posted on 2018-09-06, 00:00authored byGuolong Zhu, Ziyang Xu, Ye Yang, Xiaobin Dai, Li-Tang Yan
Harnessing
anisotropic interactions in a DNA-mediated nanoparticle
assembly holds great promise as a rational strategy to advance this
important area. Here, using molecular dynamics simulations, we report
the formation of novel hierarchical crystalline assemblies of Janus
nanoparticles functionalized with two types of DNA chains (DNA-JNPs).
We find that in addition to the primary nanoparticle crystallization
into face-centered cubic (FCC) structure, sequence-specific DNA hybridization
events further direct the rotational orientation of the DNA-JNPs to
diverse secondary crystalline phases including simple cubic (SC),
tetragonally ordered cylinder (P4), and lamella (L) structures, which
are mapped in the phase diagrams relating to various asymmetric parameters.
The crystallization dynamics of such hierarchical crystals is featured
by two consequent processes: entropy-dominated translational order
for the primary crystalline structure and enthalpy-dominated rotational
order for the secondary crystalline structure. For DNA-JNPs with high
asymmetry in DNA sequence length, tetrahedral nanoclusters tend to
be favored, which is revealed to be governed by the conformational
entropy penalty caused by bounded DNA chains. This work might bear
important consequences for constructing new classes of nanoparticle
crystals with designed structures and properties at multiple levels
and in a predictable manner.