Effect of gold and graphene oxide nanoparticles on the thermo- and photo-actuation of monodomain liquid crystal elastomers
Monodomain liquid crystal elastomers (m-LCEs) were synthesized from polymethylhydrosiloxane (PMHS), two distinct vinyl-functionalized mesogens (benzoate and azobenzene) and one crosslinking monomer, using the hydrosilylation reaction. Gold or amino-functionalized graphene oxide nanoparticles (NP) we...
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Veröffentlicht in: | Polymer (Guilford) 2020-09, Vol.205, p.122837, Article 122837 |
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Sprache: | eng |
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Zusammenfassung: | Monodomain liquid crystal elastomers (m-LCEs) were synthesized from polymethylhydrosiloxane (PMHS), two distinct vinyl-functionalized mesogens (benzoate and azobenzene) and one crosslinking monomer, using the hydrosilylation reaction. Gold or amino-functionalized graphene oxide nanoparticles (NP) were in-situ incorporated into the m-LCEs, aiming to enhance their response to thermal and optical stimuli. All m-LCEs exhibited a degradation temperature of ~310 °C and a mesomorphic behavior over a wide temperature range (clearing temperature around 100 °C). The inclusion of nanoparticles stiffened the m-LCEs, although they induced a highly randomized ordering of mesogens at the nematic to isotropic transition, resulting in a higher specimen contraction; a schematic model is proposed in this concern. The photo-actuation (bending) of the m-LCEs/NP composites resulted rather diminished as they became stiffer than the neat m-LCEs, although the increasing content of azobenzene units allowed higher bending angles that could be suitable for remote actuation applications.
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•Monodomain liquid crystal elastomers (m-LCEs) carrying benzoate and azobenzene-type mesogens were synthesized.•Small amounts of Au or GO nanoparticles were dispersed into m-LCE aiming to enhance the response to external stimuli.•A good polymer-particle interaction is favorable for thermo-actuation but detrimental for photo-actuation.•A new model is proposed for explaining the enhancement in thermal contraction. |
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ISSN: | 0032-3861 1873-2291 |
DOI: | 10.1016/j.polymer.2020.122837 |