Chai Yu, Hasnain Jaffar, Bahl Kushaan, Wong Matthew, Li Dong, Geissler Phillip, Kim Paul Y, Jiang Yufeng, Gu Peiyang, Li Siqi, Lei Dangyuan, Helms Brett A, Russell Thomas P, Ashby Paul D
The Molecular Foundry, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720, USA.
Department of Physics, The City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong, China.
Sci Adv. 2020 Nov 25;6(48). doi: 10.1126/sciadv.abb8675. Print 2020 Nov.
Electrostatic interactions between nanoparticles (NPs) and functionalized ligands lead to the formation of NP surfactants (NPSs) that assemble at the water-oil interface and form jammed structures. To understand the interfacial behavior of NPSs, it is necessary to understand the mechanism by which the NPSs attach to the interface and how this attachment depends on the areal coverage of the interface. Through direct observation with high spatial and temporal resolution, using laser scanning confocal microscopy and in situ atomic force microscopy (AFM), we observe that early-stage attachment of NPs to the interface is diffusion limited and with increasing areal density of the NPSs, further attachment requires cooperative displacement of the previously assembled NPSs both laterally and vertically. The unprecedented detail provided by in situ AFM reveals the complex mechanism of attachment and the deeply nonequilibrium nature of the assembly.
纳米颗粒(NPs)与功能化配体之间的静电相互作用导致形成纳米颗粒表面活性剂(NPSs),这些NPSs在水-油界面处组装并形成堵塞结构。为了理解NPSs的界面行为,有必要了解NPSs附着到界面的机制以及这种附着如何依赖于界面的面积覆盖率。通过使用激光扫描共聚焦显微镜和原位原子力显微镜(AFM)进行具有高空间和时间分辨率的直接观察,我们发现NPs在早期附着到界面是受扩散限制的,并且随着NPSs面积密度的增加,进一步的附着需要先前组装的NPSs在横向和垂直方向上协同位移。原位AFM提供的前所未有的细节揭示了附着的复杂机制以及组装的深度非平衡性质。