Format

Send to

Choose Destination
ACS Nano. 2019 Feb 26;13(2):1412-1420. doi: 10.1021/acsnano.8b07027. Epub 2018 Dec 26.

Controlled Symmetry Breaking in Colloidal Crystal Engineering with DNA.

Author information

1
X-Ray Science Division , Argonne National Laboratory , Argonne , Illinois 60439 , United States.

Abstract

The programmed crystallization of particles into low-symmetry lattices represents a major synthetic challenge in the field of colloidal crystal engineering. Herein, we report an approach to realizing such structures that relies on a library of low-symmetry Au nanoparticles, with synthetically adjustable dimensions and tunable aspect ratios. When modified with DNA ligands and used as building blocks for colloidal crystal engineering, these structures enable one to expand the types of accessible lattices and to answer mechanistic questions about phase transitions that break crystal symmetry. Indeed, crystals formed from a library of elongated rhombic dodecahedra yield a rich phase space, including low-symmetry lattices (body-centered tetragonal and hexagonal planar). Molecular dynamics simulations corroborate and provide insight into the origin of these phase transitions. In particular, we identify an unexpected asymmetry in the DNA shell, distinct from both the particle and lattice symmetries, which enables directional, nonclose-packed interactions.

KEYWORDS:

Au nanoparticle; DNA; anisotropy; colloidal crystal engineering; programmable atom equivalent; symmetry breaking

PMID:
30585476
DOI:
10.1021/acsnano.8b07027

Supplemental Content

Full text links

Icon for American Chemical Society
Loading ...
Support Center