Mix-and-Melt Colloidal Engineering

被引:35
作者
Hueckel, Theodore [1 ]
Sacanna, Stefano [1 ]
机构
[1] NYU, Dept Chem, Mol Design Inst, 29 Washington Pl, New York, NY 10003 USA
关键词
anisotropic colloids; self-assembly; shape-changing; core-shell; patchy particles; CORE-SHELL PARTICLES; MULTIPHOTON LITHOGRAPHY; PHOTONIC CRYSTALS; PATCHY PARTICLES; CLUSTERS; NANOPARTICLES; POLYHEDRA; TITANIA; SPHERES; SHAPE;
D O I
10.1021/acsnano.8b00521
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Increasing significance is being placed on the synthesis of smart colloidal particles, since the route to various meta-materials has been outlined through their bottom-up self-assembly. Unfortunately, making particles with well-defined shape and surface chemistry often requires considerable effort and time, and as such, they are available only in restrictive yields. Here we report a synthetic methodology, which we refer to as mix-and-melt reactions (MMR), that allows for rapid prototyping and mass production of anisotropic core shell colloids. MMR take advantage of the synergistic properties between common colloidal suspensions by aggregating then reconfiguring polystyrene shell particles onto core particle substrates. By systematically exchanging cores and shells, the resultant core shell particle's properties are manipulated in a modular fashion. The influence of the constituent particles' size ratio is extensively explored, which is shown to tune shell thickness, change the aspect ratio of shells on anisotropic cores, and access specific shapes such as tetrahedra. Beyond particle shape, mixed shell systems are utilized to create regular surface patches. Surface Evolver simulations are used to demonstrate how randomly packed clusters melt into regular shapes via a shell compartmentalization mechanism.
引用
收藏
页码:3533 / 3540
页数:8
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