Bicomponent Random Approach for the Synthesis of Donor Polymers for Efficient All-Polymer Solar Cells Processed from...

All-polymer solar cells (all-PSCs) can offer unique merits of high morphological stability to thermal and mechanical stress. To realize their full potential as flexible or wearable devices, it is highly desirable that the all-PSCs can be fabricated from a green solvent with simple post-treatment to avoid thermal annealing on the flexible substrate. This posed a severe challenge on material design to tune their properties with suitable solubility, aggregation, and morphology. To address this challenge, here, a simple bicomponent random approach on a D-A-type polymer donor was developed by just varying the D-A molar ratio. Under this approach, a series of new random polymers PBDT-TPD with different molar ratios of the D component of 2D-benzo[1,2-b:4,5-b']dithiophene (BDT) and A component of thieno[3,4-c]pyrrole-4,6-dione (TPD) were designed and synthesized. The energy levels, light absorption, solubility, and packing structure of random donors PBDT-TPD were found to vary substantially with the various D-A molar ratios. The devices based on PBDT-TPD/P(NDI2HD-T) were fabricated to explore the synergistic effects of the processing solvent and composition of D-A-type random polymers. The results show that nanoscale morphology, balanced miscibility/crystallinity of blend, and photovoltaic properties could be rationally optimized by tuning the composition of random donors. As a result, as-cast all-PSC-based optimal donor PBDT₅-TPD₄ achieves the best power conversion efficiency (PCE) of 8.20% processed from a green solvent, which performs better than that the reference polymer (PCE: 6.41%). This efficiency is the highest value for all-PSCs from BDT-TPD-based donors. Moreover, the optimized devices were relatively insensitive to the thickness of the active layer and exhibited good stability.