Tailoring molecular structure and electromechanical properties of polydimethylsiloxane elastomer for enhanced energy conversion efficiency

IF 3.2 4区 工程技术 Q2 ENGINEERING, CHEMICAL
Om Prakash Prabhakar, Raj Kumar Sahu
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引用次数: 0

Abstract

The molecular structure of dielectric elastomers dictates their mechanical, electrical, and properties to react under external stimuli, influencing their suitability for applications such as actuators, sensors, and energy harvesting devices. The molecular structure of polymers can be tailored by incorporating plasticizers and particulate fillers to achieve multifunctional properties. However, achieving a balance between flexibility and maintaining mechanical strength due to incorporation of fillers induced phase separation and compromised intermolecular interactions remains challenging. In the present work, polydimethylsiloxane (PDMS) composites are synthesized using plasticizer and particulate fillers, polyethylene glycol (H‐(OCH2CH2)nOH) and titanium diboride (TiB2) respectively in various concentrations using shear mixing and doctor blade casting technique. Molecular structure of synthesized PDMS composite is confirmed by observing peaks of Raman spectra sift, which exhibits robust CO bonds dominating for both fillers. Chain entanglement due to filler incorporation significantly affects the crosslink density of PDMS composite, it increases with the concentration of plasticizer and possesses inverse relation for particulate. Furthermore, interdependence of the filler types and concentration are found on the mechanical as well as electrical properties. The specific deformation energy exhibits a significant increase of 118.9% when comparing particulate to the plasticizer at concentration of 8 wt.%. Although plasticizer increases the actuation strain and energy conversion efficiency but decreases the electrical breakdown voltage in comparison to particulate. By systematically varying fillers concentration, subtle changes in multifunctional properties are achieved. Overall, this investigation provides a framework for tailoring dielectric elastomer composites with desired electromechanical characteristics through the amalgamation of filler types and crosslinking densities, all intricately tied to the molecular architecture for electromechanical sensors.Highlights Filler incorporation changes DE molecular structure and materials properties. Formation of additional bonds and micro‐capacitors in DE enhances capacitance. Actuation strain in DE depends on filler type and concentration. Energy conversion efficiency varies with the concentration of filler.
调整聚二甲基硅氧烷弹性体的分子结构和机电特性以提高能量转换效率
介电弹性体的分子结构决定了其在外部刺激下的机械、电气和反应特性,从而影响其在致动器、传感器和能量收集装置等应用中的适用性。聚合物的分子结构可通过加入增塑剂和微粒填料进行定制,以实现多功能特性。然而,由于填料的加入会导致相分离和分子间相互作用受到影响,因此要在柔性和保持机械强度之间取得平衡仍具有挑战性。在本研究中,采用剪切混合和刮刀浇铸技术,分别使用不同浓度的增塑剂和颗粒填料、聚乙二醇(H-(OCH2CH2)nOH)和二硼化钛(TiB2)合成了聚二甲基硅氧烷(PDMS)复合材料。通过观察拉曼光谱筛分的峰值,证实了合成的 PDMS 复合材料的分子结构,两种填料都表现出强大的 CO 键。填料加入导致的链缠结极大地影响了 PDMS 复合材料的交联密度,交联密度随增塑剂浓度的增加而增加,与颗粒的交联密度呈反比关系。此外,填料类型和浓度对机械和电气性能也有影响。当颗粒与增塑剂的浓度为 8 wt.% 时,比变形能显著增加了 118.9%。与微粒相比,增塑剂增加了致动应变和能量转换效率,但降低了电击穿电压。通过系统地改变填料的浓度,可以实现多功能特性的微妙变化。总之,这项研究提供了一个框架,可通过混合填料类型和交联密度来定制具有所需机电特性的介电弹性体复合材料,所有这些都与机电传感器的分子结构密切相关。在 DE 中形成附加键和微型电容器可提高电容。DE 中的致动应变取决于填料类型和浓度。能量转换效率随填料浓度的变化而变化。
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来源期刊
Polymer Engineering and Science
Polymer Engineering and Science 工程技术-高分子科学
CiteScore
5.40
自引率
18.80%
发文量
329
审稿时长
3.7 months
期刊介绍: For more than 30 years, Polymer Engineering & Science has been one of the most highly regarded journals in the field, serving as a forum for authors of treatises on the cutting edge of polymer science and technology. The importance of PE&S is underscored by the frequent rate at which its articles are cited, especially by other publications - literally thousand of times a year. Engineers, researchers, technicians, and academicians worldwide are looking to PE&S for the valuable information they need. There are special issues compiled by distinguished guest editors. These contain proceedings of symposia on such diverse topics as polyblends, mechanics of plastics and polymer welding.
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