Hyperbranched conjugated polymers based on 4,7-di(thiophen-2-yl)benzo [c] [1,2,5]thiadiazole for ternary organic solar cells

被引:6
|
作者
Luo, Dong [1 ]
Ma, Dongyu [1 ,2 ]
Tan, Qinglan [1 ]
Li, Wenlang [1 ,2 ]
Lu, Jiang [1 ]
Chi, Zhenguo [1 ,2 ]
Liang, Hui [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem, GD HPPC Lab, PCFM Lab, Guangzhou 510275, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Guangdong Engn Technol Res Ctr High Performance O, Sch Chem, State Key Lab Optoelect Mat & Technol, Guangzhou 510275, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Hyperbranched conjugated polymer; Ternary organic solar cells; AB(2) monomer; Sonogashira coupling; EFFICIENCY; POLYMERIZATION; ACCEPTOR; COMPLEX;
D O I
10.1016/j.dyepig.2020.108524
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A new class of end-modifiable hyperbranched conjugated polymer (HBCP-Br) was synthesized from an AB(2) monomer, and the end-modification of HBCP-Br was carried out by substituting the end-Br with a donor group to give the end-modified HBCPs (HBCP-OR). Both polymers had relatively good thermal stability (T-d > 350 degrees C) and deep HOMO energy levels (-5.40 eV for HBCP-OR, -5.45 eV for HBCP-Br). Besides, the other two similar small molecular acceptors (IDTOTZ and IDTCPT) were synthesized to construct ternary organic solar cells (OSCs) with HBCP-OR or HBCP-Br. Owing to the favorable spectral and energy levels matching and relatively regular morphology, the ternary OSCs based on HBCP-OR/IDTOTZ/IDTCPT obtained an optimized PCE of 4.86% (with an open-circuit voltage (V-OC) of 0.893 V, a short-circuit current density (J(SC)) of 11.71 mA, and a fill factor (FF) of 45.18%), which performed better than the devices based on HBCP-Br/IDTOTZ/IDTCPT with a PCE of 2.33%. In addition, the HBCP-Br also exhibited photovoltaic activity when used as acceptors in the ternary OSCs based on small molecular donors, which demonstrated that HBCPs could play different roles in the OSCs.
引用
收藏
页数:7
相关论文
共 50 条
  • [41] Thick Film Polymer Solar Cells Based on Naphtho[1,2-c:5,6-c]bis[1,2,5]thiadiazole Conjugated Polymers with Efficiency over 11%
    Jin, Yaocheng
    Chen, Zhiming
    Xiao, Manjun
    Peng, Jiajun
    Fan, Baobing
    Ying, Lei
    Zhang, Guichuan
    Jiang, Xiao-Fang
    Yin, Qingwu
    Liang, Ziqi
    Huang, Fei
    Cao, Yong
    ADVANCED ENERGY MATERIALS, 2017, 7 (22)
  • [42] Organic sensitizers with modified di(thiophen-2-yl)phenylamine donor units for dye-sensitized solar cells: a computational study
    Supawadee Namuangruk
    Jittima Meeprasert
    Siriporn Jungsuttiwong
    Vinich Promarak
    Nawee Kungwan
    Theoretical Chemistry Accounts, 2014, 133
  • [43] Organic sensitizers with modified di(thiophen-2-yl)phenylamine donor units for dye-sensitized solar cells: a computational study
    Namuangruk, Supawadee
    Meeprasert, Jittima
    Jungsuttiwong, Siriporn
    Promarak, Vinich
    Kungwan, Nawee
    THEORETICAL CHEMISTRY ACCOUNTS, 2014, 133 (09) : 1 - 15
  • [44] New Low Bandgap Conjugated Polymer Derived from 2, 7-Carbazole and 5, 6-Bis(octyloxy)-4, 7-di(thiophen-2-yl) Benzothiadiazole: Synthesis and Photovoltaic Properties
    Ding, Ping
    Chu, Cheng-Che
    Zou, Yingping
    Xiao, Dequan
    Pan, Chunyue
    Hsu, Chain-Shu
    JOURNAL OF APPLIED POLYMER SCIENCE, 2012, 123 (01) : 99 - 107
  • [45] The structure of 4,7-bis((trimethylsilyl)ethynyl)benzo[c][1,2,5]thiadiazole and identification of a widespread S•••N structural motif
    Boudebous, Amar
    Constable, Edwin C.
    Housecroft, Catherine E.
    Neuburger, Markus
    Schaffner, Silvia
    AUSTRALIAN JOURNAL OF CHEMISTRY, 2008, 61 (10) : 755 - 757
  • [46] Effects of solvent vapour annealing on the performances of benzo[1,2-b:4,5-b′] dithiophene and 4,7-di(4-hexyl-thiophen-2-yl)-5,6-difluorine-2,1,3-benzothiadiazole-based alternating polymer solar cells with different configurations
    Chen, Mingyao
    Zhao, Baofeng
    Xin, Jinming
    Cong, Zhiyuan
    Li, Xiaoyu
    Yang, Langlei
    Ma, Wei
    Wei, Wei
    Gao, Chao
    DYES AND PIGMENTS, 2019, 161 : 58 - 65
  • [47] New compounds based on quaterthiophene and benzo[1,2,5] thiadiazole for solar cells application: correlation structure/electronic properties
    El Alamy, A.
    Amine, A.
    Bouzzine, S. M.
    Hamidi, M.
    Bouachrine, M.
    MOROCCAN JOURNAL OF CHEMISTRY, 2015, 3 (04): : 688 - 697
  • [48] Efficient polymer solar cells based on dialkoxynaphthalene and benzo[c][1,2,5]thiadiazole: A new approach for simple donor-acceptor pair
    Kim, Seul-Ong
    Chung, Dae Sung
    Cha, Hyojung
    Hwang, Moon Chan
    Park, Jong-Won
    Kim, Yun-Hi
    Park, Chan Eon
    Kwon, Soon-Ki
    SOLAR ENERGY MATERIALS AND SOLAR CELLS, 2011, 95 (07) : 1678 - 1685
  • [49] A red thermally activated delayed fluorescence emitter based on benzo[c] [1,2,5]thiadiazole
    Ma, You-Ping
    Wang, Guoliang
    Zhao, Min
    Shi, Zi-Fa
    Miao, Yanqin
    Cao, Xiao-Ping
    Zhang, Hao-Li
    DYES AND PIGMENTS, 2023, 212
  • [50] Benzo[1,2-c;4,5-c ']Bis[1,2,5]Thiadiazole in Organic Optoelectronics: A Mini-Review
    Tam, Teck Lip Dexter
    Wu, Jishan
    JOURNAL OF MOLECULAR AND ENGINEERING MATERIALS, 2015, 3 (1-2)