Electrochromic Device

Abstract

To provide an electrochromic device that can prevent generation of a remaining phenomenon.SOLUTION: The electrochromic device includes: a first electrode; an electrochromic layer on the first electrode; a second electrode; and an electrolyte layer between the electrochromic layer and the second electrode. The electrolyte layer contains a basic compound.SELECTED DRAWING: None

Description

[Technical field]

[0001] The present invention ,workman Lectrochromic elements To the child Regarding. [Background technology]

[0002] In conventional electrochromic elements, when subjected to high load environments such as repeated driving many times, continuous driving for long periods of time, or driving in high temperature environments, the color remains after it has been colored once, and it is unable to return to a transparent state. This phenomenon occurs when the charge balance between a pair of electrodes is disrupted, and is thought to be caused by charge remaining on one of the electrodes. This phenomenon is called "residual fade (or residual color)." This residual fade phenomenon has led to the problem that it has not been possible to provide an electrochromic element with a sufficiently long life.

[0003] As a means for solving the above-mentioned residual color phenomenon, there is a method for eliminating the residual charge by applying an excessively high bleaching voltage, but the application of a high voltage causes an unexpected reaction in the material inside the element, which deteriorates the electrochromic element and shortens its lifespan. Therefore, as a means for preventing such deterioration while solving the residual color phenomenon, for example, a method has been proposed in which a third electrode is placed in addition to the pair of electrodes to allow the residual charge to escape (for example, see Patent Document 1).

[0004] Also, a method has been proposed that uses a material that is more reactive than the electrochromic material and does not change color due to the reaction (for example, see Patent Document 2). This method is called a "redox buffer," and even if a charge remains, the "redox buffer," not the electrochromic material, retains the charge, so the electrochromic element can maintain its decolorized state. Summary of the Invention [Problem to be solved by the invention]

[0005] An object of the present invention is to provide an electrochromic element capable of preventing the occurrence of the residual light disappearance phenomenon. [Means for solving the problem]

[0006] The electrochromic element of the present invention as a means for solving the above problems comprises a first electrode, an electrochromic layer provided on the first electrode, a second electrode, and an electrolyte layer between the electrochromic layer and the second electrode, wherein the electrolyte layer contains a basic compound. Effect of the Invention

[0007] According to the present invention, it is possible to provide an electrochromic element capable of preventing the occurrence of the residual light phenomenon. [Brief description of the drawings]

[0008] [Figure 1] FIG. 1 is a schematic cross-sectional view showing an example of an electrochromic element according to a first embodiment. [Diagram 2] FIG. 2 is a schematic cross-sectional view showing another example of the electrochromic element according to the second embodiment. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0009] (Electrochromic element) The electrochromic element of the present invention comprises a first electrode, an electrochromic layer provided on the first electrode, a second electrode, and an electrolyte layer between the electrochromic layer and the second electrode, the electrolyte layer containing a basic compound, and further comprising other components as necessary.

[0010] The conventional technology described in Patent Document 1 (Patent Publication No. 6597373) has a configuration in which a third electrode is arranged, which places limitations on the thickness and shape of the electrochromic element, and therefore has the problem that it is not possible to provide an electrochromic element suitable for expected applications. Furthermore, the conventional technology described in Patent Document 2 (US Patent No. 6,188,505) has the drawback that the amount of current required for color development increases and power consumption increases because the "redox buffer" reacts even during normal color development. Also, when color development is resumed after some of the "redox buffer" has already reacted, the distribution of the charge input to the "redox buffer" and the electrochromic material differs from the initial state, making it impossible to maintain the expected color development state.

[0011] Therefore, in the present invention, a first electrode, an electrochromic layer provided on the first electrode, a second electrode, and an electrolyte layer between the electrochromic layer and the second electrode are provided, and the electrolyte layer contains a basic compound, thereby preventing the charge balance from being disturbed and preventing the occurrence of the residual charge phenomenon, and as a result, an electrochromic element with a long life can be provided.

[0012] The electrolyte composition of the present invention used in the electrochromic device of the present invention will be described in detail below.

[0013] (Electrolyte composition) The electrolyte composition of the present invention contains an electrolyte and a basic compound, and further contains other components as required.

[0014] <Electrolytes> Examples of the electrolyte include inorganic ion salts such as alkali metal salts and alkaline earth metal salts, quaternary ammonium salts, and supporting salts of acids and alkalis. Examples of the electrolyte include LiClO4, LiBF4, LiAsF6, LiPF6, LiCF3SO3, LiCF3COO, KCl, NaClO3, NaCl, NaBF4, NaSCN, KBF4, Mg(ClO4)2, Mg(BF4)2, etc. These may be used alone or in combination of two or more.

[0015] In addition, an ionic liquid can also be used as the electrolyte. There is no particular limitation on the ionic liquid, and any substance that has been generally studied or reported may be used. In particular, organic ionic liquids have a molecular structure that exhibits liquidity over a wide temperature range, including room temperature. The molecular structure of the ionic liquid may include, as a cationic component, for example, imidazole derivatives such as N,N-dimethylimidazole salt, N,N-methylethylimidazole salt, and N,N-methylpropylimidazole salt; aromatic salts such as pyridinium derivatives such as N,N-dimethylpyridinium salt and N,N-methylpropylpyridinium salt; and aliphatic quaternary ammonium compounds such as tetraalkylammoniums such as trimethylpropylammonium salt, trimethylhexylammonium salt, and triethylhexylammonium salt. As the anion component, a compound containing fluorine is preferable in terms of stability in the atmosphere, for example, BF4 - , CF3SO3 - , PF4 - , (CF3SO2)2N - , T.C.B. - , F.S.I. - , TFSI - , T.C.H.B. - , T.C.F.B. - Ionic liquids formulated by combining these cationic components and anionic components can be used.

[0016] Examples of the ionic liquid include ethylmethylimidazolium tetracyanoborate, ethylmethylimidazolium bistrifluoromethanesulfonimide, ethylmethylimidazolium tripentafluoroethyl trifluorophosphate, ethylmethylimidazolium bis(fluorosulfonyl)imide, ethylmethylimidazolium diethylphosphate, butylmethylimidazolium hexafluorophosphate, ethylmethylimidazolium trifluoromethanesulfonate, and ethylmethylimidazolium. Examples of the fluorine-containing amines include acetate, ethylmethylimidazolium tricyanomethanide, ethylmethylimidazolium dicyanamide, methyloctylimidazolium hexafluorophosphate, methylpropylpyrrolidinium bisfluorosulfonimide, butylmethylimidazolium tetrafluoroborate, butylmethylimidazolium bis(trifluoromethanesulfonyl)imide, hexylmethylimidazolium bis(trifluoromethylsulfonyl)imide, and allylbutylimidazolium tetrafluoroborate. These may be used alone or in combination of two or more.

[0017] <Basic compounds> Examples of the basic compound include nitrogen-containing amines, amides, heterocyclic compounds, basic organic phosphorus compounds, and conjugate salts of organic acids. Examples of basic compounds include ethylamine, diethylamine, triethylamine, ethyldiisopropylamine, 1,4-diazabicyclo[2.2.2]octane, ethanolamine, diethanolamine, triethanolamine, aniline, 1,8-bis(dimethylamino)naphthalene, pyrrolidine, pyrrole, N-methylpyrrolidone, 1-methyl-2-pyrrolidone, N-methylacetamide, N-methylformamide, pyridine, imidazole, pyrimidine, pyrazine, indole, diaza Examples of the compounds include bicycloundecene, 1,10-phenanthroline, triphenylphosphine, triethylphosphine, sodium acetate, sodium citrate, tetramethylammonium acetate, betaine, 2-(dimethylamino)ethyl acrylate, N-[3-(dimethylamino)propyl]acrylamide, N,N-dimethylacrylamide, 3-[(3-acrylamidopropyl)dimethylammonio]propanoate, 4-acryloylmorpholine, and 2-(dimethylamino)methacrylate. These compounds may be used alone or in combination of two or more. Among these compounds, compounds having a pyridine group in the structure are preferred.

[0018] Examples of compounds having a pyridine group include pyridine, 4-dimethylaminopyridine, 2,6-lutidine, bipyridine, fluoropyridine, 4-tert-butylpyridine, 2,6-di-tert-butylpyridine, 5-ethyl-2-pyridineethanol, ethyl 4-pyridyl acetate, ethyl 3-pyridyl acetate, ethyl 2-pyridyl acetate, 4-benzylpyridine, 3-benzylpyridine, 2-benzylpyridine, 4-(3-phenylpropyl)pyridine, 4-pyridylethyl acetate, etc. These may be used alone or in combination of two or more.

[0019] The basic compound is preferably a basic polymer, since diffusion to the electrode surface is suppressed, so that the basic compound itself undergoes little reaction and is less likely to deteriorate. The weight average molecular weight of the basic polymer is preferably from 10,000 to 1,000,000, and more preferably from 10,000 to 200,000. If the weight-average molecular weight is less than 10,000, it may diffuse in the electrolyte composition and cause an unexpected reaction on the electrode surface, leading to deterioration, whereas if the weight-average molecular weight exceeds 1,000,000, the solubility may be insufficient. The weight average molecular weight can be measured, for example, by gel permeation chromatography (GPC). Examples of the basic polymer include polyvinylpyridines such as poly(4-vinylpyridine) and poly(2-vinylpyridine), poly(4-vinylpyridine-co-styrene), poly(2-vinylpyridine-co-styrene), poly(4-vinylpyridine-co-butyl methacrylate), polyacrylamide, poly(dimethylaminoethyl methacrylate), polyamines, etc. Among these, polyvinylpyridine is preferred since it does not affect the polymerization reactivity during polymer polymerization and has good solubility in the electrolyte composition.

[0020] The basic polymer may be mixed directly into the electrolyte composition, or may be incorporated as a copolymer unit into a polymer chain for retaining the electrolyte and the solvent. To incorporate it as a copolymerization unit into a polymer chain, a basic polymer is synthesized by polymerizing a basic monomer, such as 2-vinylpyridine, 4-vinylpyridine, dimethylaminopropylacrylamide, 2-(dimethylamino)ethyl acrylate, or 3-[(3-acrylamidopropyl)dimethylammonio]propanoate.

[0021] The content of the basic compound is not particularly limited and can be appropriately selected depending on the purpose, but is preferably from 0.01% by mass to 10% by mass, and more preferably from 0.01% by mass to 2% by mass, based on the total amount of the electrolyte composition.

[0022] -Electrolyte solvent- Examples of the electrolyte solvent include propylene carbonate, acetonitrile, γ-butyrolactone, ethylene carbonate, sulfolane, dioxolane, tetrahydrofuran, 2-methyltetrahydrofuran, dimethylsulfoxide, 1,2-dimethoxyethane, 1,2-ethoxymethoxyethane, polyethylene glycol, alcohols, and mixed solvents thereof. When an ionic liquid is used as the electrolyte, it is not necessarily necessary to use a separate electrolyte solvent because the ionic liquid also serves as the electrolyte solvent.

[0023] The electrolyte composition does not need to be a low-viscosity liquid, and can take various forms such as a gel, a polymer crosslinked type, a liquid crystal dispersion type, etc. Among these, from the viewpoint of ease of handling and prevention of liquid leakage, a solid or gel is preferable. By forming it into a gel or solid form, advantages such as improved element strength and improved reliability can be obtained. As a solidification method, it is preferable to hold the electrolyte, the basic compound, and the electrolyte solvent in a binder resin, because this provides high ionic conductivity and solid strength.

[0024] The binder resin is not particularly limited and can be appropriately selected according to the purpose, and examples thereof include acrylic resin, polyester resin, urethane resin, polyether resin, polyamide resin, polysaccharide resin such as cellulose derivative, polyacrylamide resin, polyvinyl ester resin, and resin obtained by polymerizing photopolymerizable monomer and photopolymerizable oligomer. In addition, a basic polymer resin can be used to serve as the basic compound of the present invention. These may be used alone or in combination of two or more. Among these, resins obtained by polymerizing photopolymerizable monomer and photopolymerizable oligomer are particularly preferred because they can be produced at a low temperature and in a short time compared to the method of forming a thin film by thermal polymerization or evaporating a solvent.

[0025] As the photopolymerizable monomer, a monofunctional photopolymerizable monomer, a difunctional photopolymerizable monomer, or a polyfunctional photopolymerizable monomer having three or more functional groups can be used.

[0026] Examples of monofunctional photopolymerizable monomers include 2-(2-ethoxyethoxy)ethyl acrylate, methoxypolyethylene glycol monoacrylate, methoxypolyethylene glycol monomethacrylate, methyl methacrylate, phenoxypolyethylene glycol acrylate, 2-acryloyloxyethyl succinate, acryloylmorpholine, 2-ethylhexyl acrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, tetrahydrofurfuryl acrylate, 2-ethylhexyl carbitol acrylate, 3-methoxybutyl acrylate, benzyl acrylate, cyclohexyl acrylate, isoamyl acrylate, isobutyl acrylate, methoxytriethylene glycol acrylate, phenoxytetraethylene glycol acrylate, cetyl acrylate, isostearyl acrylate, stearyl acrylate, or styrene monomer. These may be used alone or in combination of two or more.

[0027] Examples of bifunctional photopolymerizable monomers include 1,3-butanediol diacrylate, 1,4-butanediol diacrylate, 1,4-butanediol dimethacrylate, 1,6-hexanediol diacrylate, 1,6-hexanediol dimethacrylate, diethylene glycol diacrylate, polyethylene glycol diacrylate, neopentyl glycol diacrylate, EO-modified bisphenol A diacrylate, EO-modified bisphenol F diacrylate, and neopentyl glycol diacrylate. These may be used alone or in combination of two or more. In the above, "EO-modified" refers to ethyleneoxy-modified, and "PO-modified" refers to propyleneoxy-modified.

[0028] Examples of photopolymerizable monomers with three or more functionalities include trimethylolpropane triacrylate (TMPTA), trimethylolpropane trimethacrylate, EO-modified trimethylolpropane triacrylate, PO-modified trimethylolpropane triacrylate, caprolactone-modified trimethylolpropane triacrylate, HPA-modified trimethylolpropane trimethacrylate, pentaerythritol triacrylate, pentaerythritol tetraacrylate (PETTA), glycerol triacrylate, ECH-modified glycerol triacrylate, EO-modified glycerol triacrylate, PO-modified glycerol triacrylate, tris Examples of the acrylate include (acryloxyethyl) isocyanurate, dipentaerythritol hexaacrylate (DPHA), caprolactone-modified dipentaerythritol hexaacrylate, dipentaerythritol hydroxypentaacrylate, alkyl-modified dipentaerythritol pentaacrylate, alkyl-modified dipentaerythritol tetraacrylate, alkyl-modified dipentaerythritol triacrylate, dimethylolpropane tetraacrylate (DTMPTA), pentaerythritol ethoxy tetraacrylate, EO-modified phosphoric acid triacrylate, and 2,2,5,5-tetrahydroxymethylcyclopentanone tetraacrylate. These may be used alone or in combination of two or more.

[0029] Examples of photopolymerizable oligomers include urethane acrylate, epoxy acrylate, acrylic acrylate, polyester acrylate, polyethylene glycol acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, and various reactive polymers.

[0030] -Other ingredients- The other components are not particularly limited and can be appropriately selected depending on the purpose. Examples of the other components include a polymerization initiator.

[0031] The polymerization initiator is not particularly limited and can be appropriately selected depending on the purpose. Examples of the polymerization initiator include radical polymerization initiators. Examples of the radical polymerization initiator include a thermal polymerization initiator and a photopolymerization initiator.

[0032] Examples of the thermal polymerization initiator include azo compounds such as 2,2'-azobisisobutyronitrile, dimethyl-2,2'-azobisisobutyrate, 2,2'-azobis(2,4-dimethylvaleronitrile), and 2,2'-azobis[2-(2-imidazolin-2-yl)propane]; and organic peroxides such as 2,5-dimethyl-2,5-bis(tert-butylperoxy)hexane and di(4-tert-butylcyclohexyl)peroxydicarbonate. These may be used alone or in combination of two or more.

[0033] Examples of the photopolymerization initiator include ketal-based photopolymerization initiators such as 2,2-dimethoxy-1,2-diphenylethan-1-one, acetophenone-based photopolymerization initiators such as 1-hydroxycyclohexyl phenyl ketone, 2,2-diethoxyacetophenone, 2,2-dimethoxy-2-phenylacetophenone, 4-phenoxydichloroacetophenone, and 4-(t-butyl)dichloroacetophenone, and benzoin ether-based photopolymerization initiators such as benzoin methyl ether, benzoin ethyl ether, benzoin propyl ether, benzoin isopropyl ether, and benzoin isobutyl ether. These may be used alone or in combination of two or more.

[0034] The content of the polymerization initiator is not particularly limited and can be appropriately selected depending on the purpose, but is preferably from 0.001 to 5 parts by mass, more preferably from 0.01 to 2 parts by mass, and particularly preferably from 0.01 to 1 part by mass, relative to 100 parts by mass of the total monomer components.

[0035] The electrolyte layer can be formed, for example, by injecting a liquid electrolyte composition into the gap between the electrochromic layer and the electrochemically active layer and solidifying it by photocuring, or by previously solidifying the electrolyte into a sheet shape and then laminating it with another layer. When a liquid electrolyte composition is used as the electrolyte composition, for example, the electrolyte composition adjusted to a liquid state can be injected into the gap between the electrochromic layer and the electrochemically active layer, and the outer periphery can be sealed and fixed with a sealant or the like to form a layer made of the electrolyte composition.

[0036] The electrolyte composition of the present invention can be suitably used in various electrochemical devices such as electrochromic elements, organic electroluminescent elements, lithium ion secondary batteries, solar cells, fuel cells, and ion-conducting actuators, but is particularly suitable for use in the electrolyte layer of an electrochromic element described below. By using the electrolyte composition of the present invention as the electrolyte layer of an electrochromic element, it is possible to prevent the charge balance in the electrochromic element from being disturbed and to prevent the occurrence of the residual charge phenomenon. As a result, it is possible to provide an electrochromic element with a long life.

[0037] The electrochromic device of the present invention preferably comprises a first electrode, an electrochromic layer provided on the first electrode, a second electrode, and an electrolyte layer between the electrochromic layer and the second electrode, and further comprises other components as necessary.

[0038] <First electrode> The material for the first electrode is not particularly limited as long as it is a transparent material having electrical conductivity, and can be appropriately selected depending on the purpose. Examples of materials for the first electrode include inorganic materials such as tin-doped indium oxide (hereinafter referred to as "ITO"), fluorine-doped tin oxide, antimony-doped tin oxide, and zinc oxide. Furthermore, an electrode having improved conductivity while maintaining transparency may be used by forming transparent carbon nanotubes or highly conductive non-transparent materials such as Au, Ag, Pt or Cu into a fine network.

[0039] The thickness of the first electrode is adjusted so as to obtain an electrical resistance value necessary for the redox reaction of the electrochromic layer. When ITO is used as the material of the first electrode, the average thickness of the first electrode is preferably 50 nm or more and 500 nm or less.

[0040] The method for producing the first electrode may be, for example, a vacuum deposition method, a sputtering method, an ion plating method, etc. There is no particular limitation as long as the material of the first electrode can be applied, and various printing methods such as a spin coating method, a casting method, a microgravure coating method, a gravure coating method, a bar coating method, a roll coating method, a wire bar coating method, a dip coating method, a slit coating method, a capillary coating method, a spray coating method, a nozzle coating method, a gravure printing method, a screen printing method, a flexographic printing method, an offset printing method, a reverse printing method, or an inkjet printing method may be used.

[0041] <Electrochromic layer> The electrochromic layer contains an electrochromic material that has the property of changing color by an electrochemical oxidation-reduction reaction, and further contains other components as required.

[0042] -Electrochromic materials- The electrochromic material is not particularly limited and can be appropriately selected depending on the purpose, but a compound that develops color through an oxidation reaction is preferred. Examples of materials that develop color through an oxidation reaction include azobenzene compounds, tetrathiafulvalene compounds, triphenylmethane compounds, triarylamine compounds, leuco dyes, etc. Among these, triarylamine compounds are more preferably used.

[0043] Examples of the triarylamine compound include compounds represented by the following general formula 1. A n -B m ...[General formula 1] However, when n=2, m is 0, and when n=1, m is 0 or 1. The A is a structure represented by the following general formula 2, and R1 to R 15 It is bonded to B at any one of the positions. The B is a structure represented by the following general formula 3, R 16 From R 21 It is bonded to A at any one of the positions.

[0044] [ka] [ka] However, R1 to R 21 It is preferable that any one of R1 to R2 is chemically bonded in the electrochromic layer via a polymerizable functional group or a functional group capable of directly or indirectly bonding to a hydroxyl group. This allows the oxidized electrochromic compound to be supported in the electrochromic layer. 21 are all monovalent organic groups and may be the same or different.

[0045] The polymerizable functional group is not particularly limited as long as it has a carbon-carbon double bond and is polymerizable, and can be appropriately selected depending on the purpose. Examples of the polymerizable functional group include a vinyl group, a styryl group, a 2-methyl-1,3-butadienyl group, a vinylcarbonyl group, an acryloyloxy group, an acryloylamide group, and a vinylthioether group.

[0046] The functional group capable of directly or indirectly bonding to the hydroxyl group is not particularly limited and may be appropriately selected depending on the purpose, so long as it is a functional group capable of directly or indirectly bonding to the hydroxyl group through hydrogen bonding, adsorption or chemical reaction. Specific examples of the structure include silyl groups (or silanol groups) such as phosphonic acid groups, phosphoric acid groups, trichlorosilyl groups, trialkoxysilyl groups, monochlorosilyl groups and monoalkoxysilyl groups, and carboxyl groups. Examples of the trialkoxysilyl group include a triethoxysilyl group and a trimethoxysilyl group. Among these, a phosphonic acid group or a silyl group (trialkoxysilyl group, or trihydroxysilyl group) that has a high bonding strength to a conductive or semiconducting nanostructure is preferred.

[0047] The monovalent organic groups each independently include a hydrogen atom, a halogen atom, a hydroxyl group, a nitro group, a cyano group, a carboxyl group, an alkoxycarbonyl group which may have a substituent, an aryloxycarbonyl group which may have a substituent, an alkylcarbonyl group which may have a substituent, an arylcarbonyl group which may have a substituent, an amido group, a monoalkylaminocarbonyl group which may have a substituent, a dialkylaminocarbonyl group which may have a substituent, a monoarylaminocarbonyl group which may have a substituent, a diarylaminocarbonyl group which may have a substituent, a sulfonic acid group, an alkoxysulfonyl group which may have a substituent, an aryloxysulfonyl group which may have a substituent, an alkylsulfonyl group which may have a substituent, a Examples of the alkyl group include an arylsulfonyl group, a sulfonamide group, a monoalkylaminosulfonyl group which may have a substituent, a dialkylaminosulfonyl group which may have a substituent, a monoarylaminosulfonyl group which may have a substituent, a diarylaminosulfonyl group which may have a substituent, an amino group, a monoalkylamino group which may have a substituent, a dialkylamino group which may have a substituent, an alkyl group which may have a substituent, an alkenyl group which may have a substituent, an alkynyl group which may have a substituent, an aryl group which may have a substituent, an alkoxy group which may have a substituent, an aryloxy group which may have a substituent, an alkylthio group which may have a substituent, an arylthio group which may have a substituent, a heterocyclic group which may have a substituent, etc. Among these, from the viewpoint of stable operation, an alkyl group, an alkoxy group, a hydrogen atom, an aryl group, an aryloxy group, a halogen atom, an alkenyl group, and an alkynyl group are preferable. Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, and a butyl group. Examples of the aryl group include a phenyl group and a naphthyl group. Examples of the aralkyl group include a benzyl group, a phenethyl group, and a naphthylmethyl group. Examples of the alkoxy group include a methoxy group, an ethoxy group, and a propoxy group. Examples of the aryloxy group include a phenoxy group, a 1-naphthyloxy group, a 2-naphthyloxy group, a 4-methoxyphenoxy group, and a 4-methylphenoxy group. Examples of the heterocyclic group include carbazole, dibenzofuran, dibenzothiophene, oxadiazole, and thiadiazole. Examples of the substituent that may be further substituted on the above-mentioned substituent include a halogen atom, a nitro group, a cyano group, an alkyl group such as a methyl group or an ethyl group, an alkoxy group such as a methoxy group or an ethoxy group, an aryloxy group such as a phenoxy group, an aryl group such as a phenyl group or a naphthyl group, and an aralkyl group such as a benzyl group or a phenethyl group.

[0048] Examples of the triarylamine compound represented by the general formula 1 include, but are not limited to, the following: In the above, Me represents a methyl group, and Et represents an ethyl group.

[0049] [Example compound 1] [ka]

[0050] [Example compound 2] [ka]

[0051] [Example compound 3] [ka]

[0052] [Example compound 4] [ka]

[0053] [Example compound 5] [ka]

[0054] [Example compound 6] [ka]

[0055] [Example compound 7] [ka]

[0056] [Example compound 8] [ka]

[0057] [Example compound 9] [ka]

[0058] [Example compound 10] [ka]

[0059] [Example compound 11] [ka]

[0060] [Example compound 12] [ka]

[0061] [Example compound 13] [ka]

[0062] [Example compound 14] [ka]

[0063] [Example compound 15] [ka]

[0064] [Example compound 16] [ka]

[0065] [Example compound 17] [ka]

[0066] [Example compound 18] [ka]

[0067] [Example compound 19] [ka]

[0068] [Example compound 20] [ka]

[0069] -Binder- The electrochromic layer may contain a binder. Examples of the binder include polymers such as polyethylene oxide, polyvinyl alcohol, polyacrylonitrile, methacrylate, acrylate, and polyvinylidene fluoride.

[0070] The electrochromic composition may contain a binder precursor instead of a binder, or may contain a binder and a binder precursor. The binder precursor may be, for example, a polymerizable compound such as a monomer.

[0071] When a polymerizable compound is used as the binder precursor, for example, an electrochromic composition in which the polymerizable compound is dissolved in a liquid is applied, and then the polymerizable compound is polymerized by heating or irradiating with non-ionizing radiation, ionizing radiation, infrared radiation, ultraviolet radiation, or the like, to produce a binder as shown in FIG. 2.

[0072] The polymerizable compound is not particularly limited as long as it has a polymerizable group, but a compound capable of being polymerized at 25°C is preferred.

[0073] The polymerizable compound may be monofunctional or polyfunctional. Note that a polyfunctional polymerizable compound means a compound having two or more polymerizable groups.

[0074] The polyfunctional polymerizable compound is not particularly limited as long as it can be polymerized by heating or by irradiating with nonionizing radiation, ionizing radiation, or infrared rays. For example, acrylate resin, methacrylate resin, urethane acrylate resin, vinyl ester resin, unsaturated polyester, epoxy resin, oxetane resin, vinyl ether, resin utilizing ene-thiol reaction, etc. are listed. Among these, acrylate resin, methacrylate resin, urethane acrylate resin, and vinyl ester resin are preferred from the viewpoint of productivity.

[0075] Examples of polyfunctional acrylate resins include difunctional acrylates such as low molecular weight compounds such as dipropylene glycol diacrylate and neopentyl glycol diacrylate, and high molecular weight compounds such as polyethylene glycol diacrylate, urethane acrylate and epoxy acrylate; trifunctional acrylates such as trimethylolpropane triacrylate and pentaerythritol triacrylate; and tetrafunctional or higher acrylates such as pentaerythritol tetraacrylate and dipentaerythritol hexaacrylate.

[0076] When the electrochromic composition contains a binder precursor, the electrochromic composition preferably contains a catalyst for the polyaddition reaction of the binder precursor and a polymerization initiator.

[0077] As the catalyst for the polyaddition reaction, any catalyst commonly used in the Michael addition reaction can be appropriately selected and used. Examples of the catalyst include amine catalysts such as diazabicycloundecene (DBU) and N-methyldicyclohexylamine, base catalysts such as sodium methoxide, sodium ethoxide, potassium t-butoxide, sodium hydroxide, and tetramethylammonium hydroxide, metallic sodium, and butyllithium.

[0078] As the polymerization initiator, for example, a photopolymerization initiator or a thermal polymerization initiator can be used.

[0079] Examples of the thermal polymerization initiator include azo compounds such as 2,2'-azobisisobutyronitrile, dimethyl-2,2'-azobisisobutyrate, 2,2'-azobis(2,4-dimethylvaleronitrile), and 2,2'-azobis[2-(2-imidazolin-2-yl)propane]; and organic peroxides such as 2,5-dimethyl-2,5-bis(tert-butylperoxy)hexane and di(4-tert-butylcyclohexyl)peroxydicarbonate. These may be used alone or in combination of two or more.

[0080] Examples of the photopolymerization initiator include ketal-based photopolymerization initiators such as 2,2-dimethoxy-1,2-diphenylethan-1-one, acetophenone-based photopolymerization initiators such as 1-hydroxycyclohexyl phenyl ketone, 2,2-diethoxyacetophenone, 2,2-dimethoxy-2-phenylacetophenone, 4-phenoxydichloroacetophenone, and 4-(t-butyl)dichloroacetophenone, and benzoin ether-based photopolymerization initiators such as benzoin methyl ether, benzoin ethyl ether, benzoin propyl ether, benzoin isopropyl ether, and benzoin isobutyl ether. These may be used alone or in combination of two or more.

[0081] The content of the polymerization initiator is not particularly limited and can be appropriately selected depending on the purpose, but is preferably from 0.001 to 5 parts by mass, more preferably from 0.01 to 2 parts by mass, and particularly preferably from 0.01 to 1 part by mass, relative to 100 parts by mass of the total monomer components.

[0082] <Other ingredients> The other components are not particularly limited and can be appropriately selected depending on the purpose. Examples of the other components include fillers, solvents, plasticizers, leveling agents, sensitizers, dispersants, surfactants, and antioxidants.

[0083] <Electrolyte layer> The electrolyte layer is a layer capable of conducting ions for supplying ions to the electrochromic layer. The electrolyte layer is preferably a transparent layer due to the nature of the electrochromic device as a display device and a light control device. The electrolyte composition of the present invention can be used as the electrolyte layer. The average thickness of the electrolyte layer is not particularly limited and may be appropriately selected depending on the purpose, but is preferably 100 nm or more and 100 μm or less.

[0084] <Second electrode> The second electrode is formed opposite the first electrode. The second electrode may be a transparent electrode like the first electrode, or a non-transparent electrode may be used. If the second electrode is transparent, inorganic materials such as indium oxide doped with tin (ITO), tin oxide doped with fluorine, tin oxide doped with antimony, zinc oxide, etc. may be used. Furthermore, an electrode having improved conductivity while maintaining transparency may be used by forming transparent carbon nanotubes or other highly conductive non-transparent materials such as Au, Ag, Pt, Cu, etc. into a fine network shape. When the electrode is not transparent, a metal plate such as Pt, Au, Cu, Al, Ti, or stainless steel can be used. The method for producing the second electrode is the same as that for the first electrode.

[0085] <Electrochemically active layer> In order to compensate for the charge used to develop the color of the electrochromic layer when the electrochromic element develops color, an electrochemically active layer is formed on the second electrode. By electrochemically active layer is meant a layer that can reversibly store or release charge electrostatically and / or by redox reaction. The electrochemically active layer preferably has a structure in which conductive or semiconductive particles are laminated. Specifically, it is produced by sintering particles with a particle size of about 5 nm to 50 nm on the electrode surface. In such a structure, it is possible to store electric charges by utilizing the large surface effect of the particles. The conductive or semiconductive fine particles are not particularly limited and may be appropriately selected depending on the purpose, but inorganic oxides are preferred. Examples of inorganic oxides include titanium oxide, zinc oxide, tin oxide, zirconium oxide, cerium oxide, yttrium oxide, boron oxide, magnesium oxide, strontium titanate, potassium titanate, barium titanate, calcium titanate, calcium oxide, ferrite, hafnium oxide, tungsten oxide, iron oxide, copper oxide, nickel oxide, cobalt oxide, barium oxide, strontium oxide, vanadium oxide, aluminosilicate, calcium phosphate, and aluminosilicate. These may be used alone or in combination of two or more. Among these, from the viewpoint of electrical properties such as electrical conductivity and physical properties such as optical properties, titanium oxide, zinc oxide, tin oxide, zirconium oxide, iron oxide, magnesium oxide, indium oxide, and tungsten oxide are preferred, and tin oxide is particularly preferred. Note that tin oxide may be doped with an element other than tin.

[0086] The conductive or semiconductive fine particles can also serve as the inorganic oxide contained in the electrochemically active layer, but the electrochemically active layer may also contain an inorganic oxide. For example, a thin film of inorganic oxide can be formed on the second electrode by a method such as vacuum deposition, sputtering, or ion plating to form an electrochemically active layer. As the inorganic oxide, for example, the same inorganic oxide as that used as the conductive or semiconductive fine particles can be used.

[0087] As long as the material of the electrochemically active layer can be applied, various printing methods can be used, such as spin coating, casting, microgravure coating, gravure coating, bar coating, roll coating, wire bar coating, dip coating, slit coating, capillary coating, spray coating, nozzle coating, gravure printing, screen printing, flexographic printing, offset printing, reverse printing, inkjet printing, etc. Among these, it is preferable to apply a particle-dispersed paste from the viewpoint of productivity. The average thickness of the electrochemically active layer is not particularly limited and can be appropriately selected depending on the purpose, but is preferably 0.2 μm or more and 5.0 μm or less. If the average thickness is less than 0.2 μm, it may be difficult to obtain a desired color density, and if it exceeds 5.0 μm, the manufacturing cost may increase and the visibility may be easily reduced.

[0088] <Counter electrochromic layer (second electrochromic layer)> The electrochemically active layer may contain an electrochromic compound for the purpose of improving the color density and controlling the color during color development. In this case, the electrochemically active layer is the second electrochromic layer (counter electrochromic layer). The electrochromic layer in contact with the first electrode (first electrochromic layer) and the second electrochromic layer are required to simultaneously change color and fade. In the present invention, since the first electrochromic layer develops color through an oxidation reaction, it is preferable that the second electrochromic layer contains an electrochromic material that develops color through a reduction reaction.

[0089] -Electrochromic material that changes color through reduction reaction- Examples of the electrochromic material contained in the second electrochromic layer that develops color through a reduction reaction include polymer-based and dye-based electrochromic compounds. Examples of electrochromic materials that develop color by reduction include low molecular weight organic electrochromic compounds such as azobenzene, anthraquinone, diarylethene, dihydroprene, dipyridine, styryl, styrylspiropyran, spirooxazine, spirothiopyran, thioindigo, tetrathiafulvalene, terephthalic acid, triphenylmethane, triphenylamine, naphthopyran, viologen, pyrazoline, phenazine, phenylenediamine, phenoxazine, phenothiazine, phthalocyanine, fluoran, fulgide, benzopyran, and metallocene, and conductive polymer compounds such as polyaniline and polythiophene. These may be used alone or in combination of two or more. Among these, viologen derivatives are preferred because they have a low color development and fading potential and show good color values. The electrochromic material that develops color through a reduction reaction is more preferably a compound having at least one of a phosphonic acid group and a phosphoric acid group so as to be adsorbed to the inorganic oxide contained in the second electrochromic layer.

[0090] Examples of electrochromic materials that develop color through a reduction reaction include, but are not limited to, the following exemplary compounds.

[0091] <Example compound R1> [ka]

[0092] <Example compound R2> [ka]

[0093] <Example compound R3> [ka]

[0094] <Other materials> The other members are not particularly limited and can be appropriately selected depending on the purpose. Examples of the other members include a support, an insulating porous layer, a deterioration prevention layer, a protective layer, and a white reflective layer.

[0095] -Support- The support is formed of a transparent material capable of supporting each layer, and is not particularly limited in shape, structure, size, material, etc., as long as it has a structure capable of supporting each layer, and can be appropriately selected depending on the purpose.

[0096] The shape of the support is not particularly limited and can be appropriately selected depending on the purpose. For example, the support may have a flat plate shape or a shape having a curved surface. The structure of the support is not particularly limited and can be appropriately selected depending on the purpose. The size of the support is not particularly limited and can be appropriately selected depending on the purpose.

[0097] The material of the support may be any transparent material, and well-known organic and inorganic materials may be used as they are. Examples of the material include glass substrates such as alkali-free glass, borosilicate glass, float glass, and soda-lime glass, and resin substrates such as polycarbonate resin, acrylic resin, polyethylene, polyvinyl chloride, polyester, epoxy resin, melamine resin, phenolic resin, polyurethane resin, and polyimide resin.

[0098] The surface of the support may be provided with a transparent insulating layer, a UV-cut layer, an anti-reflection layer, or the like in order to improve water vapor barrier properties, gas barrier properties, ultraviolet resistance, and visibility.

[0099] -Insulating porous layer- The insulating porous layer separates the first electrode layer and the second electrode layer so as to be electrically insulated from each other, and has a function of retaining an electrolyte. The material of the insulating porous layer is not particularly limited as long as it is porous and can be appropriately selected, but it is preferable to use an organic material, an inorganic material, or a composite thereof that has high insulating properties and durability and excellent film-forming properties. Examples of methods for forming the insulating porous layer include a sintering method (using holes generated between particles by partially fusing polymer fine particles or inorganic particles with the addition of a binder or the like), an extraction method (forming a layer of a composition using organic or inorganic substances soluble in a solvent and a binder or the like insoluble in the solvent, and then dissolving the organic or inorganic substances with a solvent to obtain pores), a foaming method, a phase inversion method in which a mixture of polymers is phase-separated by manipulating a good solvent and a poor solvent, and a radiation irradiation method in which various types of radiation are radiated to form pores.

[0100] -Deterioration prevention layer- The role of the degradation prevention layer is to undergo a reverse chemical reaction with the electrochromic layer, balance the charge, and prevent the first electrode layer and the second electrode layer from corroding or deteriorating due to an irreversible oxidation-reduction reaction. Note that the reverse reaction includes not only the case where the degradation prevention layer undergoes oxidation-reduction, but also the case where the layer acts as a capacitor. The material for the degradation prevention layer is not particularly limited as long as it is a material that plays a role in preventing corrosion due to irreversible oxidation-reduction reactions of the first electrode layer and the second electrode layer, and can be appropriately selected depending on the purpose. Examples of the material include antimony tin oxide, nickel oxide, titanium oxide, zinc oxide, tin oxide, and conductive or semiconductive metal oxides containing a plurality of these. The deterioration prevention layer can be composed of a porous thin film that does not inhibit the injection of electrolyte. For example, conductive or semiconducting metal oxide fine particles such as antimony tin oxide, nickel oxide, titanium oxide, zinc oxide, tin oxide, etc. can be fixed to the second electrode with a binder resin such as an acrylic, alkyd, isocyanate, urethane, epoxy, or phenol, to obtain a suitable porous thin film that has electrolyte permeability and satisfies the function of an deterioration prevention layer.

[0101] -Protective layer- The role of the protective layer is to protect the element from external stress and chemicals used in the cleaning process, to prevent electrolyte leakage, and to prevent the intrusion of substances unnecessary for stable operation of the electrochromic element, such as moisture and oxygen in the air. The average thickness of the protective layer is not particularly limited and may be appropriately selected depending on the purpose, but is preferably 1 μm or more and 200 μm or less. The material for the protective layer may be, for example, an ultraviolet-curable or thermosetting resin, and specific examples thereof include an acrylic resin, a urethane resin, and an epoxy resin.

[0102] The electrochromic element of the present invention preferably has a decolorization rate represented by the following formula 1 of 95% or more, and more preferably 97% or more. [Formula 1] Decolorization rate (%)=(T2 / T1)×100 A voltage of 1.2 V was applied between a pair of opposing electrodes of the electrochromic element for 1 hour to drive the element to develop color, and then the pair of electrodes was short-circuited for 30 minutes to drive the element to decolorize. The luminous transmittance before the color development drive was defined as T1, and the luminous transmittance after the decolorization drive was defined as T2.

[0103] Here, an embodiment of the electrochromic element of the present invention will be described with reference to the drawings. In the drawings, the same components are denoted by the same reference numerals, and duplicated explanations may be omitted.

[0104] <First embodiment> Fig. 1 is a schematic diagram showing an example of an electrochromic element according to a first embodiment. The electrochromic element in Fig. 1 has a first electrode 1, an electrochromic layer 2 provided on the first electrode, a second electrode 5, an electrochemically active layer 4 containing an inorganic oxide on the second electrode, and an electrolyte layer 3 between the electrochromic layer and the second electrode.

[0105] <Second embodiment> Fig. 2 is a schematic diagram showing an example of an electrochromic element according to a second embodiment. In the electrochromic element of Fig. 2, the electrochemically active layer 4 becomes an opposing electrochromic layer (second electrochromic layer) 6. The first electrochromic layer 2 and the second electrochromic layer 6 in contact with the first electrode 1 are required to simultaneously change color and fade. Therefore, since the first electrochromic layer 2 develops color through an oxidation reaction, it is preferable that the second electrochromic layer 6 contains an electrochromic material that develops color through a reduction reaction.

[0106] (Electrochromic light control device) The electrochromic light control device of the present invention comprises the electrochromic element of the present invention, and further comprises other members as necessary. The other means are not particularly limited and can be appropriately selected depending on the application. Examples of the other means include a power source, a fixing means, and a control means. Examples of the electrochromic light control device include anti-glare mirrors, light control glass, light control spectacles, binoculars, opera glasses, bicycle goggles, and watches.

[0107] (Electrochromic Display Device) The electrochromic display device of the present invention comprises the electrochromic element of the present invention, and further comprises other means as necessary. The other means are not particularly limited and can be appropriately selected depending on the application. Examples of the other means include a power source, a fixing means, and a control means. Examples of electrochromic devices include electronic paper, electronic albums, electronic billboards, and displays. EXAMPLES

[0108] Examples of the present invention will be described below, but the present invention is not limited to these examples.

[0109] Example 1 <Preparation of electrochromic element> - Formation of the first electrode and electrochromic layer - A glass substrate with a size of 40 mm x 40 mm and an average thickness of 0.7 mm was prepared as a transparent support. An ITO film was formed on the transparent support by sputtering to an average thickness of about 100 nm to form a first electrode. The sheet resistance of the first electrode was 40 Ω / □. Next, polyethylene oxide diacrylate (PEG400DA, manufactured by Nippon Kayaku Co., Ltd.), a photopolymerization initiator (IRG184, manufactured by BASF), a triarylamine compound represented by the following structural formula A, a triarylamine compound represented by the following structural formula B, and cyclohexanone (manufactured by Kanto Chemical Co., Ltd.) were mixed in a mass ratio of (20:1:14:6:500) to prepare an electrochromic solution. Next, the prepared electrochromic solution was applied onto the first electrode and cured by UV irradiation in a nitrogen atmosphere to form an electrochromic layer in the electrochromic reaction area (30 mm x 30 mm) on the surface of the ITO film. The average thickness of the electrochromic layer was 1.3 μm.

[0110] [Structural formula A] [ka]

[0111] [Structural formula B] [ka]

[0112] - Formation of the second electrode - Similarly to the first electrode, an ITO film was formed by sputtering to an average thickness of about 100 nm on a glass substrate of 40 mm×40 mm and an average thickness of 0.7 mm to form a second electrode.

[0113] - Formation of an electrochemically active layer - A thickener was added to a tin oxide particle dispersion (methanol dispersion, solid content concentration 50% by mass, average particle diameter: 18 nm), and the mixture was applied to the second electrode by screen printing. A tin oxide particle film with an average thickness of about 3.5 μm was obtained by further annealing at 120° C. for 15 minutes, and an electrochemically active layer was formed in the electrochromic reaction area (30 mm × 30 mm) on the surface of the ITO film.

[0114] - Formation of electrolyte layer - Polyethylene glycol diacrylate (PEG400DA, manufactured by Nippon Kayaku Co., Ltd.), a photopolymerization initiator (IRG184, manufactured by BASF), and an electrolyte (1-ethyl-3-methylimidazolium bisfluorosulfonimide, manufactured by Kanto Chemical Co., Ltd.) were mixed in a mass ratio of 100:5:100 to prepare an electrolyte precursor. The electrolyte precursor and a basic compound (poly(4-vinylpyridine), weight average molecular weight (Mw) 60,000, manufactured by Sigma-Aldrich) were mixed in a mass ratio (electrolyte precursor:basic compound) = 100:0.05 to prepare a solution. The solution was applied onto the electrochromic layer on a glass substrate using a dispenser, and the glass substrate having the electrochemically active layer was bonded to the glass substrate using a vacuum bonding device, followed by ultraviolet (UV) curing to form an electrolyte layer. Thereafter, the periphery of the element was sealed with a UV adhesive (Photolec E, low moisture permeability type, manufactured by Sekisui Chemical Co., Ltd.) In this manner, an electrochromic element of Example 1 as shown in FIG.

[0115] Example 2 An electrochromic element of Example 2 as shown in FIG. 2 was produced in the same manner as in Example 1, except that a second electrochromic layer was formed by subjecting the tin oxide particle layer to an additional treatment as described below. <Formation of the second electrochromic layer> A 2,2,3,3-tetrafluoropropanol solution containing 2.0 mass% of a reduction-reactive electrochromic compound represented by the following structural formula C was applied by spin coating to a tin oxide particle layer obtained by the same process as in Example 1, and then annealed at 120°C for 10 minutes to adsorb the compound onto the tin oxide particle layer, thereby forming a reduction-reactive second electrochromic layer.

[0116] [Structural formula C] [ka]

[0117] (Examples 3, 5, 7, 14, 15, 20, 22, 31, 33, and 35) Electrochromic elements of Examples 3, 5, 7, 14, 15, 20, 22, 31, 33, and 35 as shown in FIG. 1 were produced in the same manner as in Example 1, except that the types and mass ratios (electrolyte precursor: basic compound B) of the basic compounds used in the electrolyte layer were changed as shown in Tables 1 and 2.

[0118] (Example 49) An electrochromic element of Example 49 as shown in FIG. 1 was produced in the same manner as in Example 1, except that the method for forming the electrochemically active layer in Example 1 was changed as follows. <Formation of electrochemically active layer> A titanium oxide nanoparticle dispersion (product name: SP210, manufactured by Showa Titanium Co., Ltd., average particle size: about 20 nm) was applied onto the second electrode by spin coating. An annealing treatment was then performed at 120°C for 15 minutes to obtain a titanium oxide particle film with an average thickness of about 2.5 μm, and an electrochemically active layer was formed in the electrochromic reaction area (30 mm × 30 mm) on the surface of the ITO film.

[0119] (Example 51) An electrochromic element of Example 51 as shown in FIG. 1 was produced in the same manner as in Example 1, except that the formation of the electrolyte layer in Example 1 was changed as follows. <Formation of electrolyte layer> Dimethoxypolyethylene glycol (Uniox MM400, NOF Corp.) and an electrolyte (1-ethyl-3-methylimidazolium bisfluorosulfonimide, Kanto Chemical Co., Ltd.) were mixed in a mass ratio of 100:100 to prepare an electrolyte precursor. The electrolyte precursor and a basic compound (poly(4-vinylpyridine), weight average molecular weight (Mw) 60,000, Sigma-Aldrich) were mixed in a mass ratio (electrolyte precursor:basic compound) of 100:0.05 to prepare a solution. The solution was applied onto the electrochromic layer on a glass substrate using a dispenser, and the glass substrate having the electrochemically active layer was bonded to the electrolyte precursor using a vacuum bonding device to form an electrolyte layer.

[0120] (Examples 52 to 54) Electrochromic elements of Examples 52 to 54 as shown in FIG. 1 were prepared in the same manner as in Example 51, except that the types and mass ratios of the basic compounds used in the electrolyte layer (electrolyte precursor: basic compound B) were changed as shown in Table 3.

[0121] (Examples 4, 6, 8-13, 16-19, 21, 23-30, 32, 34, and 36-48) Electrochromic elements of Examples 4, 6, 8 to 13, 16 to 19, 21, 23 to 30, 32, 34, and 36 to 48 as shown in FIG. 2 were produced in the same manner as in Example 2, except that the types and mass ratios (electrolyte precursor: basic compound B) of the basic compounds used in the electrolyte layer were changed as shown in Tables 1 and 2.

[0122] (Example 50) An electrochromic device of Example 50 as shown in FIG. 2 was produced in the same manner as in Example 2, except that the method for forming the electrochemically active layer in Example 2 was changed as follows. <Formation of electrochemically active layer> A titanium oxide nanoparticle dispersion (product name: SP210, manufactured by Showa Titanium Co., Ltd., average particle size: about 20 nm) was applied onto the second electrode by spin coating. An annealing treatment was then performed at 120°C for 15 minutes to obtain a titanium oxide particle film with an average thickness of about 2.5 μm, and an electrochemically active layer was formed in the electrochromic reaction area (30 mm × 30 mm) on the surface of the ITO film.

[0123] (Example 55) An electrochromic element of Example 55 as shown in FIG. 2 was produced in the same manner as in Example 2, except that the formation of the electrolyte layer in Example 2 was changed as follows. <Formation of electrolyte layer> Dimethoxypolyethylene glycol (Uniox MM400, NOF Corp.) and an electrolyte (1-ethyl-3-methylimidazolium bisfluorosulfonimide, Kanto Chemical Co., Ltd.) were mixed in a mass ratio of 100:100 to prepare an electrolyte precursor. The electrolyte precursor and a basic compound (poly(4-vinylpyridine), weight average molecular weight (Mw) 60,000, Sigma-Aldrich) were mixed in a mass ratio (electrolyte precursor:basic compound) of 100:0.05 to prepare a solution. The solution was applied onto the electrochromic layer on a glass substrate using a dispenser, and the glass substrate having the electrochemically active layer was bonded to the electrolyte precursor using a vacuum bonding device to form an electrolyte layer.

[0124] (Examples 56 to 71) Electrochromic elements of Examples 56 to 71 as shown in FIG. 2 were produced in the same manner as in Example 55, except that the types and mass ratios of the basic compounds used in the electrolyte layer (electrolyte precursor: basic compound B) were changed as shown in Table 3.

[0125] Comparative Example 1 An electrochromic element of Comparative Example 1 as shown in FIG. 1 was produced in the same manner as in Example 1, except that, as shown in Table 2, no basic compound was added to the electrolyte layer.

[0126] Comparative Example 2 An electrochromic element of Comparative Example 2 as shown in FIG. 2 was produced in the same manner as in Example 2, except that, as shown in Table 2, no basic compound was added to the electrolyte layer.

[0127] Comparative Example 3 An electrochromic element of Comparative Example 3 as shown in FIG. 2 was produced in the same manner as in Example 2, except that, in Example 2, an acidic compound, ethyl phosphate (manufactured by Tokyo Chemical Industry Co., Ltd.), was used in the electrolyte layer as shown in Table 2.

[0128] Comparative Example 4 An electrochromic element of Comparative Example 4 as shown in FIG. 1 was produced in the same manner as in Example 51, except that in Example 51, a basic compound was not added to the electrolyte layer as shown in Table 3.

[0129] Comparative Example 5 An electrochromic element of Comparative Example 5 as shown in FIG. 2 was produced in the same manner as in Example 55, except that, as shown in Table 3, no basic compound was added to the electrolyte layer.

[0130] Next, a color development / discoloration driving test was carried out on each of the produced electrochromic elements as follows. The results are shown in Tables 1 to 3.

[0131] <Color development and erasing driving test> For each electrochromic element produced, a constant voltage (1.2V) was applied between a pair of opposing electrodes for 1 hour to cause color development (color development drive). After that, the electrodes were short-circuited for 30 minutes to cause color loss (color loss drive). The luminous transmittance of the element before and after the color development drive and color loss drive was calculated from the transmission spectrum measured using an Ocean Optics USB4000. The visual transmittance before the color development / discoloration drive test was T1, and the visual transmittance after the color development / discoloration drive test was T2, and the color disappearance rate A [%] was calculated by the following formula 1. If no residual color disappearance occurs and the color disappears completely, the visual transmittance does not change before and after the color development / discoloration drive test, so T1 and T2 have the same value and the color disappearance rate A is 100%. The closer the value of the color disappearance rate A is to 100, the less residual color disappearance there is in an electrochromic element. [Formula 1] Decolorization rate A(%)=(T2 / T1)×100

[0132] [Judgment criteria] ○: The color erasing rate A was 95% or more, and the color was properly erased. ×: The color erasing rate A was less than 95%, and the color could not be erased and the color remained.

[0133] [Table 1]

[0134] [Table 2]

[0135] [Table 3]

[0136] From the results in Tables 1 to 3, it was found that in Examples 1 to 71, the inclusion of a basic compound in the electrolyte layer made it possible to prevent the occurrence of the residual discharge phenomenon, and as a result, made it possible to realize an electrochromic element with a long life.

[0137] For example, aspects of the present invention are as follows. <1> A first electrode; an electrochromic layer disposed on the first electrode; A second electrode; an electrolyte layer between the electrochromic layer and the second electrode; having The electrochromic element is characterized in that the electrolyte layer contains a basic compound. <2> The basic compound is a compound having a pyridine skeleton. <1> 1 is an electrochromic device according to the present invention. <3> The basic compound is a basic polymer. <1> from <2> The electrochromic device according to any one of the above items. <4> The basic compound is polyvinylpyridine. <1> from <3> The electrochromic device according to any one of the above items. <5> the second electrode having an electrochemically active layer comprising an inorganic oxide on the second electrode; <1> from <4> The electrochromic device according to any one of the above items. <6> The inorganic oxide is tin oxide. <5> 1 is an electrochromic device according to the present invention. <7> the electrochemically active layer comprises an electrochromic material; <5> from <6> The electrochromic device according to any one of the above items. <8> The electrochromic material is a compound having at least one of a phosphonic acid group and a phosphoric acid group. <7> 1 is an electrochromic device according to the present invention. <9> The electrochromic material is a viologen derivative. <7> from <8> The electrochromic device according to any one of the above items. <10> The color erasing rate represented by the following formula 1 is 95% or more. <1> from <9> The electrochromic device according to any one of the above items. [Formula 1] Decolorization rate (%)=(T2 / T1)×100 A voltage of 1.2 V was applied between a pair of opposing electrodes of the electrochromic element for 1 hour to drive the element to develop color, and then the pair of electrodes was short-circuited for 30 minutes to drive the element to decolorize. The luminous transmittance before the color development drive was defined as T1, and the luminous transmittance after the decolorization drive was defined as T2. <11> The above <1> from <10> 1 is a schematic diagram showing an electrochromic display device according to the first embodiment of the present invention; <12> The above <1> from <10> 1. An electrochromic light control device comprising the electrochromic element according to any one of claims 1 to 9. <13> The electrolyte composition is characterized by containing an electrolyte and a basic compound. <14> The basic compound is a compound having a pyridine skeleton. <13> The electrolyte composition according to claim 1, <15> The basic compound is a basic polymer. <13> from <14> The electrolyte composition according to any one of claims 1 to 5, <16> The basic compound is polyvinylpyridine. <13> from <15> The electrolyte composition according to any one of claims 1 to 5, <17> The content of the basic compound is 0.01% by mass or more and 2% by mass or less. <13> from <16> The electrolyte composition according to any one of claims 1 to 5, <18> The above is in a liquid, gel or solid form. <13> from <17> The electrolyte composition according to any one of claims 1 to 5, <19> The above-mentioned electrochromic device <13> from <18> The electrolyte composition according to any one of claims 1 to 5,

[0138] The above <1> from <10> The electrochromic element according to any one of the preceding claims. <11> The electrochromic display device according to <12> The electrochromic light control device according to claim 1, <13> from <19> According to the electrolyte composition described in any one of the above, the conventional problems can be solved and the object of the present invention can be achieved. [Explanation of symbols]

[0139] 1 First electrode 2 Electrochromic Layer (First Electrochromic Layer) 3 Electrolyte layer 4. Electrochemically active layer 5 Second electrode 6 Counter electrochromic layer (second electrochromic layer) [Prior art documents] [Patent documents]

[0140] [Patent Document 1] Patent No. 6597373 [Patent Document 2] U.S. Patent No. 6,188,505

Claims

1. A first electrode; an electrochromic layer disposed on the first electrode; A second electrode; and an electrolyte layer between the electrochromic layer and the second electrode; An electrochromic device having an electrochemically active layer comprising an inorganic oxide on the second electrode; Electrochromic device, characterized in that the electrolyte layer contains a basic compound.

2. 2. The electrochromic device according to claim 1, wherein the basic compound is a compound having a pyridine skeleton.

3. 3. The electrochromic device according to claim 1, wherein the basic compound is a basic polymer.

4. 4. The electrochromic device according to claim 1, wherein the basic compound is polyvinylpyridine.

5. An electrochromic element described in any one of claims 1 to 4, wherein the inorganic oxide is a conductive fine particle or a semiconducting fine particle.

6. 6. The electrochromic device of claim 5, wherein the inorganic oxide is tin oxide.

7. 7. An electrochromic device according to claim 5, wherein the electrochemically active layer comprises an electrochromic material.

8. 8. The electrochromic device according to claim 7, wherein the electrochromic material is a compound having at least one of a phosphonic acid group and a phosphoric acid group.

9. 9. The electrochromic device according to claim 7, wherein the electrochromic material is a viologen derivative.

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