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Energetically Preferred Bilayered Coacervation of Oppositely Charged ZrHP Nanoplatelets

机译:能量上优选的相反电荷的ZRHP纳米型纳米片的双层凝聚

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摘要

A platform is introduced for bilayered coacervation of oppositely charged nanoplatelets (NPLs) at the oil–water interface. To this end, we synthesized two types of zirconium hydrogen phosphate (ZrHP) NPLs, cationically charged NPLs (CNPLs), and anionically charged NPLs (ANPLs) by conducting surface-initiated atom transfer radical polymerization. Taking advantage of the platelet geometry and controlled wettability, we demonstrated that ANPLs and CNPLs coacervate themselves to form a bilayered NPL membrane at the interface, which was directly confirmed by confocal laser scanning microscopy. Via theoretical consideration using the hit-and-miss Monte Carlo method, we determined that electrostatic attraction-driven coacervation of ANPLs and CNPLs at the interface shows a minimum attachment energy of ~ ?10~(6)k _(B)T, which is comparable to the cases where NPLs charged with the same type of ions are attached. Finally, this unique and novel interfacial coacervation behavior allowed us to develop a pH-responsive smart Pickering emulsion system.
机译:介绍了一种用于在油-水界面上对带电纳米片(NPLs)进行双层凝聚的平台。为此,我们通过进行表面引发的原子转移自由基聚合,合成了两种类型的磷酸氢锆(ZrHP)NPLs,阳离子电荷NPLs(CNPLs)和阴离子电荷NPLs(ANPLs)。利用血小板的几何形状和可控的润湿性,我们证明了ANPLs和CNPLs在界面处凝聚形成双层NPL膜,这一点由共焦激光扫描显微镜直接证实。通过使用命中和未命中蒙特卡罗方法进行理论考虑,我们确定,ANPLs和CNPLs在界面处的静电引力驱动凝聚显示最小附着能为~?10~(6)k_B(B)T,这与附加相同类型离子的NPL的情况相当。最后,这种独特且新颖的界面凝聚行为使我们能够开发一种pH响应的智能Pickering乳液系统。

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