The interaction between multiwalled carbon nanotubes (MWCNTs) and aqueous poly(diallyl dimethylammonium) chloride (PDDA) was studied by X-ray photoelectron (XPS) and photoacoustic Fourier transform infrared (PA-FTIR) spectroscopies. We have found that the mild sonication of MWCNTs in aqueous PDDA results in a significant improvement of CNT dispersibility and greatly enhances their adhesion to Au and Si substrates. The MWCNT-PDDA interaction is due to the presence of an unsaturated contaminant in the PDDA chain, as confirmed by both XPS and PA-FTIR, which enters into a pi-pi interaction with the CNTs. Electrostatic group repulsions of the coated CNTs then provide the dispersibility and adhesion.

Sonication has been widely used in the dispersal of carbon nanotubes (CNTs) in various liquids as well as in their functionalization in aqueous acids. Here, for the first time, we study the sonication of multiwalled CNTs (MWCNTs) in deionized water. Our results indicate an improvement in the aqueous dispersal of MWCNTs as well as an increase in their adhesive interaction with Au substrates. Field emission scanning electron and high-resolution transmission electron microscopies as well as X-ray photoelectron, photoacoustic Fourier transform IR, and Raman spectroscopies have shown this to be due to the production of low concentrations of O-containing functionalizations (alcohol, carbonyl, acid, with the total O concentration being approximately 2%), without damaging the basic CNT structure; this production of functional groups is mirrored by the disappearance of -CH(n) groups existing on the pristine CNTs. These new functional groups are capable of hydrogen bonding, which plays an important role in their aqueous dispersal and enhanced substrate interactions.

The chemical and morphological modifications of multiwalled carbon nanotubes (MWCNTs), by 2 keV Ar(+) treatment, have been followed by field emission scanning (FESEM) and high-resolution transmission (HRTEM) electron microscopies and by X-ray photoelectron (XPS) and Raman spectroscopies. Morphological changes were followed, both in situ and on subsequent air exposure, and the data indicate that free radical defects, initially produced under low Ar(+) treatment doses ( approximately 10(13) ions/cm(2)), act as the nuclei for the formation of localized asperities that form along the walls of the CNTs. Continued treatment results in their stublike elongation that continues with further treatment, forming extensions under heavy treatment doses. The chemical changes that occur, on reaction with air, reveal that the defects initially created are secondary C atoms, formed when a single bond breaks; further treatment breaks an additional bond to form primary C atoms; free radical fragments, lost when the third bond breaks, condense on the free radical defects to form the asperities. The extent of primary and secondary C atoms, and thus their functionalization on air exposure, may be controlled by the extent of treatment, offering a method for the controlled surface functionalization of CNTs by low-energy Ar(+) treatment.