Boz Emre B, Boillat Pierre, Forner-Cuenca Antoni
Electrochemical Materials and Systems, Department of Chemical Engineering and Chemistry, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven, The Netherlands.
Eindhoven Institute for Renewable Energy Systems, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven, The Netherlands.
ACS Appl Mater Interfaces. 2022 Sep 21;14(37):41883-41895. doi: 10.1021/acsami.2c08211. Epub 2022 Sep 7.
The surface properties of porous carbonaceous electrodes govern the performance, durability, and ultimately the cost of redox flow batteries (RFBs). State-of-the-art carbon fiber-based electrode interfaces suffer from limited kinetic activity and incomplete wettability, fundamentally limiting the performance. Surface treatments for electrodes such as thermal and acid activation are a common practice to make them more suitable for aqueous RFBs; however, these treatments offer limited control over the desired functional properties. Here, we propose, for the first time, electrografting as a facile, rapid, and versatile technique to enable task-specific functionalization of porous carbonaceous electrodes for use in RFBs. Electrografting allows covalent attachment of organic molecules on conductive substrates upon application of an electrochemical driving force, and the vast library of available organic molecules can unlock a broad range of desired functional properties. To showcase the potential of electrografting for RFBs, we elect to investigate taurine, an amine with a highly hydrophilic sulfonic acid tail. Oxidative electrografting with cyclic voltammetry allows covalent attachment of taurine through the amine group to the fiber surface, resulting in taurine-functionalized carbon cloth electrodes. In situ polarization and impedance spectroscopy in single-electrolyte flow cells reveal that taurine-treated cloth electrodes result in 40% lower charge transfer and 25% lower mass transfer resistances than off-the-shelf cloth electrodes. We find that taurine-treated electrode interfaces promote faster Fe reduction reaction kinetics as the electrochemical surface area normalized current densities are 2-fold and 4-fold higher than oxidized and untreated glassy carbon surfaces, respectively. Improved mass transfer of taurine-treated electrodes is attributed to their superior wettability, as revealed by operando neutron radiography within a flow cell setup. Through demonstrating promising results for aqueous systems with the model molecule taurine, this work aims to bring forth electrografting as a facile technique to tailor electrode surfaces for other RFB chemistries and electrochemical technologies.
多孔碳质电极的表面性质决定了氧化还原液流电池(RFB)的性能、耐久性以及最终成本。基于碳纤维的电极界面目前存在动力学活性有限和润湿性不完全的问题,从根本上限制了电池性能。对电极进行诸如热活化和酸活化等表面处理是使其更适合水性RFB的常见做法;然而,这些处理对所需功能特性的控制有限。在此,我们首次提出电接枝作为一种简便、快速且通用的技术,用于实现多孔碳质电极的特定任务功能化,以应用于RFB。电接枝能够在施加电化学驱动力时将有机分子共价连接到导电基底上,并且大量可用的有机分子可以实现广泛的所需功能特性。为了展示电接枝对RFB的潜力,我们选择研究牛磺酸,一种带有高度亲水性磺酸尾的胺。通过循环伏安法进行氧化电接枝可使牛磺酸通过胺基共价连接到纤维表面,从而得到牛磺酸功能化的碳布电极。在单电解质流动池中进行的原位极化和阻抗谱表明,与现成的碳布电极相比,经牛磺酸处理的碳布电极的电荷转移电阻降低了40%,传质电阻降低了25%。我们发现,经牛磺酸处理的电极界面促进了更快的铁还原反应动力学,因为电化学表面积归一化电流密度分别比氧化和未处理的玻碳表面高2倍和4倍。流动池装置中的操作中子射线成像显示,经牛磺酸处理的电极传质性能的改善归因于其优异的润湿性。通过用模型分子牛磺酸展示水性体系的良好结果,这项工作旨在将电接枝作为一种简便技术推广,用于为其他RFB化学和电化学技术定制电极表面。