In-Silico Design of a Donor–Antenna–Acceptor Supramolecular Complex for Photoinduced Charge Separation

Abstract

We investigate via density functional theory a series of donor–antenna–acceptor molecular rectifiers designed as modules for artificial photosynthesis devices. We consider triad modules containing phenothiazine (PTZ) as the electron donor and different derivatives of naphthalene diimide (NDI) as the antenna and secondary electron acceptor. The choice of the molecular components in the triad is guided by the redox and optical properties of each subunit. Using time-dependent DFT in combination with the long-range corrected xc-functional CAM-B3LYP we investigate how photoinduced charge transfer states are affected by systematic modifications of the triad molecular structure. In particular, we show how by controlling the length of the molecular bridges connecting the different charge separator subunits it is possible to control the driving force for the relaxation of the excitonic state into the full charge-separated state. On the basis of these findings we propose a supramolecular triad consisting of inexpensive and readily available molecular components that can find its implementation in artificial devices for solar energy transduction.