Huang Xiao-Wei, Peng Yi, Huang Jian-Hua, Luo Meng-Bo
Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou 310018, China.
Phys Chem Chem Phys. 2017 Nov 15;19(44):29975-29983. doi: 10.1039/c7cp05514e.
The effect of nanoparticles (NPs) on the diffusivity of polymers in crowded environments is complicated. We study the diffusivity of polymers in the environment with periodically distributed immobile NPs by using off-lattice Monte Carlo simulations. Results show that the diffusion coefficient D of polymers at low temperature is dependent on the inter-particle distance d and polymer length N or end-to-end distance of polymers in dilute solution R. At low temperature, D is large at both small and large d and a minimum is observed at intermediate d. The nonmonotonic behavior of D is due to the reason that there are two kinds of diffusion modes for the polymers at low temperature: NP-exchange motion for R > d and adsorption-and-desorption motion for R < d. Moreover, we observe the oscillation of D with N at a relatively low temperature. The novel behavior is relevant to the adsorption of polymers on NPs and is explained from the free energy barrier for polymers jumping from the ground state to others.
纳米颗粒(NPs)对聚合物在拥挤环境中扩散率的影响较为复杂。我们通过非晶格蒙特卡罗模拟研究了聚合物在具有周期性分布的固定NPs的环境中的扩散率。结果表明,低温下聚合物的扩散系数D取决于颗粒间距离d以及聚合物长度N或稀溶液中聚合物的端到端距离R。在低温下,d较小时和较大时D都较大,而在中间d值时观察到最小值。D的这种非单调行为是由于低温下聚合物存在两种扩散模式:R > d时的NP交换运动和R < d时的吸附-解吸运动。此外,我们在相对较低温度下观察到D随N的振荡。这种新行为与聚合物在NPs上的吸附有关,并从聚合物从基态跃迁到其他状态的自由能垒角度进行了解释。