Surface Activity and Aggregation Behavior of Polyhydroxylated Fullerenes in Aqueous Solutions

Polyhydroxylated fullerene (PHF) surface activity and aggregation behavior at the air-water interface were examined using surface tension and resonance-enhanced second harmonic generation (SHG). Surface tension data showed that PHFs are surface active with a limiting surface excess corresponding to 130 angstrom(2)/molecule in aqueous (Millipore water) solutions. Increasing the solution-phase ionic strength (through the addition of NaCl) reduces the PHF surface excess. Conductivity measurements show that PHFs carry a single charge, presumably negative. Surface-specific SHG experiments show a small but measurable fixed wavelength, nonlinear response from solutions having surface excess coverages as low as similar to 400 angstrom(2)/molecule. The SHG response of PHF solutions in the low-concentration limit shows unexpected behavior, implying that at bulk concentrations below 0.06 mg/mL, PHF monomers adsorb to the surface and interfere destructively with the intrinsic nonlinear susceptibility of the aqueous/vapor interface, leading to a similar to 75% reduction in the SH signal. Above a PHF concentration of 0.0.06 mg/mL, the SH signal begins to rise in the Millipore and 50 mM NaCl solutions but remains very low in the 500 mM NaCl solutions. From this behavior, we infer that an increased nonlinear optical response is due to adsorbed aggregates.