Modification of the N-methyl-4,5-diazacarbazole D-π-A with a π-conjugated bridge to enhance excited-state properties for superior utilization in green energy applications: A theoretical approach

Abstract

In organic photovoltaic technology, tailoring the acceptor or donor unit to enhance intramolecular charge transfer is a well-known approach, however, the effect of modifying conjugated bridge units is an underdeveloped phenomenon. In this study, this approach has been focused, where a series of conjugated bridges including, a) electron-excessive heterocycles, b) electron-deficient heterocycles, and c) short-chain unsaturated hydrocarbons have been substituted from thiophene bridge-containing D-π-A; N-methyl-4,5-diazacarbazole (donor) and bay-annulated indigo (acceptor) molecule. This quantum chemical study aims to investigate the effect of various types of π-conjugated bridges on the electronic structure and solar cell activity of already reported material. The selected π-conjugated bridges include electron-excessive (furan, pyrrole, & thiophene) and electro-deficient (diazine, tetrazine, & pyridine) heterocycles, and short-chain hydrocarbons (ethylene & ethyne). The optimized structural parameters e.g., dihedral angles (θ), distortion energies (Edis), & bond distances (d), and electronic behaviour i.e., Frontier Molecular Orbitals (FMO), Electrostatic Potentials (ESP), Density of States (DOS) spectra, dipole moments (μ), and absorption spectra of the hypothetically designed molecules are estimated using density functional theory calculations. The solar cell proficiency is investigated with transition dipole moment (μT), reorganization energy (RE), Transition density matrix (TDM), exciton binding energy (Eb), and open circuit voltage (Voc). Our finding encompassed that our designed D-π-A molecules show significant improvement in their electronic behaviour, especially when the thiophene bridge of the reference molecule is substituted with the excess electron heterocycles, especially pyrrole. The HOMO-LUMO gap of this particular molecule (MPy) is reduced to 2.07 eV, resulting in the significant charge transfer between donor and acceptor units (0.15 e-). Moreover, the results of RE, TDM, Eb, and Voc also support the high solar cell efficiency of pyrrole-containing molecules.