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Updated: Jun 4, 2025

Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
Published on: September 26, 2016
Investigation of Polymer Chain Diffusion Behavior in Thin Slits Formed by Patch-Patterned Surfaces: Influence of
Hao-Nan Zhang1, Guo-Ao Wang1, Hang-Kai Qi2
1Department of Physics, Hangzhou Dianzi University, Hangzhou 310018, China.
Abstract:
The diffusion dynamics of polymer chains within a narrow slit formed by two patch-patterned surfaces is investigated utilizing Langevin dynamics simulations. These surfaces feature periodically arranged attractive patches of size L and period d, with a staggered configuration of (0.5d, 0.5d) offsets along the x and y axes. When d is fixed, the polymer chain exhibits normal diffusion over long time scales, with the translational diffusion coefficient D gradually decreasing to zero as L increases. Notably, our findings reveal four distinct diffusion modes: free-diffusion mode for L ≤ L1, where the polymer chain is mainly in a desorption state; adsorption-desorption mode for L1 < L ≤ L2, involving transitions from a single-patch adsorption state to a desorption state; exchange-patch mode for L2 < L ≤ L3, where the polymer chain switches between a single-patch adsorption state and an upper-lower double-patch adsorption state by exchanging patches; and nondiffusion mode for L > L3, where the polymer chain is primarily in a pinned state. Furthermore, as the patch attraction strength εps increases, D decreases due to an increase in the adsorption time of the polymer chain. Simultaneously, critical patch size thresholds L1, L2, and L3, exhibit a decreasing trend. These observations highlight the significant influence of the confining slit and patch properties on the diffusion behavior of polymer chains.
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