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首页> 外文期刊>Journal of the American Chemical Society >Selective Charging Behavior in an Ionic Mixture Electrolyte-Supercapacitor System for Higher Energy and Power
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Selective Charging Behavior in an Ionic Mixture Electrolyte-Supercapacitor System for Higher Energy and Power

机译:离子混合物电解质-超级电容器系统中较高能量和功率的选择性充电行为

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摘要

Ion–ion interactions in supercapacitor (SC) electrolytes are considered to have significant influence over the charging process and therefore the overall performance of the SC system. Current strategies used to weaken ionic interactions can enhance the power of SCs, but consequently, the energy density will decrease due to the increased distance between adjacent electrolyte ions at the electrode surface. Herein, we report on the simultaneous enhancement of the power and energy densities of a SC using an ionic mixture electrolyte with different types of ionic interactions. Two types of cations with stronger ionic interactions can be packed in a denser arrangement in mesopores to increase the capacitance, whereas only cations with weaker ionic interactions are allowed to enter micropores without sacrificing the power density. This unique selective charging behavior in different confined porous structure was investigated by solid-state nuclear magnetic resonance experiments and further confirmed theoretically by both density functional theory and molecular dynamics simulations. Our results offer a distinct insight into pairing ionic mixture electrolytes with materials with confined porous characteristics and further propose that it is possible to control the charging process resulting in comprehensive enhancements in SC performance.
机译:超级电容器(SC)电解质中的离子-离子相互作用被认为对充电过程以及SC系统的整体性能具有重大影响。用于削弱离子相互作用的当前策略可以增强SC的功率,但是由于电极表面上相邻电解质离子之间距离的增加,能量密度将降低。在本文中,我们报道了使用具有不同类型离子相互作用的离子混合物电解质同时提高SC的功率和能量密度的方法。可以将具有较强离子相互作用的两种类型的阳离子密集排列在中孔中以增加电容,而只有具有较弱离子相互作用的阳离子才可以进入微孔而不牺牲功率密度。通过固态核磁共振实验研究了在不同的受限多孔结构中这种独特的选择性充电行为,并通过密度泛函理论和分子动力学模拟从理论上进一步证实了这一点。我们的结果为将离子混合物电解质与具有受限多孔特性的材料配对提供了独特的见解,并进一步提出可以控制充电过程,从而全面提高SC性能。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2017年第51期|18681-18687|共7页
  • 作者单位

    Department of Chemical Engineering, Norwegian University of Science and Technology, 7491 Trondheim, Norway,Department of Materials Science and Engineering and A. J. Drexel Nanomaterials Institute, Drexel University, Philadelphia, Pennsylvania 19104, United States;

    Department of Chemical Engineering, Norwegian University of Science and Technology, 7491 Trondheim, Norway;

    SINTEF Materials and Chemistry, Blindern, 0314 Oslo, Norway;

    Department of Materials Science and Engineering and A. J. Drexel Nanomaterials Institute, Drexel University, Philadelphia, Pennsylvania 19104, United States;

    Department of Materials Science and Engineering and A. J. Drexel Nanomaterials Institute, Drexel University, Philadelphia, Pennsylvania 19104, United States;

    Department of Chemistry, Department of Chemical and Environmental Engineering, University of California, Riverside, California 92521, United States;

    Department of Chemistry, Department of Chemical and Environmental Engineering, University of California, Riverside, California 92521, United States;

    Department of Electronic Systems, Norwegian University of Science and Technology, 7491 Trondheim, Norway;

    SINTEF Materials and Chemistry, 7491 Trondheim, Norway;

    Department of Chemical Engineering, Norwegian University of Science and Technology, 7491 Trondheim, Norway;

    Department of Chemistry, Department of Chemical and Environmental Engineering, University of California, Riverside, California 92521, United States;

    Department of Chemistry, Department of Chemical and Environmental Engineering, University of California, Riverside, California 92521, United States;

    Department of Materials Science and Engineering and A. J. Drexel Nanomaterials Institute, Drexel University, Philadelphia, Pennsylvania 19104, United States;

    Department of Chemical Engineering, Norwegian University of Science and Technology, 7491 Trondheim, Norway;

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  • 正文语种 eng
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