IOP PUBLISHING NANOTECHNOLOGY
Nanotechnology 18 (2007) 405706 (5pp) doi:10.1088/0957-4484/18/40/405706
A Raman probe for selective wrapping of
single-walled carbon nanotubes by DNA
Quan-Hong Yang
1,2,7
, Nittaya Gale
3
, Claudio J Oton
2
, Feng Li
4
,
Alun Vaughan
5
, Riichiro Saito
6
, Iris S Nandhakumar
3
,
Zhi-Yuan Tang
1
, Hui-Ming Cheng
4
, Tom Brown
3
and Wei H Loh
2
1
School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072,
People’s Republic of China
2
Optoelectronics Research Centre, The University of Southampton, Southampton SO17 1BJ,
UK
3
School of Chemistry, The University of Southampton, Southampton SO17 1BJ, UK
4
Shenyang National Laboratory for Materials Science, Institute of Metal Research,
Chinese Academy of Sciences, Shenyang 100016, People’s Republic of China
5
School of Electronics and Computer Science, The University of Southampton, Southampton
SO17 1BJ, UK
6
Department of Physics, Tohoku University and CREST, JST, Sendai 980-8578, Japan
E-mail: qhyangcn@tju.edu.cn
Received 13 June 2007, in final form 6 August 2007
Published 20 September 2007
Online at stacks.iop.org/Nano/18/405706
Abstract
In this paper, we discuss nanotube diameter selectivity in DNA wrapping of
single-walled carbon nanotubes (SWNTs) under high-shear sonication and
present Raman evidence for the selective wrapping. The DNA wrapping
induces an upshift (an increase in wavenumber) of the radial breathing mode
(RBM) bands in the Raman spectra of SWNTs, which indicates strong
interaction between nanotubes and DNA. The extent of the upshift correlates
well with the change in the intensity of the RBM bands upon DNA wrapping,
and larger upshifts correspond to larger intensity changes. The intensity
changes represent wrapping selectivity, and differ from tube to tube due to
varying diameters and electronic properties. The shift of the RBM bands thus
represents a practical probe for wrapping selectivity and the extent of the
shifts indicates different electronic structures of core nanotubes hybridized
with DNA.
S Supplementary data are available from stacks.iop.org/Nano/18/405706
(Some figures in this article are in colour only in the electronic version)
1. Introduction
Considerable progress has been made in the study of
complexes between single-walled carbon nanotubes (SWNTs)
and DNA [1–5], with the aim of developing applications
in the field of detection of DNA [2, 3] and structure-based
sorting of SWNTs [4, 5]. The hybridization of SWNTs with
single-stranded DNA (ss-DNA) was recently achieved through
noncovalent aromatic interactions between nucleobases and
nanotube sidewalls [4–8]. During high-shear sonication,
ss-DNA forms a stable complex with individual SWNTs
7
Author to whom any correspondence should be addressed.
(SWNT–DNA hybrid) as a result of helical wrapping of the
macromolecule around the SWNTs. In this process, most
of bundled nanotubes are isolated into individual entities and
the SWNT–DNA hybrid becomes uniformly dispersible in
aqueous solutions. The ease of formation of stable SWNT–
DNA hybrids has motivated intensive investigations into both
the fundamental properties of such systems and their potential
use in applications such as gas sensors [9], biosensors [10],
liquid-crystals [11], drug delivery vehicles [12] and electronic
switches [13]. However, many fundamental issues still have
to be addressed before we are fully able to understand and
characterize the DNA wrapping process of SWNTs. One such
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