New photoluminescent carbon dots with intriguing photoluminescent properties were prepared from carboxylated carbon nanoparticles via covalent bonding of p-phenylenediamine oligomers.

Donor-acceptor molecules (D-π-A) built by connecting a diphenylhydrazone block to a dicyanovinyl acceptor group via various thiophene-based π-conjugating spacers (1-5) were synthesized from mono- or dialdehydes by a simple metal-free procedure. Cyclic voltammetry and UV/Vis absorption spectroscopy show that the extension and/or increase of the donor strength of the spacer produces a decrease of the HOMO and LUMO energy level, a red shift of the absorption spectrum and an increase of the molecular absorption coefficient. Compared to solutions, the optical spectra of spin-cast thin films of compounds 1-3 show a broadening and red shift of the absorption bands, consistent with the formation of J-aggregates. In contrast the blue shift observed for the EDOT-containing compounds 4 and 5 suggests the presence of H-aggregates. Solution-cast and vacuum-deposited films of donors 1-5 were evaluated in solar cells with fullerene C60 as acceptor. A power-conversion efficiency among the highest reported for bilayer devices of basic configuration was obtained with compound 2. On the other hand, the results obtained with 4 and 5 suggest that the presence of EDOT in the structure can have deleterious effects on the organization and performances of the donor material.