posted on 2014-12-30, 00:00authored byOnajite Shemi, Michael J. Solomon
The noncovalent binding of the gold
hemispheres of polystyrene/gold
colloidal Janus spheres in aqueous solution was found to depend more
significantly on the deposition thickness of the particle’s
gold layer than the chemistry of a covalently affixed self-assembled
monolayer on the gold. By means of two-channel confocal laser scanning
microscopy, salt-induced clustering was observed and quantified for
Janus particles with gold hemispheres functionalized with a thiol
self-assembled monolayer that varied in hydrophobicity and chain length.
The thickness of the gold layer on the Janus particles was also varied
from 10 to 40 nm. The measured cluster distributions were strongly
salt dependent, with clustering absent at 1 mM salt but present at
salt concentrations in the range of 2–3 mM. For Janus spheres
with a 40 nm thick gold hemisphere, the effects of both thiol monolayer
hydrophobicity and chain length were modest. Varying the gold layer
thickness from 10 to 40 nm, however, had a significant effect on the
cluster distribution; the most abundant cluster size shifted from
one to seven particles as the gold layer thickness increased from
10 to 40 nm. Thus, the gold layer thickness had an effect stronger
than that of either self-assembled monolayer hydrophobicity or chain
length on the self-assembly of metallodielectric Janus particles into
clusters. The dominant effect of the metallic layer thickness suggests
that van der Waals forces between metallic surfaces are more important
than hydrophobic interactions in determining the pair potential interactions
of metallodielectric Janus particles.