Liquid crystal elastomers (LCEs) are of interest for applications such as soft robotics and shape‐morphing devices. Among the different actuation mechanisms, light offers advantages such as spatial and local control of actuation via the photothermal effect. However, the unwanted aggregation of the light‐absorbing nanoparticles in the LCE matrix will limit the photothermal response speed, actuation performance, and repeatability. Herein, a near‐infrared‐responsive LCE composite consisting of up to 0.20 wt% poly(ethylene glycol)‐modified gold nanorods (AuNRs) without apparent aggregation is demonstrated. The high Young's modulus, 20.3 MPa, and excellent photothermal performance render repeated and fast actuation of the films (actuation within 5 s and recovery in 2 s) when exposed to 800 nm light at an average output power of ≈1.0 W cm−2, while maintaining a large actuation strain (56%). Further, it is shown that the same sheet of AuNR/LCE film (100 µm thick) can be morphed into different shapes simply by varying the motifs of the photomasks.
Fibers capable of generating axial contraction are commonly seen in nature and engineering applications. Despite the broad applications of fiber actuators, it is still very challenging to fabricate fiber actuators with combined large actuation strain, fast response speed, and high power density. Here, we report the fabrication of a liquid crystal elastomer (LCE) microfiber actuators using a facile electrospinning technique. Owing to the extremely small size of the LCE microfibers, they can generate large actuation strain (~60 percent) with a fast response speed (<0.2 second) and a high power density (400 watts per kilogram), resulting from the nematic-isotropic phase transition of liquid crystal mesogens. Moreover, no performance degradation is detected in the LCE microfibers after 106cycles of loading and unloading with the maximum strain of 20 percent at high temperature (90 degree Celsius). The small diameter of the LCE microfiber also results in a self-oscillatory behavior in a steady temperature field. In addition, with a polydopamine coating layer, the actuation of the electrospun LCE microfiber can be precisely and remotely controlled by a near-infrared laser through photothermal effect. Using the electrospun LCE microfiber actuator, we have successfully constructed a microtweezer, a microrobot, and a light-powered microfluidic pump.
more » « less- Award ID(s):
- 1762560
- NSF-PAR ID:
- 10289899
- Publisher / Repository:
- American Association for the Advancement of Science (AAAS)
- Date Published:
- Journal Name:
- Science Robotics
- Volume:
- 6
- Issue:
- 57
- ISSN:
- 2470-9476
- Page Range / eLocation ID:
- Article No. eabi9704
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Soft robots, with their agile locomotion and responsiveness to environment, have attracted great interest in recent years. Liquid crystal elastomers (LCEs), known for their reversible and anisotropic deformation, are promising candidates as embedded intelligent actuators in soft robots. So far, most studies on LCEs have focused on achieving complex deformation in thin films over centimeter‐scale areas with relatively small specific energy densities. Herein, using an extrusion process, meter‐long LCE composite filaments that are responsive to both infrared light and electrical fields are fabricated. In the composite filaments, a small quantity of cellulose nanocrystals (CNCs) is incorporated to facilitate the alignment of liquid crystal molecules along the long axis of the filament. Up to 2 wt% carbon nanotubes (CNTs) is introduced into a LCE matrix without aggregation, which in turn greatly improves the mechanical property of filaments and their actuation speed, where the Young's modulus along the long axis reaches 40 MPa, the electrothermal response time is within 10 s. The maximum work capacity is 38 J kg−1with 2 wt% CNT loading. Finally, shape transformation and locomotion in several soft robotics systems achieved by the dual‐responsive LCE/CNT composite filament actuators are demonstrated.
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