Fullerene binding effects in Al(III)/Zn(II) Porphyrin/Phthalocyanine photophysical properties and charge transport.

We evaluate the fullerene C binding effect; through the metal (Al) and through the ligand (Pc,TPP), on the photophysical and charge transport properties of M-porphyrin(TPP)/phthalocyanine(Pc) (M = Al(III), Zn(II)). We perform density functional theory (DFT) and time-dependent DFT calculations for the macrocycle-C dyads, showing that all systems studied are thermodynamically favorable. The C binding effect on the absorption spectrum is a red-shift of the Q and Soret (B) bands of TPPs and Pcs. The Pc-dyads show longer λ for Q bands (673 nm) than those with TPP (568 nm). AlTPP-C and ZnTPP-C show a more favorable electron injection to TiO than the analogs Pcs, and the regeneration of the dye is preferred in AlTPP-C and AlPc-C. Zero-bias conductance is computed (10-10 G) for the dyads using molecular junctions with Au(111)-based electrodes. When a bias voltage of around 0.6 V up to 1 V is applied, an increase in current is obtained for AlTPP-C (10 A), ZnTPP-C (10 A), and AlPc-C (10 A). Although there is not a unique trend in the behavior of the dyads, Pcs have better photophysical properties than TPPs and the latter are better in the charge transport. We conclude that AlTPP(ZnTPP)-C dyads are an excellent alternative for designing new materials for dye-sensitized solar cells or optoelectronic devices.