Bioinspired, Cysteamine-Catalyzed Co-Silicification of (1H, 1H, 2H, 2H-Perfluorooctyl)triethoxysilane and Tetraethyl Orthosilicate: Formation of Superhydrophobic Surfaces

被引:5
|
作者
Park, Ji Hun [1 ,2 ]
Kim, Ji Yup [1 ,2 ]
Cho, Woo Kyung [3 ]
Choi, Insung S. [1 ,2 ]
机构
[1] Korea Adv Inst Sci & Technol, Ctr Cell Encapsulat Res, Taejon 305701, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Chem, Mol Level Interface Res Ctr, Taejon 305701, South Korea
[3] Chungnam Natl Univ, Dept Chem, Taejon 305764, South Korea
基金
新加坡国家研究基金会;
关键词
cysteamine; fluorination; glass sponge; silicification; superhydrophobicity; SILICA NANOPARTICLES; FREE-ENERGY; FUNCTIONALIZATION; BIOSILICIFICATION; MINERALIZATION; ENCAPSULATION; MICROSPHERES; CHEMISTRY; ALPHA; CELLS;
D O I
10.1002/asia.201301213
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bioinspired silicification attracts a great deal of interest because of its physiologically relevant, mild conditions for hydrolysis and condensation of silica precursors, which makes the bioinspired approach superior to the conventional sol-gel process, particularly when dealing with biological entities. However, the morphological control of silica structures with incorporation of functional groups in the bioinspired silicilication has been unexplored. In this work, we co-silicificated (1H, 1H, 2H, 2H-perfluorooctyl)triethoxysilane and tetraethyl orthosilicate to investigate the morphological evolution of fluorinated silica structures in the cetyltrimethylammonium bromide-mediated, cysteamine-catalyzed silicification. The generated micrometer-long worm-like and spherical silica structures display superhydrophobicity after film formation. Interestingly, the measurement of dynamic water contact angles shows that the morphological difference leads to a different wetting state, either the self-cleaning or the pinning state of the superhydrophobic surface.
引用
收藏
页码:764 / 768
页数:5
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