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

We evaluate the fullerene C-60 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-60 dyads, showing that all systems studied are thermodynamically favorable. The C-60 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 k for Q bands (673 nm) than those with TPP (568 nm). AlTPP-C-60 and ZnTPP-C-60 show a more favorable electron injection to TiO2 than the analogs Pcs, and the regeneration of the dye is preferred in AlTPP-C-60 and AlPc-C-60. Zero-bias conductance is computed (10(-4)-10(-7) G(0)) for the dyads using molecular junctions with Au(1 1 1)-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-60 (10(-7) A), ZnTPP-C-60 (10(-7) A), and AlPc-C-60 (10(-8) 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-60 dyads are an excellent alternative for designing new materials for dye-sensitized solar cells or optoelectronic devices. (C) 2021 Elsevier B.V. All rights reserved.