Molecular dynamics simulations of carbon nanotube dispersions in water: Effects of nanotube length, diameter, chirality and surfactant structures

Abstract

Molecular dynamics simulations are used to compute the potential of mean force (PMF) governing the interactions between carbon nanotubes (CNTs) in water/surfactant systems. The effects of CNT length, diameter, chirality (armchair and zigzag) and surfactant structures on CNT interaction and dispersion in water/surfactant systems are investigated for (5, 5), (5, 0), and (10, 10) single walled CNTs with two commonly used surfactants [viz., sodium dodecyl sulfate (SDS) and sodium dodecylbenzene sulfonate (SDBS)] at room conditions. An adaptive biasing force method was used to speed up the calculations. Simulations revealed that CNT length and diameter as well as optimum amount of surfactant addition and its structures can significantly affect CNT interactions (i.e., PMFs vary significantly). Surfactant molecules were found to adsorb at the CNT surface and reduced interaction strength between CNTs. SDBS surfactant contributed weaker interactions between CNTs as compared with that of SDS surfactant by a factor of about 10 indicating that SDBS is better than SDS for dispersing CNTs in an aqueous suspension. This phenomenon agrees qualitatively with the experimental results reported in the literature. The understanding of detailed atomic arrangements and atomic interactions between CNTs and surrounding molecules reported in this study is significantly helpful to computationally screening different surfactants and improving the CNT dispersion in aqueous solution. The method will also facilitate the reduction of time and cost required to produce CNT reinforced nanocomposite materials as well as homogeneous CNT dispersed solutions for many biological applications.