| Abstract | A new dyad of fullerene/disperse-red, denoted as PCBDR, strongly absorbs visible light in the range of 400-600 nm. PCBDR showed advantages over PCBM in several aspects such as enhanced visible-light absorption, improved solubility, and the possibility to facilitate cascaded electron transfer. P3HT:PCBDR bulk heterojunction (BHJ) solar cells, nevertheless, so far have not outperformed P3HT:PCBM BHJ solar cells under similar conditions. Among factors that affect the efficiency of P3HT:PCBDR BHJ solar cells, the suppression of the interchain interaction of P3HT in the P3HT:PCBDR blend played a major role, presumably due to better interfacial miscibility between P3HT and PCBDR than that in blends of P3HT:PCBM. In contrast, benzoporphyrin (BP), due to its unique crystallinity, morphology, and nonsolubility, afforded a better control of the morphology and the interface of the p/n junctions. As a consequence, the performance of solar cells with BP/PCBDR as the active layer was comparable to that of BP/PCBM solar cells. These results suggest that a synergistic approach of synthetic design and morphological control in devices is critical to develop new electron acceptors for highly efficient organic/polymer solar cells. |
