Fluorine/bromine/selenium multi-heteroatoms substituted dual-asymmetric electron acceptors for o-xylene processed organic solar cells with 19.12% efficiency
摘要
The development of high-performance near-infrared (NIR) absorbing electron acceptors is a major challenge in achieving high short-circuit current density (JSC) to increase power conversion efficiency (PCE) of organic solar cells (OSCs). Herein, three new multi-heteroatomized Y-series acceptors (bi-asy-Y-Br, bi-asy-Y-FBr, and bi-asy-Y-FBrF) were developed by combining dual-asymmetric selenium-fused core and brominated end-groups with different numbers of fluorine substitutions. With gradually increasing fluorination, three acceptors exhibit red-shift absorption. Among them, bi-asy-Y-FBrF presents planar molecular geometry, the maximum average electrostatic potential, and the minimum molecular dipole moment, which are conducive to intramolecular packing and charge transport. Moreover, D18:bi-asy-Y-FBrF active layer presents higher crystallinity, more suitable phase separation, and reduced charge recombination compared to D18:bi-asy-Y-Br and D18:bi-asy-Y-FBr blends. Consequently, among theses binary OSCs, D18:bi-asy-Y-FBrF device achieves a higher PCE of 15.74% with an enhanced JSC of 26.28 mA cm−2, while D18:bi-asy-Y-Br device obtains a moderate PCE of 15.04% with the highest open-circuit voltage (VOC) of 0.926 V. Inspired by its high VOC and complementary absorption with NIR-absorbing BTP-eC9 as acceptor, bi-asy-Y-Br is introduced into binary D18:BTP-eC9 to construct ternary OSCs, achieving a further boosted PCE of 19.12%, which is among the top values for the reported green solvent processed OSCs.