posted on 2015-12-16, 22:45authored byKyle J. M. Bishop, Nicolas R. Chevalier, Bartosz A. Grzybowski
Like-sized,
oppositely charged nanoparticles are known to assemble
into large crystals with diamond-like (ZnS) ordering, in sharp contrast
to analogous molecular ions and micrometer-scale colloids, which invariably
favor more closely packed structures (NaCl or CsCl). Here, we show
that these experimental observations can be understood as a consequence
of ionic screening and the slight asymmetry in surface charge present
on the assembling particles. With this asymmetry taken into account,
free-energy calculations predict that the diamond-like ZnS lattice
is more favorable than other 1:1 ionic structures, namely, NaCl or
CsCl, when the Debye screening length is considerably larger than
the particle size. A thermodynamic model describes how the presence
of neutralizing counterions within the interstitial regions of the
crystal acts to bias the formation of low-volume-fraction structures.
The results provide general insights into the self-assembly of non-close-packed
structures via electrostatic interactions.