How to design an icosahedral quasicrystal through directional bonding

被引:35
作者
Noya, Eva G. [1 ]
Wong, Chak Kui [2 ]
Llombart, Pablo [1 ]
Doye, Jonathan P. K. [2 ]
机构
[1] CSIC, Consejo Super Invest Cient, Inst Quim Fis Rocasolano, Madrid, Spain
[2] Univ Oxford, Dept Chem, Phys & Theoret Chem Lab, Oxford, England
关键词
PATCHY PARTICLES; DNA; SIMULATIONS; RANGE; ORDER;
D O I
10.1038/s41586-021-03700-2
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
Icosahedral quasicrystals (IQCs) are materials that exhibit long-range order but lack periodicity in any direction. Although IQCs were the first reported quasicrystals(1), they have been experimentally observed only in metallic alloys(2), not in other materials. By contrast, quasicrystals with other symmetries (particularly dodecagonal) have now been found in several soft-matter systems(3-5). Here we introduce a class of IQCs built from model patchy colloids that could be realized experimentally using DNA origami particles. Our rational design strategy leads to systems that robustly assemble in simulations into a target IQC through directional bonding. This is illustrated for both body-centred and primitive IQCs, with the simplest systems involving just two particle types. The key design feature is the geometry of the interparticle interactions favouring the propagation of an icosahedral network of bonds, despite this leading to many particles not being fully bonded. As well as furnishing model systems in which to explore the fundamental physics of IQCs, our approach provides a potential route towards functional quasicrystalline materials. Model patchy colloids with directional bonding are designed that assemble into icosahedral quasicrystals through the propagation of an icosahedral network of bonds and may be realized using DNA origami particles.
引用
收藏
页码:367 / +
页数:18
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