An asymmetric A-DA′D-π-A type non-fullerene acceptor for high-performance organic solar cells

Under the guidance of a symmetry-breaking and pi-bridge-extending strategy, three asymmetric and symmetric non-fullerene acceptors (L1, L2, and L3) with DA'D core units and two 2-(5,6-difluoro-3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile electron-withdrawing units (A) have been designed and synthesized via changing the alkoxy-substituted thiophene bridge unit. The asymmetric A-DA'D-pi-A-type non-fullerene acceptor (NFA) L2 displays much improved solubility and a slightly larger molar absorption coefficient than its symmetric counterparts (L1 and L3). In addition, blend film based on the asymmetric NFA L2 shows suitable nanoscale phase morphology and much higher and more balanced hole and electron mobilities. Hence, compared with L1- and L3-based organic solar cells (OSCs), optimal L2-based devices can deliver a high power-conversion efficiency (PCE) of 14.06% with simultaneously enhanced current density and fill factor values. Our study indicates that a combined symmetry-breaking and pi-bridge-extending strategy is powerful for the design of high-performance NFAs.

Automated summary

By breaking the symmetry and extending the pi-bridge, three asymmetric and symmetric non-fullerene acceptors have been designed and synthesized, with the asymmetric acceptor L2 showing improved solubility, larger molar absorption coefficient, suitable phase morphology, and higher electron mobilities, leading to enhanced power-conversion efficiency in organic solar cells.