Single-Molecule Charge Transport and Electrochemical Gating in Redox-Active Perylene Diimide Junctions

A series of redox-active perylene tetracarboxylic diimide (PTCDI) derivatives have been synthesized and studied by electrochemical cyclic voltammetry and electrochemical scanning tunnelling microscopy break junction techniques. These PTCDI molecules feature the substitution of pyrrolidine at the bay (1,7-) position of perylene and are named pyrrolidine-PTCDIs. These moieties exhibit a small bandgap (2.1 eV) compared with the “normal” (unsubstituted) PTCDI molecule (2.5 eV). Pyrrolidine-PTCDIs were functionalized with different anchoring groups (thiol, amine, pyridine) for building metal−molecule−metal (m−M−m) junctions. The single-molecule conductance values of pyrrolidinePTCDIs have been determined by analyzing a large number of molecular (m−M−m) junctions created between an STM tip and substrate using a statistical method. Furthermore, we studied the gate dependence of the single-molecule conductance by trapping a molecule between the two electrodes and recording the current as a function of electrochemical gate potential. The experimentally determined conductance values for these bay-substituted pyrrolidine-PTCDI molecules are about twice as much as the unsubstituted PTCDI molecules. The present work shows that single-molecule conductance can be tuned by the bandgap of a molecular system without significantly altering the conductance pathway.