Enhanced Gating Performance of Single-Molecule Conductance by Heterocyclic Molecules

Enhancing the gating performance of single-molecule conductance is significant for realizing molecular transistors. Herein, we report a new strategy to improve the electrochemical gating efficiency of single-molecule conductance with fused molecular structures consisting of heterocyclic rings of furan, thiophene, or selenophene. One order magnitude of gating ratio is achieved within a potential window of 1.2 V for the selenophene-based molecule, which is significantly greater than that of other heterocyclic and benzene ring molecules. This is caused by the different electronic structures of heterocyclic molecules and transmission coefficients T(E), and preliminary resonance tunneling is achieved through the highest occupied molecular orbital at high potential. The current work experimentally shows that electrochemical gating performance can be significantly modulated by the alignment of the conducting orbital of the heterocyclic molecule relative to the metal Fermi energy.

Automated summary

This study presents a new strategy to improve the electrochemical gating efficiency of single-molecule conductance, achieving a significant gating ratio through fused molecular structures. The research demonstrates that electrochemical gating performance can be significantly modulated by adjusting the alignment of the conducting orbital of the heterocyclic molecule relative to the metal Fermi energy.