Issue 13, 2012

Synthesis of vertically aligned polyaniline (PANI) nanofibers, nanotubes on APTMS monolayer and their field emission characteristics

Abstract

Growth of aligned polyaniline (PANI) nanostructures on silicon modified with amino-silane self-assembled (3-aminopropyl)trimethoxysilane (APTMS) monolayer has been carried out by chemical polymerization in the presence of strong (HCl) and weak (CH3COOH) acids as dopant. Self assembly of aniline monomer leading to formation of aligned nanostructures on the APTMS monolayer is due to the amino (–NH2) moieties acting as growth centers. Interestingly, the nature of dopant acid (strong/weak) is found to determine the resultant form of the PANI nanostructures, either as nanofibers or nanotubes. The formation of PANI nanofibers and nanotubes has been revealed by scanning and transmission electron microscopy, whereas confirmation of the conducting phase of PANI is obtained from UV-visible and FTIR analysis. A plausible explanation illustrating the growth mechanism has been presented. Field emission studies of the PANI films have been carried out in a planar diode configuration at base pressure of ∼1 × 10−8 mbar. The turn-on field required to draw an emission current of 1 nA was found to 1.6 and 2.4 V μm−1 for aligned nanofibers and nanotubes, respectively. Interestingly, both the emitters exhibit good stability of the emission current over a duration of 4 h. The ease of the synthesis route and interesting field emission characteristics indicate the aligned PANI nanofibers and nanotubes as promising materials for field emission based applications.

Graphical abstract: Synthesis of vertically aligned polyaniline (PANI) nanofibers, nanotubes on APTMS monolayer and their field emission characteristics

Article information

Article type
Paper
Submitted
13 Dec 2011
Accepted
06 Apr 2012
First published
11 Apr 2012

RSC Adv., 2012,2, 5822-5827

Synthesis of vertically aligned polyaniline (PANI) nanofibers, nanotubes on APTMS monolayer and their field emission characteristics

S. S. Patil, S. P. Koiry, P. Veerender, D. K. Aswal, S. K. Gupta, D. S. Joag and M. A. More, RSC Adv., 2012, 2, 5822 DOI: 10.1039/C2RA01294D

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