Charge Transfer in Self-Assembled Fullerene-Tetraphenylporphyrin Non-Covalent Multilayer

Abstract

Self-assembly of organic molecules is a promising method for generating multilayer systems for fabrication of functional devices. In particular, fullerene (C60) and porphyrin molecules offer a variety of binding modes, including π–π interactions, dipole electrostatic attraction, and hydrogen bonding, to tailor the charge separation and charge recombination limiting device performance. Here, we investigate multilayer systems obtained by the sequential physical vapor deposition of C60 and tetraphenylporphyrin (H2TPP) layers, focusing on the effect of the interfaces on the charge transfer processes. Absorbance spectra indicate noncovalent-like π-stacking, with the increment of fullerene interfaces shifting the porphyrin Soret band toward the blue. Similarly, surface photovoltage measurements in the multilayer systems show that as the number of interfaces increases, so does the photogeneration of charge. Charge separation follows carrier generation given that the recombination time, associated to trap states, decreases. This behavior indicates that the Donor-Acceptor nature of the fullerene-porphyrin bilayer system is conserved, and even enhanced in the multilayer film, and that the number of interfaces aids to the formation of selective paths for charge carrier collection, demonstrating its potential in optoelectronic devices.