Iron(II) complexes bearing N-heterocyclic carbene (NHC) ligands have emerged as promising earth-abundant dye sensitizers for applications in dye-sensitized solar cells (DSSCs). In this work, we present a computational study of a set of 42 Fe–NHC dyes derived from seven ligand frameworks, systematically functionalized with donor, acceptor, and donor–acceptor groups to tune or enhance their photophysical properties. The calculated geometries reveal that substitution modulates Fe–N bond lengths and ligand dihedral angles only slightly, preserving the structural integrity of the complexes. TD-DFT calculations show clear and predictable electronic trends: donor groups raise the HOMO, acceptor groups lower the LUMO, and the combined push–pull configuration produces the most pronounced HOMO–LUMO gap narrowing and largest redshifts in MLCT transitions. Key DSSC performance descriptors, including electron-injection and dye-regeneration free energies, light-harvesting efficiency, excited-state lifetimes, and hole-transport reorganization energies, collectively identify the double-acceptor and push–pull derivatives as the most promising candidates across multiple frameworks.
Helal et al. (2026) studied this question.