Reconfigurable materials can do amazing things. Flat sheets transform into a face. An extruded cube transforms into dozens of different shapes. But there’s one thing a reconfigurable material has yet to be able to change: its underlying topology. A reconfigurable material with 100 cells will always have 100 cells, even if those cells are stretched or squashed. Now, researchers from the Harvard John A. Paulson School of Engineering and Applied Sciences (SEAS) have developed a method to change a cellular material’s fundamental topology at the microscale. The research is published in Nature.
“Creating cellular structures capable of dynamically changing their topology will open new opportunities in developing active materials with information encryption, selective particle trapping, as well as tunable mechanical, chemical and acoustic properties,” said Joanna Aizenberg, the Amy Smith Berylson Professor of Materials Science at SEAS and Professor of Chemistry & Chemical Biology and senior author of the paper.
The researchers harnessed the same physics that clumps our hair together when it gets wet — capillary force. Capillary force works well on soft, compliant material, like our hair, but struggles with stiff cellular structures that require the bending, stretching or folding of walls, especially around strong, connected nodes. Capillary force is also temporary, with materials tending to return to their original configuration after drying.
In order to develop a long-lasting yet reversible method to transform the topology of stiff cellular microstructures, the researchers developed a two-tiered dynamic strategy. They began with a stiff, polymeric cellular microstructure with a triangular lattice topology, and exposed it to droplets of a volatile solvent chosen to swell and soften the polymer at the molecular scale. This made the material temporarily more flexible and in this flexible state, the capillary forces imposed by the evaporating liquid drew the edges of the triangles together, changing their connections with one another and transforming them into hexagons. Then, as the solvent rapidly evaporated, the material dried and was trapped in its new configuration, regaining its stiffness. The whole process took a matter of seconds.
“When you think about applications, it’s really important not to lose a material’s mechanical properties after the transformation process,” said Shucong Li, a graduate student in the Aizenberg Lab and co-first author of the paper. “Here, we showed that we can start with a stiff material and end with a stiff material through the process of temporarily softening it at the reconfiguration stage.”
The new topology of the material is so durable it can withstand heat or be submerged in some liquids for days without disassembling. Its robustness actually posed a problem for the researchers who had hoped to make the transformation reversible.
To return to the original topology, the researchers developed a technique that combines two liquids. The first temporarily swells the lattice, which peels apart the adhered walls of the hexagons and allows the lattice to return to its original triangular structure. The second, less volatile liquid delays the emergence of capillary forces until the first liquid has evaporated and the material has regained its stiffness. In this way, the structures can be assembled and disassembled repeatedly and trapped in any in-between configuration.