EP2638577A2 - Générateur photovoltaïque organique et procédé de fabrication - Google Patents
Générateur photovoltaïque organique et procédé de fabricationInfo
- Publication number
- EP2638577A2 EP2638577A2 EP12746750.4A EP12746750A EP2638577A2 EP 2638577 A2 EP2638577 A2 EP 2638577A2 EP 12746750 A EP12746750 A EP 12746750A EP 2638577 A2 EP2638577 A2 EP 2638577A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- layer
- solar photovoltaic
- photovoltaic cell
- poly
- ito
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
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- 229920000642 polymer Polymers 0.000 description 28
- -1 poly(3-hexylthiophene) Polymers 0.000 description 27
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 19
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- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
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- 229920000144 PEDOT:PSS Polymers 0.000 description 3
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- 230000000149 penetrating effect Effects 0.000 description 3
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 3
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- 238000005204 segregation Methods 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
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- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 3
- 239000004709 Chlorinated polyethylene Substances 0.000 description 2
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 2
- 239000004713 Cyclic olefin copolymer Substances 0.000 description 2
- 229920000106 Liquid crystal polymer Polymers 0.000 description 2
- 239000004977 Liquid-crystal polymers (LCPs) Substances 0.000 description 2
- UUIQMZJEGPQKFD-UHFFFAOYSA-N Methyl butyrate Chemical compound CCCC(=O)OC UUIQMZJEGPQKFD-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 239000004697 Polyetherimide Substances 0.000 description 2
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- 238000005265 energy consumption Methods 0.000 description 2
- 229910003472 fullerene Inorganic materials 0.000 description 2
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
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- 239000000203 mixture Substances 0.000 description 2
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- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 description 2
- 229920001652 poly(etherketoneketone) Polymers 0.000 description 2
- 239000005014 poly(hydroxyalkanoate) Substances 0.000 description 2
- 229920002492 poly(sulfone) Polymers 0.000 description 2
- 229920002239 polyacrylonitrile Polymers 0.000 description 2
- 229920006260 polyaryletherketone Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920001748 polybutylene Polymers 0.000 description 2
- 239000005023 polychlorotrifluoroethylene (PCTFE) polymer Substances 0.000 description 2
- 229920001123 polycyclohexylenedimethylene terephthalate Polymers 0.000 description 2
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- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
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- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical compound FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
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- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y10/00—Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K71/00—Manufacture or treatment specially adapted for the organic devices covered by this subclass
- H10K71/10—Deposition of organic active material
- H10K71/12—Deposition of organic active material using liquid deposition, e.g. spin coating
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K2102/00—Constructional details relating to the organic devices covered by this subclass
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
- H10K30/30—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation comprising bulk heterojunctions, e.g. interpenetrating networks of donor and acceptor material domains
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
- H10K30/50—Photovoltaic [PV] devices
-
- 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
- H10K85/10—Organic polymers or oligomers
- H10K85/111—Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
- H10K85/113—Heteroaromatic compounds comprising sulfur or selene, e.g. polythiophene
-
- 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
- H10K85/10—Organic polymers or oligomers
- H10K85/111—Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
- H10K85/113—Heteroaromatic compounds comprising sulfur or selene, e.g. polythiophene
- H10K85/1135—Polyethylene dioxythiophene [PEDOT]; Derivatives thereof
-
- 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
- H10K85/20—Carbon compounds, e.g. carbon nanotubes or fullerenes
- H10K85/211—Fullerenes, e.g. C60
- H10K85/215—Fullerenes, e.g. C60 comprising substituents, e.g. PCBM
-
- 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
-
- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Definitions
- the poly (3,4) ethylenedioxythiophene:poly-styrenesulfonate mixed with 5 vol.% of dimethylsulfoxide was prepared diluting the poly (3,4) ethylenedioxythiophene:poly- styrenesulfonate filtering the diluted poly (3,4) ethylenedioxythiophene:poly-styrenesulfonate through a 0.45 ⁇ filter, and mixing the dimethylsulfoxide into the diluted poly (3,4) ethylenedioxythiophene:poly-styrenesulfonate.
- this cathodic layer has a thickness of about 100nm to about 700nm, and may be 600nm in some variations. Exemplary thicknesses include 200nm, 250nm, 300nm, 350nm, 400nm, 450nm, 550nm, 600nm, 650nm, and 700nm.
- the l-V was measured by shining light from m- PEDOT side.
- the device was analyzed by exposing the cell to continuous radiation.
- the current-voltage (l-V) characterization of the solar array was performed with a 1.6 KW solar simulator under AM1 .5 irradiance of 100 mW/cm 2 (Newport Corp., Franklin MA). No spectral mismatch with the standard solar spectrum was corrected in the power conversion efficiency (PCE) calculation.
- the incident photon converted electron (IPCE), or the external quantum efficiency, of the device was measured using 250W tungsten halogen lamp coupled with a monochromator (Newport Oriel Cornerstone 1/4 m).
- the photocurrent was detected by a UV enhanced silicon detector connected with a Keithley 2000 multimeter.
- the second annealing step at 160°C worsens the device performance, mainly due to unfavorable change of film morphology, which was confirmed in AFM images (data not shown).
- the PCE of 1 -step annealing at 160°C was in between that of 1 -step annealing at 120°C and 2-step annealing, yet the device has the worst FF.
- Table 1 listed the details of the IV characteristics of these three test cells.
- IPCE measurement shows 2-step annealing was worse than 1 step annealing, seen in Figure 9, which was consistent with IV measurements (data not shown).
- IPCE measurement was done under illumination from Tungsten lamp, whereas IV was done under solar simulator which has different spectrum than that of the tungsten lamp. Nevertheless, the integration of IPCE should be proportional to l sc .
- the 1-step annealing at 120°C showed the improved film roughness and the best phase segregation of P3HT and PCBM, which explains why the device performance was the best, seen in Figures 8 and 9.
- Device by 2-step annealing has the smoothest film, however, the phase segregation was much less distinct. This indicates that P3HT chains and PCBM molecules are penetrating through each other more after the second annealing at 160°C, and form much smaller nano-domains, which are favorable for charge transport between the domains (Kline and McGehee, Morphology and Charge Transport in Conjugated Polymers. J of Macromol Sci, Part C: Polymer Reviews, 2006, 46(1): 27-45).
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Nanotechnology (AREA)
- Physics & Mathematics (AREA)
- Mathematical Physics (AREA)
- Theoretical Computer Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Photovoltaic Devices (AREA)
Abstract
La présente invention se rapporte à la fabrication et à la caractérisation d'un générateur solaire organique inversé de grande taille à l'aide d'un procédé de pulvérisation et qui se compose de quatre couches : ITO-Cs2CO3-(P3HT:PCBM)-PEDPT:PSS modifié, sur un substrat. Avec la couche PEDPT:PSS comme anode, le générateur solaire encapsulé présente une transmission supérieure à 30 % dans la plage visible proche de l'infrarouge (IR). L'optimisation par un recuit thermique est réalisée sur la base de générateurs à une seule cellule ou à multiples cellules. L'éclairage solaire a été démontré pour améliorer l'efficacité du générateur solaire jusqu'à 250 % avec une efficacité du dispositif de 1,80 % sous un éclairage énergétique de AM : 1,5. L'amélioration de la performance sous un éclairage se produit seulement avec des dispositifs pulvérisés, indiquant une amélioration du dispositif sous la lumière du soleil, ce qui est bénéfique pour des applications d'énergie solaire. La propriété semi-transparente du module solaire permet des applications sur des fenêtres et des pare-brises, des applications intérieures et des substances de tissu souple telles que des tentes, des sacs à dos militaires ou des tenues de combat, ce qui permet de fournir une alimentation électrique renouvelable aisément transportable pour les forces militaires déployées.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US201161442561P | 2011-02-14 | 2011-02-14 | |
PCT/US2012/025028 WO2012112533A2 (fr) | 2011-02-14 | 2012-02-14 | Générateur photovoltaïque organique et procédé de fabrication |
Publications (1)
Publication Number | Publication Date |
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EP2638577A2 true EP2638577A2 (fr) | 2013-09-18 |
Family
ID=46673118
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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EP12746750.4A Withdrawn EP2638577A2 (fr) | 2011-02-14 | 2012-02-14 | Générateur photovoltaïque organique et procédé de fabrication |
Country Status (5)
Country | Link |
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EP (1) | EP2638577A2 (fr) |
JP (1) | JP2014505378A (fr) |
CN (1) | CN103262281B (fr) |
CA (1) | CA2820090A1 (fr) |
WO (1) | WO2012112533A2 (fr) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2014505371A (ja) | 2011-02-01 | 2014-02-27 | ユニバーシティー オブ サウス フロリダ | 自己組織化単分子膜を使用する部分スプレー式有機太陽電池および製造方法 |
JP6027641B2 (ja) * | 2015-03-10 | 2016-11-16 | 株式会社東芝 | 光電変換素子および太陽電池 |
CN105355795A (zh) * | 2015-12-01 | 2016-02-24 | 电子科技大学 | 基于共轭聚合物-纳米晶叠层式自装配功能薄膜的光电探测器阵列制造方法 |
JP7413833B2 (ja) * | 2020-02-27 | 2024-01-16 | 株式会社リコー | 光電変換素子及び光電変換モジュール |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007527109A (ja) * | 2003-07-07 | 2007-09-20 | ダウ・コ−ニング・コ−ポレ−ション | 太陽電池の封入 |
CN100505367C (zh) * | 2007-01-22 | 2009-06-24 | 铼德科技股份有限公司 | 有机太阳能电池及其制作方法 |
WO2009094663A2 (fr) * | 2008-01-25 | 2009-07-30 | University Of Washington | Dispositifs photovoltaïques comportant des couches de transport d'électrons en oxyde métallique |
US20090229667A1 (en) * | 2008-03-14 | 2009-09-17 | Solarmer Energy, Inc. | Translucent solar cell |
KR20100130514A (ko) * | 2009-06-03 | 2010-12-13 | 삼성전자주식회사 | 유기 태양 전지 및 그 제조방법 |
CA2812559A1 (fr) * | 2010-09-30 | 2012-04-05 | University Of South Florida | Panneau solaire organique transparent par pulverisation a encapsulation |
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2012
- 2012-02-14 JP JP2013553654A patent/JP2014505378A/ja active Pending
- 2012-02-14 EP EP12746750.4A patent/EP2638577A2/fr not_active Withdrawn
- 2012-02-14 CN CN201280004152.8A patent/CN103262281B/zh not_active Expired - Fee Related
- 2012-02-14 WO PCT/US2012/025028 patent/WO2012112533A2/fr active Application Filing
- 2012-02-14 CA CA2820090A patent/CA2820090A1/fr not_active Abandoned
Non-Patent Citations (1)
Title |
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See references of WO2012112533A3 * |
Also Published As
Publication number | Publication date |
---|---|
CA2820090A1 (fr) | 2012-08-23 |
CN103262281A (zh) | 2013-08-21 |
WO2012112533A3 (fr) | 2012-11-22 |
CN103262281B (zh) | 2017-02-08 |
JP2014505378A (ja) | 2014-02-27 |
WO2012112533A2 (fr) | 2012-08-23 |
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