Dynamics in adsorbed homopolymer layers: Understanding complexity from simple starting points

被引:42
作者
Santore, MM [1 ]
机构
[1] Univ Massachusetts, Dept Polymer Sci, Amherst, MA 01003 USA
关键词
D O I
10.1016/j.cocis.2005.05.005
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Now more than ever, smart material interfaces in a variety of applications demand control over complex interfacial processes, often involving adsorbed polymers. To this end, this opinion article addresses the dynamic complexity in homopolymer layers adsorbed at liquid-solid interfaces, summarizing some of the simplest examples and examining the potential impact of specific complicating mechanisms: The distinction between diffusion limited (in free solution) and surface-controlled chain release is made, and then for the latter, several different cases of single-exponential desorption, self-exchange, and displacement are compared: Though the systems present great chemical variety, they have either a limited number of or a weak energy of segment- surface contacts. Increasing the strength and/or numbers of these contacts complicates dynamics, as does increasing molecular weight which can introduce chain pinning. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:176 / 183
页数:8
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