Science
9 October 2015:
Vol. 350 no. 6257
DOI: 10.1126/science.1242477
Vol. 350 no. 6257
DOI: 10.1126/science.1242477
Nonadditivity of nanoparticle interactions
+ Author Affiliations
Abstract
Understanding interactions between
inorganic nanoparticles (NPs) is central to comprehension of
self-organization processes
and a wide spectrum of physical, chemical, and
biological phenomena. However, quantitative description of the
interparticle
forces is complicated by many obstacles that are
not present, or not as severe, for microsize particles (μPs). Here we
analyze
the sources of these difficulties and chart a
course for future research. Such difficulties can be traced to the
increased
importance of discreteness and fluctuations
around NPs (relative to μPs) and to multiscale collective effects.
Although these
problems can be partially overcome by modifying
classical theories for colloidal interactions, such an approach fails to
manage
the nonadditivity of electrostatic, van der
Waals, hydrophobic, and other interactions at the nanoscale. Several
heuristic
rules identified here can be helpful for
discriminating between additive and nonadditive nanoscale systems.
Further work on
NP interactions would benefit from embracing NPs
as strongly correlated reconfigurable systems with diverse physical
elements
and multiscale coupling processes, which will
require new experimental and theoretical tools. Meanwhile, the
similarity between
the size of medium constituents and NPs makes
atomic simulations of their interactions increasingly practical.
Evolving experimental
tools can stimulate improvement of existing
force fields. New scientific opportunities for a better understanding of
the electronic
origin of classical interactions are converging
at the scale of NPs.
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