College of Chemistry and Chemical Engineering, Jiangsu Key Laboratory of Environmental Engineering and Monitoring, Yangzhou University, 180 Si-Wang-Ting Road, Yangzhou 225002, China.
J Colloid Interface Sci. 2011 Feb 1;354(1):219-25. doi: 10.1016/j.jcis.2010.10.050. Epub 2010 Oct 28.
With water droplets as sacrificed templates at a particular humidity, micro-porous solid thin films were successfully fabricated by self-assembly using an amphiphilic block polymer, polystyrene-b-polyacrylic acid (PS-b-PAA). Interface interactions between the micro-porous thin film and a cationic surfactant, cetyltrimethylammonium bromide (CTAB), are investigated by in-situ AFM in aqueous solutions. An interesting phenomenon was observed in water and CTAB solution, which the dimensions of the micropores are remarkably larger than the dimensions of those in air. The solid thin films exhibit different surface morphologies in response to stimulus by different concentrations of CTAB. These observations were explained by positing that the PAA chains in the micropores stretch and contract with interface interactions between PAA and CTAB. A promising electrochemical application of this film is suggested. This study is aimed at strategies for the functionalization of stimulus-responsive micro-porous solid thin films with tunable surface morphologies, and exploring new smart materials.
以水滴为牺牲模板,在特定湿度下,通过使用两亲嵌段聚合物聚苯乙烯-聚(丙烯酸)(PS-b-PAA)的自组装,成功制备了微孔固体薄膜。通过在水溶液中的原位 AFM 研究了微孔薄膜与阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)之间的界面相互作用。在水中和 CTAB 溶液中观察到了一个有趣的现象,即微孔的尺寸明显大于空气中的尺寸。固体薄膜在不同浓度的 CTAB 刺激下表现出不同的表面形态。这些观察结果可以通过假设微孔中的 PAA 链在 PAA 和 CTAB 之间的界面相互作用下伸缩来解释。该薄膜具有很有前途的电化学应用。本研究旨在为具有可调表面形态的刺激响应性微孔固体薄膜的功能化提供策略,并探索新型智能材料。