WO2021232682A1 - 一种柔性太阳能电池及其制备方法 - Google Patents

一种柔性太阳能电池及其制备方法 Download PDF

Info

Publication number
WO2021232682A1
WO2021232682A1 PCT/CN2020/124969 CN2020124969W WO2021232682A1 WO 2021232682 A1 WO2021232682 A1 WO 2021232682A1 CN 2020124969 W CN2020124969 W CN 2020124969W WO 2021232682 A1 WO2021232682 A1 WO 2021232682A1
Authority
WO
WIPO (PCT)
Prior art keywords
layer
solar cell
flexible
flexible solar
transport layer
Prior art date
Application number
PCT/CN2020/124969
Other languages
English (en)
French (fr)
Inventor
秦校军
王绍民
赵志国
董超
熊继光
Original Assignee
中国华能集团有限公司
中国华能集团清洁能源技术研究院有限公司
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 中国华能集团有限公司, 中国华能集团清洁能源技术研究院有限公司 filed Critical 中国华能集团有限公司
Priority to DE212020000612.1U priority Critical patent/DE212020000612U1/de
Publication of WO2021232682A1 publication Critical patent/WO2021232682A1/zh

Links

Images

Classifications

    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K77/00—Constructional details of devices covered by this subclass and not covered by groups H10K10/80, H10K30/80, H10K50/80 or H10K59/80
    • H10K77/10—Substrates, e.g. flexible substrates
    • H10K77/111—Flexible substrates
    • 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
    • H10K30/80—Constructional details
    • H10K30/88—Passivation; Containers; Encapsulations
    • 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
    • H10K85/50—Organic perovskites; Hybrid organic-inorganic perovskites [HOIP], e.g. CH3NH3PbI3
    • 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
    • H10K30/50—Photovoltaic [PV] devices
    • 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
    • H10K71/40—Thermal treatment, e.g. annealing in the presence of a solvent vapour
    • 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 invention belongs to the field of design and preparation of thin-film solar cell devices, and relates to a flexible solar cell and a preparation method thereof.
  • a type of thin-film battery represented by perovskite batteries has good flexibility and shapeability due to its core functional layer material thickness is micron level.
  • its components can also be used in military and civilian fields such as outdoor tents.
  • perovskite solar cells with most structures can easily obtain higher photoelectric conversion efficiency, the efficiency of the battery device is A significant drop will occur. Therefore, poor stability is one of the biggest obstacles affecting the practical application of perovskite solar cells.
  • Perovskite-type solar cells have poor stability, and the packaging of their cells is an important issue. The packaging steps should be optimized to obtain better water and oxygen barrier properties and improve cell stability.
  • the purpose of the present invention is to overcome the above shortcomings of the prior art and provide a flexible solar cell and a preparation method thereof.
  • the battery has better water and oxygen barrier properties, higher battery stability, and a simple preparation method.
  • the flexible solar cell of the present invention includes a first encapsulation layer, a first electrode layer, a PET layer, a second encapsulation layer, a second electrode layer, a hole transport layer, a perovskite photoelectric active layer, and electron Transmission layer and flexible PET substrate;
  • the PET layer, the second encapsulation layer, the second electrode layer, the hole transport layer, the perovskite photoelectric active layer, the electron transport layer, the first electrode layer, the flexible PET substrate, and the first encapsulation layer are sequentially distributed from top to bottom .
  • the materials of the first encapsulation layer and the second encapsulation layer are both alumina.
  • the flexible PET substrate and the first electrode layer are both flexible structures.
  • the thickness of the electron transport layer is 15-40 nm.
  • the thickness of the perovskite photoelectric active layer is 400-600nm.
  • the thickness of the hole transport layer is 30-80 nm.
  • the thickness of the second electrode layer is 50-80 nm.
  • the thickness of the first encapsulation layer and the second encapsulation layer are both 20-30 nm.
  • the preparation method of the flexible solar cell of the present invention includes the following steps:
  • the electron transport layer is prepared by atomic deposition, vapor deposition, magnetron sputtering or spin coating;
  • the hole transport layer is prepared by the solution spin coating method
  • the second electrode layer is prepared by spin coating
  • the material of the electron transport layer is tin oxide
  • the material of the perovskite photoelectric active layer is CH 3 NH 3 PbBrI 2 ;
  • the material of the hole transport layer is cuprous thiocyanide, cuprous iodide, Spiro-OMeTAD or PEDOT.
  • the flexible solar cell and the preparation method thereof of the present invention include a PET layer, a second encapsulation layer, a second electrode layer, a hole transport layer, a perovskite photoelectric active layer,
  • the electron transmission layer, the first electrode layer, the flexible PET substrate and the first encapsulation layer, the first encapsulation layer and the second encapsulation layer adopt a sandwich structure to block water and oxygen and other factors that are likely to cause battery aging to further improve the overall device
  • the PET layer is provided on the outside of the second encapsulation layer, which can effectively improve the weather resistance and mechanical strength of the overall battery device, and at the same time improve the operability and ease of use of the battery.
  • the preparation is carried out by conventional methods, and the preparation is relatively simple.
  • Figure 1 is a schematic diagram of the structure of the present invention.
  • 102 is the first encapsulation layer
  • 104 is the flexible PET substrate
  • 106 is the first electrode layer
  • 108 is the electron transport layer
  • 110 is the perovskite photoelectric active layer
  • 112 is the hole transport layer
  • 114 is the second electrode layer
  • 116 is the second encapsulation layer
  • 118 is the PET layer.
  • the flexible solar cell of the present invention includes a first encapsulation layer 102, a first electrode layer 106, a PET layer 118, a second encapsulation layer 116, a second electrode layer 114, a hole transport layer 112, and a perovskite Photoelectric active layer 110, electron transport layer 108 and flexible PET substrate 104; among them, PET layer 118, second encapsulation layer 116, second electrode layer 114, hole transport layer 112, perovskite photoelectric active layer 110, electron transport layer 108.
  • the first electrode layer 106, the flexible PET substrate 104, and the first encapsulation layer 102 are sequentially distributed from top to bottom.
  • the preparation method of the flexible solar cell of the present invention includes the following steps:
  • Flexible PET substrate 104 and second packaging layer 116 are flexible PET substrate 104 and second packaging layer 116:
  • the ITO transparent electrode deposited on a transparent PET resin film is used as the substrate of the device.
  • the area is not limited. Such products are commercially available products that can be used directly.
  • deionized water on the electrode surface Before use, use deionized water on the electrode surface. , Acetone and isopropanol ultrasonic treatment for 15 minutes, and then use a UV cleaner to clean for 10 minutes, and then blow dry by nitrogen flow for use.
  • the flexible PET substrate 104 and the first electrode layer 106 are both flexible structures, which greatly improves the fragility of the traditional semiconductor metal oxide transparent electrode.
  • the electron transport layer 108 formed on the first electrode layer 106 is the electron transport layer 108 formed on the first electrode layer 106:
  • the material of the electron transport layer 108 is tin oxide (SnO 2 ) or titanium oxide (TiO 2 ). Tin oxide can be easily prepared into a flat film with uniform thickness and good electronic conductivity. The fluorescence lifetime test shows that it is more compatible with the energy level of the perovskite photoelectric active layer 110, which can improve the final efficiency of the battery.
  • the electron transport layer 108 made of tin oxide has stable properties, while the electron transport layer 108 made of titanium oxide is easily affected by ultraviolet rays and causes performance degradation. Therefore, tin oxide is preferred as the electron transport layer in the present invention. Material of layer 108.
  • the electron transport layer 108 is prepared by atomic deposition, vapor deposition, magnetron sputtering, or spin coating.
  • the electron transport layer 108 is prepared by a solution spin coating method.
  • a suspension of commercial tin oxide nanoparticles (1-25 nm in diameter) is directly used as the spin coating liquid, and the substrate is used at 3000-5500 rpm, 20
  • the spin coating parameters of -60 s are used to prepare the electron transport layer 108 (15-40 nm) with different thicknesses.
  • the spin coating parameters of 4500 rpm and 50 s are used to obtain the electron transport layer 108 with a thickness of about 30 nm.
  • the hole transport layer 112 is characterized by hole transport materials that match the energy level of the perovskite active material, such as cuprous thiocyanide (CuSCN), cuprous iodide (CuI), Spiro-OMeTAD, PEDOT: PSS, etc.
  • the material, inorganic salt has more stable physical and chemical properties, and its weather resistance under strong ultraviolet light environment is significantly enhanced, and the cost is very low, and the final battery efficiency is not significantly reduced.
  • the cuprous thiocyanate layer can be prepared by a solution spin coating method.
  • the cuprous thiocyanate is prepared into a slurry with a mass fraction of 3-8%, preferably 4%, and the solvent is two Ethyl sulfide;
  • the hole transport layer 112 is prepared on the substrate at 3500-5000rpm, 30-60s spin-coating parameters, with a thickness of 30-80nm; in particular, using 4000rpm, 40s spin-coating parameters to obtain a thickness of about
  • the hole transport layer 112 is about 50 nm.
  • the material of the second electrode layer 114 is a commercial silver nanowire sol, the solvent is isopropanol, the concentration is 50-100 g/L, the diameter of the silver nanowire is about 100-200 nm, and the length is 50-100 ⁇ m.
  • the blade coating speed is 5-20mm/s, preferably 15mm/s; the coating temperature is room temperature; the distance between the blade and the substrate is 50 ⁇ m; after coating, it is annealed at 90-100°C in nitrogen for 10-20 minutes, preferably 90°C Anneal for 15 minutes, the thickness is about 50-80nm.
  • Adopting a "sandwich structure" the flexible PET substrate 104, the second electrode layer 114, the hole transport layer 112, the perovskite photoelectric active layer 110, the electron transport layer 108 and the first encapsulation layer 102 and the second encapsulation layer 116 are used to cover
  • the first electrode layer 106 has an encapsulation effect and blocks water and oxygen for the entire device, which are likely to cause battery aging, and further improves the stability of the entire device.
  • the material used for the encapsulation layer is aluminum oxide (Al 2 O 3 ), and the preparation method is atomic layer deposition.
  • the two reaction gases are nitrogen (N 2 , purity ⁇ 99.999%) containing trimethylaluminum (Al(CH 3 ) 3 ), and water (H 2 O); the two are charged alternately in the form of pulses
  • the pulse time is preferably 0.02s
  • the residence time is 60s
  • one cycle is alternately. It can be considered to use 50-500 cycles to prepare aluminum oxide layers of different thicknesses, preferably 200 times, and the aluminum oxide layer is 20- Around 30nm.
  • the first encapsulation layer 102 and the second encapsulation layer 116 can be combined with conventional encapsulating materials such as EVA, UV encapsulating glue, and silicone for further encapsulation. Compared with conventional encapsulation methods, the encapsulation effect will be significantly improved, so they are very suitable for general stability.
  • the field of perovskite-type solar cells are nitrogen (N 2 , purity ⁇ 99.999%) containing trimethylaluminum (Al(CH 3 ) 3 ), and water (
  • a PET layer 118 is prepared outside the second encapsulation layer 116:
  • Glue bonding and other methods can be used to cover another layer of PET polymer film with higher water and oxygen barrier capacity on the outer layer of alumina, further improving the weather resistance and mechanical strength of the overall battery device, and at the same time improving the battery’s performance.
  • the operability and ease of use facilitate the subsequent productization work.
  • This type of material layer has mature commercial products, which can be selected and replaced according to the use of the product, or not.

Landscapes

  • Physics & Mathematics (AREA)
  • Electromagnetism (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Photovoltaic Devices (AREA)

Abstract

本发明公开了一种柔性太阳能电池及其制备方法，包括第一封装层、第一电极层、PET层、第二封装层、第二电极层、空穴传输层、钙钛矿光电活性层、电子传输层及柔性PET基底；其中，PET层、第二封装层、第二电极层、空穴传输层、钙钛矿光电活性层、电子传输层、第一电极层、柔性PET基底及第一封装层自上到下依次分布，该电池具有较好的水氧阻隔性，电池的稳定性较高，同时制备方法较为简单。

Description

一种柔性太阳能电池及其制备方法 技术领域
本发明属于薄膜太阳能电池器件的设计和制备领域，涉及一种柔性太阳能电池及其制备方法。
背景技术
随着化石能源的日益枯竭和其使用所带来的高昂的环境成本，可再生清洁能源的开发和利用受到广泛的关注。太阳能光伏发电技术和产品在全球范围内得到了高速增长，成为最具潜力的清洁能源。近年来发现的钙钛矿型太阳能电池由于高转换效率、低成本、环境友善、可挠式产品化等优点备受关注。目前主流的晶硅电池由于其硅片本身易碎、易折断的特性，使用时只能将其封装在玻璃基底的电池组件中进行使用，难以弯折或轻量化，这就限制其只能够被用在集中及分布式电站之中。而钙钛矿电池为代表的一类薄膜电池，由于其核心功能层材料厚度为微米级别，因而具有良好的柔性可塑形性质，除了电站以外，其组件还可以在军用、民用领域物品如户外帐篷、衣服、背包等场景使用，以及一些具有不规则或曲面表面的建筑物外立面使用，极大程度上拓展了光伏产品的应用场景。
同时，在目前的研发过程中，人们发现大部分结构的钙钛矿型太阳能电池虽然能够较为容易的获得较高的光电转换效率，但是，在测试和保存较长一段时间之后，电池器件的效能会发生明显的下降。因此稳定性差是影响钙钛矿型太阳能电池走向实际化应用的最大阻碍之一。钙钛 矿型太阳能电池稳定性不佳，其电池的封装是一个重要问题，应优化封装步骤以获得更好的水、氧阻隔性，提高电池稳定性。
发明内容
本发明的目的在于克服上述现有技术的缺点，提供了一种柔性太阳能电池及其制备方法，该电池具有较好的水氧阻隔性，电池的稳定性较高，同时制备方法较为简单。
为达到上述目的，本发明所述的柔性太阳能电池包括第一封装层、第一电极层、PET层、第二封装层、第二电极层、空穴传输层、钙钛矿光电活性层、电子传输层及柔性PET基底；
其中，PET层、第二封装层、第二电极层、空穴传输层、钙钛矿光电活性层、电子传输层、第一电极层、柔性PET基底及第一封装层自上到下依次分布。
第一封装层及第二封装层的材质均为氧化铝。
柔性PET基底及第一电极层均为柔性结构。
电子传输层的厚度为15-40nm。
钙钛矿光电活性层的厚度为400-600nm。
空穴传输层的厚度为30-80nm。
第二电极层的厚度为50-80nm。
第一封装层及第二封装层的厚度均为20-30nm。
本发明所述柔性太阳能电池的制备方法包括以下步骤：
1)选取柔性PET基底，再在柔性PET基底上制备第一电极层；
2)采用原子沉积、气相沉积、磁控溅射或旋涂的方法制备电子传输 层；
3)采用旋涂的方法制备钙钛矿光电活性层；
4)采用溶液旋涂法制备空穴传输层；
5)采用旋涂的方法制备第二电极层；
6)采用原子层沉积法制备第一封装层及第二封装层；
7)采用胶水粘合的方式固定PET层，得柔性太阳能电池。
电子传输层的材质为氧化锡；
钙钛矿光电活性层的材质为CH 3NH 3PbBrI 2；
空穴传输层的材质为硫氰化亚铜、碘化亚铜、Spiro-OMeTAD或PEDOT。
本发明具有以下有益效果：
本发明所述的柔性太阳能电池及其制备方法在具体操作时，包括自上到下依次分布的PET层、第二封装层、第二电极层、空穴传输层、钙钛矿光电活性层、电子传输层、第一电极层、柔性PET基底及第一封装层，第一封装层及第二封装层采用夹心结构，为整个器件阻隔水及氧等易于引起电池老化的因素，进一步提高整体器件的稳定性，另外，第二封装层的外侧设置有PET层，可以有效的提升整体电池器件的耐候性和机械强度，并同时提升电池的可操作性和易用性，另外，在制备过程中，采用常规的方法进行制备，制备较为简单。
附图说明
图1为本发明的结构示意图。
其中，102为第一封装层、104为柔性PET基底、106为第一电极 层、108为电子传输层、110为钙钛矿光电活性层、112为空穴传输层、114为第二电极层、116为第二封装层、118为PET层。
具体实施方式
下面结合附图对本发明做进一步详细描述：
参考图1，本发明所述的柔性太阳能电池包括第一封装层102、第一电极层106、PET层118、第二封装层116、第二电极层114、空穴传输层112、钙钛矿光电活性层110、电子传输层108及柔性PET基底104；其中，PET层118、第二封装层116、第二电极层114、空穴传输层112、钙钛矿光电活性层110、电子传输层108、第一电极层106、柔性PET基底104及第一封装层102自上到下依次分布。
本发明所述柔性太阳能电池的制备方法包括以下步骤：
柔性PET基底104及第二封装层116：
采用沉积在透明的PET树脂薄膜上的ITO透明电极为器件的基底，面积不限，此类产品有规模化量产的商品化产品可以直接使用，使用前，将电极表面依次分别使用去离子水、丙酮及异丙醇超声处理15min，然后使用紫外光清洗机清洁10min，再通过氮气流吹干备用。
柔性PET基底104及第一电极层106均为柔性结构，大大改善了传统半导体金属氧化物透明电极的易碎性。
在第一电极层106上形成的电子传输层108：
电子传输层108的材质为氧化锡(SnO 2)或氧化钛(TiO 2)等材料。氧化锡可以较为容易的制备成为平面薄膜，厚度均一且电子传导性好，荧光寿命测试表明其与钙钛矿光电活性层110能级更为匹配，可以提高 电池的最终效率。此外，相对于常用的氧化钛，氧化锡材质的电子传输层108的性质稳定，而氧化钛材质的电子传输层108容易受到紫外线的影响而导致性能下降，因此本发明中优选氧化锡作为电子传输层108的材料。电子传输层108采用原子沉积、气相沉积、磁控溅射或旋涂的方法进行制备。优选的，采用溶液旋涂方法制备电子传输层108，在具体操作时，将商品化的氧化锡纳米粒子(直径1-25nm)悬浮液直接作为旋涂液，在基底上以3000-5500rpm，20-60s的旋涂参数进行不同厚度电子传输层108(15-40nm)的制备，特别的，优选的，采用4500rpm，50s的旋涂参数获得厚度约为30nm的电子传输层108。
在电子传输层108上制备的钙钛矿光电活性层110：
钙钛矿光电活性层110的结构为(RNH 3)AX mY nZ 3-m-n，R＝烃基；A＝Pb，Sn等；X，Y，Z＝Cl，Br，I；m，n为0-3的实数且m+n≤3，优选的为CH 3NH 3PbBrI 2，溶剂为DMF:DMSO＝95:5的混合溶剂，配成质量分数为20-40％的浆料，优选的为25％的浆料；刮刀涂布速度为5-20mm/s，优选为10mm/s；涂布温度为室温；刮刀与基底之间的间距为50μm；涂布后在氮气中110-140℃退火20-40min，优选的为氮气中130℃退火30min，得到厚度约为400-600nm的钙钛矿光电活性层110。
在钙钛矿光电活性层110上形成的空穴传输层112：
空穴传输层112的特点为与钙钛矿活性材料能级相匹配的空穴传输材料，如硫氰化亚铜(CuSCN)、碘化亚铜(CuI)、Spiro-OMeTAD、PEDOT：PSS等材料，无机盐的物理、化学性质更加稳定，在强紫外光环境下的耐候性明显增强，且成本很低，同时最终电池效率并无显著降低。本发 明中，硫氰化亚铜层可采用溶液旋涂法进行制备，具体的，将硫氰化亚铜配成质量分数为3-8％的浆料，优选的为4％，溶剂为二乙基硫；在基底上以3500-5000rpm，30-60s的旋涂参数进行该空穴传输层112的制备，厚度为30-80nm；特别的，采用4000rpm，40s的旋涂参数获得厚度约为50nm左右的空穴传输层112。
在空穴传输层112上形成的第二电极层114：
第二电极层114的材料为商品化银纳米线溶胶，溶剂为异丙醇，浓度为50-100g/L，银纳米线的直径约为100-200nm，长度为50-100μm。刮刀涂布速度为5-20mm/s，优选为15mm/s；涂布温度为室温；刮刀与基底间距为50μm；涂布后经氮气中90-100℃退火10-20分钟，优选为90℃退火15分钟，厚度约为50-80nm。
第一封装层102及第二封装层116的制备：
采用“夹心结构”，利用第一封装层102及第二封装层116包覆柔性PET基底104、第二电极层114、空穴传输层112、钙钛矿光电活性层110、电子传输层108及第一电极层106，起到封装效果，为整个器件阻隔水及氧等易于引起电池老化的因素，进一步提高整体器件的稳定性。本发明中，封装层使用材料为氧化铝(Al 2O 3)，制备方法为原子层沉积法。具体为：两种反应气体分别为氮气(N 2，纯度≥99.999％)载三甲基铝(Al(CH 3) 3)，和水(H 2O)；两者交替以脉冲的形式充入反应室，脉冲时间优选为0.02s，停留时间为60s，交替一次为一个循环，可考虑使用50-500次循环制备不同厚度的氧化铝层，优选为200次，制得氧化铝层为20-30nm左右。此外，第一封装层102及第二封装层116可结合EVA、 紫外封装胶、有机硅胶等常规封装材料进行进一步封装，相对于常规封装方法将显著提高封装效果，因此非常适合于稳定性较为一般的钙钛矿型太阳能电池领域。
第二封装层116外侧制备PET层118：
可采用胶水粘合等方式将另一层具有较高水、氧组隔能力的PET高分子薄膜覆盖于氧化铝外层，进一步提升整体电池器件的耐候性和机械强度，并同时提升电池的可操作性和易用性，便于进行后续的产品化工作，此类材料层有成熟的商业化产品，可以依照产品用途进行选择替换，也可以不用。

Claims (10)

  1. 一种柔性太阳能电池，其特征在于，包括第一封装层(102)、第一电极层(106)、PET层(118)、第二封装层(116)、第二电极层(114)、空穴传输层(112)、钙钛矿光电活性层(110)、电子传输层(108)及柔性PET基底(104)；
    其中，PET层(118)、第二封装层(116)、第二电极层(114)、空穴传输层(112)、钙钛矿光电活性层(110)、电子传输层(108)、第一电极层(106)、柔性PET基底(104)及第一封装层(102)自上到下依次分布。
  2. 根据权利要求1所述的柔性太阳能电池，其特征在于，第一封装层(102)及第二封装层(116)的材质均为氧化铝。
  3. 根据权利要求1所述的柔性太阳能电池，其特征在于，柔性PET基底(104)及第一电极层(106)均为柔性结构。
  4. 根据权利要求1所述的柔性太阳能电池，其特征在于，电子传输层(108)的厚度为15-40nm。
  5. 根据权利要求1所述的柔性太阳能电池，其特征在于，钙钛矿光电活性层(110)的厚度为400-600nm。
  6. 根据权利要求1所述的柔性太阳能电池，其特征在于，空穴传输层(112)的厚度为30-80nm。
  7. 根据权利要求1所述的柔性太阳能电池，其特征在于，第二电极层(114)的厚度为50-80nm。
  8. 根据权利要求1所述的柔性太阳能电池，其特征在于，第一封装层(102)及第二封装层(116)的厚度均为20-30nm。
  9. 一种权利要求1所述柔性太阳能电池的制备方法，其特征在于，包括以下步骤：
    1)选取柔性PET基底(104)，再在柔性PET基底(104)上制备第一电极层(106)；
    2)采用原子沉积、气相沉积、磁控溅射或旋涂的方法制备电子传输层(108)；
    3)采用旋涂的方法制备钙钛矿光电活性层(110)；
    4)采用溶液旋涂法制备空穴传输层(112)；
    5)采用旋涂的方法制备第二电极层(114)；
    6)采用原子层沉积法制备第一封装层(102)及第二封装层(116)；
    7)采用胶水粘合的方式固定PET层(118)，得柔性太阳能电池。
  10. 根据权利要求9所述的柔性太阳能电池的制备方法，其特征在于，
    电子传输层(108)的材质为氧化锡；
    钙钛矿光电活性层(110)的材质为CH 3NH 3PbBrI 2；
    空穴传输层(112)的材质为硫氰化亚铜、碘化亚铜、Spiro-OMeTAD或PEDOT。
PCT/CN2020/124969 2020-05-18 2020-10-29 一种柔性太阳能电池及其制备方法 WO2021232682A1 (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DE212020000612.1U DE212020000612U1 (de) 2020-05-18 2020-10-29 Flexible Solarzelle

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN202010421625.0A CN111477751A (zh) 2020-05-18 2020-05-18 一种柔性太阳能电池及其制备方法
CN202010421625.0 2020-05-18

Publications (1)

Publication Number Publication Date
WO2021232682A1 true WO2021232682A1 (zh) 2021-11-25

Family

ID=71762428

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2020/124969 WO2021232682A1 (zh) 2020-05-18 2020-10-29 一种柔性太阳能电池及其制备方法

Country Status (3)

Country Link
CN (1) CN111477751A (zh)
DE (1) DE212020000612U1 (zh)
WO (1) WO2021232682A1 (zh)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111477751A (zh) * 2020-05-18 2020-07-31 中国华能集团有限公司 一种柔性太阳能电池及其制备方法
CN112599674A (zh) * 2020-12-14 2021-04-02 华能新能源股份有限公司 一种柔性钙钛矿太阳能电池及其制备方法
CN113013334A (zh) * 2021-02-05 2021-06-22 中山大学 一种光电转换器件及其制备方法、装置和系统

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110246968A (zh) * 2019-06-17 2019-09-17 中国华能集团有限公司 一种两面受光的钙钛矿太阳能电池
CN110637376A (zh) * 2017-04-14 2019-12-31 熙太阳能有限责任公司 光伏器件封装
CN111477751A (zh) * 2020-05-18 2020-07-31 中国华能集团有限公司 一种柔性太阳能电池及其制备方法
CN211743192U (zh) * 2020-05-18 2020-10-23 中国华能集团有限公司 一种柔性太阳能电池

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109216556A (zh) * 2018-08-31 2019-01-15 武汉理工大学 一种特定结构的钙钛矿太阳能电池及其制备方法
CN109273611A (zh) * 2018-11-28 2019-01-25 中国华能集团有限公司 一种钙钛矿太阳能电池结构及其制备方法
CN110350092B (zh) * 2019-07-19 2023-03-24 陕西师范大学 一种具有双电子传输层和双空穴传输层的钙钛矿太阳电池及其制备方法
CN110838547A (zh) * 2019-11-08 2020-02-25 福仕保(江苏)新材料有限公司 有机电子器件真空溅射混合光固化树脂封装工艺

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110637376A (zh) * 2017-04-14 2019-12-31 熙太阳能有限责任公司 光伏器件封装
CN110246968A (zh) * 2019-06-17 2019-09-17 中国华能集团有限公司 一种两面受光的钙钛矿太阳能电池
CN111477751A (zh) * 2020-05-18 2020-07-31 中国华能集团有限公司 一种柔性太阳能电池及其制备方法
CN211743192U (zh) * 2020-05-18 2020-10-23 中国华能集团有限公司 一种柔性太阳能电池

Also Published As

Publication number Publication date
DE212020000612U1 (de) 2021-12-20
CN111477751A (zh) 2020-07-31

Similar Documents

Publication Publication Date Title
WO2021232682A1 (zh) 一种柔性太阳能电池及其制备方法
CN104091888B (zh) 一种钙钛矿型太阳能电池及其制备方法
CN103700768A (zh) 一种钙钛矿结构太阳能电池及其制备方法
CN107565024B (zh) 一种阶梯式吸收层结构的钙钛矿太阳能电池及其制备方法
CN106025085A (zh) 基于Spiro-OMeTAD/CuXS复合空穴传输层的钙钛矿太阳能电池及其制备方法
CN107331775B (zh) 一种高质量电子传输层的钙钛矿太阳电池及其制备方法
CN111864079B (zh) 一种双电子传输层柔性钙钛矿太阳能电池及其制备方法
CN109103280B (zh) 全无机钙钛矿铁电纤维复合结构的太阳能电池及制备方法
CN116546867A (zh) 柔性钙钛矿太阳能电池的制备方法
CN109817810A (zh) 一种掺杂三唑离子液体的钙钛矿太阳能电池及制备方法
CN104167492A (zh) 一种钙钛矿电池、及其制备方法
CN111029470B (zh) 基于纳米草状介孔层的钙钛矿太阳能电池及其制备方法
CN107369768A (zh) 一种基于新有机铅源的钙钛矿太阳能电池的制备方法
CN110767777B (zh) 可降低成本提高转换效率的叠层太阳电池的制备方法
CN109638161A (zh) 一种高效钙钛矿太阳能电池的制备方法及钙钛矿太阳能电池
CN109166972A (zh) 一种双缓冲层钙钛矿太阳能电池制造方法
CN211743192U (zh) 一种柔性太阳能电池
CN102751096B (zh) 一种双面透光染料敏化太阳能电池光阳极
CN104916714B (zh) 以La‑TiO2为电子传输层的有机光伏电池及其制备方法
CN116634823A (zh) 一种制备钝化层的方法及晶硅/钙钛矿叠层太阳能电池
CN102683032B (zh) 叶片状二氧化钛纳米阵列薄膜电极制备及其在染料敏化太阳电池中的应用
CN109830604A (zh) 一种以聚氧化乙烯薄膜钝化电子传输层与光敏层间界面的钙钛矿光伏电池及其制备方法
CN109326718A (zh) 一种双缓冲层钙钛矿太阳能电池制造方法
CN112614942B (zh) 一种peg修饰的碳电极、其制备方法及利用其制得的钙钛矿电池
CN108281551A (zh) 基于光子晶体异质结的反式三维钙钛矿太阳能电池及其制备方法

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 20936544

Country of ref document: EP

Kind code of ref document: A1

122 Ep: pct application non-entry in european phase

Ref document number: 20936544

Country of ref document: EP

Kind code of ref document: A1