JP2010265458A - 有機色素および光電変換装置 - Google Patents
有機色素および光電変換装置 Download PDFInfo
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- JP2010265458A JP2010265458A JP2010112235A JP2010112235A JP2010265458A JP 2010265458 A JP2010265458 A JP 2010265458A JP 2010112235 A JP2010112235 A JP 2010112235A JP 2010112235 A JP2010112235 A JP 2010112235A JP 2010265458 A JP2010265458 A JP 2010265458A
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- 238000006243 chemical reaction Methods 0.000 title claims abstract description 60
- 239000001257 hydrogen Substances 0.000 claims description 27
- 150000002431 hydrogen Chemical class 0.000 claims description 27
- 229910052739 hydrogen Inorganic materials 0.000 claims description 27
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 claims description 21
- 125000006651 (C3-C20) cycloalkyl group Chemical group 0.000 claims description 21
- 125000003545 alkoxy group Chemical group 0.000 claims description 21
- 125000003118 aryl group Chemical group 0.000 claims description 21
- 125000001072 heteroaryl group Chemical group 0.000 claims description 21
- 125000002723 alicyclic group Chemical group 0.000 claims description 20
- 229910052736 halogen Inorganic materials 0.000 claims description 20
- 150000002367 halogens Chemical class 0.000 claims description 20
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 20
- 125000003277 amino group Chemical group 0.000 claims description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
- 229910052783 alkali metal Inorganic materials 0.000 claims description 7
- 150000001340 alkali metals Chemical class 0.000 claims description 7
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 7
- APVPOHHVBBYQAV-UHFFFAOYSA-N n-(4-aminophenyl)sulfonyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 APVPOHHVBBYQAV-UHFFFAOYSA-N 0.000 claims description 5
- 239000012860 organic pigment Substances 0.000 claims description 4
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- 229910052744 lithium Inorganic materials 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 239000011591 potassium Substances 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 abstract description 20
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical group C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 abstract description 8
- 238000010521 absorption reaction Methods 0.000 abstract description 6
- 125000006850 spacer group Chemical group 0.000 abstract description 3
- 239000000975 dye Substances 0.000 description 46
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 16
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 14
- MZRVEZGGRBJDDB-UHFFFAOYSA-N n-Butyllithium Substances [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 12
- 229940035422 diphenylamine Drugs 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 10
- -1 heptoxy group Chemical group 0.000 description 9
- 0 *C(*N(c1ccccc1)c1ccccc1)=C(C(*)=O)C#N Chemical compound *C(*N(c1ccccc1)c1ccccc1)=C(C(*)=O)C#N 0.000 description 8
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 8
- 239000000706 filtrate Substances 0.000 description 8
- 238000001914 filtration Methods 0.000 description 8
- 239000012074 organic phase Substances 0.000 description 8
- 239000003960 organic solvent Substances 0.000 description 8
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 238000001816 cooling Methods 0.000 description 6
- 230000008878 coupling Effects 0.000 description 6
- 238000010168 coupling process Methods 0.000 description 6
- 238000005859 coupling reaction Methods 0.000 description 6
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 229910010413 TiO 2 Inorganic materials 0.000 description 4
- 229910052786 argon Inorganic materials 0.000 description 4
- DLEDOFVPSDKWEF-UHFFFAOYSA-N lithium butane Chemical compound [Li+].CCC[CH2-] DLEDOFVPSDKWEF-UHFFFAOYSA-N 0.000 description 4
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 4
- 150000002900 organolithium compounds Chemical class 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 239000008151 electrolyte solution Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000003504 photosensitizing agent Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 230000032258 transport Effects 0.000 description 3
- SQTLUXJWUCHKMT-UHFFFAOYSA-N 4-bromo-n,n-diphenylaniline Chemical compound C1=CC(Br)=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 SQTLUXJWUCHKMT-UHFFFAOYSA-N 0.000 description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004440 column chromatography Methods 0.000 description 2
- MLIREBYILWEBDM-UHFFFAOYSA-N cyanoacetic acid Chemical compound OC(=O)CC#N MLIREBYILWEBDM-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 229910052707 ruthenium Inorganic materials 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000006478 transmetalation reaction Methods 0.000 description 2
- QWAFPTWWKUWNDC-UHFFFAOYSA-N 2-(4-carboxypyridin-2-yl)pyridine-4-carboxylic acid;ruthenium Chemical compound [Ru].OC(=O)C1=CC=NC(C=2N=CC=C(C=2)C(O)=O)=C1 QWAFPTWWKUWNDC-UHFFFAOYSA-N 0.000 description 1
- LTNAYKNIZNSHQA-UHFFFAOYSA-L 2-(4-carboxypyridin-2-yl)pyridine-4-carboxylic acid;ruthenium(2+);dithiocyanate Chemical compound N#CS[Ru]SC#N.OC(=O)C1=CC=NC(C=2N=CC=C(C=2)C(O)=O)=C1.OC(=O)C1=CC=NC(C=2N=CC=C(C=2)C(O)=O)=C1 LTNAYKNIZNSHQA-UHFFFAOYSA-L 0.000 description 1
- MFOWHGLWSHZGCA-UHFFFAOYSA-N 9h-fluorene-1-carbaldehyde Chemical compound C1C2=CC=CC=C2C2=C1C(C=O)=CC=C2 MFOWHGLWSHZGCA-UHFFFAOYSA-N 0.000 description 1
- OOCYPUXBFBGIPL-UHFFFAOYSA-N CC(c1c-2[s]c(-c(cc3)ccc3N(c3ccccc3)c3ccccc3)c1)(c1c-2[s]c([Sn](C)(C)C)c1)I Chemical compound CC(c1c-2[s]c(-c(cc3)ccc3N(c3ccccc3)c3ccccc3)c1)(c1c-2[s]c([Sn](C)(C)C)c1)I OOCYPUXBFBGIPL-UHFFFAOYSA-N 0.000 description 1
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 238000005401 electroluminescence Methods 0.000 description 1
- 238000004134 energy conservation Methods 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000005281 excited state Effects 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 230000005525 hole transport Effects 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000001792 phenanthrenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C=CC12)* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
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Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6576—Polycyclic condensed heteroaromatic hydrocarbons comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D495/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- 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
-
- 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
- Y02E10/549—Organic PV cells
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Hybrid Cells (AREA)
- Photovoltaic Devices (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Description
で示されることを特徴とする有機色素を提供する。
で示される有機色素を提供する。
で示される有機色素を提供する。
式(I):
化合物W−01の合成
まず、8gのDOCPDT(4,4−ジオクチル−4H−シクロペンタ[2,1−b;3,4−b’]−ジチオフェン)を100mLの反応ビンに加え、50mLのTHF(テトラヒドロフラン)を用いて溶解した。次に、7.95mLのn−BuLi(n−ブチルリチウム)を−78℃で反応ビンに加えた。2時間攪拌した後、4.36gのMe3SnCl(10mLのTHFに溶解)を反応ビンに加えた。−78℃で2時間、室温で10時間反応させた後、水を反応ビンに加えて反応を終了させ、CH2Cl2を用いて混合物を抽出した。有機相を分離し、MgSO4で乾燥させた。濾過後、濾液を濃縮して有機溶媒を除去し、TMSn−CPDT(4,4−ジオクチル−2−トリメチルスタンナニル−4H−シクロ−ペンタ[2,1−b;3,4−b’]−ジチオフェン)を得た。
化合物W−05の合成
まず、8gのDOCPDT(4,4−ジオクチル−4H−シクロペンタ[2,1−b;3,4−b’]−ジチオフェン)を反応ビンに加え、50mLのTHF(テトラヒドロフラン)を用いて溶解した。次に、7.95mLのn−BuLi(n−ブチルリチウム)を−78℃で反応ビンに加えた。2時間攪拌した後、4.36gのMe3SnCl(10mLのTHFに溶解)を反応ビンに加えた。−78℃で2時間、室温で10時間反応させた後、水を反応ビンに加えて反応を終了させ、CH2Cl2を用いて混合物を抽出した。有機相を分離し、MgSO4で乾燥させた。濾過後、濾液を濃縮して有機溶媒を除去し、TMSn−CPDT(4,4−ジオクチル−2−トリメチルスタンナニル−4H−シクロ−ペンタ[2,1−b;3,4−b’]−ジチオフェン)を得た。
≪実施例17≫
実施例1で合成された有機色素W−01を用いて、図1に示すような色素増感型太陽電池100を作製した。この作製方法は、下記の工程を含んでいた。
まず、予め準備された作用電極10(透明導電基板12および多孔質酸化チタン(TiO2)層14を含む)を、有機色素16(実施例5で合成された有機色素W−05)を含む溶液に数分間浸漬した。ここで、有機色素16は、自己組織化により、TiO2層14の表面に吸着された。次に、作用電極10を溶媒で洗浄した。乾燥後、作用電極10をエポキシ樹脂または紫外線硬化剤により対向電極20で密閉した。次に、電解液(0.5M LiI/0.05M I2/0.5M TBP/アセトニトリル)30をセル内に充填した後、開口部を密封することにより、色素増感型太陽電池Bの作製を完成した。次に、色素増感型太陽電池Bの開路電圧、短絡電流および光電変換効率を測定した。その結果を表6に示す。
実施例19〜24は、有機色素W−01を有機色素W−11、W−12、W−13、W−14、W−15およびW−16にそれぞれ置き換えたこと以外は、実施例17と同様にして行った。次に、得られた色素増感型太陽電池の開路電圧、短絡電流および光電変換効率を測定した。その結果を表7に示す。
Claims (13)
- 下記式(I):
で示されることを特徴とする有機色素。 - 下記式(II):
で示される請求項1に記載の有機色素。 - 下記式(III):
で示される請求項1に記載の有機色素。 - nが4である請求項1に記載の有機色素。
- nが5である請求項1に記載の有機色素。
- nが6である請求項1に記載の有機色素。
- Zがリチウム、ナトリウムまたはカリウムである請求項1〜3のいずれか1項に記載の有機色素。
- 請求項1〜7のいずれか1項に記載の有機色素を含むことを特徴とする光電変換装置。
- フラットディスプレイ装置を含む請求項8に記載の光電変換装置。
- 有機エレクトロルミネッセンス素子を含む請求項8に記載の光電変換装置。
- 有機光電変換素子を含む請求項8に記載の光電変換装置。
- 太陽電池を含む請求項8に記載の光電変換装置。
- 色素増感型太陽電池を含む請求項8に記載の光電変換装置。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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TW098116139 | 2009-05-15 | ||
TW098116139A TWI458787B (zh) | 2009-05-15 | 2009-05-15 | 有機染料及包含其之光電轉換裝置 |
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JP2010265458A true JP2010265458A (ja) | 2010-11-25 |
JP5325161B2 JP5325161B2 (ja) | 2013-10-23 |
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Country | Link |
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US (2) | US8969593B2 (ja) |
JP (1) | JP5325161B2 (ja) |
TW (1) | TWI458787B (ja) |
Cited By (5)
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JP2012031373A (ja) * | 2010-07-09 | 2012-02-16 | Toyo Ink Sc Holdings Co Ltd | 光機能材料 |
WO2012132735A1 (ja) * | 2011-03-31 | 2012-10-04 | 富士フイルム株式会社 | 色素、光電変換素子及び光電気化学電池 |
WO2013042414A1 (ja) * | 2011-09-22 | 2013-03-28 | 日本電気株式会社 | ジチエノピロール系化合物、光電変換素子用色素、これを用いた光電変換素子用半導体電極、および光電変換素子 |
WO2013129605A1 (ja) * | 2012-03-01 | 2013-09-06 | 関東天然瓦斯開発株式会社 | 色素増感型光電変換素子用の非平面型構造を有する完全有機色素化合物、およびそれを用いた光電変換素子 |
JP2013181108A (ja) * | 2012-03-01 | 2013-09-12 | Kanto Natural Gas Development Co Ltd | 色素増感型光電変換素子用の高活性完全有機色素化合物、およびそれを用いた光電変換素子 |
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WO2012049167A1 (en) * | 2010-10-11 | 2012-04-19 | Universite De La Mediterranee Aix-Marseille Ii | Novel oligothiophene derivatives, their process of preparation and their uses |
KR102052565B1 (ko) * | 2013-07-24 | 2019-12-06 | 덕산네오룩스 주식회사 | 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치 |
ITMI20131899A1 (it) | 2013-11-15 | 2015-05-16 | C N R S Ct Nat De La Rec Herche Scienti | Colorante organico per una cella solare sensibilizzata da colorante |
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JP2012031373A (ja) * | 2010-07-09 | 2012-02-16 | Toyo Ink Sc Holdings Co Ltd | 光機能材料 |
WO2012132735A1 (ja) * | 2011-03-31 | 2012-10-04 | 富士フイルム株式会社 | 色素、光電変換素子及び光電気化学電池 |
JP2012214671A (ja) * | 2011-03-31 | 2012-11-08 | Fujifilm Corp | 色素、光電変換素子及び光電気化学電池 |
GB2507661A (en) * | 2011-03-31 | 2014-05-07 | Fujifilm Corp | Pigment, photoelectric converter, and photoelectrochemical cell |
WO2013042414A1 (ja) * | 2011-09-22 | 2013-03-28 | 日本電気株式会社 | ジチエノピロール系化合物、光電変換素子用色素、これを用いた光電変換素子用半導体電極、および光電変換素子 |
WO2013129605A1 (ja) * | 2012-03-01 | 2013-09-06 | 関東天然瓦斯開発株式会社 | 色素増感型光電変換素子用の非平面型構造を有する完全有機色素化合物、およびそれを用いた光電変換素子 |
JP2013181108A (ja) * | 2012-03-01 | 2013-09-12 | Kanto Natural Gas Development Co Ltd | 色素増感型光電変換素子用の高活性完全有機色素化合物、およびそれを用いた光電変換素子 |
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Also Published As
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US20130144069A1 (en) | 2013-06-06 |
TWI458787B (zh) | 2014-11-01 |
TW201040230A (en) | 2010-11-16 |
JP5325161B2 (ja) | 2013-10-23 |
US8969593B2 (en) | 2015-03-03 |
US20100292488A1 (en) | 2010-11-18 |
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