The colloidal stabilization of carbon with carbon: carbon nanobubbles as both dispersant and glue for carbon nanotubes.

The superior physical properties of carbon nanotubes (CNTs) have led to their broad application. Intrinsically, CNTs tend to agglomerate from hydrophobic interactions, which is highly undesirable for solution processing and device fabrication. Commonly, a stabilizer consisting of organic surfactants or polymers is used to disperse CNTs. Recently, we synthesized nitrogen-doped carbon hollow nanospheres (25-90 nm), termed carbon "nanobubbles". They bear superior dispersability in water and distinctive graphitic order. Herein, we describe the nanobubble-assisted dispersion of CNTs in aqueous solution upon sonication. This process relies on the π-π interaction between the two aromatic carbon nanostructures, which can process their carbon mixture in water into conductive filter membranes, ink, and discs. This stabilization can be extended to other aromatic carbons. In addition, the π-π interaction may create a new type of carbon p-n junction that can be used to improve charge separation.

Water dispersible, highly graphitic and nitrogen-doped carbon nanobubbles.

Dispersible, highly graphitic, and nitrogen-doped carbon hollow nanospheres (25-90 nm), termed 'nanobubbles', are prepared via confined carbonization through a silica nanocasting technique. Poly(ionic liquid) nanoparticles are employed as easy-to-make and multifunctional templates, which simultaneously act as both the carbon and nitrogen source. The promising potential of the nanobubbles in oxygen reduction reactions for fuel cells is demonstrated.

Double Stimuli-Responsive Copolymer Stabilizers for Multiwalled Carbon Nanotubes.

A unique copolymer stabilizer is presented that can be used to stabilize multiwalled carbon nanotubes in aqueous solution to form "smart" dispersions. They showed double stimuli-responsive behavior (in dependence of temperature and ionic strength) and allowed for accurate control of the transition (exfoliated → agglomerated) temperature of nanotubes over a wide temperature range. In spite of its effective dispersion strength, the copolymer was easily synthesized in one step via free radical copolymerization of N-isopropylacrylamide and 1-ethyl-3-vinylimidazolium bromide.

Self-assembly of poly(ionic liquid)s: polymerization, mesostructure formation, and directional alignment in one step.

This paper reports on the highly ordered and tunable inner structure of poly(ionic liquid) nanoparticles, which formed spontaneously by precipitation polymerization from water. Without added stabilizer, these "latexes" are much smaller (20-40 nm in diameter) than usual polymer latexes and exhibit either multilamellar or unilamellar vesicular morphology, depending on the tail length of the quaternizing alkyl chains. The simplicity in the synthesis and composition and the high complexity of the ordered structures that resemble liposomes expand the classical profile of homopolymer self-assembly. In addition, unidirectional superassembly to a nanoworm mesostructure is found at elevated concentrations, indicating that the ionic liquid liposomes are apt to integrate into further hierarchical assembly schemes.