Dimerized Acceptors with Conjugate‐Break Linker Enable Highly Efficient and Mechanically Robust Organic Solar Cells

Abstract Designing new acceptors is critical for intrinsically stretchable organic solar cells (IS‐OSCs) with high efficiency and mechanical robustness. However, nearly all stretchable polymer acceptors exhibit limited efficiency and high‐performance small molecular acceptors are very brittle. In this regard, we select thienylene‐alkane‐thienylene (TAT) as the conjugate‐break linker and synthesize four dimerized acceptors by the regulation of connecting sites and halogen substitutions. It is found that the connecting sites and halogen substitutions considerably impact the overall electronic structures, aggregation behaviors, and charge transport properties. Benefiting from the optimization of the molecular structure, the dimerized acceptor exhibits rational phase separation within the blend films, which significantly facilitates exciton dissociation while effectively suppressing charge recombination processes. Consequently, FDY‐m‐TAT‐based rigid OSCs render the highest power conversion efficiency (PCE) of 18.07 % among reported acceptors containing conjugate‐break linker. Most importantly, FDY‐m‐TAT‐based IS‐OSCs achieve high PCE (14.29 %) and remarkable stretchability (crack‐onset strain COS=18.23 %), significantly surpassing Y6‐based counterpart (PCE=12.80 % and COS=8.50 %). To sum up, these findings demonstrate that dimerized acceptors containing conjugate‐break linkers have immense potential in developing highly efficient and mechanically robust OSCs.