4.8 Article

Dual-Additive-Driven Morphology Optimization for Solvent-Annealing-Free All-Small-Molecule Organic Solar Cells

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume -, Issue -, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202303307

Keywords

all-small-molecule organic solar cells; capacitance spectroscopy; femtosecond transient absorption spectroscopy; x-ray scattering

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This study develops a dual-additive-driven morphology optimization method for all-small-molecule organic solar cells (ASM-OSCs). By incorporating 1,4-diiodobenzene (DIB) and diiodomethane (DIM) as additives, the intermolecular interactions and acceptor phase separation can be modulated, while the over-aggregation of the donor is suppressed. The optimized ASM-OSC device achieves a power conversion efficiency (PCE) of 15.2%, one of the highest PCE reported for binary ASM-OSCs without solvent annealing treatment. This work demonstrates the potential of morphology tuning via the incorporation of dual additives into ASM-OSCs, enabling comparable efficiencies to those of conventional polymer/small-molecule based OSCs.
All-small-molecule organic solar cells (ASM-OSCs), which consist of small-molecule donors and acceptors, have recently been studied extensively to eliminate the batch-to-batch variation from polymer-based donor or acceptor. On the other hand, the control of their active layer morphology is more challenging due to the similar chemical structure and miscibility of small-molecule donor and small-molecule accepter. Hence, this study develops a dual-additive-driven morphology optimization method for ASM-OSCs based on BTR-Cl:Y6. One solid additive - 1,4-diiodobenzene (DIB) and one liquid additive - diiodomethane (DIM) are selected, making use of their distinct interaction mechanisms with Y6 and BTR-Cl. It is found that DIB can form a eutectic phase with Y6, which can increase the intermolecular interactions and modulate the acceptor phase separation, while the simultaneous volatilization of DIM suppresses the over-aggregation of BTR-Cl during the film casting process. As a result of the synergistic morphology tuning, the optimized device delivers a power conversion efficiency (PCE) as high as 15.2%, among the highest PCE reported to date for binary ASM-OSCs without solvent annealing treatment. This work demonstrates the potential of morphology tuning via the incorporation of dual additives into ASM-OSCs, enabling them to achieve comparable efficiencies to those of conventional polymer/small-molecule based OSCs.

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