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Selenium-Functionalized Main-Chain Twisted Molecules with High Melting Points Enable Efficient and Stable Ternary Organic Solar Cells

  • Weiping Wang
  • , Shujuan Liu
  • , Yuchen Zhou
  • , Zhiyuan Cong
  • , Haimei Wu
  • , Chao Gao*
  • , Zhi Yang
  • , Zihui Meng*
  • *Corresponding author for this work
  • Beijing Institute of Technology
  • Xi’an Key Laboratory of Liquid Crystal and Organic Photovoltaic Materials
  • Xi'an Modern Chemistry Research Institute

Research output: Contribution to journal › Article › peer-review

Abstract

Although organic solar cells (OSCs) based on Y6 and its derivatives have achieved rapid development, their intrinsically low open-circuit voltage (VOC), which limits the power conversion efficiency (PCE), and the poor long-term stability remain two major obstacles to their application. To address these challenges, two selenium-functionalized main-chain twisted small molecules, i-DA and i-EA, were designed and synthesized. These molecules exhibit strong absorption in the 500−700 nm region and exhibit up-shifted LUMO energy levels, which facilitate cascading energy alignment and enhanced VOC in ternary devices. Notably, they exhibit intrinsically high melting points (Tm) of 312.1 °C (i-DA) and 344.9 °C (i-EA) with large melting enthalpies (ΔHm of 50.02 and 95.61 J g−1), reflecting strong intermolecular cohesion. When incorporated into the PM6:Y6 as the third component, both i-DA and i-EA function as crystallization modulators that optimize the molecular packing and film morphology, leading to improved and more simultaneously balanced hole/electron mobilities. Consequently, the PM6:Y6:i-DA and PM6:Y6:i-EA ternary devices achieve promising PCEs of 19.09% and 19.35%, respectively, with simultaneously enhanced VOC, short-circuit current density (JSC), and fill factor (FF), surpassing the binary device (18.44%). Moreover, the PM6:Y6:i-DA and PM6:Y6:i-EA ternary devices exhibit significantly improved thermal stability (T80 of 840 h and 910 h) compared with the PM6:Y6 control device (T80 of 300 h). The effectiveness of these two molecules is further validated in the D18:L8-BO system, realizing excellent PCEs of 20.33% and 20.50% with i-DA- and i-EA-based ternary devices, respectively. This work demonstrates that high Tm, backbone-twisted small molecular acceptors represent a potential strategy for simultaneously optimizing morphology and charge transport toward high-performance and stable ternary OSCs.

Original languageEnglish
Pages (from-to)51071-51082
Number of pages12
JournalACS Applied Materials and Interfaces
Volume18
Issue number37
DOIs
Publication statusPublished - 23 Sept 2026
Externally publishedYes

Keywords

  • backbone-twisted small molecules
  • long-term stability
  • organic solar cells
  • power conversion efficiency
  • ternary solar cells

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