Universal Scaling of Polymer Diffusion in Nanocomposites.

Universal Scaling of Polymer Diffusion in Nanocomposites.
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DOI:
10.1021/mz400064w
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发表时间:
2013-03
期刊:
影响因子:
5.8
通讯作者:
Jihoon Choi;Michael J. A. Hore;J. Meth;N. Clarke;K. Winey;R. Composto
Jihoon Choi;Michael J. A. Hore;J. Meth;N. Clarke;K. Winey;R. Composto
中科院分区:
化学1区
文献类型:
--
作者:
Jihoon Choi;Michael J. A. Hore;J. Meth;N. Clarke;K. Winey;R. Composto

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Nanoparticles are new and valuable additives that can favorably tune thermomechanical, electric, optical, and magnetic properties of polymeric materials. The addition of nanoparticles can also enhance or slow down polymer dynamics depending on the mixture thermodynamics and key length scales, namely, nanoparticle size, interparticle spacing (ID), and the polymer radius of gyration (Rg). Presently, a framework for understanding how nanoparticles affect polymer dynamics is not available, in part, because of a lack of wide-ranging experimental studies. Here, tracer diffusion is studied in model nanocomposites containing silica nanoparticles grafted with either polymer brushes (soft nanoparticles) or short ligands (hard nanoparticles). Over a wide range of tracer molecular weights and nanoparticle loadings, the normalized diffusion coefficient collapses onto a universal curve for both soft and hard nanoparticles when plotted against a confinement parameter, defined as ID/Rg, which accounts for tracer penetration into the brush. These experimental results provide new insights into the fundamental principles required to construct predictive models of polymer dynamics in nanocomposites.