Abstract
Optoelectronic properties of triphenylamine dyes arising from the embedded five-membered π-linkers C
4
H
4
X (X = O, NH, S, Se, Te) and varying anchoring groups, cyanoacrylic acid and hydantoin, in D-π-π-A model are examined. The reported properties for both, isolated dyes and dye@TiO
2
complexes, are realized through density functional theory (DFT) and time-dependent DFT. The study reveals that chalcogen doping (X = S, Se, Te) enhances absorption and fluorescent emission spectra in the visible and NIR regions. The adsorption of the dyes on the TiO
2
cluster has been simulated. Alteration of the UV-Vis spectra and electron density redistribution for the complexes from individual dyes are examined and analyzed. The binding energies relate to the nature of the heteroatoms X; the complexes dye@TiO
2
with heavier heteroatoms Se and Te demonstrate stronger binding.
Graphical abstract