盐溶液中阴离子交换膜驱动的实验表征

Nicco Ulbricht, A. Boldini, Chulsung Bae, T. Wallmersperger, M. Porfiri
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引用次数: 0

摘要

离子交换膜除了用于分离和过滤过程之外,由于其独特的电化学和力学耦合,已被用作软机器人和生物医学工程中的电活性聚合物致动器。驱动是由阳离子和阴离子运输的不对称性产生的,因为两种离子中的一种与膜骨干结合,而另一种可以在整个膜中移动。通常,电极被镀在膜上,以使外部电场的应用成为可能。一种新的,有前途的水下应用的非接触式驱动配置包括将裸露的膜浸入电解质溶液中,在外部电极之间。当电场施加在电极上时,观察到宏观弯曲变形。尽管在理解阳离子交换膜(固定阴离子)的驱动方面取得了重大进展,但阴离子交换膜(固定阳离子)的驱动几乎是一个未开发的领域。在这项工作中,我们实验研究阴离子交换膜的非接触驱动。在实验中,我们系统地改变了外溶液和膜内的阴离子,以揭示它们对膜驱动的影响。在所有测试的组合中,与阳离子交换膜相比,膜总是向相反的方向弯曲。此外,我们发现外部阴离子对致动强度有显著影响,这与先前将致动归因于溶剂化效应的理论一致。我们的研究结果有助于揭示阴离子交换膜的化学电力学,使其更多地被用作软致动器。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Experimental characterization of actuation of anion-exchange membranes in salt solution
Besides their use in separation and filtration processes, ion-exchange membranes have been adopted as electroactive polymer actuators in soft robotics and biomedical engineering, due to their unique coupling between electrochemistry and mechanics. Actuation is generated by the asymmetry in cations and anions transport, as one of the two species is bonded to the membrane backbone, whereas the other can move throughout the membrane. Typically, electrodes are plated on the membrane to enable application of an external electric field. A new, promising contactless actuation configuration for underwater applications consists of immersing a bare membrane in an electrolyte solution, between external electrodes. When an electric field is imposed across the electrodes, a macroscopic bending deformation is observed. Despite major advances in understanding the actuation of cation-exchange membranes (with fixed anions), the actuation of anion-exchange membranes (with fixed cations) is an almost untapped field. In this work, we experimentally investigate the contactless actuation of anion-exchange membranes. In the experiments, we systematically vary the anions in the external solution and inside the membrane, to unravel their effects on membrane actuation. In all tested combinations, the membrane always bends in the opposite direction compared to cation-exchange membranes. Additionally, we find a prominent influence of the external anions on the actuation strength, consistent with previous theories that attribute actuation to solvation effects. Our results help shade light on the chemoelectromechanics of anion-exchange membranes, toward their increase adoption as soft actuators.
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