Quantum modelling of multi-directional fused-ring electron acceptors for organic photovoltaics

Abstract

Multi-directional fused-ring electron acceptors (FREAs) feature a fused-ring backbone that extends in multiple directions through bridging and acceptor units. This unique structural design imparts several advantageous properties, like increased light absorption, precise energy level adjustments, improved electron mobility, reduced energy loss, and enhanced efficiency in organic photovoltaic (OPV) devices. In this study, we designed seven novel multi-directional FREAs and conducted a comprehensive computational analysis using Density Functional Theory (DFT) and Time-Dependent DFT (TD-DFT). The designed molecules feature a benzotrithienopyrrole central core connected to a π-bridge acceptor, either benzothiadiazole or benzotriazole, and three varying terminal acceptors, including malononitrile, 2-(5,6-difluoro-3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile, and 2-(3-methyl-4-oxothiazolidin-2-ylidene)malononitrile. Our investigation encompassed the evaluation of geometry, frontier molecular orbitals (FMOs), optical properties, density of states (DOS), charge mobilities, dipole moment, global reactivity descriptors, molecular electrostatic potential (MEP), transition density matrix (TDM), and OPV device-related parameters. The results revealed significant potential of the designed molecules as FREAs for OPVs, thus highlighting their suitability for further experimental exploration.