Effects of Thieno[3,2-b]thiophene Number on Narrow-Bandgap Fused-Ring Electron Acceptors

被引:1
|
作者
Tengfei Li [1 ,2 ]
Guilong Cai [3 ]
Yuze Lin [2 ]
Xinhui Lu [3 ]
Xiaowei Zhan [1 ]
机构
[1] Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, School of Materials Science and Engineering, Peking University
[2] Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences
[3] Department of Physics, The Chinese University of Hong Kong
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
D O I
暂无
中图分类号
O626.12 [硫杂茂(噻吩)族]; TM914.4 [太阳能电池];
学科分类号
摘要
We synthesize and compare four near-infrared absorbing fused-ring electron acceptors named as n TTIC(n=2, 3, 4, and 5), based on different number of thieno[3,2-b]thiophene(TT) unit as the electron-donating core. With increasing the TT unit, absorption spectrum of the TTIC series red shifts, and the highest occupied molecular orbital(HOMO) upshifts notably. It is worth noting that 4TTIC and 5TTIC exhibit absorption edges approaching 1100 nm, which is the photoresponse limit of solar cells based on crystal silicon. When the TTIC series acceptors are blended with polymer donor PM6, the binary-blend organic solar cells based on 3TTIC show the best power conversion efficiency(PCE) of 13.1%. In contrast, 2TTIC-based devices exhibit relatively lower PCE of 8.32%, mainly caused by the larger energy loss and blue-shifted absorption. Due to insufficient driving force of charge separation caused by very high HOMO, 4TTIC and 5TTIC show poor PCEs lower than 3%.
引用
收藏
页码:914 / 920
页数:7
相关论文
共 50 条
  • [41] Dialkyl-substituted thieno[3,2-b]thiophene-based polymers containing 2,2'-bithiophene, thieno[3,2-b]thiophene, and ethynylene spacers
    Miguel, Lidaris San
    Matzger, Adam J.
    MACROMOLECULES, 2007, 40 (26) : 9233 - 9237
  • [42] 2,5-Bis(trimethylsilylethynyl)thieno[3,2-b]thiophene
    Khan, MS
    Al-Naamani, RS
    Ahrens, B
    Raithby, PR
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2004, 60 : O1202 - O1203
  • [43] Thieno[3,2-b]pyrrolo Donor Fused with Benzothiadiazolo, Benzoselenadiazolo and Quinoxalino Acceptors: Synthesis, Characterization, and Molecular Properties
    Cheng, Yen-Ju
    Chen, Chiu-Hsiang
    Ho, Yu-Ju
    Chang, Shu-Wei
    Witek, Henryk A.
    Hsu, Chain-Shu
    ORGANIC LETTERS, 2011, 13 (20) : 5484 - 5487
  • [44] IMPROVED SYNTHESES OF THIENO[2,3-B]-FUSED AND [3,2-B]-FUSED NAPHTHYRIDINES
    BJORK, P
    AAKERMANN, T
    HORNFELDT, AB
    GRONOWITZ, S
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 1995, 32 (03) : 751 - 754
  • [45] Butterfly Effects Arising from Starting Materials in Fused-Ring Electron Acceptors
    Li, Tengfei
    Wu, Yao
    Zhou, Jiadong
    Li, Mengyang
    Wu, Jingnan
    Hu, Qin
    Jia, Boyu
    Pan, Xiran
    Zhang, Maojie
    Tang, Zheng
    Xie, Zengqi
    Russell, Thomas P.
    Zhan, Xiaowei
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2020, 142 (47) : 20124 - 20133
  • [46] Selenopheno[3,2-b]thiophene-Based Narrow-Bandgap Nonfullerene Acceptor Enabling 13.3% Efficiency for Organic Solar Cells with Thickness-Insensitive Feature
    Wang, Jin-Liang
    Liu, Kai-Kai
    Hong, Ling
    Ge, Gao-Yang
    Zhang, Chao
    Hou, Jianhui
    ACS ENERGY LETTERS, 2018, 3 (12): : 2967 - 2976
  • [47] A fused-ring non-fullerene acceptor based on a benzo[1,2-b:4,5-b′]dithiophene central core with a thieno[3,2-b]thiophene side-chain for highly efficient organic solar cells
    Jia, Yu
    Zhang, Yun
    Jiang, Wei
    Su, Bin
    Liu, Chunbo
    Zhu, Enwei
    Che, Guangbo
    JOURNAL OF MATERIALS CHEMISTRY A, 2019, 7 (18) : 10905 - 10911
  • [48] Synthesis of a Novel Fused Thiophene-thieno[3,2-b]thiophene-thiophene Donor Monomer and Co-polymer for Use in OPV and OFETs
    Bronstein, Hugo
    Ashraf, Raja Shahid
    Kim, Youngju
    White, Andrew J. P.
    Anthopoulos, Thomas
    Song, Kigook
    James, David
    Zhang, Weimin
    McCulloch, Iain
    MACROMOLECULAR RAPID COMMUNICATIONS, 2011, 32 (20) : 1664 - 1668
  • [49] Highly transmissive blue electrochromic polymers based on thieno[3,2-b]thiophene
    Xu, Panpan
    Murtaza, Imran
    Shi, Jingjing
    Zhu, Mengmeng
    He, Yaowu
    Yu, Hongtao
    Goto, Osamu
    Meng, Hong
    POLYMER CHEMISTRY, 2016, 7 (34) : 5351 - 5356
  • [50] Influence of the substituent on the chiroptical properties of poly(thieno[3,2-b]thiophene)s
    De Crerner, Lieven
    Verbiest, Thierry
    Koeckelberghs, Guy
    MACROMOLECULES, 2008, 41 (03) : 568 - 578