| Home > Publications database > Pressure-Dependent Diffusion of PEG-Functionalized Gold Nanoparticles Probed by X-ray Photon Correlation Spectroscopy |
| Typ | Amount | VAT | Currency | Share | Status | Cost centre |
| Hybrid-OA | 0.00 | 0.00 | EUR | (Publish and Read) | 810 / 476152 | |
| Hybrid-OA | -1400.00 | 0.00 | EUR | (Storniert) | 810 / 476152 | |
| Hybrid-OA | 1400.00 | 0.00 | EUR | (Bestellt) | 28902 / 476152 | |
| Sum | 0.00 | 0.00 | EUR | |||
| Total | 0.00 |
| Journal Article | PUBDB-2026-01815 |
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2026
Americal Chemical Society
Washington, DC
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Please use a persistent id in citations: doi:10.1021/acs.jpcb.6c03752 doi:10.3204/PUBDB-2026-01815
Abstract: Dynamic properties of nanoparticles under high pressure are poorly understood due to experimental challenges. Here, we use X-ray photon correlation spectroscopy (XPCS) to investigate the diffusion dynamics of polyethylene glycol (PEG)-functionalized gold nanoparticles dispersed in water at pressures up to 6 kbar. Complementary small-angle X-ray scattering reveals no measurable pressure-induced changes in the gold core size, confirming structural stability across the studied pressure range. XPCS measurements show a systematic slowing down of nanoparticle dynamics with increasing pressure, with relaxation rates retaining the expected q$^2$-dependence characteristic of Brownian motion. The extracted diffusion coefficients decrease continuously with pressure and align with predictions based on the pressure-dependent viscosity of water and the Stokes–Einstein relation, assuming a constant hydrodynamic particle size. Within experimental uncertainty, no additional contribution from pressure-induced ligand-shell modifications is observed in these dilute dispersions.
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