Direct measurements of structural forces and twist transitions in cholesteric liquid crystal films with a surface force apparatus.

Using a surface force apparatus, a cholesteric liquid crystal was confined between two crossed cylindrical surfaces that induced strong planar anchoring and normal alignment of the chiral helix. The film thickness and total twist angle of the chiral molecular structure were simultaneously measured using multiple-beam optical interference. As the film thickness was increased and the chiral structure deformed, the twist angle remained almost unchanged until discontinuous changes occurred at critical distances that were equally spaced by one cholesteric half-pitch length. Structural deformations generated oscillatory elastic forces with periodically spaced maxima corresponding to twist transitions. These findings were reproduced using an equilibrium model of cholesteric confinement and force generation. The analysis indicates that the strength of the azimuthal surface anchoring on mica is high, exceeding 0.2 mJ m-2.

Surface forces generated by the action of electric fields across liquid films.

We explore the force generation and surface interactions arising when electric fields are applied across fluid films. Using a surface force balance (SFB) we measure directly the force between two electrodes in crossed-cylinder geometry across dielectric and electrolytic fluids. In the case of dielectric films the field between the electrodes exerts a force which can be well explained using classic expressions and with no fitting parameters. However when the electrodes are separated by a film of electrolyte, an alternating electric field induces a force which diverges substantially from the calculated static response of the electrolyte. The magnitude of the force is larger than predicted, and the interaction can switch from attractive to repulsive. Furthermore, the approach to steady state in electrolyte takes place over 102-103 s which is very slow compared to both the charging and viscous timescales of the system. The non-trivial electrolyte response in AC electric fields, measured here directly, is likely to underlie several recent reports of unexpected and bifurcating forces driving colloids in AC fields. Our measurements suggest ways to control colloidal and soft matter using electric fields, as well as providing a direct measure of the length- and time-scales relevant in AC electrochemical and electrokinetic systems.