Regulation of Side-Chain Symmetry for Delaying Triplet Formation and Suppressing Non-Radiative Loss in Organic Solar Cells

Huanhuan Gao, Qian Li, Baobing Fan*, Zhaozhao Bi, Wenlin Jiang, Sen Zhang, Qunping Fan, Tianqi Chen, Francis R. Lin, Bin Kan, Dangyuan Lei, Wei Ma, Alex K.-Y. Jen*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

4 Citations (Scopus)

Abstract

The structural revolutions of non-fullerene acceptors (NFAs) have driven continuous efficiency breakthroughs in organic solar cells (OSCs). Rational regulation of NFA structures toward efficient exciton dissociation and mitigated non-radiative recombination is pivotal for OSCs. The incorporation of asymmetric side chains on NFAs can often achieve these goals by inducing a desirable aggregate state. However, it lacks the studies to directly correlate the side-chain symmetry of NFAs with the exciton delocalization and triplet dynamics in OSCs. Herein, The influence of structural symmetry on the aggregate properties is systematically investigated and exciton/charge dynamics based on two developed biaxial-conjugated NFAs with varied side-chain symmetry. The symmetric NFA having diverse molecular packing orientations can form multiple charge transfer channels in its blend with polymer donor, which cannot be found in that comprising the asymmetric ones. Moreover, a slower rate and lower ratio of the spin-triplet state are formed in the blend of symmetric NFA, resulting in a much lower non-radiative voltage loss in corresponding OSCs. This study reveals the distinct advantages of symmetric NFAs in both aggregate properties and exciton/charge dynamics over those of asymmetric ones, paving the way for developing high-performance OSCs using easier-to-prepare, low-cost symmetric materials. © 2024 Wiley-VCH GmbH.
Original languageEnglish
Article number2403121
JournalAdvanced Energy Materials
DOIs
Publication statusOnline published - 27 Sept 2024

Funding

H.G. and Q.L. contributed equally to this work. A.K.-Y.J. thanks the sponsorship of the Lee Shau-Kee Chair Professor (Materials Science), and the support from the APRC Grant of the City University of Hong Kong (9380086, 9610419, 9610492, 9610508); the TCFS Grant (GHP/018/20SZ) and MRP Grant (MRP/040/21X) from the Innovation and Technology Commission of Hong Kong; the Green Tech Fund (202020164) from the Environment and Ecology Bureau of Hong Kong; the GRF grant (11307621, 11316422) from the Research Grants Council of Hong Kong; the CRF grant (C6023-19GF) from the Research Grants Council of Hong Kong; Shenzhen Science and Technology Program (SGDX20201103095412040); Guangzhou Huangpu Technology Bureau (2022GH02), and Guangdong Major Project of Basic and Applied Basic Research (2019B030302007). H.G. acknowledges the financial support of the Hong Kong Scholar program (XJ2021-038), Young Talent Fund of Xi'an Association for Science and Technology (959202313080). D.Y.L. acknowledges the financial support from the Research Grants Council of the Hong Kong through a Collaborative Research Equipment Grant (C1015-21EF). X-ray data was acquired at beamlines 7.3.3 at the Advanced Light Source, which is supported by the Director, Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231. The authors thank Dr. Eric Schaible and Dr. Chenhui Zhu at beamline 7.3.3 for assistance with data acquisition.

Research Keywords

  • non-fullerene acceptor
  • non-radiative loss
  • organic solar cell
  • side-chain symmetry
  • triplet formation

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