Multiple-Asymmetric Molecular Engineering Enables Regioregular Selenium-Substituted Acceptor with High Efficiency and
Can Yang1, Yuan Gao2, Heng Zhang1
1Key Laboratory of Cluster Science of Ministry of Education, Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, 100081, China.
Abstract:
Asymmetric molecular engineering is utilized for developing efficient small molecular acceptors (SMAs), whereas adopting multiple asymmetric strategies at the terminals, side chains, and cores of efficient SMAs remains a challenge, and effects on reducing energy loss (Eloss) have been rarely investigation. Herein, four regioregular multiple-asymmetric SMAs (DASe-4F, DASe-4Cl, TASe-2Cl2F, and TASe-2F2Cl) are constructed by delicately manipulating the number and position of F and Cl on end groups. Triple-asymmetric TASe-2F2Cl not only exhibits a unique and most compact 3D network crystal stacking structure but also possesses excellent crystallinity and electron mobility in neat film. Surprisingly, the PM1:TASe-2F2Cl-based binary organic solar cells (OSCs) yield a champion power conversion efficiencies (PCEs) of 19.32%, surpassing the PCE of 18.27%, 17.25%, and 16.30% for DASe-4F, DASe-4Cl, and TASe-2Cl2F-based devices, which attributed to the optimized blend morphology with proper phase separation and more ordered intermolecular stacking and excellent charge transport. Notably, the champion PCE of 19.32% with ultralow nonradiative recombination energy loss (ΔE3) of 0.179 eV marks a record-breaking result for selenium-containing SMAs in binary OSCs. Our innovative multiple-asymmetric molecular engineering of precisely modulating the number and position of fluorinated/chlorinated end groups is an effective strategy for obtaining highly-efficient and minimal ΔE3 of selenium-substituted SMAs-based binary OSCs simultaneously.
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