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Shuttlecock-Shaped Molecular Rectifier: Asymmetric Electron Transport Coupled with Controlled Molecular Motion
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Title
Shuttlecock-Shaped Molecular Rectifier: Asymmetric Electron Transport Coupled with Controlled Molecular Motion
Issued Date
2017-07
Citation
Ryu, Taek Hee. (2017-07). Shuttlecock-Shaped Molecular Rectifier: Asymmetric Electron Transport Coupled with Controlled Molecular Motion. Nano Letters, 17(7), 4061–4066. doi: 10.1021/acs.nanolett.7b00596
Type
Article
Author Keywords
Molecular rectifierasymmetric I-V curveE-field-induced orientation switchingself-assembled monolayerdensity functional theorynonequilibrium Green&aposs function formalismmolecular dynamics simulation
Keywords
CHARGE-TRANSPORTRECTIFICATIONMONOLAYERDYNAMICSSWITCHFIELD
ISSN
1530-6984
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. © 2017 American Chemical Society.
URI
http://hdl.handle.net/20.500.11750/5651
DOI
10.1021/acs.nanolett.7b00596
Publisher
American Chemical Society
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Jang, Yun Hee장윤희

Department of Energy Science and Engineering

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