Liquid-crystal-mediated self-assembly at nanodroplet interfaces

• J. A. Moreno-Razo,
• E. J. Sambriski,
• N. L. Abbott,
• J. P. Hernández-Ortiz
• & J. J. de Pablo

• Affiliations
• Contributions
• Corresponding author

Nature

 

485,

 

86–89

 

(03 May 2012)

 

doi:10.1038/nature11084

Received

 

10 October 2011 

Accepted

 

19 March 2012 

Published online

 

02 May 2012

Technological applications of liquid crystals have generally relied on control of molecular orientation at a surface or an interface^1, 2. Such control has been achieved through topography, chemistry and the adsorption of monolayers or surfactants^2, 3. The role of the substrate or interface has been to impart order over visible length scales and to confine the liquid crystal in a device. Here, we report results from a computational study of a liquid-crystal-based system in which the opposite is true: the liquid crystal is used to impart order on the interfacial arrangement of a surfactant. Recent experiments on macroscopic interfaces have hinted that an interfacial coupling between bulk liquid crystal and surfactant can lead to a two-dimensional phase separation of the surfactant at the interface⁴, but have not had the resolution to measure the structure of the resulting phases. To enhance that coupling, we consider the limit of nanodroplets, the interfaces of which are decorated with surfactant molecules that promote local perpendicular orientation of mesogens within the droplet. In the absence of surfactant, mesogens at the interface are all parallel to that interface. As the droplet is cooled, the mesogens undergo a transition from a disordered (isotropic) to an ordered (nematic or smectic) liquid-crystal phase. As this happens, mesogens within the droplet cause a transition of the surfactant at the interface, which forms new ordered nanophases with morphologies dependent on surfactant concentration. Such nanophases are reminiscent of those encountered in block copolymers⁵, and include circular, striped and worm-like patterns.