etc., a mixed liquid was first prepared by adding the ionic liquid A1 to A3 to the organic solvent.
A titanium oxide paste (Ti-Nanoxide D, manufactured by Solaronix S.A.) was coated on transparent conductive glass (FTO glass, surface resistance: 15 Ω/square, manufactured by Nippon Sheet Glass Co., Ltd.) and dried at room temperature, and thereafter was sintered for 30 minutes at a temperature of 450° C. Thereby, a photoelectrode having a titanium oxide porous film formed on transparent conductive glass was fabricated.
The fabricated photoelectrode was then immersed for four hours in a ruthenium complex dye (cis-(dithiocyanate)-N,N′-bis(2,2′-bipyridyl-4,4′-dicarboxylic acid)ruthenium(II)complex) (Ruthenium 535-bis TBA, manufactured by Solaronix S.A.) butyl alcohol/acetonitrile solution (Specific volume: 1/1; Concentration: 3×10−4 mol/L).
Thereafter, the product was washed using acetonitrile and dried in a dark location under a stream of nitrogen. Thus a photoelectrode carrying a photosensitized dye in a titanium oxide electrode of a photoelectrode was used as the photoelectrode.
The prepared electrolyte was applied on the photoelectrode carrying the photosensitized dye, and this and a platinum counterelectrode formed by forming a platinum film having a thickness of about 100 nm on a surface of a transparent conductive glass plate using a sputtering method (indium oxide doped with tin on a conductive face, sheet resistance: 8 Ω/square, manufactured by Nippon Sheet Glass Co., Ltd.) were bonded. When bonding, a thermal fusion bonding film was interposed between the photoelectrode and the platinum counterelectrode. Thermal fusion bonding was performed at 150° C. and a seal was formed between the electrodes. Thus, the dye-sensitized solar cell (photosensitized dye: ruthenium complex dye) was obtained.
Other than using an indoline-based dye (D205, manufactured by Mitsubishi Paper Mills Limited) in place of the ruthenium complex dye, a dye-sensitized solar cell (photosensitized dye: organic dye) was fabricated according to the same method used in the fabrication of the dye-sensitized solar cell (photosensitized dye: ruthenium complex dye).
The photoelectric conversion efficiency of the obtained two types of dye-sensitized solar cells and maintenance factor thereof were measured and evaluated according to the methods described below. The results are shown in Table 1, etc.
As illustrated in
The dye-sensitized solar cell that was measured for photoelectric conversion efficiency was left for 1,000 hours at a temperature of 40° C. and an RH of 85% and, thereafter, was measured again for photoelectric conversion efficiency according to the same method described above. The maintenance factor (post-humidifying photoelectric conversion efficiency/pre-humidifying photoelectric conversion efficiency) was calculated.
When the calculated results of the maintenance factor of photoelectric conversion efficiency was 0.80 or greater, the moisture resistance was evaluated as being superior.
The same evaluation was performed after allowing the dye-sensitized solar cell to be left for 1,500 hours.
The components shown in Table 1, etc. are as follows.
Ionic liquid A1: N-methyl-3-propyl imidazolium iodide (manufactured by Tokyo Chemical Industry Co., Ltd.)
Ionic liquid A2: N-ethyl-3-methyl imidazolium bis(trifluoromethylsulphonyl)imide (manufactured by Solvent Innovation)
Ionic liquid A3: N-ethyl-3-methylimidazolium tetracyanoborate (manufactured by Merck)
Lamellar clay mineral B1: Silane-treated organic bentonite treated with quaternary ammonium and alkyltrialkoxysilane (manufactured by Hojun Co., Ltd.)
Lamellar clay mineral 1: Synthetic smectite (trade name: Lucentite SPN, manufactured by Co-op Chemical Co., Ltd. (organically modified lamellar clay mineral of organically modified Lucentite SWN (average particle size: 0.02 μm, also manufactured by Co-op Chemical Co., Ltd.)))
Organic solvent C1: Methoxypropionitrile (boiling point: 166° C., relative dielectric constant: 25)
As is clear from the results shown in Table 1, etc., the electrolytes of Comparative Examples 1 and 2 that were prepared without including the lamellar clay mineral containing an alkylsilyl group experienced about a 60% decline in photoelectric conversion efficiency after moisturization and had inferior moisture resistance. It is also clear that the electrolytes of Comparative Examples 3 and 4 in which the type of ionic liquid was changed, the electrolyte of Comparative Example 5 in which an organic solvent was also used, and the electrolytes of Comparative Examples 6 and 7 in which the type of photosensitized dye was changed experienced the same results. Note that in Comparative Example 7 where an organic dye was used as the photosensitized dye, the maintenance factor of the photoelectric conversion efficiency after moisturization was higher than that of Comparative Example 6. Based on this, it is thought that the elution of the organic dye was suppressed due to the usage of the organic solvent.
On the other hand, it is clear that the electrolytes of Working Examples 1 to 6 that were prepared using the lamellar clay mineral (B) containing an alkylsilyl group displayed the same level of photoelectric conversion efficiency as that of Comparative Examples 1 and 2, and displayed high photoelectric conversion efficiency after moisturizing and also superior moisture resistance. Likewise, it is clear that the electrolytes of Working Examples 7 to 10 in which the type of ionic liquid was changed displayed the same level of photoelectric conversion efficiency as that of Comparative Examples 3 and 4, and displayed high photoelectric conversion efficiency after moisturizing and also superior moisture resistance.
Additionally, it is clear that the electrolytes of Working Examples 11 to 14 that were prepared also using the organic solvent (C) displayed moisture resistance that was as superior as that of Working Examples 1 to 6 and also displayed a higher photoelectric conversion efficiency.
On the other hand, it is clear that the electrolytes of Working Examples 15 to 19 in which the organic dye was used as the photosensitized dye displayed superior moisture resistance. Particularly, it is clear that the electrolytes of Working Examples 16 to 19 in which the organic solvent (C) was also used displayed moisture resistance superior to that of Working Example 15, and that the maintenance factor of the photoelectric conversion efficiency after moisturization was higher.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2010-064068 | Mar 2010 | JP | national |
| 2010-243682 | Oct 2010 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2011/055100 | 3/4/2011 | WO | 00 | 9/13/2012 |
