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Unusual packing of soft-shelled nanocubes
Author(s) -
Fang Lu,
Thi Vo,
Yugang Zhang,
Alex Frenkel,
Kevin G. Yager,
Sanat K. Kumar,
Oleg Gang
Publication year - 2019
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.aaw2399
Subject(s) - nanoscopic scale , anisotropy , shell (structure) , curvature , tetragonal crystal system , materials science , nanoparticle , zigzag , chemical physics , nanotechnology , crystallography , condensed matter physics , geometry , physics , chemistry , optics , crystal structure , composite material , mathematics
Space-filling generally governs hard particle packing and the resulting phases and interparticle orientations. Contrastingly, hard-shaped nanoparticles with grafted soft-ligands pack differently since the energetically interacting soft-shell is amenable to nanoscale sculpturing. While the interplay between the shape and soft-shell can lead to unforeseen packing effects, little is known about the underlying physics. Here, using electron microscopy and small-angle x-ray scattering, we demonstrate that nanoscale cubes with soft, grafted DNA shells exhibit remarkable packing, distinguished by orientational symmetry breaking of cubes relative to the unit cell vectors. This zigzag arrangement occurs in flat body-centered tetragonal and body-centered cubic phases. We ascribe this unique arrangement to the interplay between shape and a spatially anisotropic shell resulting from preferential grafting of ligands to regions of high curvature. These observations reveal the decisive role played by shell-modulated anisotropy in nanoscale packing and suggest a plethora of new spatial organizations for molecularly decorated shaped nanoparticles.

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