论文标题

用热响应PS/PNIPAM聚合物混合物覆盖的激光 - 微结构的硅的功能表面:在亲水性和疏水性之间可逆地切换

Functional surfaces of laser-microstructured silicon coated with thermoresponsive PS/PNIPAM polymer blends: switching reversibly between hydrophilicity and hydrophobicity

论文作者

Kanidi, Maria, Papagiannopoulos, Aristeidis, Matei, Andreea, Dinescu, Maria, Pispas, Stergios, Kandyla, Maria

论文摘要

我们开发了与聚苯乙烯(PS)和聚(N-异丙基丙烯酰胺)(PNIPAM)混合的激光微结构的硅的功能表面,我们研究了它们在亲水性和疏水性之间的切换润湿行为。硅的大面积用可重复的表面微形状处理,并用两个混合比的PS/PNIPAM混合物旋转。表面地形和表面化学效应的组合可以改变表面的润湿行为。 PS/PNIPAM膜铸造在具有或没有天然SIO2层的平坦和微结构硅底物上。所有薄膜对温度的刺激以及用天然SIO2层在微结构硅底物上施放的膜的刺激作出反应,大概是因为它们采用了更有利的结构,因此均显示出最高的热回应性。微观结构提供了一个较大的特定区域,该区域扩展了根据Wenzel模型扩展PNIPAM链与水分子的接触,从而增加了膜的热响应性,从而导致从亲水性到加热后从亲水性到疏水性的可逆过渡。来自硅底物的天然SIO2层的不存在会影响膜中的PS和PNIPAM排列,从而增加了PNIPAM的临界溶液温度下方和高于较低的临界溶液温度并降低其热响应性。

We developed functional surfaces of laser-microstructured silicon coated with blends of polystyrene (PS) and poly(N-isopropylacrylamide) (PNIPAM) and we study their switching wetting behavior between hydrophilicity and hydrophobicity. Large areas of silicon are processed with reproducible surface micromorphology and spin-coated with PS/PNIPAM blends of two blend ratios. The wetting behavior of the surfaces is modified by the combination of surface topography and surface chemistry effects. PS/PNIPAM films are casted on flat and microstructured silicon substrates with or without a native SiO2 layer. All films respond to the stimulus of temperature and films casted on microstructured silicon substrates with a native SiO2 layer show the highest thermoresponsiveness presumably because they adopt a more favorable structure. Microstructuring provides a large specific area that extends the contact of PNIPAM chains with water molecules according to the Wenzel model, and thus increasing the film thermoresponsiveness, resulting in a reversible transition from hydrophilicity to hydrophobicity upon heating. The absence of the native SiO2 layer from the silicon substrates affects the PS and PNIPAM arrangement in the films, increasing the water contact angle both below and above the lower critical solution temperature of PNIPAM and decreasing their thermoresponsiveness.

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