Effect of the Selective Halogenation of Small Molecule Acceptors on the Blend Morphology and Voltage Loss of High‐Performance Solar Cells

Abstract

AbstractHerein, the impacts of the selective halogenation at two different positions of dicyanomethylene‐3‐indanone (IC) end groups and inner side chains of small molecular acceptors (SMAs) on the PD:SMA interfacial interactions, blend morphology, and resulting photovoltaic properties are described. In this study, four different SMAs (A1, A2, A3, and A4) with the same molecular backbone, but with different degrees of halogenation, are synthesized. The IC end groups on the backbones of the A1 and A3, and A2 and A4 SMAs are chlorinated and fluorinated, respectively; in addition, 6‐phenoxyhexyl inner side chains of the A3 and A4 are chlorinated. The SMAs are paired with a chlorinated PBDT‐Cl PD to construct organic solar cells (OSCs). The PBDT‐Cl:A4‐based OSC exhibits the highest power conversion efficiency of 17.2%, outperforming the PBDT‐Cl:A1‐(13.3%), PBDT‐Cl:A2‐(15.6%), and PBDT‐Cl:A3‐based OSC (16.5%). The Cl atoms on the side chains in the A3 and A4 SMAs enhance the molecular/energetic interactions at the PD:SMA interfaces and improve the blend morphology in terms of domain purity and spacing. These effects lead to the improved fill factors and reduced voltage loss of the PBDT‐Cl:A3‐ and PBDT‐Cl:A4‐based OSCs. This study demonstrates the importance of appropriate halogenation of SMAs in optimizing the blend morphology, reducing voltage loss, and improving OSC performance.