XPCS at the Microsecond Frontier: Diffusion of PEGylated Nanoparticles in Water

Abstract

Probing nanoscale transport in liquids under extreme thermodynamic conditions is essential for understanding soft matter and nanomaterials. However, accessing intrinsic microsecond dynamics of nanometre-sized objects remains challenging for synchrotron-based X-ray photon correlation spectroscopy (XPCS) because of limitations of coherent flux and detector repetition rates. Here, we investigate the diffusion of dilute polyethylene glycol (PEG)-coated gold nanoparticles dispersed in water over a wide temperature range, including the supercooled regime using XPCS. The measured dynamics exhibit purely diffusive behaviour, with relaxation rates scaling as q 2 , and the extracted diffusion coefficients quantitatively follow the Stokes-Einstein relation with no slip boundary. Viscosity values derived from nanoparticle motion agree with established literature data, confirming that PEGylated nanoparticles act as reliable nanoscopic viscosity probes without evidence of ligand shell compression or structural changes. Using event-based XPCS with next-generation detectors, we access microsecond dynamics approaching the intrinsic Brownian timescale of nanometer-sized particles. These results establish PEGylated gold nanoparticles as robust probes of nanoscale transport and demonstrate the capability of advanced XPCS instrumentation to investigate fast dynamics in soft and nanoscale materials.