Xu Yaxin, Choi Kyu Hwan, Nagella Sachit G, Takatori Sho C
Department of Chemical Engineering, University of California, Santa Barbara, Santa Barbara, CA, USA.
Soft Matter. 2023 Aug 2;19(30):5692-5700. doi: 10.1039/d3sm00673e.
Understanding pairwise interactions between colloidal particles out of equilibrium has a profound impact on dynamical processes such as colloidal self assembly. However, traditional colloidal interactions are effectively quasi-static on colloidal timescales and cannot be modulated out of equilibrium. A mechanism to dynamically tune the interactions during colloidal contacts can provide new avenues for self assembly and material design. In this work, we develop a framework based on polymer-coated colloids and demonstrate that in-plane surface mobility and mechanical relaxation of polymers at colloidal contact interfaces enable an effective, dynamic interaction. Combining analytical theory, simulations, and optical tweezer experiments, we demonstrate precise control of dynamic pair interactions over a range of pico-Newton forces and seconds timescales. Our model helps further the general understanding of out-of-equilibrium colloidal assemblies while providing extensive design freedom interface modulation and nonequilibrium processing.
理解非平衡态下胶体颗粒之间的成对相互作用,对诸如胶体自组装等动力学过程具有深远影响。然而,传统的胶体相互作用在胶体时间尺度上实际上是准静态的,无法在非平衡态下进行调制。一种在胶体接触过程中动态调节相互作用的机制,可以为自组装和材料设计提供新途径。在这项工作中,我们基于聚合物包覆的胶体开发了一个框架,并证明了在胶体接触界面处聚合物的面内表面迁移率和机械弛豫能够实现有效的动态相互作用。结合分析理论、模拟和光镊实验,我们展示了在一系列皮牛顿力和秒级时间尺度上对动态成对相互作用的精确控制。我们的模型有助于进一步全面理解非平衡态胶体组装,同时提供广泛的界面调制和非平衡处理设计自由度。