JP2013211473A - 有機薄膜太陽電池モジュールおよびその製造方法 - Google Patents
有機薄膜太陽電池モジュールおよびその製造方法 Download PDFInfo
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- 125000002350 geranyl group Chemical group [H]C([*])([H])/C([H])=C(C([H])([H])[H])/C([H])([H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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- 239000001257 hydrogen Substances 0.000 description 1
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- BDAGIHXWWSANSR-NJFSPNSNSA-N hydroxyformaldehyde Chemical compound O[14CH]=O BDAGIHXWWSANSR-NJFSPNSNSA-N 0.000 description 1
- SKWCWFYBFZIXHE-UHFFFAOYSA-K indium acetylacetonate Chemical compound CC(=O)C=C(C)O[In](OC(C)=CC(C)=O)OC(C)=CC(C)=O SKWCWFYBFZIXHE-UHFFFAOYSA-K 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
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- LZKLAOYSENRNKR-LNTINUHCSA-N iron;(z)-4-oxoniumylidenepent-2-en-2-olate Chemical compound [Fe].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O LZKLAOYSENRNKR-LNTINUHCSA-N 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
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- 239000003446 ligand Substances 0.000 description 1
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- 125000003588 lysine group Chemical group [H]N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 description 1
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- 230000003287 optical effect Effects 0.000 description 1
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- SCRKTTJILRGIEY-UHFFFAOYSA-N pentanedioic acid;zinc Chemical compound [Zn].OC(=O)CCCC(O)=O SCRKTTJILRGIEY-UHFFFAOYSA-N 0.000 description 1
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- DFLCZDIXTAAMLZ-UHFFFAOYSA-N phthalic acid;sodium Chemical compound [Na].OC(=O)C1=CC=CC=C1C(O)=O DFLCZDIXTAAMLZ-UHFFFAOYSA-N 0.000 description 1
- CLYVDMAATCIVBF-UHFFFAOYSA-N pigment red 224 Chemical compound C=12C3=CC=C(C(OC4=O)=O)C2=C4C=CC=1C1=CC=C2C(=O)OC(=O)C4=CC=C3C1=C42 CLYVDMAATCIVBF-UHFFFAOYSA-N 0.000 description 1
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- 235000010332 potassium propionate Nutrition 0.000 description 1
- RWMKSKOZLCXHOK-UHFFFAOYSA-M potassium;butanoate Chemical compound [K+].CCCC([O-])=O RWMKSKOZLCXHOK-UHFFFAOYSA-M 0.000 description 1
- LBYLQJKRTJQVDQ-UHFFFAOYSA-M potassium;hydron;propanedioate Chemical compound [K+].OC(=O)CC([O-])=O LBYLQJKRTJQVDQ-UHFFFAOYSA-M 0.000 description 1
- 125000001844 prenyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- TVOIPJPTFTYKQM-UHFFFAOYSA-N propanedioic acid;zinc Chemical compound [Zn].OC(=O)CC(O)=O TVOIPJPTFTYKQM-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- CPNGPNLZQNNVQM-UHFFFAOYSA-N pteridine Chemical compound N1=CN=CC2=NC=CN=C21 CPNGPNLZQNNVQM-UHFFFAOYSA-N 0.000 description 1
- 150000003220 pyrenes Chemical class 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- SVOOVMQUISJERI-UHFFFAOYSA-K rhodium(3+);triacetate Chemical compound [Rh+3].CC([O-])=O.CC([O-])=O.CC([O-])=O SVOOVMQUISJERI-UHFFFAOYSA-K 0.000 description 1
- WPFGFHJALYCVMO-UHFFFAOYSA-L rubidium carbonate Chemical compound [Rb+].[Rb+].[O-]C([O-])=O WPFGFHJALYCVMO-UHFFFAOYSA-L 0.000 description 1
- 229910000026 rubidium carbonate Inorganic materials 0.000 description 1
- 229940102127 rubidium chloride Drugs 0.000 description 1
- 150000003298 rubidium compounds Chemical class 0.000 description 1
- RTHYXYOJKHGZJT-UHFFFAOYSA-N rubidium nitrate Inorganic materials [Rb+].[O-][N+]([O-])=O RTHYXYOJKHGZJT-UHFFFAOYSA-N 0.000 description 1
- 229910000344 rubidium sulfate Inorganic materials 0.000 description 1
- ZIMBPNXOLRMVGV-UHFFFAOYSA-M rubidium(1+);formate Chemical compound [Rb+].[O-]C=O ZIMBPNXOLRMVGV-UHFFFAOYSA-M 0.000 description 1
- GANPIEKBSASAOC-UHFFFAOYSA-L rubidium(1+);sulfate Chemical compound [Rb+].[Rb+].[O-]S([O-])(=O)=O GANPIEKBSASAOC-UHFFFAOYSA-L 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- KZUNJOHGWZRPMI-UHFFFAOYSA-N samarium atom Chemical compound [Sm] KZUNJOHGWZRPMI-UHFFFAOYSA-N 0.000 description 1
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical compound [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 description 1
- 239000010944 silver (metal) Substances 0.000 description 1
- CQLFBEKRDQMJLZ-UHFFFAOYSA-M silver acetate Chemical compound [Ag+].CC([O-])=O CQLFBEKRDQMJLZ-UHFFFAOYSA-M 0.000 description 1
- 229940071536 silver acetate Drugs 0.000 description 1
- CHACQUSVOVNARW-LNKPDPKZSA-M silver;(z)-4-oxopent-2-en-2-olate Chemical compound [Ag+].C\C([O-])=C\C(C)=O CHACQUSVOVNARW-LNKPDPKZSA-M 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 229960004249 sodium acetate Drugs 0.000 description 1
- MFBOGIVSZKQAPD-UHFFFAOYSA-M sodium butyrate Chemical compound [Na+].CCCC([O-])=O MFBOGIVSZKQAPD-UHFFFAOYSA-M 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 150000003388 sodium compounds Chemical class 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- PRWXGRGLHYDWPS-UHFFFAOYSA-L sodium malonate Chemical compound [Na+].[Na+].[O-]C(=O)CC([O-])=O PRWXGRGLHYDWPS-UHFFFAOYSA-L 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- ZNCPFRVNHGOPAG-UHFFFAOYSA-L sodium oxalate Chemical compound [Na+].[Na+].[O-]C(=O)C([O-])=O ZNCPFRVNHGOPAG-UHFFFAOYSA-L 0.000 description 1
- 229940039790 sodium oxalate Drugs 0.000 description 1
- JXKPEJDQGNYQSM-UHFFFAOYSA-M sodium propionate Chemical compound [Na+].CCC([O-])=O JXKPEJDQGNYQSM-UHFFFAOYSA-M 0.000 description 1
- 239000004324 sodium propionate Substances 0.000 description 1
- 235000010334 sodium propionate Nutrition 0.000 description 1
- 229960003212 sodium propionate Drugs 0.000 description 1
- 229940074404 sodium succinate Drugs 0.000 description 1
- ZDQYSKICYIVCPN-UHFFFAOYSA-L sodium succinate (anhydrous) Chemical compound [Na+].[Na+].[O-]C(=O)CCC([O-])=O ZDQYSKICYIVCPN-UHFFFAOYSA-L 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- AIWZOHBYSFSQGV-LNKPDPKZSA-M sodium;(z)-4-oxopent-2-en-2-olate Chemical compound [Na+].C\C([O-])=C\C(C)=O AIWZOHBYSFSQGV-LNKPDPKZSA-M 0.000 description 1
- UJRAXLUXHBUNDO-UHFFFAOYSA-M sodium;hydron;oxalate Chemical compound [Na+].OC(=O)C([O-])=O UJRAXLUXHBUNDO-UHFFFAOYSA-M 0.000 description 1
- LXWZLYDXYCQRJT-UHFFFAOYSA-M sodium;hydron;propanedioate Chemical compound [H+].[Na+].[O-]C(=O)CC([O-])=O LXWZLYDXYCQRJT-UHFFFAOYSA-M 0.000 description 1
- 125000003696 stearoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([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
- 210000002784 stomach Anatomy 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- YJPVTCSBVRMESK-UHFFFAOYSA-L strontium bromide Chemical compound [Br-].[Br-].[Sr+2] YJPVTCSBVRMESK-UHFFFAOYSA-L 0.000 description 1
- 229910001625 strontium bromide Inorganic materials 0.000 description 1
- 229940074155 strontium bromide Drugs 0.000 description 1
- 229910000018 strontium carbonate Inorganic materials 0.000 description 1
- 229910001631 strontium chloride Inorganic materials 0.000 description 1
- 150000003438 strontium compounds Chemical class 0.000 description 1
- AHBGXTDRMVNFER-UHFFFAOYSA-L strontium dichloride Chemical compound [Cl-].[Cl-].[Sr+2] AHBGXTDRMVNFER-UHFFFAOYSA-L 0.000 description 1
- FVRNDBHWWSPNOM-UHFFFAOYSA-L strontium fluoride Chemical compound [F-].[F-].[Sr+2] FVRNDBHWWSPNOM-UHFFFAOYSA-L 0.000 description 1
- 229910001637 strontium fluoride Inorganic materials 0.000 description 1
- KRIJWFBRWPCESA-UHFFFAOYSA-L strontium iodide Chemical compound [Sr+2].[I-].[I-] KRIJWFBRWPCESA-UHFFFAOYSA-L 0.000 description 1
- 229910001643 strontium iodide Inorganic materials 0.000 description 1
- KQAGKTURZUKUCH-UHFFFAOYSA-L strontium oxalate Chemical compound [Sr+2].[O-]C(=O)C([O-])=O KQAGKTURZUKUCH-UHFFFAOYSA-L 0.000 description 1
- UMBFGWVRZIHXCK-FDGPNNRMSA-L strontium;(z)-4-oxopent-2-en-2-olate Chemical compound [Sr+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O UMBFGWVRZIHXCK-FDGPNNRMSA-L 0.000 description 1
- CRLDSNGPLRRUQU-UHFFFAOYSA-L strontium;butanedioate Chemical compound [Sr+2].[O-]C(=O)CCC([O-])=O CRLDSNGPLRRUQU-UHFFFAOYSA-L 0.000 description 1
- ITUCOQTVTSFGRJ-UHFFFAOYSA-L strontium;butanoate Chemical compound [Sr+2].CCCC([O-])=O.CCCC([O-])=O ITUCOQTVTSFGRJ-UHFFFAOYSA-L 0.000 description 1
- FXWRHZACHXRMCI-UHFFFAOYSA-L strontium;diformate Chemical compound [Sr+2].[O-]C=O.[O-]C=O FXWRHZACHXRMCI-UHFFFAOYSA-L 0.000 description 1
- AYNNBBQUOJKZJU-UHFFFAOYSA-L strontium;pentanedioate Chemical compound [Sr+2].[O-]C(=O)CCCC([O-])=O AYNNBBQUOJKZJU-UHFFFAOYSA-L 0.000 description 1
- KGCOMQDJRDGWDD-UHFFFAOYSA-L strontium;phthalate Chemical compound [Sr+2].[O-]C(=O)C1=CC=CC=C1C([O-])=O KGCOMQDJRDGWDD-UHFFFAOYSA-L 0.000 description 1
- LVZZABGEQTZXHP-UHFFFAOYSA-L strontium;propanedioate Chemical compound [Sr+2].[O-]C(=O)CC([O-])=O LVZZABGEQTZXHP-UHFFFAOYSA-L 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- OKUCEQDKBKYEJY-UHFFFAOYSA-N tert-butyl 3-(methylamino)pyrrolidine-1-carboxylate Chemical compound CNC1CCN(C(=O)OC(C)(C)C)C1 OKUCEQDKBKYEJY-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003518 tetracenes Chemical class 0.000 description 1
- NLDYACGHTUPAQU-UHFFFAOYSA-N tetracyanoethylene Chemical group N#CC(C#N)=C(C#N)C#N NLDYACGHTUPAQU-UHFFFAOYSA-N 0.000 description 1
- PCCVSPMFGIFTHU-UHFFFAOYSA-N tetracyanoquinodimethane Chemical compound N#CC(C#N)=C1C=CC(=C(C#N)C#N)C=C1 PCCVSPMFGIFTHU-UHFFFAOYSA-N 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- 229910052716 thallium Inorganic materials 0.000 description 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- QKTRRACPJVYJNU-UHFFFAOYSA-N thiadiazolo[5,4-b]pyridine Chemical compound C1=CN=C2SN=NC2=C1 QKTRRACPJVYJNU-UHFFFAOYSA-N 0.000 description 1
- WEQHQGJDZLDFID-UHFFFAOYSA-J thorium(iv) chloride Chemical compound Cl[Th](Cl)(Cl)Cl WEQHQGJDZLDFID-UHFFFAOYSA-J 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- HLLICFJUWSZHRJ-UHFFFAOYSA-N tioxidazole Chemical compound CCCOC1=CC=C2N=C(NC(=O)OC)SC2=C1 HLLICFJUWSZHRJ-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- YJGJRYWNNHUESM-UHFFFAOYSA-J triacetyloxystannyl acetate Chemical compound [Sn+4].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O YJGJRYWNNHUESM-UHFFFAOYSA-J 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical compound BrC1=CC=CC(C=2N=C3N=CN[N+]3=C(NCC=3C=CN=CC=3)C=2)=C1 YWBFPKPWMSWWEA-UHFFFAOYSA-O 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000006617 triphenylamine group Chemical group 0.000 description 1
- KHAUBYTYGDOYRU-IRXASZMISA-N trospectomycin Chemical compound CN[C@H]([C@H]1O2)[C@@H](O)[C@@H](NC)[C@H](O)[C@H]1O[C@H]1[C@]2(O)C(=O)C[C@@H](CCCC)O1 KHAUBYTYGDOYRU-IRXASZMISA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000001039 wet etching Methods 0.000 description 1
- YZYKBQUWMPUVEN-UHFFFAOYSA-N zafuleptine Chemical compound OC(=O)CCCCCC(C(C)C)NCC1=CC=C(F)C=C1 YZYKBQUWMPUVEN-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- SRWMQSFFRFWREA-UHFFFAOYSA-M zinc formate Chemical compound [Zn+2].[O-]C=O SRWMQSFFRFWREA-UHFFFAOYSA-M 0.000 description 1
- AGFGXVAAIXIOFZ-UHFFFAOYSA-L zinc;butanedioate Chemical compound [Zn+2].[O-]C(=O)CCC([O-])=O AGFGXVAAIXIOFZ-UHFFFAOYSA-L 0.000 description 1
- WDHVIZKSFZNHJB-UHFFFAOYSA-L zinc;butanoate Chemical compound [Zn+2].CCCC([O-])=O.CCCC([O-])=O WDHVIZKSFZNHJB-UHFFFAOYSA-L 0.000 description 1
- ZPEJZWGMHAKWNL-UHFFFAOYSA-L zinc;oxalate Chemical compound [Zn+2].[O-]C(=O)C([O-])=O ZPEJZWGMHAKWNL-UHFFFAOYSA-L 0.000 description 1
- UXDZLUCNRYCZCG-UHFFFAOYSA-L zinc;phthalate Chemical compound [Zn+2].[O-]C(=O)C1=CC=CC=C1C([O-])=O UXDZLUCNRYCZCG-UHFFFAOYSA-L 0.000 description 1
- XDWXRAYGALQIFG-UHFFFAOYSA-L zinc;propanoate Chemical compound [Zn+2].CCC([O-])=O.CCC([O-])=O XDWXRAYGALQIFG-UHFFFAOYSA-L 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
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- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K39/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic radiation-sensitive element covered by group H10K30/00
- H10K39/10—Organic photovoltaic [PV] modules; Arrays of single organic PV cells
- H10K39/12—Electrical configurations of PV cells, e.g. series connections or parallel connections
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- 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
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- Y02E10/549—Organic PV cells
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Abstract
【解決手段】透明基板上に複数個の単位素子が平面的に配列され、少なくとも、第1の電極、光電変換層、および第2の電極とを備えた単位素子が、透明基板上に複数個前記複数個の平面的に配列され、一方の単位素子の第2の電極が、光電変換層および保護層を貫通する加工線を通して隣り合う他方の単位素子の第1の電極と直接接触することにより直列に接続することで形成された集積構造を有する。
【選択図】図1
Description
互いに直列接続された一方の単位素子に、光電変換層および保護層を貫通する溝部分が形成されており、互いに直列接続された他方の単位素子の第1の電極が前記溝部分の底部にまで延在し、前記一方の単位素子の第2の電極が前記溝部分を通じて前記他方の単位素子の第1の電極と電気的に接続していることを特徴とする。
M(X)a (1)
上記(1)式において、Mはアルカリ金属、アルカリ土類金属、2B、3B族の金属、遷移金属から成る群より選ばれ、Xはハロゲン、カルボキシラート基、アルコキシ基、アルキル基、および下式で表されるアセトナート基から選ばれ、aはMの価数に応じて決まる、正の整数である。
Zn(X)2 (1−1)
上記(1−1)式において、Xはハロゲン、カルボキシラート基、アルコキシ基、アルキル基、および上述したアセトナート基から選ばれる。
Mg(X)2 (1−2)
上記(1−2)式において、Xはハロゲン、カルボキシラート基、アルコキシ基、アルキル基、および上述したアセトナート基から選ばれる。
<負極の形成>
透明基板20としてガラス基板(面抵抗値15Ω/□)を用い、当該ガラス基板にITOをスパッタ法により成膜した後、洗浄して負極(電子取出電極)用電極用の金属層を形成した。
<負極のパターニング>
上記負極用電極用の金属層を表1に示す加工条件でレーザースクライブ加工を実施し、パターニング電極(第1の電極)を得た(加工線P1加工)。
<電子取出層の形成>
(1)電子輸送層の形成
溶液塗布法により電子輸送層80を作製した。具体的には、酢酸亜鉛・2水和物(アルドリッチ社製)を濃度20mg/mlになるように2−メトキシエタノール中に溶解させ、さらに、モノエタノールアミンを添加(55μl/ml)して溶液を調製した。上述したパターニング電極のITO上に、前記溶液を2000rpm(30秒)でスピンコートし、ホットプレート上で120℃、5分間熱処理して電子輸送層を形成した。熱処理後の電子輸送層80の膜厚は30nmであった。
(2)伝導帯下端エネルギー調整層の形成
炭酸セシウム(アルドリッチ社製)を濃度1.86mg/mlになるように2−エトキシエタノール中に溶解させ、溶液を調製した。上述の方法で形成した電子輸送層80の上に、当該溶液を5000rpm(30秒)でスピンコートし、ホットプレート上で150℃、10分間熱処理することで伝導帯下端エネルギー調整層90を形成した。熱処理後の伝導帯下端エネルギー調整層90の膜厚は5nmであった。
<光電変換層の形成>
p型有機半導体材料としてポリ(3−ヘキシルチオフェン)(P3HT)とn型有機半導体材料としてIndene−C60 bisadduct(ICBA)を質量比1:1で混合し、合計濃度が2.5質量%となるようにオルトジクロロベンゼンに溶解させた。上記伝導帯下端エネルギー調整層を形成した基板上に750rpm(10秒)でスピンコートし、光電変換層50を形成した。光電変換層50の膜厚は200nmであった。
<保護層の形成>
光電変換層50を作製した基板上にWO3(保護層60)を抵抗加熱法により真空蒸着した。WO3層の膜厚は10nmであった。蒸着時の真空度は10−6Torr以下とした。さらに、上記WO3層上にAgを抵抗加熱法により真空蒸着した。Ag層の膜厚は50nmである。蒸着時の真空度は10−6Torr以下とした。
<光電変換層、保護層のパターニング>
上記で保護層まで作製した基板を表1に示す加工条件でレーザースクライブ加工を実施し、光電変換層、保護層のパターニング基板を得た(加工線P2加工)。
<正極の形成>
上記パターニング基板上にAgを抵抗加熱法により真空蒸着した。Ag層の膜厚は100nmである。蒸着時の真空度は10−6Torr以下とした。
<正極のパターニング>
上記正極形成基板を表1に示す加工条件でレーザースクライブ加工を実施し、光電変換層、保護層、正極(第2の電極70)のパターニングを行った(加工線P3加工)。
<封止処理>
上記のように作製した有機薄膜太陽電池モジュールを、熱硬化性封止剤320を用いてカバーガラス310と貼り合せ、100℃2h熱処理して封止モジュールを得た。
実施例2の有機薄膜太陽電池モジュールの作製方法は、保護層としてWO3層だけを形成したことを除き、実施例1と同様である。また、実施例3の有機薄膜太陽電池モジュールの作製方法は、気体のブローをしなかったことを除き、実施例2と同様である。また、実施例4の有機薄膜太陽電池モジュールの作製方法は、集塵をしなかったことを除き、実施例2と同様である。実施例5の有機薄膜太陽電池モジュールの作製方法は、気体のブロー、集塵の両方をしなかったことを除き、実施例2と同様である。
図5は、比較例1の有機薄膜太陽電池モジュールの構成を示す断面図である。比較例1の有機薄膜太陽電池モジュール200の作製方法は、WO3層を製膜せずに光電変換層のパターニング加工(加工線P2加工)を行った後、WO3層、正極の製膜を行い、加工線P3に対する加工を行ったこと以外は実施例1と同様である。また、比較例2は、N2ブロー、集塵の方向を反対にしたこと以外は比較例1と同様である。また、比較例3は、封止材として、紫外線硬化型封止材を用いた以外は、比較例1と同様である。
初期状態の実施例1〜5、および比較例1〜3の有機薄膜太陽電池モジュールについて、室温で1000W/m2疑似太陽光を照射しながら電流電圧特性を測定した。得られた電流−電圧特性より太陽電池の光電変換効率および開放電圧を算出した。光電変換効率、開放電圧について得られた結果を表2に示す。
電子取出層および電子輸送層の伝導帯下端エネルギーの評価には、紫外光電子分光法により求めたイオン化ポテンシャル、および紫外・可視吸収スペクトルより求めたバンドギャップを用いておこなった(参考文献:T.C.Nguyen著“Electronic Properties of Conjugated Polyelectrolyte Thin Film” J.AM.CHEM.SOC. 2008, 130, 10042−10043)。紫外光電子分光器としてKratos社製AXIS Ultraを用い、エネルギー21.22エレクトロンボルトのHe(I)励起の紫外光電子分光法により電子取出層及び電子輸送層の光電子スペクトルを測定した。得られた光電子スペクトルの高束縛エネルギー側カットオフエネルギーより、イオン化ポテンシャルを評価した。紫外・可視吸収スペクトル測定には、日立ハイテクノロジーズ社製U−4100を用いた。得られた吸収スペクトルの長波長側カットオフより、バンドギャップを評価した。イオン化ポテンシャルから光学バンドギャップを差し引くことで、伝導帯下端エネルギーを算出した。このようにして算出した実施例、比較例の電子取出層の伝導帯下端エネルギーは2.9eVであった。なお、光電変換素子に組み込まれた電子取出層および電子輸送層の伝導帯下端エネルギーを測定する場合は、光電変換素子のカバーガラスの一方を剥ぎ取り、光電変換層をo−ジクロロベンゼンで溶解除去した後、基板上に残った、電子取出層付基板を用いて、Arスパッタリングにより膜厚方向に掘り進めながら、上記方法で伝導帯下端エネルギーを算出する。
A.J.Bard著「Electochemical Methods: Fundamentals and Applicaitons」を参考に以下のように実施した。
図6は、実施例1および比較例3の有機薄膜太陽電池モジュールの耐熱試験結果を示すグラフである。耐熱試験は恒温槽を用いて作製した有機薄膜太陽電池モジュールを開回路状態で85℃の暗所放置を行った。
Claims (2)
- 透明基板上に複数個の単位素子が平面的に配列され、前記単位素子が、前記透明基板の側から順に、少なくとも、第1の電極、光電変換層、保護層および第2の電極とを備え、前記複数個の単位素子のうち少なくとも2個の単位素子が直列に接続された有機薄膜太陽電池モジュールであって、
互いに直列接続された一方の単位素子に、光電変換層および保護層を貫通する溝部分が形成されており、
互いに直列接続された他方の単位素子の第1の電極が前記溝部分の底部にまで延在し、
前記一方の単位素子の第2の電極が前記溝部分を通じて前記他方の単位素子の第1の電極と電気的に接続していることを特徴とする有機薄膜太陽電池モジュール。 - 透明基板上に複数個の単位素子が平面的に配列され、前記単位素子が、前記透明基板の側から順に、少なくとも第1の電極、光電変換層、保護層および第2の電極とを備え、前記複数個の単位素子のうち少なくとも2個の単位素子が直列に接続された有機薄膜太陽電池モジュールの製造方法であって、
パターニングされた前記第1の電極の上に少なくとも前記光電変換層と前記保護層を設ける工程と、
任意の単位素子の前記光電変換層および前記保護層をレーザーによりスクライブすることで前記光電変換層および前記保護層を貫通し、当該単位素子と直列接続される他の単位素子の第2の電極が底部に延在する溝部分を形成する工程と、
当該単位素子の前記保護層の上および前記溝部分に、第2の電極を形成し、当該単位素子の第2の電極を前記溝部分を通じて他の単位素子の第1の電極と電気的に接続させる工程と、
を備えることを特徴とする有機薄膜太陽電池モジュールの製造方法。
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016063972A1 (ja) * | 2014-10-24 | 2016-04-28 | 昭和電工株式会社 | 樹脂添加剤、それを用いた樹脂組成物及びその製造方法 |
JP2016111153A (ja) * | 2014-12-04 | 2016-06-20 | 住友化学株式会社 | 太陽電池モジュール及びその製造方法 |
KR20170113193A (ko) * | 2016-03-25 | 2017-10-12 | 코오롱인더스트리 주식회사 | 유기태양전지 및 이의 제조방법 |
US9899618B2 (en) | 2015-03-19 | 2018-02-20 | Kabushiki Kaisha Toshiba | Photoelectric conversion device and manufacturing method thereof |
JP2020053616A (ja) * | 2018-09-28 | 2020-04-02 | 株式会社リコー | 太陽電池モジュール |
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---|---|---|---|---|
EP2983209A1 (en) * | 2014-08-07 | 2016-02-10 | Koninklijke Philips N.V. | Organic electronics device, method and system for producing the same |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005014083A (ja) * | 2003-06-30 | 2005-01-20 | Fuji Electric Holdings Co Ltd | レーザ加工装置およびレーザ加工方法 |
JP2010287800A (ja) * | 2009-06-12 | 2010-12-24 | Tokki Corp | 有機デバイスの製造装置並びに有機デバイスの製造方法 |
JP2011119695A (ja) * | 2009-10-29 | 2011-06-16 | Sumitomo Chemical Co Ltd | 有機薄膜太陽電池モジュールの製造方法 |
JP2012004239A (ja) * | 2010-06-15 | 2012-01-05 | Fujifilm Corp | 有機薄膜太陽電池 |
-
2012
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-
2013
- 2013-03-29 WO PCT/JP2013/002175 patent/WO2013145775A1/ja active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005014083A (ja) * | 2003-06-30 | 2005-01-20 | Fuji Electric Holdings Co Ltd | レーザ加工装置およびレーザ加工方法 |
JP2010287800A (ja) * | 2009-06-12 | 2010-12-24 | Tokki Corp | 有機デバイスの製造装置並びに有機デバイスの製造方法 |
JP2011119695A (ja) * | 2009-10-29 | 2011-06-16 | Sumitomo Chemical Co Ltd | 有機薄膜太陽電池モジュールの製造方法 |
JP2012004239A (ja) * | 2010-06-15 | 2012-01-05 | Fujifilm Corp | 有機薄膜太陽電池 |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016063972A1 (ja) * | 2014-10-24 | 2016-04-28 | 昭和電工株式会社 | 樹脂添加剤、それを用いた樹脂組成物及びその製造方法 |
JPWO2016063972A1 (ja) * | 2014-10-24 | 2017-08-03 | 昭和電工株式会社 | 樹脂添加剤、それを用いた樹脂組成物及びその製造方法 |
JP2020094181A (ja) * | 2014-10-24 | 2020-06-18 | 昭和電工株式会社 | 樹脂組成物の製造方法および樹脂添加剤 |
JP2016111153A (ja) * | 2014-12-04 | 2016-06-20 | 住友化学株式会社 | 太陽電池モジュール及びその製造方法 |
US9899618B2 (en) | 2015-03-19 | 2018-02-20 | Kabushiki Kaisha Toshiba | Photoelectric conversion device and manufacturing method thereof |
US10305055B2 (en) | 2015-03-19 | 2019-05-28 | Kabushiki Kaisha Toshiba | Photoelectric conversion device and manufacturing method thereof |
KR20170113193A (ko) * | 2016-03-25 | 2017-10-12 | 코오롱인더스트리 주식회사 | 유기태양전지 및 이의 제조방법 |
JP2020053616A (ja) * | 2018-09-28 | 2020-04-02 | 株式会社リコー | 太陽電池モジュール |
WO2020067188A1 (en) * | 2018-09-28 | 2020-04-02 | Ricoh Company, Ltd. | Solar cell module |
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