A Non-fullerene Acceptor with Enhanced Intermolecular π-Core Interaction for High-Performance Organic Solar Cells

Abstract

Understanding the molecular structure and self-assembly of thiadiazole-derived non-fullerene acceptors (NFAs) is very critical for elucidating the origin of their extraordinary charge generation and transport properties that enable high power conversion efficiencies to be achieved in these systems. A comprehensive crystallographic study on a state-of-the-art NFA, Y6, and its selenium analog, <b>CH1007</b>, has been conducted which revealed that the <i>face-to-face</i> π-core interaction induced by benzo[2,1,3]thiadiazole S-N-containing moieties plays a significant role in governing the molecular geometries and unique packing of Y6 and <b>CH1007</b> to ensure their superior charge-transport properties. Moreover, benefitting from the red-shifted optical absorption via selenium substitution, photovoltaic devices based on a PM6:<b>CH1007</b>:PC₇₁BM ternary blend delivered an exceptionally high short-circuit current of 27.48 mA/cm² and a power conversion efficiency of 17.08%.