Journal
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 8, Issue 12, Pages 2629-2633Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.7b01049
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- National Science Foundation of China [11404288]
- Science Foundation of Zhejiang Sci-Tech University
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Controlling the nanoparticle (NP) diffusion in polymers is a prerequisite to obtain polymer nanocomposites (PNCs) with desired dynamical and rheological properties and to achieve targeted delivery of nanomedicine in biological systems. Here we determine the suppression mechanism of direct NP polymer attraction to hamper the NP mobility in adsorbing polymers and then quantify the dependence of the effective viscosity eta(eff) felt by the NP on the adsorption duration tau(ads) of polymers on the NP using scaling theory analysis and molecular dynamics simulations. 8 We propose and confirm that participation of adsorbed chains in the NP motion break up at time intervals beyond tau(ads) due to the rearrangement of polymer segments at the NP surface, which accounts for the onset of Fickian NP diffusion on a time scale of t approximate to tau(ads). We develop a power law, eta(eff) similar to (tau(ads))(nu), where nu is the scaling exponent of the dependence of polymer coil size on the chain length, which leads to a theoretical basis for the design of PNCs and nanomedicine with desired applications through tuning the polymer adsorption duration.
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