应用化学 ›› 2019, Vol. 36 ›› Issue (9): 1023-1034.DOI: 10.11944/j.issn.1000-0518.2019.09.190048

• 研究论文 • 上一篇    下一篇

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

张小梅ab,李淼淼ab*(),王琪ab,江宇c,耿延候ab   

  1. a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
    b天津大学天津化学化工协同创新中心 天津 300072
    c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
  • 收稿日期:2019-02-23 接受日期:2019-03-22 出版日期:2019-09-05 发布日期:2019-09-05
  • 通讯作者: 李淼淼
  • 基金资助:
    国家自然科学基金资助项目(51703158)

Near-infrared Absorbing Non-fullerene Acceptors with Dithienopyrrole as π Spacer for Organic Solar Cells

ZHANG Xiaomeiab,LI Miaomiaoab*(),WANG Qiab,JIANG Yuc,GENG Yanhouab   

  1. aSchool of Materials Science and Engineering and Tianjin Key Laboratory of Molecular Optoelectronic Science,Tianjin University,Tianjin 300072,China
    bCollaborative Innovation Center of Chemical Science and Engineering(Tianjin),Tianjin University,Tianjin 300072,China
    cState Key Laboratory of Polymer Physics and Chemistry,Changchun Institute of Applied Chemistry,Chinese Academy of Sciences,Changchun 130022,China
  • Received:2019-02-23 Accepted:2019-03-22 Published:2019-09-05 Online:2019-09-05
  • Contact: Miaomiao LI
  • Supported by:
    Supported by the National Natural Science Foundation of China(No.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

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%.

Key words: organic solar cell, non-fullerene acceptor, dithienopyrrole, alky side chain, power conversion efficiency