Hierarchical self-assembly of hard cube derivatives

被引:7
|
作者
Harper, Eric S. [1 ]
Waters, Brendon [2 ]
Glotzer, Sharon C. [1 ,2 ,3 ,4 ]
机构
[1] Univ Michigan, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Phys, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Biointerfaces Inst, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
MOLECULAR-DYNAMICS SIMULATIONS; CRYSTALLINE; SUPERLATTICE; BEHAVIOR; ENTROPY; !text type='PYTHON']PYTHON[!/text;
D O I
10.1039/c8sm02619j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hierarchical, self-assembled structures are ordered on multiple scales, and formed by objects comprised of even smaller elements. Such structures are widely reported for nanoparticles, macromolecules, and peptides, and even in entropy-driven hard particle assembly hierarchical colloidal crystals have been reported. Here we consider the hierarchical self-assembly of a cubic colloidal crystal from congruent hard cube derivatives, and investigate how various ways of slicing and dicing a cube can affect the ability of the pieces to entropically re-assemble the initial colloidal crystal formed from perfect cubes. We present design rules that support heuristics reported for different systems, and present evidence for a previously unreported cubatic phase from 2 : 1 rectangular prisms.
引用
收藏
页码:3733 / 3739
页数:7
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