Goodrich Carl P, Brenner Michael P
School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138;
Kavli Institute of Bionano Sciences and Technology, Harvard University, Cambridge, MA 02138.
Proc Natl Acad Sci U S A. 2017 Jan 10;114(2):257-262. doi: 10.1073/pnas.1608838114. Epub 2016 Dec 29.
Controlling motion at the microscopic scale is a fundamental goal in the development of biologically inspired systems. We show that the motion of active, self-propelled colloids can be sufficiently controlled for use as a tool to assemble complex structures such as braids and weaves out of microscopic filaments. Unlike typical self-assembly paradigms, these structures are held together by geometric constraints rather than adhesive bonds. The out-of-equilibrium assembly that we propose involves precisely controlling the 2D motion of active colloids so that their path has a nontrivial topology. We demonstrate with proof-of-principle Brownian dynamics simulations that, when the colloids are attached to long semiflexible filaments, this motion causes the filaments to braid. The ability of the active particles to provide sufficient force necessary to bend the filaments into a braid depends on a number of factors, including the self-propulsion mechanism, the properties of the filament, and the maximum curvature in the braid. Our work demonstrates that nonequilibrium assembly pathways can be designed using active particles.
在微观尺度上控制运动是受生物启发系统发展的一个基本目标。我们表明,活性自推进胶体的运动可以得到充分控制,用作从微观细丝组装复杂结构(如辫子和织物)的工具。与典型的自组装范式不同,这些结构是通过几何约束而非粘合剂结合在一起的。我们提出的非平衡组装涉及精确控制活性胶体的二维运动,使其路径具有非平凡拓扑结构。我们通过原理验证布朗动力学模拟表明,当胶体附着在长的半柔性细丝上时,这种运动会使细丝编织在一起。活性粒子提供将细丝弯曲成辫子所需足够力的能力取决于许多因素,包括自推进机制、细丝的特性以及辫子中的最大曲率。我们的工作表明,可以使用活性粒子设计非平衡组装途径。