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Significantly Improve Electromechanical Performance of Dielectric Elastomer via Alkyl Side-Chain Engineering

Abstract

Dielectric elastomers (DEs) can be deformed in response to electric field. Combining many muscle-like attributes like mechanical compliancy, very fast response, large actuation strain, high energy density, noiseless actuation, and light weight, DEs are considered to be leading materials for “artificial muscles”. Herein, we report a new strategy to significantly improve electromechanical performance of an elastomer by decreasing chain entanglement density. A series of symmetric polystyrene-polyalkylacrylate-polystyrene triblock copolymers was synthesized by reversible additional fragmental transfer polymerization, where the chain entanglement density was varied by changing the bulkiness of side groups of polyalkylacrylate. It is found that the voltage-induced maximum strain and energy density both quickly increase because the modulus is quickly decreased while the electric breakdown is little affected with increase of the bulkiness of the alkyl side groups. The maximum actuation strain of polystyrene-poly(2-ethylhexyl acrylate)-polystyrene (SEHAS, 25% at 28 kV/mm, without prestretch) and energy density (4.4 kJ/m3) are significantly higher than those of the state-of-art single component thermal plastic DEs. The actuation performance of SEHAS is comparable to that of the mammalian skeletal muscle. The other attractive attributes of SEHAS include thermal plasticity, relatively high tensile strength and very low glass temperature (-68oC) of the elastic phase.

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Publication details

The article was received on 23 Mar 2017, accepted on 12 Jun 2017 and first published on 12 Jun 2017


Article type: Paper
DOI: 10.1039/C7TC01221G
Citation: J. Mater. Chem. C, 2017, Accepted Manuscript
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    Significantly Improve Electromechanical Performance of Dielectric Elastomer via Alkyl Side-Chain Engineering

    J. Mao, T. Li and Y. Luo, J. Mater. Chem. C, 2017, Accepted Manuscript , DOI: 10.1039/C7TC01221G

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