Non-equilibrium dynamics of single polymer adsorption to solid surfaces

被引:32
|
作者
Panja, Debabrata [1 ]
Barkema, Gerard T. [2 ,3 ]
Kolomeisky, Anatoly B. [4 ]
机构
[1] Univ Amsterdam, Inst Theoret Phys, NL-1018 XE Amsterdam, Netherlands
[2] Univ Utrecht, Inst Theoret Phys, NL-3584 CE Utrecht, Netherlands
[3] Leiden Univ, Inst Lorentz, NL-2333 CA Leiden, Netherlands
[4] Rice Univ, Dept Chem, Houston, TX 77005 USA
基金
美国国家科学基金会;
关键词
CHAINS; TIMES;
D O I
10.1088/0953-8984/21/24/242101
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
The adsorption of polymers to surfaces is crucial for understanding many fundamental processes in nature. Recent experimental studies indicate that the adsorption dynamics is dominated by non-equilibrium effects. We investigate the adsorption of a single polymer of length N to a planar solid surface in the absence of hydrodynamic interactions. We find that for weak adsorption energies the adsorption timescales similar to N(1+2 nu)/(1+nu), where nu is the Flory exponent for the polymer. We argue that in this regime the single chain adsorption is closely related to a field-driven polymer translocation through narrow pores. Surprisingly, for high adsorption energies the adsorption time becomes longer, as it scales as similar to N1+nu, which is explained by strong stretching of the unadsorbed part of the polymer close to the adsorbing surface. These two dynamic regimes are separated by an energy scale that is characterized by non-equilibrium contributions during the adsorption process.
引用
收藏
页数:6
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