Effect of Polymer Chain Length on the Superlattice Assembly of Functionalized Gold Nanoparticles

We report on the assembly of gold nanoparticle (AuNPs) superlattices at the liquid/vapor interface and in the bulk of their suspensions. Interparticle distances in the assemblies are achieved on multiple length scales by varying chain lengths of surface grafted AuNPs by polyethylene glycol (PEG) with molecular weights in the range 2000-40,000 Da. Crystal structures and lattice constants in both 2D and 3D assemblies are determined by synchrotron-based surface-sensitive and small-angle X-ray scattering. Assuming knowledge of grafting density, we show that experimentally determined interparticle distances are adequately modeled by spherical brushes close to the theta point (Flory-Huggins parameter, chi approximate to 1/2) for 2D superlattices at a liquid interface and a nonsolvent (chi = infinity) for the 3D dry superlattices.

Automated summary

The assembly of gold nanoparticle superlattices at liquid/vapor interface and in suspensions is achieved by varying chain lengths of surface grafted AuNPs by polyethylene glycol. Crystal structures and lattice constants in both 2D and 3D assemblies are determined by synchrotron-based surface-sensitive and small-angle X-ray scattering. The experimentally determined interparticle distances are adequately modeled by spherical brushes for 2D superlattices at a liquid interface and a nonsolvent for 3D dry superlattices, assuming knowledge of grafting density.