Ma Jihong, Carrillo Jan-Michael Y, Do Changwoo, Chen Wei-Ren, Falus Péter, Shen Zhiqiang, Hong Kunlun, Sumpter Bobby G, Wang Yangyang
Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA.
Neutron Scattering Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA.
Phys Rev E. 2021 Aug;104(2-1):024503. doi: 10.1103/PhysRevE.104.024503.
The spatial correlations of entangled polymer dynamics are examined by molecular dynamics simulations and neutron spin-echo spectroscopy. Due to the soft nature of topological constraints, the initial spatial decays of intermediate scattering functions of entangled chains are, to the first approximation, surprisingly similar to those of an unentangled system in the functional forms. However, entanglements reveal themselves as a long tail in the reciprocal-space correlations, implying a weak but persistent dynamic localization in real space. Comparison with a number of existing theoretical models of entangled polymers suggests that they cannot fully describe the spatial correlations revealed by simulations and experiments. In particular, the strict one-dimensional diffusion idea of the original tube model is shown to be flawed. The dynamic spatial correlation analysis demonstrated in this work provides a useful tool for interrogating the dynamics of entangled polymers. Lastly, the failure of the investigated models to even qualitatively predict the spatial correlations of collective single-chain density fluctuations points to a possible critical role of incompressibility in polymer melt dynamics.
通过分子动力学模拟和中子自旋回波光谱研究了缠结聚合物动力学的空间相关性。由于拓扑约束的软性,缠结链的中间散射函数的初始空间衰减,在一阶近似下,其函数形式与非缠结系统的惊人相似。然而,缠结在倒易空间相关性中表现为长尾巴,这意味着在实空间中存在微弱但持续的动态局域化。与一些现有的缠结聚合物理论模型的比较表明,它们不能完全描述模拟和实验所揭示的空间相关性。特别是,原始管模型中严格的一维扩散概念被证明是有缺陷的。这项工作中展示的动态空间相关性分析为研究缠结聚合物的动力学提供了一个有用的工具。最后,所研究的模型甚至在定性预测集体单链密度涨落的空间相关性方面的失败,表明不可压缩性在聚合物熔体动力学中可能起关键作用。