WO2025079168A1 - バリア膜およびそれを具備する太陽電池 - Google Patents

バリア膜およびそれを具備する太陽電池 Download PDF

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Publication number
WO2025079168A1
WO2025079168A1 PCT/JP2023/036862 JP2023036862W WO2025079168A1 WO 2025079168 A1 WO2025079168 A1 WO 2025079168A1 JP 2023036862 W JP2023036862 W JP 2023036862W WO 2025079168 A1 WO2025079168 A1 WO 2025079168A1
Authority
WO
WIPO (PCT)
Prior art keywords
layer
barrier film
barrier
sealing layer
film according
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.)
Pending
Application number
PCT/JP2023/036862
Other languages
English (en)
French (fr)
Japanese (ja)
Inventor
直美 信田
勝之 内藤
智博 戸張
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toshiba Corp
Toshiba Energy Systems and Solutions Corp
Original Assignee
Toshiba Corp
Toshiba Energy Systems and Solutions Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Toshiba Corp, Toshiba Energy Systems and Solutions Corp filed Critical Toshiba Corp
Priority to CN202380091551.0A priority Critical patent/CN120660467A/zh
Priority to JP2025551256A priority patent/JPWO2025079168A1/ja
Priority to EP23955419.9A priority patent/EP4633332A1/en
Priority to PCT/JP2023/036862 priority patent/WO2025079168A1/ja
Publication of WO2025079168A1 publication Critical patent/WO2025079168A1/ja
Priority to US19/266,583 priority patent/US20250344552A1/en
Anticipated expiration legal-status Critical
Pending legal-status Critical Current

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Classifications

    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K30/00Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
    • H10K30/80Constructional details
    • H10K30/88Passivation; Containers; Encapsulations
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10FINORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F77/00Constructional details of devices covered by this subclass
    • H10F77/50Encapsulations or containers
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10FINORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F77/00Constructional details of devices covered by this subclass
    • H10F77/20Electrodes
    • H10F77/244Electrodes made of transparent conductive layers, e.g. transparent conductive oxide [TCO] layers
    • H10F77/247Electrodes made of transparent conductive layers, e.g. transparent conductive oxide [TCO] layers comprising indium tin oxide [ITO]
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K30/00Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
    • H10K30/40Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation comprising a p-i-n structure, e.g. having a perovskite absorber between p-type and n-type charge transport layers
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K30/00Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
    • H10K30/50Photovoltaic [PV] devices

Definitions

  • the first embodiment relates to a barrier film that has high gas barrier properties and high resistance to moisture, and therefore also has excellent weather resistance and durability.
  • the configuration of the barrier film of this embodiment will be described below.
  • the barrier film according to the embodiment may be provided with one or more additional barrier layers on the opposite side of the contact surface a of the inorganic barrier layer, and may be provided with one or more additional sealing layers on the opposite side of the contact surface a of the sealing layer.
  • an additional barrier layer 103 and an additional sealing layer 104 are shown as examples, but these may be omitted, and two or more additional barrier layers or additional sealing layers may be laminated.
  • the inorganic barrier layer may be disposed on a substrate (not shown).
  • the substrate may be glass or a resin such as polyethylene terephthalate (PET) or polyethylene naphthalate (PEN).
  • PET polyethylene terephthalate
  • PEN polyethylene naphthalate
  • a substrate containing a resin containing a halogen element is preferable, and the substrate may be composed of only a resin having a halogen element.
  • the resin constituting the substrate it is more preferable to use a resin having flame retardancy with an oxygen index of 22% or more, for example, polyvinyl chloride (PVC), polyvinylidene chloride (PVDC), silicone resin, polyvinylidene fluoride (PVDF), polyimide (PI), and polycarbonate (PC).
  • PVC polyvinyl chloride
  • PVDC polyvinylidene chloride
  • silicone resin silicone resin
  • PVDF polyvinylidene fluoride
  • PI polyimide
  • PC polycarbonate
  • the substrate may be a composite material combining multiple members.
  • graphene has a skeleton in which carbon atoms are bonded in a planar shape, and is preferably chemically modified.
  • One of the preferred graphenes has a structure in which polyalkyleneimine, particularly polyethyleneimine chains, are bonded as shown in the following formula:
  • graphene When graphene has such a structure, its water dispersibility is improved, so when a film is formed by coating, coating becomes easier and the zeta potential can be made positive.
  • silicon oxide or silicon nitride When silicon oxide or silicon nitride is used for the inorganic barrier film, their zeta potential is negative, so the adhesion between the inorganic barrier layer and the sealing layer is improved, and therefore graphene having a structure in which polyethyleneimine chains are bonded is preferable.
  • Such maxine having a hydroxyl group is preferred because the layered structure of the maxine particles is easily maintained by interlayer hydrogen bonds.
  • a nitrogen-containing compound is present on the surface of the maxine particle, it is preferred because it can make the zeta potential of maxine positive and make it easier to adsorb ions.
  • one or more additional sealing layers may be laminated on the opposite side of the contact surface a of the sealing layer.
  • the material for the additional sealing layer can be selected from the materials listed as the sealing layer materials.
  • the sealing layer is formed from a two-dimensional material that swells with water vapor, the two-dimensional material swells when it comes into contact with water vapor, narrowing the gaps between particles and making it easier to reduce the water vapor permeability. Therefore, it is preferable that the sealing layer is formed from a two-dimensional material that swells with water vapor.
  • the sheet resistance of the sealing layer is preferably 10 4 to 10 12 ⁇ , and more preferably 10 4 to 10 8 ⁇ .
  • Two-dimensional materials have excellent gas shielding properties in areas without defects, making them suitable as materials for forming sealing layers. Furthermore, they are particles with a high aspect ratio, specifically widths on the order of ⁇ m and thicknesses on the order of nm, and by applying a dispersion of these particles, it is easy to form a large-area, flexible sealing layer.
  • a strong barrier film can be formed by layering a layer (barrier layer) of aluminum oxide or titanium oxide with a positive zeta potential on silicon oxide (additional barrier layer) with a negative zeta potential, layering a layer (sealing layer) of maxine with a negative zeta potential on top of that, and then layering a layer (additional sealing layer) of graphene bonded to polyethyleneimine chains with a positive zeta potential on top of that.
  • the zeta potential of the surface of a flat sample can be measured by electrophoretic light scattering (ELS) using a Zetasizer Nano ZS (Malvern Instruments). Specifically, it is measured using a flat zeta potential measurement cell and polystyrene latex as tracer particles.
  • the pH when measuring the zeta potential can be adjusted by adding dilute hydrochloric acid and dilute potassium hydroxide aqueous solution to pure water.
  • the zeta potential of a powdered sample can be measured by electrophoretic light scattering (ELS) using a Zetasizer Nano ZS (Malvern Instruments).
  • ELS electrophoretic light scattering
  • the cell used is a capillary cell.
  • the zeta potentials of the inorganic barrier layer, the additional barrier layer, the sealing layer, and the additional sealing layer at their respective contact interfaces can be evaluated using flat plate samples if they can be peeled off at the interfaces, or can be evaluated using flat plate or powder samples containing each material separately.
  • DMF N,N-dimethylformamide
  • DMSO dimethyl sulfoxide
  • 2-propanol 2-propanol
  • ⁇ -butyrolactone can also be used.
  • solvents can be used alone or in combination. There are no particular restrictions on the solvent as long as it can dissolve the material and does not damage the material.
  • the second electrode 205 preferably contains a transparent conductive material.
  • the second electrode 205 of this embodiment may be made of the same material as the first electrode 203.
  • the second electrode 205 may be formed by a vacuum deposition method, a sputtering method, an ion plating method, a plating method, a coating method, or the like, similarly to the first electrode 203.
  • a protective film or the like may be provided between the solar cell power generating section 201 and the barrier film 100, or the solar cell power generating section 201 and the barrier film 100 may be in direct contact with each other.
  • Example 1 A barrier film 300 having the structure shown in FIG. 3 is formed.
  • a polycarbonate (PC) film having a thickness of 100 ⁇ m is prepared as a substrate 301, and a barrier layer 302 made of a silicon oxide film having a thickness of 100 nm is formed by sputtering three times on the surface of this substrate 301.
  • the zeta potential of the silicon oxide film 302 in water of pH 6 is negative.
  • the resulting barrier film 300 has an excellent barrier property with a WVTR of 4 ⁇ 10 ⁇ 3 g/m 2 /day, and even when a bending test is performed 100 times using a glass rod with a diameter of 5 mm, the WVTR increases by only 10%.
  • maxine titanium carbide
  • the resulting barrier film 400 has an excellent barrier property with a WVTR of 5 ⁇ 10 ⁇ 3 g/m 2 /day, and even when a bending test is performed 100 times using a glass rod with a diameter of 5 mm, the WVTR increases by only 8%.
  • Example 4 A barrier film 600 having the structure shown in FIG. 6 is prepared. First, a 100 ⁇ m thick polyethylene phthalate (PET) film is prepared as the substrate 601, and a 150 nm thick crystalline ITO film 602 is formed on the back surface. A 100 nm thick silicon oxide film 603 is formed on the surface of this substrate 601 by three sputtering processes. A 50 nm thick titanium oxide film 604 is formed on top of this by two sputtering processes to form a barrier layer 605. The zeta potential of titanium oxide 603 in water with a pH of 6 is positive. The titanium oxide film also serves as an ultraviolet absorbing layer.
  • PET polyethylene phthalate
  • Example 6 A solar cell 700 shown in FIG. 7 is produced.
  • a transparent electrode (second electrode) 72 of indium tin oxide (ITO) (200 nm) is formed by sputtering on a PC film (substrate 701) with a hard coat layer having a thickness of 100 ⁇ m.
  • a toluene solution of C 60 -PCBM is applied to this transparent electrode 702 with a bar coater and dried to form an electron injection layer 703.

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  • Physics & Mathematics (AREA)
  • Electromagnetism (AREA)
  • Laminated Bodies (AREA)
  • Photovoltaic Devices (AREA)
PCT/JP2023/036862 2023-10-11 2023-10-11 バリア膜およびそれを具備する太陽電池 Pending WO2025079168A1 (ja)

Priority Applications (5)

Application Number Priority Date Filing Date Title
CN202380091551.0A CN120660467A (zh) 2023-10-11 2023-10-11 阻隔膜及具备该阻隔膜的太阳能电池
JP2025551256A JPWO2025079168A1 (https=) 2023-10-11 2023-10-11
EP23955419.9A EP4633332A1 (en) 2023-10-11 2023-10-11 Barrier film and solar cell equipped with same
PCT/JP2023/036862 WO2025079168A1 (ja) 2023-10-11 2023-10-11 バリア膜およびそれを具備する太陽電池
US19/266,583 US20250344552A1 (en) 2023-10-11 2025-07-11 Barrier film and solar cell including same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2023/036862 WO2025079168A1 (ja) 2023-10-11 2023-10-11 バリア膜およびそれを具備する太陽電池

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US19/266,583 Continuation US20250344552A1 (en) 2023-10-11 2025-07-11 Barrier film and solar cell including same

Publications (1)

Publication Number Publication Date
WO2025079168A1 true WO2025079168A1 (ja) 2025-04-17

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PCT/JP2023/036862 Pending WO2025079168A1 (ja) 2023-10-11 2023-10-11 バリア膜およびそれを具備する太陽電池

Country Status (5)

Country Link
US (1) US20250344552A1 (https=)
EP (1) EP4633332A1 (https=)
JP (1) JPWO2025079168A1 (https=)
CN (1) CN120660467A (https=)
WO (1) WO2025079168A1 (https=)

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20130106121A (ko) * 2012-03-19 2013-09-27 한국과학기술연구원 다층 나노 구조의 고투광율 광촉매 박막과 그 제조방법
US20160087573A1 (en) * 2014-09-19 2016-03-24 Institute Of Nuclear Energy Research, Atomic Energy Council, Exec. Yuan, R.O.C. Multi-function floating solar power generating system
CN106290253A (zh) * 2016-11-02 2017-01-04 中国计量大学 一种测量空气中相对湿度的光纤型传感器
JP2019103990A (ja) * 2017-12-14 2019-06-27 株式会社東芝 光触媒付基材およびその製造方法及び光触媒装置
JP2019165144A (ja) 2018-03-20 2019-09-26 積水化学工業株式会社 太陽電池
CN110548530A (zh) * 2019-08-27 2019-12-10 生态环境部南京环境科学研究所 一种改性氧化石墨烯紫外光催化膜及其制备方法
CN210379071U (zh) * 2019-07-03 2020-04-21 福建金石能源有限公司 一种有效防水防藻类的海上柔性太阳能电池组件
US20230076330A1 (en) * 2021-07-27 2023-03-09 Jilin University Near-infrared photothermal catalyst and preparation method and use thereof
CN116284934A (zh) * 2022-12-12 2023-06-23 山东大学 一种氧化石墨烯辅助多重交联MXene复合薄膜及其应用
CN116850795A (zh) * 2022-03-28 2023-10-10 中国华能集团清洁能源技术研究院有限公司 一种纳滤复合膜及其制备方法

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20130106121A (ko) * 2012-03-19 2013-09-27 한국과학기술연구원 다층 나노 구조의 고투광율 광촉매 박막과 그 제조방법
US20160087573A1 (en) * 2014-09-19 2016-03-24 Institute Of Nuclear Energy Research, Atomic Energy Council, Exec. Yuan, R.O.C. Multi-function floating solar power generating system
CN106290253A (zh) * 2016-11-02 2017-01-04 中国计量大学 一种测量空气中相对湿度的光纤型传感器
JP2019103990A (ja) * 2017-12-14 2019-06-27 株式会社東芝 光触媒付基材およびその製造方法及び光触媒装置
JP2019165144A (ja) 2018-03-20 2019-09-26 積水化学工業株式会社 太陽電池
CN210379071U (zh) * 2019-07-03 2020-04-21 福建金石能源有限公司 一种有效防水防藻类的海上柔性太阳能电池组件
CN110548530A (zh) * 2019-08-27 2019-12-10 生态环境部南京环境科学研究所 一种改性氧化石墨烯紫外光催化膜及其制备方法
US20230076330A1 (en) * 2021-07-27 2023-03-09 Jilin University Near-infrared photothermal catalyst and preparation method and use thereof
CN116850795A (zh) * 2022-03-28 2023-10-10 中国华能集团清洁能源技术研究院有限公司 一种纳滤复合膜及其制备方法
CN116284934A (zh) * 2022-12-12 2023-06-23 山东大学 一种氧化石墨烯辅助多重交联MXene复合薄膜及其应用

Non-Patent Citations (1)

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Title
See also references of EP4633332A1

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Publication number Publication date
US20250344552A1 (en) 2025-11-06
CN120660467A (zh) 2025-09-16
JPWO2025079168A1 (https=) 2025-04-17
EP4633332A1 (en) 2025-10-15

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