Exploring the Impact of Structural Modifications of Phenothiazine-Based Novel Compounds for Organic Solar Cells: DFT Investigations.

This paper explores a novel group of D-π-A configurations that has been specifically created for organic solar cell applications. In these material compounds, the phenothiazine, the furan, and two derivatives of the thienyl-fused IC group act as the donor, the π-conjugated spacer, and the end-group acceptors, respectively. We assess the impact of substituents by introducing bromine atoms at two potential substitution sites on each end-group acceptor (EG1 and EG2). With the donor and π-bridge held constant, we have employed density functional theory and time-dependent DFT simulations to explore the photophysical and optoelectronic properties of tailored compounds (M1-M6). We have demonstrated how structural modifications influence the optoelectronic properties of materials for organic solar cells. Moreover, all proposed compounds exhibit a greater V exceeding 1.5 V, a suitable HOMO-LUMO energy gap (2.14-2.30 eV), and higher dipole moments (9.23-10.90 D). Various decisive key factors that are crucial for exploring the properties of tailored compounds-frontier molecular orbitals, transition density matrix, electrostatic potential, open-circuit voltage, maximum absorption, reduced density gradient, and charge transfer length (D)-were also explored. Our analysis delivers profound insights into the design principles of optimizing the performance of organic solar cell applications based on halogenated material compounds.