4.8 Article

Heteroheptacene-based acceptors with thieno[3,2-b]pyrrole yield high-performance polymer solar cells

Journal

NATIONAL SCIENCE REVIEW
Volume 9, Issue 7, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nsr/nwac076

Keywords

thieno[3; 2-b]pyrrole; small-molecule acceptors; energy loss; intramolecular non-covalent interactions; polymer solar cells

Funding

  1. National Key Research and Development Program of China - Ministry of Science and Technology [2019YFA0705900]
  2. Basic and Applied Research Major Programme of Guangdong Province [2019B030302007]
  3. National Natural Science Foundation of China [91433202]
  4. Shenzhen Technology and Innovation Commission through Shenzhen Fundamental Research Program [JCYJ20200109140801751]
  5. Hong Kong Innovation and Technology Commission [ITC-CNERC14SC01]
  6. Foshan-HKUST [FSUST19-CAT0202]
  7. Hong Kong Research Grants Council (RIF project) [R6021-18]
  8. Hong Kong Research Grants Council (CRF project) [C6023-19G]
  9. Hong Kong Research Grants Council (GRF project) [16310019, 16310020]

Ask authors/readers for more resources

Rationally utilizing and developing synthetic units is crucial for designing high-performance non-fullerene small-molecule acceptors. In this study, four acceptors were developed based on a thieno[3,2-b]pyrrole synthetic unit, showing improved photovoltaic properties and energy utilization compared to the standard acceptor IT-4Cl. The ThPy3-based device achieved the highest PCE and excellent FF, while the ThPy4-based device achieved the lowest energy loss and smallest optical band gap.
Rationally utilizing and developing synthetic units is of particular significance for the design of high-performance non-fullerene small-molecule acceptors (SMAs). Here, a thieno[3,2-b]pyrrole synthetic unit was employed to develop a set of SMAs (ThPy1, ThPy2, ThPy3 and ThPy4) by changing the number or the position of the pyrrole ring in the central core based on a standard SMA of IT-4Cl, compared to which the four thieno[3,2-b]pyrrole-based acceptors exhibit bathochromic absorption and upshifted frontier orbital energy level due to the strong electron-donating ability of pyrrole. As a result, the polymer solar cells (PSCs) of the four thieno[3,2-b]pyrrole-based acceptors yield higher open-circuit voltage and lower energy loss relative to those of the IT-4Cl-based device. What is more, the ThPy3-based device achieves a power conversion efficiency (PCE) (15.3%) and an outstanding fill factor (FF) (0.771) that are superior to the IT-4Cl-based device (PCE = 12.6%, FF = 0.758). The ThPy4-based device realizes the lowest energy loss and the smallest optical band gap, and the ternary PSC device based on PM6:BTP-eC9:ThPy4 exhibits a PCE of 18.43% and a FF of 0.802. Overall, this work sheds light on the great potential of thieno[3,2-b]pyrrole-based SMAs in realizing low energy loss and high PCE. Four heteroheptacene-based acceptors using thieno[3,2-b]pyrrole building block were developed for the first time, and all the four acceptors-based devices realized high performance and low energy loss.

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