Organo-disulfide-based particles enable controlled stimulus-triggered cleaning of electrode surfaces†

Hongyi Zhang, Garrett L. Grocke, Samuel S. Kopfinger, Yilin Wang, Arnav Brahmasandra, Randy H. Ewoldt, Stuart J. Rowan and Shrayesh N. Patel
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Abstract

Electrode fouling resulting in reduced performance is an ongoing challenge in electrochemical flow cells based on redox active polymers (RAPs). An avenue that holds substantial promise yet remains relatively unexplored involves the strategic design of RAPs capable of undergoing electrochemical stimulation to facilitate in situ electrode cleaning within a flow cell. Herein, a new electrode cleaning strategy is demonstrated through the application of redox-active poly(glycidyl methacrylate) particles crosslinked with 2-amino-1,3,4-thiadiazole disulfide (PGMA–ATDDS). The resulting particles can de-crosslink through cleavage of the disulfide bond using stimuli, such as electrochemical reduction or UV photoexcitation. Using a custom flow cell, applying such a stimulus to an ITO electrode artificially fouled with PGMA–ATDDS in the presence of a fluid flow leads to a significant particle removal (80%) that is over six times more efficient relative to the case when no stimulus is applied. Confocal fluorescence imaging of the electrochemically stimulated electrode highlighted localized disulfide reduction of particles near the electrode surface. It is posited that this selective de-crosslinking and concomitant electrolyte swelling at the particle/electrode interface facilitate particle removal in the presence of a fluid flow. In addition, the regeneration of electrode performance upon cleaning was demonstrated through charging of a redox-active particle suspension of poly(vinylbenzyl chloride) functionalized with dimethylaminoferrocene (PVBC–Fc). Upon electrochemical cleaning of the fouled ITO electrode, the accessible charge of PVBC–Fc was statistically equivalent to the accessible charge measured using a pristine ITO electrode. Overall, this study introduces a new approach for leveraging stimulus-responsive chemistries for RAPs to impart inherent functionality to facilitate in-line electrode cleaning in electrochemical flow cells.

Abstract Image

基于有机二硫化物的颗粒可实现受控刺激触发的电极表面清洁†。
在基于氧化还原活性聚合物 (RAP) 的电化学流动池中,电极堵塞导致性能下降是一个持续的挑战。一种前景广阔但相对尚未开发的途径是战略性地设计能够进行电化学刺激的 RAP,以促进流动池内的原位电极清洁。本文通过应用与 2-氨基-1,3,4-噻二唑二硫化物(PGMA-ATDDS)交联的氧化还原活性聚甲基丙烯酸缩水甘油酯颗粒,展示了一种新的电极清洁策略。通过电化学还原或紫外光激发等刺激,二硫键会裂解,从而使产生的颗粒解除交联。使用定制的流动池,在有流体流动的情况下,对被 PGMA-ATDDS 人为弄脏的 ITO 电极施加这种刺激,可显著去除粒子(80%),其效率是不施加刺激情况下的六倍多。电化学刺激电极的共焦荧光成像突出显示了电极表面附近颗粒的局部二硫化物还原。据推测,这种选择性脱交联以及颗粒/电极界面处随之而来的电解质溶胀有助于在流体流动的情况下去除颗粒。此外,通过对二甲氨基二茂铁功能化聚(乙烯基氯苄)氧化还原活性颗粒悬浮液(PVBC-Fc)充电,证明了清洁后电极性能的再生。在对污损的 ITO 电极进行电化学清洗后,PVBC-Fc 的可触及电荷在统计学上与使用原始 ITO 电极测得的可触及电荷相当。总之,这项研究引入了一种新方法,利用 RAPs 的刺激响应化学特性赋予其固有功能,从而促进电化学流动池中的在线电极清洁。
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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