Electro-induced orientational ordering of anisotropic pigment nanoparticles.

The response of anisotropic pigment particle suspensions to externally applied electric fields has been explored for possible application in reflective display technologies. Three different types of pigment particle were suspended in dodecane, using a polymeric stabilizer, and showed Schlieren textures between crossed polarizers at high concentrations (greater than 25-30 wt%), indicating the formation of colloidal nematic phases. Orientational order parameters were determined by X-ray scattering, and the influence of polydispersity on the values is discussed. X-ray scattering measurements also demonstrated a change in the structure factor consistent with the onset of a colloidal nematic phase. In addition, the pigment particles were dispersed into various liquid crystal hosts at low concentrations (less than 5 wt%) with and without the presence of mesogenic mimic stabilizers. However, the influence of these stabilizers on orientational ordering could not be confirmed. The electro-induced ordering determined via scattering was related to the electro-optical response of each suspension using a simple model. The particles in nematic hosts not only showed a high degree of orientational ordering at lower electric field strengths, but also showed a reduction in stability. Although these systems have shown strong orientational ordering, the optical response has been limited by the intrinsic shape of the pigment particles and the distribution of the transition dipoles moments within them. Nevertheless, the feasibility of developing materials for display applications has been demonstrated.

Nematic director-induced switching of assemblies of hexagonally packed gold nanorods.

Self-assembled disc-shaped clusters of hexagonally packed, thiol-functionalized gold nanorods are prepared and dispersed in thermotropic nematic liquid crystals. The resultant hybrid complex fluids exhibit colloidal anisotropy with very high orientational order and are characterized by SAXS as shown in the figure. Precise, reconfigurable control of the cluster orientation at very low electric field strengths (0.18 V µm(-1) ) is achieved.