Mitigation of the impact of single-walled carbon nanotubes on a freshwater green algae: Pseudokirchneriella subcapitata.

This study investigates the biological response of Pseudokirchneriella subcapitata to single-walled carbon nanotubes (SWNTs) suspended in gum Arabic (GA), using typical 96-hour algal bioassays and long-term growth studies. Changes in algal biomass and cell morphology associated with specific SWNT-treatments were monitored and the mechanisms of observed biological responses investigated through a combination of biochemical and spectroscopic methods. Results from short-term bioassays showed a growth inhibition in culture media containing >0.5 mg SWNT/L and a final GA concentration of 0.023% (v/v). Interestingly, the observed toxicity disappears when GA concentrations are brought to levels ≥ 0.046%. Long-term experiments based on toxic combination of SWNTs and GA showed that P. subcapitata would easily recover from an initial growth inhibition effect. Overall, these findings point to the possibility of GA to mitigate the toxicity of SWNTs, making it an ideal surfactant if SWNT suspension in GA does not alter the performance sought from these nanotubes.

Spectroscopic properties of nanotube-chromophore hybrids.

Recently, individual single-walled carbon nanotubes (SWNTs) functionalized with azo-benzene chromophores were shown to form a new class of hybrid nanomaterials for optoelectronics applications. Here we use a number of experimental and computational techniques to understand the binding, orientation, and nature of coupling between chromophores and the nanotubes, all of which are relevant to future optimization of these hybrid materials. We find that the binding energy between chromophores and nanotubes depends strongly on the type of tether that is used to bind the chromophores to the nanotubes. The pyrene tethers form a much stronger attachment to nanotubes compared to anthracene or benzene rings, resulting in more than 80% retention of bound chromophores post-processing. Density functional theory (DFT) calculations show that the binding energy of the chromophores to the nanotubes is maximized for chromophores parallel to the nanotube sidewall, even with the use of tethers; optical second harmonic generation measurements show that there is nonetheless a partial radial orientation of the chromophores on the nanotubes. We find weak electronic coupling between the chromophores and the SWNTs, consistent with noncovalent binding. This weak coupling is still sufficient to quench the chromophore fluorescence through a combination of static and dynamic processes. Photoluminescence measurements show a lack of significant energy transfer from the chromophores to isolated semiconducting nanotubes.

Solvatochromic shifts of single-walled carbon nanotubes in nonpolar microenvironments.

Single-walled carbon nanotubes (SWNTs) are encapsulated with microenvironments of nonpolar solvent, providing a new method to measure the photophysical properties of nanotubes in environments with known properties. Photoluminescence (PL) and absorbance spectra of SWNTs show solvatochromic shifts in 16 nonpolar solvents, which are proportional to the solvent induction polarization. The shifts in the emission energies (DeltaE(11)) range from approximately 25 to 100 meV and the smallest diameter SWNTs have the largest shifts. The PL intensity of SWNTs is very sensitive to changes in polarity. For example, SWNTs encapsulated with chloroform (epsilon approximately 5) show substantial reductions in intensity. The solvatochromic shifts of SWNTs were used to determine the relationship between the longitudinal polarizability, band gap and radius, alpha(11,||) proportional to 1/(R(2)E(11)(3)).

Coating individual single-walled carbon nanotubes with nylon 6,10 through emulsion polymerization.

Solvent microenvironments are formed around individual single-walled carbon nanotubes (SWNTs) by mixing SWNT suspensions with water-immiscible organic solvents. These microenvironments are used to encapsulate the SWNTs with the monomer sebacoyl chloride. Hexamethylene diamine is then injected into the aqueous phase so the formation of nylon 6,10 is restricted to the interface between the microenvironment and water. This emulsion polymerization process results in uniform coatings of nylon 6,10 around individual SWNTs. The nylon-coated SWNTs remain dispersed in the aqueous phase and are highly luminescent at pH values ranging from 3 to 12. This emulsion polymerization method provides a general approach to coat nanotubes with various polymers.

Swelling the micelle core surrounding single-walled carbon nanotubes with water-immiscible organic solvents.

Solvatochromic shifts in the absorbance and fluorescence spectra are observed when surfactant-stabilized aqueous single-walled carbon nanotube (SWNT) suspensions are mixed with immiscible organic solvents. When aqueous surfactant-suspended SWNTs are mixed with o-dichlorobenzene, the spectra closely match the peaks for SWNTs dispersed in only pure o-dichlorobenzene. These spectral changes suggest that the hydrophobic region of the micelle surrounding SWNTs swells with the organic solvent when mixed. The solvatochromic shifts of the aqueous SWNT suspensions are reversible once the solvent evaporates. However, some surfactant-solvent systems show permanent changes to the fluorescence emission intensity after exposure to the organic solvent. The intensity of some large diameter SWNT (n, m) types increase by more than 175%. These differences are attributed to surfactant reorganization, which can improve nanotube coverage, resulting in decreased exposure to quenching mechanisms from the aqueous phase.

Improving the effectiveness of interfacial trapping in removing single-walled carbon nanotube bundles.

Single-walled carbon nanotube (SWNT) bundles are selectively removed from an aqueous dispersion containing individually suspended carbon nanotubes coated with gum Arabic via interfacial trapping. The suspensions are characterized with absorbance, fluorescence, and Raman spectroscopy as well as atomic force microscopy (AFM) and rheology. The resulting aqueous suspensions have better dispersion quality after interfacial trapping and can be further improved by altering the processing conditions. A two-step extraction process offers a simple and fast approach to preparing high-quality dispersions of individual SWNTs comparable to ultracentrifugation. Partitioning of SWNTs to the liquid-liquid interface is described by free energy changes. SWNT bundles prefer to reside at the interface over individually suspended SWNTs because of greater free energy changes.