Department of Applied Science and Technology, University of California , Berkeley 94720 United States.
Material Sciences Division, Lawrence Berkeley National Laboratory , Berkeley 94720, United States.
ACS Appl Mater Interfaces. 2017 Sep 27;9(38):33327-33332. doi: 10.1021/acsami.7b10981. Epub 2017 Sep 13.
The self-assembly and interfacial jamming of spherical Janus nanoparticles (JNPs) at the water/oil interface were investigated. Polymeric JNPs, made by cross-linking polystyrene-block-polybutadiene-block-poly(methyl methacrylate) (PS-PB-PMMA), with a high interfacial activity assemble at the water/oil interface. During the self-assembly at the interface, the interfacial energy was reduced and a dynamic interlayer was observed that is responsive to the pH of the aqueous phase. Unlike hard particles, the JNPs are composed of polymer chains that can spread at the liquid-liquid interface to maximize coverage at relatively low areal densities. In a pendant drop geometry, the interfacial area of a water droplet in oil was significantly decreased and the JNPs were forced to pack more closely. Entangling of the polymer chains causes the JNPs to form a solid-like interfacial assembly, resulting in the formation of wrinkles when the interfacial area is decreased. The wrinkling behavior, the retention of the wrinkles, or the slow relaxation of the liquid drop back to its original equilibrium shape was found to depend upon the pH.
我们研究了球形单壁纳米粒子(JNPs)在油水界面处的自组装和界面堵塞。通过交联聚苯乙烯-聚丁二烯-聚甲基丙烯酸甲酯(PS-PB-PMMA)制备的具有高界面活性的聚合物 JNPs 在油水界面处组装。在界面处自组装过程中,界面能降低,并观察到一个对水相 pH 值有响应的动态夹层。与硬颗粒不同,JNPs 由聚合物链组成,这些聚合物链可以在液-液界面上展开,以在相对较低的比表面积密度下实现最大覆盖。在悬滴几何形状中,油中水滴的界面面积显著减小,迫使 JNPs 更紧密地堆积。聚合物链的缠结导致 JNPs 形成固态界面组装,当界面面积减小时形成皱纹。发现皱折行为、皱折的保留或液滴缓慢恢复到其原始平衡形状取决于 pH 值。