Single-molecule transistors incorporating trimetal molecules of Cu(3)(dpa)(4)Cl(2) and Ni(3)(dpa)(4)Cl(2) (dpa = 2,2'-dipyridylamide) have been fabricated. Conductance is measured as a function of bias and gate voltages at low temperature, showing single-electron tunneling behavior through the molecules. Additional structures corresponding to the excitations in the molecules are observed, which can be attributed to intramolecular vibrational excitations coupled to the electron tunneling processes. The energies of the vibrational states are dependent on the redox state of the included molecules.

We have fabricated single-electron transistors by alkanedithiol molecular self-assembly. The devices consist of spontaneously formed ultrasmall Au nanoparticles linked by alkanedithiols to nanometer-spaced Au electrodes created by electromigration. The devices reproducibly exhibit addition energies of a few hundred meV, which enables the observation of single-electron tunneling at room temperature. At low temperatures, tunneling through discrete energy levels in the Au nanoparticles is observed, which is accompanied by the excitations of molecular vibrations at large bias voltage.

Precise graphene patterning is of critical importance for tailor-made and sophisticated two-dimensional nanoelectronic and optical devices. However, graphene-based heterostructures have been grown by delicate multistep chemical vapor deposition methods, limiting preparation of versatile heterostructures. Here, we report one-pot synthesis of graphene/amorphous carbon (a-C) heterostructures from a solid source of polystyrene via selective photo-cross-linking process. Graphene is successfully grown from neat polystyrene regions, while patterned cross-linked polystyrene regions turn into a-C because of a large difference in their thermal stability. Since the electrical resistance of a-C is at least 2 orders of magnitude higher than that for graphene, the charge transport in graphene/a-C heterostructure occurs through the graphene region. Measurement of the quantum Hall effect in graphene/a-C lateral heterostructures clearly confirms the reliable quality of graphene and well-defined graphene/a-C interface. The direct synthesis of patterned graphene from polymer pattern could be further exploited to prepare versatile heterostructures.