Solvent exchange kinetics in poly(N-isopropylacrylamide) microgel-based etalons

被引:11
作者
Smiley-Wiens, Janelle B. [1 ]
Serpe, Michael J. [1 ]
机构
[1] Univ Alberta, Dept Chem, Edmonton, AB T6G 2G2, Canada
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
Poly(N-isopropylacrylamide) microgels; Color-tunable materials; Fabry-Perot etalon; Stimuli-responsive polymers; Metal-polymer hybrid structures; Microgel deswelling kinetics; Solvent exchange; COIL-TO-GLOBULE; ORGANIC-DYE REMOVAL; N-ISOPROPYLACRYLAMIDE; THIN-FILMS; COLLOIDAL MICROGELS; AQUEOUS-SOLUTIONS; IONIC-STRENGTH; GOLD-FILMS; WATER; TEMPERATURE;
D O I
10.1007/s00396-012-2818-4
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
Poly (N-isopropylacrylamide)-co-acrylic acid (pNIPAm-co-AAc) microgel-based etalons are constructed by depositing thin Au layers (mirrors) on either side of a planar microgel layer. When immersed in water, the microgel layer swells and the etalon exhibits visual color. The thermoresponsivity of the pNIPAm-based microgels allows the Au mirror spacing, and hence the device color, to be dynamically modulated. Necessarily, when the mirror spacing is modulated solvent in the microgel layer must be expelled to the surroundings. Previously, we determined that the etalon deswelling kinetics depended critically on the thickness of the Au layer covering the microgels. Here, we report on solvent exchange kinetics. We found that the time required for solvent entry into the microgel layer is much longer than solvent exit. In addition, the rate was found to again depend critically on the thickness of the Au layer covering the microgel layer; thicker Au layers corresponded to slower solvent exchange kinetics.
引用
收藏
页码:971 / 979
页数:9
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