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Ion Dynamics of Water-in-Salt Electrolyte with Organic Solvents in Nanoporous Supercapacitor Electrodes

机译:纳米多孔超级电容器电极有机溶剂水 - 盐电解液的离子动力学

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摘要

Water-in-salt electrolytes blended with organics solvents, that is, organic solvent/water mixed electrolytes, are promising for applications in next-generation energy storage devices vitally needed for industrial electrification and decarbonization. However, the electrolyte ion diffusion behaviors within nanoporous supercapacitor electrodes are poorly understood. Here a systematic investigation into supercapacitor resistances and ion kinetics is carried out experimentally and with numerical simulations. The electrochemical results on the nanoporous electrodes reveal a nonmonotonic (decreasing, increasing, and then decreasing) trend of supercapacitor resistances with increasing solvent mobility, challenging the long-held views that supercapacitor resistances decrease with elevated mobility of organic solvent. The abnormal trend is examined by numerical molecular dynamics simulations of electrolyte ion diffusion within 0.95 nm nanochannels. The electrolyte conductivity is related to cation-anion interactions within nanochannels. We further confirm the crucial interplay of the van der Waals sizes of solvent molecules and channel width in determining electrolyte conductivity in nanoporous electrodes.
机译:与有机溶剂混合的盐水电解质,即有机溶剂/水混合电解质,是在工业电气化和脱碳所需的下一代能量存储装置中的应用。然而,纳米多孔超级电容器电极内的电解质离子扩散行为差不多理解。此处实验和数值模拟进行了对超级电容器电阻和离子动力学进行了系统的调查。纳米多孔电极上的电化学结果揭示了超级电容(减小,增加,然后降低)超级涂物电阻的趋势,随着溶剂迁移率挑战,使超级电容器电阻随着有机溶剂的升高而降低。通过在0.95nm纳米中的电解质离子扩散的数值分子动力学模拟来检查异常趋势。电解质电导率与纳米通道内的阳离子阴离子相互作用有关。我们进一步证实了Van der WaaS尺寸的溶剂分子和通道宽度的关键相互作用在确定纳米多孔电极中的电解质电导率。

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