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离子型聚二甲基硅氧烷-二氧化硅纳米复合材料:分散与自愈

Ionic poly(dimethylsiloxane)-silica nanocomposites: Dispersion and self-healing.

作者信息

Mugemana Clément, Moghimikheirabadi Ahmad, Arl Didier, Addiego Frédéric, Schmidt Daniel F, Kröger Martin, Karatrantos Argyrios V

机构信息

Materials Research and Technology, Luxembourg Institute of Science and Technology, Esch-sur-Alzette, Luxembourg.

Polymer Physics, Department of Materials, ETH Zürich, Zurich, Switzerland.

出版信息

MRS Bull. 2022;47(12):1185-1197. doi: 10.1557/s43577-022-00346-x. Epub 2022 Sep 16.

Abstract

ABSTRACT

Poly(dimethylsiloxane) (PDMS)-based nanocomposites have attracted increasing attention due to their inherent outstanding properties. Nevertheless, the realization of high levels of dispersion of nanosilicas in PDMS represents a challenge arising from the poor compatibility between the two components. Herein, we explore the use of ionic interactions located at the interface between silica and a PDMS matrix by combining anionic sulfonate-functionalized silica and cationic ammonium-functionalized PDMS. A library of ionic PDMS nanocomposites was synthesized and characterized to highlight the impact of charge location, density, and molecular weight of ionic PDMS polymers on the dispersion of nanosilicas and the resulting mechanical reinforcement. The use of reversible ionic interactions at the interface of nanoparticles-polymer matrix enables the healing of scratches applied to the surface of the nanocomposites. Molecular dynamics simulations were used to estimate the survival probability of ionic cross-links between nanoparticles and the polymer matrix, revealing a dependence on polymer charge density.

IMPACT STATEMENT

Poly(dimethylsiloxane) (PDMS) has been widely used in diverse applications due to its inherent attractive and multifunctional properties including optical transparency, high flexibility, and biocompatibility. The combination of such properties in a single polymer matrix has paved the way toward a wide range of applications in sensors, electronics, and biomedical devices. As a liquid at room temperature, the cross-linking of the PDMS turns the system into a mechanically stable elastomer for several applications. Nanofillers have served as a reinforcing agent to design PDMS nanocomposites. However, due to significant incompatibility between silica and the PDMS matrix, the dispersion of nanosilica fillers has been challenging. One of the existing strategies to improve nanoparticle dispersion consists of grafting oppositely charged ionic functional groups to the nanoparticle surface and the polymer matrix, respectively, creating nanoparticle ionic materials. Here, this approach has been explored further to improve the dispersion of nanosilicas in a PDMS matrix. The designed ionic PDMS nanocomposites exhibit self-healing properties due to the reversible nature of ionic interactions. The developed synthetic approach can be transferred to other kinds of inorganic nanoparticles dispersed in a PDMS matrix, where dispersion at the nanometer scale is a prerequisite for specific applications such as encapsulants for light-emitting diodes (LEDs).

SUPPLEMENTARY INFORMATION

The online version contains supplementary material available at 10.1557/s43577-022-00346-x.

摘要

摘要

基于聚二甲基硅氧烷(PDMS)的纳米复合材料因其固有的优异性能而受到越来越多的关注。然而,要实现纳米二氧化硅在PDMS中的高度分散是一项挑战,因为这两种组分之间的相容性较差。在此,我们通过将阴离子磺酸酯官能化二氧化硅和阳离子铵官能化PDMS相结合,探索利用位于二氧化硅与PDMS基体界面处的离子相互作用。合成并表征了一系列离子型PDMS纳米复合材料,以突出离子型PDMS聚合物的电荷位置、密度和分子量对纳米二氧化硅分散性以及由此产生的机械增强作用的影响。在纳米颗粒 - 聚合物基体界面使用可逆离子相互作用能够修复施加在纳米复合材料表面的划痕。利用分子动力学模拟来估计纳米颗粒与聚合物基体之间离子交联的存活概率,揭示了其对聚合物电荷密度的依赖性。

影响声明

聚二甲基硅氧烷(PDMS)因其固有的吸引人的多功能特性,包括光学透明性、高柔韧性和生物相容性,已在各种应用中广泛使用。在单一聚合物基体中结合这些特性为在传感器、电子和生物医学设备中的广泛应用铺平了道路。作为室温下的液体,PDMS的交联使该系统转变为适用于多种应用的机械稳定弹性体。纳米填料已用作增强剂来设计PDMS纳米复合材料。然而,由于二氧化硅与PDMS基体之间存在显著的不相容性,纳米二氧化硅填料的分散一直具有挑战性。现有的改善纳米颗粒分散的策略之一是分别将带相反电荷的离子官能团接枝到纳米颗粒表面和聚合物基体上,从而制备纳米颗粒离子材料。在此,进一步探索了这种方法以改善纳米二氧化硅在PDMS基体中的分散性。由于离子相互作用的可逆性,所设计的离子型PDMS纳米复合材料具有自修复性能。所开发的合成方法可转移到分散在PDMS基体中的其他种类无机纳米颗粒上,其中纳米级分散是诸如发光二极管(LED)密封剂等特定应用的先决条件。

补充信息

在线版本包含可在10.1557/s43577 - 022 - 00346 - x获取的补充材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3607/9947054/7140d302b14a/43577_2022_346_Fig1_HTML.jpg

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