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On the Dynamics of Charging in Nanoporous Carbon-Based Supercapacitors

机译:纳米多孔碳基超级电容器的充电动力学

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Supercapacitors are electricity storage systems with high power performances. Their short charge/discharge times are due to fast adsorption/desorption rates for the ions of the electrolyte on the electrode surface. Nanoporous carbon electrodes, which give larger capacitances than simpler geometries, might be expected to show poorer power performances because of the longer times taken by the ions to access the electrode interior. Experiments do not show such trends, however, and this remains to be explained at the molecular scale. Here we show that carbide-derived carbons exhibit heterogeneous and fast charging dynamics. We perform molecular dynamics simulations, with realistically modeled nanoporous electrodes and an ionic liquid electrolyte, in which the system, originally at equilibrium in the uncharged state, is suddenly perturbed by the application of an electric potential difference between the electrodes. The electrodes respond by charging progressively from the interface to the bulk as ions are exchanged between the nanopores and the electrolyte region. The simulation results are then injected into an equivalent circuit model, which allows us to calculate charging times for macroscopic-scale devices
机译:超级电容器是具有高功率性能的蓄电系统。它们的短充电/放电时间归因于电极表面上的电解质离子的快速吸附/解吸速率。纳米多孔碳电极比简单的几何形状具有更大的电容,但由于离子进入电极内部所花费的时间较长,因此可能会表现出较差的功率性能。实验没有显示出这种趋势,但是,这仍需要在分子水平上加以解释。在这里,我们表明,碳化物衍生的碳表现出非均质的快速充电动力学。我们使用逼真的建模的纳米多孔电极和离子液体电解质进行分子动力学模拟,其中最初处于未充电状态的平衡状态的系统突然由于电极之间的电势差而受到干扰。当离子在纳米孔和电解质区域之间交换时,电极通过从界面到主体逐渐充电来响应。然后将仿真结果注入等效电路模型,这使我们能够计算宏观设备的充电时间

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