A green route to water soluble carbon nanotubes and in situ loading of silver nanoparticles.

A green approach has been developed to synthesize water soluble multi-walled carbon nanotubes (MWNTs). Ag nanoparticles have been loaded on the as-synthesized MWNTs via the in situ solution method. The strategy is based on the introduction of hydroxyl and carboxyl groups through a mild modification of MWNTs via polycondensation of citric acid and D-sorbitol, improving the water solubility of MWNTs, giving rise to preferred sites of Ag nucleation, and providing mild in situ reducing agents. The modification of MWNTs and loading of Ag nanoparticles on MWNTs were demonstrated by Fourier transform infrared spectroscopy, thermogravimetric analysis, transmission electron microscopy, and scanning electron microscopy.

The preparation of highly water-soluble multi-walled carbon nanotubes by irreversible noncovalent functionalization with a pyrene-carrying polymer.

Multi-walled carbon nanotubes (MWNTs) have been solubilized in water via a noncovalent method of exfoliation and centrifugation cycles with the assistance of hydrolyzed poly(styrene-co-maleic anhydride) carrying pyrene (HPSMAP). After the obtained solution was micro-filtered and dried, a water-soluble complex of HPSMAP-MWNTs was obtained. The solubility of HPSMAP-MWNTs was measured to be 46.2 mg ml(-1) with a net MWNT concentration of 7.4 mg ml(-1) in water. Thermal gravimetric analyses showed that there was a large amount of polymer remaining on the surface of MWNTs irreversibly after thoroughly removing the free polymer. Other characterizations using transmission electron microscopy, Fourier transform infrared (FTIR) spectroscopy, fluorescence spectra, and fluorescence decay were conducted.

Well-defined nanoarrays from an n-type organic perylene-diimide derivative for photoconductive devices.

Well-defined one-dimensional (1D) perylene-diimide derivative (PDD) nanowire arrays were prepared via a simple electrophoretic deposition method by using anodic aluminum oxide (AAO) templates. The morphology of the as-deposited films was characterized by field emission scanning electron microscope and transmission electron microscopy. The highly ordered nanoarrays were free-standing after removing the AAO supports. Further studies revealed that the growth process of the nanowires in the AAO pores followed a 'bottom-up' growth model. A photoreceptor with PDD nanowire arrays as the charge generation layer was fabricated. It exhibited a better photoconductivity under light illumination when compared to that of its bulk counterpart. Our results suggested that electron-accepting PDD nanowire arrays can be used as a potential candidate for photoconduction devices, which would facilitate further exploration of new technological applications of the photoimaging process.