It has been a challenge to achieve
deoxyribonucleic acid (DNA)
metallization and mass production with a high quality. The main aim
of this study was to develop a large-scale production method of metal-ion-coated
DNA hybrid fibers, which can be useful for the development of physical
devices and sensors. Cetyltrimethylammonium-chloride-modified DNA
molecules (CDNA) coated with metal ions through self-metallization
exhibit enhanced optical and magnetic properties and thermal stability.
In this paper, we present a simple synthesis route for Cu2+-coated CDNA hybrid fibers through ion exchange followed by self-metallization
and analyze their structural and chemical composition (by X-ray diffraction
(XRD), high-resolution field emission transmission electron microscopy
(FETEM), and energy-dispersive X-ray spectroscopy (EDS)) and optical
(by ultraviolet (UV)–visible absorption, Fourier transform
infrared (FTIR), and X-ray photoelectron spectroscopies (XPS)), magnetic
(by vibrating-sample magnetometry), and thermal (by a thermogravimetric
analysis) characteristics. The XRD patterns, high-resolution FETEM
images, and selected-area electron diffraction patterns confirmed
the triclinic structure of Cu2+ in CDNA. The EDS results
revealed the formation of Cu2+-coated CDNA fibers with
a homogeneous distribution of Cu2+. The UV–vis,
FTIR, and XPS spectra showed the electronic transition, interaction,
and energy transfer between CDNA and Cu2+, respectively.
The Cu2+-coated CDNA fibers exhibited a ferromagnetic nature
owing to the presence of Cu2+. The magnetization of the
Cu2+-coated CDNA fibers increased with the concentration
of Cu2+ and decreased with the increase in temperature.
Endothermic (absorbed heat) and exothermic (released heat) peaks in
the differential thermal analysis curve were observed owing to the
interaction of Cu2+ with the phosphate backbone.