Structurally tunable two-dimensional (2D) arrays of nanoscale objects are important for modulating functional responses of thin films. We demonstrate that such tunable and ordered nanoparticles (NP) arrays can be assembled at charged air-water interfaces from nanoparticles coated with polyelectrolyte chains, DNA. The electrostatic attraction between the negatively charged nonhybridizing DNA-coated gold NPs and a positively charged lipid layer at the interface facilitates the formation of a 2D hexagonally closed packed (HCP) nanoparticle lattice. We observed about 4-fold change of the monolayer nanoparticle density by varying the ionic strength of the subphase. The tunable NP arrays retain their structure reasonably well when transferred to a solid support. The influence of particle's DNA corona and lipid layer composition on the salt-induced in-plane and normal structural evolution of NP arrays was studied in detail using a combination of synchrotron-based in situ surface scattering methods, grazing incidence X-ray scattering (GISAXS), and X-ray reflectivity (XRR). Comparative analysis of the interparticle distances as a function of ionic strength reveals the difference between the studied 2D nanoparticle arrays and analogous bulk polyelectrolyte star polymers systems, typically described by Daoud-Cotton model and power law scaling. The observed behavior of the 2D nanoparticle array manifests a nonuniform deformation of the nanoparticle DNA corona due to its electrostatically induced confinement at the lipid interface. The present study provides insight on the interfacial properties of the NPs coated with charged soft shells.
Keywords: charged nanoparticle; lipid membrane; liquid interfaces; self-assembly.