Journal
ADVANCED FUNCTIONAL MATERIALS
Volume -, Issue -, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202312545
Keywords
electron-deficient; molecular rigidity and planarity; non-covalent intramolecular interactions; polymer donors; ternary polymerization
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Ternary polymerization is a feasible method to optimize the properties of polymer matrix. By introducing the DDT unit as the third component, two terpolymer donors, L1 and L2, with deeper energy levels, enhanced molecular rigidity, and planarity are developed. The L1-based polymer solar cells blended with L8-BO exhibit well-defined nanofibrous morphology, face-on orientation, and record power conversion efficiency of up to 18.75%.
Ternary polymerization are demonstrated as a feasible and successful method of optimizing absorption, energy level, and crystallinity by maintaining the excellent properties of a polymer matrix. However, the third unit inevitably interrupts the periodic sequence distribution of the ordering packing of conjugated backbones, and thus balancing the trade-off between the advantages of the third component and the disruption caused by the nonperiodic sequence distribution remains a great challenge. Herein, two terpolymer donors L1 and L2 are developed by introducing diethyl-5,5 '-dibromo-4,4 '-bis(2-ethylhexyl)-[2,2 ':5 ',2 ''-terthiophene]-3 ',4 '-dicarboxylate (DDT) unit as the third component. Owing to the electron-deficient ability and S center dot center dot center dot O non-covalent intramolecular interactions of DDT, terpolymers L1 and L2 displays deeper energy levels, enhanced molecular rigidity, and planarity than PM6. After blending with L8-BO, the L1-based polymer solar cells exhibit well miscibility with L8-BO, leading to a more well-defined nanofibrous morphology, face-on orientation, and a slight energy loss in the blend films. As a result, the optimized L1:L8-BO-based device achieves a record power conversion efficiency (PCE) as high as 18.75%. This work provides a feasible strategy to develop high-performance polymer donors via utilizing S center dot center dot center dot O non-covalent intramolecular interactions to improve the planarity of polymer donors. Two terpolymer donors L1 and L2 are developed by combined esterylthiophene-based DDT unit as the third component to polymer matrix PM6. Thanks to the S center dot center dot center dot O non-covalent intramolecular interactions of DDT unit, the L1:L8-BO-based device exhibit well-defined nanofibrous morphology and preference face-on orientation, yielding a record power conversion efficiency of up to 18.75%.image
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