Jitvisate Monchai
School of Physics, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima, 30000, Thailand.
J Phys Chem Lett. 2024 Sep 26;15(38):9637-9643. doi: 10.1021/acs.jpclett.4c02428. Epub 2024 Sep 16.
Differential capacitance is a crucial parameter that connects the experimental observation of electrical double-layer behavior with theoretical models. However, the current number of reported differential capacitance values for deep eutectic solvents remains limited, making it challenging to verify or refute existing models. In this study, we systematically investigate the differential capacitance in deep eutectic solvents using chronoamperometry. By comparing metal and glassy carbon electrodes across various liquid combinations and ion concentrations, we observed a range of distinct capacitance characteristics. While some findings align with the existing mean-field model for ionic liquids, others clearly reflect the influence of electrode materials, with certain cases resisting full explanation by current theoretical models. These results underscore the importance of selecting appropriate electrode materials in experimental studies of such electrolytes and highlight the need for further theoretical advancements in understanding this complex liquid system.
微分电容是一个关键参数,它将双电层行为的实验观测与理论模型联系起来。然而,目前报道的深共熔溶剂的微分电容值数量仍然有限,这使得验证或反驳现有模型具有挑战性。在本研究中,我们使用计时电流法系统地研究了深共熔溶剂中的微分电容。通过比较各种液体组合和离子浓度下的金属电极和玻碳电极,我们观察到了一系列不同的电容特性。虽然一些发现与现有的离子液体平均场模型一致,但其他发现清楚地反映了电极材料的影响,某些情况目前的理论模型无法完全解释。这些结果强调了在这类电解质的实验研究中选择合适电极材料的重要性,并突出了在理解这个复杂液体系统方面进一步理论进展的必要性。