Abstract
A fullerene derivative with five hydroxyphenyl groups attached around a pentagon, (4-HOC6H4)5HC60 (1), has shown an asymmetric current-voltage (I-V) curve in a conducting atomic force microscopy experiment on gold. Such molecular rectification has been ascribed to the asymmetric distribution of frontier molecular orbitals over its shuttlecock-shaped structure. Our nonequilibrium Green's function (NEGF) calculations based on density functional theory (DFT) indeed exhibit an asymmetric I-V curve for 1 standing up between two Au(111) electrodes, but the resulting rectification ratio (RR ∼ 3) is insufficient to explain the wide range of RR observed in experiments performed under a high bias voltage. Therefore, we formulate a hypothesis that high RR (>10) may come from molecular orientation switching induced by a strong electric field applied between two electrodes. Indeed, molecular dynamics simulations of a self-assembled monolayer of 1 on Au(111) show that the orientation of 1 can be switched between standing-up and lying-on-the-side configurations in a manner to align its molecular dipole moment with the direction of the applied electric field. The DFT-NEGF calculations taking into account such field-induced reorientation between up and side configurations indeed yield RR of ∼13, which agrees well with the experimental value obtained under a high bias voltage.
| Original language | English |
|---|---|
| Pages (from-to) | 4061-4066 |
| Number of pages | 6 |
| Journal | Nano Letters |
| Volume | 17 |
| Issue number | 7 |
| DOIs | |
| State | Published - 12 Jul 2017 |
Bibliographical note
Publisher Copyright:© 2017 American Chemical Society.
Keywords
- E-field-induced orientation switching
- Molecular rectifier
- asymmetric I-V curve
- density functional theory
- molecular dynamics simulation
- nonequilibrium Green's function formalism
- self-assembled monolayer