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Research > Novel smectic liquid crystal phases and Materials
Liquid crystal phases are ordered fluid phases which occur between the solid and liquid phases of matter. They are formed from anisotropic molecules (i.e. not globular or spherical) which pack together to form an anisotropic phase. The phases formed are typically birefringent (i.e. they have two different refractive indices) and are now used everywhere in the form of LCDs (although they also have many other applications)

A molecule which forms liquid crystal phases in bulk by packing in an ordered fashion may change it's packing arrangement as a function of concentration in a solvent (lyotropic liquid crystals) or as a function of temperature (Thermotropic liquid crystals).

Our group works on both forms of liquid crystal material. Thermotropics will be discussed on this page, see the section on lipids and membranes for an example of lyotropic liquid crystals.

Thermotropic Phases

Rod-like molecules will form either a nematic phase (molecules orient themselves in a preferred direction) or a smectic-type phase (molecules have a preferred direction and also arrange themselves into fluid-like layers). Some material have a rich phase diagram, exhibiting several different smectic phases at different temperatures. T

If the molecules are chiral they may exhibit ferroelectric switching. In this case a bulk molecular motion is induced by an applied electric field across the material. By moving the molecules in bulk the transmission of polarised light through the materials can be moduated - resulting in an optical switch.

collings and Hird

A good introduction to the physics of liquid crystals and their synthesis can be found in the book “An introduction to Liquid Crystals” by Peter Collins and Mike Hird.

 

Bent-Core Liquid Crystalline Phases (or Banana phases)

We are currently investigating a relatively new class of materials "Bent-Core" liquid crystals, in which the central rigid core of the molecule has a significant bend angle. This bend can be symmetric or asymmetric and molecular structure plays an important role in bulk phase morphology, as with all liquid crystal materials.

There are 8 known B phases to date, although on-going research in this area is sure to reveal more. We currently focus on the B1 and B2 phases which have demonstrated electrical switching properties and using electro-optical measurements and x-ray diffraction we are looking at structural changes in the B phases as a function of applied electric fields.This work may eventually lead to new, low energy materials for display devices or other optical modulators.

Recent projects:

  • Switching studies of the B1 phase have revealed a field induced transition to the B2 phase at surprisingly low eletric field strengths. J. Kirchhoff, K.M. Fergusson, M. Hird and L.S. Hirst, APPL. PHYS. LETT. 90, 161905 (2007) PDF
  • A study of the effects of chiral and achiral dopants on the B1 and B2 liquid crystalline phases.

B1  transition

An electric field induced phase transition from the columnar B1 phase to a new switching phase.


Ferroelectric phase (SmC*)


Antiferroelectric phase (SmC*A)

layer spacing measurment

Smectic layer spacing as a function of temperature (deg C from the SmA transition) for a ferroelectric material. measured using x-ray diffraction.

Chiral Smectic Phases

We are interested in a class of phases called the chiral tilted smectic phases (SmC*). In these phases, molecules are tilted with respect to the layer normal. There are several variants to the tilted smectic phases, characterized by the progression of molecular orientation from layer to layer. For example the antiferroelectric phase exhibits a two layer orientational super-lattice. Other interesting and more complicated phases include the the ferrielectric (intermediate) phases (SmC*FI1 and SmC*FI2) and the alpha phase (SmC*a). The detailed structures of the ferrielectric and alpha phases were only recently described and we are interested in understanding their stability. These phases may also have important device applicatons as many different stable orientational states can be accessed by varying an applied electric field.

One of the key methods used to elucidate the molecular arrangement in a phase is resonant x-ray scattering. This is a synchrotron technique which used labeled molecules to determine teh superlattice structure of a phase. For more details on this take a look at our recent review article

"Resonant x-ray Scattering: a tool for structure elucidation in liquid crystals"
H.F.Gleeson and L.S. Hirst, CHEM PHYS CHEM, 7, 321-328 (2006) PDF

antiferroelectric liquid crystal film

A free-standing antiferroelectric liquid crystal film

Combining smectic layer spacing measurements with synchrotron studies of molecular orientation we hope to learn more about the stability of these interesting layered phases and their electrical properties.

The layer orientation in liquid crystal devices (i.e. between glass plates) can also be investigated via conventional small angle x-ray scattering. This measurement provides important information on the behavior of materials in commercial geometries (e.g. in LCDs).

Recent projects:

  • A study of the effects of chiral and achiral dopants on the smectic C* sub-phases. We have shown that the intermediate (also known as ferrielectric) liquid crystal phases can be significantly broadened by the addition of achiral dopants.
    J. Kirchhoff and L.S. Hirst, PHYS. REV. E, 76, 051704 (2007) PDF
  • Resonant scattering experiments at the Brookhaven synchrotron facility (NSLS)) have revealed the orientational molecular progressions in each smectic C* sub-phase.
    L.S. Hirst, S.J.Watson, H.F.Gleeson, P. Cluzeau, P. Barois, R. Pindak, P. Mach, J. Pitney, P. Johnson, C.C. Huang, G. Srajer, J. Pollmann, A-M. Levelut, and W. Caleibe. PHYS. REV. E. 65 (4): art. no. 041705 Part 1 APR 2002 PDF
  • A study of smectic layer arrangement in a liquid crystal device in different phases as a function of applied electric field.
    L.S. Matkin, H.F. Gleeson, L.J. Baylis, S.J. Watson and N. Bowring. APPL. PHYS. LETT. Vol 77, No 3 (17th July 2000) PDF

 


 

 

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