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Materials that undergo reversible changes in form typically require top-down processing to program the microstructure of the material. As a result, it is difficult to program microscale, 3D shape-morphing materials that undergo non-uniaxial deformations. Here, a simple bottom-up fabrication approach to prepare bending microactuators is described. Spontaneous self-assembly of liquid crystal (LC) monomers with controlled chirality within 3D micromold results in a change in molecular orientation across thickness of the microstructure. As a result, heating induces bending in these microactuators. The concentration of chiral dopant is varied to adjust the chirality of the monomer mixture. Liquid crystal elastomer (LCE) microactuators doped with 0.05 wt% of chiral dopant produce needle-shaped actuators that bend from flat to an angle of 27.2 ± 11.3° at 180 °C. Higher concentrations of chiral dopant lead to actuators with reduced bending, and lower concentrations of chiral dopant lead to actuators with poorly controlled bending. Asymmetric molecular alignment inside 3D structure is confirmed by sectioning actuators. Arrays of microactuators that all bend in the same direction can be fabricated if symmetry of geometry of the microstructure is broken. It is envisioned that the new platform to synthesize microstructures can further be applied in soft robotics and biomedical devices.
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http://dx.doi.org/10.1002/smll.202302774 | DOI Listing |
Adv Mater
September 2025
Key Lab of Artificial Micro- and Nano-Structures of Ministry of Education of China, School of Physics and Technology, Wuhan University, Wuhan, 430072, China.
Sequential deposition technique is widely used to fabricate perovskite films with large grain size in perovskite solar cells (PSCs). Residual lead halide (PbI) in the perovskite film tends to be decomposed into metallic lead (Pb) under long-term heating or light soaking. Here, a chiral levetiracetam (LEV) dopant containing α-amide and pyrrolidone groups is introduced into the PbI precursor solution.
View Article and Find Full Text PDFAdv Mater
August 2025
6128 Burke Laboratory, Department of Chemistry, Dartmouth College, Hanover, NH, 03755, USA.
The development of light-tunable ferroelectric nematic liquid crystals (NLCs) will allow for the multi-stimuli control over the properties of this newly discovered LC phase. Here on the development of photoresponsive chiral ferroelectric nematic liquid crystals (N LCs) is reported by incorporating chiral triptycene/hydrazone-based bistable photoswitchable dopants into the polar liquid crystal mesogen DIO. The propeller-like dopants exhibit high helical twisting powers with values of 13.
View Article and Find Full Text PDFNano Lett
September 2025
Tata Institute of Fundamental Research (TIFR), Hyderabad 500046, India.
MoS monolayers (MS) having magnetic impurities as dopants can bring about time-reversal asymmetry and hence room temperature magnetism. Here, we demonstrated the synthesis of Cr substitutionally doped (∼1%) MS (CrMS) along with its vanadium-doped MS counterpart (VMS) and investigated their suitability for valleytronics by studies based on chirality-selective photoluminescence, time-resolved transient absorption spectroscopy, and spin Hall effect of light (SHEL). While VMS showed room temperature valley splitting, no such shift was observed in CrMS although with their expected similarity.
View Article and Find Full Text PDFSupramolecular functional helical superstructures are typical structures exhibiting many fascinating properties and performances. In nature, cholesteric liquid crystals (CLCs) are self-assembled soft helical superstructures that display orientation-dependent features of supramolecular helical architectures and have potential scientific applications. The most intriguing applications of CLCs primarily depend on the various orientations of their helical axis.
View Article and Find Full Text PDFSoft Matter
August 2025
Guangdong Provincial Key Laboratory of Optical Information Materials and Technology & Institute of Electronic Paper Displays, South China Academy of Advanced Optoelectronics, South China Normal University, Guangzhou 510006, China.
The rational molecular engineering of cholesteryl azobenzene dimers provides an effective strategy for designing precisely tunable photo-switchable materials with controllable chiral optical responses. This study systematically explores how spacer length parity and terminal group polarity dictate phase transitions, helical twisting power (HTP) and photoisomerization kinetics of cholesteryl azobenzene dimers, enabling predictive control over their functional performance. A key finding is an odd-even effect of the spacer length, which determines the sign of the helical twisting power change in liquid crystals (LC) upon UV irradiation.
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