Assembly of planar chiral superlattices from achiral building blocks

被引:36
|
作者
Cheng, Zhihua [1 ]
Jones, Matthew R. [1 ,2 ]
机构
[1] Rice Univ, Dept Chem, Houston, TX 77005 USA
[2] Rice Univ, Dept Mat Sci & Nanoengn, Houston, TX 77005 USA
关键词
CETYLTRIMETHYLAMMONIUM BROMIDE; QUASI-CRYSTALLINE; NANOCRYSTALS; PATCHINESS; FORCES; NANOSTRUCTURES; NANOPARTICLES; TETRAHEDRA; PACKINGS; MICELLE;
D O I
10.1038/s41467-022-31868-2
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
The formation of nanostructures with chiral symmetry often requires chiral directing agents at a smaller length scale. Here, the authors report the self-assembly of 2D chiral superlattices from achiral tetrahedron-shaped building blocks. The spontaneous assembly of chiral structures from building blocks that lack chirality is fundamentally important for colloidal chemistry and has implications for the formation of advanced optical materials. Here, we find that purified achiral gold tetrahedron-shaped nanoparticles assemble into two-dimensional superlattices that exhibit planar chirality under a balance of repulsive electrostatic and attractive van der Waals and depletion forces. A model accounting for these interactions shows that the growth of planar structures is kinetically preferred over similar three-dimensional products, explaining their selective formation. Exploration and mapping of different packing symmetries demonstrates that the hexagonal chiral phase forms exclusively because of geometric constraints imposed by the presence of constituent tetrahedra with sharp tips. A formation mechanism is proposed in which the chiral phase nucleates from within a related 2D achiral phase by clockwise or counterclockwise rotation of tetrahedra about their central axis. These results lay the scientific foundation for the high-throughput assembly of planar chiral metamaterials.
引用
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页数:11
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