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基于二噻吩并吡咯π桥的窄带隙非富勒烯受体材料在有机太阳能电池中的应用
引用本文:张小梅,李淼淼,王琪,江宇,耿延候. 基于二噻吩并吡咯π桥的窄带隙非富勒烯受体材料在有机太阳能电池中的应用[J]. 应用化学, 2019, 36(9): 1023-1034. DOI: 10.11944/j.issn.1000-0518.2019.09.190048
作者姓名:张小梅  李淼淼  王琪  江宇  耿延候
作者单位:天津大学材料科学与工程学院,分子光电科学重点实验 天津 300072;天津大学天津化学化工协同创新中心 天津 300072;中国科学院长春应用化学研究所,高分子物理与化学国家重点实验室 长春 130022
基金项目:国家自然科学基金资助项目(51703158)
摘    要:以不同烷基取代的二噻吩并吡咯(DTP)为π桥,连接吲哒省并二噻吩(IDT)中间单元和氰基茚酮(IC)或二氟代氰基茚酮(2F-IC)末端基团,设计并合成了6个窄带隙的非富勒烯受体材料。 其中,IDTDTP-C2C2-H和IDTDTP-C2C2-F中的DTP单元以1-乙基丙基为侧链,IDTDTP-C6C6-H和IDTDTP-C6C6-F中的DTP单元以1-己基庚基为侧链,IDTDTP-C12-H和IDTDTP-C12-F中的DTP单元以十二烷基为侧链。 6个分子均具有较窄的光学带隙(1.37~1.44 eV)。 相比于以IC为末端基团的分子(IDTDTP-C2C2-H、IDTDTP-C6C6-H和IDTDTP-C12-H),由于氟原子的拉电子效应,以2F-IC为末端基团的分子(IDTDTP-C2C2-F、IDTDTP-C6C6-F和IDTDTP-C12-F)具有红移的吸收光谱,以及更低的最高分子占有轨道能级(HOMO)和最低分子空轨道(LUMO)能级。 以宽带隙聚合物聚[2,6-(4,8-双(5-(2-乙基己基))噻吩-2-基)-苯并[1,2-b:4,5-b']二噻吩-alt-5,5-(1',3'-二-2-噻吩)-5',7'-双(2-乙基己基)-苯并[1',2'-c:4',5'-c']二噻吩-4,8-二酮](PBDB-T)为给体材料,制备了有机太阳能电池器件。 PBDB-T:IDTDTP-C6C6-F共混薄膜具有较高且更平衡的空穴/电子迁移率,以及良好的形貌,基于PBDB-T:IDTDTP-C6C6-F的有机太阳能电池获得了6.94%的能量转换效率,开路电压为0.86 V,短路电流密度为13.56 mA/cm2,填充因子为59.5%。

关 键 词:有机太阳能电池  非富勒烯受体  二噻吩并吡咯  烷基侧链  能量转换效率  
收稿时间:2019-02-23

Near-infrared Absorbing Non-fullerene Acceptors with Dithienopyrrole as π Spacer for Organic Solar Cells
ZHANG Xiaomei,LI Miaomiao,WANG Qi,JIANG Yu,GENG Yanhou. Near-infrared Absorbing Non-fullerene Acceptors with Dithienopyrrole as π Spacer for Organic Solar Cells[J]. Chinese Journal of Applied Chemistry, 2019, 36(9): 1023-1034. DOI: 10.11944/j.issn.1000-0518.2019.09.190048
Authors:ZHANG Xiaomei  LI Miaomiao  WANG Qi  JIANG Yu  GENG Yanhou
Affiliation:School of Materials Science and Engineering and Tianjin Key Laboratory of Molecular Optoelectronic Science,Tianjin University,Tianjin 300072,China;Collaborative Innovation Center of Chemical Science and Engineering(Tianjin),Tianjin University,Tianjin 300072,China;State Key Laboratory of Polymer Physics and Chemistry,Changchun Institute of Applied Chemistry,Chinese Academy of Sciences,Changchun 130022,China
Abstract:A series of non-fullerene acceptors with dithieno[3,2-b:2',3'-d]pyrrole(DTP) π bridge to link indacenodithiophene(IDT) core and 3-(dicyanomethylidene)indan-1-one(IC) or difluorinated IC(2F-IC) terminals, i.e. IDTDTP-C2C2-H and IDTDTP-C2C2-F with 1-ethylpropyl on DTP, IDTDTP-C6C6-H and IDTDTP-C6C6-F with 1-hexylheptyl on DTP, and IDTDTP-C12-H and IDTDTP-C12-F with n-dodecyl on DTP, was designed and synthesized. These molecules achieved low optical band gaps(1.37~1.44 eV). Compared with the IC-terminated molecules(IDTDTP-C2C2-H, IDTDTP-C6C6-H and IDTDTP-C12-H), IDTDTP-C2C2-F, IDTDTP-C6C6-F and IDTDTP-C12-F with 2F-IC as terminals show red-shifted absorption spectra and down-shifted the highest occupied molecular orbitals(HOMO) and the lowest unoccupied molecular orbitals(LUMO) energy levels owing to the electron-withdrawing ability of F substituents. Organic solar cells(OSCs) based on these acceptors were fabricated with the wide-bandgap polymer poly[2,6-(4,8-bis(5-(2-ethylhexyl))thiophen-2-yl)-benzo[1,2-b:4,5-b']dithiophene-alt-5,5-(1',3'-di-2-thienyl)-5',7'-bis(2-ethylhexyl)-benzo[1',2'-c:4',5'-c']dithiophene-4,8-dione](PBDB-T) as the donor. Owing to the higher and more balanced hole and electron mobilities, and a proper phase-separated morphology in the blend film, IDTDTP-C6C6-F with 1-hexylheptyl on DTP unit achieved a maximum power conversion efficiency(PCE) of 6.94% with an open-circuit voltage(Voc) of 0.86 V, a short circuit current density(Jsc) of 13.56 mA/cm2 and a fill factor(FF) of 59.5%.
Keywords:organic solar cell  non-fullerene acceptor  dithienopyrrole  alky side chain  power conversion efficiency  
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