Issue 3, 2015

Silicon-pyrene/perylene hybrids as molecular rectifiers

Abstract

We have synthesized two alkenyl (C-6 and C-11 chains) pyrenes and one alkenyl (C-11 chain) perylene as the σ–π systems, which were electro-grafted on H-terminated Si surfaces to form the respective monolayers. The IV characteristics of the monolayers revealed pronounced rectification in forward bias with a maximum rectification ratio (RR) of 2.5 × 105 at 2.5 V for the C-6-pyrene 4b, 1000 at 1.5 V for the C-11-pyrene 4a and 3000–5000 at 1.75 V for the C-11-perylene 3. The higher RR of the devices containing 4b compared to those of 4a and 3 is possibly due to better alignment and packing of the 4b-monolayers on the Si substrate. The rectification was explained using the ab initio molecular-orbital calculations.

Graphical abstract: Silicon-pyrene/perylene hybrids as molecular rectifiers

Supplementary files

Article information

Article type
Paper
Submitted
09 Sep 2014
Accepted
18 Nov 2014
First published
26 Nov 2014

Phys. Chem. Chem. Phys., 2015,17, 1891-1899

Author version available

Silicon-pyrene/perylene hybrids as molecular rectifiers

K. Garg, C. Majumder, S. K. Nayak, D. K. Aswal, S. K. Gupta and S. Chattopadhyay, Phys. Chem. Chem. Phys., 2015, 17, 1891 DOI: 10.1039/C4CP04044A

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