We have made significant advancements beyond the state of the art in several areas:
1. Halogen Bonding in Dynamic Liquid Crystal Elastomers (Angewandte Chemie International Edition, 2023). This promising approach allows materials to respond to moderate energy inputs, such as heat from a human palm, and introduces self-healing properties. Looking ahead, we believe functionalization with halogen bonding to lead to liquid crystal elastomers without covalent crosslinking, an important step towards recyclability and reprocessing.
2. Multiresponsive and Multifunctional Actuators. We developed photochemical actuators that respond to light and magnetic fields (ACS Applied Materials & Interfaces, 2025), and light and humidity (Journal of Materials Chemistry B, 2024). We also designed systems that integrate shape memory programming with reversible actuation (Advanced Functional Materials, 2024) by combining permanent covalent and dynamic supramolecular crosslinks. Future work will extend these design principles to cholesteric liquid crystal elastomers to create materials with dynamic color-changing properties.
3. Light-Driven Toroidal Structures for Microscale Swimming (Nature Materials, 2024). Movement in viscous environments poses a significant challenge for microscopic organisms, as highlighted by Purcell’s Scallop Theorem. We introduced a solution to this challenge, toroidal LCN structure that leverage zero-elastic-energy-modes (ZEEMs) to achieve autonomous locomotion in various environments. These ZEEM-driven LCNs can move toward or away from light, whether on solid surfaces or in liquid media. Most notably, powered by continuous optical input, they exhibit untethered swimming in the Stokes regime, navigating with remarkable agility in three dimensions at a Reynolds number as low as 0.0001.
4. Photoswitching via Sensitized Isomerization (Science, 2023). One of the major challenges in photoswitchable compounds is the reliance on UV light to control molecular and material properties. In a collaboration led by Prof. Rafal Klajn, we developed an indirect sensitized isomerization method that eliminates this limitation, enabling efficient photoswitching with any visible, or even near-infrared, light. We recently integrated this approach, termed Disequilibration by Sensitization under Confinement (DESC), into polymers (unpublished), aiming to use low-energy light to precisely control their structure and functionality.