From a two-dimensional chemical pattern to a three-dimensional topology through selective inversion of a liquid-liquid bilayer

被引:40
作者
Leopoldes, Julien [1 ]
Damman, Pascal [1 ]
机构
[1] Univ Mons, Lab Physicochim Polymeres, B-7000 Mons, Belgium
关键词
D O I
10.1038/nmat1787
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
Soft organic surfaces with more and more complex topologies are required daily to engineer appropriate microstructures for many different applications such as DNA array technology, biological optics for advanced photonic systems and microfluidics. Complementarily to conventional lithographic processes, several pioneering methods have been developed recently, by controlling phase separation of polymer blends, spinodal decomposition of homopolymers or by using the action of additional external forces driving diverse instabilities. Here we present a method that not only provides original concepts towards the three-dimensional (3D) structuring of liquids, on the basis of the synergistic effects of molecular diffusion and confined nucleation, but also suggests original solutions for the transport, mixing and filtering of small volumes of liquid. Through the intrinsic destabilization of a liquid-liquid bilayer, the 2D pattern of a chemically structured surface with hydrophilic and hydrophobic domains is transferred to a solid/liquid interface as a 3D topography with either positive or negative replication. This easy-to-use process has potential applications in various technological realms requiring a specific topography at interfaces such as microfluidics orbiosensors. © 2006 Nature Publishing Group.
引用
收藏
页码:957 / 961
页数:5
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