Magnetic field-driven assembly and reconfiguration of multicomponent supraparticles

被引:41
|
作者
Al Harraq, A. [1 ]
Lee, J. G. [1 ]
Bharti, B. [1 ]
机构
[1] Louisiana State Univ, Cain Dept Chem Engn, Baton Rouge, LA 70803 USA
关键词
ANISOTROPY; CRYSTALS; BINDING;
D O I
10.1126/sciadv.aba5337
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Suprastructures at the colloidal scale must be assembled with precise control over local interactions to accurately mimic biological complexes. The toughest design requirements include breaking the symmetry of assembly in a simple and reversible fashion to unlock functions and properties so far limited to living matter. We demonstrate a simple experimental technique to program magnetic field-induced interactions between metallodielectric patchy particles and isotropic, nonmagnetic "satellite" particles. By controlling the connectivity, composition, and distribution of building blocks, we show the assembly of three-dimensional, multicomponent supraparticles that can dynamically reconfigure in response to change in external field strength. The local arrangement of building blocks and their reconfigurability are governed by a balance of attraction and repulsion between oppositely polarized domains, which we illustrate theoretically and tune experimentally. Tunable, bulk assembly of colloidal matter with predefined symmetry provides a platform to design functional microstructured materials with preprogrammable physical and chemical properties.
引用
收藏
页数:9
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