Self-propelled, endlessly programmable artificial cilia: Simple microstructures that bend, twist and perform stroke-like motions could be used for soft robotics, medical devices and more

Now, researchers from the Harvard John A. Paulson School of Engineering and Applied Sciences (SEAS) have developed a single-material, single-stimuli microstructure that can outmaneuver even living cilia. These programmable, micron-scale structures could be used for a range of applications, including soft robotics, biocompatible medical devices, and even dynamic information encryption.

The research is published in Nature.

“Innovations in adaptive self-regulated materials that are capable of a diverse set of programmed motions represent a very active field, which is being tackled by interdisciplinary teams of scientists and engineers,” said Joanna Aizenberg, the Amy Smith Berylson Professor of Materials Science and Professor of Chemistry & Chemical Biology at SEAS and senior author of the paper. “Advances achieved in this field may significantly impact the ways we design materials and devices for a variety of applications, including robotics, medicine and information technologies.”

Unlike previous research, which relied mostly on complex multi-component materials to achieve programmable movement of reconfigurable structural elements, Aizenberg and her team designed a microstructure pillar made of a single material — a photoresponsive liquid crystal elastomer. Because of the way the fundamental building blocks of the liquid crystal elastomer are aligned, when light hits the microstructure, those building blocks realign and the structure changes shape.

As this shape change occurs, two things happen. First, the spot where the light hits becomes transparent, allowing the light to penetrate further into the material, causing additional deformations. Second, as the material deforms and the shape moves, a new spot on the pillar is exposed to light, causing that area to also change shape.

This feedback loop propels the microstructure into a stroke-like cycle of motion.

“This internal and external feedback loop gives us a self-regulating material. Once you turn the light on, it does all its own work,” said Shucong Li, a graduate student in the Department of Chemistry and Chemical Biology at Harvard and co-first author of the paper.

When the light turns off, the material snaps back to its original shape.

The material’s specific twists and motions change with its shape, making these simple structures endlessly reconfigurable and tunable. Using a model and experiments, the researchers demonstrated the movements of round, square, L- and T-shaped, and palm-tree-shaped structures and laid out all the other ways the material can be tuned.

“We showed that we can program the choreography of this dynamic dance by tailoring a range of parameters, including illumination angle, light intensity, molecular alignment, microstructure geometry, temperature, and irradiation intervals and duration,” said Michael M. Lerch, a postdoctoral fellow in the Aizenberg Lab and co-first author of the paper.

To add another layer of complexity and functionality, the research team also demonstrated how these pillars interact with each other as part of an array.

“When these pillars are grouped together, they interact in very complex ways because each deforming pillar casts a shadow on its neighbor, which changes throughout the deformation process,” said Li. “Programming how these shadow-mediated self-exposures change and interact dynamically with each other could be useful for such applications as dynamic information encryption.”

“The vast design space for individual and collective motions is potentially transformative for soft robotics, micro-walkers, sensors, and robust information encryption systems,” said Aizenberg.

The paper was co-authored by James T. Waters, Bolei Deng, Reese S. Martens, Yuxing Yao, Do Yoon Kim, Katia Bertoldi, Alison Grinthal and Anna C. Balazs. It was supported in part by the U.S. Army Research Office, under grant number W911NF-17-1-0351 and the National Science Foundation through the Harvard University Materials Research Science and Engineering Center under award DMR-2011754.