Eva-Kristina Fleischmann

Liquid-crystalline ordering as a concept in materials science: from semiconductors to stimuli-responsive devices.

While the unique optical properties of liquid crystals (LCs) are already well exploited for flat-panel displays, their intrinsic ability to self-organize into ordered mesophases, which are intermediate states between crystal and liquid, gives rise to a broad variety of additional applications. The high degree of molecular order, the possibility for large scale orientation, and the structural motif of the aromatic subunits recommend liquid-crystalline materials as organic semiconductors, which are solvent-processable and can easily be deposited on a substrate. The anisotropy of liquid crystals can further cause a stimuli-responsive macroscopic shape change of cross-linked polymer networks, which act as reversibly contracting artificial muscles. After illustrating the concept of liquid-crystalline order in this Review, emphasis will be placed on synthetic strategies for novel classes of LC materials, and the design and fabrication of active devices.

One-piece micropumps from liquid crystalline core-shell particles

Responsive polymers are low-cost, light weight and flexible, and thus an attractive class of materials for the integration into micromechanical and lab-on-chip systems. Triggered by external stimuli, liquid crystalline elastomers are able to perform mechanical motion and can be utilized as microactuators. Here we present the fabrication of one-piece micropumps from liquid crystalline core-shell elastomer particles via a microfluidic double-emulsion process, the continuous nature of which enables a low-cost and rapid production. The liquid crystalline elastomer shell contains a liquid core, which is reversibly pumped into and out of the particle by actuation of the liquid crystalline shell in a jellyfish-like motion. The liquid crystalline elastomer shells have the potential to be integrated into a microfluidic system as micropumps that do not require additional components, except passive channel connectors and a trigger for actuation. This renders elaborate and high-cost micromachining techniques, which are otherwise required for obtaining microstructures with pump function, unnecessary.

Microactuators from a main-chain liquid crystalline elastomer via thiol–ene “click” chemistry

Recently it has been described that liquid crystalline elastomer (LCE) particles of the side-chain type can be prepared in microfluidic devices. Here we present the preparation of micrometer-sized LCE particles of the main-chain type by thiol–ene chemistry. The LCE particles are UV-crosslinked via thiol–ene click chemistry of the nematic monomer, carrying terminal thiol and ene groups, and non-mesogenic tetrathiol and tetraene crosslinkers. The preparation of the LCE particles with a microfluidic device by a continuous “on the fly” technique allows their fast processing with an irradiation time of less than 2 seconds. The resulting particles undergo a temperature-driven volume change up to 25% upon the nematic–isotropic phase transition and the extent of the shape change can be controlled by adjusting the microfluidic parameters. The reversibility of the shape change and the chemical durability of the thiol–ene network towards reducing agents demonstrate the usability of the LCE particles as soft microactuators.

Better Actuation Through Chemistry: Using Surface Coatings to Create Uniform Director Fields in Nematic Liquid Crystal Elastomers.

Controlling the molecular alignment of liquid crystal monomers (LCMs) within nano- and microstructures is essential in manipulating the actuation behavior of nematic liquid crystal elastomers (NLCEs). Here, we study how to induce uniformly vertical alignment of nematic LCMs within a micropillar array to maximize the macroscopic shape change using surface chemistry. Landau-de Gennes numerical modeling suggests that it is difficult to perfectly align LCMs vertically in every pore within a poly(dimethylsiloxane) (PDMS) mold with porous channels during soft lithography. In an untreated PDMS mold that provides homeotropic anchoring of LCMs, a radially escaped configuration of LCMs is observed. Vertically aligned LCMs, a preferred configuration for actuation, are only observed when using a PDMS mold with planar anchoring. Guided by the numerical modeling, we coat the PDMS mold with a thin layer of poly(2-hydroxyethyl methacrylate) (PHEMA), leading to planar anchoring of LCM. Confirmed by polarized optical microscopy, we observe monodomains of vertically aligned LCMs within the mold, in agreement with modeling. After curing and peeling off the mold, the resulting NLCE micropillars showed a relatively large and reversible radial strain (∼30%) when heated above the nematic to isotropic transition temperature.

Towards micrometer sized core-shell actuators from liquid crystalline elastomers by a continuous flow synthesis

We present here the successful preparation of liquid crystalline core-shell elastomers via a microfluidic double-emulsion process. The customized set-up allows for a temperature-controlled fabrication of the core-shell particles from a thermoresponsive mesogenic monomer. The nematic liquid crystalline shell is filled with a non-mesogenic core of silicone oil. To verify the core-shell structure with optical microscopy, we prepared particles with a colored core using a red dye. We were also able to micro-manipulate the particles and penetrate them with a small glass capillary to extract the liquid core.