Enhancing Mechanical and Actuation Properties of Silicone Dielectric Elastomers by Polarizable Small Molecule Doping.

IF 4.3 3区 化学 Q2 POLYMER SCIENCE
Zhengdong Wang, Libin Yang, Kai Yang, Bo Sun, Yingge Xu, Xuefeng Zhang
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引用次数: 0

Abstract

Dielectric elastomers, with their high deformability, high energy density, and flexibility, are ideal candidates for applications such as artificial muscles, flexible robots, and wearable devices. However, high drive voltages and complex preparation processes have limited their development for large-scale practical applications. In this work, we used a simple reaction blending method to introduce acrylonitrile with high polarizability and 3,7-dimethyl-6-octenitrile into silicone rubber, respectively, to prepare dielectric elastomers with excellent mechanical and electro-mechanical properties. Experimental results show that both mechanical and electro-mechanical properties are synergistically enhanced, with the elastic modulus reduced to 0.53 MPa, and the maximum electro-mechanical sensitivity reaching 17.36 times that of unmodified silicone rubber. Under an electric field strength of 35.3 kV/mm, the maximum driving strain of the unstressed film can reach 13.19%, which is 599% that of ordinary silicone rubber. This work provides new insights for the development of novel dielectric elastomers suitable for low drive voltages, low elastic moduli, and high drive strains.

利用可极化小分子掺杂增强有机硅介电弹性体的力学和驱动性能。
介电弹性体具有高可变形性、高能量密度和灵活性,是人造肌肉、柔性机器人和可穿戴设备等应用的理想候选者。然而,高驱动电压和复杂的制备工艺限制了其大规模实际应用的发展。本文采用简单的反应共混方法,将高极化率的丙烯腈和3,7-二甲基-6-辛腈分别引入硅橡胶中,制备出具有优异力学性能和机电性能的介电弹性体。实验结果表明,改性硅橡胶的力学性能和机电性能协同提高,弹性模量降至0.53 MPa,最大机电灵敏度达到未改性硅橡胶的17.36倍。在35.3 kV/mm的电场强度下,无应力膜的最大驱动应变可达13.19%,是普通硅橡胶的599%。这项工作为开发适用于低驱动电压、低弹性模量和高驱动应变的新型介电弹性体提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Macromolecular Rapid Communications
Macromolecular Rapid Communications 工程技术-高分子科学
CiteScore
7.70
自引率
6.50%
发文量
477
审稿时长
1.4 months
期刊介绍: Macromolecular Rapid Communications publishes original research in polymer science, ranging from chemistry and physics of polymers to polymers in materials science and life sciences.
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