Three Regimes of Polymer Surface Dynamics under Crowded Conditions

被引:21
|
作者
Morrin, Gregory T. [1 ]
Schwartz, Daniel K. [1 ]
机构
[1] Univ Colorado, Dept Chem & Biol Engn, Boulder, CO 80309 USA
关键词
SINGLE-MOLECULE DIFFUSION; STRONG ADSORPTION SITES; POLY(ETHYLENE GLYCOL); ANOMALOUS DIFFUSION; POLYETHYLENE OXIDE; CHAIN DENSITY; SILICA; RELAXATION; TRACKING; KINETICS;
D O I
10.1021/acs.macromol.7b02453
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Single-molecule tracking was used to characterize the mobility of poly(ethylene glycol) chains at a solid-liquid interface over a wide range of surface coverage. Trajectories exhibited intermittent motion consistent with a generalized continuous time random walk (CTRW) model, where strongly confined "waiting times" alternated with rapid flights. The presence of three characteristic regimes emerged as a function of surface coverage, based on an analysis of effective short-time diffusion coefficients, mean-squared displacement, and CTRW distributions. The dilute "site-blocking" regime exhibited increasing short-time diffusion, less confined behavior, and shorter waiting times with higher surface coverage, as anomalously strong adsorption sites were increasingly passivated. At intermediate values of surface coverage, the "crowding" regime was distinguished by the exact opposite trends (slower, more confined mobility), presumably due to increasing intermolecular interactions. The trends reversed yet again in the "brush" regime, where adsorbing molecules interacted weakly with a layer of extended overlapping chains.
引用
收藏
页码:1207 / 1214
页数:8
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