Zhu, H. H.; Wang, J. Y.; Deng, N. K.; Huang, J. X.; Hou, Y. N.; Wang, M.; Liu, Z. Y.; Huang, S. Thermoplastic liquid crystal elastomers based on ABA-type triblock copolymers. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3752-0
Heng-Hui Zhu, Jin-Yu Wang, Nan-Kai Deng, et al. Thermoplastic Liquid Crystal Elastomers Based on ABA-type Triblock Copolymers[J/OL]. Chinese Journal of Polymer Science, 2026, 441-9.
Zhu, H. H.; Wang, J. Y.; Deng, N. K.; Huang, J. X.; Hou, Y. N.; Wang, M.; Liu, Z. Y.; Huang, S. Thermoplastic liquid crystal elastomers based on ABA-type triblock copolymers. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3752-0DOI:
Heng-Hui Zhu, Jin-Yu Wang, Nan-Kai Deng, et al. Thermoplastic Liquid Crystal Elastomers Based on ABA-type Triblock Copolymers[J/OL]. Chinese Journal of Polymer Science, 2026, 441-9.DOI: 10.1007/s10118-026-3752-0.
Thermoplastic Liquid Crystal Elastomers Based on ABA-type Triblock Copolymers
Liquid crystal elastomers (LCEs) are compelling smart materials for soft robotics and flexible electronics. However
both conventional and dynamically crosslinked LCE systems fundamentally rely on chemically crosslinked networks
which has long been regarded as a prerequisite for their reversible actuation. While thermoplastic elastomers based on bl
ock copolymers offer a structural model for constructing robust physically crosslinked networks
it remains a significant challenge to transplant this design strategy into LCEs to realize reversible actuation in non-covalently crosslinked system. Herein
we develop a physically crosslinked thermoplastic LCE system based on ABA-type triblock copolymers (PS-
effectively replacing permanent covalent bonds. We systematically investigated the regulatory effect of the PS block content on the microstructure
mechanical properties
and thermally responsive actuation of the materials. By achieving an optimal balance between physical network confinement and the segment mobility of the liquid crystal phase
the resultant elastomer exhibits excellent reversible thermally driven actuation
well-balanced mechanical properties and solvent recyclability with high mechanical retention. Furthermore
the material demonstrates prominent wide-temperature-range damping performance attributed to the synergistic energy dissipation of the physical network and mesogen rotation. This work offers a feasible molecular design strategy for sustainable and multifunctional LCEs to break the dependence on chemical crosslinking for reversible actuation.
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references
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