Optically induced transport through semiconductor-based molecular electronics

• Published in: The Journal of chemical physics Vol. 142; no. 15; p. 154111
• Main Authors: Li, Guangqi, Fainberg, Boris D., Seideman, Tamar
• Format: Journal Article
• Language: English
• Published: United States American Institute of Physics 21.04.2015
• Subjects: Coupling (molecular); Current carriers; Dipole interactions; Electrodes; Markov processes; Molecular electronics; Perturbation theory; Photons
• ISSN: 0021-9606; 1089-7690; 1089-7690
• DOI: 10.1063/1.4917029

A tight binding model is used to investigate photoinduced tunneling current through a molecular bridge coupled to two semiconductor electrodes. A quantum master equation is developed within a non-Markovian theory based on second-order perturbation theory with respect to the molecule-semiconductor electrode coupling. The spectral functions are generated using a one dimensional alternating bond model, and the coupling between the molecule and the electrodes is expressed through a corresponding correlation function. Since the molecular bridge orbitals are inside the bandgap between the conduction and valence bands, charge carrier tunneling is inhibited in the dark. Subject to the dipole interaction with the laser field, virtual molecular states are generated via the absorption and emission of photons, and new tunneling channels open. Interesting phenomena arising from memory are noted. Such a phenomenon could serve as a switch.