Gold Nanoparticle–Polyelectrolyte Complexes with Tunable Structure Probed by Synchrotron Small-Angle X-ray Scattering: Implications for the Production of Colloidal Crystals-Based Nanophotonic Materials
Résumé
Close-packed colloidal crystals of gold nanoparticles (AuNPs) are of great interest in the field of nanophotonics due to their lattice pattern dependent optical properties. One challenge resides in producing such crystalline assemblies by a scalable approach involving polydisperse AuNPs obtained by standard synthesis routes and structuring natural molecules in water at room temperature. Electrostatic complexation between functionalized AuNPs and oppositely charged polyelectrolytes (PELs) is a very simple way to create AuNP self-assemblies of different morphologies and compactness. Our work investigates, using synchrotron small-angle X-ray scattering, their structure as a function of concentration, PEL persistence length and ionic strength. By decreasing the radius, R, of the positively charged gold nanoparticles to a few nm (R ≤ 3 nm) and increasing the polyelectrolyte persistence length, LT, substituting flexible sodium polystyrene sulfonate for natural semi-flexible hyaluronan, we tuned the characteristic ratio LT/R up to values ≥ 1.85. Such ratios allow the successful formation of a new AuNPs arrangement with a high degree of short-range order at low ionic strength and of crystalline order when interactions are screened by addition of salt. This approach involving commercially available natural water-soluble semi-flexible PELs, opens a low-cost and promising way for the one-step production of gold colloidal crystals, which can be of ubiquitous utility in nanophotonics.
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