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Boosting power conversion efficiency (PCE) of organic solar cells (OSCs) has been restricted by its undesirably high energy loss, especially for those nonhalogenated solvent-processed ones. Here,a dichloro-methoxylated terminal group in an asymmetric small molecular acceptor design, which realizes a significantly reduced non-radiative energy loss (0.179 eV) compared to its symmetric counterpart (0.202 eV), is reported. Consequently, the device efficiency is improved by up to 20% for PM6:BTP-eC9-4ClO, without sacrificing the photon harvest or charge transport ability of the control system PM6:BTP-eC9. Further characterizations reveal the asymmetric acceptor BTP-eC9-4ClO's blend film demonstrates a suppressed triplet state formation, enabled by an enhanced electron delocalization. In addition, the asymmetric BTP-eC9-4ClO is found to be thermally stabler than BTP-eC9, and thus providing an improved device stability, whose T80 value reaches > 7800 h under 80 °C anneal in N2 via linear extrapolation. This work represents state-of-the-art device performance for nonhalogenated solvent-processed binary OSCs with certified results (19.45%).
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Ruijie Ma
University of Science and Technology Liaoning
Bosen Zou
Hong Kong Polytechnic University
Yulong Hai
Guangzhou University
Advanced Materials
University of Hong Kong
Hong Kong University of Science and Technology
Hong Kong Polytechnic University
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Ma et al. (Sun,) studied this question.
synapsesocial.com/papers/69d84fe652654bb436d190ee — DOI: https://doi.org/10.1002/adma.202500861