Drops of liquid crystal molecules branch out into strange structures

While many scientific achievements come from long years of careful planning, once in a while researchers stumble onto something completely unexpected. “At the beginning, we were looking to create a particular effect,” says graduate student Wei-Shao Wei. “Then, we observed something weird.”

A new study in

Nature

details this “weird” finding by showing how droplets containing chain-like liquid crystal molecules transform into complex shapes when the temperature drops. Conducted by Wei, graduate student Sophie Ettinger, Ph.D. alum Yu Xia, Shu Yang, and Arjun Yodh, this unexpected discovery provides new understanding about how molecular polydispersity–a condition where the lengths of liquid crystal molecules vary widely–can drive simple droplets to change into unusual shapes.

Liquid crystals are composed of rod- or disc-like molecules called mesogens, and, as a result of the alignment of these mesogens, exhibit remarkable physical properties in between those of a solid and a liquid. The liquid crystals used in this study have similar characteristics to the ones used in LCD screens but are instead made of oligomers, flexible short-chain polymers comprised of smaller rod-like molecular building blocks.

Wei’s initial goal was to use this type of liquid crystal from Yang’s lab to create Janus droplets, which contain two different types of materials on opposite sides of the drop–in this case, one half would be a rubbery network called a liquid crystal elastomer, made by “locking” liquid crystal molecules in place with cross-linking, and the other half would be silicone.

Wei quickly discovered that the droplets were instead transforming into strange filamentous structures. At first the researchers thought that what they were seeing was an experimental error, but because the results were repeatable, they realized it was something remarkably new that they should try to understand.

“It was a visually spectacular effect. I wasn’t expecting it at all,” says Yodh. “We were trying to make designer drops, but in the process, we saw something interesting and different.”

Both amazed and puzzled by their strange results, the researchers began a rigorous investigation to explain what they were seeing. With the help of the Yang lab, Wei studied droplets that contained different mixtures of liquid crystal oligomers made of mesogens of varying lengths. The researchers varied oligomer chain length, used different surfactants to hold the droplets together, and explored simple theoretical models to make sense of their findings.

The essential feature of the model the researchers developed is that the structure of the droplet is driven by two forces: surface tension, the tendency of fluid surfaces to shrink into the smallest area possible, and elastic energy, with one example being the mechanical energy stored in bendable objects like bed springs or an archer’s bow. To keep surface energy to a minimum, the liquid crystal droplet normally forms a sphere, the shape with the smallest surface-to-volume ratio. Inside the droplet, however, the individual rods want to be both perpendicular to the sphere’s surface while also sitting parallel with other rods.

With these opposing forces at play, at high temperatures (~90 C/~194 F), the liquid crystal droplets are spherical and have a classic “radial hedgehog” internal structure, where all of the rods point towards the center, a configuration that requires elastic energy to form. Then, when the temperature decreases, surface tension and elastic energy change, and both the shape of the droplet and the alignment of the rods inside the droplet transform to minimize total energy cost.

By happenstance, the resulting droplet structures form a stunning array of complex shapes, from “flowers” that resemble microscopic chrysanthemums to massive “Medusa” networks of intertwining fibers. The effects are also reversible–droplets can go from spheres to tangled networks and then back again.

In addition to the remarkable new droplet morphologies, one of the surprising findings of this work was that the key to this strange phenomenon was having both long-chain and short-chain rods in the drop–in scientific terms, having a liquid crystal system with polydispersity.

When the rod-like mesogens were of similar length, no strange effects were seen, but if they had many different lengths, then the rods would move to different places inside the droplet based on their length. Rods made of smaller chains preferentially moved to where the elastic energy is larger, near the center of the droplet, while those made of larger chains moved to the surface.

“Usually when your sample contains a mixture of constituents of different size, or length, or even composition, then phase transitions or self-assembly events are smeared out or prevented altogether,” explains Yodh, “But here, polydispersity in the mixture helps to drive the effect, because chains of different length can move to different parts of the drop. This doesn’t happen for the homogenous, monodisperse system.”

While many questions still remain, like why, exactly, the droplets branch out in strange ways that make the material seem alive, the researchers hope to use these insights to explore new applications and concepts.

“One reason we decided to use these particular liquid crystal oligomers is that we can cross-link them and make them into an elastomer,” says Yodh, adding that these and other similar kinds of chain-like liquid crystal molecules could be used to create new types of soft materials, like actuatable fibers that could move and change shapes in response to temperature or moisture.

The researchers are also thinking about other phenomena where polydispersity plays a role in driving a material’s assembly and shaping its structure and function. Molecular heterogeneity in biology is potentially related to what the researchers found with the polydisperse chain-like liquid crystal molecules and might facilitate ways to synthesize and pattern materials based on what already exists in the living world–many polymers found in nature, like natural rubber, wood cellulose, and silk, are themselves polydisperse.

“In general, scientists tend to control things–you want to control so you can understand it, and thus we usually try to make and work with monodisperse systems,” says Yang. “But in biology, the source materials are sometimes a mixture of molecules with different chain lengths and functions: They can have different stiffness, hydrophobicity, or hydrophilicity, and that’s why it’s so complicated to understand.”

The researchers hope that this study, which was done in the collaborative “MRSEC spirit” by uniting efforts in materials science and engineering with physics, will encourage others to see new implications and possible benefits of polydispersity.

“This work was fun,” adds Yodh. “It was fun to be surprised in the beginning, and then frustratingly fun to try to understand it for so long. And it’s fun looking back. The disorder of the polymers makes something that’s different.”

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This research was supported by National Science Foundation grants MRSEC DMR-1720530 and DMR16-07378 and NASA grant 80NSSC19K0348.

This part of information is sourced from https://www.eurekalert.org/pub_releases/2019-12/uop-dol121619.php

Erica K. Brockmeier
215-898-8562
[email protected]
http://www.upenn.edu/pennnews 

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