WO2000054361A1 - Dispositifs de conversion photoelectrique fabriques au moyen d'electrolytes etheres - Google Patents
Dispositifs de conversion photoelectrique fabriques au moyen d'electrolytes etheres Download PDFInfo
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- WO2000054361A1 WO2000054361A1 PCT/JP2000/001379 JP0001379W WO0054361A1 WO 2000054361 A1 WO2000054361 A1 WO 2000054361A1 JP 0001379 W JP0001379 W JP 0001379W WO 0054361 A1 WO0054361 A1 WO 0054361A1
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- Prior art keywords
- formula
- photoelectric conversion
- compound
- electrolyte
- conversion element
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- 238000006243 chemical reaction Methods 0.000 title claims abstract description 40
- 239000003792 electrolyte Substances 0.000 title claims abstract description 38
- -1 ether compound Chemical class 0.000 claims abstract description 48
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 40
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 14
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 11
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 10
- 239000011630 iodine Substances 0.000 claims abstract description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 8
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 7
- 150000002497 iodine compounds Chemical class 0.000 claims abstract description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 229940126062 Compound A Drugs 0.000 claims 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims 1
- 230000007774 longterm Effects 0.000 abstract description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 1
- 235000019256 formaldehyde Nutrition 0.000 abstract 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 36
- 239000000203 mixture Substances 0.000 description 22
- 150000001875 compounds Chemical class 0.000 description 21
- 239000004065 semiconductor Substances 0.000 description 17
- 230000015572 biosynthetic process Effects 0.000 description 12
- 238000003786 synthesis reaction Methods 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 239000011521 glass Substances 0.000 description 10
- 239000008188 pellet Substances 0.000 description 10
- 238000004821 distillation Methods 0.000 description 9
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 8
- 150000002500 ions Chemical class 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 7
- HSZCZNFXUDYRKD-UHFFFAOYSA-M lithium iodide Chemical compound [Li+].[I-] HSZCZNFXUDYRKD-UHFFFAOYSA-M 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 238000003756 stirring Methods 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 229910052697 platinum Inorganic materials 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 3
- 239000004745 nonwoven fabric Substances 0.000 description 3
- 238000001308 synthesis method Methods 0.000 description 3
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000010416 ion conductor Substances 0.000 description 2
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- 125000000858 thiocyanato group Chemical group *SC#N 0.000 description 2
- 229910001930 tungsten oxide Inorganic materials 0.000 description 2
- HQOKJWBWTJVHNJ-UHFFFAOYSA-N 1,3-bis[2-(2-methoxyethoxy)ethoxy]propan-2-ol Chemical compound COCCOCCOCC(O)COCCOCCOC HQOKJWBWTJVHNJ-UHFFFAOYSA-N 0.000 description 1
- XTIGGAHUZJWQMD-UHFFFAOYSA-N 1-chloro-2-methoxyethane Chemical compound COCCCl XTIGGAHUZJWQMD-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- ZNSMNVMLTJELDZ-UHFFFAOYSA-N Bis(2-chloroethyl)ether Chemical compound ClCCOCCCl ZNSMNVMLTJELDZ-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229910004613 CdTe Inorganic materials 0.000 description 1
- 241000282693 Cercopithecidae Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- DKNPRRRKHAEUMW-UHFFFAOYSA-N Iodine aqueous Chemical compound [K+].I[I-]I DKNPRRRKHAEUMW-UHFFFAOYSA-N 0.000 description 1
- QPFYXYFORQJZEC-FOCLMDBBSA-N Phenazopyridine Chemical compound NC1=NC(N)=CC=C1\N=N\C1=CC=CC=C1 QPFYXYFORQJZEC-FOCLMDBBSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- SWJBITNFDYHWBU-UHFFFAOYSA-N [I].[I] Chemical compound [I].[I] SWJBITNFDYHWBU-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 1
- 229910002113 barium titanate Inorganic materials 0.000 description 1
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000003487 electrochemical reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 238000002847 impedance measurement Methods 0.000 description 1
- 150000002496 iodine Chemical class 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 150000002605 large molecules Chemical class 0.000 description 1
- 230000004298 light response Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910001511 metal iodide Inorganic materials 0.000 description 1
- PJSOCBVWZJGTHW-UHFFFAOYSA-N n-(1h-indazol-5-yl)-5-[3-methoxy-4-[2-(2-methoxyethoxy)ethoxy]phenyl]-1,3-oxazol-2-amine Chemical compound C1=C(OC)C(OCCOCCOC)=CC=C1C(O1)=CN=C1NC1=CC=C(NN=C2)C2=C1 PJSOCBVWZJGTHW-UHFFFAOYSA-N 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 239000005518 polymer electrolyte Substances 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Substances [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229940070891 pyridium Drugs 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- YAYGSLOSTXKUBW-UHFFFAOYSA-N ruthenium(2+) Chemical compound [Ru+2] YAYGSLOSTXKUBW-UHFFFAOYSA-N 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- VEALVRVVWBQVSL-UHFFFAOYSA-N strontium titanate Chemical compound [Sr+2].[O-][Ti]([O-])=O VEALVRVVWBQVSL-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/20—Light-sensitive devices
- H01G9/2027—Light-sensitive devices comprising an oxide semiconductor electrode
- H01G9/2031—Light-sensitive devices comprising an oxide semiconductor electrode comprising titanium oxide, e.g. TiO2
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/20—Light-sensitive devices
- H01G9/2004—Light-sensitive devices characterised by the electrolyte, e.g. comprising an organic electrolyte
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/542—Dye sensitized solar cells
Definitions
- the present invention relates to a photoelectric conversion element using an electrolyte of an ether compound having high ionic conductivity.
- electrolytes in which iodine and potassium iodide are added to an organic solvent such as carbonate and tetrahydrofuran have been proposed as ion conductors for photoelectric conversion elements used for solar cells.
- these electrolytes have a high vapor pressure and hinder the durability of the photoelectric conversion element.
- durability of 10 years or more is required, and ion conductivity, An electrolyte with excellent safety and seal stability is desired.
- the present inventors have proposed that a redox couple (B) composed of a combination of iodine and an iodine compound or a combination of bromine and a bromine compound is added to an ether compound (I), (11), (III) or (IV): (A). ) Can be obtained to obtain a desired electrolyte. Further, the inventors have found that this electrolyte is useful for application to a photoelectric conversion element such as a solar cell, and completed the present invention. That is, the present invention provides a photoelectric conversion element having excellent long-term stability by using an electrolyte having sufficient ion conductivity and excellent stability.
- the present invention provides a photoelectric conversion element having excellent long-term stability by using an electrolyte having sufficient ion conductivity and excellent stability.
- R 13 , R 14 , R 15 , R 16 , R 10 R 102 , R 103 , R 104 , and R 105 are a hydrogen atom or -0 A 1 (where A 1 is an alkyl group or an alkenyl group, and a is 1 to 12).
- a 1 is an alkyl group or an alkenyl group, and a is 1 to 12.
- R 10 ⁇ R 1Q5 are hydrogen atoms at the same time.
- a photoelectric conversion element using an electrolyte comprising:
- FIG. 1 is a cross-sectional view of the photoelectric conversion element obtained in Example 4.
- the total number of ethylene oxide units (_CH 2 CH 2 0—) in the ether compound is:! -20, for example, 3-12.
- R 17 , R 18 and R 19 are groups selected from an alkyl group having 1 to 6 carbon atoms or an alkyl group having 2 to 6 carbon atoms. 1, m and n are 0-12. However, all of 1, m and n are not 0 at the same time. ]
- the sum of 1 + m + n is preferably 2 or more, and more preferably 3 or more.
- the method for synthesizing the ether compound represented by the formula (II-1) having the structural formula of the formula (II) is as follows.
- R 2. And R 2 R 22 and R 23 are groups selected from an alkyl group having 1 to 6 carbon atoms or an alkenyl group having 2 to 6 carbon atoms. o, p, q, r, s are 0-12. However, all of o, p, q, r, and s cannot be 0 at the same time. ]
- the sum of o + p + q + r + s is preferably 2 or more, more preferably 3 or more, for example, 4 or more.
- the alcohols of (e) and (f) are synthesized.
- R 24 , R 25 , R 26 and R 27 are groups selected from an alkyl group having 1 to 6 carbon atoms or a alkenyl group having 2 to 6 carbon atoms.
- t, u, v, w are 0-12. However, t, u, v, and w are not all 0 at the same time.
- the sum of t + u + v + w is preferably 2 or more, more preferably 3 or more, for example, 4 or more.
- the ether compound of the formula (II) can be obtained by the same operation as described above.
- the redox couple ( ⁇ ) in the present invention is a pair of compounds that perform a reversible redox reaction, and when acid and reductants are independently added to the system, an electrochemical equilibrium is quickly reached.
- Means a substance that A redox couple is a combination of an iodine-iodine compound or a combination of a bromine-bromine compound.
- Iodine - ® ⁇ redox couple of a combination of iodine compounds for example, I 2 and L i I, Na I, KI , C s I, combinations of metal iodides such as Ca 1 2 or 1 2 and ⁇ Rukiruan, It is preferably composed of a combination of an iodine salt of a quaternary ammonium compound such as monodimodide and pyridinumodide or a high molecular compound having these in a side chain.
- the redox couple of the combination of bromine one bromine compound for example, B r 2 and L i B r, N a B r, KB r, C s B r, C a B r 2 of a metal such as a bromide,, B r 2 And a quaternary ammonium compound such as alkylammonium bromide and pyridium bromide, or a high molecular weight compound having a side chain thereof.
- the mixing ratio of the redox couple can be arbitrarily selected with the ether compound to be mixed. come. In general, an electrolyte having higher ionic conductivity can be obtained as the amount of the redox couple increases. However, if the mixing amount is too large, the dissociation of ions becomes difficult to occur, and the conductivity decreases. If the equilibrium potential of the redox couple is a problem, the mixing amount can be adjusted to obtain the required equilibrium potential.
- the amount of the redox couple may be 1 to 50 parts by weight, for example, 5 to 35 parts by weight, based on 100 parts by weight of the ether compound.
- the molar ratio of iodine: iodine compound (and bromine: bromine compound) in the redox couple is preferably 1: 5 to 5: 1.
- the method for producing the electrolyte of the present invention is not particularly limited, but usually, it is sufficient that the ether compound (A) and the redox couple (B) can be mixed.
- the method of mixing the redox couple (B) with the ether compound (A) is not particularly limited.
- the method of directly mixing the redox couple (B) with the ether compound (A), the organic containing the redox couple (B) There is a method of mixing an ether compound (A) with a solvent.
- the organic solvent is removed after the production of the electrolyte using an organic solvent (eg, acetonitrile).
- a photoelectric conversion element is an element that converts photoenergy into electric energy by utilizing an electrochemical reaction between electrodes.
- the photoelectric conversion element When the photoelectric conversion element is irradiated with light, electrons are generated at one electrode and move to the counter electrode through an electric wire provided between the electrodes.
- the electrons transferred to the counter electrode reduce a redox couple in the electrolyte comprising the ether compound of the present invention.
- the reduced redox couple travels from one electrode to the other as an anion in the electrolyte made of the ether compound, reaches the other electrode, and returns itself to the oxidized body, thereby transferring the electron to the other.
- the photoelectric conversion element of the present invention is an element or a sensor that can convert light energy into electric energy. It also has a function as an optical sensor because it responds to light.
- the photoelectric conversion element has an ether compound electrolyte and a pair (two) of electrodes.
- Examples of the electrode include a conductor attached to a glass plate (a transparent protective material that transmits light).
- a glass plate having electrodes is a glass plate coated with a conductive material (for example, a metal, an oxide semiconductor, particularly indium-tin oxide (ITO)). Good.
- Oxide semiconductors such as titanium oxide, zinc oxide, tungsten oxide, barium titanate, strontium titanate, potassium titanate, potassium tantalate, tungsten oxide, iron oxide, cadmium sulfide, CdTe, C
- a semiconductor such as silicon, a lid, cyan, polychenylene, polypyrrole, or polyaniline, or a material obtained by sensing the above-mentioned oxide semiconductor or semiconductor with a dye or other inorganic substance is supported. A more preferable photoelectric conversion element is obtained.
- the photoelectric conversion element of the present invention includes an electrolyte made of an ether compound, one electrode containing a semiconductor (for example, an n-type semiconductor or a p-type semiconductor), and a semiconductor (for example, a p-type semiconductor or an n-type semiconductor). Alternatively, it may have one counter electrode made of metal.
- An oxide semiconductor is preferable as the semiconductor to be supported on the electrode, and titanium oxide or titanium oxide sensitized with a dye is particularly preferable in terms of stability, safety, and price.
- Dyes include organometallic complexes, for example, ruthenium-biviridine complexes, especially cis-di (thiocyanato) -N, N'-bis (2,2'-biviridyl-4,4'-dicarbonic acid) noretium (II ) (cis-di (thiocyanato) - N, N '- bis (2, 2' - bipyridyl-4, 4 '-dicarboxyl ic acicD rutheniunn, II)) provided on the electrode that force monkey 0 electrolytes use Rereru the
- ruthenium-biviridine complexes especially cis-di (thiocyanato) -N, N'-bis (2,2'-biviridyl-4,4'-d
- the photoelectric conversion element When the electrolyte of the ether compound of the present invention is used for a photoelectric conversion element, the photoelectric conversion element has excellent ion conductivity and excellent stability, so that a photoelectric conversion element having good conversion efficiency can be obtained. .
- the photoelectric conversion element of the present invention can be used as a solar cell, an optical sensor, or the like.
- FIG. 1 is a cross-sectional view of the photoelectric conversion element obtained in Example 4.
- the photoelectric conversion element has glass plates 1 and 6, electrodes 2 and 5, a semiconductor layer 3, and an electrolyte layer 4 of an ether compound.
- the transparent glass plates 1 and 6 protect the photoelectric conversion element and transmit light.
- the thickness of the glass plates 1 and 6 may be 0.1-5 mm.
- Electrode 2 is transparent IT O (indium monotin oxide) may be used. The thickness of the electrode 2 may be between 2 and 100 / m.
- Layer 3 is made of porous Ti 2 and emits holes and electrons from light.
- the electrolyte layer 4 is composed of an athenole compound and an electrolyte compound, and functions as a carrier layer for ions. The thickness of the electrolyte layer 4 may be between 5 and 1 000 / m.
- Electrode 5 is preferably made of a metal (eg, gold and platinum). The thickness of the electrode 5 may be between 2 and 100 m.
- the side surface of the photoelectric conversion element is sealed with resin 7.
- resin ⁇ are an epoxy resin and an acrylic resin.
- a lead wire 8 is connected to the electrodes 2 and 5.
- Lead 8 is attached to electrodes 2 and 5 by a conductive paste (not shown).
- the conductive paste include a silver paste and a power paste.
- the properties of the ether compound were measured as follows.
- Ionic conductivity (conductivity ⁇ ) was determined by complex impedance measurement. The measurement was performed using an alternating current method at 40 ° C, a voltage of 10 mV, and a frequency of 5 Hz to 13 MHz.
- the 1,3-bis [2- (2-methoxyethoxy) ethoxy] obtained in Step 1 was added to 100 g (0.34 monole) of propanol and 20.4 g of NaOH (pellet) in the form of pellets. 51 mol), and 48.2 g (0.51 mol) of 2-chloroethyl methyl ether was added dropwise little by little while stirring at 60 ° C. After completion of the dropwise addition, the mixture was stirred for about 2 hours.
- Ether compound prepared in Synthesis Example 2 (ii) lg, mixed lithium iodide 40 Omg ⁇ beauty iodine 10 Omg, was 8. 2 X10- 3 S "cm was measured ionic conductivity.
- Ether compound prepared in Synthesis Example 3 (iii) was measured in the same manner Ion conductivity as in Example 2, 9. 2 X10- 3 S, was cm.
- the nonwoven fabric was impregnated with the electrolyte compound, and then exposed to an iodine atmosphere for 2 hours.
- Titanium oxide suspended on a transparent glass plate (glass plate thickness: 2 mm, ITO film thickness: 20 ⁇ m) coated with ITO (indium monotin oxide) by sputtering as a counter electrode. Apply a suspension, dry, and sinter to form a porous titanium oxide film
- the light response of the current was measured by irradiating light of 96 WZm 2 with a solar simulator of AM I.5 as the light 3 ⁇ 4g.
- a photoelectric conversion element having a semiconductor layer 3 and an electrolyte layer 4 using an ether compound (ii) and using an ether compound (i ii)
- the photoelectric conversion element of the present invention using an electrolyte having excellent stability can continuously flow a DC current by light irradiation and efficiently transport ions.
- the photoelectric conversion element of the present invention functions well as a solar cell.
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Abstract
L'invention concerne des dispositifs de conversion photoélectrique fabriqués au moyen d'électrolytes contenant les constituants (A) et (B) suivants, et qui présentent une excellente stabilité à long terme : (A) est un composé éthéré représenté par les formules générales (I), (II), (III) ou (IV) dans lesquelles R?1 à R16 et R101 à R105¿ sont chacun hydrogène ou O(CH¿2?CH2O)a-A?1 (où A1¿ est alkyle ou alcényle ; et a est un nombre compris entre 1 et 12), à condition que dans chacune des formules (I) à (IV), R?1 à R16 et R101 à R105¿ ne soient pas tous simultanément hydrogène; et A est (CH¿2?)b-( b étant un nombre entier compris entre 1 et 12) ou O(CH2CH2O)c- (c étant un nombre compris entre 1 et 12)] ; et (B) est un couple redox composé d'iode et d'un composé iodé ou de brome et d'un composé bromé.
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JP2000604485A JP4538955B2 (ja) | 1999-03-10 | 2000-03-08 | エーテル化合物の電解質を用いた光電変換素子 |
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JP11/63080 | 1999-03-10 | ||
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010050575A1 (fr) | 2008-10-29 | 2010-05-06 | 富士フイルム株式会社 | Colorant, élément de conversion photoélectrique et cellule photoélectrochimique comprenant chacun le colorant, et procédé de fabrication du colorant |
EP2302650A2 (fr) | 2009-09-28 | 2011-03-30 | Fujifilm Corporation | Procédé de production d'un élément de conversion photoélectrique, élément de conversion photoélectrique et cellule photoélectricochimique |
EP2306479A2 (fr) | 2009-09-28 | 2011-04-06 | Fujifilm Corporation | Procédé de production d'un élément de conversion photoélectrique, élément de conversion photoélectrique et cellule photoélectricochimique |
CN102471417A (zh) * | 2009-07-15 | 2012-05-23 | 巴斯夫欧洲公司 | 共聚物、其作为增稠剂的用途及其制备方法 |
WO2012132855A1 (fr) | 2011-03-30 | 2012-10-04 | 富士フイルム株式会社 | Convertisseur photoélectrique et cellule photoélectrochimique |
WO2014129575A1 (fr) | 2013-02-22 | 2014-08-28 | 富士フイルム株式会社 | Élément de conversion photoélectrique, procédé de fabrication d'élément de conversion photoélectrique et cellule solaire à colorant |
Citations (4)
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US5084365A (en) * | 1988-02-12 | 1992-01-28 | Michael Gratzel | Photo-electrochemical cell and process of making same |
EP0720189A2 (fr) * | 1994-12-29 | 1996-07-03 | Ishihara Sangyo Kaisha, Ltd. | Matériau composite (matériau poreux - électrolyte polymérique solide), méthode de fabrication et dispositif de conversion photoélectrique utilisant celui-ci |
JPH09245848A (ja) * | 1996-03-14 | 1997-09-19 | Shin Etsu Chem Co Ltd | 光充電式薄型電源素子 |
JPH09259943A (ja) * | 1996-03-19 | 1997-10-03 | Tokyo Gas Co Ltd | 湿式太陽電池 |
Family Cites Families (1)
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JPH08236165A (ja) * | 1994-12-29 | 1996-09-13 | Ishihara Sangyo Kaisha Ltd | 高分子固体電解質およびその製造方法ならびにそれを用いた光電変換素子 |
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2000
- 2000-03-08 WO PCT/JP2000/001379 patent/WO2000054361A1/fr active Application Filing
- 2000-03-08 JP JP2000604485A patent/JP4538955B2/ja not_active Expired - Fee Related
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5084365A (en) * | 1988-02-12 | 1992-01-28 | Michael Gratzel | Photo-electrochemical cell and process of making same |
EP0720189A2 (fr) * | 1994-12-29 | 1996-07-03 | Ishihara Sangyo Kaisha, Ltd. | Matériau composite (matériau poreux - électrolyte polymérique solide), méthode de fabrication et dispositif de conversion photoélectrique utilisant celui-ci |
JPH09245848A (ja) * | 1996-03-14 | 1997-09-19 | Shin Etsu Chem Co Ltd | 光充電式薄型電源素子 |
JPH09259943A (ja) * | 1996-03-19 | 1997-10-03 | Tokyo Gas Co Ltd | 湿式太陽電池 |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010050575A1 (fr) | 2008-10-29 | 2010-05-06 | 富士フイルム株式会社 | Colorant, élément de conversion photoélectrique et cellule photoélectrochimique comprenant chacun le colorant, et procédé de fabrication du colorant |
EP2845882A2 (fr) | 2008-10-29 | 2015-03-11 | Fujifilm Corporation | Colorant, élément de conversion photoélectrique et cellule photoélectrochimique |
CN102471417A (zh) * | 2009-07-15 | 2012-05-23 | 巴斯夫欧洲公司 | 共聚物、其作为增稠剂的用途及其制备方法 |
CN102471417B (zh) * | 2009-07-15 | 2015-08-19 | 巴斯夫欧洲公司 | 共聚物、其作为增稠剂的用途及其制备方法 |
EP2302650A2 (fr) | 2009-09-28 | 2011-03-30 | Fujifilm Corporation | Procédé de production d'un élément de conversion photoélectrique, élément de conversion photoélectrique et cellule photoélectricochimique |
EP2306479A2 (fr) | 2009-09-28 | 2011-04-06 | Fujifilm Corporation | Procédé de production d'un élément de conversion photoélectrique, élément de conversion photoélectrique et cellule photoélectricochimique |
WO2012132855A1 (fr) | 2011-03-30 | 2012-10-04 | 富士フイルム株式会社 | Convertisseur photoélectrique et cellule photoélectrochimique |
WO2014129575A1 (fr) | 2013-02-22 | 2014-08-28 | 富士フイルム株式会社 | Élément de conversion photoélectrique, procédé de fabrication d'élément de conversion photoélectrique et cellule solaire à colorant |
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