Artificial muscles based on liquid crystal elastomers

Author(s):  
Min-Hui Li ◽  
Patrick Keller

This paper presents our results on liquid crystal (LC) elastomers as artificial muscle, based on the ideas proposed by de Gennes. In the theoretical model, the material consists of a repeated series of main-chain nematic LC polymer blocks, N, and conventional rubber blocks, R, based on the lamellar phase of a triblock copolymer RNR. The motor for the contraction is the reversible macromolecular shape change of the chain, from stretched to spherical, that occurs at the nematic-to-isotropic phase transition in the main-chain nematic LC polymers. We first developed a new kind of muscle-like material based on a network of side-on nematic LC homopolymers. Side-on LC polymers were used instead of main-chain LC polymers for synthetic reasons. The first example of these materials was thermo-responsive, with a typical contraction of around 35–45% and a generated force of around 210 kPa. Subsequently, a photo-responsive material was developed, with a fast photochemically induced contraction of around 20%, triggered by UV light. We then succeeded in preparing a thermo-responsive artificial muscle, RNR, with lamellar structure, using a side-on nematic LC polymer as N block. Micrometre-sized artificial muscles were also prepared. This paper illustrates the bottom-up design of stimuli-responsive materials, in which the overall material response reflects the individual macromolecular response, using LC polymer as building block.

2014 ◽  
Vol 896 ◽  
pp. 322-326 ◽  
Author(s):  
Supardi ◽  
Harsojo ◽  
Yusril Yusuf

Liquid crystal elastomers (LCEs), either side-chain LCEs (SCLCEs) or main-chain LCEs (MCLCEs), possess a combination of LC and elastic properties, and are expected to be used as artificial muscles. We experimentally investigated the thermo-induced mechanical effects showed by MCLCEs with four different crosslinker concentrations, i.e., 8%, 12%, 14% and 16%. The samples were heated up to the critical temperature and the images were recorded. The samples made the contraction in direction parallel to the director and the expansion in direction perpendicular to the director. Drastic changes occured when approaching the critical temperature, the greater the crosslinkers concentration the bigger the maximum contraction and expansion. The shape anisotropy expression showed that heating up to the critical temperature caused the system no longer in anisotropic state.


Soft Matter ◽  
2021 ◽  
Vol 17 (11) ◽  
pp. 3128-3136
Author(s):  
Suzuka Okamoto ◽  
Shinichi Sakurai ◽  
Kenji Urayama

Stretching angle for a main-chain liquid crystal elastomer has pronounced effects on the width of the stress plateau as well as the ultimate elongation, while it has no effect on the plateau height.


Molecules ◽  
2021 ◽  
Vol 26 (20) ◽  
pp. 6193
Author(s):  
Kyosun Ku ◽  
Kyohei Hisano ◽  
Kyoko Yuasa ◽  
Tomoki Shigeyama ◽  
Norihisa Akamatsu ◽  
...  

Chiral nematic (N*) liquid crystal elastomers (LCEs) are suitable for fabricating stimuli-responsive materials. As crosslinkers considerably affect the N*LCE network, we investigated the effects of crosslinking units on the physical properties of N*LCEs. The N*LCEs were synthesized with different types of crosslinkers, and the relationship between the N*LC polymeric system and the crosslinking unit was investigated. The N*LCEs emit color by selective reflection, in which the color changes in response to mechanical deformation. The LC-type crosslinker decreases the helical twisting power of the N*LCE by increasing the total molar ratio of the mesogenic compound. The N*LCE exhibits mechano-responsive color changes by coupling the N*LC orientation and the polymer network, where the N*LCEs exhibit different degrees of pitch variation depending on the crosslinker. Moreover, the LC-type crosslinker increases the Young’s modulus of N*LCEs, and the long methylene chains increase the breaking strain. An analysis of experimental results verified the effect of the crosslinkers, providing a design rationale for N*LCE materials in mechano-optical sensor applications.


Soft Matter ◽  
2018 ◽  
Vol 14 (29) ◽  
pp. 6024-6036 ◽  
Author(s):  
Daniel R. Merkel ◽  
Nicholas A. Traugutt ◽  
Rayshan Visvanathan ◽  
Christopher M. Yakacki ◽  
Carl P. Frick

Actuation temperature was controlled without influencing total actuation performance in liquid crystal elastomers fabricated by a two-stage reaction scheme.


Soft Matter ◽  
2018 ◽  
Vol 14 (31) ◽  
pp. 6449-6462 ◽  
Author(s):  
D. Rogez ◽  
S. Krause ◽  
P. Martinoty

The shear and Young moduli, the poly-domain to mono-domain transition, the Poisson ratio and the supercritical or subcritical nature of main-chain and side-chain liquid-crystal elastomers are characterized with various mechanical experiments.


2011 ◽  
Vol 21 (23) ◽  
pp. 8436 ◽  
Author(s):  
Maria Amela-Cortés ◽  
Duncan W. Bruce ◽  
Kenneth E. Evans ◽  
Christopher W. Smith

2021 ◽  
Vol 7 (30) ◽  
pp. eabg3677
Author(s):  
Shuo Li ◽  
Hedan Bai ◽  
Zheng Liu ◽  
Xinyue Zhang ◽  
Chuqi Huang ◽  
...  

Artificial muscles based on stimuli-responsive polymers usually exhibit mechanical compliance, versatility, and high power-to-weight ratio, showing great promise to potentially replace conventional rigid motors for next-generation soft robots, wearable electronics, and biomedical devices. In particular, thermomechanical liquid crystal elastomers (LCEs) constitute artificial muscle-like actuators that can be remotely triggered for large stroke, fast response, and highly repeatable actuations. Here, we introduce a digital light processing (DLP)–based additive manufacturing approach that automatically shear aligns mesogenic oligomers, layer-by-layer, to achieve high orientational order in the photocrosslinked structures; this ordering yields high specific work capacity (63 J kg−1) and energy density (0.18 MJ m−3). We demonstrate actuators composed of these DLP printed LCEs’ applications in soft robotics, such as reversible grasping, untethered crawling, and weightlifting. Furthermore, we present an LCE self-sensing system that exploits thermally induced optical transition as an intrinsic option toward feedback control.


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