A topic
related to the previous one concerns the molecular mechanisms which
produce tilted structures in Langmuir monolayers, which are monolayers
of surfactant molecules deposited on a water surface. These essentially
two-dimensional systems also exhibit a significant variety of phases,
differing in the nature of both translational and orientational ordering.
In tilt-ordered phases, which are similar to smectic-C phases, the molecules
are on average tilted uniformly with respect to the surface normal:
the azimuthal direction of the tilt can be either toward nearest-neighbors,
next-nearest neighbors, or in some intermediate direction. We have studied
the origin of tilt-ordering using a rigid-rod model, where each surfactant
molecules is composed of a chain of Lennard-Jones atoms, and replacing
the aqueous substrate by a continuum (described by external fields).
These studies have examined the roles of various features of the molecular
architecture in producing tilt-ordering, particularly the effects of
size mismatch between the hydrophillic head groups and hydrophobic tail
units. Here we have used both ground-state analysis (See
details) and Monte-Carlo simulation methods (See
details).

Simulated
Langmuir monolayer