CN108276560B - 基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物及在单组分有机太阳电池的应用 - Google Patents

基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物及在单组分有机太阳电池的应用 Download PDF

Info

Publication number
CN108276560B
CN108276560B CN201810038793.4A CN201810038793A CN108276560B CN 108276560 B CN108276560 B CN 108276560B CN 201810038793 A CN201810038793 A CN 201810038793A CN 108276560 B CN108276560 B CN 108276560B
Authority
CN
China
Prior art keywords
indacene
main chain
acid imide
organic photovoltaic
containing benzotriazole
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.)
Active
Application number
CN201810038793.4A
Other languages
English (en)
Other versions
CN108276560A (zh
Inventor
黄飞
胡志诚
应磊
曹镛
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.)
Dongguan volt ampere Photoelectric Technology Co., Ltd
Original Assignee
South China Institute of Collaborative Innovation
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 South China Institute of Collaborative Innovation filed Critical South China Institute of Collaborative Innovation
Priority to CN201810038793.4A priority Critical patent/CN108276560B/zh
Publication of CN108276560A publication Critical patent/CN108276560A/zh
Application granted granted Critical
Publication of CN108276560B publication Critical patent/CN108276560B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
    • C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
    • C08G61/126—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds with a five-membered ring containing one sulfur atom in the ring
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
    • C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
    • C08G61/124—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds with a five-membered ring containing one nitrogen atom in the ring
    • 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
    • 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
    • H10K85/151—Copolymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10—Definition of the polymer structure
    • C08G2261/12—Copolymers
    • C08G2261/126—Copolymers block
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10—Definition of the polymer structure
    • C08G2261/14—Side-groups
    • C08G2261/145—Side-chains containing sulfur
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/32—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
    • C08G2261/322—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
    • C08G2261/3223—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed containing one or more sulfur atoms as the only heteroatom, e.g. thiophene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/32—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
    • C08G2261/324—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain condensed
    • C08G2261/3241—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain condensed containing one or more nitrogen atoms as the only heteroatom, e.g. carbazole
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/32—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
    • C08G2261/324—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain condensed
    • C08G2261/3243—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain condensed containing one or more sulfur atoms as the only heteroatom, e.g. benzothiophene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/34—Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain
    • C08G2261/344—Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain containing heteroatoms
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/40—Polymerisation processes
    • C08G2261/41—Organometallic coupling reactions
    • C08G2261/414—Stille reactions
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/90—Applications
    • C08G2261/91—Photovoltaic applications
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Electromagnetism (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Photovoltaic Devices (AREA)

Abstract

本发明属于高分子光电材料技术领域，公开了一种基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物及其在单组分有机太阳电池中的应用。本发明基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物结构如下：其中，聚合度n为小于100万的正整数，0＜x＜1，R1、R2、R3、R4相同或不同的分别为烷基链。本发明的基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物可应用于单组分有机太阳电池中，特别是应用于有机光伏器件中，应用于活性层。本发明共聚物可单独作为有机太阳电池活性层，而不需采用给受体共混的本体异质结；采用单一组分做为活性层便于更好的控制活性层的形貌，且对于器件的稳定性具有重要的作用。

Description

基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物 及在单组分有机太阳电池的应用
技术领域
本发明属于高分子光电材料技术领域，特别涉及一种基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物及其在单组分有机太阳电池中的应用。
背景技术
随着全球对于能源需求的逐年增加，石油、煤炭等传统能源的日益枯竭，以及对保护地球生态环境的需要，全世界越来越多的科学家将研究集中在氢气、太阳能等取之不尽用之不竭的可再生清洁能源。
已经成熟的无机硅、砷化镓、磷化铟等基于无机材料的光伏器件已经在市场上占有主导地位，然而由于其对于材料纯度的要求高，加工过程中会产生高能耗及污染等问题，且其价格非常昂贵，因此在追求低成本和绿色环保的今天，其大规模应用受到了限制。
有机光伏器件作为一种新型薄膜光伏电池技术，具有全固态、光伏材料性质可调范围宽、可实现半透明、柔性电池、具有大面积低成本制备潜力等突出优点。有机材料的光伏性能可调范围宽，可利用化学手段对材料的能级、载流子迁移率以及吸收等性能进行有效的调控。有机/聚合物光伏器件可采用打印、印刷等方法进行加工，可借鉴传统塑料的加工工艺，通过卷对卷滚动加工流程制造大面积、柔性的薄膜光伏器件，该生产工艺能够有效降低光伏电池的制造成本。有机光伏器件几乎不受环境和场地限制，在许多场合可将光能转换为电能，同时与无机半导体光伏器件有非常强的互补性，无疑具有巨大的商业开发价值和市场竞争力。因此有机光伏器件的研究引起了广泛关注，以有机光伏器件为核心的科学研究已经成为一个世界范围内竞争激烈的材料科学前沿研究领域。
有机太阳电池活性层经历了从单组分到双组分以及多组分共混体系的发展。目前，代表性的结构为由一个给体和一个受体共同组成的本体异质结结构，展现出了优良的光电转化效率。但是由于活性层是由给受体两个材料组成，两个材料的聚集会有差异使得活性层的形貌不好调控。受本体异质结启发，人们设计了一个分子中同时含有给受体的嵌段共轭聚合物作为有机太阳电池活性层，而不需采用给受体共混的本体异质结。采用单一的一种材料作为有机太阳电池器件的活性层便于更好的控制活性层的形貌；此外，采用单一组分做为活性层对于器件的稳定性具有重要的作用。
发明内容
为了克服上述现有技术的缺点与不足，本发明的首要目的在于提供一种基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物。
本发明另一目的在于提供上述基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物在单组分有机太阳电池中的应用。
本发明的目的通过下述方案实现：
一种基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物，结构如下：
其中，聚合度n为小于100万的正整数，0＜x＜1，R1、R2、R3、R4相同或不同的分别为烷基链。
进一步地，所述的R1、R2、R3、R4相同或不同的分别为C1～40的直链、支链或者环状烷基链，所述C1～40的直链、支链或者环状烷基链中的一个或一个以上的碳原子可被氧原子、烯基、炔基、芳基、羟基、氨基、羰基、羧基、酯基、氰基、甲基、乙基、甲氧基或硝基取代；所述C1～40的直链、支链或者环状烷基链中的一个或一个以上氢原子可被氟原子、氧原子、烯基、炔基、芳基、羟基、氨基、羰基、羧基、酯基、氰基、甲基、乙基、甲氧基或硝基取代。
本发明的基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物可通过Stille聚合反应得到。
本发明的基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物可应用于单组分有机太阳电池中，特别是应用于有机光伏器件中，应用于活性层。本发明共聚物可单独作为有机太阳电池活性层，而不需采用给受体共混的本体异质结。采用单一的一种材料作为有机太阳电池器件的活性层便于更好的控制活性层的形貌；此外，采用单一组分做为活性层对于器件的稳定性具有重要的作用。
上述应用中，所述有机光伏器件的结构如图1所示，由衬底、阳极、阳极界面层、光吸收层、阴极界面层、阴极依次层叠构成。所述光吸收层含有本发明的基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物。
所述阳极的材料优选为铝、银、金、钙/铝合金或钙/银合金。
所述的阳极界面层优选为有机共轭聚合物(如聚3,4-乙撑二氧噻吩/聚苯乙烯磺酸盐)或无机半导体。
所述的阴极优选为金属、金属氧化物(如氧化铟锡导电膜(ITO)，掺杂二氧化锡(FTO)，氧化锌(ZnO)，铟镓锌氧化物(IGZO))和石墨烯及其衍生物中的至少一种。
所述的衬底优选为玻璃、柔性材料(如聚酰亚胺、聚对苯二甲酸乙二醇酯、乙烯对苯二甲酸酯、聚萘二甲酸乙二醇酯或其他聚酯材料)、金属、合金和不锈钢薄膜中的至少一种。
本发明相对于现有技术，具有如下的优点及有益效果：
(1)本发明设计了主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物，所述共轭聚合物可单独作为有机太阳电池活性层，而不需要额外的给体或受体。
(2)所述嵌段共聚物主链含引达省氰基茚酮，可以有效拓宽吸收光谱，增强吸收系数。
(3)采用单一的一种材料作为有机太阳电池器件的活性层便于更好的控制活性层的形貌。
(4)采用单一组分做为活性层对于器件的长期稳定性具有重要的作用。
附图说明
图1为有机光伏器件结构示意图。
图2为本发明基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物(P1、P2)的紫外-可见光-近红外吸收谱图。
图3为电池结构为ITO阳极/阳极界面层/活性层/阴机界面层/阴极(正装结构)时，活性层含本发明的主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物(P1、P2)时电池器件的电流-电压曲线图。
图4为本发明基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物的合成路线图。
具体实施方式
下面结合实施例对本发明作进一步详细的描述，但本发明的实施方式不限于此。下列实施例中涉及的物料均可从商业渠道获得。
实施例1
合成路线见图4：
(1)单体M1参考按照文献[Journal of Materials Chemistry A,2014,2(23):8773-8781.]公开的方法合成。
(2)单体M2按照文献[Energy&Environmental Science,2017,10(5):1243-1251.]公开的方法合成。
(3)单体M3、M4按照文献[ACS Applied Materials&Interfaces,2017,9(10):8838-8847.]公开的方法合成。
(4)聚合物P1、P2的合成：
将单体M1(0.5mmol)、M2(0.15mmol)、M3(0.35mmol)加入到25mL两口烧瓶中，通入氮气保护，加入6mL甲苯。抽换气两次后加入5mg Pd(PPh3)4，95℃反应12h后用甲醇将聚合物沉淀出来，洗涤三次。得深色聚合物P1，产率88.2.7％。1H NMR(CDCl3 500MHz):δ:7.43-7.74(m,38H),6.10-6.38(m,33H),4.10-3.85(m,26H),2.10-1.95(m,44H),1.15-1.40(br,390H),0.875(t,111H).GPC:Mn＝35.4KDa,Mw＝89.6KDa,PDI＝2.53.Elem.Anal.:C,74.36；H7.97；N,1.85；O,3.16；S,12.67.
将单体M1(0.5mmol)、M2(0.15mmol)、M4(0.35mmol)加入到25mL两口烧瓶中，通入氮气保护，加入12mL甲苯。抽换气两次后加入7mg Pd(PPh3)4，95℃反应12h后用甲醇将聚合物沉淀出来，洗涤三次。得深色聚合物P2，产率86.9％。1H NMR(CDCl3 500MHz):δ:7.45-7.76(m,94H),6.14-6.42(m,33H),4.14-3.89(m,54H),2.16-2.05(m,44H),1.15-1.40(br,194H),0.875(t,111H).GPC:Mn＝32.5KDa,Mw＝80.9KDa,PDI＝2.49.Elem.Anal.:C,75.13；H6.91；N,1.87；O,3.21；S,12.87.
将所得的聚合物进行溶液的吸收光谱的测定，如图2所示。从溶液的浓度(0.02mg/mL)和所测得的吸收值可以计算出聚合物P1、P2的吸收系数。P1、P2在最高峰的吸收系数分别为6.37×105cm-1，6.21×105cm-1。
实施例2
以实施例1所合成的共轭聚合物P1、P2作为活性层在有机光伏器件(ITO阳极/阳极界面层/活性层/阴机界面层/阴极)中应用
将ITO导电玻璃，方块电阻～20欧/平方厘米，预切成15毫米×15毫米方片。依次用丙酮、微米级半导体专用洗涤剂、去离子水、异丙醇超声清洗，氮气吹哨后置于恒温烘箱备用。在ITO上旋凃一层20nm厚的PEDOT:PSS，然后旋涂活性层材料P1，P2，厚度均为100nm。然后旋涂一层5nm厚的PFN-Br，最后蒸镀Al电极。所有制备过程均在提供氮气氛围的手套箱内进行。所制备的正装电池器件的电流-电压曲线如图3、表1所示。
表1含本发明共轭聚合物的有机光伏器件的性能参数
效率(％) 短路电流(mA/cm<sup>2</sup>) 开路电压(V) 填充因子
P1 6.73 16.5 0.68 0.60
P2 6.91 16.4 0.68 0.62
上述实施例为本发明较佳的实施方式，但本发明的实施方式并不受上述实施例的限制，其他的任何未背离本发明的精神实质与原理下所作的改变、修饰、替代、组合、简化，均应为等效的置换方式，都包含在本发明的保护范围之内。

Claims (9)

1.一种基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物，其特征在于结构如下：
其中，聚合度n为小于100万的正整数，0＜x＜1，R1、R2、R3、R4相同或不同的分别为烷基链。
2.根据权利要求1所述的基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物，其特征在于：所述的R1、R2、R3、R4相同或不同的分别为C1～40的直链、支链或者环状烷基链。
3.根据权利要求2所述的基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物，其特征在于：所述C1～40的直链、支链或者环状烷基链中的一个或一个以上氢原子被氟原子、氧原子、烯基、炔基、芳基、羟基、氨基、羰基、羧基、酯基、氰基、甲基、乙基、甲氧基或硝基取代。
4.根据权利要求1所述的基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物，其特征在于通过Stille聚合反应得到。
5.权利要求1～4任一项所述的基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物在单组分有机太阳电池中的应用。
6.权利要求1～4任一项所述的基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物在有机光伏器件中的应用。
7.根据权利要求6所述的基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物在有机光伏器件中的应用，其特征在于：所述有机光伏器件由衬底、阳极、阳极界面层、光吸收层、阴极界面层、阴极依次层叠构成。
8.根据权利要求7所述的基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物在有机光伏器件中的应用，其特征在于：所述光吸收层含有权利要求1～4任一项所述的基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物。
9.根据权利要求7所述的基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物在有机光伏器件中的应用，其特征在于：所述阳极的材料为铝、银、金、钙/铝合金或钙/银合金；
所述的阳极界面层为有机共轭聚合物或无机半导体；
所述的阴极为金属、金属氧化物石墨烯及其衍生物中的至少一种；
所述的衬底为玻璃、柔性材料、金属、合金和不锈钢薄膜中的至少一种。
CN201810038793.4A 2018-01-16 2018-01-16 基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物及在单组分有机太阳电池的应用 Active CN108276560B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810038793.4A CN108276560B (zh) 2018-01-16 2018-01-16 基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物及在单组分有机太阳电池的应用

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810038793.4A CN108276560B (zh) 2018-01-16 2018-01-16 基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物及在单组分有机太阳电池的应用

Publications (2)

Publication Number Publication Date
CN108276560A CN108276560A (zh) 2018-07-13
CN108276560B true CN108276560B (zh) 2019-09-17

Family

ID=62803665

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810038793.4A Active CN108276560B (zh) 2018-01-16 2018-01-16 基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物及在单组分有机太阳电池的应用

Country Status (1)

Country Link
CN (1) CN108276560B (zh)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020058860A1 (en) * 2018-09-19 2020-03-26 Eni S.P.A. Conjugated polymers including an indacen-4-one derivative, procedure for their preparation and photovoltaic devices comprising the same
CN112876656B (zh) * 2021-01-15 2022-10-28 东华大学 一种电子传输型聚合物及其制备方法、电子传输型薄膜和有机光伏电池器件
CN113817142B (zh) * 2021-10-13 2022-06-14 福州大学 芴基氰基茚酮类共轭聚合物及其制备方法
CN113943311A (zh) * 2021-11-22 2022-01-18 北京航空航天大学 一种新型非富勒烯小分子的制备与应用

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102050940A (zh) * 2011-01-28 2011-05-11 华南理工大学 含6-R基-[1,2,5]噻唑[3,4-g]苯并三唑的有机半导体材料及其应用
CN104744675A (zh) * 2015-03-30 2015-07-01 华南理工大学 含6H–吡咯并[3,4–f]苯并三唑–5,7–二酮的共轭聚合物及其应用
CN106977704A (zh) * 2017-03-31 2017-07-25 华南理工大学 一种含三唑并异吲哚‑5,7（2h，6h）‑二酮单元的三元共聚物及其制备方法与应用

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102050940A (zh) * 2011-01-28 2011-05-11 华南理工大学 含6-R基-[1,2,5]噻唑[3,4-g]苯并三唑的有机半导体材料及其应用
CN104744675A (zh) * 2015-03-30 2015-07-01 华南理工大学 含6H–吡咯并[3,4–f]苯并三唑–5,7–二酮的共轭聚合物及其应用
CN106977704A (zh) * 2017-03-31 2017-07-25 华南理工大学 一种含三唑并异吲哚‑5,7（2h，6h）‑二酮单元的三元共聚物及其制备方法与应用

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
High-Performance Nonfullerene Polymer Solar Cells based on Imide-Functionalized Wide-Bandgap Polymers;Baobing Fan,et al.;《Adv. Mater.》;20170323;第29卷;第1606396页

Also Published As

Publication number Publication date
CN108276560A (zh) 2018-07-13

Similar Documents

Publication Publication Date Title
CN108276560B (zh) 基于主链含苯并三唑酰亚胺和引达省氰基茚酮的嵌段共聚物及在单组分有机太阳电池的应用
CN109749059A (zh) 一种主链含氰基茚酮的稠环n型聚合物及其应用
Dong et al. Efficient organic-inorganic hybrid cathode interfacial layer enabled by polymeric dopant and its application in large-area polymer solar cells
Ono et al. Efficient crystalline Si/poly (ethylene dioxythiophene): poly (styrene sulfonate): graphene oxide composite heterojunction solar cells
CN112646129B (zh) 含苯并双噻二唑的n型水/醇溶共轭聚电解质及其制备与应用
CN109021214A (zh) 含寡聚乙二醇基侧链修饰萘二酰亚胺单元的n-型共轭聚合物及其在有机光电器件中的应用
CN108034042B (zh) 一种主链给体-侧链受体型共轭聚合物及其制备和应用
CN107325266A (zh) 含醌式结构的n型共轭聚合物及其在有机光电器件中的应用
CN104140521A (zh) 宽吸收谱的三元共轭聚合物给体材料及其制备方法和用途
CN105237745A (zh) 含季膦盐基团共轭聚电解质及其在有机光电器件中的应用
CN108084405A (zh) 基于主链结构为萘二酰亚胺和引达省氰基茚酮的嵌段共聚物及其在有机光伏器件中的应用
CN114883500A (zh) 一种非卤素溶剂加工的基于聚噻吩体系的有机太阳电池及其制备方法
CN109244242B (zh) 一种有机太阳电池及其制备方法
CN107674183B (zh) 含萘[1,2-c；5,6-c]二[1,2,5]噻二唑的共轭聚合物及制备方法和应用
CN107674180A (zh) 基于共轭π桥相连呋喃的n型共轭聚合物及其在有机光电器件中的应用
CN112646130B (zh) 基于双自由基苯并双噻二唑的n型水/醇溶共轭聚电解质及其制备与应用
CN107793423B (zh) 新型n型醌式结构小分子及其在有机光电器件中的应用
CN109749060A (zh) 一种侧链支化点可调的萘酰亚胺n型共轭聚合物及其应用
CN107778457A (zh) 基于连呋喃的n型共轭聚合物及其在有机光电器件中的应用
CN105384930B (zh) 共轭-非共轭n型聚电解质及其在有机光电器件中的应用
CN109232527B (zh) 自掺杂型富勒烯吡啶盐电子传输材料及其构成的有机太阳电池
CN109694463B (zh) 含硅氧烷侧链的萘二酰亚胺n型共聚物及其在有机光电器件中的应用
CN108084406B (zh) 基于侧链含吸光型受体的n型共轭聚合物及其制备和应用
CN102311535B (zh) 含芴、蒽和噻吩并吡嗪单元的聚合物、制备方法及其应用
CN110649164B (zh) 聚合物太阳能电池及其制备方法

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20210630

Address after: 523808 room 236, building 15, No.1 Xuefu Road, Songshanhu Park, Dongguan City, Guangdong Province

Patentee after: Dongguan Hua Gong Cooperative Innovation Technology Development Co.,Ltd.

Patentee after: Huang Fei

Patentee after: Ying Lei

Address before: 523808 room 168, productivity building, Songshan Lake high tech Industrial Development Zone, Dongguan, Guangdong

Patentee before: SOUTH CHINA INSTITUTE OF COLLABORATIVE INNOVATION

TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20210819

Address after: 523808 room 533, building 15, No.1 Xuefu Road, Songshanhu Park, Dongguan City, Guangdong Province

Patentee after: Dongguan volt ampere Photoelectric Technology Co., Ltd

Address before: 523808 room 236, building 15, No.1 Xuefu Road, Songshanhu Park, Dongguan City, Guangdong Province

Patentee before: Dongguan Hua Gong Cooperative Innovation Technology Development Co.,Ltd.

Patentee before: Huang Fei

Patentee before: Ying Lei