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Single-Molecule Observation of Long Jumps in Polymer Adsorption

2013/06/22 by Changqian Yu, Juan Guan, Yu, Changqian +7
Biochemistry, Genetics and Molecular Biology · Materials Science · Physics and Astronomy · #Advanced Fluorescence Microscopy Techniques #FOS: Physical sciences #Force Microscopy Techniques and Applications #Polymer Surface Interaction Studies #Soft Condensed Matter (cond-mat.soft) #cond-mat.soft

paper · pdf · doi:10.48550/arxiv.1306.5738

arxiv created 2013/06/22 · openalex publication_date 2013/06/22 · arxiv updated 2013/06/26 · openalex created_date 2025/10/10 · openalex updated_date 2026/08/01

Abstract

Single-molecule fluorescence imaging of adsorption onto initially-bare surfaces shows that polymer chains need not localize immediately after arrival. In a system optimized to present limited adsorption sites (quartz surface to which polyethylene glycol (PEG) is exposed in aqueous solution at pH = 8.2) we find that some chains diffuse back into bulk solution and re-adsorb at some distance away, sometimes multiple times before either they localize at a stable position or else diffuse away into bulk solution. This mechanism of surface diffusion is considerably more rapid than the classical model in which adsorbed polymers crawl on surfaces while the entire molecule remains adsorbed. The trajectories with jumps follow a truncated Levy distribution of step size with limiting slope -2.5, consistent with a well-defined, rapid surface diffusion coefficient over the times we observe.

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