Near-Infrared Nonfullerene Acceptors Based on 4H-Cyclopenta[1,2-b:5,4-b']dithiophene for Organic Solar Cells and Organic Field-Effect Transistors.

Abstract

The development of nonfullerene small molecular acceptors (NF-SMAs) has dominated the improvement of efficiencies for organic solar cells and the near-infrared (NIR) absorption is the primary feature of NF-SMAs compared with fullerene derivatives. In this article, a series of acceptor-donor-acceptor-structured NF-SMAs (named CPICs) containing 4H-cyclopenta[1,2-b : 5,4-b']dithiophene (CPDT) electron donor and F-substituted 2-(3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile (2FIC) as electron acceptor were designed and synthesized. With the increase of CPDT units, the elongated conjugations broadened the absorption range of the acceptors and tuned their energy levels sequentially. Therefore, their charge-transporting polarities switched from electron-only type to bipolar mode in organic field-effect transistors. Moreover, these changes also influenced the voltages, current densities, and eventual PCEs of their corresponding cells. When blending with PBDB-T, a champion efficiency of 10.01% was achieved in CPIC-2 based cells. This work demonstrated the importance of absorptions, suitable energy levels and charge transports in improving the efficiencies of organic solar cells.