Selective layer-by-layer self-assembly on patterned porous films modulated by Cassie-Wenzel transition

被引:40
|
作者
Ke, Bei-Bei [1 ]
Wan, Ling-Shu [1 ]
Li, Yang [1 ]
Xu, Ming-Yao [1 ]
Xu, Zhi-Kang [1 ]
机构
[1] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
POLYMER-FILMS; RAFT POLYMERIZATION; SOFT LITHOGRAPHY; BREATH FIGURES; HONEYCOMB FILMS; CROSS-LINKING; FABRICATION; CONSTRUCTION; ORGANIZATION; PROTEINS;
D O I
10.1039/c0cp01229g
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
We describe a robust and facile approach to the selective modification of patterned porous films via layer-by-layer (LBL) self-assembly. Positively charged honeycomb-patterned films were prepared from polystyrene-block-poly(N,N-dimethyl-aminoethyl methacrylate) (PS-b-PDMAEMA) and a PS/PDMAEMA blend by the breath figure method followed by surface quaternization. Alginate and chitosan were alternately deposited on the films via LBL self-assembly. The assembly on the PS-b-PDMAEMA film exhibits two stages with different growth rates, as elucidated by water contact angles, fluorescence microscopy, and quartz crystal microbalance results. The assembly can be controlled on the top surface or across all surfaces of the film by changing the number of deposition cycles. We confirm that there exists a Cassie-Wenzel transition with an increase in deposition cycles, which is responsible for the tunable assembly. For the PS/PDMAEMA film, the pores can be completely wetted and the polyelectrolytes selectively assemble inside the pores, instead of on the top surface. The controllable selective assembly forms unique hierarchical structures and opens a new route for surface modification of patterned porous films.
引用
收藏
页码:4881 / 4887
页数:7
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